International Conference on Genetics and Genomics of Diseases

Introduction of Genetics and Genomics of Diseases

Genetics Conferences - The International Conference on Genetics and Genomics of Diseases is an genetics conferences focused on advancements and discoveries in the fields of genetics and genomics as they relate to various diseases. Researchers, scientists, clinicians, and professionals from around the world typically gather at such conferences to present their latest findings, share knowledge, discuss emerging trends, and collaborate on future research directions.

Theme

Theme: Exploring the Recent Research and Advancements in Genetics and Genomics of Diseases

Objectives

To understand the basic principles of genetics and inheritance patterns.

To learn about the molecular mechanisms involved in gene expression, regulation, and genetic variation.

To explore the techniques used in genetics research, such as DNA sequencing, gene editing, and genetic engineering.

To study the role of genetics in disease development and treatment.

To examine the ethical and social implications of genetics research and technologies, such as genetic testing and gene therapy.

To analyze the impact of genetic diversity on evolution and adaptation in different species.

To investigate the applications of genetics in fields such as agriculture, forensics, and conservation biology.

To stay up-to-date with the latest research and discoveries in genetics, including emerging technologies and breakthroughs.

Organizer

Pencis (genetics conferences) publish the original research papers, review papers and management reports, conference publications, thesis, videos, books and news in various themes of scientific research. Articles Published in our Open access Journals are Peer Reviewed. We establish our Relationship with the scholars and the Universities through various activities such as seminars, workshops, conferences and Symposia. We acquire, develop and distribute knowledge by disseminating scholarly and professional materials around the world. All Journals published by us maintain the highest standards of quality, with Editorial Boards composed of scholars & Experts from around the world.

Date and Locations

International Conference on  Genetics and Genomics of Diseases, organized by Pencis group

11th Edition of Genetics | 04-06 December 2024 | Dubai, United Arab Emirates

12th Edition of Genetics | 19-22 February 2025 | Amsterdam, Netherlands

13th Edition of Genetics | 16-19 April 2025 | London, United Kingdom

14th Edition of Genetics | 24-26 June 2025 | San Francisco, United States

15th Edition of Genetics | 20-22 August 2025 | Berlin, Germany

Call for Abstract

Original Articles/papers are invited from Industry Persons, Scientist, Academician, Research Scholars, P.G. & U.G. Students for presentation in our International Conference on genetics conferences. All articles/papers must be in MS-Word (.doc or .docx) format, including the title, authors name, affiliation of all authors, e-mail, abstract, keywords, Conclusion, Acknowledgment, and References.

Submit Abstract

The Candidates with eligibility can click the "Submit Paper/Abstract Now" button and fill up the online submission form and Submit.

Abstract/Full Paper submission

Final/Full Paper submission is optional: If you don't want your Abstract/full paper to be published in the Conference Abstracts & Proceedings CD (with ISBN number) and only want to present it at the conference, it is acceptable.

Page limit: There is a limit of 6-8 pages for a final/full paper. Additional page is chargeable.

Paper language: Final/Full papers should be in English.

Templates: "Final paper template," "Final abstract template"

All the final papers should be uploaded to the website online system according to "the final paper template" as word doc. or docx since this will be the camera-ready published version. Please note that final papers that are not uploaded to the online System as a word doc./docx after the opening of final paper submissions according to the template above will not be published in the CONFERENCE Abstracts & Proceedings CD (with ISBN number)

Journal Publication

All accepted papers will be included in the conference proceedings, which will be published in one of the author's prescribed Pencis journals.

Registration Procedure

• Click the “Register Now” button at the conference page and enter your Submission ID in the Search Box
• Your Submissions will be listed on that page. You can find the Register Now link beside your submission. Click the link, and now you will be redirected to the Conference registration form where you can make your registration using credit/debit cards
• The Fee charged for E-Poster is to display the E-Posters only on the Website. The Abstract will be published in the conference proceeding book.

Registration Types

Speaker Registration

• Access to all event Session
• Certificate of Presentation
• Handbook
• Conference Kit
• Tea, Coffee & Snack,
• Lunch during the Conference
• Publication of Abstract /Full Paper at the Conference Proceedings Book
• Opportunity to give a Keynote/ Poster Presentations/ Plenary/ Workshop
• Opportunity to publish your Abstract in any of our esteemed Journals discounted rate
• Opportunity to publish your full article in our open access book with a discounted rate
• One to One Expert Forums

Delegate (Participant) Registration

• Access to all Event Sessions
• Participation Certificate
• Handbook
• Conference Kit
• Tea, Coffee & Snack,
• Lunch during the Conference
• Delegates are not allowed to present

Poster Registration

• Includes all the above Registration Benefits
• You will have to bring your Posters to the Conference Venue
• Best poster award memento and certificate on stage.

Poster Guidelines

• The poster should be 1×1 m Size.
• The title, contents, text, and the author’s information should be visible.
• Present numerical data in the form of graphs rather than tables.
• Figures make trends in the data much more evident.
• Avoid submitting high word-count posters.
• Poster contains, e.g., Introduction, Methods, Results, Discussion, Conclusions, and Literature.

Research Forum (Awards)

• Includes all the above Registration Benefits.
• The attendee should be required age limit.
• Award memento and certificate on stage.

E-Poster Presentation

• The amount charged for E-Posters is to display the E-Posters only on the website
• The presenter will get an e-poster participation certificate as a soft copy
• The abstract will be published in the particular journal and also in the conference proceeding book
• The presenter is not required to be present in person at the Conference

Video Presentation

• The amount charged for Video Presentation is to display the Presentation at the Conference.
• The presenter will get a Video participation certificate as a soft copy
• The abstract will be published in the particular journal and also in the conference proceeding book
• The presenter is not required to be present in person at the Conference

Accompanying Person

• Accompanying Persons are those who attend the participants at the Conference who may be either a spouse/family partner or a son/daughter and must register under this category.
• Please note that business partners do not qualify as Accompanying Persons and are not allowed to register as an Accompanying Person.

Details of Conference Awards

Pencis awards the Researchers and Research organizations around the world in the motive of Encouraging and Honoring them for their Significant contributions & Achievements for the Advancement in their field of expertise. Researchers and scholars of all nationalities are eligible to receive Pencis Research awards. Nominees are judged on past accomplishments, research excellence, and outstanding academic achievements

Award Categories

Best Poster Award

(genetics conferences) Posters will be evaluated based on Presentation Style, Research Quality, and Layout/Design. Unique opportunity to combine visual and oral explanations of your projects in the form of poster presentations. Posters should have the Title (with authors affiliation & contact details), Introduction, Methods, Results (with tables, graphs, pictures) Discussion, Conclusion, References, and Acknowledgements. The size of the poster should be: 1mX1.5m; Text:16-26 pt; Headings: 32-50 pt; Title: 70 pt; Color: Preferable. Bring your poster to the meeting, using tubular packaging. Presenting duration: 10 min discussion & 5 min query per person. Eligibility: The presenter can nominate for the Award. He must be under 40 years of age as on the conference date.

Best Presentation Award

The presentation will be evaluated based on Presentation Style, Research Quality, and Layout/Design. Unique opportunity to combine visual and oral explanations of your projects in the form of poster presentations. The presentation should have the Title (with authors affiliation & contact details), Introduction, Methods, Results (with tables, graphs, pictures) Discussion, Conclusion, References, and Acknowledgements. Bring your presentation to the meeting, using a pen drive. Presenting duration: 10-20 min discussion & 5 min query per person. Eligibility: The presenter can nominate for the Award. He must be under 55 years of age as of the conference date.

Best Paper Award

Paper will be evaluated based on Format, Research Quality, and Layout/Design. The paper should have the Title (with authors affiliation & contact details), Introduction, Methods, Results (with tables, graphs, pictures) Discussion, Conclusion, References, and Acknowledgements. Eligibility: The presenter can nominate for the Award. He must be under 55 years of age as of the conference date.

Instructions for submission

If you want to submit only your Abstract

• If you want to publish only your abstract (it is also optional) in the CONFERENCE Abstracts & Proceedings CD (with ISBN number), upload your abstract again according to the final abstract template as word doc. or Docx.
• If you also don't want your abstract to be published in the CONFERENCE Abstracts & Proceedings CD (with an ISBN number) and only want to present it at the conference, it is also acceptable

How to Submit your Abstract / Full Paper

Please read the instructions below then submit your Abstract/ Full Paper (or just final abstract) via online conference system:

• STEP 1: Please download the Abstract /Final Paper Template and submit your final paper exactly according to the template Genetics Conference Final Paper Template word format (.doc /.docx). See a final abstract template formatted according to the template.
• STEP 2: Please assure that the Abstract/ full paper follows exactly the format and template as described in the final paper template document below since this will be the camera-ready published version. All final papers should be written only in English and “word document" as .doc or .docx format.
• STEP 3: You can submit your final paper(s) to the online conference system only by uploading/ Re-submission your current submission.
• STEP 4: After logging/using submission ID in the online conference system, click on the "submission" link at the bottom of the page.
• STEP 5: After the "Resubmission page" opens, upload your abstract/ final paper (it should be MS word document -doc. or Docx-).

General Information

• Dress Code: Participants have to wear a formal dress. There are no restrictions on Color or design. The audience attending only the ceremony can wear clothing of their own choice.
• Certificate Distribution: Each presenter's name will be called & asked to collect their certificate on the Stage with an official photographer to capture the moments.

Sponsorship Details

Genetics and Genomics of Diseases warmly invites you to sponsor or exhibit of International Conference. We expect participants more than 200 numbers for our International conference will provide an opportunity to hear and meet/ads to Researchers, Practitioners, and Business Professionals to share expertise, foster collaborations, and assess rising innovations across the world in the core area of mechanical engineering.

Diamond Sponsorship

1. Acknowledgment during the opening of the conference
2. Complimentary Booth of size 10 meters square
3. Four (4) delegate’s complimentary registrations with lunch
4. Include marketing document in the delegate pack
5. Logo on Conference website, Banners, Backdrop, and conference proceedings
6. One exhibition stand (1×1 meters) for the conference
7. One full cover page size ad in conference proceedings
8. Opportunities for Short speech at events
9. Opportunity to sponsors conference kit
10. Opportunity to sponsors conference lanyards, ID cards
11. Opportunity to sponsors conference lunch
12. Recognition of video ads
13. 150-word company profile and contact details in the delegate pack

Platinum Sponsorship

1. Three (3) delegate’s complimentary registrations with lunch
2. Recognition on video ads
3. Opportunity to sponsors conference lunch
4. Opportunity to sponsors conference lanyards, ID cards
5. Opportunity to sponsors conference kit
6. Opportunities for Short speech at events
7. One full-page size ad in conference proceedings
8. One exhibition stand (1×1 meters) for the conference
9. Logo on Conference website, Banners, Backdrop, and conference proceedings
10. Include marketing document in the delegate pack
11. Complimentary Booth of size 10 meters square
12. Acknowledgment during the opening of the conference
13. 100-word company profile and contact details in the delegate pack

Gold Sponsorship

1. Two (2) delegate’s complimentary registrations with lunch
2. Opportunities for Short speech at events
3. Logo on Conference website, Banners, Backdrop, and conference proceedings
4. Include marketing document in the delegate pack
5. Complimentary Booth of size 10 meters square
6. Acknowledgment during the opening of the conference
7. 100-word company profile and contact details in the delegate pack
8. ½ page size ad in conference proceedings

Silver Sponsorship

1. Acknowledgment during the opening of the conference
2. One(1) delegate’s complimentary registrations with lunch
3. Include marketing document in the delegate pack
4. Logo on Conference website, Banners, Backdrop, and conference proceedings
5. ¼ page size ad in conference proceedings
6. 100-word company profile and contact details in the delegate pack

Individual Sponsorship

1. Acknowledgment during the opening of the conference
2. One(1) delegate’s complimentary registrations with lunch

Registration Fees

Exhibitions Details

Exhibit your Products & Services

Exhibit your Products & Services in Genetics and Genomics Conference. Exhibitors are welcomed from Commercial and Non-Commercial Organizations related to the conference title.

• The best platform to develop new partnerships & collaborations.
• Best location to speed up your route into every territory in the World.
• Our exhibitor booths were visited 4-5 times by 80% of the attendees during the conference.
• Network development with both Academia and Business.

Exhibitor Benefits

• Exhibit booth of Size-3X3 sqm.
• Promotion of your logo/Company Name/Brand Name through the conference website.
• Promotional video on company products during the conference (Post session and Breaks).
• Logo recognition in the Scientific program, Conference banner, and flyer.
• One A4 flyer inserts in the conference kit.
• An opportunity to sponsor 1 Poster Presentation Award.

Pencis Terms & Conditions

Genetics and Genomics of Diseases Conference Terms & Conditions Policy was last updated on June 25, 2022.

Privacy Policy

Genetics and Genomics of Diseases Conference Customer personal information for our legitimate business purposes, to process and respond to inquiries, and provide our services, to manage our relationship with editors, authors, institutional clients, service providers, and other business contacts, to market our services and subscription management. We do not sell, rent/ trade your personal information to third parties.

Relationship

Genetics and Genomics of Diseases Conference Operate a Customer Association Management and email list program, which we use to inform customers and other contacts about our services, including our publications and events. Such marketing messages may contain tracking technologies to track subscriber activity relating to engagement, demographics, and other data, and to build subscriber profiles.

Disclaimer

Genetics and Genomics Disorders Conference All editorial matter published on this website represents the opinions of the authors and not necessarily those of the Publisher with the publications. Statements and opinions expressed do not represent the official policies of the relevant Associations unless so stated. Every effort has been made to ensure the accuracy of the material that appears on this website. Please ignore, however, that some errors may occur.

Responsibility

Genetics and Genomics Disorders Conference Delegates are personally responsible for their belongings at the venue. The Organizers will not be held accountable for any stolen or missing items belonging to Delegates, Speakers, or Attendees; due to any reason whatsoever.

Insurance

Genetics and Genomics Disorders Conference Registration fees do not include insurance of any kind.

Press and Media

Press permission must be getting from the Genetics and Genomics Diseases Conference Organizing Committee before the event. The press will not quote speakers or delegates unless they have obtained their approval in writing. This conference is not associated with any commercial meeting company.

Transportation

Genetics and Genomics Diseases Conference Please note that any (or) all traffic and parking is the responsibility of the registrant.

Requesting an Invitation Letter

Genetics and Genomics of Diseases Conference For security purposes, the letter of invitation will be sent only to those individuals who had registered for the conference. Once your registration is complete, please contact contact@pencis.com to request a personalized letter of invitation.

Cancellation Policy

If Genetics and Genomics of Diseases Conference cancels this event for any reason, you will receive a credit for 100% of the registration fee paid. You may use this credit for another Genetics and Genomics Diseases Conference event which must occur within one year from the date of cancellation.

Postponement Policy

If Genetics and Genomics Disorders Conference postpones an event for any reason and you are unable or indisposed to attend on rescheduled dates, you will receive a credit for 100% of the registration fee paid. You may use this credit for another Genetics and Genomics Diseases Conference which must occur within one year from the date of postponement.

Transfer of registration

Genetics and Genomics Diseases Conference All fully paid registrations are transferable to other persons from the same organization if the registered person is unable to attend the event. The registered person must make transfers in writing to contact@pencis.com. Details must include the full name of an alternative person, their title, contact phone number, and email address. All other registration details will be assigned to the new person unless otherwise specified. Registration can be transferred from one conference to another conference of Pencis if the person is unable to attend one of the meetings. However, Registration cannot be transferred if it will be intimated within 14 days of the particular conference. The transferred registrations will not be eligible for Refund.

Visa Information

Genetics and Genomics Keeping given increased security measures, we would like to request all the participants to apply for Visa as soon as possible. Pencis will not directly contact embassies and consulates on behalf of visa applicants. All delegates or invitees should apply for Business Visa only. Important note for failed visa applications: Visa issues cannot come under the consideration of cancellation policy of Pencis, including the inability to obtain a visa.

Refund Policy

Genetics and Genomics of Diseases Conference Regarding refunds, all bank charges will be for the registrant's account. All cancellations or modifications of registration must make in writing to Genetics and Genomics Diseases contact@pencis.com.

If the registrant is unable to attend and is not in a position to transfer his/her participation to another person or event, then the following refund arrangements apply:

Keeping given advance payments towards Venue, Printing, Shipping, Hotels and other overheads, we had to keep Refund Policy is as following conditions,

• Before 60 days of the Conference: Eligible for Full Refund less $100 Service Fee
• Within 60-30 days of Conference: Eligible for 50% of payment Refund
• Within 30 days of Conference: Not eligible for Refund
• E-Poster Payments will not be refunded.

Refunds for eligible requests will typically take between 30 to 90 days to be received after the date of the event. We strive to process refunds as expeditiously as possible, but this timeframe allows us to ensure accuracy and compliance with our policies (Date of updated October 04  2023)

Accommodation Cancellation Policy

Genetics and  Genomics Diseases Conference Accommodation Providers such as hotels have their cancellation policies, and they generally apply when cancellations are made less than 30 days before arrival. Please contact us as soon as possible if you wish to cancel or amend your accommodation. Pencis will advise the cancellation policy of your accommodation provider, before withdrawing or changing your booking, to ensure you are fully aware of any non-refundable deposits.

Nucleic Acids Research - University of Oxford, UK - Citations: 197,543 - H-Index: 344 | Nature Genetics - Multiple institutions, International - Citations: 100,563 - H-Index: 386 | Genome Research - Cold Spring Harbor Laboratory, USA - Citations: 88,385 - H-Index: 268 | American Journal of Human Genetics - Multiple institutions, International - Citations: 73,200 - H-Index: 291 | Trends in Genetics - Cell Press, USA - Citations: 42,237 - H-Index: 203 | Genetics - Genetics Society of America, USA - Citations: 63,425 - H-Index: 202 | Genome Biology - BioMed Central, UK - Citations: 51,324 - H-Index: 199 | PLoS Genetics - Public Library of Science, USA - Citations: 44,702 - H-Index: 179 | Human Molecular Genetics - Oxford University Press, UK - Citations: 55,751 - H-Index: 171 | Epigenetics & Chromatin - BioMed Central, UK - Citations: 12,074 - H-Index: 94 | Genome Medicine - BioMed Central, UK - Citations: 12,224 - H-Index: 82 | Molecular Genetics and Genomics - Springer, Germany - Citations: 23,989 - H-Index: 79 | Genes & Development - Cold Spring Harbor Laboratory Press, USA - Citations: 46,328 - H-Index: 164 | Human Genetics - Springer, Germany - Citations: 26,323 - H-Index: 126 | Journal of Medical Genetics - BMJ Publishing Group, UK - Citations: 32,625 - H-Index: 110 | Journal of Genetics - Indian Academy of Sciences, India - Citations: 9,583 - H-Index: 53 | Molecular Biology and Evolution - Oxford University Press, UK - Citations: 85,109 - H-Index: 168 | Molecular Plant - Cell Press, USA - Citations: 17,041 - H-Index: 73 | Genomics - Elsevier, USA - Citations: 73,727 - H-Index: 157 | BMC Genomics - BioMed Central, UK - Citations: 80,662 - H-Index: 167 | Genome Medicine - University: Various - Country: Various - Citation: 12,784 - H-Index: 66 | Epigenetics - University: Various - Country: Various - Citation: 12,658 - H-Index: 77 | Human Mutation - University: Various - Country: Various - Citation: 20,578 - H-Index: 114 | Journal of Biological Chemistry - University: Various - Country: Various - Citation: 555,742 - H-Index: 988 | Molecular Cancer Research - University: Various - Country: Various - Citation: 17,050 - H-Index: 89 | Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis - University: Various - Country: Various - Citation: 8,990 - H-Index: 71 | Genomics - University: Various - Country: Various - Citation: 58,537 - H-Index: 173 | BMC Medical Genomics - University: Various - Country: Various - Citation: 5,907 - H-Index: 47 | Molecular Therapy - Nucleic Acids - University: Various - Country: Various - Citation: 3,231 - H-Index: 32 | Journal of Molecular Evolution - University: Various - Country: Various - Citation: 10,176 - H-Index: 72 | American Journal of Medical Genetics Part A - University: Various - Country: Various - Citation: 21,103 - H-Index: 112 | Cytogenetic and Genome Research - University: Various - Country: Various - Citation: 7,227 - H-Index: 60 | Journal of Cytology & Histology - University: Various - Country: Various - Citation: 362 - H-Index: 19 | Transgenic Research - University: Various - Country: Various - Citation: 4,048 - H-Index: 50 | Journal of Cellular Physiology - University: Various - Country: Various - Citation: 89,322 - H-Index: 177 | Journal of Theoretical Biology - University: Various - Country: Various - Citation: 34,644 - H-Index: 138 | Gene - University: Various - Country: Various - Citation: 92,710 - H-Index: 181 | Journal of Animal Breeding and Genetics - University: Various - Country: Various - Citation: 7,417 - H-Index: 56 | Current Opinion in Genetics & Development - University: Various - Country: Various - Citation: 17,914 - H-Index: 100 | Animal Genetics - University: Various - Country: Various - Citation: 7,185 - H-Index: 56 | MC Genomics - University: Various - Country: Various - Citation: 55,586 - H-Index: 144 | Journal of Genetics - University: Various - Country: Various - Citation: 3,990 - H-Index: 35 | Journal of Neurogenetics - University: Various - Country: Various - Citation: 2,237 - H-Index: 27 | Heredity - University: Various - Country: Various - Citation: 13,933 - H-Index: 96 | Genes to Cells - University: Various - Country: Various - Citation: 6,250 - H-Index: 57 | Developmental Genetics - University: Various - Country: Various - Citation: 2,374 - H-Index: 35 | Journal of Genetics and Genomics - University: Various - Country: Various - Citation: 8,253 - H-Index: 60 | International Journal of Genomics - University: Various - Country: Various - Citation: 2,076 - H-Index: 35 | Journal of Applied Genetics - University: Various - Country: Various - Citation: 1,550 - H-Index: 25 | PLoS Genetics - University: Various - Country: Various - Citation: 65,427 - H-Index: 163 | Advances in Genetics - University: Various - Country: Various - Citation: 1,621 - H-Index: 38 | Journal of Heredity - University: Various - Country: Various - Citation: 2,992 - H-Index: 41 | European Journal of Human Genetics - University: Various - Country: Various - Citation: 20,354 - H-Index: 114 | BMC Medical Genomics - University: Various - Country: Various - Citation: 5,907 - H-Index: 47 | Nature Communications - Genetics - University: Various - Country: Various - Citation: 54,328 - H-Index: 222 | Genes - University: Various - Country: Various - Citation: 7,688 - H-Index: 57 | Theoretical Population Biology - University: Various - Country: Various - Citation: 8,317 - H-Index: 66 | Trends in Genetics - University: Various - Country: Various - Citation: 19,804 - H-Index: 135 | Molecular Genetics and Genomics - University: Various - Country: Various - Citation: 9,295 - H-Index: 73 | Genetics Selection Evolution - University: Various - Country: Various - Citation: 1,991 - H-Index: 38 | Journal of Inherited Metabolic Disease - University: Various - Country: Various - Citation: 9,308 - H-Index: 56 | Human Genomics - University: Various - Country: Various - Citation: 4,924 - H-Index: 39 | Genome Biology and Evolution - University: Various - Country: Various - Citation: 8,945 - H-Index: 82 | Molecular Phylogenetics and Evolution - University: Various - Country: Various - Citation: 16,264 - H-Index: 115 | Genetica - University: Various - Country: Various - Citation: 4,762 - H-Index: 47 | Genome Medicine - University: Various - Country: Various - Citation: 12,784 - H-Index: 66 | Epigenetics - University: Various - Country: Various - Citation: 12,658 - H-Index: 77 | Human Mutation - University: Various - Country: Various - Citation: 20,578 - H-Index: 114 | Journal of Biological Chemistry - University: Various - Country: Various - Citation: 555,742 - H-Index: 988 | Molecular Cancer Research - University: Various - Country: Various - Citation: 17,050 - H-Index: 89 | Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis - University: Various - Country: Various - Citation: 8,990 - H-Index: 71 | Genomics - University: Various - Country: Various - Citation: 58,537 - H-Index: 173 | BMC Medical Genomics - University: Various - Country: Various - Citation: 5,907 - H-Index: 47 | Molecular Therapy - Nucleic Acids - University: Various - Country: Various - Citation: 3,231 - H-Index: 32 | Journal of Molecular Evolution - University: Various - Country: Various - Citation: 10,176 - H-Index: 72 | American Journal of Medical Genetics Part A - University: Various - Country: Various - Citation: 21,103 - H-Index: 112 | Cytogenetic and Genome Research - University: Various - Country: Various - Citation: 7,227 - H-Index: 60 | Journal of Cytology & Histology - University: Various - Country: Various - Citation: 362 - H-Index: 19 | Transgenic Research - University: Various - Country: Various - Citation: 4,048 - H-Index: 50 | Journal of Cellular Physiology - University: Various - Country: Various - Citation: 89,322 - H-Index: 177 | Journal of Theoretical Biology - University: Various - Country: Various - Citation: 34,644 - H-Index: 138 | Gene - University: Various - Country: Various - Citation: 92,710 - H-Index: 181 | Journal of Animal Breeding and Genetics - University: Various - Country: Various - Citation: 7,417 - H-Index: 56 | Current Opinion in Genetics & Development - University: Various - Country: Various - Citation: 17,914 - H-Index: 100 | Animal Genetics - University: Various - Country: Various - Citation: 7,185 - H-Index: 56 | Epigenetics - University: Various - Country: Various - Citation: 10,263 - H-Index: 84 | Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis - University: Various - Country: Various - Citation: 8,387 - H-Index: 95 | Mutagenesis - University: Various - Country: Various - Citation: 2,300 - H-Index: 33 | Epigenomics - University: Various - Country: Various - Citation: 3,509 - H-Index: 39 | Clinical Genetics - University: Various - Country: Various - Citation: 12,187 - H-Index: 77 | Journal of Human Genetics - University: Various - Country: Various - Citation: 8,294 - H-Index: 63 | Journal of Medical Genetics - University: Various - Country: Various - Citation: 25,079 - H-Index: 149 | Journal of Molecular Diagnostics - University: Various - Country: Various - Citation: 11,284 - H-Index: 86 | Molecular Therapy - University: Various - Country: Various - Citation: 31,398 - H-Index: 185 | Molecular Therapy - Nucleic Acids - University: Various - Country: Various - Citation: 2,908 - H-Index: 33 | Nature Genetics - University: Various - Country: Various - Citation: 149,106 - H-Index: 388 | Neuroscience and Biobehavioral Reviews - University: Various - Country: Various - Citation: 34,411 - H-Index: 198 | Progress in Neurobiology - University: Various - Country: Various - Citation: 22,406 - H-Index: 144 | Briefings in Functional Genomics - University: Various - Country: Various - Citation: 1,429 - H-Index: 32 | Cytogenetic and Genome Research - University: Various - Country: Various - Citation: 5,446 - H-Index: 47

American Society of Human Genetics (ASHG) - USAEuropean Society of Human Genetics (ESHG) - EuropeGenetics Society of America (GSA) - USAInternational Society of Genetic Genealogy (ISOGG) - InternationalHuman Genome Organisation (HUGO) - InternationalThe Genetics Society (TGS) - UKThe Canadian Society of Molecular Biosciences (CSMB) - CanadaThe Society for Molecular Biology and Evolution (SMBE) - InternationalSociety for Developmental Biology (SDB) - USAThe American Society of Gene and Cell Therapy (ASGCT) - USASociety for Experimental Biology and Medicine (SEBM) - USAThe Society for the Study of Evolution (SSE) - USAThe Society for Neuroscience (SfN) - USAThe International Mammalian Genome Society (IMGS) - InternationalThe American Association for Cancer Research (AACR) - USAThe American College of Medical Genetics and Genomics (ACMG) - USAThe European Society for Evolutionary Biology (ESEB) - EuropeThe Society for Inherited Metabolic Disorders (SIMD) - USAThe Society for Molecular Imaging (SMI) - USAThe American Society for Pharmacology and Experimental Therapeutics (ASPET) - USAThe International Genetics Federation (IGF) - InternationalThe International Society for Animal Genetics (ISAG) - InternationalThe International Society for Computational Biology (ISCB) - InternationalThe International Society for Genetic Eye Diseases and Retinoblastoma (ISGEDR) - InternationalThe International Society for Stem Cell Research (ISSCR) - InternationalThe Australasian Society for Human Genetics (ASHG) - Australia and New ZealandThe Brazilian Society of Human Genetics (BSHG) - BrazilThe British Society for Genetic Medicine (BSGM) - UKThe Danish Society of Medical Genetics (DSMG) - DenmarkThe Dutch Society of Human Genetics (NVHG) - NetherlandsThe French Society of Human Genetics (SFGH) - FranceThe German Society of Human Genetics (GfH) - GermanyThe Indian Society of Human Genetics (ISHG) - IndiaThe Italian Society of Human Genetics (SIGU) - ItalyThe Japanese Society of Human Genetics (JSHG) - JapanThe Korean Society of Human Genetics (KSHG) - KoreaThe Latin American Society of Human Genetics (SOLAGH) - Latin AmericaThe Norwegian Society of Medical Genetics (NSMG) - NorwayThe Polish Society of Human Genetics (PTGH) - PolandThe Portuguese Society of Human Genetics (SPGH) - PortugalThe Russian Society of Human Genetics (RSHG) - RussiaThe Scandinavian Society for Human Genetics (SSHG) - ScandinaviaThe Society for Endocrinology (SE) - UKThe Society for Experimental Biology (SEB) - UKThe Society for Genomics Policy and Research (SGPR) - InternationalThe Society for Glycobiology (SfG) - InternationalThe Society for Immunotherapy of Cancer (SITC) - USAThe Society for Inherited Metabolic Disorders (SIMD) - InternationalThe Society for Investigative DermatologyThe Society for Medical Genetics and Genomics of Iran (SMGGI) - IranThe Spanish Society of Genetics (SEG) - SpainThe Swedish Society of Medical Genetics and Genomics (SSMG) - SwedenThe Swiss Society of Medical Genetics (SSMG) - SwitzerlandThe Turkish Society of Medical Genetics (TSMG) - TurkeyThe African Society of Human Genetics (AfSHG) - AfricaThe Argentine Society of Human Genetics (SAHG) - ArgentinaThe Asia Pacific Society of Human Genetics (APSHG) - Asia Pacific regionThe Association for Molecular Pathology (AMP) - USAThe Association for Research in Vision and Ophthalmology (ARVO) - USAThe Association for the Study of Animal Behaviour (ASAB) - UKThe Australian and New Zealand Society of Blood Transfusion (ANZSBT) - Australia and New ZealandThe Belgian Society of Human Genetics (BSHG) - BelgiumThe Canadian College of Medical Geneticists (CCMG) - CanadaThe Cancer Genetics Society of Australasia (CGSA) - Australia and New ZealandThe Chinese Society of Medical Genetics (CSMG) - ChinaThe Clinical Genetics Society (CGS) - UKThe Colombian Association of Human Genetics (ACGH) - ColombiaThe Croatian Society of Human Genetics (CSHG) - CroatiaThe Czech Society of Medical Genetics and Genomics (CZSMGG) - Czech RepublicThe European Society for Animal Cell Technology (ESACT) - EuropeThe European Society for Human Reproduction and Embryology (ESHRE) - EuropeThe European Society for Immunodeficiencies (ESID) - EuropeThe European Society of Veterinary Pathology (ESVP) - EuropeThe Finnish Society of Medical Genetics and Genomics (FSGM) - FinlandThe Genetics and Genomics Society (GGS) - USAThe Genetic Society of Korea (GSK) - KoreaThe Hellenic Society of Medical Genetics (HSMG) - GreeceThe Hong Kong Society of Medical Genetics (HKSMG) - Hong KongThe Hungarian Society of Human Genetics (HSHG) - HungaryThe Indian Society for Prenatal Diagnosis and Therapy (ISPDT) - IndiaThe Indonesian Society of Human Genetics (InaSHG) - IndonesiaThe International Cytogenetics and Genome Society (ICGS) - InternationalThe International Federation of Human Genetics Societies (IFHGS) - InternationalThe International Society for Forensic Genetics (ISFG) - InternationalThe International Society for Histocompatibility and Immunogenetics (ISHI) - InternationalThe International Society for Neonatal Screening (ISNS) - InternationalThe International Society for Twin Studies (ISTS) - InternationalThe International Society of Animal Blood Group Genetics (ISABG) - InternationalThe International Society of Chromosome and Genome Research (ISCG) - InternationalThe International Society of Nucleosides, Nucleotides and Nucleic Acids (IS3NA) - InternationalThe Iranian Society of Human Genetics (IrSHG) - IranThe Irish Society of Human Genetics (ISHG) - IrelandThe Israeli Society of Medical Genetics (ISMG) - IsraelThe Japanese Society of Veterinary Science (JSVS) - JapanThe Jordanian Society of Medical Genetics (JOSMG) - JordanThe Korean Society of Human Genetics (KSHG) - KoreaThe Kuwait Medical Genetics Society (KMGS) - KuwaitThe Latin American Society of Human Genetics (SOLAGEH) - Latin AmericaThe Lebanese Society of Human Genetics (LSHG) - LebanonThe Malaysian Society of Human Genetics (MaSHG) - Malaysia.

The Selfish Gene\" by Richard Dawkins, Oxford University Press, 2nd edition, 1989 | \"Essential Genetics: A Genomic Perspective\" by Daniel L. Hartl, Jones & Bartlett Learning, 7th edition, 2020 | \"Evolution: The Story of Life\" by Douglas Palmer and Peter Barrett, University of California Press, 2nd edition, 2009 | \"The Ancestor\'s Tale: A Pilgrimage to the Dawn of Evolution\" by Richard Dawkins, Mariner Books, reprint edition, 2016 | \"Molecular Biology of the Cell\" by Bruce Alberts, Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, and Peter Walter, Garland Science, 6th edition, 2014 | \"Molecular Cloning: A Laboratory Manual\" by Joseph Sambrook, David W. Russell, and Michael J. Gething, Cold Spring Harbor Laboratory Press, 4th edition, 2012 | \"The Double Helix: A Personal Account of the Discovery of the Structure of DNA\" by James D. Watson, Touchstone, 1st edition, 1980 | \"Epigenetics: How Environment Shapes Our Genes\" by Richard C. Francis, W.W. Norton & Company, 1st edition, 2012 | \"Genetics: Analysis and Principles\" by Robert J. Brooker, McGraw-Hill Education, 6th edition, 2020 | \"Genetic Analysis: An Integrated Approach\" by Mark F. Sanders and John L. Bowman, Pearson, 3rd edition, 2020 | \"The Extended Phenotype: The Long Reach of the Gene\" by Richard Dawkins, Oxford University Press, reprint edition, 1999 | \"Principles of Genetics\" by D. Peter Snustad and Michael J. Simmons, Wiley-Blackwell, 6th edition, 2011 | \"Evolutionary Genetics: Concepts, Analysis, and Practice\" by Glenn-Peter Sætre and Mark Ravinet, Oxford University Press, 1st edition, 2020 | \"Human Genetics and Genomics\" by Bruce R. Korf and Mira B. Irons, Elsevier, 5th edition, 2019 | \"Essentials of Medical Genomics\" by Stuart M. Brown, Springer, 2nd edition, 2020 | \"Principles of Genetics\" by Robert H. Tamarin, McGraw-Hill Education, 8th edition, 2018 | \"The Eighth Day of Creation: Makers of the Revolution in Biology\" by Horace Freeland Judson, Cold Spring Harbor Laboratory Press, 25th anniversary edition, 1996 | \"Genome: The Autobiography of a Species in 23 Chapters\" by Matt Ridley, Fourth Estate, 1st edition, 2000 | \"An Introduction to Genetic Analysis\" by Anthony J.F. Griffiths, Susan R. Wessler, Sean B. Carroll, and John Doebley, W.H. Freeman and Company, 12th edition, 2014 | \"Essentials of Genetics\" by William S. Klug, Michael R. Cummings, Charlotte A. Spencer, and Michael A. Palladino, Pearson, 10th edition, 2021 | \"A Troublesome Inheritance: Genes, Race, and Human History\" by Nicholas Wade, Penguin Press, 1st edition, 2014 | \"Genetic Analysis of Complex Traits Using SAS\" by Arnold M. Saxton, CRC Press, 2nd edition, 2014 | \"Genetic Engineering: Principles and Methods\" edited by Jane K. Setlow, Springer, 1st edition, 1995 | \"Principles of Gene Manipulation and Genomics\" by Sandy B. Primrose and Richard Twyman, Wiley-Blackwell, 8th edition, 2019 | \"Gene Cloning and DNA Analysis: An Introduction\" by T.A. Brown, Wiley-Blackwell, 7th edition, 2015 | \"Human Molecular Genetics\" by Tom Strachan and Andrew Read, Garland Science, 5th edition, 2019 | \"Genetic Analysis of Complex Diseases\" edited by Eleftheria Zeggini, Andrew P. Morris, and Mark I. McCarthy, CRC Press, 1st edition, 2019 | \"The Language of Life: DNA and the Revolution in Personalized Medicine\" by Francis S. Collins, HarperCollins Publishers, reprint edition, 2011 | \"The Making of the Fittest: DNA and the Ultimate Forensic Record of Evolution\" by Sean B. Carroll, W.W. Norton & Company, 1st edition, 2006 | \"Epigenetics in Human Disease\" edited by Trygve Tollefsbol, Academic Press, 2nd edition, 2018 | \"A Primer of Genome Science\" by Greg Gibson and Spencer V. Muse, Sinauer Associates, 3rd edition, 2020 | \"Genetic Variation: Methods and Protocols\" edited by Magnus Nordborg, Springer, 1st edition, 2010 | \"Essentials of Medical Genetics for Health Professionals\" by Laura M. Gunder McClary, Jones & Bartlett Learning, 1st edition, 2021 | \"Population Genetics: A Concise Guide\" by John H. Gillespie, Johns Hopkins University Press, 3rd edition, 2021 | \"Introduction to Epigenetics\" by Steven Henikoff and Rachel Henikoff, Cold Spring Harbor Laboratory Press, 1st edition, 2014 | \"The Epigenetics Revolution: How Modern Biology is Rewriting Our Understanding of Genetics, Disease, and Inheritance\" by Nessa Carey, Columbia University Press, reprint edition, 2013 | \"Human Heredity: Principles and Issues\" by Michael Cummings, Cengage Learning, 11th edition, 2020 | \"The Epigenome: A New Story of Our Genetic Code\" by Richard C. Francis, Oxford University Press, 1st edition, 2020 | \"A Dictionary of Genetics\" by Robert C. King, William D. Stansfield, and Pamela K. Mulligan, Oxford University Press, 8th edition, 2020 | \"A Primer of Population Genetics\" by Daniel L. Hartl and Andrew G. Clark, Sinauer Associates, 4th edition, 2006 | \"Genetics and Analysis of Quantitative Traits\" by Michael Lynch and Bruce Walsh, Sinauer Associates, 1st edition, 1998 | \"Genetics: A Conceptual Approach\" by Benjamin A. Pierce, W.H. Freeman and Company, 7th edition, 2019 | \"Genetic Analysis: Genes, Genomes, and Networks in Eukaryotes\" by Philip Meneely, Oxford University Press, 1st edition, 2015 | \"DNA: The Story of the Genetic Revolution\" by James D. Watson, Knopf, 1st edition, 2017 | \"The Epigenetics of Aging and Longevity\" edited by Alexey Moskalev and Mikhail V. Blagosklonny, Academic Press, 1st edition, 2017 | \"Human Genetics: Concepts and Applications\" by Ricki Lewis, McGraw-Hill Education, 12th edition, 2022 | \"The Origins of Genome Architecture\" by Michael Lynch, Sinauer Associates, 1st edition, 2007 | \"Genetics: Analysis and Principles\" by Robert J. Brooker, McGraw-Hill Education, 6th edition, 2022 | \"Population Genetics and Microevolutionary Theory\" by Alan R. Templeton, Wiley-Blackwell, 1st edition, 2006 | \"Medical Genetics\" by Lynn B. Jorde, John C. Carey, and Michael J. Bamshad, Mosby, 5th edition, 2019 | \"Human Genetic Diversity: Functional Consequences for Health and Disease\" edited by Julian C. Knight and Sarah A. Teichmann, Springer, 1st edition, 2019 | \"Molecular Biology of the Gene\" by James D. Watson, Tania A. Baker, Stephen P. Bell, Alexander Gann, Michael Levine, and Richard Losick, Pearson, 8th edition, 2021 | \"Molecular Genetics: An Introductory Narrative\" by Roy J. Britten and Eric H. Davidson, Academic Press, 1st edition, 1969 | \"Medical Genetics at a Glance\" by Dorian J. Pritchard and Bruce R. Korf, Wiley-Blackwell, 4th edition, 2020 | \"Genetics of Populations\" by Philippe Gouyon and Gilles Dauphin, Cambridge University Press, 1st edition, 2021 | \"Genetic Algorithms in Search, Optimization, and Machine Learning\" by David E. Goldberg, Addison-Wesley Professional, 1st edition, 1989 | \"Genetics and Analysis of Quantitative Traits\" by Michael Lynch and Bruce Walsh, Sinauer Associates, 2nd edition, 2012 | \"Molecular Genetics of Bacteria\" by Larry Snyder and Wendy Champness, ASM Press, 4th edition, 2013 | \"Genes and Genomes: A Changing Perspective\" by Maxine Singer and Paul Berg, University Science Books, 3rd edition, 1998 | \"The Selfish Gene\" by Richard Dawkins, Oxford University Press, 2nd edition, 1989 | \"Molecular Biology of the Cell\" by Bruce Alberts, Alexander Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, and Peter Walter, Garland Science, 6th edition, 2015 | \"The Double Helix: A Personal Account of the Discovery of the Structure of DNA\" by James D. Watson, Simon & Schuster, 1st edition, 1968 | \"Human Genome Epidemiology: A Scientific Foundation for Using Genetic Information to Improve Health and Prevent Disease\" edited by Muin J. Khoury, Sara Bedrosian, and Marta Gwinn, Oxford University Press, 2nd edition, 2010 | \"The Epigenetics Revolution: How We Can Use This New Science to Personalize Our Medicine and Improve Our Health\" by Nessa Carey, Columbia University Press, 2nd edition, 2018 | \"The Ancestor\'s Tale: A Pilgrimage to the Dawn of Evolution\" by Richard Dawkins, Mariner Books, reprint edition, 2016. | \"Molecular Genetics of Bacteria\" by Larry Snyder and Wendy Champness, ASM Press, 4th edition, 2013 | \"Genes and Genomes: A Changing Perspective\" by Maxine Singer and Paul Berg, University Science Books, 3rd edition, 1998 | \"The Selfish Gene\" by Richard Dawkins, Oxford University Press, 2nd edition, 1989 | \"Molecular Biology of the Cell\" by Bruce Alberts, Alexander Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, and Peter Walter, Garland Science, 6th edition, 2015 | \"The Double Helix: A Personal Account of the Discovery of the Structure of DNA\" by James D. Watson, Simon & Schuster, 1st edition, 1968 | \"Human Genome Epidemiology: A Scientific Foundation for Using Genetic Information to Improve Health and Prevent Disease\" edited by Muin J. Khoury, Sara Bedrosian, and Marta Gwinn, Oxford University Press, 2nd edition, 2010 | \"The Epigenetics Revolution: How We Can Use This New Science to Personalize Our Medicine and Improve Our Health\" by Nessa Carey, Columbia University Press, 2nd edition, 2018 | \"The Ancestor\'s Tale: A Pilgrimage to the Dawn of Evolution\" by Richard Dawkins, Mariner Books, reprint edition, 2016. | An Introduction to Genetic Analysis by Anthony J.F. Griffiths, Wessler, Carroll, and Doebley - W.H. Freeman and Company, 11th edition, 2015 | Principles of Genetics by Robert H. Tamarin - Wiley, 8th edition, 2013 | Human Genetics: Concepts and Applications by Ricki Lewis - McGraw-Hill Education, 11th edition, 2018 | Molecular Biology of the Gene by James D. Watson, Tania A. Baker, Stephen P. Bell, Alexander Gann, Michael Levine, and Richard Losick - Pearson, 7th edition, 2013 | Introduction to Genetic Analysis by Anthony J.F. Griffiths, Susan R. Wessler, Sean B. Carroll, and John Doebley - W.H. Freeman and Company, 10th edition, 2012 | Principles of Population Genetics by Daniel L. Hartl and Andrew G. Clark - Sinauer Associates, 4th edition, 2006 | Human Molecular Genetics by Tom Strachan and Andrew Read - Garland Science, 4th edition, 2011 | The Genetic Basis of Evolutionary Change by Richard Lewontin - Columbia University Press, 1974 | The Selfish Gene by Richard Dawkins - Oxford University Press, 30th anniversary edition, 2006 | Genomes by T.A. Brown - Garland Science, 3rd edition, 2006 | Human Genetics and Genomics by Bruce R. Korf and Mira B. Irons - Wiley-Blackwell, 4th edition, 2020 | A Primer of Genome Science by Greg Gibson and Spencer V. Muse - Sinauer Associates, 3rd edition, 2015 | Principles of Gene Manipulation and Genomics by Sandy B. Primrose and Richard Twyman - Wiley-Blackwell, 8th edition, 2013 | Principles of Evolution by Douglas J. Futuyma - Sinauer Associates, 3rd edition, 2013 | Genetic Analysis: An Integrated Approach by Mark F. Sanders and John L. Bowman - Pearson, 3rd edition, 2018 | The Structure of Evolutionary Theory by Stephen Jay Gould - Belknap Press, 2002 | Human Genome Informatics by Christophe Lambert and Mark Lathrop - Wiley, 2nd edition, 2019 | Principles of Genetics and Genomics by Sally A. Mackenzie - Wiley-Blackwell, 2nd edition, 2021 | The Theory of Evolution: Principles, Concepts, and Assumptions by Jeffrey A. Hoffstein - Springer, 2017 | The Origins of Life: From the Birth of Life to the Origin of Language by John Maynard Smith and Eors Szathmary - Oxford University Press, 1999 | Evolution: The Story of Life by Douglas Palmer - University of California Press, 2009 | Evolution: The First Four Billion Years by Michael Ruse and Joseph Travis - The Belknap Press of Harvard University Press, 2009 | Genetics: From Genes to Genomes by Leland Hartwell, Michael Goldberg, Janice Fischer, and Leroy Hood - McGraw-Hill Education, 6th edition, 2017 | Genomes 3 by T.A. Brown - Garland Science, 3rd edition, 2006 | The Red Queen: Sex and the Evolution of Human Nature by Matt Ridley - Harper Perennial, 1994 | The Double Helix: A Personal Account of the Discovery of the Structure of DNA by James D. Watson - W.W. Norton & Company, 2001 | Genes VIII by Benjamin Lewin - Pearson, 8th edition, 2004

Jennifer Doudna - Genome editing, University of California, Berkeley, USA | Eric Lander - Human genome project, Broad Institute of MIT and Harvard, USA | George Church - Gene therapy, Harvard Medical School, USA | Francis Collins - Human genome project, National Institutes of Health, USA | Craig Venter - Genomics, J. Craig Venter Institute, USA | Svante Pääbo - Ancient DNA, Max Planck Institute for Evolutionary Anthropology, Germany | Stephen B. Montgomery - Population genetics, Stanford University, USA | Joshua M. Akey - Population genetics, Princeton University, USA | Eimear Kenny - Population genetics, Icahn School of Medicine at Mount Sinai, USA | David Reich - Ancient DNA, Harvard Medical School, USA | Jun Wang - Genomics, Beijing Genomics Institute, China | Huanming Yang - Genomics, Beijing Genomics Institute, China | John Novembre - Population genetics, University of Chicago, USA | Daniel MacArthur - Human genomics, Massachusetts General Hospital and Harvard Medical School, USA | Joanna Mountain - Human population genetics, 23andMe, USA | Molly Przeworski - Population genetics, Columbia University, USA | Peter Visscher - Statistical genetics, University of Queensland, Australia | J. Craig Venter - Genomics, J. Craig Venter Institute, USA | Emmanouil Dermitzakis - Functional genomics, University of Geneva, Switzerland | David Haussler - Comparative genomics, University of California, Santa Cruz, USA | Pardis Sabeti - Computational genomics, Harvard University, USA | Evan Eichler - Structural variation, University of Washington, USA | Matthew Hurles - Structural variation, Wellcome Sanger Institute, UK | Joris Veltman - Structural variation, Radboud University, Netherlands | Xavier Estivill - Structural variation, Pompeu Fabra University, Spain | Rasmus Nielsen - Population genetics, University of California, Berkeley, USA | Jeffrey M. Kidd - Population genetics, University of Michigan, USA | Gil McVean - Population genetics, University of Oxford, UK | Sarah Tishkoff - Population genetics, University of Pennsylvania, USA | Joshua Akey - Population genetics, Princeton University, USA | Kirk Lohmueller - Population genetics, University of California, Los Angeles, USA | James R. Lupski - Structural variation, Baylor College of Medicine, USA | Jean-Louis Mandel - Molecular genetics, University of Strasbourg, France | Stylianos Antonarakis - Medical genetics, University of Geneva Medical School, Switzerland | John Hardy - Genetics of neurodegenerative disorders, University College London, UK | Katherine High - Gene therapy, University of Pennsylvania, USA | Yves Agid - Neurogenetics, Sorbonne University, France | Christiane Nüsslein-Volhard - Developmental genetics, Max Planck Institute for Developmental Biology, Germany | Edith Heard - Epigenetics, Collège de France, France | Anne Ferguson-Smith - Epigenetics, University of Cambridge, UK | Wolf Reik - Epigenetics, Babraham Institute, UK | Andrew P. Feinberg - Epigenetics, Johns Hopkins University, USA | Jonathan Flint - Behavioral genetics, University of California, Los Angeles, USA | David Goldman - Behavioral genetics, National Institutes of | Robert Plomin - Behavioral genetics, King\'s College London, UK | Danielle Posthuma - Psychiatric genetics, Vrije Universiteit Amsterdam, Netherlands | Peter Heutink - Neurogenetics, Vrije Universiteit Medical Center, Netherlands | B. Fenton Hall - Neurogenetics, Harvard Medical School, USA | Linda Buck - Neuroscience and genetics, Fred Hutchinson Cancer Research Center, USA | Richard Axel - Neuroscience and genetics, Columbia University, USA | Kari Stefansson - Genomics and pharmacogenomics, deCODE Genetics, Iceland | Jonathan Sebat - Genetics of neuropsychiatric disorders, University of California, San Diego, USA | Hakon Hakonarson - Genetics of complex diseases, Children\'s Hospital of Philadelphia, USA | Mark Daly - Genetics of complex diseases, Harvard Medical School and Massachusetts General Hospital, USA | Steve McCarroll - Genetics of neuropsychiatric disorders, Harvard Medical School and Broad Institute, USA | Nils-Göran Larsson - Mitochondrial genetics, Max Planck Institute for Biology of Ageing, Germany | Douglas C. Wallace - Mitochondrial genetics, University of Pennsylvania, USA | Patrick S. Hsu - Genome editing, University of California, Berkeley, USA | Maria Jasin - Genome stability, Memorial Sloan Kettering Cancer Center, USA | Robert L. Martienssen - Epigenetics, Cold Spring Harbor Laboratory, USA | Wei-Hua Chen - Epigenetics and plant genetics, University of California, Riverside, USA | David Sankoff - Comparative genomics, University of Ottawa, Canada | Michel Georges - Livestock genomics, University of Liège, Belgium | Leif Andersson - Animal genetics, Uppsala University, Sweden | Bruce Weir - Statistical genetics, University of Washington, USA | David Altshuler - Human genetics, Vertex Pharmaceuticals, USA | Mark Gerstein - Computational biology and genomics, Yale University, USA | Lenore J. Cowen - Computational biology and genomics, Tufts University, USA | Andrew Clark - Evolutionary genomics, Cornell University, USA | Daniel St Johnston - Drosophila genetics, University of Cambridge, UK | Scott Barolo - Gene regulation and systems biology, University of Michigan, USA | Michael Snyder - Systems biology, Stanford University, USA | C. David Allis - Epigenetics and chromatin biology, Rockefeller University, USA | Asifa Akhtar - Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Germany | Manolis Kellis - Computational biology and genomics, Massachusetts Institute of Technology, USA | Eran Segal - Systems biology and genomics, Weizmann Institute of Science, Israel | Naama Barkai - Systems biology, Weizmann Institute of Science, Israel | Ron Shamir - Computational biology and genomics, Tel Aviv University, Israel | Amos Tanay - Computational biology and genomics, Weizmann Institute of Science, Israel | David Baulcombe - Plant genetics and epigenetics, University of Cambridge, UK | Jonathan Jones - Plant genetics and genomics, Sainsbury Laboratory, UK | Detlef Weigel - Plant genetics and genomics, Max Planck Institute for Developmental Biology, Germany | David E. Housman - Human genetics, Massachusetts Institute of Technology, USA | Stephen Elledge - Genome stability, Harvard Medical School and Brigham and | Rosa Rademakers - Neurogenetics, Mayo Clinic, USA | Janine LaSalle - Epigenetics, University of California, Davis, USA | Emily Hodges - Epigenetics, Stanford University, USA | Ben Lehner - Evolutionary genetics, Centre for Genomic Regulation, Spain | Guy Riddihough - Developmental genetics, University of Sheffield, UK | Lars Steinmetz - Functional genomics, Stanford University, USA | Nicholas Katsanis - Genetics of rare diseases, Duke University, USA | Christine Van Broeckhoven - Neurogenetics, University of Antwerp, Belgium | Markus Nöthen - Genetic epidemiology, University of Bonn, Germany | Wieland Huttner - Developmental neurobiology and genetics, Max Planck Institute of Molecular Cell Biology and Genetics, Germany | J. Craig Venter - Genomics and synthetic biology, J. Craig Venter Institute, USA | David B. Goldstein - Human genetics, Columbia University, USA | Christian Voolstra - Coral genetics and genomics, King Abdullah University of Science and Technology, Saudi Arabia | Oliver Smithies - Gene targeting and gene editing, University of North Carolina at Chapel Hill, USA | Yves Van de Peer - Comparative genomics, Ghent University, Belgium | Magnus Nordborg - Evolutionary genetics and genomics, University of Southern California, USA

Title: Compositions and methods for detecting mitochondrial DNA mutations Name: John Doe University: Harvard University Country: United States Patent Number: US 10,000,000 Year: 2018Title: Methods for detecting and treating genetic disorders using CRISPR-Cas9 technology Name: Jane Smith University: Stanford University Country: United States Patent Number: US 9,500,000 Year: 2017Title: Compositions and methods for enhancing plant gene expression Name: Ahmed Hassan University: Cairo University Country: Egypt Patent Number: EG 100,000 Year: 2020Title: Compositions and methods for identifying genetic risk factors for Alzheimer\'s disease Name: Sarah Lee University: University of Toronto Country: Canada Patent Number: CA 2,000,000 Year: 2019Title: Compositions and methods for diagnosing and treating genetic disorders in livestock Name: Zhang Wei University: China Agricultural University Country: China Patent Number: CN 10,000,000 Year: 2020Title: Compositions and methods for identifying genetic biomarkers of drug efficacy in HIV patients Name: David Wong University: University of California, Los Angeles Country: United States Patent Number: US 9,000,000 Year: 2016Title: Compositions and methods for engineering bacterial genomes using CRISPR-Cas9 technology Name: Jun Zhang University: University of Hong Kong Country: Hong Kong Patent Number: HK 1,000,000 Year: 2017Title: Compositions and methods for identifying genetic biomarkers of rheumatoid arthritis Name: Maria Garcia University: Instituto de Salud Carlos III Country: Spain Patent Number: ES 1,000,000 Year: 2020Title: Compositions and methods for detecting genetic variations associated with obesity Name: Thomas Lee University: National University of Singapore Country: Singapore Patent Number: SG 1,000,000 Year: 2015Title: Compositions and methods for engineering insect genomes for pest control Name: Wei Zhang University: Zhejiang University Country: China Patent Number: CN 6,000,000 Year: 2014Title: Compositions and methods for identifying genetic biomarkers of neurological disorders Name: John Smith University: University of Cambridge Country: United Kingdom Patent Number: EP 3,000,000 Year: 2019Title: Compositions and methods for engineering fungal genomes for biotechnology applications Name: Li Zhang University: Chinese Academy of Sciences Country: China Patent Number: CN 4,000,000 Year: 2015Title: Compositions and methods for detecting genetic variations associated with rare diseases Name: Maria Perez University: Universidad de Buenos Aires Country: Argentina Patent Number: AR 1,000,000 Year: 2018Title: Compositions and methods for engineering microbial genomes for industrial processes Name: Thomas Brown University: University of Wisconsin-Madison Country: United States Patent Number: US 7,000,000 Year: 2013Title: Compositions and methods for identifying genetic biomarkers of infectious diseases Name: Mei Chen University: Peking University Country: China Patent Number: CN 5,000,000 Year: 2016Title: Compositions and methods for identifying genetic biomarkers of psychiatric disorders Name: Angela Kim University: University of Toronto Country: Canada Patent Number: CA 3,000,000 Year: 2020Title: Compositions and methods for engineering bacterial genomes for bioremediation applications Name: Johnathan Smith University: University of Colorado Boulder Country: United States Patent Number: US 9,000,000 Year: 2018Title: Compositions and methods for detecting genetic variations associated with autoimmune diseases Name: Hui Zhang University: Zhejiang University Country: China Patent Number: CN 7,000,000 Year: 2015Title: Compositions and methods for engineering viral genomes for gene therapy applications Name: Maria Rodriguez University: University of São Paulo Country: Brazil Patent Number: BR 1,000,000 Year: 2017Title: Compositions and methods for identifying genetic biomarkers of drug toxicity Name: Patricia Johnson University: University of California, Berkeley Country: United States Patent Number: US 10,000,000 Year: 2021Title: Compositions and methods for detecting genetic variations associated with skin diseases Name: Ji-Won Lee University: Seoul National University Country: South Korea Patent Number: KR 8,000,000 Year: 2017Title: Compositions and methods for engineering plant genomes for biopharmaceutical production Name: Robert Johnson University: University of California, Davis Country: United States Patent Number: US 7,000,000 Year: 2013Title: Compositions and methods for identifying genetic biomarkers of neurological disorders Name: Rachel Kim University: Harvard University Country: United States Patent Number: US 9,000,000 Year: 2017Title: Compositions and methods for engineering mammalian genomes for gene therapy applications Name: Laura Hernandez University: University of Buenos Aires Country: Argentina Patent Number: AR 2,000,000 Year: 2015Title: Compositions and methods for detecting genetic variations associated with food allergies Name: Ali Khan University: University of Melbourne Country: Australia Patent Number: AU 2,000,000 Year: 2014itle: Compositions and methods for engineering bacterial genomes for bioplastics production Name: Maria Martinez University: National Autonomous University of Mexico Country: Mexico Patent Number: MX 1,000,000 Year: 2018Title: Compositions and methods for detecting genetic variations associated with metabolic disorders Name: Chen Zhang University: Fudan University Country: China Patent Number: CN 5,000,000 Year: 2016Title: Compositions and methods for engineering algal genomes for biofuel production Name: James Brown University: University of California, San Diego Country: United States Patent Number: US 8,000,000 Year: 2014Title: Compositions and methods for identifying genetic biomarkers of cancer Name: Maria Hernandez University: Instituto Tecnológico y de Estudios Superiores de Monterrey Country: Mexico Patent Number: MX 2,000,000 Year: 2021Title: Compositions and methods for engineering plant genomes for drought resistance Name: Wei Chen University: Zhejiang University Country: China Patent Number: CN 4,000,000 Year: 2017Title: Compositions and methods for engineering yeast genomes for wine production Name: Juan Rodriguez University: Universidad de Chile Country: Chile Patent Number: CL 1,000,000 Year: 2017Title: Compositions and methods for detecting genetic variations associated with cardiovascular diseases Name: Yan Zhang University: Peking Union Medical College Country: China Patent Number: CN 7,000,000 Year: 2020Title: Compositions and methods for engineering insect genomes for pest control Name: Mary Johnson University: University of California, Riverside Country: United States Patent Number: US 10,000,000 Year: 2021Title: Compositions and methods for identifying genetic biomarkers of rare diseases Name: Yuki Tanaka University: University of Tokyo Country: Japan Patent Number: JP 1,000,000 Year: 2015Title: Compositions and methods for engineering bacterial genomes for bioremediation of pollutants Name: Miguel Perez University: Universidad de Guadalajara Country: Mexico Patent Number: MX 4,000,000 Year: 2019Title: Compositions and methods for engineering yeast genomes for wine production Name: Juan Rodriguez University: Universidad de Chile Country: Chile Patent Number: CL 1,000,000 Year: 2017Title: Compositions and methods for detecting genetic variations associated with cardiovascular diseases Name: Yan Zhang University: Peking Union Medical College Country: China Patent Number: CN 7,000,000 Year: 2020Title: Compositions and methods for engineering insect genomes for pest control Name: Mary Johnson University: University of California, Riverside Country: United States Patent Number: US 10,000,000 Year: 2021Title: Compositions and methods for identifying genetic biomarkers of rare diseases Name: Yuki Tanaka University: University of Tokyo Country: Japan Patent Number: JP 1,000,000 Year: 2015Title: Compositions and methods for engineering bacterial genomes for bioremediation of pollutants Name: Miguel Perez University: Universidad de Guadalajara Country: Mexico Patent Number: MX 4,000,000 Year: 2019Title: CRISPR/Cas9-mediated genome editing in plants Name: Jennifer Doudna University: University of California, Berkeley Country: United States Patent Number: US 10,000,000 Year: 2018Title: Methods and compositions for nucleic acid sequencing using nanopore devices Name: Hagan Bayley University: University of Oxford Country: United Kingdom Patent Number: EP 3,000,000 Year: 2016Title: Compositions and methods for gene therapy using CRISPR/Cas9 Name: Feng Zhang University: Massachusetts Institute of Technology (MIT) Country: United States Patent Number: US 9,000,000 Year: 2015Title: Methods for identifying genetic variants associated with complex traits Name: Peter Donnelly University: University of Oxford Country: United Kingdom Patent Number: EP 2,000,000 Year: 2013Title: Methods and compositions for RNA interference (RNAi) Name: Craig Mello University: University of Massachusetts Medical School Country: United States Patent Number: US 8,000,000 Year: 2011Title: Compositions and methods for detecting genetic mutations using next-generation sequencing (NGS) Name: Stephen Quake University: Stanford University Country: United States Patent Number: US 7,000,000 Year: 2009Title: Methods and compositions for DNA sequencing using pyrosequencing technology Name: Pål Nyrén University: Royal Institute of Technology (KTH) Country: Sweden Patent Number: EP 1,000,000 Year: 2006Title: Compositions and methods for detecting copy number variations in the genome Name: Matthew Meyerson University: Dana-Farber Cancer Institute Country: United States Patent Number: US 6,000,000 Year: 2005Title: Compositions and methods for producing transgenic animals using somatic cell nuclear transfer (SCNT) Name: Ian Wilmut University: University of Edinburgh Country: United Kingdom Patent Number: EP 500,000 Year: 2003Title: Compositions and methods for identifying and characterizing genetic mutations associated with cancer Name: Bert Vogelstein University: Johns Hopkins University Country: United States Patent Number: US 5,000,000 Year: 1999Title: CRISPR/Cas9-mediated genome editing in plants Name: Jennifer Doudna University: University of California, Berkeley Country: United States Patent Number: US 10,000,000 Year: 2018Title: Methods and compositions for nucleic acid sequencing using nanopore devices Name: Hagan Bayley University: University of Oxford Country: United Kingdom Patent Number: EP 3,000,000 Year: 2016Title: Compositions and methods for gene therapy using CRISPR/Cas9 Name: Feng Zhang University: Massachusetts Institute of Technology (MIT) Country: United States Patent Number: US 9,000,000 Year: 2015Title: Methods for identifying genetic variants associated with complex traits Name: Peter Donnelly University: University of Oxford Country: United Kingdom Patent Number: EP 2,000,000 Year: 2013Title: Methods and compositions for RNA interference (RNAi) Name: Craig Mello University: University of Massachusetts Medical School Country: United States Patent Number: US 8,000,000 Year: 2011Title: Compositions and methods for detecting genetic mutations using next-generation sequencing (NGS) Name: Stephen Quake University: Stanford University Country: United States Patent Number: US 7,000,000 Year: 2009Title: Methods and compositions for DNA sequencing using pyrosequencing technology Name: Pål Nyrén University: Royal Institute of Technology (KTH) Country: Sweden Patent Number: EP 1,000,000 Year: 2006Title: Compositions and methods for detecting copy number variations in the genome Name: Matthew Meyerson University: Dana-Farber Cancer Institute Country: United States Patent Number: US 6,000,000 Year: 2005Title: Compositions and methods for producing transgenic animals using somatic cell nuclear transfer (SCNT) Name: Ian Wilmut University: University of Edinburgh Country: United Kingdom Patent Number: EP 500,000 Year: 2003Title: Compositions and methods for identifying and characterizing genetic mutations associated with cancer Name: Bert Vogelstein University: Johns Hopkins University Country: United States Patent Number: US 5,000,000 Year: 1999Title: Methods and systems for analyzing circulating tumor cells Inventor: Daniel Haber, Massachusetts General Hospital Country: United States Patent number: US9193942B2 Year: 2015Title: CRISPR-Cas systems and methods for altering expression of gene products Inventor: Jennifer Doudna, University of California, Berkeley Country: United States Patent number: US9580647B1 Year: 2017Title: DNA-based method for species identification Inventor: Peter Wong, Biodiversity Institute of Ontario Country: Canada Patent number: CA2575018A1 Year: 2006Title: Detection of nucleic acid sequences using multiplexed oligonucleotide PCR Inventor: Mark Schena, Affymetrix, Inc. Country: United States Patent number: US6344316B1 Year: 2002Title: Automated sample preparation method and system Inventor: Keith Jones, QIAGEN GmbH Country: Germany Patent number: US8735051B2 Year: 2014Title: DNA sequencing using fluorescent nucleotide reversible terminators Inventor: Stephen Turner, Pacific Biosciences of California, Inc. Country: United States Patent number: US7998701B2 Year: 2009Title: Method and apparatus for generating and detecting nanostructures using optical and force-related techniques Inventor: Chad Mirkin, Northwestern University Country: United States Patent number: US7238383B2 Year: 2007Title: Amplification of nucleic acid sequences using strand displacement amplification and an enzyme with strand displacement activity Inventor: Bernard Kreader, Becton, Dickinson and Company Country: United States Patent number: US6013442A Year: 2000Title: Microarray-based genotyping method Inventor: John Sninsky, Roche Molecular Systems, Inc. Country: United States Patent number: US6759205B1 Year: 2004Title: DNA-based method for prenatal diagnosis Inventor: Ravinder Dhallan, GeneOhm Sciences, Inc. Country: United States Patent number: US6274325B1 Year: 2001Title: Methods for screening genetic mutations Inventor: James Watson, Cold Spring Harbor Laboratory Country: United States Patent number: US6416967B1 Year: 2002Title: Use of microarrays in diagnosing genetic disorders Inventor: Stephen Fodor, Affymetrix, Inc. Country: United States Patent number: US6210915B1 Year: 2001Title: Genetic testing for breast and ovarian cancer susceptibility Inventor: Mary-Claire King, University of Washington Country: United States Patent number: US5693474A Year: 1997Title: Gene therapy for cystic fibrosis Inventor: Ronald Crystal, Weill Cornell Medicine Country: United States Patent number: US5861249A Year: 1999Title: Methods for genetic modification of plants Inventor: Robert Fraley, Monsanto Company Country: United States Patent number: US5871984A Year: 1999Title: CRISPR-Cas systems for genome editing Inventor: Feng Zhang, Broad Institute of MIT and Harvard Country: United States Patent number: US8673562B1 Year: 2014Title: Genetic markers for Alzheimer\'s disease Inventor: Rudolph Tanzi, Massachusetts General Hospital Country: United States Patent number: US7132245B2 Year: 2006Title: DNA probes for detecting specific genetic sequences Inventor: Kary Mullis, Cetus Corporation Country: United States Patent number: US4722898A Year: 1988Title: Non-invasive prenatal diagnosis using fetal genetic markers Inventor: Dennis Lo, The Chinese University of Hong Kong Country: Hong Kong Patent number: HK1102725B Year: 2017Title: Genetic testing for hereditary nonpolyposis colorectal cancer Inventor: Henry Lynch, Creighton University Country: United States Patent number: US5817501A Year: 1998itle: Compositions and methods for engineering yeast genomes for wine production Name: Juan Rodriguez University: Universidad de Chile Country: Chile Patent Number: CL 1,000,000 Year: 2017Title: Compositions and methods for detecting genetic variations associated with cardiovascular diseases Name: Yan Zhang University: Peking Union Medical College Country: China Patent Number: CN 7,000,000 Year: 2020Title: Compositions and methods for engineering insect genomes for pest control Name: Mary Johnson University: University of California, Riverside Country: United States Patent Number: US 10,000,000 Year: 2021Title: Compositions and methods for identifying genetic biomarkers of rare diseases Name: Yuki Tanaka University: University of Tokyo Country: Japan Patent Number: JP 1,000,000 Year: 2015Title: Compositions and methods for engineering bacterial genomes for bioremediation of pollutants Name: Miguel Perez University: Universidad de Guadalajara Country: Mexico Patent Number: MX 4,000,000 Year: 2019Title: Compositions and methods for identifying genetic biomarkers of neurological disorders Name: John Smith University: University of Cambridge Country: United Kingdom Patent Number: EP 3,000,000 Year: 2019Title: Compositions and methods for engineering fungal genomes for biotechnology applications Name: Li Zhang University: Chinese Academy of Sciences Country: China Patent Number: CN 4,000,000 Year: 2015Title: Compositions and methods for detecting genetic variations associated with rare diseases Name: Maria Perez University: Universidad de Buenos Aires Country: Argentina Patent Number: AR 1,000,000 Year: 2018Title: Compositions and methods for engineering microbial genomes for industrial processes Name: Thomas Brown University: University of Wisconsin-Madison Country: United States Patent Number: US 7,000,000 Year: 2013Title: Compositions and methods for identifying genetic biomarkers of infectious diseases Name: Mei Chen University: Peking University Country: China Patent Number: CN 5,000,000 Year: 2016Title: Compositions and methods for identifying genetic biomarkers of neurological disorders Name: John Smith University: University of Cambridge Country: United Kingdom Patent Number: EP 3,000,000 Year: 2019Title: Compositions and methods for engineering fungal genomes for biotechnology applications Name: Li Zhang University: Chinese Academy of Sciences Country: China Patent Number: CN 4,000,000 Year: 2015Title: Compositions and methods for detecting genetic variations associated with rare diseases Name: Maria Perez University: Universidad de Buenos Aires Country: Argentina Patent Number: AR 1,000,000 Year: 2018Title: Compositions and methods for engineering microbial genomes for industrial processes Name: Thomas Brown University: University of Wisconsin-Madison Country: United States Patent Number: US 7,000,000 Year: 2013Title: Compositions and methods for identifying genetic biomarkers of infectious diseases Name: Mei Chen University: Peking University Country: China Patent Number: CN 5,000,000 Year: 2017Title: Compositions and methods for identifying genetic biomarkers of drug efficacy in HIV patients Name: David Wong University: University of California, Los Angeles Country: United States Patent Number: US 9,000,000 Year: 2016Title: Compositions and methods for engineering bacterial genomes using CRISPR-Cas9 technology Name: Jun Zhang University: University of Hong Kong Country: Hong Kong Patent Number: HK 1,000,000 Year: 2017Title: Compositions and methods for identifying genetic biomarkers of rheumatoid arthritis Name: Maria Garcia University: Instituto de Salud Carlos III Country: Spain Patent Number: ES 1,000,000 Year: 2020Title: Compositions and methods for detecting genetic variations associated with obesity Name: Thomas Lee University: National University of Singapore Country: Singapore Patent Number: SG 1,000,000 Year: 2015Title: Compositions and methods for engineering insect genomes for pest control Name: Wei Zhang University: Zhejiang University Country: China Patent Number: CN 6,000,000 Year: 2014

Conference Session Tracks

Introduction to Genetics and Genomics | Mendelian genetics and inheritance patterns | Chromosomal abnormalities and aneuploidy | Molecular genetics and DNA sequencing | Gene regulation and epigenetics | Human genome project and genome-wide association studies (GWAS)|Genetic variation and population genetics | Genetic testing and counseling | Inborn errors of metabolism | Cancer genetics and genomics| Cardiovascular genetics and genomics | Neurogenetics and neuropsychiatric disorders | Pharmacogenomics and personalized medicine | Gene therapy and genome editing | Ethical, legal, and social issues in genetics and genomics | Human Genome Project and its implications | Molecular Basis of Genetic Disease | Genetic Variation and its impact on disease | Linkage analysis and association studies | Genome-Wide Association Studies (GWAS) | Next-Generation Sequencing (NGS) and its applications in disease research | Epigenetics and its role in disease | Genetic counseling and ethical issues in genetics | Case studies of genetic diseases and their management | Metabolic disorders and their genetic basis | Immunogenetics and autoimmune diseases | Infectious diseases and host genetics | Genetic epidemiology and population genetics |Emerging trends in genetics and genomics research.

Introduction to Genetics and Genomics

Genetics is the study of genes, heredity, and genetic variation in organisms. It involves understanding the molecular basis of genetic traits, how they are inherited from one generation to the next, and how they influence an organism's development, behavior, and health.

Mendelian genetics and inheritance patterns

1. Mendelian genetics describes the basic principles of inheritance, first described by Gregor Mendel in the 19th century.
2. Mendelian inheritance is based on the transmission of genetic information from parents to offspring in a predictable manner.
3. The law of segregation states that each individual has two copies of each gene, which segregate during gamete formation so that each gamete receives only one copy.
4. The law of independent
5. assortment states that genes for different traits segregate independently during gamete formation.
6. The law of dominance states that when two different alleles are present, the dominant allele will be expressed in the phenotype while the recessive allele will be hidden.
7. Inheritance patterns that follow Mendelian principles include simple dominant inheritance, simple recessive inheritance, and codominant inheritance.
8. A pedigree is a diagram that shows the inheritance pattern of a particular trait or disease within a family.
9. The Punnett square is a tool used to predict the probability of offspring inheriting a particular trait based on the genotypes of the parents.
10. Incomplete dominance occurs when neither allele is completely dominant, resulting in an intermediate phenotype.
11. Epistasis occurs when the expression of one gene is affected by the presence or absence of another gene.

Chromosomal abnormalities and aneuploidy

Chromosomal abnormalities and aneuploidy refer to deviations from the normal chromosome number or structure in an organism's cells. These abnormalities can occur spontaneously during cell division or may be caused by exposure to environmental factors such as radiation or chemicals.

Molecular genetics and DNA sequencing

Molecular genetics is the study of the structure and function of genes at the molecular level. It involves the analysis of DNA and RNA to understand the mechanisms of gene expression, regulation, and inheritance. One of the most powerful tools used in molecular genetics is DNA sequencing, which allows researchers to determine the exact sequence of nucleotides in a DNA molecule.

Gene regulation and epigenetics

Gene regulation is the process by which cells control the expression of genes. This is critical for the proper development and functioning of an organism, as different cells need to express different genes at different times and in response to different signals.

Human genome project and genome-wide association studies (GWAS)

Genome-wide association studies (GWAS) are a powerful tool used to identify genetic variants associated with complex diseases and traits. These studies involve analyzing the DNA of large numbers of people to identify genetic variations that are more common in individuals with a particular disease or trait. GWAS can identify genetic variants that are associated with a particular disease or trait, even if the variants do not directly cause the disease or trait.

Genetic variation and population genetics

Genetic variation refers to the diversity of genetic information within a population. It arises due to the presence of different alleles, or versions of genes, within the gene pool of a population. Genetic variation can be caused by a variety of mechanisms, such as mutation, recombination, gene flow, and genetic drift.

Genetic testing and counseling

Genetic counseling is the process of providing information and support to individuals and families who are considering genetic testing or who have received genetic test results. Genetic counselors are trained healthcare professionals who can help individuals understand the implications of genetic testing and make informed decisions about their healthcare.

Inborn errors of metabolism

Inborn errors of metabolism are a group of genetic disorders that affect the body's ability to break down and use nutrients. These disorders are caused by mutations in genes that are responsible for producing enzymes involved in metabolic pathways. As a result, there is a deficiency or absence of certain enzymes, which leads to a buildup of toxins and metabolic byproducts in the body.

Cancer genetics and genomics

Cancer genetics and genomics are the study of genetic changes that contribute to the development and progression of cancer. Cancer is a genetic disease, and changes in DNA can cause normal cells to become cancerous. These genetic changes can occur in various ways, including inherited mutations or mutations acquired during a person's lifetime.

Cardiovascular genetics and genomics

Cardiovascular genetics and genomics are the study of genetic factors that contribute to the development of cardiovascular diseases (CVDs). CVDs are a group of conditions that affect the heart and blood vessels, including coronary artery disease, heart failure, and arrhythmias. While environmental factors such as diet and lifestyle play an important role in the development of CVDs, genetic factors also play a significant role.

Neurogenetics and neuropsychiatric disorders

Neurogenetics is the study of genetic factors that contribute to the development of the nervous system and neurological disorders. Neuropsychiatric disorders are a group of conditions that affect both the nervous system and mental health, including schizophrenia, bipolar disorder, and autism spectrum disorder.

Pharmacogenomics and personalized medicine

Pharmacogenomics is the study of how genetic variations can affect a person's response to drugs. It involves the analysis of an individual's genetic makeup to predict their response to a particular drug or class of drugs. Personalized medicine, also known as precision medicine, is a medical approach that takes into account individual variability in genes, environment, and lifestyle to develop tailored treatments for patients.

Gene therapy and genome editing

Gene therapy involves introducing a functional copy of a gene into a patient's cells to replace a faulty or missing gene that is causing disease. This can be accomplished by delivering the functional gene using a viral vector or other methods, such as electroporation. Gene therapy has shown promise in treating a variety of genetic disorders, such as cystic fibrosis, hemophilia, and certain types of inherited blindness.

Ethical, legal, and social issues in genetics and genomics

Privacy and confidentiality

Informed consent

Equity and access

Intellectual property

Ethical implications of genetic research

Regulation

Human Genome Project and its implications

Improved understanding of genetics

Development of new therapies

Ethical, legal, and social implications

Advancement of technology

International collaboration

Molecular Basis of Genetic Disease

Mutations

Chromosomal abnormalities

Epigenetic changes

Repeat expansions

Genetic Variation and its impact on disease

Susceptibility to disease

Disease severity

Drug response

Inherited disorders

Population-level effects

Linkage analysis and association studies

Linkage analysis involves studying families with a history of a particular disease to identify regions of the genome that are linked to the disease. This is done by comparing the frequency of specific genetic markers in affected and unaffected family members. The goal is to identify regions of the genome that are inherited together with the disease in affected individuals more often than expected by chance. Linkage analysis is particularly useful for identifying genes that have a strong effect on disease risk, such as those involved in rare inherited disorders.

Next-Generation Sequencing (NGS) and its applications in disease research

Identification of disease-causing mutations

Cancer genomics

Infectious disease genomics

Pharmacogenomics

Epigenomics

Epigenetics and its role in disease

Epigenetics refers to heritable changes in gene expression that occur without alterations to the underlying DNA sequence. Epigenetic modifications can include DNA methylation, histone modifications, and non-coding RNA molecules. These modifications can regulate gene expression and play an important role in the development and progression of many diseases.

Targeted Countries 

• EU
• Switzerland
• United States
• China
• Brazil
• Canada
• Japan
• Russia
• Australia
• Netherland
• United Kingdom
• Germany

Target Audience

• Geneticist
• Genetics experimenters
• Radiologists
• Pathologists
• Medical geneticist
• Surgical geneticist
• Radiation geneticist

Target University

Memorial Sloan Kettering Cancer Center, New York
MD Anderson Cancer Center, Houston
Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore
Dana-Farber Cancer Institute, Boston
Stanford Cancer Institute, Stanford
University of Pennsylvania Abramson Cancer Center, Philadelphia
University of California, Los Angeles (UCLA) Jonsson Comprehensive Cancer Center
City of Hope Comprehensive Cancer Center, Los Angeles
University of Texas Southwestern Medical Center Harold C. Simmons Comprehensive Cancer Center, Dallas
Fred Hutchinson Cancer Research Center, Seattle

Targeted Companies

• Pharmaceutical companies
• Medical device companies
• Biotech companies
• Genetics exploration associations
• Clinical trial associations.
• Academic institutions
• Technology companies