Sidra Batool | DNA Sequencing | Women Researcher Award 

Dr. Sidra Batool | DNA Sequencing | Women Researcher Award 

Abdul Wali Khan University Mardan | Pakistan

Author Profile

Scopus 

📜 SIDRA BATOOL: A DEDICATED RESEARCHER AND LEADER

🎓 EARLY ACADEMIC PURSUITS

Sidra Batool, born on January 30, 1997, in Kohat, Khyber Pakhtunkhwa, Pakistan, has pursued a solid academic career. She completed her Matriculation in 2014 with an A1 grade from the BISE Kohat. Continuing her journey, she earned her Intermediate qualification in 2016, achieving an A grade from the BISE Kohat. Her academic foundation, especially in sciences, laid the groundwork for her future research endeavors.

💼 PROFESSIONAL ENDEAVORS

Sidra has demonstrated a diverse range of experiences across academia and business. She has worked as a Research Assistant under Prof. Dr. Sadaf Niaz in the Department of Zoology at Abdul Wali Khan University Mardan. Her key responsibilities included conducting Field Surveys, performing DNA Extraction, PCR Sequencing, and Bioinformatics Analysis. This hands-on experience with advanced laboratory techniques enabled her to contribute significantly to the understanding of tick infestations and related biosecurity measures.

🔬 CONTRIBUTIONS AND RESEARCH FOCUS ON DNA SEQUENCING

Sidra’s primary research focuses on molecular biology, toxicology, and bioinformatics. Her work emphasizes the taxonomic and molecular characterization of ticks, along with the ecological impacts of various species on livestock. This research is crucial for understanding and controlling tick-borne diseases, especially in rural and under-researched regions of Pakistan. She is proficient in a variety of advanced laboratory techniques, including DNA Extraction, Gel Electrophoresis, PCR, and bioinformatics tools like R Programming, Python, BioEdit, and BEAST. Sidra has also made notable contributions to genomic databases, with several GenBank submissions to her credit, such as OR665376.1, PP565365.1, and PP477083.1.

🌍 IMPACT AND INFLUENCE

Sidra’s research has a direct impact on the field of zoology, particularly in understanding tick infestations and improving livestock health in Pakistan. Her work contributes to sustainable livestock management, helping rural communities mitigate the risks posed by pathogens. Her technical expertise in bioinformatics and molecular biology enables her to explore the genomics of species that directly affect public health and the agricultural economy. Additionally, Sidra’s leadership qualities are evident as she currently manages a team of four, further solidifying her role as a guide and mentor for younger researchers.

🏅 ACADEMIC CITES

Sidra Batool has already started to make her mark in the academic world, with her work receiving citations across various research publications and genomic repositories. Her GenBank submissions and collaborative research papers reflect her growing academic influence. Her participation in conferences and seminars has allowed her to present her findings on a national level, further expanding her recognition in the scientific community.

🏛️ LEGACY AND FUTURE CONTRIBUTIONS

Sidra’s legacy will be defined by her commitment to molecular biology and her efforts to advance research in tick-borne diseases, biosecurity, and ecological conservation. As a young researcher, her potential for contributing to both academic and practical solutions in the field of zoology is immense. In the future, Sidra aspires to expand her research beyond the borders of Pakistan, focusing on international collaborations that address global challenges in zoonotic diseases and biosecurity. With her solid academic background, practical experience, and leadership qualities, she is well-positioned to contribute to global scientific advancements.

✨ PERSONAL SKILLS AND ACHIEVEMENTS

Sidra is proficient in multiple languages, including Pashto, Urdu, and English. Her strong communication skills, both in written and spoken formats, complement her ability to present complex scientific data clearly. She has also garnered a fully funded scholarship through the Ehsaas Undergraduate Scholarship Program for her bachelor’s studies, underscoring her academic excellence. Sidra’s diverse skill set extends to computational tools, where she excels in software like Microsoft Office, FinchTV, Latex, Mesquite, and Figtree, adding value to her research in bioinformatics and computational biology.

📑NOTABLE PUBLICATIONS 

“Infestation prevalence, spatio-temporal distribution, phylogenetic positioning, and pathogen investigation of Argas persicus ticks in domestic hens (Gallus gallus domesticus) from Pakistan” 

  • Authors: Tsai, K.-H., Batool, S., Khan, A.,  Ben Said, M., Khan, A.
  • Journal: Veterinary Parasitology
  • Year: 2024

Giulia Pascolini | Neurodevelopmental Disorders | Best Researcher Award 

Dr. Giulia Pascolini | Neurodevelopmental Disorders | Best Researcher Award 

Dermopathic Institute of the Immaculate, IDI-IRCC | Italy 

Author Profile

Scopus 

Orcid ID

Google Scholar

🌟 Biography of Giulia Pascolini, MD, PhD

🎓 EARLY ACADEMIC PURSUITS

Giulia Pascolini's journey in medical science began with a Degree in Medicine from Sapienza University of Rome in 2008, which she completed with honors. Following this, she pursued specialization in Medical Genetics at Tor Vergata University of Rome, graduating with honors in 2015 after five years of in-depth study. Driven by her passion for genetics, Dr. Pascolini went on to earn her Ph.D. in Medical Genetics from Sapienza University in 2019, establishing her expertise in a rapidly advancing field. In 2022, she further expanded her knowledge with a Master of II level in Rare Diseases, also from Sapienza University, solidifying her role as a leading expert in rare genetic disorders.

🩺 PROFESSIONAL ENDEAVORS

Dr. Pascolini's professional career is marked by extensive experience across multiple prestigious institutions. Currently, she is a Clinical Geneticist and head of the Clinical Genetics Service at the Istituto Dermopatico dell'Immacolata (IDI-IRCCS) in Rome, Italy. Since September 2023, she also holds a position as Professor of Medical Genetics at the Faculty of Medicine and Surgery at Tor Vergata University of Rome. Over the years, she has held various roles, including serving as a clinical geneticist at Bambino Gesù Children’s Hospital and a researcher at San Camillo-Forlanini Hospital. Her long-standing commitment to clinical genetics spans over 15 years, with a focus on intellectual disability syndromes, dysmorphology, and developmental disorders.

🔬 CONTRIBUTIONS AND RESEARCH FOCUS ON NEURODEVELOPMENTAL DISORDERS 

Dr. Pascolini's research primarily centers around Developmental Disorders of Chromatin Remodeling (DDCRs), intellectual disability (ID) syndromes, and genodermatoses. She has played a crucial role in the study of the skin phenotype in rare genetic diseases, and her work on deep learning technologies for diagnosing genetic syndromes using facial phenotype recognition is groundbreaking. Her involvement with FDNA Inc. and the DeepGestalt technology is a testament to her contributions to advancing medical genetics through innovative platforms. She is also a principal investigator for multiple research projects, including studies on rare cutaneous tumors and familial melanoma, with funding of over €47,000 for these projects.

🌍 IMPACT AND INFLUENCE

As a Scientific Board Member of the ADNP Syndrome Italian Association and an editorial board member of the Journal of Pediatric Genetics, Dr. Pascolini has made significant contributions to the broader medical community. Her work has helped shape new approaches to the clinical understanding of complex genetic disorders, particularly in rare diseases and neurodevelopmental syndromes. Through her collaborative efforts with international organizations and her academic roles, she continues to influence both current medical practices and future research directions.

📚 ACADEMIC CITES AND PUBLICATIONS

Dr. Pascolini has authored several impactful works, including her involvement in the DeepGestalt technology article on SETD5-associated intellectual disability published in the Journal of Translational Genetics and Genomics. Her contributions to book chapters, such as her writing on Genomic Copy Number Variants (CNVs) and Autism Spectrum Disorder (ASD), have added substantial value to academic literature. Her expertise has also been recognized through invitations to write for special issues in leading journals, enhancing her standing as a key voice in her field.

🏅 AWARDS AND RECOGNITION

In 2019, Dr. Pascolini was awarded the Franca Dagna Bricarelli Award for her clinical research on genetic mutations associated with the BAF complex. This prestigious award highlights her excellence in medical genetics and clinical research. Her contributions to the field, recognized by peers and institutions alike, reflect her profound impact on the study and treatment of genetic disorders.

🌟 LEGACY AND FUTURE CONTRIBUTIONS

With her leadership in clinical genetics, active research on rare skin diseases, and innovative work in genetic syndrome diagnostics, Dr. Pascolini is poised to continue shaping the future of medical genetics. Her contributions to understanding the genetic basis of intellectual disabilities and her work on cutting-edge diagnostic technologies ensure her legacy as a pioneering figure in genetics. As she continues her role in both clinical and academic settings, her future contributions will likely further advance the study and treatment of rare genetic conditions, helping countless individuals worldwide.

📑NOTABLE PUBLICATIONS 

"The face of Non-photosensitive trichothiodystrophy phenotypic spectrum: A subsequent study on paediatric population" 

  • Authors: Pascolini, G. , Lipari, M. , Gaudioso, F. , Di Zenzo, G. , Didona, B.
  • Journal: Molecular Genetics and Genomic Medicine
  • Year: 2024

"Usmani-Riazuddin syndrome can have a recognizable phenotype: Report of a novel AP1G1 variant" 

  • Authors: Gnazzo, M. , Pascolini, G. , Parlapiano, G. , Novelli, A. , Baban, A.
  • Journal: Clinical Genetics
  • Year: 2024

"Extended phenotypic characterization of a novel Helsmoortel-van der Aa syndrome case series" 

  • Authors: Pascolini, G., Di Zenzo, G., Panebianco, A., Didona, B., Gozes, I.
  • Journal: American Journal of Medical Genetics
  • Year: 2024

"Ectoderm-derived findings in Aymè-Gripp syndrome" 

  • Authors: Pascolini, G., Di Zenzo, G., Morani, P., Didona, B., Panebianco, A.
  • Journal: Journal of Dermatology
  • Year: 2024

"Defining the clinical spectrum of ichthyosis follicularis, atrichia and photophobia clinical association type 1 (IFAP1)" 

  • Authors: Pascolini, G., Fortugno, P., Chandramouli, B., Didona, B., Castiglia, D.
  • Journal: European Journal of Dermatology
  • Year: 2023