Zhe Zhang | Cardiovascular Genetics | Outstanding Scientist Award

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Dr. Zhe Zhang | Cardiovascular Genetics | Outstanding Scientist Award

Zhuhai People’s Hospital | China

Dr. Zhe Zhang, MD, PhD, is a distinguished Chinese physician–scientist and attending cardiologist at the Department of Cardiology, Zhuhai People’s Hospital, where she also serves as an associate researcher. Trained at Xi’an Jiaotong University School of Medicine, she holds a PhD in Cardiology along with advanced degrees in medical imaging, nuclear medicine, and clinical medicine. Dr. Zhang’s research centers on cardiovascular genetics and the genomics of diseases, integrating clinical cardiology with whole-genome sequencing, single-cell RNA sequencing, and multi-omics approaches to uncover molecular mechanisms underlying congenital and inherited heart diseases. She has authored influential publications in leading journals such as Scientific Data, Cell Reports, and Clinical and Translational Medicine, and has contributed valuable public genomic datasets to the global research community. Her translational work effectively bridges experimental genomics and clinically relevant cardiovascular phenotypes, positioning her as a strong candidate for the Outstanding Scientist Award.

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Abdul Karim Khalid | Host Genetics | Best Paper Award

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Mr. Abdul Karim Khalid | Host Genetics | Best Paper Award

Huazhong Agricultural University | China

Abdul Karim Khalid is a veterinary researcher specializing in preventive veterinary medicine, microbial pathogenesis, and host–microbe interactions, currently based in Wuhan, China. He earned his Master’s degree in Preventive Veterinary Medicine from Huazhong Agricultural University with a strong academic record, where his thesis focused on elucidating the role of the secreted protein MbovP537 as a virulence factor and diagnostic antigen in Mycoplasma bovis pathogenesis. His research integrates molecular microbiology, immunology, and translational One Health approaches, encompassing gene cloning, protein expression, mammalian cell culture, and advanced immunological assays. Abdul has contributed to multiple high-impact peer-reviewed publications in journals such as Veterinary Microbiology, eLife, Cells, and Frontiers in Immunology. He also holds a Doctor of Veterinary Medicine degree from Gomal University, Pakistan, and brings valuable clinical experience alongside strong bioinformatics and statistical analysis skills.

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Harshitha Dudipala | Cancer Genetics | Research Excellence Award

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Dr. Harshitha Dudipala | Cancer Genetics | Research Excellence Award

University of California San Diego | United States

Dr. Harshitha R. Dudipala, MD, is a board-certified physician in Internal Medicine and a highly accomplished Hematology & Oncology Fellow at the University of California, San Diego (Moores Cancer Center), with fellowship completion expected. She completed her Internal Medicine residency at Boston University Medical Center and earned her MD from Northeast Ohio Medical University, following a BS in Natural Sciences from the University of Akron. Dr. Dudipala has an extensive research portfolio spanning genitourinary oncology, lung cancer, immunotherapy biomarkers, molecular profiling, health disparities, and quality improvement, with multiple peer-reviewed publications in high-impact journals and presentations at ASCO, EACR, AAMC, and AMA. Her work has been featured in ASCO Daily News, and she has received numerous honors, including the Alice Jacobs Citizenship Award. An active leader and educator, she holds key roles in fellowship wellness, women in medicine, medical education, advocacy, and community health, reflecting a career dedicated to academic excellence, equity in cancer care, and physician leadership.

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Helala AlShehri | Cancer Genetics | Research Excellence Award

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Assist. Prof. Dr. Helala AlShehri | Cancer Genetics | Research Excellence Award

Jubail Industrial College | Saudi Arabia

Assist. Prof. Dr. Helala Mohammad AlShehri is an Assistant Professor of Computer Science and Deputy for Planning and Development at Jubail Industrial College, Saudi Arabia. She earned her PhD in Computer Science from King Saud University and brings together strong academic leadership with advanced research expertise in artificial intelligence and deep learning. Dr. AlShehri has held several senior administrative roles, including department chair and head of student and academic affairs, contributing significantly to institutional planning, quality assurance, and academic accreditation. Her research focuses on AI-driven medical image analysis, particularly histopathological image classification for cancer diagnosis, explainable AI, and computer-aided decision support. She has published nine peer-reviewed articles in SCI- and Scopus-indexed journals, with over 140 citations. Dr. AlShehri actively collaborates with national and international researchers and serves as a peer reviewer for leading AI and medical imaging journals.

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Jacob Raber | Cancer Genetics | Research Excellence Award

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Prof. Jacob Raber | Cancer Genetics | Research Excellence Award

OHSU | United States

Prof. Jacob Raber, Ph.D., is a distinguished Professor with interdisciplinary expertise spanning Behavioral Neuroscience, Neurology, Psychiatry, and Radiation Medicine. He serves as an Affiliated Scientist in the Division of Neuroscience at the Oregon National Primate Research Center (ONPRC), Oregon Health & Science University (OHSU), and holds a courtesy appointment as Professor of Pharmaceutical Sciences at Oregon State University. Dr. Raber earned his BSc in Chemistry and MSc in Pharmacochemistry from the Free University of Amsterdam, where his early research focused on β2-adrenergic receptor desensitization, complemented by training in immunochemistry and Yiddish language and literature. He completed his Ph.D. in Molecular Genetics and Virology at the Weizmann Institute of Science in Israel, investigating interferon-regulated pathways under the mentorship of Dr. Michel Revel. His work integrates molecular genetics with translational neuroscience to advance understanding of brain function and disease.

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William Hanna Kutteh | Chromosomal Abnormalities | Excellence in Research 

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Prof Dr. William Hanna Kutteh | Chromosomal Abnormalities | Excellence in Research 

University of Tennessee HSC and Baptist Women's Hospital | Unites States

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🌟 Biography of William Hanna Kutteh, MD, PhD, HCLD, CC 🌟

William Hanna Kutteh is a distinguished physician, scientist, and educator with an exceptional career in reproductive endocrinology, obstetrics, and gynecology. His contributions span across academic research, clinical excellence, and education, solidifying his legacy as a pioneer in reproductive health.

🏛️ EARLY ACADEMIC PURSUITS

William Hanna Kutteh embarked on his academic journey at Wake Forest University, earning a Bachelor of Arts in Biology with a minor in Chemistry (1971-1975). His keen interest in immunology led him to pursue graduate studies at Duke University, where he took advanced courses in immunology under the mentorship of Dr. Jeff Dawson (1975-1978).

He furthered his research with a Ph.D. in Molecular Cell Biology and Immunology from the University of Alabama at Birmingham (1978-1981), mentored by Dr. Jiri Mestecky. Following this, he achieved his MD at the Wake Forest University School of Medicine (1981-1985).

🩺 PROFESSIONAL ENDEAVORS

Key Positions

Dr. Kutteh has held prominent positions across leading institutions:

  • Founding Partner & Director at the Fertility Associates of Memphis
  • Professor of Obstetrics and Gynecology, University of Tennessee Health Sciences Center
  • Clinical Professor, Vanderbilt University Medical Center
  • Consulting Gynecologist, St. Jude Children’s Research Hospital, where he founded the Fertility Preservation Program

Special Roles

  • Director of Reproductive Endocrinology and Infertility at Baptist Memorial Hospital
  • Director of Resident Research Program, fostering the next generation of reproductive specialists
  • Director of EMIGS Simulation Training, advancing minimally invasive gynecologic surgery training

🔬 CONTRIBUTIONS AND RESEARCH FOCUS ON CHROMOSOMAL ABNORMALITIES

Dr. Kutteh’s research encompasses:

  1. Reproductive Immunology: Exploring immunological causes of recurrent pregnancy loss.
  2. Fertility Preservation: Pioneering techniques for cancer patients.
  3. Endocrine Disorders: Advancing treatments in reproductive endocrinology and infertility.
  4. Minimally Invasive Surgery: Innovating gynecological surgical techniques.

His dedication to translational medicine bridges the gap between laboratory research and clinical application, improving patient outcomes.

🌍 IMPACT AND INFLUENCE

Dr. Kutteh has significantly impacted:

  • Patient Care: As a reproductive endocrinologist, he has transformed the lives of countless families.
  • Medical Education: Training residents and fellows in cutting-edge reproductive techniques.
  • Research: Leading groundbreaking studies funded by the NIH, such as a prestigious R01 grant from the National Institutes of Child Health and Human Development (1995-1999).

📚 ACADEMIC CITATIONS

Dr. Kutteh's scholarly contributions include:

  • Numerous peer-reviewed publications in high-impact journals.
  • Regular faculty roles at national and international conferences such as ASRM, ESHRE, and FASEB, where his expertise in early pregnancy and immunology is widely sought after.
  • Recognition by Newsweek and US News & World Report as one of the top reproductive endocrinologists in America.

🏅 HONORS AND AWARDS

Dr. Kutteh's accolades include:

  • America’s Top Doctors by Castle Connolly (1996-2022)
  • Top Reproductive Endocrinologist by US News & World Report (2012)
  • Louie C. Henry Faculty Award for excellence in clinical teaching (2024)

He has also received numerous Sigma Xi Research Awards and service awards from professional societies, such as the American Society for Reproductive Medicine (ASRM).

💡 LEGACY AND FUTURE CONTRIBUTIONS

Dr. Kutteh’s legacy is marked by his dual commitment to advancing reproductive medicine and mentoring future leaders in the field. His ongoing work in fertility preservation, reproductive immunology, and minimally invasive surgery ensures his enduring influence.

As a visionary, he continues to push the boundaries of reproductive health through research, innovation, and education, shaping a brighter future for patients and practitioners alike.

📑NOTABLE PUBLICATIONS 

"Response: Would surgical retrieval of product of conception for the purpose of genetic analysis increase the risk of intra uterine adhesions?" 

  • Authors: Kutteh, W.H. , Maisenbacher, M. , Dahdouh, E.M.
  • Journal: Reproductive BioMedicine Online
  • Year: 2024

"Cell-Free DNA Analysis of Fetal Aneuploidies in Early Pregnancy Loss" 

  • Authors: Kutteh, W.H. , Miller, C.E. , Park, J.K. , Bhatt, S. , Keefe, D.L.
  • Journal: Journal of Clinical Medicine
  • Year: 2024

"Role of genetic analysis of products of conception and PGT in managing early pregnancy loss" 

  • Authors: Kutteh, W.H. , Papas, R.S. , Maisenbacher, M.K. , Dahdouh, E.M.
  • Journal: Reproductive BioMedicine Online
  • Year: 2024

"Expanding the role of chromosomal microarray analysis in the evaluation of recurrent pregnancy loss" 

  • Authors: Eliwa, J. , Papas, R.S. , Kutteh, W.H.
  • Journal: Journal of Reproductive Immunology
  • Year: 2024

"Is it time for new guidelines for recurrent pregnancy loss integrating genetic testing of products of conception and preimplantation genetic testing?" 

  • Authors: Kutteh, W.H. , Papas, R.S. , Dahdouh, E.M.
  • Journal: Fertility and Sterility
  • Year: 2024

Sami Nassar | Cancer Genetics and Genomics | Best Researcher Award

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Dr. Sami Nassar | Cancer Genetics and Genomics | Best Researcher Award

Medical University of South Carolina | United States

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🌟 SAMI I. NASSAR: A DEDICATED JOURNEY IN MEDICINE AND RESEARCH

EARLY ACADEMIC PURSUITS 🎓

Sami I. Nassar began his academic journey at Columbia University, where he majored in Neuroscience and Behavior, graduating Cum Laude in 2019 with an impressive GPA of 3.94/4.00. His academic excellence earned him a place in the Psi Chi International Honor Society in Psychology for his outstanding achievements. This strong foundation in neuroscience laid the groundwork for his future medical career. He is currently pursuing his MD at Wayne State University, School of Medicine, where he is on track to graduate in June 2024, having achieved a Step 2 Score of 258—a testament to his dedication to medical excellence.

PROFESSIONAL ENDEAVORS 👨‍⚕️

Throughout his career, Nassar has actively engaged in clinical and research positions across prestigious institutions. His experience as a Research Fellow at the Medical University of South Carolina since 2024 has enabled him to delve into otolaryngological topics, including vertiginous disorders and suicide risk in head and neck cancer patients. At the Henry Ford Health System and Karmanos Cancer Institute, he contributed to significant research on molecular biomarkers and substance use among cancer patients, helping to push the boundaries of cancer research and patient care. His earlier roles, including work at Generation Next Fertility and Columbia University, demonstrate his practical skills in clinical and laboratory settings, offering a holistic approach to patient care and research. These roles also gave him experience in collaborating with medical professionals and managing clinical trials, which have been integral to his development as a medical researcher.

CONTRIBUTIONS AND RESEARCH FOCUS ON CANCER GENETICS AND GENOMICS 🔬

Nassar’s research has focused heavily on otolaryngology, head and neck cancer, and HPV-related carcinomas. His work on identifying molecular biomarkers and risk factors in cancer patients, such as those for suicide and substance use, has been groundbreaking. His research not only seeks to understand the molecular foundations of cancer but also aims to improve the quality of life for cancer patients. His investigations into tinnitus and vertiginous disorders add further depth to his research portfolio, contributing to patient outcomes in the field of ear, nose, and throat (ENT) medicine.

IMPACT AND INFLUENCE 🏆

Nassar's research has been widely recognized within the medical community, as seen through numerous awards. His work has been presented at leading conferences, such as the American Head and Neck Society's 11th International Conference, where he won the 3rd place poster award in the Education/Care Delivery category. His earlier recognition by the American Journal of Gastroenterology in 2021 further highlights his ability to contribute to diverse fields of medicine. His influence extends to peer-reviewed academic journals, where his manuscripts and abstracts have garnered attention, solidifying his reputation as a promising researcher.

ACADEMIC CITES 📚

Nassar’s work has been cited in reputable journals, including Cancer Epidemiology, Biomarkers & Prevention, and the American Journal of Gastroenterology. His published work on topics like teduglutide therapy for Short Bowel Syndrome and cancer epidemiology reflects his ability to contribute to high-impact scientific literature. These citations, alongside his ongoing manuscripts on suicide and substance use in cancer patients, illustrate his influence on ongoing medical research.

LEGACY AND FUTURE CONTRIBUTIONS 🌍

As a young and promising researcher, Nassar is poised to make even more significant contributions to the field of medicine. His research on biomarkers and immunochemotherapy for cancer treatment, as well as his ongoing investigation into the psychological aspects of cancer care, will likely have a lasting impact on both academic research and clinical practice. His focus on improving patient quality of life through research on mental health and substance use demonstrates his commitment to a holistic approach to medicine, one that integrates both physical and mental health outcomes. His legacy will undoubtedly include shaping future practices in otolaryngology, head and neck oncology, and biomolecular cancer therapy. With his continued drive and dedication, Nassar’s future contributions to medical science promise to push boundaries and pave the way for innovative treatments and care models.

NOTABLE PUBLICATIONS 📑

"S3030 Safety and Efficacy of Teduglutide Therapy for Management of Short Bowel Syndrome After Intestinal Transplantation" 

  • Authors: Sami I. Nassar; Syed-Mohammed Jafri
  • Journal: American Journal of Gastroenterology
  • Year: 2021

"Abstract C067: Disparities in health literacy in patients with head and neck cancer: Considerations for understanding" 

  • Authors: Aleksandra Vidovich; Amy Williams; Samantha H. Tam; Mary K. Miller; Maria Olex; Sami Nassar; Alex Rodriguez; Eric Adjei Boakye
  • Journal: Cancer Epidemiology, Biomarkers & Prevention
  • Year: 2023

"The Role of ctDNA and Liquid Biopsy in the Diagnosis and Monitoring of Head and Neck Cancer: Towards Precision Medicine"

  • Authors: Sami I. Nassar; Amber Suk; Shaun A. Nguyen, MD; Dauren Adilbay; John Pang; Cherie-Ann Nathan
  • Journal: Cancer
  • Year: 2024

Flavio Faletra | Cardiovascular Genetics and Genomics | Best Researcher Award 

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Dr. Flavio Faletra | Cardiovascular Genetics and Genomics | Best Researcher Award 

University Health Authority of Central Friuli | Italy

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Biography of Flavio Faletra: A Leader in Medical Genetics 🧬

EARLY ACADEMIC PURSUITS 🎓

Flavio Faletra began his distinguished academic journey at the University of Trieste, where he earned a Degree in Medicine and Surgery in 2005. He further specialized in Medical Genetics at the same institution, completing his specialization in 2009. Demonstrating a strong commitment to his field, Faletra pursued advanced education with a Second-level Master’s degree in Clinical Genetics from the University of Siena in 2011. His foundational academic achievements laid the groundwork for a career focused on the intersection of genetics and clinical medicine.

PROFESSIONAL ENDEAVORS 🏥

Flavio Faletra has held multiple pivotal roles in medical genetics. Since August 2023, he has been an Expert in Genetics at the Regional Health Coordination Agency (ARCS) in Friuli Venezia Giulia, Italy. Alongside his expert role, he has been a University Lecturer on contract at the University of Trieste from 2018 to 2023, contributing to the academic growth of students in the field of genetics. His professional journey includes numerous positions as a Medical Director I Level in Medical Genetics, starting with the IRCCS Burlo Garofolo (2013–2017) and progressing through roles in University Health Authority Friuli Centrale and IRCCS Burlo Garofolo until his current position, reflecting his leadership in the medical genetics field.

CONTRIBUTIONS AND RESEARCH FOCUS ON CARDIOVASCULAR GENETICS AND GENOMICS  🔬

Faletra’s research focus spans various critical areas of medical genetics, from pediatric endocrinology to rare genetic diseases. He has contributed extensively to genetic counseling and clinical genetics, with a strong emphasis on pediatric genetic disorders. His work as a Thesis Co-Surveyor and PhD Supervisor at the University of Trieste demonstrates his dedication to nurturing the next generation of geneticists. Through courses such as the Genetic Consulting in Medical Genetics Specialization School, he has shaped the landscape of medical genetics education. His involvement in pediatric endocrinology through ADE courses has brought syndromic genetic disorders to the forefront, significantly impacting the medical community’s approach to these conditions.

IMPACT AND INFLUENCE 🌍

Faletra’s influence extends beyond academia into clinical practice, where his expertise has helped shape genetic diagnostic strategies across Italy. His participation in national conferences, such as the National Congress of Human Genetics and seminars on genetic syndromes and diagnostics, marks him as a key figure in Italian medical genetics. Faletra's teaching and research efforts have particularly impacted the areas of growth retardation, fetal malformations, and syndromic genetic disorders, positioning him as a central figure in advancing genetic medicine in pediatrics.

ACADEMIC CITES 📚

Flavio Faletra's work has been cited in numerous academic publications, with topics ranging from genetic diagnostic methods to therapeutic approaches for rare genetic disorders. His research in exome sequencing and next-generation sequencing techniques has had a broad impact, being referenced widely in the fields of human genetics and pediatric medicine.

LEGACY AND FUTURE CONTRIBUTIONS 🏅

Faletra’s legacy lies in his dedication to medical genetics, particularly in the areas of pediatric syndromic diseases and clinical genetics. His contribution to education, research, and clinical practice has left an indelible mark on the field. Looking ahead, his ongoing role as an expert and lecturer promises continued contributions to genomic medicine and the advancement of personalized treatment for genetic disorders. Through his continuous involvement in research, teaching, and clinical practice, Faletra remains at the forefront of innovation in medical genetics, with the potential to further revolutionize the diagnosis and treatment of complex genetic diseases.

NOTABLE PUBLICATIONS 📑

"SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability" 

  • Authors: Bogaert, E., Garde, A., Gautier, T., Dermaut, B., Vitobello, A.
  • Journal: American Journal of Human Genetics
  • Year: 2023

"Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders" 

  • Authors:Di Stazio, M., Zanus, C., Faletra, F., d’Adamo, A.P., Musante, L.
  • Journal: Genes
  • Year: 2023

"A new neurodevelopmental disorder linked to heterozygous variants in UNC79"

  • Authors: A., Liu, Z., Luo, S., Liao, W., & Ren, D.
  • Journal: Genetics in Medicine
  • Year: 2023

"The clinical impact of the first-trimester nuchal translucency between the 95th–99th percentiles"

  • Authors: Fantasia, I., Catagini, S., Zamagni, G., Feresin, A., & Stampalija, T.
  • Journal: Prenatal Diagnosis
  • Year: 2023

"A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases"

  • Authors: Zucco, J., Baldan, F., Allegri, L., Damante, G., Mio, C.
  • Journal: Journal of Human Genetics
  • Year: 2024