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  1. A-Z Directory
  2. Ahmad Abou Tayoun
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Ahmad Abou Tayoun Biography Academic Appointments Professional Education Teaching Experience Honors and Awards Publications Membership of Professional Bodies/Associations Research Interest Clinical and Community Service
Professor - Genetics

Ahmad Abou Tayoun

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Ahmad Abou Tayoun is an American board-certified (ABMGG) clinical molecular geneticist dedicated to advancing genomic medicine through research, innovation, and equitable clinical implementation. His work focuses on genomic discovery and translational research to improve the diagnosis and management of genetic disorders, while building capacity and expanding access to high-quality clinical genomics services, particularly in the Middle East. Professor Abou Tayoun is committed to translating scientific discoveries into clinical practice through multidisciplinary collaboration, innovative technologies, and sustainable implementation

Academic Appointments

2026 - Present

Professor of Genetics

Mohammed Bin Rashid University of Medicine and Health Sciences, UAE

2020 - 2026

Associate Professor of Genetics

Mohammed Bin Rashid University of Medicine and Health Sciences, UAE

2015 - 2018

Assistant Professor of Pathology & Lab Medicine

University of Pennsylvania, USA

Professional Education

2015

Fellowship - Clinical Molecular Genetics

Harvard Medical School, USA

2013

Fellowship - Molecular Diagnostics

Dartmouth Medical School, USA

2011

Doctor of Philosophy (PhD) - Genetics

Dartmouth College, USA

2003

Masters of Science (MSc) - Molecular Biology

American University of Beirut, Lebanon

2003

Bachelors of Science - Biology

American University of Beirut, Lebanon

Teaching Experience

  • Teaching Genetics and Molecular Biology to undergraduate medical students.
  • Teaching Molecular Genomics to postgraduate students.
  • Mentoring and co-supervising master’s and PhD students.

Honors and Awards

2025

Hamdan Award for Best Arab Research in Healthcare

Hamdan Bin Rashid Al Maktoum Award for Distinguished Academic Performance

2021 - 2022

Hamdan Award for Outstanding Clinical Department in the Public Sector in the United Arab Emirates

Hamdan Bin Rashid Al Maktoum Award for Distinguished Academic Performance

2005 - 2011

Graduate school student Scholarship

Dartmouth College, USA

2004 - 2005

Suaad Al Sabbah Award, Best Master’s Thesis in Biomedical Sciences

American University of Beirut, Lebanon

1999

Top three student in national high school exam

Prime Minister Rafic Hariri Scholarship Award, Lebanon

Publications

Genetic variant pathogenicity prediction trained using large-scale disease specific clinical sequencing datasets.

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FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature.

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Diagnosing Cornelia de Lange Syndrome and related neurodevelopmental disorders using RNA-sequencing.

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Genomics of rare diseases in the Greater Middle East

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Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases.

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Genetic and Clinical characteristics of Patients in the Middle East With Multisystem Inflammatory Syndrome in Children.

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Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populations.

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The genomic landscape of rare disease in the Middle East.

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A draft human pangenome reference.

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Citywide premarital genomic screening in a Middle Eastern population.

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View all publications on PubMed

Membership of Professional Bodies/Associations

  • Fellow of the American College of Medical Genetics and Genomics (ACMG).
  • Diplomate of the American Board of Medical Genetics and Genomics (ABMGG).
  • Hearing Loss Expert Panel, The Clinical Genome Consortium (ClinGen), USA
  • Sequence Variant Interpretation (SVI) Workgroup, ClinGen, USA
  • Sequence Variant Classification (SVC) Workgroup: ACMG, ClinGen, AMP (Association for Molecular Pathology), CAP (College of American Pathologists).
  • Human Pangenome Reference Consortium (HPRC), USA.
  • World Health Organization (WHO), Geneva

Research Interest

  • Characterizing the genomic landscape and epidemiology of rare diseases in the Middle East.
  • Developing new diagnostic and screening tools using mutli-OMICs and long-read sequencing technologies.
  • Citywide implementation of genomic medicine throughout an individual’s lifecycle, including premarital carrier screening, rapid whole genome sequencing (rWGS) in intensive care units, genomic newborn screening (gNBS), genomic diagnostics in pediatrics, and cancer genomics.
  • Discovery and functional characterization of novel disease genes or biomarkers using patients induced pluripotent stems cells (iPSCs) and animal models.
  • Preclinical characterization of therapeutic agents.

Clinical and Community Service

  • Premarital genomic screening, supporting family medicine at Dubai Health.
  • Prenatal genetics (non-invasive screening and diagnostics), supporting OB/GYN at Dubai Health.
  • Rapid whole genome sequencing (rWGS) supporting neonatal and pediatric intensive care units (NICU/PICU) at Dubai Health.
  • Genomic diagnostics supporting pediatrics at Dubai Health.
  • Cancer genomics supporting Dubai Health oncology services.
  • Hamdan Bin Mohammed College of Dental Medicine
  • Hind Bint Maktoum College of Nursing and Midwifery
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