Prof. Majid Alfadhel
Chairman, Genetics & Precision Medicine | Professor of Medical Genetics, KSAU-HS | Deputy Executive Director, KAIMRC
Prof. Majid Alfadhel is the Chairman of the Genetics and Precision Medicine Department at King Abdullah Specialized Children Hospital, Riyadh, and Professor of Medical Genetics at King Saud bin Abdulaziz University for Health Sciences (KSAU-HS).
He also serves as Deputy Executive Director of King Abdullah International Medical Research Centre (KAIMRC) and Director of its Medical Genomic Research Laboratory. Prof. Alfadhel is internationally recognized for his contributions to medical genetics and precision medicine.
In 2024, he received the Founders’ Award for Career Achievement from the Canadian College of Medical Geneticists (CCMG). In recognition of his scientific contributions, two syndromes were named after him in the OMIM database: Alfadhel Syndrome and Umair-Alfadhel Neurodevelopmental Disorder.
Prof. Zuhair Al-Hassnan
Consultant, Medical Genomics; Professor, Alfaisal University; Scientist, Translational Genomics, King Faisal Specialist Hospital & Research Centre (KFSH&RC), Riyadh, Saudi Arabia
He is a leading medical geneticist and professor at Alfaisal University, and a consultant in the Department of Medical Genomics at KFSH&RC, Riyadh. He completed his medical genetics fellowship at Johns Hopkins University and holds multiple board certifications in clinical biochemical and molecular genetics.
Prof. Al-Hassnan has extensive experience in clinical genomics, newborn screening, and rare genetic disorders. He leads national and international research initiatives, contributes to policy and ethics in genomic medicine, and has received numerous awards for his work in genetic research and clinical innovation in Saudi Arabia.
Prof. Fuad Almutairi
Senior Medical Genetics Consultant | Associate Professor of Pediatrics | Genetics & Precision Medicine Department, KASCH
Prof. Fuad Almutairi is a Senior Medical Genetics Consultant and Associate Professor of Pediatrics in the Genetics and Precision Medicine Department at King Abdullah Specialized Children Hospital (KASCH), affiliated with King Saud bin Abdulaziz University for Health Sciences in Riyadh, Saudi Arabia.
He earned his MBBS degree from King Saud University and completed his Pediatrics Residency at Prince Sultan Military Medical City (PSMMC), Riyadh. He later pursued fellowship training in Biochemical Genetics at the University of British Columbia.
Prof. Almutairi is actively involved in clinical genetics education and training and currently chairs the National Medical Genetics Fellowship Program at the Saudi Commission for Health Specialties (SCFHS). He is also a member of the Board of Directors of the Saudi Society of Medical Genetics and contributes to several regional and international scientific initiatives.
His research interests focus on neurogenetic disorders, inborn errors of metabolism, and the discovery of novel disease-associated genes through local and international collaborations. He has published numerous scientific articles in high-impact journals and continues to contribute extensively to research and precision medicine initiatives in Saudi Arabia.
Prof. Malak Alghamdi
Head of Medical Genetics Division | Senior Medical Genetics Consultant & Associate Professor, King Saud University, Riyadh,KSA
She is Head of the Medical Genetics Division at King Khalid University Hospital and Senior Medical Genetics Consultant and Associate Professor at King Saud University, Riyadh. She earned her MD from KSU, holds Arab and Saudi Board certifications in Pediatrics, and is board-certified in Medical Genetics (FCCMG, Canada).
She completed a fellowship in Clinical Biochemical Genetics at British Columbia Children’s Hospital, Canada. Prof. Alghamdi established the clinical and academic Medical Genetics Division at KSUMC, with research and clinical focus on neurogenetic disorders and inborn errors of metabolism, and has several publications in the field. She actively mentors fellows, residents, and medical students.
Dr. Mohammed Almuqbil
Consultant Pediatric Neurology & Neurogenetics, King Abdullah Specialized Children’s Hospital | Assistant Professor, KSAU-HS
Dr. Mohammed Almuqbil is a Consultant in Pediatric Neurology and Neurogenetics at King Abdullah Specialized Children’s Hospital (KASCH), Riyadh, Saudi Arabia, and an Assistant Professor at King Saud bin Abdulaziz University for Health Sciences .
He specializes in pediatric neurological and neurogenetic disorders, with expertise in medical genetics, biochemical genetics, and rare neurological diseases.
Dr. Almuqbil completed his Pediatric Neurology residency at McGill University in 2016, followed by board training in Medical Genetics and Genomics at Harvard Medical School in 2018, and a fellowship in Medical Biochemical Genetics at Johns Hopkins University in 2019.
He is actively involved in clinical research, medical education, and international scientific collaborations, with numerous publications in high-impact journals focusing on neurogenetics, mitochondrial disorders, leukodystrophies, and rare genetic diseases.
Dr. Almuqbil also serves on the boards of several scientific societies and contributes extensively to resident and fellow training programs.
Dr. Mohammed Almannai
Consultant, Genetics & Precision Medicine | Program Director, Clinical Genetics & Genomics Fellowship Program
Dr. Mohammed AlMannai completed his Medical Doctor (MD) degree at Arabian Gulf University. He completed his medical internship and Pediatrics Residency at Salmaniya Medical Complex, Ministry of Health, Bahrain, before continuing his pediatric training at the University of South Alabama.
He later received specialty training in Medical Genetics and Medical Biochemical Genetics at Baylor College of Medicine.
Dr. AlMannai currently serves as a Consultant in the Genetics and Precision Medicine Department at King Abdulaziz Medical City, Riyadh, and is the Program Director of the Clinical Genetics and Genomics Fellowship Program at the same institution.
He is actively involved in scientific research and has contributed to numerous publications in the fields of medical genetics and genomic medicine.
Dr. Bader Almuzaini
Deputy Chairman, Medical Genomic Research Department, KAIMRC | Consultant Clinical Scientist | Director of Novogenomic Lab
Dr. Bader Almuzaini is a certified Clinical Laboratory Consultant and Research Scientist with more than twenty years of experience in diagnostic conventional cytogenetics, genomic and epigenomic research, including whole genome sequencing (WGS), transcriptome analysis, microarray technologies, and molecular diagnostics.
He currently serves as Deputy Chairman of the Medical Genomic Research Department at King Abdullah International Medical Research Center (KAIMRC), Director of Novogenomic Lab, and Consultant Clinical Scientist in Genetic Laboratory Medicine at King Abdulaziz Medical City, Riyadh.
Dr. Almuzaini earned his PhD in Cell and Molecular Genetics from the Karolinska Institute and holds a Master’s degree in Medical Genetics from the University of Glasgow.
His research focuses on identifying genetic and epigenetic signatures underlying cancer genetics and rare genetic disorders. He has led and co-investigated several funded research projects and has extensive scientific publications in genomics, molecular pathology, and precision medicine.
In addition to his research and clinical work, Dr. Almuzaini is actively involved in teaching, mentorship, and national scientific committees related to laboratory medicine, genomics, and healthcare quality standards in Saudi Arabia.
Dr. Maha AlOtaibi
Consultant in Medical Genetics & Genomic Medicine | King Saud Medical City, Riyadh, Saudi Arabia
Dr. Maha AlOtaibi is a Consultant in Medical Genetics and Genomic Medicine at King Saud Medical City, specializing in inherited metabolic disorders, rare genetic diseases, and genomic diagnostics.
She is actively involved in clinical genetics practice and precision medicine initiatives, with a strong focus on improving diagnostic pathways for patients with rare and hereditary disorders.
Dr. AlOtaibi has contributed to several research projects and scientific publications in the fields of neurogenetics, metabolic disorders, and genomic medicine. She also participates in national initiatives related to genetic disease awareness and newborn screening programs.
Dr. Aqeela Alhashim
Consultant Pediatric Neurologist & Neurogeneticist | National Neuroscience Institute, King Fahad Medical City
Dr. Aqeela Alhashim is a Consultant Pediatric Neurologist and Neurogeneticist at the National Neuroscience Institute, King Fahad Medical City.
She earned her MBBS degree from King Faisal University and completed her Pediatric Residency training in Riyadh, followed by the Saudi and Arab Boards in Pediatrics. She later obtained the Fellowship of the Royal College of Physicians and Surgeons of Canada (FRCPC) in Child Neurology and completed a Neurogenetics Fellowship in Clinical and Molecular Genetics Research at The Hospital for Sick Children.
Dr. Alhashim has extensive expertise in pediatric neurology, neurogenetics, and rare neurological disorders. She is actively involved in clinical research, medical education, and international scientific collaborations, with multiple publications and presentations in the fields of neurogenetics and inherited neurological diseases.
She has also participated as a speaker and faculty member in numerous regional and international conferences focused on pediatric neurology and rare diseases.
Dr. Mohammed Al-Dubayee
Professor and Consultant Pediatric Endocrinology
Professor Mohammed Al-Dubayee is a Saudi physician specializing in Pediatric Endocrinology and Diabetes, with a special interest in lipid disorders, inherited metabolic diseases, and precision medicine in children
and adolescents.
He is actively involved in advancing pediatric endocrine and metabolic healthcare services in Saudi Arabia through clinical practice, academic leadership, research, and medical education.
Professor Al-Dubayee has contributed to several scientific and collaborative initiatives focused on pediatric diabetes, dyslipidemia, obesity, and genomic medicine, with particular interest in improving early diagnosis and
long-term outcomes for children with rare and hereditary metabolic disorders. He is also actively engaged in postgraduate medical training, healthcare quality improvement, and the development of specialized pediatric service
Dr. Hamad Althiyab
Consultant Genetic & Metabolic Physician | King Abdulaziz Medical City
Dr. Hamad Althiyab is a Consultant Genetic and Metabolic Physician at King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
He earned his Bachelor of Medicine and Bachelor of Surgery (MBBS) from King Saud bin Abdulaziz University for Health Sciences (KSAU-HS). He completed his Pediatrics Residency and obtained the Saudi Pediatric Board certification, followed by a Clinical Genetics and Metabolic Disorders Fellowship accredited by the Saudi Commission for Health Specialties (SCFHS). He later completed a Biochemical Genetics Fellowship at BC Children’s Hospital, Canada.
Dr. Althiyab has contributed to several scientific publications and research projects in the fields of metabolic and genetic disorders, including leukodystrophies, neuronal ceroid lipofuscinosis, and rare neurodevelopmental syndromes.
He is actively involved in academic activities, committee work, and continuing medical education, with presentations delivered at regional and international conferences related to inborn errors of metabolism and pediatric genetics. His professional interests focus on genetic and metabolic disorders, newborn screening, and rare disease diagnostics.
Dr. Muhammad Umair
Research Scientist | Team Leader, Functional Studies | Human Molecular Genetics & Rare Genetic Disorders Specialist
Dr. Muhammad Umair is a Research Scientist and Team Leader of Functional Studies at King Abdullah International Medical Research Center (KAIMRC), specializing in human molecular genetics and rare genetic disorders.
His research focuses on novel gene discovery, neurodevelopmental disorders, skeletal disorders, and translational genomics using advanced next-generation sequencing technologies.
Dr. Umair has published more than 200 peer-reviewed scientific articles and has contributed to the identification of 27 novel disease-associated genes. He also serves as an editor and reviewer for several international scientific journals.
His work integrates clinical genomics, functional characterization, and precision medicine approaches to improve the diagnosis and understanding of rare human genetic disorders.
Dr. Ahmed Alodaib
Consultant Clinical Scientist in Clinical Biochemistry & Biochemical Genetics | Head of Metabolomics Section, KFSHRC
Dr. Alodaib is a Consultant Clinical Scientist in clinical biochemistry and biochemical genetics and currently serves as the Head of the Metabolomics Section, including the Biochemical Genetics Unit, within the Precision Medicine Laboratory Department at the Genomic Medicine Center of Excellence at King Faisal Specialist Hospital & Research Centre (KFSHRC). He is also an Adjunct Assistant Professor at the University of Pittsburgh and Alfaisal University.
Dr. Alodaib graduated from the College of Science, Department of Biochemistry at King Saud University in 2003. In 2008, he completed his Bachelor’s Honors degree in Health Science at the University of Melbourne, followed by a Master’s degree in Human Genetics from the University of Sydney in 2010.
In 2015, he earned his PhD in Human Genetics from the University of Sydney, where he utilized advanced next-generation sequencing technologies to identify disease-causing genes in rare Mendelian disorders. He later completed the American Board of Medical Genetics and Genomics (ABMGG) Clinical Fellowship Training in Biochemical Genetics in 2019.
Dr. Alodaib is the Founder and Director of the Fellowship Training Program in Clinical Biochemical Genetics (Laboratory-based) at KFSHRC. He has played an active role in regional and national health research and has published extensively in leading scientific journals, with presentations at numerous national and international conferences and workshops.
His professional interests focus on expanding the biochemical characterization of inborn errors of metabolism through advanced next-generation metabolic screening platforms and emerging biochemical technologies.
Dr. Hajar Alakeel
Board-Certified Geneticist | Clinical Geneticist & Genomic Medicine Consultant
Dr. Hajar Alakeel is a board-certified geneticist and genomic medicine consultant currently undertaking her second fellowship in Clinical Molecular Genetics and Genomics at King Faisal Specialist Hospital & Research Centre (KFSHRC), following the completion of her Clinical Genetics and Genomics Fellowship at King Abdullah Specialized Children’s Hospital (NGHA).
Prior to her subspecialty training, she completed her pediatric residency at NGHA and earned the Saudi Board of Pediatrics certification in 2021.
Throughout her training, Dr. Alakeel has been recognized for her clinical and academic excellence, receiving multiple distinctions, including the Best Resident Award. Her research has been presented at leading international conferences, including the American Society of Human Genetics (ASHG), the European Society of Human Genetics (ESHG), as well as regional MENA meetings.
Dr. Abdullah Alfalah
Physician Specializing in Medical & Molecular Genetics | Rare Diseases & Clinical Genomics
Dr. Abdullah Alfalah is a physician specializing in medical and molecular genetics, with particular expertise in rare diseases, genomic diagnostics, and clinical genomics.
He is actively involved in genomic research and multidisciplinary rare disease initiatives, with a focus on advanced genomic interpretation, reanalysis strategies, and improving diagnostic yield in complex genetic disorders.
Dr. Alfalah has contributed to several research projects and scientific presentations in the fields of pediatric genetics, neurogenetics, and precision medicine. He is also passionate about integrating genomics into clinical care and advancing medical education in the field of genetics.Bottom of Form
Dr. Ali Tabish
Consultant Clinical Geneticist
Dr. Ali Tabish is a Consultant Clinical Geneticist in Saudi Arabia, holding an MD and PhD with a strong academic and clinical focus on clinical genetics and genomic medicine.
He has a special interest in advancing the application of genomics in clinical practice, with a focus on improving the diagnosis and management of inherited and complex genetic disorders. His work is centered on integrating modern genomic technologies into patient care to support precision medicine and enhance clinical outcomes.
Dr. Tabish is passionate about the field of genomics and continues to contribute to the growing understanding of genetic diseases through clinical practice and scientific engagement. He is committed to advancing genetic healthcare services and supporting the development of precision medicine approaches in the region.
Dr. Najim Ameziane
Senior Director Bioinformatics | Molecular Biologist with Self-Taught Bioinformatics Expertise
Najim Ameziane is a passionate molecular biologist and bioinformatics expert with extensive leadership experience in developing innovative methods and advanced tools for clinical molecular genetic testing.
He has successfully led high-performing teams of bioinformaticians and data scientists, optimizing workflows for maximum efficiency and implementing forward-thinking strategies to support organizational growth and scientific advancement.
His expertise spans genomic research, drug development, and advanced sequencing technologies, including next-generation sequencing (NGS), whole genome sequencing (WGS), and RNA sequencing (RNA-seq). Through his multidisciplinary experience, he continues to contribute to the advancement of precision medicine and translational genomics.