Dr. Ahmad is Director of the Genetics Laboratory at Al Jalila Children’s. He completed his doctoral studies (PhD) at Dartmouth College in the USA followed by a fellowship in molecular diagnostics at Dartmouth Medical School. In 2013, he joined Harvard Medical School where he completed his clinical molecular genetics fellowship and, in 2015, became board-certified by the American Board of Medical Genetics and Genomics (ABMGG). Dr. Abou Tayoun is a fellow of the American College of Medical Genetics and Genomics.
Prior to joining Al Jalila Children’s, he was a director in the Division of Genomic Diagnostics at the Children’s Hospital of Philadelphia, and also an assistant professor of Pathology and Laboratory Medicine at the University of Pennsylvania Perelman School of Medicine. To support clinicians in various specialties at CHOP, Dr. Ahmad developed genomic sequencing-based diagnostic tests for a range of pediatric disorders. He also developed and published several tools and assays involving next generation sequencing and variant interpretation. Dr. Abou Tayoun is a co-chair of the Clinical Genome Resource (ClinGen) Hearing Loss Expert Group, and is a member of the ClinGen Sequence Variant Interpretation group. In both capacities, Dr. Abou Tayoun is working with international experts to establish guidelines and recommendations for sequence variant interpretation in general, and in the hearing loss disease area specifically.
Alan Taylor is an American board certified genetic counsellor who received his MS in Genetic Counseling from Northwestern University in 2016. After graduation, he held a joint position between the Epilepsy Genetics Program at Boston Children’s Hospital and Claritas Genomics, a genetic testing laboratory. In his role at Boston Children’s, he provided genetic counselling to patients and families within the clinic while in his role at Claritas, he interpreted and reported genomic test results. In 2017, he expanded his clinical experience by joining the Neurometabolic and Mitochondrial Disease Program at Boston Children’s Hospital. Alan joined Al Jalila Children’s in 2018 and provides genetic counselling to families who have a genetic diagnosis or are planning to pursue genetic testing.
Divin joined Al Jalila Children’s Specialty Hospital as Genomics Laboratory Supervisor in 2018. He has over 11 years of experience in clinical and research lab management in diverse settings that includes mid-size and established organizations. He is specialized in Next Generation Sequencing technologies and has extensive hands-on experience in state of art Next Generation Sequencers, Lab automations and different Next Generation Sequencing library preparation methods. Divin holds a Master of Science degree in Biotechnology from Bharathiar University, India.
Maha El Naofal joined the Al Jalila Children's Genomics Centre as Molecular Technologist in 2018. Maha is involved in the daily running of the laboratory but her primary responsibility is the execution of the assays in the lab including Next Generation Sequencing and Chromosomal Microarrays. She has previously worked as research assistant at the Houston Methodist Research Institute and undergone clinical rotations at top tier genetic laboratories including Baylor Miraca and MD Anderson Cancer Center in America. Maha El Naofal is certified in Molecular Biology (MB) and Cytogenetics (CG) by the American Society of Clinical Pathology (ASCP). She earned her Master’s Degree in Diagnostic Genetics from the University of Texas MD Anderson Cancer Center SHP.
Ruchi Jain is responsible for the analysis, interpretation and identification of pathogenic variants within the genomic data generated from clinical samples. She is also involved in research projects including sequencing of the UAE Covid-19 strain and analysing Transcriptome data. Ruchi obtained her PhD in bioinformatics from the Bharathiar University, India, in 2015. After her PhD she joined Indian Institute of Science as a Post-Doctoral Associate and bioinformatician where she led various next generation sequencing, microarray and epigenetics projects. Her post-doctoral research was focused on identification and validation of the genes and pathways in triple negative breast cancers. She has authored several peer- reviewed scientific publications. Ruchi joined the genomics team at Al Jalila Children’s Hospital in April 2020.
Sathishkumar Ramaswamy is responsible for analyzing next-generation sequencing and chromosomal microarray data, including whole genome, clinical exome and gene panels. He is actively involved in developing the bioinformatics pipelines for genomic analysis. He closely works with the IT team to setting up the servers and analysis platforms for the Genomic Lab. He holds a PhD in Bioinformatics from Bharathiar University, India. His PhD research was focused on molecular dynamics and simulation of potential inhibitors for neurodegenerative disease. He has held various scientific positions in both academia and biotech industry with a total experience of 11 years in the field of bioinformatics and Next Generation Sequencing. He has worked on various challenging projects involving Whole Exome Sequencing, RNAseq, ChipSeq and genome assembly from a range of organisms. He has successfully developed and optimized analysis pipelines for nanopore sequencing data. He was awarded a research fellowship from the Department of Information Technology and Department of Biotechnology from the Indian Government for his research.
Yasmeen is a molecular Biology Technologist at the Genomics Centre of Al Jalila Children Specialty Hospital. She currently works as both a molecular technologist and a quality coordinator within the centre. She is a motivated, self-driven biotechnology graduate who earned her Bachelor's degree from the University of Sharjah. Yasmeen previously worked at the Dubai Health Authority in 2015 as a laboratory technologist before joining Al Jalila Children's in 2016. She participated in the CAP inspection in 2018 as a lab technologist. Her ambition to proceed in her field drove her to join the Al Jalila Children's Genomics Centre.