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Frontiers in Cardiovascular Medicine|October 24, 2022
Identification of distinct circulating microRNAs in acute ischemic stroke patients with type 2 diabetes mellitusSalman M Toor, Eman K Aldous, Aijaz Parray, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndromeSmail Hadj-Rabia, Gaelle Brideau, Yasser Al-Sarraj, et al.
Human Mutation|February 3, 2022
Qatar genome: Insights on genomics from the Middle EastHamdi Mbarek, Geethanjali Devadoss Gandhi, Senthil Selvaraj, et al.
Frontiers in Genetics|April 4, 2024
The genetic landscape of autism spectrum disorder in the Middle Eastern populationYasser Al-Sarraj, Rowaida Z Taha, Eman Al-Dous, et al.
Annals of Clinical and Translational Neurology|January 13, 2017
Biallelic SCN10A mutations in neuromuscular disease and epileptic encephalopathyMarios Kambouris, Julien Thevenon, Ariane Soldatos, et al.
NPJ Genomic Medicine|January 20, 2022
The QChip1 knowledgebase and microarray for precision medicine in QatarJuan L Rodriguez-Flores, Radja Messai-Badji, Amal Robay, et al.
Nature Medicine|April 18, 2025
Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgeryJakob German, Mattia Cordioli, Veronica Tozzo, et al.
Medrxiv : the Preprint Server for Health Sciences|September 24, 2024
Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery: a multi-ancestry study in 10 960 individuals from 9 biobanksJakob German, Mattia Cordioli, Veronica Tozzo, et al.
Frontiers in Cellular and Infection Microbiology|December 6, 2021
One Year of SARS-CoV-2: Genomic Characterization of COVID-19 Outbreak in QatarFatiha M Benslimane, Hebah A Al Khatib, Ola Al-Jamal, et al.
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