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Molecular Neurobiology|April 30, 2025
Mitochondrial DNA Copy Number as a Hidden Player in the Progression of Multiple Sclerosis: A Bidirectional Two-Sample Mendelian Randomization StudyHani Sabaie, Ali Taghavi Rad, Motahareh Shabestari, et al.Scientific Reports|February 27, 2024
The Tehran longitudinal family-based cardiometabolic cohort study sheds new light on dyslipidemia transmission patternsMahdi Akbarzadeh, Parisa Riahi, Amir Hossein Saeidian, et al.Scientific Reports|August 27, 2024
Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in IranSara Asgarian, Hossein Lanjanian, Shiva Rahimipour Anaraki, et al.Journal, Genetic Engineering & Biotechnology|December 12, 2025
Within-family analysis of PRS313: insights into breast cancer risk predictionHossein Lanjanian, Sahand Tehrani Fateh, Mahdi Akbarzadeh, et al.Human Genomics|September 10, 2024
The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetesMahmoud Amiri Roudbar, Seyed Milad Vahedi, Jin Jin, et al.Plos Genetics|September 2, 2015
A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery DiseaseSolveig Gretarsdottir, Hannes Helgason, Anna Helgadottir, et al.European Journal of Epidemiology|May 11, 2023
Cohort profile update: Tehran cardiometabolic genetic studyMaryam S Daneshpour, Mahdi Akbarzadeh, Hossein Lanjanian, et al.Nature Communications|November 2, 2019
Associations of autozygosity with a broad range of human phenotypesDavid W Clark, Yukinori Okada, Kristjan H S Moore, et al.Pageof 39