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Causal effect of serum 25 hydroxyvitamin D concentration on cardioembolic stroke: Evidence from two-sample Mendelian randomization.
Habibi D, Teymoori F, Ebrahimi N, Fateh ST, Najd-Hassan-Bonab L, Saeidian AH, Soleymani Taloubaghi A, Asgarian S, Hosseinpanah F, Hakonarson H, Azizi F, Hedayati M, Daneshpour MS, Akbarzadeh M, Mansourian M. Habibi D, et al. Among authors: fateh st. Nutr Metab Cardiovasc Dis. 2024 May;34(5):1305-1313. doi: 10.1016/j.numecd.2024.02.013. Epub 2024 Feb 28. Nutr Metab Cardiovasc Dis. 2024. PMID: 38508993
The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes.
Amiri Roudbar M, Vahedi SM, Jin J, Jahangiri M, Lanjanian H, Habibi D, Masjoudi S, Riahi P, Fateh ST, Neshati F, Zahedi AS, Moazzam-Jazi M, Najd-Hassan-Bonab L, Mousavi SF, Asgarian S, Zarkesh M, Moghaddas MR, Tenesa A, Kazemnejad A, Vahidnezhad H, Hakonarson H, Azizi F, Hedayati M, Daneshpour MS, Akbarzadeh M. Amiri Roudbar M, et al. Among authors: fateh st. Hum Genomics. 2024 Sep 11;18(1):98. doi: 10.1186/s40246-024-00669-7. Hum Genomics. 2024. PMID: 39256828 Free PMC article.
Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG).
Ghasemi MR, Fateh ST, Ben-Mahmoud A, Gupta V, Stühn LG, Lesca G, Chatron N, Platzer K, Edery P, Sadeghi H, Isidor B, Cogné B, Schulz HL, Krauspe-Stübecke I, Periyasamy R, Nampoothiri S, Mirfakhraie R, Alijanpour S, Syrbe S, Pfeifer U, Spranger S, Grundmann-Hauser K, Haack TB, Papadopoulou MT, da Silva Gonçalves T, Panagiotakaki E, Arzimanoglou A, Tonekaboni SH, Rossi M, Korenke GC, Lacassie Y, Jang MH, Layman LC, Miryounesi M, Kim HG. Ghasemi MR, et al. Among authors: fateh st. Am J Med Genet A. 2024 Dec 20:e63963. doi: 10.1002/ajmg.a.63963. Online ahead of print. Am J Med Genet A. 2024. PMID: 39707601
13 results