Showing results (1531-1540 of 1,657) with videos related to
Sort By:
Pageof 166
Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.Nature Communications|March 2, 2025
Multimodal histopathologic models stratify hormone receptor-positive early breast cancerKevin M Boehm, Omar S M El Nahhas, Antonio Marra, et al.The EMBO Journal|February 19, 2026
TRPML1 suppresses pulmonary fibrosis by limiting collagen and elastin depositionEva-Maria Weiden, Zala Serianz, Yvonne Klingl, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2022
Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalitiesJoseph S Leslie, Rim Hjeij, Asaf Vivante, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 26, 2022
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasisAmar J Majmundar, Eugen Widmeier, John F Heneghan, et al.The New England Journal of Medicine|May 7, 2010
L-histidine decarboxylase and Tourette's syndromeA Gulhan Ercan-Sencicek, Althea A Stillman, Ananda K Ghosh, et al.Hypertension (Dallas, Tex. : 1979)|February 28, 2018
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic SyndromeJillian K Warejko, Markus Schueler, Asaf Vivante, et al.Nature|August 24, 2010
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformationsKaya Bilgüvar, Ali Kemal Oztürk, Angeliki Louvi, et al.Journal of the American Society of Nephrology : JASN|July 1, 2018
<i>GAPVD1</i> and <i>ANKFY1</i> Mutations Implicate RAB5 Regulation in Nephrotic SyndromeTobias Hermle, Ronen Schneider, David Schapiro, et al.Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.Pageof 166