Showing results (2231-2240 of 2,288) with videos related to

Sort By:
Pageof 229
American Journal of Human Genetics|April 17, 2018
Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar AtaxiaClaire Guissart, Xenia Latypova, Paul Rollier, et al.
JAMA Network Open|July 26, 2022
Association of Assisted Reproductive Technology With Offspring Growth and Adiposity From Infancy to Early AdulthoodAhmed Elhakeem, Amy E Taylor, Hazel M Inskip, et al.
NPJ Genomic Medicine|March 1, 2024
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomaliesJil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, et al.
Communications Biology|November 9, 2022
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophyEnrico Mingardo, Glenda Beaman, Philip Grote, et al.
BMC Medicine|November 7, 2018
Gestational weight gain charts for different body mass index groups for women in Europe, North America, and OceaniaSusana Santos, Iris Eekhout, Ellis Voerman, et al.
Plos Medicine|February 12, 2019
Maternal body mass index, gestational weight gain, and the risk of overweight and obesity across childhood: An individual participant data meta-analysisEllis Voerman, Susana Santos, Bernadeta Patro Golab, et al.
Mutation Research. Reviews in Mutation Research|June 11, 2022
Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylationOlivia Solomon, Karen Huen, Paul Yousefi, et al.
The Journal of Allergy and Clinical Immunology|December 24, 2018
Epigenome-wide meta-analysis of DNA methylation and childhood asthmaSarah E Reese, Cheng-Jian Xu, Herman T den Dekker, et al.
Genome Medicine|November 26, 2020
DNA methylation and body mass index from birth to adolescence: meta-analyses of epigenome-wide association studiesFlorianne O L Vehmeijer, Leanne K Küpers, Gemma C Sharp, et al.
HGG Advances|February 24, 2022
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1BJan Gehlen, Ann-Sophie Giel, Ricarda Köllges, et al.
Pageof 229