Showing results (1621-1630 of 1,712) with videos related to
Sort By:
Pageof 172
Nature Human Behaviour|May 7, 2025
Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestryAnna Gui, Anja Hollowell, Emilie M Wigdor, et al.Nature|September 17, 2025
CRISPR activation for SCN2A-related neurodevelopmental disordersSerena Tamura, Andrew D Nelson, Perry W E Spratt, et al.Nature Genetics|August 4, 2014
A framework for the interpretation of de novo mutation in human diseaseKaitlin E Samocha, Elise B Robinson, Stephan J Sanders, et al.Circulation Research|September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataJoseph T Glessner, Alexander G Bick, Kaoru Ito, et al.Trends in Neurosciences|April 26, 2018
Progress in Understanding and Treating SCN2A-Mediated DisordersStephan J Sanders, Arthur J Campbell, Jeffrey R Cottrell, et al.Blood|June 1, 1996
Outcome of unrelated donor bone marrow transplantation in 40 children with Hurler syndromeC Peters, M Balthazor, E G Shapiro, 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.Cell Stem Cell|February 21, 2024
Thalamocortical organoids enable in vitro modeling of 22q11.2 microdeletion associated with neuropsychiatric disordersDavid Shin, Chang N Kim, Jayden Ross, et al.Genome Biology|March 7, 2017
Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genomeRyan L Collins, Harrison Brand, Claire E Redin, et al.Nature Communications|March 9, 2019
Role of carbonate burial in Blue Carbon budgetsV Saderne, N R Geraldi, P I Macreadie, et al.Pageof 172