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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.
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.
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.
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