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Nature Neuroscience|November 8, 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general populationAndrea Ganna, Giulio Genovese, Daniel P Howrigan, et al.American Journal of Medical Genetics. Part A|October 21, 2016
Implication of LRRC4C and DPP6 in neurodevelopmental disordersGilles Maussion, Cristiana Cruceanu, Jill A Rosenfeld, et al.Medrxiv : the Preprint Server for Health Sciences|March 18, 2024
Genome-wide association study identifies new loci associated with OCDNora I Strom, Matthew W Halvorsen, Chao Tian, et al.Nature Medicine|May 29, 2020
The effect of LRRK2 loss-of-function variants in humansNicola Whiffin, Irina M Armean, Aaron Kleinman, et al.American Journal of Human Genetics|June 5, 2018
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic SpectrumAndrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, et al.Molecular Psychiatry|October 28, 2015
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorderJ Song, S E Bergen, A Di Florio, et al.Human Molecular Genetics|January 30, 2014
An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosisDerek W Morris, Richard D Pearson, Paul Cormican, et al.Medrxiv : the Preprint Server for Health Sciences|May 7, 2024
Genome-wide association study identifies 30 obsessive-compulsive disorder associated lociNora I Strom, Zachary F Gerring, Marco Galimberti, et al.Nature Genetics|May 13, 2025
Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorderNora I Strom, Zachary F Gerring, Marco Galimberti, et al.Pageof 3