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Cell|August 1, 2023
Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancerRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.Nature Genetics|March 29, 2024
Protein-altering variants at copy number-variable regions influence diverse human phenotypesMargaux L A Hujoel, Robert E Handsaker, Maxwell A Sherman, et al.Biorxiv : the Preprint Server for Biology|June 19, 2023
Hidden protein-altering variants influence diverse human phenotypesMargaux L A Hujoel, Robert E Handsaker, Maxwell A Sherman, et al.Nature Neuroscience|January 12, 2021
Large mosaic copy number variations confer autism riskMaxwell A Sherman, Rachel E Rodin, Giulio Genovese, et al.Nature Neuroscience|February 5, 2021
Activity-dependent regulome of human GABAergic neurons reveals new patterns of gene regulation and neurological disease heritabilityGabriella L Boulting, Ershela Durresi, Bulent Ataman, et al.Nature Genetics|March 20, 2019
Linked-read analysis identifies mutations in single-cell DNA-sequencing dataCraig L Bohrson, Alison R Barton, Michael A Lodato, et al.Nature Neuroscience|January 12, 2021
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencingRachel E Rodin, Yanmei Dou, Minseok Kwon, et al.Science (New York, N.Y.)|December 9, 2017
Aging and neurodegeneration are associated with increased mutations in single human neuronsMichael A Lodato, Rachel E Rodin, Craig L Bohrson, et al.Cell Genomics|August 21, 2023
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptionsEduardo A Maury, Maxwell A Sherman, Giulio Genovese, et al.Nature Neuroscience|September 28, 2022
Developmental dynamics of RNA translation in the human brainErin E Duffy, Benjamin Finander, GiHun Choi, et al.Pageof 3