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Nature Genetics|June 2, 2022
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sexDanny Antaki, James Guevara, Adam X Maihofer, et al.Molecular Psychiatry|March 17, 2021
Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signalingMegha Amar, Akula Bala Pramod, Nam-Kyung Yu, et al.Nature Genetics|October 25, 2022
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16pDaniel J Weiner, Emi Ling, Serkan Erdin, et al.Translational Psychiatry|April 1, 2024
Effects of genetically predicted posttraumatic stress disorder on autoimmune phenotypesAdam X Maihofer, Andrew Ratanatharathorn, Sian M J Hemmings, et al.Neuron|December 21, 2024
snRNA-seq stratifies multiple sclerosis patients into distinct white matter glial responsesWill Macnair, Daniela Calini, Eneritz Agirre, et al.Biorxiv : the Preprint Server for Biology|October 9, 2023
Disease-specific selective vulnerability and neuroimmune pathways in dementia revealed by single cell genomicsJessica E Rexach, Yuyan Cheng, Lawrence Chen, et al.Research Square|December 8, 2025
Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortexKuldeep Kumar, Sayeh Kazem, Guillaume Huguet, 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.Cell Reports. Medicine|March 19, 2025
T-bet+ CXCR3+ B cells drive hyperreactive B-T cell interactions in multiple sclerosisIvan Jelcic, Reza Naghavian, Imran Fanaswala, et al.Cell|September 12, 2024
Cross-disorder and disease-specific pathways in dementia revealed by single-cell genomicsJessica E Rexach, Yuyan Cheng, Lawrence Chen, et al.Pageof 12