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Proceedings of the National Academy of Sciences of the United States of America|March 3, 2015
Rare variants in neuronal excitability genes influence risk for bipolar disorderSeth A Ament, Szabolcs Szelinger, Gustavo Glusman, et al.
Nature Medicine|May 30, 2018
Convergence of placenta biology and genetic risk for schizophreniaGianluca Ursini, Giovanna Punzi, Qiang Chen, et al.
Nature Neuroscience|July 28, 2018
Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesisAndrew E Jaffe, Richard E Straub, Joo Heon Shin, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Transcriptomic and protein analysis of human cortex reveals genes and pathways linked to NPTX2 disruption in Alzheimer's diseaseYuelin Lao, Mei-Fang Xiao, Shiyu Ji, et al.
Nature Communications|May 30, 2024
Gene expression signatures in blood from a West African sepsis cohort define host response phenotypesJosh G Chenoweth, Carlo Colantuoni, Deborah A Striegel, et al.
Stem Cell Reports|August 16, 2024
Individual variation in the emergence of anterior-to-posterior neural fates from human pluripotent stem cellsSuel-Kee Kim, Seungmae Seo, Genevieve Stein-O'Brien, et al.
Research Square|July 29, 2026
Clinical, cellular, and genomic consequences of a population-enriched SETD1A missense variantSeth Ament, Robert Lease, Rediet Oshone, et al.
Circulation|March 27, 2023
Impaired Reorganization of Centrosome Structure Underlies Human Infantile Dilated CardiomyopathyYoung Wook Chun, Matthew Miyamoto, Charles H Williams, et al.
Nature|October 7, 2021
A transcriptomic and epigenomic cell atlas of the mouse primary motor cortexZizhen Yao, Hanqing Liu, Fangming Xie, et al.
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