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Biorxiv : the Preprint Server for Biology|July 15, 2025
Uncovering Heterogeneous Effects via Localized Feature SelectionXiaoxia Liu, Jiaqi Gu, Zhaomeng Chen, et al.Trials|August 6, 2024
Study protocol: perinatal mood treatment studyKate Wolitzky-Taylor, Misty C Richards, Amelia Welborn, et al.Biological Psychiatry|December 21, 2010
TTC12-ANKK1-DRD2 and CHRNA5-CHRNA3-CHRNB4 influence different pathways leading to smoking behavior from adolescence to mid-adulthoodFrancesca Ducci, Marika Kaakinen, Anneli Pouta, et al.Journal of Geriatric Psychiatry and Neurology|November 25, 2005
Middle-aged children of Alzheimer parents, a pilot study: stable neurocognitive performance at 20-year follow-upLissy F Jarvik, Asenath La Rue, Izabella Gokhman, et al.Human Molecular Genetics|October 13, 2006
Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analysesDianne Keen-Kim, Carol A Mathews, Victor I Reus, et al.Addiction Biology|August 25, 2010
Glucocorticoid receptor (NR3C1) gene polymorphisms and onset of alcohol abuse in adolescentsSylvane Desrivières, Anbarasu Lourdusamy, Christian Müller, et al.Nature Communications|November 23, 2022
GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studiesZihuai He, Linxi Liu, Michael E Belloy, et al.Translational Psychiatry|September 23, 2021
Increased activation product of complement 4 protein in plasma of individuals with schizophreniaAgnieszka Kalinowski, Joanna Liliental, Lauren A Anker, et al.Molecular Cancer Therapeutics|August 24, 2011
A molecular screening approach to identify and characterize inhibitors of glioblastoma stem cellsKoppany Visnyei, Hideyuki Onodera, Robert Damoiseaux, et al.Genome Biology|July 14, 2026
CIT-Lasso: a scalable approach beyond guilty by association for identifying causal variants from genome-wide summary statisticsZihuai He, Benjamin Chu, James Yang, et al.Pageof 15