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Nature Communications|November 4, 2020
Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traitsBryan C Quach, Michael J Bray, Nathan C Gaddis, et al.Journal of Medicinal Chemistry|January 13, 2016
Discovery of 1-{(3R,4R)-3-[({5-Chloro-2-[(1-methyl-1H-pyrazol-4-yl)amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}oxy)methyl]-4-methoxypyrrolidin-1-yl}prop-2-en-1-one (PF-06459988), a Potent, WT Sparing, Irreversible Inhibitor of T790M-Containing EGFR MutantsHengmiao Cheng, Sajiv K Nair, Brion W Murray, et al.Medrxiv : the Preprint Server for Health Sciences|September 15, 2025
DNA Methylation Signatures of Alcohol Use Disorder - A large-scale Meta-Analysis in the Psychiatric Genomics ConsortiumLea Zillich, Sofia D'Augello, Diana Avetyan, et al.Molecular Psychiatry|April 26, 2017
Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritabilityL E Duncan, A Ratanatharathorn, A E Aiello, et al.JAMA Neurology|February 3, 2015
A genome-wide association study of myasthenia gravisAlan E Renton, Hannah A Pliner, Carlo Provenzano, et al.Journal of the National Cancer Institute|April 16, 2015
CHRNA5 risk variant predicts delayed smoking cessation and earlier lung cancer diagnosis--a meta-analysisLi-Shiun Chen, Rayjean J Hung, Timothy Baker, et al.Molecular Psychiatry|August 5, 2015
Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African AmericansE Olfson, N L Saccone, E O Johnson, et al.The Lancet. Neurology|March 13, 2012
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyElisa Majounie, Alan E Renton, Kin Mok, et al.Journal of the American College of Cardiology|December 14, 2020
Global Burden of Cardiovascular Diseases and Risk Factors, 1990-2019: Update From the GBD 2019 StudyGregory A Roth, George A Mensah, Catherine O Johnson, et al.Nature|August 2, 2023
Africa-specific human genetic variation near CHD1L associates with HIV-1 loadPaul J McLaren, Immacolata Porreca, Gennaro Iaconis, et al.Pageof 154