Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: CHRD[original query] |
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De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects. PLoS genetics 2016 Apr 12 (4): e1005963. Priest James R, Osoegawa Kazutoyo, Mohammed Nebil, Nanda Vivek, Kundu Ramendra, Schultz Kathleen, Lammer Edward J, Girirajan Santhosh, Scheetz Todd, Waggott Daryl, Haddad Francois, Reddy Sushma, Bernstein Daniel, Burns Trudy, Steimle Jeffrey D, Yang Xinan H, Moskowitz Ivan P, Hurles Matthew, Lifton Richard P, Nickerson Debbie, Bamshad Michael, Eichler Evan E, Mital Seema, Sheffield Val, Quertermous Thomas, Gelb Bruce D, Portman Michael, Ashley Euan |
Evaluation of Gene-Based Family-Based Methods to Detect Novel Genes Associated With Familial Late Onset Alzheimer Disease. Frontiers in neuroscience 2018 4 12 209. Fernández Maria V, Budde John, Del-Aguila Jorge L, Ibañez Laura, Deming Yuetiva, Harari Oscar, Norton Joanne, Morris John C, Goate Alison M, , , Cruchaga Carl |
Dynamics of the personalities of PCSK9 on missense variants (rs505151 and rs562556) from elderly cohort studies in Brazil. Journal of biomolecular structure & dynamics 2023 4 1-9. Galvão Lopes Vitor, Fernandes de Oliveira Victor, Mendonça Munhoz Dati Livia, Naslavsky Michel Satya, Ferreira Glaucio Monteiro, Hirata Mario Hiroyu |
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