Human Genome Epidemiology Literature Finder
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Integrative analysis of genome-wide association studies and gene expression profiles identified candidate genes for osteoporosis in Kashin-Beck disease patients. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2015 Oct . Wen Y, Guo X, Hao J, Xiao X, Wang W, Wu C, Wang S, Yang T, Shen H, Chen X, Tan L, Tian Q, Deng H-W, Zhang |
Risk prediction of pulmonary tuberculosis using genetic and conventional risk factors in adult Korean population.
PloS one 2017 12 (3): e0174642. Hong Eun Pyo, Go Min Jin, Kim Hyung-Lae, Park Ji W |
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. Journal of the American College of Cardiology 2017 Feb 69 (7): 823-836. Webb Thomas R, Erdmann Jeanette, Stirrups Kathleen E, Stitziel Nathan O, Masca Nicholas G D, Jansen Henning, Kanoni Stavroula, Nelson Christopher P, Ferrario Paola G, König Inke R, Eicher John D, Johnson Andrew D, Hamby Stephen E, Betsholtz Christer, Ruusalepp Arno, Franzén Oscar, Schadt Eric E, Björkegren Johan L M, Weeke Peter E, Auer Paul L, Schick Ursula M, Lu Yingchang, Zhang He, Dube Marie-Pierre, Goel Anuj, Farrall Martin, Peloso Gina M, Won Hong-Hee, Do Ron, van Iperen Erik, Kruppa Jochen, Mahajan Anubha, Scott Robert A, Willenborg Christina, Braund Peter S, van Capelleveen Julian C, Doney Alex S F, Donnelly Louise A, Asselta Rosanna, Merlini Pier A, Duga Stefano, Marziliano Nicola, Denny Josh C, Shaffer Christian, El-Mokhtari Nour Eddine, Franke Andre, Heilmann Stefanie, Hengstenberg Christian, Hoffmann Per, Holmen Oddgeir L, Hveem Kristian, Jansson Jan-Håkan, Jöckel Karl-Heinz, Kessler Thorsten, Kriebel Jennifer, Laugwitz Karl L, Marouli Eirini, Martinelli Nicola, McCarthy Mark I, Van Zuydam Natalie R, Meisinger Christa, Esko Tõnu, Mihailov Evelin, Escher Stefan A, Alver Maris, Moebus Susanne, Morris Andrew D, Virtamo Jarma, Nikpay Majid, Olivieri Oliviero, Provost Sylvie, AlQarawi Alaa, Robertson Neil R, Akinsansya Karen O, Reilly Dermot F, Vogt Thomas F, Yin Wu, Asselbergs Folkert W, Kooperberg Charles, Jackson Rebecca D, Stahl Eli, Müller-Nurasyid Martina, Strauch Konstantin, Varga Tibor V, Waldenberger Melanie, , Zeng Lingyao, Chowdhury Rajiv, Salomaa Veikko, Ford Ian, Jukema J Wouter, Amouyel Philippe, Kontto Jukka, , Nordestgaard Børge G, Ferrières Jean, Saleheen Danish, Sattar Naveed, Surendran Praveen, Wagner Aline, Young Robin, Howson Joanna M M, Butterworth Adam S, Danesh John, Ardissino Diego, Bottinger Erwin P, Erbel Raimund, Franks Paul W, Girelli Domenico, Hall Alistair S, Hovingh G Kees, Kastrati Adnan, Lieb Wolfgang, Meitinger Thomas, Kraus William E, Shah Svati H, McPherson Ruth, Orho-Melander Marju, Melander Olle, Metspalu Andres, Palmer Colin N A, Peters Annette, Rader Daniel J, Reilly Muredach P, Loos Ruth J F, Reiner Alex P, Roden Dan M, Tardif Jean-Claude, Thompson John R, Wareham Nicholas J, Watkins Hugh, Willer Cristen J, Samani Nilesh J, Schunkert Heribert, Deloukas Panos, Kathiresan Sekar, |
Revisiting Non-BRCA1/2 Familial Whole Exome Sequencing Datasets Implicates NCK1 as a Cancer Gene. Frontiers in genetics 2019 10 527. Yin Jie, Wu Kai, Ma Qingyang, Dong Hang, Zhu Yufei, Hu Landian, Kong Xiangy |
Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants. American journal of surgery 2021 7 223 (1): 182-186. Schwab Marisa E, Dong Shan, Lianoglou Billie R, Aguilar Lucero Alessandra F, Schwartz Grace B, Norton Mary E, MacKenzie Tippi C, Sanders Stephan |
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