Human Genome Epidemiology Literature Finder
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Query Trace: Rare Diseases and KDR[original query] |
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Bayesian Inference Associates Rare KDR Variants with Specific Phenotypes in Pulmonary Arterial Hypertension. Circulation. Genomic and precision medicine 2020 12 14 (1): e003155. Swietlik Emilia M, Greene Daniel, Zhu Na, Megy Karyn, Cogliano Marcella, Rajaram Smitha, Pandya Divya, Tilly Tobias, Lutz Katie A, Welch Carrie C L, Pauciulo Michael W, Southgate Laura, Martin Jennifer M, Treacy Carmen M, Penkett Christopher J, Stephens Jonathan C, Bogaard Harm J, Church Colin, Coghlan Gerry, Coleman Anna W, Condliffe Robin, Eichstaedt Christina A, Eyries Mélanie, Gall Henning, Ghio Stefano, Girerd Barbara, Grünig Ekkehard, Holden Simon, Howard Luke, Humbert Marc, Kiely David G, Kovacs Gabor, Lordan Jim, Machado Rajiv D, Mackenzie Ross Robert V, McCabe Colm, Moledina Shahin, Montani David, Olschewski Horst, Pepke-Zaba Joanna, Price Laura, Rhodes Christopher J, Seeger Werner, Soubrier Florent, Suntharalingam Jay, Toshner Mark R, Vonk Noordegraaf Anton, Wharton John, Wild James M, Wort Stephen John, Lawrie Allan, Wilkins Martin R, Trembath Richard C, Shen Yufeng, Chung Wendy K, Swift Andrew J, Nichols William C, Morrell Nicholas W, Gräf Stef |
Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH. Genome medicine 2021 May 13 (1): 80. Zhu Na, Swietlik Emilia M, Welch Carrie L, Pauciulo Michael W, Hagen Jacob J, Zhou Xueya, Guo Yicheng, Karten Johannes, Pandya Divya, Tilly Tobias, Lutz Katie A, Martin Jennifer M, Treacy Carmen M, Rosenzweig Erika B, Krishnan Usha, Coleman Anna W, Gonzaga-Jauregui Claudia, Lawrie Allan, Trembath Richard C, Wilkins Martin R, , , , , Morrell Nicholas W, Shen Yufeng, Gräf Stefan, Nichols William C, Chung Wendy |
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