HuGE Literature Finder
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| 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-Juaregui Claudia, Lawrie Allan, Trembath Richard C, Wilkins Martin R, , , , , Morrell Nicholas W, Shen Yufeng, Gräf Stefan, Nichols William C, Chung Wendy |
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.
The Lancet. Respiratory medicine 2018 Dec . Rhodes Christopher J, Batai Ken, Bleda Marta, Haimel Matthias, Southgate Laura, Germain Marine, Pauciulo Michael W, Hadinnapola Charaka, Aman Jurjan, Girerd Barbara, Arora Amit, Knight Jo, Hanscombe Ken B, Karnes Jason H, Kaakinen Marika, Gall Henning, Ulrich Anna, Harbaum Lars, Cebola Inês, Ferrer Jorge, Lutz Katie, Swietlik Emilia M, Ahmad Ferhaan, Amouyel Philippe, Archer Stephen L, Argula Rahul, Austin Eric D, Badesch David, Bakshi Sahil, Barnett Christopher, Benza Raymond, Bhatt Nitin, Bogaard Harm J, Burger Charles D, Chakinala Murali, Church Colin, Coghlan John G, Condliffe Robin, Corris Paul A, Danesino Cesare, Debette Stéphanie, Elliott C Gregory, Elwing Jean, Eyries Melanie, Fortin Terry, Franke Andre, Frantz Robert P, Frost Adaani, Garcia Joe G N, Ghio Stefano, Ghofrani Hossein-Ardeschir, Gibbs J Simon R, Harley John, He Hua, Hill Nicholas S, Hirsch Russel, Houweling Arjan C, Howard Luke S, Ivy Dunbar, Kiely David G, Klinger James, Kovacs Gabor, Lahm Tim, Laudes Matthias, Machado Rajiv D, Ross Robert V MacKenzie, Marsolo Keith, Martin Lisa J, Moledina Shahin, Montani David, Nathan Steven D, Newnham Michael, Olschewski Andrea, Olschewski Horst, Oudiz Ronald J, Ouwehand Willem H, Peacock Andrew J, Pepke-Zaba Joanna, Rehman Zia, Robbins Ivan, Roden Dan M, Rosenzweig Erika B, Saydain Ghulam, Scelsi Laura, Schilz Robert, Seeger Werner, Shaffer Christian M, Simms Robert W, Simon Marc, Sitbon Olivier, Suntharalingam Jay, Tang Haiyang, Tchourbanov Alexander Y, Thenappan Thenappan, Torres Fernando, Toshner Mark R, Treacy Carmen M, Noordegraaf Anton Vonk, Waisfisz Quinten, Walsworth Anna K, Walter Robert E, Wharton John, White R James, Wilt Jeffrey, Wort Stephen J, Yung Delphine, Lawrie Allan, Humbert Marc, Soubrier Florent, Trégouët David-Alexandre, Prokopenko Inga, Kittles Richard, Gräf Stefan, Nichols William C, Trembath Richard C, Desai Ankit A, Morrell Nicholas W, Wilkins Martin R, , , |
| Genetic Risk Factors for Intracranial Aneurysm in the Kazakh Population. Journal of molecular neuroscience : MN 2018 Aug . Zholdybayeva Elena V, Medetov Yerkin Z, Aitkulova Akbota M, Makhambetov Yerbol T, Akshulakov Serik K, Kaliyev Assylbek B, Talzhanov Yerkebulan A, Kulmambetova Gulmira N, Iskakova Aisha N, Ramankulov Yerlan |
| Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease. Genome medicine 2018 Jul 10 (1): 56. Zhu Na, Welch Carrie L, Wang Jiayao, Allen Philip M, Gonzaga-Jauregui Claudia, Ma Lijiang, King Alejandra K, Krishnan Usha, Rosenzweig Erika B, Ivy D Dunbar, Austin Eric D, Hamid Rizwan, Pauciulo Michael W, Lutz Katie A, Nichols William C, Reid Jeffrey G, Overton John D, Baras Aris, Dewey Frederick E, Shen Yufeng, Chung Wendy |
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- Page last updated:Nov 29, 2022
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