Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and SOX17[original query] |
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Susceptibility loci for intracranial aneurysm in European and Japanese populations.
Nature genetics 2008 Dec 40 (12): 1472-7. Bilguvar Kaya, Yasuno Katsuhito, Niemelä Mika, Ruigrok Ynte M, von Und Zu Fraunberg Mikael, van Duijn Cornelia M, van den Berg Leonard H, Mane Shrikant, Mason Christopher E, Choi Murim, Gaál Emília, Bayri Yasar, Kolb Luis, Arlier Zulfikar, Ravuri Sudhakar, Ronkainen Antti, Tajima Atsushi, Laakso Aki, Hata Akira, Kasuya Hidetoshi, Koivisto Timo, Rinne Jaakko, Ohman Juha, Breteler Monique M B, Wijmenga Cisca, State Matthew W, Rinkel Gabriel J E, Hernesniemi Juha, Jääskeläinen Juha E, Palotie Aarno, Inoue Ituro, Lifton Richard P, Günel Mur |
| Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk.
Stroke; a journal of cerebral circulation 2012 Nov 43 (11): 2846-52. Foroud Tatiana, Koller Daniel L, Lai Dongbing, Sauerbeck Laura, Anderson Craig, Ko Nerissa, Deka Ranjan, Mosley Thomas H, Fornage Myriam, Woo Daniel, Moomaw Charles J, Hornung Richard, Huston John, Meissner Irene, Bailey-Wilson Joan E, Langefeld Carl, Rouleau Guy, Connolly E Sander, Worrall Bradford B, Kleindorfer Dawn, Flaherty Matthew L, Martini Sharyl, Mackey Jason, De Los Rios La Rosa Felipe, Brown Robert D, Broderick Joseph P, |
| Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux. Pediatric nephrology (Berlin, Germany) 2015 Sep . Elahi Shan, Homstad Alison, Vaidya Himani, Stout Jennifer, Hall Gentzon, Wu Guanghong, Conlon Peter, Routh Jonathan C, Wiener John S, Ross Sherry S, Nagaraj Shashi, Wigfall Delbert, Foreman John, Adeyemo Adebowale, Gupta Indra R, Brophy Patrick D, Rabinovich C Egla, Gbadegesin Rasheed |
| Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract. Journal of the American Society of Nephrology : JASN 2017 May . Heidet Laurence, Morinière Vincent, Henry Charline, De Tomasi Lara, Reilly Madeline Louise, Humbert Camille, Alibeu Olivier, Fourrage Cécile, Bole-Feysot Christine, Nitschké Patrick, Tores Frédéric, Bras Marc, Jeanpierre Marc, Pietrement Christine, Gaillard Dominique, Gonzales Marie, Novo Robert, Schaefer Elise, Roume Joëlle, Martinovic Jelena, Malan Valérie, Salomon Rémi, Saunier Sophie, Antignac Corinne, Jeanpierre Céci |
| 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 |
| Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.
Circulation 2019 Jan 139 (5): 620-635. Sabater-Lleal Maria, Huffman Jennifer E, de Vries Paul S, Marten Jonathan, Mastrangelo Michael A, Song Ci, Pankratz Nathan, Ward-Caviness Cavin K, Yanek Lisa R, Trompet Stella, Delgado Graciela E, Guo Xiuqing, Bartz Traci M, Martinez-Perez Angel, Germain Marine, de Haan Hugoline G, Ozel Ayse B, Polasek Ozren, Smith Albert V, Eicher John D, Reiner Alex P, Tang Weihong, Davies Neil M, Stott David J, Rotter Jerome I, Tofler Geoffrey H, Boerwinkle Eric, de Maat Moniek P M, Kleber Marcus E, Welsh Paul, Brody Jennifer A, Chen Ming-Huei, Vaidya Dhananjay, Soria José Manuel, Suchon Pierre, van Hylckama Vlieg Astrid, Desch Karl C, Kolcic Ivana, Joshi Peter K, Launer Lenore J, Harris Tamara B, Campbell Harry, Rudan Igor, Becker Diane M, Li Jun Z, Rivadeneira Fernando, Uitterlinden André G, Hofman Albert, Franco Oscar H, Cushman Mary, Psaty Bruce M, Morange Pierre-Emmanuel, McKnight Barbara, Chong Michael R, Fernandez-Cadenas Israel, Rosand Jonathan, Lindgren Arne, , Gudnason Vilmundur, Wilson James F, Hayward Caroline, Ginsburg David, Fornage Myriam, Rosendaal Frits R, Souto Juan Carlos, Becker Lewis C, Jenny Nancy S, März Winfried, Jukema J Wouter, Dehghan Abbas, Trégouët David-Alexandre, Morrison Alanna C, Johnson Andrew D, O'Donnell Christopher J, Strachan David P, Lowenstein Charles J, Smith Nicholas |
| 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, MacKenzie Ross Robert V, 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, Vonk Noordegraaf Anton, 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, , , |
| Genes that drive the pathobiology of pediatric pulmonary arterial hypertension. Pediatric pulmonology 2020 1 56 (3): 614-620. Welch Carrie L, Austin Eric D, Chung Wendy |
| 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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