Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Congenital heart[original query] |
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X-chromosome association studies of congenital heart defects.
American journal of medical genetics. Part A 2019 11 182 (1): 250-254. Agopian A J, Hoang Thanh T, Goldmuntz Elizabeth, Hakonarson Hakon, Musfee Fadi I, Mitchell Laura E, |
| Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Nature genetics 2013 Jul 45 (7): 822-4. Cordell Heather J, Bentham Jamie, Topf Ana, Zelenika Diana, Heath Simon, Mamasoula Chrysovalanto, Cosgrove Catherine, Blue Gillian, Granados-Riveron Javier, Setchfield Kerry, Thornborough Chris, Breckpot Jeroen, Soemedi Rachel, Martin Ruairidh, Rahman Thahira J, Hall Darroch, van Engelen Klaartje, Moorman Antoon F M, Zwinderman Aelko H, Barnett Phil, Koopmann Tamara T, Adriaens Michiel E, Varro Andras, George Alfred L, dos Remedios Christobal, Bishopric Nanette H, Bezzina Connie R, O'Sullivan John, Gewillig Marc, Bu'Lock Frances A, Winlaw David, Bhattacharya Shoumo, Devriendt Koen, Brook J David, Mulder Barbara J M, Mital Seema, Postma Alex V, Lathrop G Mark, Farrall Martin, Goodship Judith A, Keavney Bernard |
| A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.
Nature genetics 2013 Jul 45 (7): 818-21. Hu Zhibin, Shi Yongyong, Mo Xuming, Xu Jing, Zhao Bijun, Lin Yuan, Yang Shiwei, Xu Zhengfeng, Dai Juncheng, Pan Shandong, Da Min, Wang Xiaowei, Qian Bo, Wen Yang, Wen Juan, Xing Jinliang, Guo Xuejiang, Xia Yankai, Ma Hongxia, Jin Guangfu, Yu Shiqiang, Liu Jiayin, Zhou Zuomin, Wang Xinru, Chen Yijiang, Sha Jiahao, Shen Hongbi |
| Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
Nature genetics 2013 Jun 45 (6): 621-31. den Hoed Marcel, Eijgelsheim Mark, Esko Tõnu, Brundel Bianca J J M, Peal David S, Evans David M, Nolte Ilja M, Segrè Ayellet V, Holm Hilma, Handsaker Robert E, Westra Harm-Jan, Johnson Toby, Isaacs Aaron, Yang Jian, Lundby Alicia, Zhao Jing Hua, Kim Young Jin, Go Min Jin, Almgren Peter, Bochud Murielle, Boucher Gabrielle, Cornelis Marilyn C, Gudbjartsson Daniel, Hadley David, van der Harst Pim, Hayward Caroline, den Heijer Martin, Igl Wilmar, Jackson Anne U, Kutalik Zoltán, Luan Jian'an, Kemp John P, Kristiansson Kati, Ladenvall Claes, Lorentzon Mattias, Montasser May E, Njajou Omer T, O'Reilly Paul F, Padmanabhan Sandosh, St Pourcain Beate, Rankinen Tuomo, Salo Perttu, Tanaka Toshiko, Timpson Nicholas J, Vitart Veronique, Waite Lindsay, Wheeler William, Zhang Weihua, Draisma Harmen H M, Feitosa Mary F, Kerr Kathleen F, Lind Penelope A, Mihailov Evelin, Onland-Moret N Charlotte, Song Ci, Weedon Michael N, Xie Weijia, Yengo Loic, Absher Devin, Albert Christine M, Alonso Alvaro, Arking Dan E, de Bakker Paul I W, Balkau Beverley, Barlassina Cristina, Benaglio Paola, Bis Joshua C, Bouatia-Naji Nabila, Brage Søren, Chanock Stephen J, Chines Peter S, Chung Mina, Darbar Dawood, Dina Christian, Dörr Marcus, Elliott Paul, Felix Stephan B, Fischer Krista, Fuchsberger Christian, de Geus Eco J C, Goyette Philippe, Gudnason Vilmundur, Harris Tamara B, Hartikainen Anna-Liisa, Havulinna Aki S, Heckbert Susan R, Hicks Andrew A, Hofman Albert, Holewijn Suzanne, Hoogstra-Berends Femke, Hottenga Jouke-Jan, Jensen Majken K, Johansson Asa, Junttila Juhani, Kääb Stefan, Kanon Bart, Ketkar Shamika, Khaw Kay-Tee, Knowles Joshua W, Kooner Angrad S, Kors Jan A, Kumari Meena, Milani Lili, Laiho Päivi, Lakatta Edward G, Langenberg Claudia, Leusink Maarten, Liu Yongmei, Luben Robert N, Lunetta Kathryn L, Lynch Stacey N, Markus Marcello R P, Marques-Vidal Pedro, Mateo Leach Irene, McArdle Wendy L, McCarroll Steven A, Medland Sarah E, Miller Kathryn A, Montgomery Grant W, Morrison Alanna C, Müller-Nurasyid Martina, Navarro Pau, Nelis Mari, O'Connell Jeffrey R, O'Donnell Christopher J, Ong Ken K, Newman Anne B, Peters Annette, Polasek Ozren, Pouta Anneli, Pramstaller Peter P, Psaty Bruce M, Rao Dabeeru C, Ring Susan M, Rossin Elizabeth J, Rudan Diana, Sanna Serena, Scott Robert A, Sehmi Jaban S, Sharp Stephen, Shin Jordan T, Singleton Andrew B, Smith Albert V, Soranzo Nicole, Spector Tim D, Stewart Chip, Stringham Heather M, Tarasov Kirill V, Uitterlinden André G, Vandenput Liesbeth, Hwang Shih-Jen, Whitfield John B, Wijmenga Cisca, Wild Sarah H, Willemsen Gonneke, Wilson James F, Witteman Jacqueline C M, Wong Andrew, Wong Quenna, Jamshidi Yalda, Zitting Paavo, Boer Jolanda M A, Boomsma Dorret I, Borecki Ingrid B, van Duijn Cornelia M, Ekelund Ulf, Forouhi Nita G, Froguel Philippe, Hingorani Aroon, Ingelsson Erik, Kivimaki Mika, Kronmal Richard A, Kuh Diana, Lind Lars, Martin Nicholas G, Oostra Ben A, Pedersen Nancy L, Quertermous Thomas, Rotter Jerome I, van der Schouw Yvonne T, Verschuren W M Monique, Walker Mark, Albanes Demetrius, Arnar David O, Assimes Themistocles L, Bandinelli Stefania, Boehnke Michael, de Boer Rudolf A, Bouchard Claude, Caulfield W L Mark, Chambers John C, Curhan Gary, Cusi Daniele, Eriksson Johan, Ferrucci Luigi, van Gilst Wiek H, Glorioso Nicola, de Graaf Jacqueline, Groop Leif, Gyllensten Ulf, Hsueh Wen-Chi, Hu Frank B, Huikuri Heikki V, Hunter David J, Iribarren Carlos, Isomaa Bo, Jarvelin Marjo-Riitta, Jula Antti, Kähönen Mika, Kiemeney Lambertus A, van der Klauw Melanie M, Kooner Jaspal S, Kraft Peter, Iacoviello Licia, Lehtimäki Terho, Lokki Marja-Liisa L, Mitchell Braxton D, Navis Gerjan, Nieminen Markku S, Ohlsson Claes, Poulter Neil R, Qi Lu, Raitakari Olli T, Rimm Eric B, Rioux John D, Rizzi Federica, Rudan Igor, Salomaa Veikko, Sever Peter S, Shields Denis C, Shuldiner Alan R, Sinisalo Juha, Stanton Alice V, Stolk Ronald P, Strachan David P, Tardif Jean-Claude, Thorsteinsdottir Unnur, Tuomilehto Jaako, van Veldhuisen Dirk J, Virtamo Jarmo, Viikari Jorma, Vollenweider Peter, Waeber Gérard, Widen Elisabeth, Cho Yoon Shin, Olsen Jesper V, Visscher Peter M, Willer Cristen, Franke Lude, , , Erdmann Jeanette, Thompson John R, , Pfeufer Arne, , Sotoodehnia Nona, , Newton-Cheh Christopher, , Ellinor Patrick T, Stricker Bruno H Ch, Metspalu Andres, Perola Markus, Beckmann Jacques S, Smith George Davey, Stefansson Kari, Wareham Nicholas J, Munroe Patricia B, Sibon Ody C M, Milan David J, Snieder Harold, Samani Nilesh J, Loos Ruth J |
| Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Human molecular genetics 2013 Jan . Cordell HJ, Töpf A, Mamasoula C, Postma AV, Bentham J, Zelenika D, Heath S, Blue G, Cosgrove C, Riveron JG, Darlay R, Soemedi R, Wilson IJ, Ayers KL, Rahman TJ, Hall D, Mulder BJ, Zwinderman AH, van Engelen K, Brook JD, Setchfield K, Bu'lock FA, Thornborough C, O'Sullivan J, Stuart AG, Parsons J, Bhattacharya S, Winlaw D, Mital S, Gewillig M, Breckpot J, Devriendt K, Moorman AF, Rauch A, Lathrop GM, Keavney BD, Goodship JA |
| A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.
Human molecular genetics 2016 Mar . Hanchard Neil A, Swaminathan Shanker, Bucasas Kristine, Furthner Dieter, Fernbach Susan, Azamian Mahshid S, Wang Xueqing, Lewin Mark, Towbin Jeffrey A, D'Alessandro Lisa C A, Morris Shaine A, Dreyer William, Denfield Susan, Ayres Nancy A, Franklin Wayne J, Justino Henri, Lantin-Hermoso M Regina, Ocampo Elena C, Santos Alexia B, Parekh Dhaval, Moodie Douglas, Jeewa Aamir, Lawrence Emily, Allen Hugh D, Penny Daniel J, Fraser Charles D, Lupski James R, Popoola Mojisola, Wadhwa Lalita, Brook J David, Bu'Lock Frances A, Bhattacharya Shoumo, Lalani Seema R, Zender Gloria A, Fitzgerald-Butt Sara, Bowman Jessica, Corsmeier Don, White Peter, Lecerf Kelsey, Zapata Gladys, Hernandez Patricia, Goodship Judith A, Garg Vidu, Keavney Bernard D, Leal Suzanne M, Cordell Heather J, Belmont John W, McBride Kim |
| Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.
Circulation. Cardiovascular genetics 2017 Jun 10 (3): e001449. Agopian A J, Goldmuntz Elizabeth, Hakonarson Hakon, Sewda Anshuman, Taylor Deanne, Mitchell Laura E, |
| A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta.
European heart journal 2018 Mar . Bjornsson Thorsteinn, Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Sulem Patrick, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Magnusdottir Audur, Danielsen Ragnar, Sigurdsson Emil L, Adalsteinsdottir Berglind, Gunnarsson Sverrir I, Jonsdottir Ingileif, Arnar David O, Helgason Hrodmar, Gudbjartsson Tomas, Gudbjartsson Daniel F, Thorsteinsdottir Unnur, Holm Hilma, Stefansson Ka |
| Congenital heart disease risk loci identified by genome-wide association study in European patients.
The Journal of clinical investigation 2020 Nov . Lahm Harald, Jia Meiwen, Dreßen Martina, Wirth Felix, Puluca Nazan, Gilsbach Ralf, Keavney Bernard D, Cleuziou Julie, Beck Nicole, Bondareva Olga, Dzilic Elda, Burri Melchior, König Karl C, Ziegelmüller Johannes A, Abou-Ajram Claudia, Neb Irina, Zhang Zhong, Doppler Stefanie A, Mastantuono Elisa, Lichtner Peter, Eckstein Gertrud, Hörer Jürgen, Ewert Peter, Priest James R, Hein Lutz, Lange Rüdiger, Meitinger Thomas, Cordell Heather J, Müller-Myhsok Bertram, Krane Mark |
| Elucidation of the genetic causes of bicuspid aortic valve disease.
Cardiovascular research 2022 Jun . Gehlen Jan, Stundl Anja, Debiec Radoslaw, Fontana Federica, Krane Markus, Sharipova Dinara, Nelson Christopher P, Al-Kassou Baravan, Giel Ann Sophie, Sinning Jan Malte, Bruenger Christopher Mh, Zelck Carolin F, Koebbe Laura L, Braund Peter S, Webb Thomas R, Hetherington Simon, Ensminger Stephan, Fujita Buntaro, Mohamed Salah A, Shrestha Malakh, Krueger Heike, Siepe Matthias, Kari Fabian Alexander, Nordbeck Peter, Buravezky Larissa, Kelm Malte, Veulemans Verena, Adam Matti, Baldus Stephan, Laugwitz Karl Ludwig, Haas Yannick, Karck Matthias, Mehlhorn Uwe, Conzelmann Lars Oliver, Breitenbach Ingo, Lebherz Corinna, Urbanski Paul, Kim Won Keun, Kandels Joscha, Ellinghaus David, Nowak-Goettl Ulrike, Hoffmann Per, Wirth Felix, Doppler Stefanie, Lahm Harald, Dreßen Martina, von Scheidt Moritz, Knoll Katharina, Kessler Thorsten, Hengstenberg Christian, Schunkert Heribert, Nickenig Georg, Nöthen Markus M, Bolger Aidan P, Abdelilah-Seyfried Salim, Samani Nilesh J, Erdmann Jeanette, Trenkwalder Teresa, Schumacher Johann |
| A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study.
American journal of medical genetics. Part A 2022 4 188 (8): 2303-2314. Rashkin Sara R, Cleves Mario, Shaw Gary M, Nembhard Wendy N, Nestoridi Eirini, Jenkins Mary M, Romitti Paul A, Lou Xiang-Yang, Browne Marilyn L, Mitchell Laura E, Olshan Andrew F, Lomangino Kevin, Bhattacharyya Sudeepa, Witte John S, Hobbs Charlotte A, |
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