Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: HEY2[original query] |
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ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresia. American journal of medical genetics. Part A 2005 Feb 133A (1): 68-70. Sarkozy Anna, Conti Emanuela, D'Agostino Rita, Digilio Maria Cristina, Formigari Roberto, Picchio Fernando, Marino Bruno, Pizzuti Antonio, Dallapiccola Bru |
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Nature genetics 2013 Sep 45 (9): 1044-9. Bezzina Connie R, Barc Julien, Mizusawa Yuka, Remme Carol Ann, Gourraud Jean-Baptiste, Simonet Floriane, Verkerk Arie O, Schwartz Peter J, Crotti Lia, Dagradi Federica, Guicheney Pascale, Fressart Véronique, Leenhardt Antoine, Antzelevitch Charles, Bartkowiak Susan, Borggrefe Martin, Schimpf Rainer, Schulze-Bahr Eric, Zumhagen Sven, Behr Elijah R, Bastiaenen Rachel, Tfelt-Hansen Jacob, Olesen Morten Salling, Kääb Stefan, Beckmann Britt M, Weeke Peter, Watanabe Hiroshi, Endo Naoto, Minamino Tohru, Horie Minoru, Ohno Seiko, Hasegawa Kanae, Makita Naomasa, Nogami Akihiko, Shimizu Wataru, Aiba Takeshi, Froguel Philippe, Balkau Beverley, Lantieri Olivier, Torchio Margherita, Wiese Cornelia, Weber David, Wolswinkel Rianne, Coronel Ruben, Boukens Bas J, Bézieau Stéphane, Charpentier Eric, Chatel Stéphanie, Despres Aurore, Gros Françoise, Kyndt Florence, Lecointe Simon, Lindenbaum Pierre, Portero Vincent, Violleau Jade, Gessler Manfred, Tan Hanno L, Roden Dan M, Christoffels Vincent M, Le Marec Hervé, Wilde Arthur A, Probst Vincent, Schott Jean-Jacques, Dina Christian, Redon Richa |
Brugada syndrome risk loci seem protective against atrial fibrillation. European journal of human genetics : EJHG 2014 Dec 22 (12): 1357-61. Andreasen Laura, Nielsen Jonas B, Darkner Stine, Christophersen Ingrid E, Jabbari Javad, Refsgaard Lena, Thiis Jens J, Sajadieh Ahmad, Tveit Arnljot, Haunsø Stig, Svendsen Jesper H, Schmitt Nicole, Olesen Morten |
Forkhead box C2 promoter variant c.-512C>T is associated with increased susceptibility to chronic venous diseases. PloS one 2014 9 (3): e90682. Surendran Sumi, Girijamma Athira, Nair Radhakrishnan, Ramegowda Kalpana S, Nair Divya H, Thulaseedharan Jissa V, Lakkappa Ravikumar B, Kamalapurkar Giridhar, Kartha Chandrasekharan |
Five endometrial cancer risk loci identified through genome-wide association analysis.
Nature genetics 2016 May . Cheng Timothy H T, Thompson Deborah J, O'Mara Tracy A, Painter Jodie N, Glubb Dylan M, Flach Susanne, Lewis Annabelle, French Juliet D, Freeman-Mills Luke, Church David, Gorman Maggie, Martin Lynn, , Hodgson Shirley, Webb Penelope M, , Attia John, Holliday Elizabeth G, McEvoy Mark, Scott Rodney J, Henders Anjali K, Martin Nicholas G, Montgomery Grant W, Nyholt Dale R, Ahmed Shahana, Healey Catherine S, Shah Mitul, Dennis Joe, Fasching Peter A, Beckmann Matthias W, Hein Alexander, Ekici Arif B, Hall Per, Czene Kamila, Darabi Hatef, Li Jingmei, Dörk Thilo, Dürst Matthias, Hillemanns Peter, Runnebaum Ingo, Amant Frederic, Schrauwen Stefanie, Zhao Hui, Lambrechts Diether, Depreeuw Jeroen, Dowdy Sean C, Goode Ellen L, Fridley Brooke L, Winham Stacey J, Njølstad Tormund S, Salvesen Helga B, Trovik Jone, Werner Henrica M J, Ashton Katie, Otton Geoffrey, Proietto Tony, Liu Tao, Mints Miriam, Tham Emma, , , Li Mulin Jun, Yip Shun H, Wang Junwen, Bolla Manjeet K, Michailidou Kyriaki, Wang Qin, Tyrer Jonathan P, Dunlop Malcolm, Houlston Richard, Palles Claire, Hopper John L, , Peto Julian, Swerdlow Anthony J, Burwinkel Barbara, Brenner Hermann, Meindl Alfons, Brauch Hiltrud, Lindblom Annika, Chang-Claude Jenny, Couch Fergus J, Giles Graham G, Kristensen Vessela N, Cox Angela, Cunningham Julie M, Pharoah Paul D P, Dunning Alison M, Edwards Stacey L, Easton Douglas F, Tomlinson Ian, Spurdle Amanda |
Common Variant Near HEY2 Has a Protective Effect on Ventricular Fibrillation Occurrence in Brugada Syndrome by Regulating the Repolarization Current. Circulation. Arrhythmia and electrophysiology 2016 Jan 9 (1): . Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Toshishige Masaaki, Tokuyama Takehito, Matsumura Hiroya, Kawazoe Hiroshi, Tomomori Shunsuke, Sairaku Akinori, Watanabe Yoshikazu, Ikenaga Hiroki, Motoda Chikaaki, Suenari Kazuyoshi, Hayashida Yasufumi, Miki Daiki, Oda Nozomu, Kishimoto Shinji, Oda Noboru, Yoshida Yukihiko, Tashiro Satoshi, Chayama Kazuaki, Kihara Yasu |
The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity. Circulation research 2017 Aug 121 (5): 537-548. Veerman Christiaan C, Podliesna Svitlana, Tadros Rafik, Lodder Elisabeth M, Mengarelli Isabella, de Jonge Berend, Beekman Leander, Barc Julien, Wilders Ronald, Wilde Arthur A M, Boukens Bastiaan J, Coronel Ruben, Verkerk Arie O, Remme Carol Ann, Bezzina Connie |
Kras upregulates Notch signaling to induce gallbladder tumorigenesis in mice. Oncoscience 2017 Sep 4 (9-10): 131-138. Chung Wen-Cheng, Wang Junqing, Zhou Yunyun, Xu Ke |
A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction. PloS one 2017 12 (1): e0170193. Jabbari Reza, Glinge Charlotte, Jabbari Javad, Risgaard Bjarke, Winkel Bo Gregers, Terkelsen Christian Juhl, Tilsted Hans-Henrik, Jensen Lisette Okkels, Hougaard Mikkel, Haunsø Stig, Engstrøm Thomas, Albert Christine M, Tfelt-Hansen Jac |
[Association between polymorphism in notch signaling pathway and lung cancer risk]. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] 2018 Mar 52 (3): 243-252. Xu Q P, Xiao R D, Xiong W M, He F, Cai |
Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest. Frontiers in physiology 2018 9 894. Andreasen Laura, Ghouse Jonas, Skov Morten W, Have Christian T, Ahlberg Gustav, Rasmussen Peter V, Linneberg Allan, Pedersen Oluf, Platonov Pyotr G, Haunsø Stig, Svendsen Jesper H, Hansen Torben, Kanters Jørgen K, Olesen Morten |
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Aug . van Walree Eva S, Dombrowsky Gregor, Jansen Iris E, Mirkov Maša Umi?evi?, Zwart Rob, Ilgun Aho, Guo Dongchuan, Clur Sally-Ann B, Amin Ahmed S, Savage Jeanne E, van der Wal Allard C, Waisfisz Quinten, Maugeri Alessandra, Wilsdon Anna, Bu'Lock Frances A, Hurles Matthew E, Dittrich Sven, Berger Felix, Audain Martinez Enrique, Christoffels Vincent M, Hitz Marc-Philip, Milewicz Dianna M, Posthuma Daniëlle, Meijers-Heijboer Hanne, Postma Alex V, Mathijssen Inge |
Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand.
Heart rhythm 2020 Jun . Makarawate Pattarapong, Glinge Charlotte, Khongphatthanayothin Apichai, Walsh Roddy, Mauleekoonphairoj John, Amnueypol Montawatt, Prechawat Somchai, Wongcharoen Wanwarang, Krittayaphong Rungroj, Anannab Alisara, Lichtner Peter, Meitinger Thomas, Tjong Fleur V Y, Lieve Krystien V V, Amin Ahmad S, Sahasatas Dujdao, Ngarmukos Tachapong, Wichadakul Duangdao, Payungporn Sunchai, Sutjaporn Boosamas, Wandee Pharawee, Poovorawan Yong, Tfelt-Hansen Jacob, Tanck Michael W T, Tadros Rafik, Wilde Arthur A M, Bezzina Connie R, Veerakul Gumpanart, Nademanee Koonlaw |
Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2020 Apr . Foddha Hajer, Bouzidi Nadia, Foddha Abdelhak, Chouchene Saoussen, Touhami Rahma, Leban Nadia, Maatoug Mohamed Faouzi, Gamra Habib, Ferchichi Salima, Chibani Jemni Ben, Khelil Amel H |
Phenotypic and Genotypic Associations Between Migraine and Lipoprotein Subfractions. Neurology 2021 10 97 (22): e2223-e2235. Guo Yanjun, Daghlas Iyas, Gormley Padhraig, Giulianini Franco, Ridker Paul M, Mora Samia, Kurth Tobias, Rist Pamela M, Chasman Daniel |
Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population. Italian journal of pediatrics 2022 7 48 (1): 124. Sarwar Sumbal, Shabana , Tahir Amna, Liaqat Zainab, Naseer Saher, Seme Rani Summeya, Mehmood Sabahat, Shahid Saleem Ullah, Hasnain Shahi |
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