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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and HEY2[original query]
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. GWAS Catalog
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
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
[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
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
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
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