Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and GOSR2[original query] |
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Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.
JCI insight 2022 2 7 (3): . Yu Mengyao, Tcheandjieu Catherine, Georges Adrien, Xiao Ke, Tejeda Helio, Dina Christian, Le Tourneau Thierry, Fiterau Madalina, Judy Renae, Tsao Noah L, Amgalan Dulguun, Munger Chad J, Engreitz Jesse M, Damrauer Scott M, Bouatia-Naji Nabila, Priest James |
| GOSR2 Lys67Arg is associated with hypertension in whites. American journal of hypertension 2009 Feb 22 (2): 163-8. Meyer Tamra E, Shiffman Dov, Morrison Alanna C, Rowland Charles M, Louie Judy Z, Bare Lance A, Ross David A, Arellano Andre R, Chasman Daniel I, Ridker Paul M, Pankow James S, Coresh Josef, Malloy Mary J, Kane John P, Ellis Stephen G, Devlin James J, Boerwinkle Er |
| Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature 2011 Oct 478 (7367): 7367. Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, Bragg-Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y, Heath S, Sõber S, Parsa A, Luan J, Arora P, Dehghan A, Zhang F, Lucas G, Hicks AA, Jackson AU, Peden JF, Tanaka T, Wild SH, Rudan I, Igl W, Milaneschi Y, Parker AN, Fava C, Chambers JC, Fox ER, Kumari M, Go MJ, van der Harst P, Kao WH, Sjögren M, Vinay DG, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup PH, Liu Y, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen KD, Lehtimäki T, Matullo G, Wu Y, Gaunt TR, Onland-Moret NC, Cooper MN, Platou CG, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund PS, Kuznetsova T, Uiterwaal CS, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer ND, Aspelund T, Garcia M, Chang YP, O'Connell JR, Steinle NI, Grobbee DE, Arking DE, Kardia SL, Morrison AC, Hernandez D, Najjar S, McArdle WL, Hadley D, Brown MJ, Connell JM, Hingorani AD, Day IN, Lawlor DA, Beilby JP, Lawrence RW, Clarke R, Hopewell JC, Ongen H, Dreisbach AW, Li Y, Young JH, Bis JC, Kähönen M, Viikari J, Adair LS, Lee NR, Chen MH, Olden M, Pattaro C, Bolton JA, Köttgen A, Bergmann S, Mooser V, Chaturvedi N, Frayling TM, Islam M, Jafar TH, Erdmann J, Kulkarni SR, Bornstein SR, Grässler J, Groop L, Voight BF, Kettunen J, Howard P, Taylor A, Guarrera S, Ricceri F, Emilsson V, Plump A, Barroso I, Khaw KT, Weder AB, Hunt SC, Sun YV, Bergman RN, Collins FS, Bonnycastle LL, Scott LJ, Stringham HM, Peltonen L, Perola M, Vartiainen E, Brand SM, Staessen JA, Wang TJ, Burton PR, Soler Artigas M, Dong Y, Snieder H, Wang X, Zhu H, Lohman KK, Rudock ME, Heckbert SR, Smith NL, Wiggins KL, Doumatey A, Shriner D, Veldre G, Viigimaa M, Kinra S, Prabhakaran D, Tripathy V, Langefeld CD, Rosengren A, Thelle DS, Corsi AM, Singleton A, Forrester T, Hilton G, McKenzie CA, Salako T, Iwai N, Kita Y, Ogihara T, Ohkubo T, Okamura T, Ueshima H, Umemura S, Eyheramendy S, Meitinger T, Wichmann HE, Cho YS, Kim HL, Lee JY, Scott J, Sehmi JS, Zhang W, Hedblad B, Nilsson P, Smith GD, Wong A, Narisu N, Stan?áková A, Raffel LJ, Yao J, Kathiresan S, O'Donnell CJ, Schwartz SM, Ikram MA, Longstreth WT, Mosley TH, Seshadri S, Shrine NR, Wain LV, Morken MA, Swift AJ, Laitinen J, Prokopenko I, Zitting P, Cooper JA, Humphries SE, Danesh J, Rasheed A, Goel A, Hamsten A, Watkins H, Bakker SJ, van Gilst WH, Janipalli CS, Mani KR, Yajnik CS, Hofman A, Mattace-Raso FU, Oostra BA, Demirkan A, Isaacs A, Rivadeneira F, Lakatta EG, Orru M, Scuteri A, Ala-Korpela M, Kangas AJ, Lyytikäinen LP, Soininen P, Tukiainen T, Würtz P, Ong RT, Dörr M, Kroemer HK, Völker U, Völzke H, Galan P, Hercberg S, Lathrop M, Zelenika D, Deloukas P, Mangino M, Spector TD, Zhai G, Meschia JF, Nalls MA, Sharma P, Terzic J, Kumar MV, Denniff M, Zukowska-Szczechowska E, Wagenknecht LE, Fowkes FG, Charchar FJ, Schwarz PE, Hayward C, Guo X, Rotimi C, Bots ML, Brand E, Samani NJ, Polasek O, Talmud PJ, Nyberg F, Kuh D, Laan M, Hveem K, Palmer LJ, van der Schouw YT, Casas JP, Mohlke KL, Vineis P, Raitakari O, Ganesh SK, Wong TY, Tai ES, Cooper RS, Laakso M, Rao DC, Harris TB, Morris RW, Dominiczak AF, Kivimaki M, Marmot MG, Miki T, Saleheen D, Chandak GR, Coresh J, Navis G, Salomaa V, Han BG, Zhu X, Kooner JS, Melander O, Ridker PM, Bandinelli S, Gyllensten UB, Wright AF, Wilson JF, Ferrucci L, Farrall M, Tuomilehto J, Pramstaller PP, Elosua R, Soranzo N, Sijbrands EJ, Altshuler D, Loos RJ, Shuldiner AR, Gieger C, Meneton P, Uitterlinden AG, Wareham NJ, Gudnason V, Rotter JI, Rettig R, Uda M, Strachan DP, Witteman JC, Hartikainen AL, Beckmann JS, Boerwinkle E, Vasan RS, Boehnke M, Larson MG, Järvelin MR, Psaty BM, Abecasis GR, Chakravarti A, Elliott P, van Duijn CM, Newton-Cheh C, Levy D, Caulfield MJ, Johnson T |
| A genetic variant in the seed region of miR-4513 shows pleiotropic effects on lipid and glucose homeostasis, blood pressure, and coronary artery disease. Human mutation 2014 Dec 35 (12): 1524-31. Ghanbari Mohsen, de Vries Paul S, de Looper Hans, Peters Marjolein J, Schurmann Claudia, Yaghootkar Hanieh, Dörr Marcus, Frayling Timothy M, Uitterlinden Andre G, Hofman Albert, van Meurs Joyce B J, Erkeland Stefan J, Franco Oscar H, Dehghan Abb |
| Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
The Journal of clinical investigation 2017 May 127 (5): 1798-1812. Wild Philipp S, Felix Janine F, Schillert Arne, Teumer Alexander, Chen Ming-Huei, Leening Maarten J G, Völker Uwe, Großmann Vera, Brody Jennifer A, Irvin Marguerite R, Shah Sanjiv J, Pramana Setia, Lieb Wolfgang, Schmidt Reinhold, Stanton Alice V, Malzahn Dörthe, Smith Albert Vernon, Sundström Johan, Minelli Cosetta, Ruggiero Daniela, Lyytikäinen Leo-Pekka, Tiller Daniel, Smith J Gustav, Monnereau Claire, Di Tullio Marco R, Musani Solomon K, Morrison Alanna C, Pers Tune H, Morley Michael, Kleber Marcus E, Aragam Jayashri, Benjamin Emelia J, Bis Joshua C, Bisping Egbert, Broeckel Ulrich, Cheng Susan, Deckers Jaap W, Del Greco M Fabiola, Edelmann Frank, Fornage Myriam, Franke Lude, Friedrich Nele, Harris Tamara B, Hofer Edith, Hofman Albert, Huang Jie, Hughes Alun D, Kähönen Mika, Investigators Knhi, Kruppa Jochen, Lackner Karl J, Lannfelt Lars, Laskowski Rafael, Launer Lenore J, Leosdottir Margrét, Lin Honghuang, Lindgren Cecilia M, Loley Christina, MacRae Calum A, Mascalzoni Deborah, Mayet Jamil, Medenwald Daniel, Morris Andrew P, Müller Christian, Müller-Nurasyid Martina, Nappo Stefania, Nilsson Peter M, Nuding Sebastian, Nutile Teresa, Peters Annette, Pfeufer Arne, Pietzner Diana, Pramstaller Peter P, Raitakari Olli T, Rice Kenneth M, Rivadeneira Fernando, Rotter Jerome I, Ruohonen Saku T, Sacco Ralph L, Samdarshi Tandaw E, Schmidt Helena, Sharp Andrew S P, Shields Denis C, Sorice Rossella, Sotoodehnia Nona, Stricker Bruno H, Surendran Praveen, Thom Simon, Töglhofer Anna M, Uitterlinden André G, Wachter Rolf, Völzke Henry, Ziegler Andreas, Münzel Thomas, März Winfried, Cappola Thomas P, Hirschhorn Joel N, Mitchell Gary F, Smith Nicholas L, Fox Ervin R, Dueker Nicole D, Jaddoe Vincent W V, Melander Olle, Russ Martin, Lehtimäki Terho, Ciullo Marina, Hicks Andrew A, Lind Lars, Gudnason Vilmundur, Pieske Burkert, Barron Anthony J, Zweiker Robert, Schunkert Heribert, Ingelsson Erik, Liu Kiang, Arnett Donna K, Psaty Bruce M, Blankenberg Stefan, Larson Martin G, Felix Stephan B, Franco Oscar H, Zeller Tanja, Vasan Ramachandran S, Dörr Marc |
| G-T haplotype established by rs3785889-rs16941382 in GOSR2 gene is associated with coronary artery disease in Chinese Han population. Oncotarget 2017 Oct 8 (47): 82165-82173. Pan Shuo, Guan Gong-Chang, Lv Ying, Liu Zhong-Wei, Liu Fu-Qiang, Zhang Yong, Zhu Shun-Ming, Zhang Rong-Huai, Zhao Na, Shi Shuang, Nakayama Tomohiro, Wang Jun-K |
| Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease.
International journal of molecular medicine 2018 Nov 42 (5): 2415-2436. Yamada Yoshiji, Kato Kimihiko, Oguri Mitsutoshi, Horibe Hideki, Fujimaki Tetsuo, Yasukochi Yoshiki, Takeuchi Ichiro, Sakuma J |
| Examination of the associations between mA-associated single-nucleotide polymorphisms and blood pressure. Hypertension research : official journal of the Japanese Society of Hypertension 2019 6 42 (10): 1582-1589. Mo Xing-Bo, Lei Shu-Feng, Zhang Yong-Hong, Zhang Hu |
| 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 |
| Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease Phenotypes.
Circulation. Genomic and precision medicine 2020 10 13 (6): e003014. Córdova-Palomera Aldo, Tcheandjieu Catherine, Fries Jason A, Varma Paroma, Chen Vincent S, Fiterau Madalina, Xiao Ke, Tejeda Heliodoro, Keavney Bernard D, Cordell Heather J, Tanigawa Yosuke, Venkataraman Guhan, Rivas Manuel A, Ré Christopher, Ashley Euan, Priest James |
| Unraveling the genomic basis of congenital heart disease. The Journal of clinical investigation 2021 Jan 131 (2): . Darbar Dawo |
| Coronary artery disease patients with rs7904519 (TCF7L2) are at a persistent risk of type 2 diabetes. Diabetes research and clinical practice 2023 12 207 111052. Cynthia Al Hageh, Siobhan O'Sullivan, Daniel E Platt, Andreas Henschel, Stephanie Chacar, Dominique Gauguier, Antoine Abchee, Eman Alefishat, Moni Nader, Pierre A Zallo |
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