Human Genome Epidemiology Literature Finder
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Records 1 - 21 (of 21 Records) |
| Query Trace: Disease and BAG3[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 |
| Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes. Human mutation 2011 Dec 32 (12): 1481-91. Arimura Takuro, Ishikawa Taisuke, Nunoda Shinichi, Kawai Sachio, Kimura Akino |
| A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
European heart journal 2011 May 32 (9): 1065-76. Villard Eric, Perret Claire, Gary Françoise, Proust Carole, Dilanian Gilles, Hengstenberg Christian, Ruppert Volker, Arbustini Eloisa, Wichter Thomas, Germain Marine, Dubourg Olivier, Tavazzi Luigi, Aumont Marie-Claude, DeGroote Pascal, Fauchier Laurent, Trochu Jean-Noël, Gibelin Pierre, Aupetit Jean-François, Stark Klaus, Erdmann Jeanette, Hetzer Roland, Roberts Angharad M, Barton Paul J R, Regitz-Zagrosek Vera, , Aslam Uzma, Duboscq-Bidot Laëtitia, Meyborg Matthias, Maisch Bernhard, Madeira Hugo, Waldenström Anders, Galve Enrique, Cleland John G, Dorent Richard, Roizes Gerard, Zeller Tanja, Blankenberg Stefan, Goodall Alison H, Cook Stuart, Tregouet David A, Tiret Laurence, Isnard Richard, Komajda Michel, Charron Philippe, Cambien Franço |
| Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy. American journal of human genetics 2011 Mar 88 (3): 273-82. Norton Nadine, Li Duanxiang, Rieder Mark J, Siegfried Jill D, Rampersaud Evadnie, Züchner Stephan, Mangos Steve, Gonzalez-Quintana Jorge, Wang Libin, McGee Sean, Reiser Jochen, Martin Eden, Nickerson Deborah A, Hershberger Ray |
| The BAG3 gene variants in Polish patients with dilated cardiomyopathy: four novel mutations and a genotype-phenotype correlation. Journal of translational medicine 2014 12 192. Franaszczyk Maria, Bilinska Zofia T, Sobieszcza?ska-Ma?ek Ma?gorzata, Michalak Ewa, Sleszycka Justyna, Sioma Agnieszka, Ma?ek ?ukasz A, Kaczmarska Dorota, Walczak Ewa, W?odarski Pawe?, Hutnik ?ukasz, Milanowska Blanka, Dzielinska Zofia, Religa Grzegorz, Grzybowski Jacek, Zieli?ski Tomasz, Ploski Raf |
| BAG3 (Bcl-2-Associated Athanogene-3) Coding Variant in Mice Determines Susceptibility to Ischemic Limb Muscle Myopathy by Directing Autophagy. Circulation 2017 Jul 136 (3): 281-296. McClung Joseph M, McCord Timothy J, Ryan Terence E, Schmidt Cameron A, Green Tom D, Southerland Kevin W, Reinardy Jessica L, Mueller Sarah B, Venkatraman Talaignair N, Lascola Christopher D, Keum Sehoon, Marchuk Douglas A, Spangenburg Espen E, Dokun Ayotunde, Annex Brian H, Kontos Christopher |
| Association of Variants in BAG3 With Cardiomyopathy Outcomes in African American Individuals. JAMA cardiology 2018 Aug . Myers Valerie D, Gerhard Glenn S, McNamara Dennis M, Tomar Dhanendra, Madesh Muniswamy, Kaniper Scott, Ramsey Frederick V, Fisher Susan G, Ingersoll Roxann G, Kasch-Semenza Laura, Wang JuFang, Hanley-Yanez Karen, Lemster Bonnie, Schwisow Jessica A, Ambardekar Amrut V, Degann Seta H, Bristow Michael R, Sheppard Richard, Alexis Jeffrey D, Tilley Douglas G, Kontos Christopher D, McClung Joseph M, Taylor Anne L, Yancy Clyde W, Khalili Kamel, Seidman Jonathan G, Seidman Christine E, McTiernan Charles F, Cheung Joseph Y, Feldman Arthur |
| Genetic basis of hypertrophic cardiomyopathy in children. Clinical research in cardiology : official journal of the German Cardiac Society 2018 Aug . Rupp Stefan, Felimban Moataz, Schänzer Anne, Schranz Dietmar, Marschall Christoph, Zenker Martin, Logeswaran Thushiha, Neuhäuser Christoph, Thul Josef, Jux Christian, Hahn Andre |
| Lack of genetic susceptibility in takotsubo cardiomyopathy: a case-control study. BMC medical genetics 2018 Mar 19 (1): 39. Mattsson Emma, Saliba-Gustafsson Peter, Ehrenborg Ewa, Tornvall P |
| Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery. Circulation 2018 Nov . Aragam Krishna G, Chaffin Mark, Levinson Rebecca T, McDermott Gregory, Choi Seung-Hoan, Shoemaker M Benjamin, Haas Mary E, Weng Lu-Chen, Lindsay Mark E, Smith J Gustav, Newton-Cheh Christopher, Roden Dan M, London Barry, Wells Quinn S, Ellinor Patrick T, Kathiresan Sekar, Lubitz Steven A, |
| Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations. Journal of the American College of Cardiology 2018 Nov 72 (20): 2471-2481. Domínguez Fernando, Cuenca Sofía, Bili?ska Zofia, Toro Rocío, Villard Eric, Barriales-Villa Roberto, Ochoa Juan Pablo, Asselbergs Folkert, Sammani Arjan, Franaszczyk Maria, Akhtar Mohammed, Coronado-Albi Maria José, Rangel-Sousa Diego, Rodriguez-Palomares Jose F, Jiménez-Jáimez Juan, Garcia-Pinilla José Manuel, Ripoll-Vera Tomás, Mogollón-Jiménez Maria Victoria, Fontalba-Romero Ana, Garcia-Medina Dolores, Palomino-Doza Julian, de Gonzalo-Calvo David, Cicerchia Marcos, Salazar-Mendiguchia Joel, Salas Clara, Pankuweit Sabine, Hey Thomas Morris, Mogensen Jens, Barton Paul J, Charron Philippe, Elliott Perry, Garcia-Pavia Pablo, |
| Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and ?-synuclein mechanisms.
Movement disorders : official journal of the Movement Disorder Society 2019 Jun 34 (6): 866-875. Blauwendraat Cornelis, Heilbron Karl, Vallerga Costanza L, Bandres-Ciga Sara, von Coelln Rainer, Pihlstrøm Lasse, Simón-Sánchez Javier, Schulte Claudia, Sharma Manu, Krohn Lynne, Siitonen Ari, Iwaki Hirotaka, Leonard Hampton, Noyce Alastair J, Tan Manuela, Gibbs J Raphael, Hernandez Dena G, Scholz Sonja W, Jankovic Joseph, Shulman Lisa M, Lesage Suzanne, Corvol Jean-Christophe, Brice Alexis, van Hilten Jacobus J, Marinus Johan, , Eerola-Rautio Johanna, Tienari Pentti, Majamaa Kari, Toft Mathias, Grosset Donald G, Gasser Thomas, Heutink Peter, Shulman Joshua M, Wood Nicolas, Hardy John, Morris Huw R, Hinds David A, Gratten Jacob, Visscher Peter M, Gan-Or Ziv, Nalls Mike A, Singleton Andrew B, |
| A single-nucleotide polymorphism induced alternative splicing in Tacr3 involves in hypoxic-ischemic brain damage. Brain research bulletin 2019 11 154 106-115. Xue Lu-Lu, Wang Fang, Xiong Liu-Lin, Du Ruo-Lan, Zhou Hao-Li, Zou Yu, Wu Ma-Xiu, Yang Ming-An, Dai Jing, He Man-Xi, Wang Ting-H |
| The Genetic Makeup of the Electrocardiogram.
Cell systems 2020 Sep 11 (3): 229-238.e5. Verweij Niek, Benjamins Jan-Walter, Morley Michael P, van de Vegte Yordi J, Teumer Alexander, Trenkwalder Teresa, Reinhard Wibke, Cappola Thomas P, van der Harst P |
| Meta-Analysis of 26 638 Individuals Identifies Two Genetic Loci Associated With Left Ventricular Ejection Fraction.
Circulation. Genomic and precision medicine 2020 Aug 13 (4): e002804. Choquet Hélène, Thai Khanh K, Jiang Chen, Ranatunga Dilrini K, Hoffmann Thomas J, Go Alan S, Lindsay Alistair C, Ehm Margaret G, Waterworth Dawn M, Risch Neil, Schaefer Catheri |
| Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
Nature communications 2020 01 11 (1): 163. Shah Sonia, Henry Albert, Roselli Carolina, Lin Honghuang, Sveinbjörnsson Garðar, Fatemifar Ghazaleh, Hedman Åsa K, Wilk Jemma B, Morley Michael P, Chaffin Mark D, Helgadottir Anna, Verweij Niek, Dehghan Abbas, Almgren Peter, Andersson Charlotte, Aragam Krishna G, Ärnlöv Johan, Backman Joshua D, Biggs Mary L, Bloom Heather L, Brandimarto Jeffrey, Brown Michael R, Buckbinder Leonard, Carey David J, Chasman Daniel I, Chen Xing, Chen Xu, Chung Jonathan, Chutkow William, Cook James P, Delgado Graciela E, Denaxas Spiros, Doney Alexander S, Dörr Marcus, Dudley Samuel C, Dunn Michael E, Engström Gunnar, Esko Tõnu, Felix Stephan B, Finan Chris, Ford Ian, Ghanbari Mohsen, Ghasemi Sahar, Giedraitis Vilmantas, Giulianini Franco, Gottdiener John S, Gross Stefan, Guðbjartsson Daníel F, Gutmann Rebecca, Haggerty Christopher M, van der Harst Pim, Hyde Craig L, Ingelsson Erik, Jukema J Wouter, Kavousi Maryam, Khaw Kay-Tee, Kleber Marcus E, Køber Lars, Koekemoer Andrea, Langenberg Claudia, Lind Lars, Lindgren Cecilia M, London Barry, Lotta Luca A, Lovering Ruth C, Luan Jian'an, Magnusson Patrik, Mahajan Anubha, Margulies Kenneth B, März Winfried, Melander Olle, Mordi Ify R, Morgan Thomas, Morris Andrew D, Morris Andrew P, Morrison Alanna C, Nagle Michael W, Nelson Christopher P, Niessner Alexander, Niiranen Teemu, O'Donoghue Michelle L, Owens Anjali T, Palmer Colin N A, Parry Helen M, Perola Markus, Portilla-Fernandez Eliana, Psaty Bruce M, , Rice Kenneth M, Ridker Paul M, Romaine Simon P R, Rotter Jerome I, Salo Perttu, Salomaa Veikko, van Setten Jessica, Shalaby Alaa A, Smelser Diane T, Smith Nicholas L, Stender Steen, Stott David J, Svensson Per, Tammesoo Mari-Liis, Taylor Kent D, Teder-Laving Maris, Teumer Alexander, Thorgeirsson Guðmundur, Thorsteinsdottir Unnur, Torp-Pedersen Christian, Trompet Stella, Tyl Benoit, Uitterlinden Andre G, Veluchamy Abirami, Völker Uwe, Voors Adriaan A, Wang Xiaosong, Wareham Nicholas J, Waterworth Dawn, Weeke Peter E, Weiss Raul, Wiggins Kerri L, Xing Heming, Yerges-Armstrong Laura M, Yu Bing, Zannad Faiez, Zhao Jing Hua, Hemingway Harry, Samani Nilesh J, McMurray John J V, Yang Jian, Visscher Peter M, Newton-Cheh Christopher, Malarstig Anders, Holm Hilma, Lubitz Steven A, Sattar Naveed, Holmes Michael V, Cappola Thomas P, Asselbergs Folkert W, Hingorani Aroon D, Kuchenbaecker Karoline, Ellinor Patrick T, Lang Chim C, Stefansson Kari, Smith J Gustav, Vasan Ramachandran S, Swerdlow Daniel I, Lumbers R Thom |
| Pathogenic Variants Associated With Dilated Cardiomyopathy Predict Outcome in Pediatric Myocarditis. Circulation. Genomic and precision medicine 2021 7 14 (4): e003250. Seidel Franziska, Holtgrewe Manuel, Al-Wakeel-Marquard Nadya, Opgen-Rhein Bernd, Dartsch Josephine, Herbst Christopher, Beule Dieter, Pickardt Thomas, Klingel Karin, Messroghli Daniel, Berger Felix, Schubert Stephan, Kühnisch Jirko, Klaassen Sabi |
| Genotype and phenotype distribution of 435 patients with Charcot-Marie-Tooth disease from central south China. European journal of neurology 2021 7 28 (11): 3774-3783. Xie Yongzhi, Lin Zhiqiang, Liu Lei, Li Xiaobo, Huang Shunxiang, Zhao Huadong, Wang Binghao, Zeng Sen, Cao Wanqian, Li Lu, Zhu Xiying, Huang Siwei, Yang Honglan, Wang Mengli, Hu Zhengmao, Wang Junling, Guo Jifeng, Shen Lu, Jiang Hong, Zuchner Stephan, Tang Beisha, Zhang Ru |
| Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation.
Circulation. Genomic and precision medicine 2021 11 14 (6): e003460. Yang Yunju, Bartz Traci M, Brown Michael R, Guo Xiuqing, Zilhão Nuno R, Trompet Stella, Weiss Stefan, Yao Jie, Brody Jennifer A, Defilippi Christopher R, Hoogeveen Ron C, Lin Henry J, Gudnason Vilmundur, Ballantyne Christie M, Dörr Marcus, Jukema J Wouter, Petersmann Astrid, Psaty Bruce M, Rotter Jerome I, Boerwinkle Eric, Fornage Myriam, Jun Goo, Yu Bi |
| Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum. medRxiv : the preprint server for health sciences 2023 7 . David S M Lee, John S DePaolo, Krishna G Aragam, Kiran Biddinger, Mitchell Conery, Ozan Dilitikas, Lily Hoffman-Andrews, Renae L Judy, Atlas Khan, Iftikhar Kulo, Mugan J Puckelwartz, Nosheen Reza, Benjamin A Satterfield, Pankhuri Singhal, , Zoltan P Arany, Thomas P Cappola, Eric Carruth, Sharlene M Day, Ron Do, Christopher M Haggarty, Jacob Joseph, Elizabeth McNally, Girish Nadkarni, Anjali T Owens, Daniel J Rader, Marylyn D Ritchie, Yan Sun, Benjamin F Voight, Michael G Levin, Scott M Damrau |
| Four cardiomyopathy patients with a heterozygous DSG2 p.Arg119Ter variant. Human genome variation 2024 12 11 (1): 47. Takuya Sumida, Shou Ogawa, Shuichiro Higo, Yuki Kuramoto, Ryo Eto, Yoshihiko Ikeda, Congcong Sun, Junjun Li, Li Liu, Tomoka Tabata, Yoshihiro Asano, Mikio Shiba, Yasuhiro Akazawa, Daisuke Nakamura, Takafumi Oka, Tomohito Ohtani, Yasushi Saka |
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