Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: FHOD3[original query] |
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Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs.
Molecular psychiatry 2011 Mar 16 (3): 321-32. Adkins D E, Aberg K, McClay J L, Bukszár J, Zhao Z, Jia P, Stroup T S, Perkins D, McEvoy J P, Lieberman J A, Sullivan P F, van den Oord E J C |
Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy. Circulation. Cardiovascular genetics 2012 Dec . Wooten EC, Hebl VB, Wolf MJ, Greytak SR, Orr N, Draper I, Calvino JE, Kapur NK, Maron MS, Kullo IJ, Ommen SR, Bos JM, Ackerman MJ, Huggins GS |
Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years.
G3 (Bethesda, Md.) 2014 Feb 4 (2): 307-14. Shaffer John R, Polk Deborah E, Wang Xiaojing, Feingold Eleanor, Weeks Daniel E, Lee Myoung-Keun, Cuenco Karen T, Weyant Robert J, Crout Richard J, McNeil Daniel W, Marazita Mary |
Dilated cardiomyopathy-associated FHOD3 variant impairs the ability to induce activation of transcription factor serum response factor. Circulation journal : official journal of the Japanese Circulation Society 2013 77 (12): 2990-6. Arimura Takuro, Takeya Ryu, Ishikawa Taisuke, Yamano Tetsuhiro, Matsuo Akiko, Tatsumi Tetsuya, Nomura Tetsuya, Sumimoto Hideki, Kimura Akino |
Whole-genome analysis in Korean patients with autoimmune myasthenia gravis. Yonsei medical journal 2014 May 55 (3): 660-8. Na Sang-Jun, Lee Ji Hyun, Kim So Won, Kim Dae-Seong, Shon Eun Hee, Park Hyung Jun, Shin Ha Young, Kim Seung Min, Choi Young-Ch |
An integrated analysis of cancer genes in thyroid cancer. Oncology reports 2016 Feb 35 (2): 962-70. Chai Li, Li Jia, Lv Zhongw |
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy. PloS one 2017 12 (3): e0172995. Esslinger Ulrike, Garnier Sophie, Korniat Agathe, Proust Carole, Kararigas Georgios, Müller-Nurasyid Martina, Empana Jean-Philippe, Morley Michael P, Perret Claire, Stark Klaus, Bick Alexander G, Prasad Sanjay K, Kriebel Jennifer, Li Jin, Tiret Laurence, Strauch Konstantin, O'Regan Declan P, Marguiles Kenneth B, Seidman Jonathan G, Boutouyrie Pierre, Lacolley Patrick, Jouven Xavier, Hengstenberg Christian, Komajda Michel, Hakonarson Hakon, Isnard Richard, Arbustini Eloisa, Grallert Harald, Cook Stuart A, Seidman Christine E, Regitz-Zagrosek Vera, Cappola Thomas P, Charron Philippe, Cambien François, Villard Er |
Genetic background of Japanese patients with pediatric hypertrophic and restrictive cardiomyopathy. Journal of human genetics 2018 Jun . Hayashi Takeharu, Tanimoto Kousuke, Hirayama-Yamada Kayoko, Tsuda Etsuko, Ayusawa Mamoru, Nunoda Shinichi, Hosaki Akira, Kimura Akino |
Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy. Journal of the American College of Cardiology 2018 Nov 72 (20): 2457-2467. Ochoa Juan Pablo, Sabater-Molina María, García-Pinilla José Manuel, Mogensen Jens, Restrepo-Córdoba Alejandra, Palomino-Doza Julián, Villacorta Eduardo, Martinez-Moreno Marina, Ramos-Maqueda Javier, Zorio Esther, Peña-Peña Maria L, García-Granja Pablo E, Rodríguez-Palomares José F, Cárdenas-Reyes Ivonne J, de la Torre-Carpente María M, Bautista-Pavés Alicia, Akhtar Mohammed M, Cicerchia Marcos N, Bilbao-Quesada Raquel, Mogollón-Jimenez Maria Victoria, Salazar-Mendiguchía Joel, Mesa Latorre José M, Arnaez Blanca, Olavarri-Miguel Ivan, Fuentes-Cañamero María E, Lamounier Arsonval, Pérez Ruiz José María, Climent-Payá Vicente, Pérez-Sanchez Inmaculada, Trujillo-Quintero Juan P, Lopes Luis R, Repáraz-Andrade Alfredo, Marín-Iglesias Rosario, Rodriguez-Vilela Alejandro, Sandín-Fuentes María, Garrote Jose A, Cortel-Fuster Alejandro, Lopez-Garrido Miguel, Fontalba-Romero Ana, Ripoll-Vera Tomás, Llano-Rivas Isabel, Fernandez-Fernandez Xusto, Isidoro-García María, Garcia-Giustiniani Diego, Barriales-Villa Roberto, Ortiz-Genga Martín, García-Pavía Pablo, Elliott Perry M, Gimeno Juan R, Monserrat Loren |
Deletions of specific exons of FHOD3 detected by next-generation sequencing are associated with hypertrophic cardiomyopathy. Clinical genetics 2020 4 98 (1): 86-90. Ochoa Juan P, Lopes Luis R, Perez-Barbeito Marlene, Cazón-Varela Laura, de la Torre-Carpente Maria M, Sonicheva-Paterson Natalia, De Uña-Iglesias David, Quinn Ellen, Kuzmina-Krutetskaya Svetlana, Garrote José A, Elliott Perry M, Monserrat Loren |
Genome-wide association study of cardiac troponin I in the general population.
Human molecular genetics 2021 . Moksnes Marta R, Røsjø Helge, Richmond Anne, Lyngbakken Magnus N, Graham Sarah E, Hansen Ailin Falkmo, Wolford Brooke N, Gagliano Taliun Sarah A, LeFaive Jonathon, Rasheed Humaira, Thomas Laurent F, Zhou Wei, Aung Nay, Surakka Ida, Douville Nicholas J, Campbell Archie, Porteous David J, Petersen Steffen E, Munroe Patricia B, Welsh Paul, Sattar Naveed, Smith George Davey, Fritsche Lars G, Nielsen Jonas B, Åsvold Bjørn Olav, Hveem Kristian, Hayward Caroline, Willer Cristen J, Brumpton Ben M, Omland Torbjø |
Variant Spectrum of Formin Homology 2 Domain-Containing 3 Gene in Chinese Patients With Hypertrophic Cardiomyopathy. Journal of the American Heart Association 2021 2 10 (5): e018236. Wu Guixin, Ruan Jieyun, Liu Jie, Zhang Channa, Kang Lianming, Wang Jizheng, Zou Yubao, Song L |
Intermediate-effect size p.Arg637Gln in FHOD3 increases risk of HCM and is associated with an aggressive phenotype in homozygous carriers. Journal of medical genetics 2023 12 . Jesús Piqueras-Flores, Eduardo Villacorta-Argüelles, Joseph Galvin, Vicente Climent-Payá, Luis Enrique Escobar-López, Almudena Amor-Salamanca, Soledad Garcia-Hernandez, Sean Esmonde, Jorge Martínez-Del Río, Maeve Soto-Pérez, Pablo Garcia-Pavia, Juan Pablo Och |
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