Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: FHL1[original query] |
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Variations in the four and a half LIM domains 1 gene (FHL1) are associated with fasting insulin and insulin sensitivity responses to regular exercise. Diabetologia 2007 Sep 50 (9): 1858-66. Teran-Garcia M, Rankinen T, Rice T, Leon AS, Rao DC, Skinner JS, Bouchard C |
Spongious hypertrophic cardiomyopathy in patients with mutations in the four-and-a-half LIM domain 1 gene. Circulation. Cardiovascular genetics 2012 Oct 5 (5): 490-502. Binder Josepha S, Weidemann Frank, Schoser Benedikt, Niemann Markus, Machann Wolfram, Beer Meinrad, Plank Gernot, Schmidt Albrecht, Bisping Egbert, Poparic Ivana, Lafer Ingrid, Stojakovic Tatjana, Quasthoff Stefan, Vincent John B, Rienmueller Rainer, Speicher Michael R, Berghold Andrea, Pieske Burkert, Windpassinger Christi |
Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy. Human molecular genetics 2012 Jul 21 (14): 3237-54. Friedrich Felix W, Wilding Brendan R, Reischmann Silke, Crocini Claudia, Lang Patrick, Charron Philippe, Müller Oliver J, McGrath Meagan J, Vollert Ingra, Hansen Arne, Linke Wolfgang A, Hengstenberg Christian, Bonne Gisèle, Morner Stellan, Wichter Thomas, Madeira Hugo, Arbustini Eloisa, Eschenhagen Thomas, Mitchell Christina A, Isnard Richard, Carrier Luc |
Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population. Clinical genetics 2016 May . Fattahi Zohreh, Kalhor Zahra, Fadaee Mahsa, Vazehan Raheleh, Parsimehr Elham, Abolhassani Ayda, Beheshtian Maryam, Zamani Gholamreza, Nafissi Shahriar, Nilipour Yalda, Akbari Mohammad R, Kahrizi Kimia, Kariminejad Ariana, Najmabadi Hosse |
Identification of RHOBTB2 aberration as an independent prognostic indicator in acute myeloid leukemia. Aging 2021 Jun 13 . Liu Peng, Ma Qinghai, Chen Hanxiang, Zhang Li, Zhang Xiaoni |
The Genetic Architecture of Hypertrophic Cardiomyopathy in Hungary: Analysis of 242 Patients with a Panel of 98 Genes. Diagnostics (Basel, Switzerland) 2022 May 12 (5): . Sepp Róbert, Hategan Lidia, Csányi Beáta, Borbás János, Tringer Annamária, Pálinkás Eszter Dalma, Nagy Viktória, Takács Hedvig, Latinovics Dóra, Nyolczas Noémi, Pálinkás Attila, Faludi Réka, Rábai Miklós, Szabó Gábor Tamás, Czuriga Dániel, Balogh László, Halmosi Róbert, Borbély Attila, Habon Tamás, Heged?s Zoltán, Nagy Istv |
Description of a novel variant in the FHL1 gene associated with hypertrophic cardiomyopathy with early and aggressive presentation. Revista espanola de cardiologia (English ed.) 2022 5 . López Blázquez María, Fernández Ávila Ana Isabel, Álvarez García-Rovés Reyes, Centeno Jiménez Miriam, Gómez González Cristina, Espinosa Castro María Ángel |
Upregulation of FHL1, SPNS3, and MPZL2 predicts poor prognosis in pediatric acute myeloid leukemia patients with FLT3-ITD mutation. Leukemia & lymphoma 2022 3 63 (8): 1897-1906. Eshibona Nasr, Giwa Abdulazeez, Rossouw Sophia Catherine, Gamieldien Junaid, Christoffels Alan, Bendou Hoci |
Autoantibodies against four-and-a-half-LIM domain 1 (FHL1) in inflammatory myopathies: results from an Australian single-centre cohort. Rheumatology (Oxford, England) 2022 1 61 (10): 4145-4154. Galindo-Feria Angeles S, Horuluoglu Begum, Day Jessica, Fernandes-Cerqueira Catia, Wigren Edvard, Gräslund Susanne, Proudman Susanna, Lundberg Ingrid E, Limaye Vid |
Identification of novel FHL1 mutations associated with X-linked scapuloperoneal myopathy in unrelated Chinese patients. Journal of human genetics 2023 3 . Lin Ying, Ban Rui, Qiao Lingya, Chen Juan, Liu Mengyang, Liu Jiaqi, Shi Qia |
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- Page last updated:Apr 22, 2024
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