HuGE Literature Finder
Records 1-21
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Wolfram syndrome 1 in the Italian population: genotype-phenotype correlations.
Pediatric research 2019 Jul . Rigoli Luciana, Aloi Concetta, Salina Alessandro, Di Bella Chiara, Salzano Giuseppina, Caruso Rosario, Mazzon Emanuela, Maghnie Mohamad, D'Annunzio Giuseppe, Lombardo Fortuna |
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Identification of a missense variant in the WFS1 gene that causes a mild form of Wolfram syndrome and is associated with risk for type 2 diabetes in Ashkenazi Jewish individuals.
Diabetologia 2018 Jul . Bansal Vikas, Boehm Bernhard O, Darvasi Ari |
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Whole exome sequencing identifies a pathogenic mutation in WFS1 in two large Chinese families with autosomal dominant all-frequency hearing loss and prenatal counseling.
International journal of pediatric otorhinolaryngology 2018 Mar 106 113-119. Cheng Hongbo, Zhang Qin, Wang Wenbin, Meng Qingxia, Wang Fuxin, Liu Minjuan, Mao Jun, Shi Yichao, Wang Wei, Li Ho |
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WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity.
Ophthalmology 2016 Jul . Grenier Joanna, Meunier Isabelle, Daien Vincent, Baudoin Corinne, Halloy François, Bocquet Béatrice, Blanchet Catherine, Delettre Cécile, Esmenjaud Etienne, Roubertie Agathe, Lenaers Guy, Hamel Christian |
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Differential promoter activity by nucleotide substitution at a type 2 diabetes genome-wide association study signal upstream of the wolframin gene.
Journal of diabetes 2015 Mar . Ryu Jihye, Lee Chaeyou |
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WFS1 mutations in hearing-impaired children.
International journal of audiology 2014 Jul 53 (7): 446-51. Häkli Sanna, Kytövuori Laura, Luotonen Mirja, Sorri Martti, Majamaa Ka |
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WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims.
Journal of human genetics 2013 Aug 58 (8): 495-500. Kytövuori Laura, Seppänen Allan, Martikainen Mika H, Moilanen Jukka S, Kamppari Seija, Särkioja Terttu, Remes Anne M, Räsänen Pirkko, Rönnemaa Tapani, Majamaa Ka |
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Genotypic classification of patients with Wolfram syndrome: insights into the natural history of the disease and correlation with phenotype.
Genetics in medicine : official journal of the American College of Medical Genetics 2013 Jul 15 (7): 497-506. de Heredia Miguel López, Clèries Ramón, Nunes Virgin |
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Association of aggression with a novel microRNA binding site polymorphism in the wolframin gene.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013 Jun 162B (4): 404-12. Kovacs-Nagy Reka, Elek Zsuzsanna, Szekely Anna, Nanasi Tibor, Sasvari-Szekely Maria, Ronai Zso |
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Association of rs734312 and rs10010131 polymorphisms in WFS1 gene with type 2 diabetes mellitus: a meta-analysis.
Endocrine journal 2012 Dec . Cheng S, Wu Y, Wu W, Zhang D |
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A predictive model of the association between gene polymorphism and the risk of noise-induced hearing loss caused by gunfire noise.
Journal of the Chinese Medical Association : JCMA 2012 Jan 75 (1): 36-9. Yuan Ben-Chih, Su Feng-Ming, Wu Wen-Tung, Liu Wen-Sheng, Chiu Kuo-Hs |
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Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotype.
Diabetes care 2011 Jul 34 (7): 1503-10. Rohayem Julia, Ehlers Christian, Wiedemann Bärbel, Holl Reinhard, Oexle Konrad, Kordonouri Olga, Salzano Giuseppina, Meissner Thomas, Burger Walter, Schober Edith, Huebner Angela, Lee-Kirsch Min Ae, |
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Detailed investigation of the role of common and low-frequency WFS1 variants in type 2 diabetes risk.
Diabetes 2010 Mar 59 (3): 741-6. Fawcett Katherine A, Wheeler Eleanor, Morris Andrew P, Ricketts Sally L, Hallmans Göran, Rolandsson Olov, Daly Allan, Wasson Jon, Permutt Alan, Hattersley Andrew T, Glaser Benjamin, Franks Paul W, McCarthy Mark I, Wareham Nicholas J, Sandhu Manjinder S, Barroso In |
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Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population.
BMC medical genetics 2010 11 (1): 81. Han Xueyao, Luo Yingying, Ren Qian, Zhang Xiuying, Wang Fang, Sun Xiuqin, Zhou Xianghai, Ji Lino |
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Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations.
Diabetologia 2008 Mar 51 (3): 458-63. Franks P W, Rolandsson O, Debenham S L, Fawcett K A, Payne F, Dina C, Froguel P, Mohlke K L, Willer C, Olsson T, Wareham N J, Hallmans G, Barroso I, Sandhu M |
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Testing of diabetes-associated WFS1 polymorphisms in the Diabetes Prevention Program.
Diabetologia 2008 Mar 51 (3): 451-7. Florez J C, Jablonski K A, McAteer J, Sandhu M S, Wareham N J, Barroso I, Franks P W, Altshuler D, Knowler W C, |
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The wolframin His611Arg polymorphism influences medication overuse headache.
Neuroscience letters 2007 Sep 424 (3): 179-84. Di Lorenzo C, Sances G, Di Lorenzo G, Rengo C, Ghiotto N, Guaschino E, Perrotta A, Santorelli F M, Grieco G S, Troisi A, Siracusano A, Pierelli F, Nappi G, Casali |
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Common variants in WFS1 confer risk of type 2 diabetes.
Nature genetics 2007 Aug 39 (8): 951-3. Sandhu Manjinder S, Weedon Michael N, Fawcett Katherine A, Wasson Jon, Debenham Sally L, Daly Allan, Lango Hana, Frayling Timothy M, Neumann Rosalind J, Sherva Richard, Blech Ilana, Pharoah Paul D, Palmer Colin N A, Kimber Charlotte, Tavendale Roger, Morris Andrew D, McCarthy Mark I, Walker Mark, Hitman Graham, Glaser Benjamin, Permutt M Alan, Hattersley Andrew T, Wareham Nicholas J, Barroso In |
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Polymorphisms in wolframin (WFS1) gene are possibly related to increased risk for mood disorders.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2005 Jun 8 (2): 235-44. Koido Kati, Kõks Sulev, Nikopensius Tiit, Maron Eduard, Altmäe Signe, Heinaste Evelin, Vabrit Kristel, Tammekivi Veronika, Hallast Pille, Kurg Ants, Shlik Jakov, Vasar Veiko, Metspalu Andres, Vasar Ee |
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Genetic variations in the WFS1 gene in Japanese with type 2 diabetes and bipolar disorder.
Molecular genetics and metabolism 2004 Jul 82 (3): 238-45. Kawamoto Takanori, Horikawa Yukio, Tanaka Takeshi, Kabe Noriko, Takeda Jun, Mikuni Masahi |
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Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populations.
Diabetes 2002 Apr 51 (4): 1287-90. Minton Jayne A L, Hattersley Andrew T, Owen Katharine, McCarthy Mark I, Walker Mark, Latif Farida, Barrett Timothy, Frayling Timothy |
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- Page last updated:Jan 23, 2020
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