Literature DB >> 18197395

Candidate gene studies reveal that the WFS1 gene joins the expanding list of novel type 2 diabetes genes.

J Wasson1, M A Permutt.   

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Year:  2008        PMID： 18197395     DOI： 10.1007/s00125-007-0920-9

Source DB:  PubMed          Journal:  Diabetologia        ISSN： 0012-186X            Impact factor:   10.122


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  19 in total

1.  A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome).

Authors:  H Inoue; Y Tanizawa; J Wasson; P Behn; K Kalidas; E Bernal-Mizrachi; M Mueckler; H Marshall; H Donis-Keller; P Crock; D Rogers; M Mikuni; H Kumashiro; K Higashi; G Sobue; Y Oka; M A Permutt
Journal:  Nat Genet       Date:  1998-10       Impact factor: 38.330

2.  Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populations.

Authors:  Jayne A L Minton; Andrew T Hattersley; Katharine Owen; Mark I McCarthy; Mark Walker; Farida Latif; Timothy Barrett; Timothy M Frayling
Journal:  Diabetes       Date:  2002-04       Impact factor: 9.461

3.  Mice conditionally lacking the Wolfram gene in pancreatic islet beta cells exhibit diabetes as a result of enhanced endoplasmic reticulum stress and apoptosis.

Authors:  A C Riggs; E Bernal-Mizrachi; M Ohsugi; J Wasson; S Fatrai; C Welling; J Murray; R E Schmidt; P L Herrera; M A Permutt
Journal:  Diabetologia       Date:  2005-10-08       Impact factor: 10.122

4.  Regulation of insulin biosynthesis in pancreatic beta cells by an endoplasmic reticulum-resident protein kinase IRE1.

Authors:  Kathryn L Lipson; Sonya G Fonseca; Shinsuke Ishigaki; Linh X Nguyen; Elizabeth Foss; Rita Bortell; Aldo A Rossini; Fumihiko Urano
Journal:  Cell Metab       Date:  2006-09       Impact factor: 27.287

5.  Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion.

Authors:  Hisamitsu Ishihara; Satoshi Takeda; Akira Tamura; Rui Takahashi; Suguru Yamaguchi; Daisuke Takei; Takahiro Yamada; Hiroshi Inoue; Hiroyuki Soga; Hideki Katagiri; Yukio Tanizawa; Yoshitomo Oka
Journal:  Hum Mol Genet       Date:  2004-03-31       Impact factor: 6.150

Review 6.  Differential diagnosis of type 1 diabetes: which genetic syndromes need to be considered?

Authors:  Timothy Geoffrey Barrett
Journal:  Pediatr Diabetes       Date:  2007-10       Impact factor: 4.866

7.  Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.

Authors:  Richa Saxena; Benjamin F Voight; Valeriya Lyssenko; Noël P Burtt; Paul I W de Bakker; Hong Chen; Jeffrey J Roix; Sekar Kathiresan; Joel N Hirschhorn; Mark J Daly; Thomas E Hughes; Leif Groop; David Altshuler; Peter Almgren; Jose C Florez; Joanne Meyer; Kristin Ardlie; Kristina Bengtsson Boström; Bo Isomaa; Guillaume Lettre; Ulf Lindblad; Helen N Lyon; Olle Melander; Christopher Newton-Cheh; Peter Nilsson; Marju Orho-Melander; Lennart Råstam; Elizabeth K Speliotes; Marja-Riitta Taskinen; Tiinamaija Tuomi; Candace Guiducci; Anna Berglund; Joyce Carlson; Lauren Gianniny; Rachel Hackett; Liselotte Hall; Johan Holmkvist; Esa Laurila; Marketa Sjögren; Maria Sterner; Aarti Surti; Margareta Svensson; Malin Svensson; Ryan Tewhey; Brendan Blumenstiel; Melissa Parkin; Matthew Defelice; Rachel Barry; Wendy Brodeur; Jody Camarata; Nancy Chia; Mary Fava; John Gibbons; Bob Handsaker; Claire Healy; Kieu Nguyen; Casey Gates; Carrie Sougnez; Diane Gage; Marcia Nizzari; Stacey B Gabriel; Gung-Wei Chirn; Qicheng Ma; Hemang Parikh; Delwood Richardson; Darrell Ricke; Shaun Purcell
Journal:  Science       Date:  2007-04-26       Impact factor: 47.728

8.  Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4.

Authors:  M H Polymeropoulos; R G Swift; M Swift
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

9.  A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.

Authors:  Laura J Scott; Karen L Mohlke; Lori L Bonnycastle; Cristen J Willer; Yun Li; William L Duren; Michael R Erdos; Heather M Stringham; Peter S Chines; Anne U Jackson; Ludmila Prokunina-Olsson; Chia-Jen Ding; Amy J Swift; Narisu Narisu; Tianle Hu; Randall Pruim; Rui Xiao; Xiao-Yi Li; Karen N Conneely; Nancy L Riebow; Andrew G Sprau; Maurine Tong; Peggy P White; Kurt N Hetrick; Michael W Barnhart; Craig W Bark; Janet L Goldstein; Lee Watkins; Fang Xiang; Jouko Saramies; Thomas A Buchanan; Richard M Watanabe; Timo T Valle; Leena Kinnunen; Gonçalo R Abecasis; Elizabeth W Pugh; Kimberly F Doheny; Richard N Bergman; Jaakko Tuomilehto; Francis S Collins; Michael Boehnke
Journal:  Science       Date:  2007-04-26       Impact factor: 47.728

10.  Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations.

Authors:  P W Franks; O Rolandsson; S L Debenham; K A Fawcett; F Payne; C Dina; P Froguel; K L Mohlke; C Willer; T Olsson; N J Wareham; G Hallmans; I Barroso; M S Sandhu
Journal:  Diabetologia       Date:  2007-11-27       Impact factor: 10.122
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  8 in total

1.  A WFS1 haplotype consisting of the minor alleles of rs752854, rs10010131, and rs734312 shows a protective role against type 2 diabetes in Russian patients.

Authors:  Dimitry A Chistiakov; Dmitry S Khodyrev; Svetlana A Smetanina; Larisa N Bel'chikova; Lyudmila A Suplotova; Valery V Nosikov
Journal:  Rev Diabet Stud       Date:  2011-02-10

2.  Gene-gene interactions lead to higher risk for development of type 2 diabetes in an Ashkenazi Jewish population.

Authors:  Rosalind J Neuman; Jon Wasson; Gil Atzmon; Julio Wainstein; Yair Yerushalmi; Joseph Cohen; Nir Barzilai; Ilana Blech; Benjamin Glaser; M Alan Permutt
Journal:  PLoS One       Date:  2010-03-26       Impact factor: 3.240

3.  Expression of the diabetes risk gene wolframin (WFS1) in the human retina.

Authors:  Rainald Schmidt-Kastner; Pawel Kreczmanski; Markus Preising; Roselie Diederen; Christoph Schmitz; Danielle Reis; Janet Blanks; C Kathleen Dorey
Journal:  Exp Eye Res       Date:  2009-06-12       Impact factor: 3.467

4.  PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population.

Authors:  Cheng Hu; Rong Zhang; Congrong Wang; Jie Wang; Xiaojing Ma; Jingyi Lu; Wen Qin; Xuhong Hou; Chen Wang; Yuqian Bao; Kunsan Xiang; Weiping Jia
Journal:  PLoS One       Date:  2009-10-28       Impact factor: 3.240

5.  Phenotypic characteristics of early Wolfram syndrome.

Authors:  Bess A Marshall; M Alan Permutt; Alexander R Paciorkowski; James Hoekel; Roanne Karzon; Jon Wasson; Amy Viehover; Neil H White; Joshua S Shimony; Linda Manwaring; Paul Austin; Timothy E Hullar; Tamara Hershey
Journal:  Orphanet J Rare Dis       Date:  2013-04-27       Impact factor: 4.123

6.  Wolfram Syndrome protein, Miner1, regulates sulphydryl redox status, the unfolded protein response, and Ca2+ homeostasis.

Authors:  Sandra E Wiley; Alexander Y Andreyev; Ajit S Divakaruni; Robert Karisch; Guy Perkins; Estelle A Wall; Peter van der Geer; Yi-Fan Chen; Ting-Fen Tsai; Melvin I Simon; Benjamin G Neel; Jack E Dixon; Anne N Murphy
Journal:  EMBO Mol Med       Date:  2013-05-24       Impact factor: 12.137

7.  Whole-exome sequencing to decipher the genetic heterogeneity of hearing loss in a Chinese family with deaf by deaf mating.

Authors:  Jie Qing; Denise Yan; Yuan Zhou; Qiong Liu; Weijing Wu; Zian Xiao; Yuyuan Liu; Jia Liu; Lilin Du; Dinghua Xie; Xue Zhong Liu
Journal:  PLoS One       Date:  2014-10-07       Impact factor: 3.240

8.  Wolfram syndrome in the Japanese population; molecular analysis of WFS1 gene and characterization of clinical features.

Authors:  Kimie Matsunaga; Katsuya Tanabe; Hiroshi Inoue; Shigeru Okuya; Yasuharu Ohta; Masaru Akiyama; Akihiko Taguchi; Yukari Kora; Naoko Okayama; Yuichiro Yamada; Yasuhiko Wada; Shin Amemiya; Shigetaka Sugihara; Yuzo Nakao; Yoshitomo Oka; Yukio Tanizawa
Journal:  PLoS One       Date:  2014-09-11       Impact factor: 3.240
  8 in total

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