HuGE Literature Finder
Records
1
-
18
| Whole-exome sequencing in Russian children with non-type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY-related and unrelated genes. Molecular medicine reports 2019 Oct . Glotov Oleg S, Serebryakova Elena A, Turkunova Mariia E, Efimova Olga A, Glotov Andrey S, Barbitoff Yury A, Nasykhova Yulia A, Predeus Alexander V, Polev Dmitrii E, Fedyakov Mikhail A, Polyakova Irina V, Ivashchenko Tatyana E, Shved Natalia Y, Shabanova Elena S, Tiselko Alena V, Romanova Olga V, Sarana Andrey M, Pendina Anna A, Scherbak Sergey G, Musina Ekaterina V, Petrovskaia-Kaminskaia Anastasiia V, Lonishin Liubov R, Ditkovskaya Liliya V, Zhelenina Liudmila ?, Tyrtova Ludmila V, Berseneva Olga S, Skitchenko Rostislav K, Suspitsin Evgenii N, Bashnina Elena B, Baranov Vladislav |
| Association of CpG-SNP and 3'UTR-SNP of WFS1 with the Risk of Type 2 Diabetes Mellitus in an Iranian Population. International journal of molecular and cellular medicine 2017 6 (4): 197-203. Torkamandi Shahram, Bastami Milad, Ghaedi Hamid, Tarighi Shahriar, Shokri Fazlollah, Javadi Abdolreza, Mirfakhraie Reza, Omrani Mir Davo |
| 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 |
| Clinical and genetic predictors of dipeptidyl peptidase-4 inhibitor treatment response in Type 2 diabetes mellitus. Pharmacogenomics 2016 Jun 0. Jamaluddin Jazlina Liza, Huri Hasniza Zaman, Vethakkan Shireene Rat |
| Multicapillary gel electrophoresis based analysis of genetic variants in the WFS1 gene. Electrophoresis 2016 09 37 (17-18): 2313-21. Elek Zsuzsanna, Dénes Réka, Prokop Susanne, Somogyi Anikó, Yowanto Handy, Luo Jane, Souquet Manfred, Guttman András, Rónai Zso |
| 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 |
| 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 |
| 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 |
| 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 |
| Association between insulin secretion, insulin sensitivity and type 2 diabetes susceptibility variants identified in genome-wide association studies. Acta diabetologica 2009 Sep 46 (3): 217-26. Ruchat Stephanie-May, Elks Cathy E, Loos Ruth J F, Vohl Marie-Claude, Weisnagel S John, Rankinen Tuomo, Bouchard Claude, Pérusse Lou |
| Association of common type 2 diabetes risk gene variants and posttransplantation diabetes mellitus in renal allograft recipients in Korea. Transplantation 2009 Sep 88 (5): 693-8. Kang Eun Seok, Kim Myoung Soo, Kim Chul Hoon, Nam Chung Mo, Han Seung Jin, Hur Kyu Yeon, Ahn Chul Woo, Cha Bong Soo, Kim Soon Il, Lee Hyun Chul, Kim Yu Se |
| Common type 2 diabetes risk gene variants associate with gestational diabetes. The Journal of clinical endocrinology and metabolism 2009 Jan 94 (1): 145-50. Lauenborg Jeannet, Grarup Niels, Damm Peter, Borch-Johnsen Knut, Jørgensen Torben, Pedersen Oluf, Hansen Torb |
| Evidence of interaction between type 2 diabetes susceptibility genes and dietary fat intake for adiposity and glucose homeostasis-related phenotypes. Journal of nutrigenetics and nutrigenomics 2009 2 (4-5): 225-34. Ruchat Stephanie-May, Elks Cathy E, Loos Ruth J F, Vohl Marie-Claude, Weisnagel S John, Rankinen Tuomo, Bouchard Claude, Pérusse Lou |
| Clinical risk factors, DNA variants, and the development of type 2 diabetes. The New England journal of medicine 2008 Nov 359 (21): 2220-32. Lyssenko Valeriya, Jonsson Anna, Almgren Peter, Pulizzi Nicoló, Isomaa Bo, Tuomi Tiinamaija, Berglund Göran, Altshuler David, Nilsson Peter, Groop Le |
| 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, |
| Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and type 2 diabetes in the Korean population. Journal of human genetics 2008 53 (11-12): 991-8. Lee Yong-Ho, Kang Eun Seok, Kim So Hun, Han Seung Jin, Kim Chul Hoon, Kim Hyeong Jin, Ahn Chul Woo, Cha Bong Soo, Nam Moonsuk, Nam Chung Mo, Lee Hyun Ch |
| 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 |
| Micro-RNA Binding Site Polymorphisms in the WFS1 Gene Are Risk Factors of Diabetes Mellitus. PloS one 0 10 (10): e0139519. Elek Zsuzsanna, Németh Nóra, Nagy Géza, Németh Helga, Somogyi Anikó, Hosszufalusi Nóra, Sasvári-Székely Mária, Rónai Zso |
- Page last reviewed:Oct 1, 2021
- Page last updated:Jun 22, 2022
- Content source: