Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 32 Records) |
Query Trace: Diabetes Mellitus and WFS1[original query] |
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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 |
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 |
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 |
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 |
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 |
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 |
A WFS1 haplotype consisting of the minor alleles of rs752854, rs10010131, and rs734312 shows a protective role against type 2 diabetes in Russian patients. The review of diabetic studies : RDS 2011 6 7 (4): 285-92. Chistiakov Dimitry A, Khodyrev Dmitry S, Smetanina Svetlana A, Bel'chikova Larisa N, Suplotova Lyudmila A, Nosikov Valery |
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 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 |
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 |
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 |
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 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 |
Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals. BMC medicine 2017 12 15 (1): 213. Bansal Vikas, Gassenhuber Johann, Phillips Tierney, Oliveira Glenn, Harbaugh Rebecca, Villarasa Nikki, Topol Eric J, Seufferlein Thomas, Boehm Bernhard |
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 |
Gene x Gene Interactions Highlight the Role of Incretin Resistance for Insulin Secretion. Frontiers in endocrinology 2019 3 10 72. Jaghutriz Benjamin Assad, Heni Martin, Lutz Stefan Zoltán, Fritsche Louise, Machicao Fausto, Staiger Harald, Peter Andreas, Häring Hans-Ulrich, Fritsche Andreas, Wagner Róbe |
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 |
Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience. Acta diabetologica 2021 8 58 (12): 1689-1700. Laimon Wafaa, El-Ziny Magdy, El-Hawary Amany, Elsharkawy Ashraf, Salem Nanees Abdel-Badie, Aboelenin Hadil Mohamed, Awad Mohammad Hosny, Flanagan Sarah E, De Franco Eli |
Unique three-site compound heterozygous mutation in the WFS1 gene in Wolfram syndrome. BMC endocrine disorders 2021 8 21 (1): 166. Ren Ziyu, Yi Jixiu, Zhong Min, Wang Yunting, Liu Qicong, Wang Xuan, Liu Dongfang, Ren W |
Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Wolfram Syndrome 1: Clinical and Genetic Findings. Investigative ophthalmology & visual science 2022 Sep 63 (10): 9. Zhang Xin, Xie Yue, Xu Ke, Chang Haoyu, Zhang Xiaohui, Li Ya |
Combined effect of pancreatic lipid content and gene variants (TCF7L2, WFS1 and 11BHSD1) on B-cell function in Middle Aged Women in a Post Hoc Analysis. Diabetology & metabolic syndrome 2022 Jul 14 (1): 106. Nádasdi Ákos, Gál Viktor, Masszi Tamás, Patócs Attila, Igaz Peter, Somogyi Anikó, Firneisz Gáb |
WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression. American journal of ophthalmology 2022 4 241 9-27. Majander Anna, Jurkute Neringa, Burté Florence, Brock Kristian, João Catarina, Huang Houbin, Neveu Magella M, Chan Choi Mun, Duncan Holly J, Kelly Simon, Burkitt-Wright Emma, Khoyratty Fadil, Lai Yoon Tse, Subash Mala, Chinnery Patrick F, Bitner-Glindzicz Maria, Arno Gavin, Webster Andrew R, Moore Anthony T, Michaelides Michel, Stockman Andrew, Robson Anthony G, Yu-Wai-Man Patri |
PPARG, TMEM163, UBE2E2, and WFS1 Gene Polymorphisms Are Not Significant Risk Factors for Gestational Diabetes in the Polish Population. Journal of personalized medicine 2022 Feb 12 (2): . Ustianowski Przemys?aw, Malinowski Damian, Safranow Krzysztof, Dziedziejko Violetta, Tarnowski Maciej, Pawlik Andrz |
Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register. Diabetologia 2022 11 66 (3): 438-449. Harsunen Minna, Kettunen Jarno L T, Härkönen Taina, Dwivedi Om, Lehtovirta Mikko, Vähäsalo Paula, Veijola Riitta, Ilonen Jorma, Miettinen Päivi J, Knip Mikael, Tuomi Tiinamai |
Comprehensive Analysis of Diabetes Mellitus-Related Gene Expression and Associated Prognoses in Human Lung Cancer. Current cancer drug targets 2023 5 . Jincheng Yang, Weilong Lin, Liming Shi, Ming Deng, Yu An, Juan Yang, Chengcheng Zhou, Qin Tong, Wenjing Ya |
Genotype and Clinical Characteristics of Patients with Wolfram Syndrome and WFS1-related Disorders. medRxiv : the preprint server for health sciences 2023 2 . Lee Evan M, Verma Megha, Palaniappan Nila, Pope Emiko M, Lee Sammie, Blacher Lindsey, Neerumalla Pooja, An William, Campbell Toko, Brown Cris, Hurst Stacy, Marshall Bess, Hershey Tamara, Nunes Virginia, de Heredia Miguel López, Urano Fumihi |
High frequency of recessive WFS1 mutations among Indian children with islet antibody-negative type 1 diabetes. The Journal of clinical endocrinology and metabolism 2023 11 . Jayakrishnan C Menon, Pratibha Singh, Archana Archana, Preeti Singh, Medha Mittal, Uma Kanga, Kausik Mandal, Anju Seth, Vijayalakshmi Bhatia, Preeti Dabadghao, Siddhnath Sudhanshu, Atul Garg, Ruchira Vishwakarma, Aditya Narayan Sarangi, Shivendra Verma, Surya Kumar Singh, Eesh Bhat |
The miR-668 binding site variant rs1046322 on WFS1 is associated with obesity in Southeast Asians. Frontiers in endocrinology 2023 10 14 1185956. Maha M Hammad, Mohamed Abu-Farha, Prashantha Hebbar, Emil Anoop, Betty Chandy, Motasem Melhem, Arshad Channanath, Fahd Al-Mulla, Thangavel Alphonse Thanaraj, Jehad Abubak |
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