HuGE Literature Finder
Records 1-89
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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 |
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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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Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India.
BMC medical genetics 2018 Feb 19 (1): 22. Mohan Viswanathan, Radha Venkatesan, Nguyen Thong T, Stawiski Eric W, Pahuja Kanika Bajaj, Goldstein Leonard D, Tom Jennifer, Anjana Ranjit Mohan, Kong-Beltran Monica, Bhangale Tushar, Jahnavi Suresh, Chandni Radhakrishnan, Gayathri Vijay, George Paul, Zhang Na, Murugan Sakthivel, Phalke Sameer, Chaudhuri Subhra, Gupta Ravi, Zhang Jingli, Santhosh Sam, Stinson Jeremy, Modrusan Zora, Ramprasad V L, Seshagiri Somasekar, Peterson Andrew |
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CDKAL1 rs7756992 is associated with diabetic retinopathy in a Chinese population with type 2 diabetes.
Scientific reports 2017 Aug 7 (1): 8812. Peng Danfeng, Wang Jie, Zhang Rong, Jiang Feng, Tam Claudia H T, Jiang Guozhi, Wang Tao, Chen Miao, Yan Jing, Wang Shiyun, Yan Dandan, He Zhen, Ma Ronald C W, Bao Yuqian, Hu Cheng, Jia Weipi |
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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 |
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Investigation of gene-diet interactions in the incretin system and risk of type 2 diabetes: the EPIC-InterAct study.
Diabetologia 2016 Sep . Authors are not available |
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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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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 |
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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 |
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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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Therapeutic implications of novel mutations of the RFX6 gene associated with early-onset diabetes.
The pharmacogenomics journal 2015 Feb 15 (1): 49-54. Artuso R, Provenzano A, Mazzinghi B, Giunti L, Palazzo V, Andreucci E, Blasetti A, Chiuri R M, Gianiorio F E, Mandich P, Monami M, Mannucci E, Giglio |
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Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing.
Hormone research in pædiatrics 2015 83 (4): 242-51. Shim Ye Jee, Kim Jung Eun, Hwang Su-Kyeong, Choi Bong Seok, Choi Byung Ho, Cho Eun-Mi, Jang Kyoung Mi, Ko Cheol W |
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The Association of Type 2 Diabetes Loci Identified in Genome-Wide Association Studies with Metabolic Syndrome and Its Components in a Chinese Population with Type 2 Diabetes.
PloS one 2015 10 (11): e0143607. Kong Xiaomu, Zhang Xuelian, Xing Xiaoyan, Zhang Bo, Hong Jing, Yang Wenyi |
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Genetic association of IDE, POU2F1, PON1, IL1? and IL1? with type 2 diabetes in Pakistani population.
Molecular biology reports 2014 May 41 (5): 3063-9. Batool Andleeb, Jahan Nusrat, Sun Yisuo, Hanif Atif, Xue Ho |
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Assessing the contribution of 38 genetic loci to the risk of type 2 diabetes in the Saudi Arabian Population.
Clinical endocrinology 2014 Apr 80 (4): 532-7. Al-Daghri Nasser M, Alkharfy Khalid M, Alokail Majed S, Alenad Amal M, Al-Attas Omar S, Mohammed Abdul Khader, Sabico Shaun, Albagha Omar M |
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Cross-sectional and longitudinal replication analyses of genome-wide association loci of type 2 diabetes in Han Chinese.
PloS one 2014 9 (3): e91790. Zhao Qi, Xiao Jianzhong, He Jiang, Zhang Xuelian, Hong Jing, Kong Xiaomu, Mills Katherine T, Weng Jianping, Jia Weiping, Yang Wenyi |
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A replication study of 19 GWAS-validated type 2 diabetes at-risk variants in the Lebanese population.
Diabetes research and clinical practice 2013 Nov 102 (2): 117-22. Almawi Wassim Y, Nemr Rita, Keleshian Sose H, Echtay Akram, Saldanha Fabiola Lisa, AlDoseri Fatima A, Racoubian Edd |
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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 study of genetic variants of 17 diabetes-related genes/loci and cardiovascular risk and diabetic nephropathy in the Chinese She population.
Journal of diabetes 2013 Jun 5 (2): 136-45. Chen Gang, Xu Yuan, Lin Yinghua, Lai Xiaolan, Yao Jin, Huang Baoying, Chen Zichun, Huang Huibin, Fu Xianguo, Lin Lixiang, Lai Shenghan, Wen Junpi |
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Polycystic ovary syndrome is not associated with genetic variants that mark risk of type 2 diabetes.
Acta diabetologica 2013 Jun 50 (3): 451-7. Saxena R, Welt C |
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Use of net reclassification improvement (NRI) method confirms the utility of combined genetic risk score to predict type 2 diabetes.
PloS one 2013 8 (12): e83093. Tam Claudia H T, Ho Janice S K, Wang Ying, Lam Vincent K L, Lee Heung Man, Jiang Guozhi, Lau Eric S H, Kong Alice P S, Fan Xiaodan, Woo Jean L F, Tsui Stephen K W, Ng Maggie C Y, So Wing Yee, Chan Juliana C N, Ma Ronald C |
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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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Evaluation of genome-wide association study-identified type 2 diabetes loci in African Americans.
American journal of epidemiology 2012 Dec 176 (11): 995-1001. Long Jirong, Edwards Todd, Signorello Lisa B, Cai Qiuyin, Zheng Wei, Shu Xiao-Ou, Blot William |
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European genetic variants associated with type 2 diabetes in North African Arabs.
Diabetes & metabolism 2012 Oct 38 (4): 316-23. Cauchi S, Ezzidi I, El Achhab Y, Mtiraoui N, Chaieb L, Salah D, Nejjari C, Labrune Y, Yengo L, Beury D, Vaxillaire M, Mahjoub T, Chikri M, Froguel |
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The association of genetic variants of type 2 diabetes with kidney function.
Kidney international 2012 Jul 82 (2): 220-5. Franceschini Nora, Shara Nawar M, Wang Hong, Voruganti V Saroja, Laston Sandy, Haack Karin, Lee Elisa T, Best Lyle G, Maccluer Jean W, Cochran Barbara J, Dyer Thomas D, Howard Barbara V, Cole Shelley A, North Kari E, Umans Jason |
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Diabetes-Associated Common Genetic Variation and Its Association With GLP-1 Concentrations and Response to Exogenous GLP-1.
Diabetes 2012 Mar . Smushkin G, Sathananthan M, Sathananthan A, Dalla Man C, Micheletto F, Zinsmeister AR, Cobelli C, Vella A |
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Genetic risk assessment of type 2 diabetes-associated polymorphisms in African Americans.
Diabetes care 2012 Feb 35 (2): 287-92. Cooke Jessica N, Ng Maggie C Y, Palmer Nicholette D, An S Sandy, Hester Jessica M, Freedman Barry I, Langefeld Carl D, Bowden Donald |
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Allele summation of diabetes risk genes predicts impaired glucose tolerance in female and obese individuals.
PloS one 2012 7 (6): e38224. Linder Katarzyna, Wagner Robert, Hatziagelaki Erifili, Ketterer Caroline, Heni Martin, Machicao Fausto, Stefan Norbert, Staiger Harald, Häring Hans-Ulrich, Fritsche Andre |
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Association of variants in genes involved in pancreatic ?-cell development and function with type 2 diabetes in North Indians.
Journal of human genetics 2011 Oct 56 (10): 695-700. Chavali Sreenivas, Mahajan Anubha, Tabassum Rubina, Dwivedi Om Prakash, Chauhan Ganesh, Ghosh Saurabh, Tandon Nikhil, Bharadwaj Dwaipay |
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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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Association study of type 2 diabetes genetic susceptibility variants and risk of pancreatic cancer: an analysis of PanScan-I data.
Cancer causes & control : CCC 2011 Jun 22 (6): 877-83. Pierce Brandon L, Austin Melissa A, Ahsan Habib |
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Replication of 13 genome-wide association (GWA)-validated risk variants for type 2 diabetes in Pakistani populations.
Diabetologia 2011 Jun 54 (6): 1368-74. Rees S D, Hydrie M Z I, Shera A S, Kumar S, O'Hare J P, Barnett A H, Basit A, Kelly M |
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Type 2 diabetes susceptibility single-nucleotide polymorphisms are not associated with polycystic ovary syndrome.
Fertility and sterility 2011 Jun 95 (8): 2538-41.e1-6. Ewens Kathryn G, Jones Michelle R, Ankener Wendy, Stewart Douglas R, Urbanek Margrit, Dunaif Andrea, Legro Richard S, Chua Angela, Azziz Ricardo, Spielman Richard S, Goodarzi Mark O, Strauss Jerome |
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Effects of 34 risk loci for type 2 diabetes or hyperglycemia on lipoprotein subclasses and their composition in 6,580 nondiabetic Finnish men.
Diabetes 2011 May 60 (5): 1608-16. Stan?áková Alena, Paananen Jussi, Soininen Pasi, Kangas Antti J, Bonnycastle Lori L, Morken Mario A, Collins Francis S, Jackson Anne U, Boehnke Michael L, Kuusisto Johanna, Ala-Korpela Mika, Laakso Mark |
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No association of risk variants for diabetes and obesity with breast cancer: the Multiethnic Cohort and PAGE studies.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011 May 20 (5): 1039-42. Chen Fang, Wilkens Lynne R, Monroe Kristine R, Stram Daniel O, Kolonel Laurence N, Henderson Brian E, Le Marchand Loïc, Haiman Christopher |
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Updated genetic score based on 34 confirmed type 2 diabetes Loci is associated with diabetes incidence and regression to normoglycemia in the diabetes prevention program.
Diabetes 2011 Apr 60 (4): 1340-8. Hivert Marie-France, Jablonski Kathleen A, Perreault Leigh, Saxena Richa, McAteer Jarred B, Franks Paul W, Hamman Richard F, Kahn Steven E, Haffner Steven, , Meigs James B, Altshuler David, Knowler William C, Florez Jose C, |
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Association of indices of liver and adipocyte insulin resistance with 19 confirmed susceptibility loci for type 2 diabetes in 6,733 non-diabetic Finnish men.
Diabetologia 2011 Mar 54 (3): 563-71. Vangipurapu J, Stan?áková A, Pihlajamäki J, Kuulasmaa T M, Kuulasmaa T, Paananen J, Kuusisto J, Ferrannini E, Laakso |
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Decreased insulin secretion and increased risk of type 2 diabetes associated with allelic variations of the WFS1 gene: the Data from Epidemiological Study on the Insulin Resistance Syndrome (DESIR) prospective study.
Diabetologia 2011 Mar 54 (3): 554-62. Cheurfa N, Brenner G M, Reis A F, Dubois-Laforgue D, Roussel R, Tichet J, Lantieri O, Balkau B, Fumeron F, Timsit J, Marre M, Velho |
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Identification of metabolic modifiers that underlie phenotypic variations in energy-balance regulation.
Diabetes 2011 Mar 60 (3): 726-34. Chang Chia Lin, Cai James J, Cheng Po Jen, Chueh Ho Yen, Hsu Sheau Yu Ted |
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Type 2 diabetes (T2D) associated polymorphisms regulate expression of adjacent transcripts in transformed lymphocytes, adipose, and muscle from Caucasian and African-American subjects.
The Journal of clinical endocrinology and metabolism 2011 Feb 96 (2): E394-403. Sharma Neeraj K, Langberg Kurt A, Mondal Ashis K, Elbein Steven C, Das Swapan |
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Genetic risk reclassification for type 2 diabetes by age below or above 50 years using 40 type 2 diabetes risk single nucleotide polymorphisms.
Diabetes care 2011 Jan 34 (1): 121-5. de Miguel-Yanes Jose M, Shrader Peter, Pencina Michael J, Fox Caroline S, Manning Alisa K, Grant Richard W, Dupuis Josèe, Florez Jose C, D'Agostino Ralph B, Cupples L Adrienne, Meigs James B, , |
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Polymorphisms associated with type 2 diabetes in familial longevity: The Leiden Longevity Study.
Aging 2011 Jan 3 (1): 55-62. Mooijaart Simon P, van Heemst Diana, Noordam Raymond, Rozing Maarten P, Wijsman Carolien A, de Craen Anton J M, Westendorp Rudi G J, Beekman Marian, Slagboom P Eli |
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Glycemia determines the effect of type 2 diabetes risk genes on insulin secretion.
Diabetes 2010 Dec 59 (12): 3247-52. Heni Martin, Ketterer Caroline, Thamer Claus, Herzberg-Schäfer Silke A, Guthoff Martina, Stefan Norbert, Machicao Fausto, Staiger Harald, Fritsche Andreas, Häring Hans-Ulri |
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Replication of recently described type 2 diabetes gene variants in a South Indian population.
Metabolism: clinical and experimental 2010 Dec 59 (12): 1760-6. Chidambaram Manickam, Radha Venkatesan, Mohan Viswanath |
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Impact of single nucleotide polymorphisms and of clinical risk factors on new?onset diabetes mellitus in HIV?infected individuals.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2010 Nov 51 (9): 1090-8. Rotger Margalida, Gsponer Thomas, Martinez Raquel, Taffé Patrick, Elzi Luigia, Vernazza Pietro, Cavassini Matthias, Bernasconi Enos, Hirschel Bernard, Furrer Hansjakob, Weber Rainer, Ledergerber Bruno, Egger Matthias, Telenti Amalio, Tarr Philip E, |
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Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population.
Diabetologia 2010 Oct 53 (10): 2155-62. Fontaine-Bisson B, Renström F, Rolandsson O, , Payne F, Hallmans G, Barroso I, Franks P |
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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
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Obesity and diabetes genetic variants associated with gestational weight gain.
American journal of obstetrics and gynecology 2010 Sep 203 (3): 283.e1-17. Stuebe Alison M, Lyon Helen, Herring Amy H, Ghosh Joyee, Wise Alison, North Kari E, Siega-Riz Anna Mar |
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Type 2 diabetes risk alleles near ADCY5, CDKAL1 and HHEX-IDE are associated with reduced birthweight.
Diabetologia 2010 Sep 53 (9): 1908-16. Andersson E A, Pilgaard K, Pisinger C, Harder M N, Grarup N, Faerch K, Poulsen P, Witte D R, Jørgensen T, Vaag A, Hansen T, Pedersen |
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Combining genetic markers and clinical risk factors improves the risk assessment of impaired glucose metabolism.
Annals of medicine 2010 Apr 42 (3): 196-206. Ruchat Stephanie-May, Vohl Marie-Claude, Weisnagel S John, Rankinen Tuomo, Bouchard Claude, Pérusse Lou |
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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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Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A, and MTNR1B affect different aspects of pancreatic beta-cell function.
Diabetes 2010 Jan 59 (1): 293-301. Simonis-Bik Annemarie M, Nijpels Giel, van Haeften Timon W, Houwing-Duistermaat Jeanine J, Boomsma Dorret I, Reiling Erwin, van Hove Els C, Diamant Michaela, Kramer Mark H H, Heine Robert J, Maassen J Antonie, Slagboom P Eline, Willemsen Gonneke, Dekker Jacqueline M, Eekhoff Elisabeth M, de Geus Eco J, 't Hart Leen |
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Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes.
Diabetes 2010 Jan 59 (1): 266-71. Lango Allen Hana, Johansson Stefan, Ellard Sian, Shields Beverley, Hertel Jens K, Raeder Helge, Colclough Kevin, Molven Anders, Frayling Timothy M, Njølstad Pål R, Hattersley Andrew T, Weedon Michael |
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Gene-gene interactions lead to higher risk for development of type 2 diabetes in an Ashkenazi Jewish population.
PloS one 2010 5 (3): e9903. Neuman Rosalind J, Wasson Jon, Atzmon Gil, Wainstein Julio, Yerushalmi Yair, Cohen Joseph, Barzilai Nir, Blech Ilana, Glaser Benjamin, Permutt M Al |
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Genetic susceptibility to type 2 diabetes is associated with reduced prostate cancer risk.
Human heredity 2010 69 (3): 193-201. Pierce Brandon L, Ahsan Habib |
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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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Obesity and diabetes genes are associated with being born small for gestational age: results from the Auckland Birthweight Collaborative study.
BMC medical genetics 2010 11 125. Morgan Angharad R, Thompson John M D, Murphy Rinki, Black Peter N, Lam Wen-Jiun, Ferguson Lynnette R, Mitchell Ed |
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Use of multiple metabolic and genetic markers to improve the prediction of type 2 diabetes: the EPIC-Potsdam Study.
Diabetes care 2009 Nov 32 (11): 2116-9. Schulze Matthias B, Weikert Cornelia, Pischon Tobias, Bergmann Manuela M, Al-Hasani Hadi, Schleicher Erwin, Fritsche Andreas, Häring Hans-Ulrich, Boeing Heiner, Joost Hans-Geo |
Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.
Nature genetics 2009 Oct 41 (10): 1110-5. Rung Johan, Cauchi Stéphane, Albrechtsen Anders, Shen Lishuang, Rocheleau Ghislain, Cavalcanti-Proença Christine, Bacot François, Balkau Beverley, Belisle Alexandre, Borch-Johnsen Knut, Charpentier Guillaume, Dina Christian, Durand Emmanuelle, Elliott Paul, Hadjadj Samy, Järvelin Marjo-Riitta, Laitinen Jaana, Lauritzen Torsten, Marre Michel, Mazur Alexander, Meyre David, Montpetit Alexandre, Pisinger Charlotta, Posner Barry, Poulsen Pernille, Pouta Anneli, Prentki Marc, Ribel-Madsen Rasmus, Ruokonen Aimo, Sandbaek Anelli, Serre David, Tichet Jean, Vaxillaire Martine, Wojtaszewski Jørgen F P, Vaag Allan, Hansen Torben, Polychronakos Constantin, Pedersen Oluf, Froguel Philippe, Sladek Robe |
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No association of multiple type 2 diabetes loci with type 1 diabetes.
Diabetologia 2009 Oct 52 (10): 2109-16. Raj S M, Howson J M M, Walker N M, Cooper J D, Smyth D J, Field S F, Stevens H E, Todd J |
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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 |
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Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men.
Diabetes 2009 Sep 58 (9): 2129-36. Stancáková Alena, Kuulasmaa Teemu, Paananen Jussi, Jackson Anne U, Bonnycastle Lori L, Collins Francis S, Boehnke Michael, Kuusisto Johanna, Laakso Mark |
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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 |
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Underlying genetic models of inheritance in established type 2 diabetes associations.
American journal of epidemiology 2009 Sep 170 (5): 537-45. Salanti Georgia, Southam Lorraine, Altshuler David, Ardlie Kristin, Barroso Inês, Boehnke Michael, Cornelis Marilyn C, Frayling Timothy M, Grallert Harald, Grarup Niels, Groop Leif, Hansen Torben, Hattersley Andrew T, Hu Frank B, Hveem Kristian, Illig Thomas, Kuusisto Johanna, Laakso Markku, Langenberg Claudia, Lyssenko Valeriya, McCarthy Mark I, Morris Andrew, Morris Andrew D, Palmer Colin N A, Payne Felicity, Platou Carl G P, Scott Laura J, Voight Benjamin F, Wareham Nicholas J, Zeggini Eleftheria, Ioannidis John P |
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A common genetic variant in WFS1 determines impaired glucagon-like peptide-1-induced insulin secretion.
Diabetologia 2009 Jun 52 (6): 1075-82. Schäfer S A, Müssig K, Staiger H, Machicao F, Stefan N, Gallwitz B, Häring H U, Fritsche |
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Genetic predisposition, Western dietary pattern, and the risk of type 2 diabetes in men.
The American journal of clinical nutrition 2009 May 89 (5): 1453-8. Qi Lu, Cornelis Marilyn C, Zhang Cuilin, van Dam Rob M, Hu Frank |
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The inhibitory effect of recent type 2 diabetes risk loci on insulin secretion is modulated by insulin sensitivity.
The Journal of clinical endocrinology and metabolism 2009 May 94 (5): 1775-80. Haupt Axel, Guthoff Martina, Schäfer Silke A, Kirchhoff Kerstin, Machicao Fausto, Gallwitz Baptist, Staiger Harald, Stefan Norbert, Fritsche Andreas, Häring Hans-Ulri |
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Joint effects of common genetic variants on the risk for type 2 diabetes in U.S. men and women of European ancestry.
Annals of internal medicine 2009 Apr 150 (8): 541-50. Cornelis Marilyn C, Qi Lu, Zhang Cuilin, Kraft Peter, Manson JoAnn, Cai Tianxi, Hunter David J, Hu Frank |
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Risk prediction of prevalent diabetes in a Swiss population using a weighted genetic score--the CoLaus Study.
Diabetologia 2009 Apr 52 (4): 600-8. Lin X, Song K, Lim N, Yuan X, Johnson T, Abderrahmani A, Vollenweider P, Stirnadel H, Sundseth S S, Lai E, Burns D K, Middleton L T, Roses A D, Matthews P M, Waeber G, Cardon L, Waterworth D M, Mooser |
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Previously associated type 2 diabetes variants may interact with physical activity to modify the risk of impaired glucose regulation and type 2 diabetes: a study of 16,003 Swedish adults.
Diabetes 2009 Mar . Brito EC, Lyssenko V, Renström F, Berglund G, Nilsson PM, Groop L, Franks PW |
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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 |
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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 |
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PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population.
PloS one 2009 4 (10): e7643. Hu Cheng, Zhang Rong, Wang Congrong, Wang Jie, Ma Xiaojing, Lu Jingyi, Qin Wen, Hou Xuhong, Wang Chen, Bao Yuqian, Xiang Kunsan, Jia Weipi |
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The search for putative unifying genetic factors for components of the metabolic syndrome.
Diabetologia 2008 Dec 51 (12): 2242-51. Sjögren M, Lyssenko V, Jonsson A, Berglund G, Nilsson P, Groop L, Orho-Melander |
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Assessing the combined impact of 18 common genetic variants of modest effect sizes on type 2 diabetes risk.
Diabetes 2008 Nov 57 (11): 3129-35. Lango Hana, , Palmer Colin N A, Morris Andrew D, Zeggini Eleftheria, Hattersley Andrew T, McCarthy Mark I, Frayling Timothy M, Weedon Michael |
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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 |
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Variants of the PPARG, IGF2BP2, CDKAL1, HHEX, and TCF7L2 genes confer risk of type 2 diabetes independently of BMI in the German KORA studies.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 2008 Oct 40 (10): 722-6. Herder C, Rathmann W, Strassburger K, Finner H, Grallert H, Huth C, Meisinger C, Gieger C, Martin S, Giani G, Scherbaum W A, Wichmann H-E, Illig |
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