HuGE Literature Finder
Records 1-30
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Next-generation sequencing identifies monogenic diabetes in 16% of patients with late adolescence/adult-onset diabetes selected on a clinical basis: a cross-sectional analysis.
BMC medicine 2019 Jul 17 (1): 132. Donath Xavier, Saint-Martin Cécile, Dubois-Laforgue Danièle, Rajasingham Ramanan, Mifsud François, Ciangura Cécile, Timsit José, Bellanné-Chantelot Christine, |
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HNF1A gene p.I27L is associated with early-onset, maturity-onset diabetes of the young-like diabetes in Turkey.
BMC endocrine disorders 2019 May 19 (1): 51. Beysel Selvihan, Eyerci Nilnur, Pinarli Ferda Alparslan, Kizilgul Muhammed, Ozcelik Ozgur, Caliskan Mustafa, Cakal Erm |
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Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population.
European journal of human genetics : EJHG 2018 Feb . Appel Emil V R, Moltke Ida, Jørgensen Marit E, Bjerregaard Peter, Linneberg Allan, Pedersen Oluf, Albrechtsen Anders, Hansen Torben, Grarup Nie |
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Maturity Onset Diabetes of the Young (MODY) in Tunisia: Low frequencies of GCK and HNF1A mutations.
Gene 2018 Feb . Ben Khelifa S, Martinez R, Dandana A, Khochtali I, Ferchichi S, Castaño |
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Glucokinase mutations in pediatric patients with impaired fasting glucose.
Acta diabetologica 2017 Oct 54 (10): 913-923. Aloi C, Salina A, Minuto N, Tallone R, Lugani F, Mascagni A, Mazza O, Cassanello M, Maghnie M, d'Annunzio |
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MODY in Ukraine: genes, clinical phenotypes and treatment.
Journal of pediatric endocrinology & metabolism : JPEM 2017 Oct 30 (10): 1095-1103. Globa Evgenia, Zelinska Nataliya, Elblova Lenka, Dusatkova Petra, Cinek Ondrej, Lebl Jan, Colclough Kevin, Ellard Sian, Pruhova Stepan |
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The prevalence of monogenic diabetes in Australia: the Fremantle Diabetes Study Phase II.
The Medical journal of Australia 2017 Oct 207 (8): 344-347. Davis Timothy Me, Makepeace Ashley E, Ellard Sian, Colclough Kevin, Peters Kirsten, Hattersley Andrew, Davis Wendy |
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Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability.
Nature genetics 2017 Sep 49 (9): 1398-1402. Ivarsdottir Erna V, Steinthorsdottir Valgerdur, Daneshpour Maryam S, Thorleifsson Gudmar, Sulem Patrick, Holm Hilma, Sigurdsson Snaevar, Hreidarsson Astradur B, Sigurdsson Gunnar, Bjarnason Ragnar, Thorsson Arni V, Benediktsson Rafn, Eyjolfsson Gudmundur, Sigurdardottir Olof, Olafsson Isleifur, Zeinali Sirous, Azizi Fereidoun, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Stefansson Ka |
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The GCKR Gene Polymorphism rs780094 is a Risk Factor for Gestational Diabetes in a Brazilian Population.
Journal of clinical laboratory analysis 2017 Mar 31 (2): . Anghebem-Oliveira Mauren Isfer, Webber Susan, Alberton Dayane, de Souza Emanuel Maltempi, Klassen Giseli, Picheth Geraldo, Rego Fabiane Gomes de Mora |
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Genetic Confirmation Rate in Clinically Suspected Maturity-Onset Diabetes of the Young.
Canadian journal of diabetes 2016 Sep . Brahm Amanda J, Wang Grace, Wang Jian, McIntyre Adam D, Cao Henian, Ban Matthew R, Hegele Robert |
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GCK Gene Mutations are a Common Cause of Childhood-Onset MODY (Maturity-Onset Diabetes Of The Young) in Turkey.
Clinical endocrinology 2016 Jun . Haliloglu Belma, Hysenaj Gerald, Atay Zeynep, Guran Tulay, Abal? Sayg?n, Turan Serap, Bereket Abdullah, Ellard Si |
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Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing.
Journal of pediatric endocrinology & metabolism : JPEM 2015 Dec . A?lad?o?lu Sebahat Y?lmaz, Aycan Zehra, Çetinkaya Semra, Ba? Veysel Nijat, Önder A?an, Peltek Kendirci Havva Nur, Do?an Haldun, Ceylaner Serd |
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Substantial proportion of MODY among multiplex families participating in a Type 1 diabetes prediction programme.
Diabetic medicine : a journal of the British Diabetic Association 2015 Dec . Petruzelkova L, Dusatkova P, Cinek O, Sumnik Z, Pruhova S, Hradsky O, Vcelakova J, Lebl J, Kolouskova |
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Association of the glucokinase gene promoter polymorphism -30G > A (rs1799884) with gestational diabetes mellitus susceptibility: a case-control study and meta-analysis.
Archives of gynecology and obstetrics 2015 Aug 292 (2): 291-8. Han Xueling, Cui Hongyan, Chen Xu, Xie Wanying, Chang Yi |
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The clinical management of hyperglycemia in pregnancy complicated by maturity-onset diabetes of the young.
American journal of obstetrics and gynecology 2015 Aug 213 (2): 236.e1-7. Bacon Siobhan, Schmid Jasmin, McCarthy Ailbhe, Edwards Jackie, Fleming Aileen, Kinsley Brendan, Firth Richard, Byrne Bridgette, Gavin Claire, Byrne Maria |
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Genetic causes of maturity onset diabetes of the young may be less prevalent in American pregnant women recently diagnosed with diabetes mellitus than in previously studied European populations.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2015 Jul 28 (10): 1113-5. Sewell M F, Presley L H, Holland S H, Catalano P |
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Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing.
Journal of pediatric endocrinology & metabolism : JPEM 2015 Jul . An?k Ahmet, Çatl? Gönül, Abac? Ayhan, Sar? Erkan, Ye?ilkaya Ediz, Korkmaz Hüseyin An?l, Demir Korcan, Alt?nc?k Ayça, Tuhan Hale Ünver, K?z?lda? Sefa, Özkan Behzat, Ceylaner Serdar, Böber E |
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Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase Mutation.
Diabetes care 2015 Jul 38 (7): 1383-92. Chakera Ali J, Steele Anna M, Gloyn Anna L, Shepherd Maggie H, Shields Beverley, Ellard Sian, Hattersley Andrew |
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Characteristics of maturity onset diabetes of the young in a large diabetes center.
Pediatric diabetes 2015 Jun . Chambers Christina, Fouts Alexandra, Dong Fran, Colclough Kevin, Wang Zhenyuan, Batish Sat Dev, Jaremko Malgorzata, Ellard Sian, Hattersley Andrew T, Klingensmith Georgeanna, Steck Andrea |
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GCK monogenic diabetes and gestational diabetes: possible diagnosis on clinical grounds.
Diabetic medicine : a journal of the British Diabetic Association 2015 Jun . Flack J R, Ross G P, Cheung N |
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Circulating ghrelin level is higher in HNF1A-MODY and GCK-MODY than in polygenic forms of diabetes mellitus.
Endocrine 2015 May . Nowak Natalia, Hohendorff Jerzy, Solecka Iwona, Szopa Magdalena, Skupien Jan, Kiec-Wilk Beata, Mlynarski Wojciech, Malecki Maciej |
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Quantitative candidate gene association studies of metabolic traits in Han Chinese type 2 diabetes patients.
Genetics and molecular research : GMR 2015 14 (4): 15471-81. Wei F J, Cai C Y, Yu P, Lv J, Ling C, Shi W T, Jiao H X, Chang B C, Yang F H, Tian Y, Li M S, Wang Y H, Zou L, Shi J M, Chen L M, Li W |
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Dual matrilineal geographic distribution of Korean type 2 diabetes mellitus-associated -11,377 G adiponectin allele.
Molecular medicine reports 2014 Dec 10 (6): 2993-3002. Choi Jee-Hye, Min Na Young, Park Sang Kil, Gavaachimed Lkhagvasuren, Ko Young Jong, Han Sung Hoon, Kim Kyung Yong, Kim Kijung, Lee Kwang Ho, Park Ae |
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Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach.
Molecular genetics and metabolism 2014 Dec 113 (4): 315-20. Alkorta-Aranburu G, Carmody D, Cheng Y W, Nelakuditi V, Ma L, Dickens Jazzmyne T, Das S, Greeley S A W, del Gaudio |
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Common genetic variation in the glucokinase gene (GCK) is associated with type 2 diabetes and rates of carbohydrate oxidation and energy expenditure.
Diabetologia 2014 Jul 57 (7): 1382-90. Muller Yunhua L, Piaggi Paolo, Hoffman Duncan, Huang Ke, Gene Brittany, Kobes Sayuko, Thearle Marie S, Knowler William C, Hanson Robert L, Baier Leslie J, Bogardus Clift |
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Association of GCK -30G> a polymorphism with gestational diabetes mellitus and type 2 diabetes mellitus risk: a meta-analysis involving 18 case-control studies.
Genetic testing and molecular biomarkers 2014 May 18 (5): 289-98. Yang Sheng, Du Qia |
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Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia.
JAMA 2014 Jan 311 (3): 279-86. Steele Anna M, Shields Beverley M, Wensley Kirsty J, Colclough Kevin, Ellard Sian, Hattersley Andrew |
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Association of common genetic variants with diabetes and metabolic syndrome related traits in the Arizona Insulin Resistance registry: a focus on Mexican American families in the Southwest.
Human heredity 2014 78 (1): 47-58. DeMenna Jacob, Puppala Sobha, Chittoor Geetha, Schneider Jennifer, Kim Joon Young, Shaibi Gabriel Q, Mandarino Lawrence J, Duggirala Ravindranath, Coletta Dawn |
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Williams-beuren syndrome is a genetic disorder associated with impaired glucose tolerance and diabetes in childhood and adolescence: new insights from a longitudinal study.
Hormone research in pædiatrics 2014 82 (1): 38-43. Stagi Stefano, Lapi Elisabetta, Cecchi Cecilia, Chiarelli Francesco, D'Avanzo Maria Gabriella, Seminara Salvatore, de Martino Mauriz |
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Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity.
Diabetes 2013 Dec . Dimas AS, Lagou V, Barker A, Knowles JW, Mägi R, Hivert MF, Benazzo A, Rybin D, Jackson AU, Stringham HM, Song C, Fischer-Rosinsky A, Boesgaard TW, Grarup N, Abbasi FA, Assimes TL, Hao K, Yang X, Lecoeur C, Barroso I, Bonnycastle LL, Böttcher Y, Bumpstead S, Chines PS, Erdos MR, Graessler J, Kovacs P, Morken MA, Narisu N, Payne F, Stancakova A, Swift AJ, Tönjes A, Bornstein SR, Cauchi S, Froguel P, Meyre D, Schwarz PE, Häring HU, Smith U, Boehnke M, Bergman RN, Collins FS, Mohlke KL, Tuomilehto J, Quertemous T, Lind L, Hansen T, Pedersen O, Walker M, Pfeiffer AF, Spranger J, Stumvoll M, Meigs JB, Wareham NJ, Kuusisto J, Laakso M, Langenberg C, Dupuis J, Watanabe RM, Florez JC, Ingelsson E, McCarthy MI, Prokopenko I |
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Prevalence, characteristics and clinical diagnosis of maturity onset diabetes of the young due to mutations in HNF1A, HNF4A, and glucokinase: results from the SEARCH for Diabetes in Youth.
The Journal of clinical endocrinology and metabolism 2013 Oct 98 (10): 4055-62. Pihoker Catherine, Gilliam Lisa K, Ellard Sian, Dabelea Dana, Davis Cralen, Dolan Lawrence M, Greenbaum Carla J, Imperatore Giuseppina, Lawrence Jean M, Marcovina Santica M, Mayer-Davis Elizabeth, Rodriguez Beatriz L, Steck Andrea K, Williams Desmond E, Hattersley Andrew T, |
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Mutations in HNF1A result in marked alterations of plasma glycan profile.
Diabetes 2013 Apr 62 (4): 1329-37. Thanabalasingham Gaya, Huffman Jennifer E, Kattla Jayesh J, Novokmet Mislav, Rudan Igor, Gloyn Anna L, Hayward Caroline, Adamczyk Barbara, Reynolds Rebecca M, Muzinic Ana, Hassanali Neelam, Pucic Maja, Bennett Amanda J, Essafi Abdelkader, Polasek Ozren, Mughal Saima A, Redzic Irma, Primorac Dragan, Zgaga Lina, Kolcic Ivana, Hansen Torben, Gasperikova Daniela, Tjora Erling, Strachan Mark W J, Nielsen Trine, Stanik Juraj, Klimes Iwar, Pedersen Oluf B, Njølstad Pål R, Wild Sarah H, Gyllensten Ulf, Gornik Olga, Wilson James F, Hastie Nicholas D, Campbell Harry, McCarthy Mark I, Rudd Pauline M, Owen Katharine R, Lauc Gordan, Wright Alan |
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Genetic polymorphism of glucokinase on the risk of type 2 diabetes and impaired glucose regulation: evidence based on 298,468 subjects.
PloS one 2013 8 (2): e55727. Fu Da, Cong Xianling, Ma Yushui, Cai Haidong, Cai Mingxiang, Li Dan, Lv Mingli, Yuan Xueyu, Huang Yinghui, Lv Zhongw |
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Large scale meta-analyses of fasting plasma glucose raising variants in GCK, GCKR, MTNR1B and G6PC2 and their impacts on type 2 diabetes mellitus risk.
PloS one 2013 8 (6): e67665. Wang Haoran, Liu Lei, Zhao Jinzhao, Cui Guanglin, Chen Chen, Ding Hu, Wang Dao W |
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Use of HbA1c in the identification of patients with hyperglycaemia caused by a glucokinase mutation: observational case control studies.
PloS one 2013 8 (6): e65326. Steele Anna M, Wensley Kirsty J, Ellard Sian, Murphy Rinki, Shepherd Maggie, Colclough Kevin, Hattersley Andrew T, Shields Beverley |
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Variations with modest effects have an important role in the genetic background of type 2 diabetes and diabetes-related traits.
Journal of human genetics 2012 Dec 57 (12): 776-9. Fujita Hayato, Hara Kazuo, Shojima Nobuhiro, Horikoshi Momoko, Iwata Minoru, Hirota Yushi, Tobe Kazuyuki, Seino Susumu, Kadowaki Takas |
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Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource.
Diabetologia 2012 Nov 55 (11): 2970-84. Liu C-T, Ng M C Y, Rybin D, Adeyemo A, Bielinski S J, Boerwinkle E, Borecki I, Cade B, Chen Y D I, Djousse L, Fornage M, Goodarzi M O, Grant S F A, Guo X, Harris T, Kabagambe E, Kizer J R, Liu Y, Lunetta K L, Mukamal K, Nettleton J A, Pankow J S, Patel S R, Ramos E, Rasmussen-Torvik L, Rich S S, Rotimi C N, Sarpong D, Shriner D, Sims M, Zmuda J M, Redline S, Kao W H, Siscovick D, Florez J C, Rotter J I, Dupuis J, Wilson J G, Bowden D W, Meigs J |
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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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Meta-Analysis of the Relationship between Common Type 2 Diabetes Risk Gene Variants with Gestational Diabetes Mellitus.
PloS one 2012 7 (9): 9. Mao H, Li Q, Gao S |
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Genetic prediction of postpartum diabetes in women with gestational diabetes mellitus.
Diabetes research and clinical practice 2012 Sep 97 (3): 394-8. Ekelund M, Shaat N, Almgren P, Anderberg E, Landin-Olsson M, Lyssenko V, Groop L, Berntorp |
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Systematic assessment of etiology in adults with a clinical diagnosis of young-onset type 2 diabetes is a successful strategy for identifying maturity-onset diabetes of the young.
Diabetes care 2012 Jun 35 (6): 1206-12. Thanabalasingham Gaya, Pal Aparna, Selwood Mary P, Dudley Christina, Fisher Karen, Bingley Polly J, Ellard Sian, Farmer Andrew J, McCarthy Mark I, Owen Katharine |
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Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism.
Diabetologia 2012 Feb 55 (2): 331-9. Walford G A, Green T, Neale B, Isakova T, Rotter J I, Grant S F A, Fox C S, Pankow J S, Wilson J G, Meigs J B, Siscovick D S, Bowden D W, Daly M J, Florez J |
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Effects of genetic variants previously associated with fasting glucose and insulin in the Diabetes Prevention Program.
PloS one 2012 7 (9): e44424. Florez Jose C, Jablonski Kathleen A, McAteer Jarred B, Franks Paul W, Mason Clinton C, Mather Kieren, Horton Edward, Goldberg Ronald, Dabelea Dana, Kahn Steven E, Arakaki Richard F, Shuldiner Alan R, Knowler William C, |
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Race-ethnic differences in the association of genetic loci with HbA1c levels and mortality in U.S. adults: the third National Health and Nutrition Examination Survey (NHANES III).
BMC medical genetics 2012 13 (1): 30. Grimsby Jonna L, Porneala Bianca C, Vassy Jason L, Yang Quanhe, Florez José C, Dupuis Josée, Liu Tiebin, Yesupriya Ajay, Chang Man-Huei, Ned Renee M, Dowling Nicole F, Khoury Muin J, Meigs James B, |
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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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Associations of common genetic variants with age-related changes in fasting and postload glucose: evidence from 18 years of follow-up of the Whitehall II cohort.
Diabetes 2011 May 60 (5): 1617-23. Jensen Anders C, Barker Adam, Kumari Meena, Brunner Eric J, Kivimäki Mika, Hingorani Aroon D, Wareham Nicholas J, Tabák Adam G, Witte Daniel R, Langenberg Claud |
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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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Glucose metabolism gene variants modulate the risk of pancreatic cancer.
Cancer prevention research (Philadelphia, Pa.) 2011 May 4 (5): 758-66. Dong Xiaoqun, Li Yanan, Chang Ping, Tang Hongwei, Hess Kenneth R, Abbruzzese James L, Li Dongh |
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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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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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Genetic predisposition to long-term nondiabetic deteriorations in glucose homeostasis: Ten-year follow-up of the GLACIER study.
Diabetes 2011 Jan 60 (1): 345-54. Renström Frida, Shungin Dmitry, Johansson Ingegerd, , Florez Jose C, Hallmans Göran, Hu Frank B, Franks Paul |
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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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Association of new loci identified in European genome-wide association studies with susceptibility to type 2 diabetes in the Japanese.
PloS one 2011 6 (10): e26911. Ohshige Toshihiko, Iwata Minoru, Omori Shintaro, Tanaka Yasushi, Hirose Hiroshi, Kaku Kohei, Maegawa Hiroshi, Watada Hirotaka, Kashiwagi Atsunori, Kawamori Ryuzo, Tobe Kazuyuki, Kadowaki Takashi, Nakamura Yusuke, Maeda Shi |
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Bioinformatics-driven identification and examination of candidate genes for non-alcoholic fatty liver disease.
PloS one 2011 6 (1): e16542. Banasik Karina, Justesen Johanne M, Hornbak Malene, Krarup Nikolaj T, Gjesing Anette P, Sandholt Camilla H, Jensen Thomas S, Grarup Niels, Andersson Asa, Jørgensen Torben, Witte Daniel R, Sandbæk Annelli, Lauritzen Torsten, Thorens Bernard, Brunak Søren, Sørensen Thorkild I A, Pedersen Oluf, Hansen Torb |
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Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations.
Pediatric diabetes 2010 Dec 11 (8): 529-35. Pruhova Stepanka, Dusatkova Petra, Sumnik Zdenek, Kolouskova Stanislava, Pedersen Oluf, Hansen Torben, Cinek Ondrej, Lebl J |
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Common variants in 40 genes assessed for diabetes incidence and response to metformin and lifestyle intervention in the diabetes prevention program.
Diabetes 2010 Oct 59 (10): 2672-81. Jablonski Kathleen A, McAteer Jarred B, de Bakker Paul I W, Franks Paul W, Pollin Toni I, Hanson Robert L, Saxena Richa, Fowler Sarah, Shuldiner Alan R, Knowler William C, Altshuler David, Florez Jose C, |
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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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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 |
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
Nature genetics 2010 Feb 42 (2): 2. Dupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL, Bouatia-Naji N, Gloyn AL, Lindgren CM, Mägi R, Morris AP, Randall J, Johnson T, Elliott P, Rybin D, Thorleifsson G, Steinthorsdottir V, Henneman P, Grallert H, Dehghan A, Hottenga JJ, Franklin CS, Navarro P, Song K, Goel A, Perry JR, Egan JM, Lajunen T, Grarup N, Sparsø T, Doney A, Voight BF, Stringham HM, Li M, Kanoni S, Shrader P, Cavalcanti-Proença C, Kumari M, Qi L, Timpson NJ, Gieger C, Zabena C, Rocheleau G, Ingelsson E, An P, O'Connell J, Luan J, Elliott A, McCarroll SA, Payne F, Roccasecca RM, Pattou F, Sethupathy P, Ardlie K, Ariyurek Y, Balkau B, Barter P, Beilby JP, Ben-Shlomo Y, Benediktsson R, Bennett AJ, Bergmann S, Bochud M, Boerwinkle E, Bonnefond A, Bonnycastle LL, Borch-Johnsen K, Böttcher Y, Brunner E, Bumpstead SJ, Charpentier G, Chen YD, Chines P, Clarke R, Coin LJ, Cooper MN, Cornelis M, Crawford G, Crisponi L, Day IN, de Geus EJ, Delplanque J, Dina C, Erdos MR, Fedson AC, Fischer-Rosinsky A, Forouhi NG, Fox CS, Frants R, Franzosi MG, Galan P, Goodarzi MO, Graessler J, Groves CJ, Grundy S, Gwilliam R, Gyllensten U, Hadjadj S, Hallmans G, Hammond N, Han X, Hartikainen AL, Hassanali N, Hayward C, Heath SC, Hercberg S, Herder C, Hicks AA, Hillman DR, Hingorani AD, Hofman A, Hui J, Hung J, Isomaa B, Johnson PR, Jørgensen T, Jula A, Kaakinen M, Kaprio J, Kesaniemi YA, Kivimaki M, Knight B, Koskinen S, Kovacs P, Kyvik KO, Lathrop GM, Lawlor DA, Le Bacquer O, Lecoeur C, Li Y, Lyssenko V, Mahley R, Mangino M, Manning AK, Martínez-Larrad MT, McAteer JB, McCulloch LJ, McPherson R, Meisinger C, Melzer D, Meyre D, Mitchell BD, Morken MA, Mukherjee S, Naitza S, Narisu N, Neville MJ, Oostra BA, Orrù M, Pakyz R, Palmer CN, Paolisso G, Pattaro C, Pearson D, Peden JF, Pedersen NL, Perola M, Pfeiffer AF, Pichler I, Polasek O, Posthuma D, Potter SC, Pouta A, Province MA, Psaty BM, Rathmann W, Rayner NW, Rice K, Ripatti S, Rivadeneira F, Roden M, Rolandsson O, Sandbaek A, Sandhu M, Sanna S, Sayer AA, Scheet P, Scott LJ, Seedorf U, Sharp SJ, Shields B, Sigurethsson G, Sijbrands EJ, Silveira A, Simpson L, Singleton A, Smith NL, Sovio U, Swift A, Syddall H, Syvänen AC, Tanaka T, Thorand B, Tichet J, Tönjes A, Tuomi T, Uitterlinden AG, van Dijk KW, van Hoek M, Varma D, Visvikis-Siest S, Vitart V, Vogelzangs N, Waeber G, Wagner PJ, Walley A, Walters GB, Ward KL, Watkins H, Weedon MN, Wild SH, Willemsen G, Witteman JC, Yarnell JW, Zeggini E, Zelenika D, Zethelius B, Zhai G, Zhao JH, Zillikens MC, Borecki IB, Loos RJ, Meneton P, Magnusson PK, Nathan DM, Williams GH, Hattersley AT, Silander K, Salomaa V, Smith GD, Bornstein SR, Schwarz P, Spranger J, Karpe F, Shuldiner AR, Cooper C, Dedoussis GV, Serrano-Ríos M, Morris AD, Lind L, Palmer LJ, Hu FB, Franks PW, Ebrahim S, Marmot M, Kao WH, Pankow JS, Sampson MJ, Kuusisto J, Laakso M, Hansen T, Pedersen O, Pramstaller PP, Wichmann HE, Illig T, Rudan I, Wright AF, Stumvoll M, Campbell H, Wilson JF, Bergman RN, Buchanan TA, Collins FS, Mohlke KL, Tuomilehto J, Valle TT, Altshuler D, Rotter JI, Siscovick DS, Penninx BW, Boomsma DI, Deloukas P, Spector TD, Frayling TM, Ferrucci L, Kong A, Thorsteinsdottir U, Stefansson K, van Duijn CM, Aulchenko YS, Cao A, Scuteri A, Schlessinger D, Uda M, Ruokonen A, Jarvelin MR, Waterworth DM, Vollenweider P, Peltonen L, Mooser V, Abecasis GR, Wareham NJ, Sladek R, Froguel P, Watanabe RM, Meigs JB, Groop L, Boehnke M, McCarthy MI, Florez JC, Barroso I |
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Chromosome 7p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy.
BMC medical genetics 2010 11 (1): 22. Leak Tennille S, Langefeld Carl D, Keene Keith L, Gallagher Carla J, Lu Lingyi, Mychaleckyj Josyf C, Rich Stephen S, Freedman Barry I, Bowden Donald W, Sale Michèle |
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Common polymorphisms in MTNR1B, G6PC2 and GCK are associated with increased fasting plasma glucose and impaired beta-cell function in Chinese subjects.
PloS one 2010 5 (7): e11428. Tam Claudia Ha Ting, Ho Janice Sin Ka, Wang Ying, Lee Heung Man, Lam Vincent Kwok Lim, Germer Soren, Martin Mitchell, So Wing Yee, Ma Ronald Ching Wan, Chan Juliana Chung Ngor, Ng Maggie Chor Y |
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Effects of GCK, GCKR, G6PC2 and MTNR1B variants on glucose metabolism and insulin secretion.
PloS one 2010 5 (7): e11761. Hu Cheng, Zhang Rong, Wang Congrong, Yu Weihui, Lu Jingyi, Ma Xiaojing, Wang Jie, Jiang Feng, Tang Shanshan, Bao Yuqian, Xiang Kunsan, Jia Weipi |
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Common genetic determinants of glucose homeostasis in healthy children: the European Youth Heart Study.
Diabetes 2009 Dec 58 (12): 2939-45. Kelliny Clara, Ekelund Ulf, Andersen Lars Bo, Brage Soren, Loos Ruth J F, Wareham Nicholas J, Langenberg Claud |
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Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type 2 diabetes among Indian Asians and European Caucasians.
Diabetes 2009 Nov 58 (11): 2703-8. Chambers John C, Zhang Weihua, Zabaneh Delilah, Sehmi Joban, Jain Piyush, McCarthy Mark I, Froguel Philippe, Ruokonen Aimo, Balding David, Jarvelin Marjo-Riitta, Scott James, Elliott Paul, Kooner Jaspal |
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Glucokinase gene mutation screening in Argentinean clinically characterized MODY patients.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2009 Sep 117 (8): 391-4. Lopez A P, Foscaldi S A, Pérez M S, Krochik G, Rodríguez M, Traversa M, Puchulu F M, Hirschler V, Bergada I, Frechtel G |
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Combined effects of single-nucleotide polymorphisms in GCK, GCKR, G6PC2 and MTNR1B on fasting plasma glucose and type 2 diabetes risk.
Diabetologia 2009 Jun . Reiling E, van 't Riet E, Groenewoud MJ, Welschen LM, van Hove EC, Nijpels G, Maassen JA, Dekker JM, 't Hart LM |
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Maturity-Onset Diabetes of the Young (MODY) in Children with Incidental Hyperglycemia. A Multicenter Italian Study on 172 families.
Diabetes care 2009 Jun . Lorini R, Klersy C, d'Annunzio G, Massa O, Minuto N, Iafusco D, Bellannè-Chantelot C, Frongia AP, Toni S, Meschi F, Cerutti F, Barbetti F |
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Mutations of maturity-onset diabetes of the young (MODY) genes in Thais with early-onset type 2 diabetes mellitus.
Clinical endocrinology 2009 Jun 70 (6): 847-53. Plengvidhya Nattachet, Boonyasrisawat Watip, Chongjaroen Nalinee, Jungtrakoon Prapaporn, Sriussadaporn Sutin, Vannaseang Sathit, Banchuin Napatawn, Yenchitsomanus Pa-th |
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A-beta-subtype of ketosis-prone diabetes is not predominantly a monogenic diabetic syndrome.
Diabetes care 2009 May 32 (5): 873-7. Haaland Wade C, Scaduto Diane I, Maldonado Mario R, Mansouri Dena L, Nalini Ramaswami, Iyer Dinakar, Patel Sanjeet, Guthikonda Anu, Hampe Christiane S, Balasubramanyam Ashok, Metzker Michael |
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Association of GCKR rs780094, alone or in combination with GCK rs1799884, with type 2 diabetes and related traits in a Han Chinese population.
Diabetologia 2009 May 52 (5): 834-43. Qi Q, Wu Y, Li H, Loos R J F, Hu F B, Sun L, Lu L, Pan A, Liu C, Wu H, Chen L, Yu Z, Lin |
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Prevalence of GCK mutations in individuals screened for fasting hyperglycaemia.
Diabetologia 2009 Jan 52 (1): 172-4. Gloyn A L, van de Bunt M, Stratton I M, Lonie L, Tucker L, Ellard S, Holman R |
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Variants in MTNR1B influence fasting glucose levels.
Nature genetics 2009 Jan 41 (1): 77-81. Prokopenko Inga, Langenberg Claudia, Florez Jose C, Saxena Richa, Soranzo Nicole, Thorleifsson Gudmar, Loos Ruth J F, Manning Alisa K, Jackson Anne U, Aulchenko Yurii, Potter Simon C, Erdos Michael R, Sanna Serena, Hottenga Jouke-Jan, Wheeler Eleanor, Kaakinen Marika, Lyssenko Valeriya, Chen Wei-Min, Ahmadi Kourosh, Beckmann Jacques S, Bergman Richard N, Bochud Murielle, Bonnycastle Lori L, Buchanan Thomas A, Cao Antonio, Cervino Alessandra, Coin Lachlan, Collins Francis S, Crisponi Laura, de Geus Eco J C, Dehghan Abbas, Deloukas Panos, Doney Alex S F, Elliott Paul, Freimer Nelson, Gateva Vesela, Herder Christian, Hofman Albert, Hughes Thomas E, Hunt Sarah, Illig Thomas, Inouye Michael, Isomaa Bo, Johnson Toby, Kong Augustine, Krestyaninova Maria, Kuusisto Johanna, Laakso Markku, Lim Noha, Lindblad Ulf, Lindgren Cecilia M, McCann Owen T, Mohlke Karen L, Morris Andrew D, Naitza Silvia, Orrù Marco, Palmer Colin N A, Pouta Anneli, Randall Joshua, Rathmann Wolfgang, Saramies Jouko, Scheet Paul, Scott Laura J, Scuteri Angelo, Sharp Stephen, Sijbrands Eric, Smit Jan H, Song Kijoung, Steinthorsdottir Valgerdur, Stringham Heather M, Tuomi Tiinamaija, Tuomilehto Jaakko, Uitterlinden André G, Voight Benjamin F, Waterworth Dawn, Wichmann H-Erich, Willemsen Gonneke, Witteman Jacqueline C M, Yuan Xin, Zhao Jing Hua, Zeggini Eleftheria, Schlessinger David, Sandhu Manjinder, Boomsma Dorret I, Uda Manuela, Spector Tim D, Penninx Brenda Wjh, Altshuler David, Vollenweider Peter, Jarvelin Marjo Riitta, Lakatta Edward, Waeber Gerard, Fox Caroline S, Peltonen Leena, Groop Leif C, Mooser Vincent, Cupples L Adrienne, Thorsteinsdottir Unnur, Boehnke Michael, Barroso Inês, Van Duijn Cornelia, Dupuis Josée, Watanabe Richard M, Stefansson Kari, McCarthy Mark I, Wareham Nicholas J, Meigs James B, Abecasis Gonçalo |
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Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study.
BMC medical genetics 2009 10 (1): 33. Ezzidi Intissar, Mtiraoui Nabil, Cauchi Stéphane, Vaillant Emmanuel, Dechaume Aurélie, Chaieb Molka, Kacem Maha, Almawi Wassim Y, Froguel Philippe, Mahjoub Touhami, Vaxillaire Marti |
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Screening of mutations in the GCK gene in Jordanian maturity-onset diabetes of the young type 2 (MODY2) patients.
Genetics and molecular research : GMR 2009 8 (2): 500-6. Khalil R, Al-Sheyab F, Khamaiseh E, Halaweh M A, Abder-Rahman H |
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Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.
PLoS genetics 2008 Dec 4 (12): e1000312. Paré Guillaume, Chasman Daniel I, Parker Alexander N, Nathan David M, Miletich Joseph P, Zee Robert Y, Ridker Paul |
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Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: linkage of candidate genes using two sib-pair based variance components analyses.
Twin research and human genetics : the official journal of the International Society for Twin Studies 2008 Oct 11 (5): 505-16. Souren Nicole Y, Zeegers Maurice P, Janssen Rob G J H, Steyls Anja, Gielen Marij, Loos Ruth J F, Beunen Gaston, Fagard Robert, Stassen Alphons P M, Aerssens Jeroen, Derom Catherine, Vlietinck Robert, Paulussen Aimee D |
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Common variants in maturity-onset diabetes of the young genes and future risk of type 2 diabetes.
Diabetes 2008 Jun 57 (6): 1738-44. Holmkvist Johan, Almgren Peter, Lyssenko Valeriya, Lindgren Cecilia M, Eriksson Karl-Fredrik, Isomaa Bo, Tuomi Tiinamaija, Nilsson Peter, Groop Le |
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The common P446L polymorphism in GCKR inversely modulates fasting glucose and triglyceride levels, and reduces type 2 diabetes risk in a prospective general French population: the D.E.S.I.R. Study.
Diabetes 2008 Jun . Vaxillaire M, Cavalcanti-Proença C, Dechaume A, Tichet J, Marre M, Balkau B, Froguel P |
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The GCKR rs780094 polymorphism is associated with elevated fasting serum triacylglycerol, reduced fasting and OGTT-related insulinaemia, and reduced risk of type 2 diabetes.
Diabetologia 2008 Jan 51 (1): 70-5. Sparsø T, Andersen G, Nielsen T, Burgdorf K S, Gjesing A P, Nielsen A L, Albrechtsen A, Rasmussen S S, Jørgensen T, Borch-Johnsen K, Sandbaek A, Lauritzen T, Madsbad S, Hansen T, Pedersen |
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Screening of mutations and polymorphisms in the glucokinase gene in Czech diabetic and healthy control populations.
Physiological research / Academia Scientiarum Bohemoslovaca 2008 57 Suppl 1 S99-108. Lukásová P, Vcelák J, Vanková M, Vejrazková D, Andelová K, Bendlová |
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The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies.
BMC medical genetics 2008 9 (1): 45. Cauchi Stéphane, Nead Kevin T, Choquet Hélène, Horber Fritz, Potoczna Natascha, Balkau Beverley, Marre Michel, Charpentier Guillaume, Froguel Philippe, Meyre Dav |
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[Glucokinase gene mutations in gestational diabetes in Polish population. Prediction of diabetes mellitus development after delivery].
Przegla?d lekarski 2007 64 (6): 401-5. Okruszko Anna, Kinalski Maciej, Ku?micki Mariusz, Miro?czuk Katarzyna, Wawrusiewicz-Kurylonek Natalia, Kinalska Ida, Kretowski Ad |
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Genetic and clinical characteristics of Korean maturity-onset diabetes of the young (MODY) patients.
Diabetes research and clinical practice 2006 Oct 74 (1): 75-81. Hwang Jin Soon, Shin Choong Ho, Yang Sei Won, Jung Sung Young, Huh N |
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Common variants in maturity-onset diabetes of the young genes contribute to risk of type 2 diabetes in Finns.
Diabetes 2006 Sep 55 (9): 2534-40. Bonnycastle Lori L, Willer Cristen J, Conneely Karen N, Jackson Anne U, Burrill Cecily P, Watanabe Richard M, Chines Peter S, Narisu Narisu, Scott Laura J, Enloe Sareena T, Swift Amy J, Duren William L, Stringham Heather M, Erdos Michael R, Riebow Nancy L, Buchanan Thomas A, Valle Timo T, Tuomilehto Jaakko, Bergman Richard N, Mohlke Karen L, Boehnke Michael, Collins Francis |
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Common variants in MODY genes increase the risk of gestational diabetes mellitus.
Diabetologia 2006 Jul 49 (7): 1545-51. Shaat N, Karlsson E, Lernmark A, Ivarsson S, Lynch K, Parikh H, Almgren P, Berntorp K, Groop |
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[Contribution of MODY2 gene to the pathogenesis of Chinese early onset familial type 2 diabetes].
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2005 Dec 37 (6): 591-4. Han Xue-yao, Ji Li-no |
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[Mutation screening of GCK gene in Chinese early-onset diabetes population].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2005 Dec 22 (6): 671-4. Zheng Tai-shan, Wu Song-hua, Yang Zhen, Lu Hui-juan, Xiang Kun-s |
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G(-30)A polymorphism in the pancreatic promoter of the glucokinase gene associated with angiographic coronary artery disease and type 2 diabetes mellitus.
Circulation 2004 Jun 109 (23): 2844-9. März Winfried, Nauck Markus, Hoffmann Michael M, Nagel Dietmar, Boehm Bernhard O, Koenig Wolfgang, Rothenbacher Dietrich, Winkelmann Bernhard |
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Screening for MODY mutations, GAD antibodies, and type 1 diabetes--associated HLA genotypes in women with gestational diabetes mellitus.
Diabetes care 2002 Jan 25 (1): 68-71. Weng Jianping, Ekelund Magnus, Lehto Markku, Li Haiyan, Ekberg Göran, Frid Anders, Aberg Anders, Groop Leif C, Berntorp Kerst |
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Routine mutation screening of HNF-1alpha and GCK genes in MODY diagnosis: how effective are the techniques of DHPLC and direct sequencing used in combination?
Diabetologia 2001 Jun 44 (6): 775-8. Boutin P, Vasseur F, Samson C, Wahl C, Froguel |
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Hepatic glucokinase promoter polymorphism is associated with hepatic insulin resistance in Asian Indians.
BMC genetics 2000 1 (): 2. Chiu K C, Chuang L M, Yoon C, Saad M |
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Characterization of glucokinase polymorphisms associated with maturity-onset diabetes of the young (MODY2) in Jordanian population.
T?Sitologii?a i genetika 0 43 (5): 58-63. Al-Sheyab Fawzi, Khamaiseh Emran, Halaweh Marwan Abu, Khaul Raida |
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