Human Genome Epidemiology Literature Finder
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Records 1 - 27 (of 27 Records) |
| Query Trace: Diabetes Mellitus and HNF4A[original query] |
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| Single nucleotide polymorphisms of the HNF4alpha gene are associated with the conversion to type 2 diabetes mellitus: the STOP-NIDDM trial. Journal of molecular medicine (Berlin, Germany) 2006 Aug 84 (8): 701-8. Andrulionyte Laura, Laukkanen Olli, Chiasson Jean-Louis, Laakso Markku, |
| 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 |
| A novel -192c/g mutation in the proximal P2 promoter of the hepatocyte nuclear factor-4 alpha gene (HNF4A) associates with late-onset diabetes. Diabetes 2006 Jun 55 (6): 1869-73. Ek Jakob, Hansen Sara P, Lajer Maria, Nicot Carine, Boesgaard Trine W, Pruhova Stepanka, Johansen Anders, Albrechtsen Anders, Yderstraede Knud, Lauenborg Jeannet, Parrizas Marcelina, Boj Sylvia F, Jørgensen Torben, Borch-Johnsen Knut, Damm Peter, Ferrer Jorge, Lebl Jan, Pedersen Oluf, Hansen Torb |
| Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1. Genomics 2008 Oct 92 (4): 226-34. Bento J L, Palmer N D, Zhong M, Roh B, Lewis J P, Wing M R, Pandya H, Freedman B I, Langefeld C D, Rich S S, Bowden D W, Mychaleckyj J |
| Interaction between HNF4A polymorphisms and physical activity in relation to type 2 diabetes-related traits: results from the Quebec Family Study. Diabetes research and clinical practice 2009 Jun 84 (3): 211-8. Ruchat Stephanie-May, Stephanie-May Ruchat, Weisnagel John S, John Weisnagel S, Rankinen Tuomo, Tuomo Rankinen, Bouchard Claude, Claude Bouchard, Vohl Marie-Claude, Marie-Claude Vohl, Pérusse Louis, Louis Pérus |
| Suggestive evidence of associations between liver X receptor ß polymorphisms with type 2 diabetes mellitus and obesity in three cohort studies: HUNT2 (Norway), MONICA (France) and HELENA (Europe). BMC medical genetics 2010 11 144. Solaas Karianne, Legry Vanessa, Retterstol Kjetil, Berg Paul R, Holven Kirsten B, Ferrières Jean, Amouyel Philippe, Lien Sigbjorn, Romeo Javier, Valtueña Jara, Widhalm Kurt, Ruiz Jonatan R, Dallongeville Jean, Tonstad Serena, Rootwelt Helge, Halvorsen Bente, Nenseter Marit S, Birkeland Kare I, Thorsby Per M, Meirhaeghe Aline, Nebb Hilde |
| Clinically-Defined Maturity Onset Diabetes of the Young in Omanis: Absence of the common Caucasian gene mutations. Sultan Qaboos University medical journal 2010 Apr 10 (1): 80-3. Woodhouse Nicholas Jy, Elshafie Omayma T, Al-Mamari Ali S, Mohammed Nagi Hs, Al-Riyami Fatma, Raeburn San |
| Thr130Ile polymorphism of HNF4A gene is associated with gestational diabetes mellitus in Mexican population. Journal of investigative medicine : the official publication of the American Federation for Clinical Research 2014 Mar 62 (3): 632-4. Monroy Virginia Sánchez, Díaz César Antonio González, Trenado Lucila Maritza Lozano, Peralta José Manuel Campos, Soto Salvador Martín Po |
| Frequency of HNF4A-P.I463V Variant in the Tunisian North-African Population and Its Relation with Diabetes Mellitus. Iranian journal of public health 2015 Mar 44 (3): 396-403. Amara Abdelbasset, Ben Charfeddine Ilhem, Ghédir Houda, Mamaï Ons, Jemni-Yacoub Saloua, Chaieb Larbi, Saad Ali, Chadli-Chaieb Molka, Gribaa Mo |
| Hepatocyte nuclear factor 4 alpha polymorphisms and the metabolic syndrome in French-Canadian youth. PloS one 2015 10 (2): e0117238. Marcil Valérie, Amre Devendra, Seidman Ernest G, Boudreau François, Gendron Fernand P, Ménard Daniel, Beaulieu Jean François, Sinnett Daniel, Lambert Marie, Levy Emi |
| Prolonged episodes of hypoglycaemia in HNF4A-MODY mutation carriers with IGT. Evidence of persistent hyperinsulinism into early adulthood. Acta diabetologica 2016 Aug . Bacon S, Kyithar M P, Condron E M, Vizzard N, Burke M, Byrne M |
| Genetic variants in KCNJ11, TCF7L2 and HNF4A are associated with type 2 diabetes, BMI and dyslipidemia in families of Northeastern Mexico: A pilot study. Experimental and therapeutic medicine 2017 Feb 13 (2): 523-529. Gallardo-Blanco Hugo Leonid, Villarreal-Perez Jesus Zacarías, Cerda-Flores Ricardo Martin, Figueroa Andres, Sanchez-Dominguez Celia Nohemi, Gutierrez-Valverde Juana Mercedes, Torres-Muñoz Iris Carmen, Lavalle-Gonzalez Fernando Javier, Gallegos-Cabriales Esther Carlota, Martinez-Garza Laura El |
| Association of recently identified type 2 diabetes gene variants with Gestational Diabetes in Asian Indian population. Molecular genetics and genomics : MGG 2017 Feb . Kanthimathi Sekar, Chidambaram Manickam, Bodhini Dhanasekaran, Liju Samuel, Bhavatharini Aruyerchelvan, Uma Ram, Anjana Ranjit Mohan, Mohan Viswanathan, Radha Venkates |
| 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 |
| High Prevalence of Diabetes-Predisposing Variants in MODY Genes Among Danish Women With Gestational Diabetes Mellitus. Journal of the Endocrine Society 2017 Jun 1 (6): 681-690. Gjesing Anette P, Rui Gao, Lauenborg Jeannet, Have Christian Theil, Hollensted Mette, Andersson Ehm, Grarup Niels, Sun Jihua, Quan Shi, Brandslund Ivan, Damm Peter, Pedersen Oluf, Wang Jun, Hansen Torb |
| Clinical and genetic characteristics of abnormal glucose tolerance in Japanese women in the first year after gestational diabetes mellitus. Journal of diabetes investigation 2018 Sep . Kasuga Yoshifumi, Miyakoshi Kei, Tajima Atsushi, Saisho Yoshifumi, Ikenoue Satoru, Ochiai Daigo, Matsumoto Tadashi, Arata Naoko, Hata Kenichiro, Tanaka Mamo |
| Heterogeneous nature of diabetes in a family with a gain-of-function mutation in the ATP-binding cassette subfamily C member 8 (ABCC8) gene. Endocrine journal 2018 8 65 (10): 1055-1059. Shima Kosuke Robert, Usuda Rika, Futatani Takeshi, Akahori Hiroshi, Kaneko Shuichi, Yorifuji Tohru, Takamura Toshina |
| Genetic basis of early-onset, maturity-onset diabetes of the young-like diabetes in Japan and features of patients without mutations in the major MODY genes: Dominance of maternal inheritance. Pediatric diabetes 2018 6 19 (7): 1164-1172. Yorifuji Tohru, Higuchi Shinji, Kawakita Rie, Hosokawa Yuki, Aoyama Takane, Murakami Akiko, Kawae Yoshiko, Hatake Kazue, Nagasaka Hironori, Tamagawa Nobuyos |
| Maturity onset diabetes of the young (MODY) in Chinese children: genes and clinical phenotypes. Journal of pediatric endocrinology & metabolism : JPEM 2019 6 32 (7): 759-765. Ming-Qiang Zhu, Yang-Li Dai, Ke Huang, Wei Wu, Jun-Fen Fu, Chao-Chun Zou, Guan-Ping Do |
| 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 |
| Association Analysis of the HNF4A Common Genetic Variants with Type 2 Diabetes Mellitus Risk. International journal of molecular and cellular medicine 2020 5 8 (Suppl1): 56-62. Azizi Seyedeh Mina, Sarhangi Negar, Afshari Mahdi, Abbasi Davood, Aghaei Meybodi Hamid Reza, Hasanzad Manda |
| Low genetic confirmation rate in South Indian subjects with a clinical diagnosis of maturity-onset diabetes of the young (MODY) who underwent targeted next-generation sequencing for 13 genes. Journal of endocrinological investigation 2021 11 45 (3): 607-615. Sampathkumar G, Valiyaparambil P P, Kumar H, Bhavani N, Nair V, Menon U, Menon A, Abraham N, Chapla A, Thomas |
| Polymorphisms in Genes of Lipid Metabolism Are Associated with Type 2 Diabetes Mellitus and Periodontitis, as Comorbidities, and with the Subjects' Periodontal, Glycemic, and Lipid Profiles. Journal of diabetes research 2021 11 2021 1049307. Nicchio Ingra G, Cirelli Thamiris, Nepomuceno Rafael, Hidalgo Marco A R, Rossa Carlos, Cirelli Joni A, Orrico Silvana R P, Barros Silvana P, Theodoro Letícia H, Scarel-Caminaga Raquel |
| Identification of Variants Responsible for Monogenic Forms of Diabetes in Brazil. Frontiers in endocrinology 2022 5 13 827325. Abreu Gabriella de Medeiros, Tarantino Roberta Magalhães, da Fonseca Ana Carolina Proença, Andrade Juliana Rosa Ferreira de Oliveira, de Souza Ritiele Bastos, Soares Camila de Almeida Pereira Dias, Cambraia Amanda, Cabello Pedro Hernan, Rodacki Melanie, Zajdenverg Lenita, Zembrzuski Verônica Marques, Campos Junior Már |
| 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 |
| Monogenic diabetes variants in Emirati women with gestational diabetes are associated with risk of non-autoimmune diabetes within 5 years after pregnancy. Metabolism open 2022 11 16 100213. Daggag Hinda, Gjesing Anette P, Mohammad Alshafi, Ängquist Lars, Shobi Bindu, Antony Suma, Haj Dalia, Al Tikriti Alia, Buckley Adam, Hansen Torben, Barakat Maha |
| Role of monogenic diabetes genes on beta cell function in Italian patients with newly diagnosed type 2 diabetes. The Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 13. Diabetes & metabolism 2022 1 48 (4): 101323. Bonetti S, Zusi C, Rinaldi E, Boselli M L, Csermely A, Malerba G, Trabetti E, Bonora E, Bonadonna R C, Trombetta |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
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