Human Genome Epidemiology Literature Finder
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Records 1 - 21 (of 21 Records) |
| Query Trace: Diabetes Mellitus and HNF1B[original query] |
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| Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association. Journal of human genetics 2009 Apr 54 (4): 236-41. Miyake Kazuaki, Yang Woosung, Hara Kazuo, Yasuda Kazuki, Horikawa Yukio, Osawa Haruhiko, Furuta Hiroto, Ng Maggie C Y, Hirota Yushi, Mori Hiroyuki, Ido Keisuke, Yamagata Kazuya, Hinokio Yoshinori, Oka Yoshitomo, Iwasaki Naoko, Iwamoto Yasuhiko, Yamada Yuichiro, Seino Yutaka, Maegawa Hiroshi, Kashiwagi Atsunori, Wang He-Yao, Tanahashi Toshihito, Nakamura Naoto, Takeda Jun, Maeda Eiichi, Yamamoto Ken, Tokunaga Katsushi, Ma Ronald C W, So Wing-Yee, Chan Juliana C N, Kamatani Naoyuki, Makino Hideichi, Nanjo Kishio, Kadowaki Takashi, Kasuga Masa |
| 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 |
| Polymorphism in microRNA-binding site in HNF1B influences the susceptibility of type 2 diabetes mellitus: a population based case-control study. BMC medical genetics 2015 16 (1): 75. Goda Naoki, Murase Haruna, Kasezawa Nobuhiko, Goda Toshinao, Yamakawa-Kobayashi Kimi |
| HNF1B, TSPAN8 and NOTCH2 gene polymorphisms in women with gestational diabetes. 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 2017 Mar 1-6. Tarnowski Maciej, Malinowski Damian, Safranow Krzysztof, Dziedziejko Violetta, Pawlik Andrz |
| 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 |
| Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1?-associated renal disease and can be symptomatic. Clinical kidney journal 2018 8 11 (4): 453-458. Clissold Rhian L, Fulford Jon, Hudson Michelle, Shields Beverley M, McDonald Timothy J, Ellard Sian, Hattersley Andrew T, Bingham Coral |
| 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 |
| Common Type 2 Diabetes Genetic Risk Variants Improve the Prediction of Gestational Diabetes. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2019 Jul . Dziedziejko Violetta, Safranow Krzysztof, Tarnowski Maciej, Pawlik Andrz |
| Searching for mutations in the HNF1B gene in a Brazilian cohort with renal cysts and hyperglycemia. Archives of endocrinology and metabolism 2019 5 63 (3): 250-257. Dotto Renata P, Santana Lucas Santos de, Lindsey Susan C, Caetano Lilian Araújo, Franco Luciana F, Moisés Regina Célia M S, Sa João R, Nishiura José Luiz, Teles Milena Gurgel, Heilberg Ita P, Dias-da-Silva Magnus R, Giuffrida Fernando M A, Reis André |
| 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 |
| Influence of IGF2BP2, HMG20A, and HNF1B genetic polymorphisms on the susceptibility to Type 2 diabetes mellitus in Chinese Han population. Bioscience reports 2020 Apr . Huang Ting, Wang Li, Bai Mei, Zheng Jianwen, Yuan Dongya, He Yongjun, Wang Yuhe, Jin Tianbo, Cui W |
| 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 |
| 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 |
| Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus. Journal of clinical research in pediatric endocrinology 2023 12 . Enver ?im?ek, Oguz Cilingir, Tulay Simsek, Sinem Kocagil, Ebru Erzurumluoglu Gokalp, Meliha Demiral, Cigdem Bin |
| Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran. Scientific reports 2024 8 14 (1): 19860. Sara Asgarian, Hossein Lanjanian, Shiva Rahimipour Anaraki, Farzad Hadaegh, Maryam Moazzam-Jazi, Leila Najd-Hassan-Bonab, Sajedeh Masjoudi, Asiyeh Sadat Zahedi, Maryam Zarkesh, Bita Shalbafan, Mahdi Akbarzadeh, Sahand Tehrani Fateh, Davood Khalili, Amirabbas Momenan, Narges Sarbazi, Mehdi Hedayati, Fereidoun Azizi, Maryam S Daneshpo |
| High prevalence of copy number variations in the Japanese participants with suspected MODY. Clinical genetics 2024 5 . Satoshi Tanaka, Hiroyuki Akagawa, Kenkou Azuma, Sayaka Higuchi, Atsushi Ujiie, Koshi Hashimoto, Naoko Iwasa |
| Molecular and clinical profiles of pediatric monogenic diabetes subtypes: comprehensive genetic analysis of 138 patients. The Journal of clinical endocrinology and metabolism 2024 11 . Qiaoli Zhou, Sama Samadli, Haoyu Zhang, Xueqin Zheng, Bixia Zheng, Aihua Zhang, Wei |
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