HuGE Literature Finder
Records 1-30
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Pathogenic variants in actionable MODY genes are associated with type 2 diabetes.
Nature metabolism 2020 Oct 2 (10): 1126-1134. Bonnefond Amélie, Boissel Mathilde, Bolze Alexandre, Durand Emmanuelle, Toussaint Bénédicte, Vaillant Emmanuel, Gaget Stefan, Graeve Franck De, Dechaume Aurélie, Allegaert Frédéric, Guilcher David Le, Yengo Loïc, Dhennin Véronique, Borys Jean-Michel, Lu James T, Cirulli Elizabeth T, Elhanan Gai, Roussel Ronan, Balkau Beverley, Marre Michel, Franc Sylvia, Charpentier Guillaume, Vaxillaire Martine, Canouil Mickaël, Washington Nicole L, Grzymski Joseph J, Froguel Philip |
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Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer.
European urology 2020 Aug . Schaid Daniel J, McDonnell Shannon K, FitzGerald Liesel M, DeRycke Lissa, Fogarty Zachary, Giles Graham G, MacInnis Robert J, Southey Melissa C, Nguyen-Dumont Tu, Cancel-Tassin Geraldine, Cussenot Oliver, Whittemore Alice S, Sieh Weiva, Ioannidis Nilah Monnier, Hsieh Chih-Lin, Stanford Janet L, Schleutker Johanna, Cropp Cheryl D, Carpten John, Hoegel Josef, Eeles Rosalind, Kote-Jarai Zsofia, Ackerman Michael J, Klein Christopher J, Mandal Diptasri, Cooney Kathleen A, Bailey-Wilson Joan E, Helfand Brian, Catalona William J, Wiklund Fredrick, Riska Shaun, Bahetti Saurabh, Larson Melissa C, Cannon Albright Lisa, Teerlink Craig, Xu Jianfeng, Isaacs William, Ostrander Elaine A, Thibodeau Stephen |
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Influence of IGF2BP2, HMG20A, and HNF1B genetic polymorphisms on the susceptibility to type 2 diabetes mellitus in Chinese Han population.
Bioscience reports 2020 Apr . Wang Li, Cui Wei, Bai Mei, Zheng Jianwen, Yuan Dongya, He Yongjun, Wang Yuhe, Jin Tian |
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Integrative Analysis of HNF1B mRNA in Human Cancers Based on Data Mining.
International journal of medical sciences 2020 17 (18): 2895-2904. Nie Chunhui, Wang Bei, Wang Baoquan, Lv Ning, Zhang Enf |
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A diabetes-associated genetic variant is associated with diastolic dysfunction and cardiovascular disease.
ESC heart failure 2019 Dec . Molvin John, Jujic Amra, Nilsson Peter M, Leosdottir Margret, Lindblad Ulf, Daka Bledar, Bennet Louise, Råstam Lennart, Lyssenko Valeriya, Magnusson Mart |
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Clinical relevance of the lnc-HNF1B-3:1 genetic polymorphisms in Western Chinese tuberculosis patients.
Journal of clinical laboratory analysis 2019 Nov e23076. Wu Qian, Zhong Huiyu, Bai Hao, Liu Tangyuheng, Song Jiajia, Wen Yang, Song Xingbo, Ying Bin |
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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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Identifying Pathogenic Variants of Monogenic Diabetes Using Targeted Panel Sequencing in an East Asian Population.
The Journal of clinical endocrinology and metabolism 2019 Apr . Park Seung Shin, Jang Se Song, Ahn Chang Ho, Kim Jung Hee, Jung Hye Seung, Cho Young Min, Lee Young Ah, Shin Choong Ho, Chae Jong Hee, Kim Jae Hyun, Choi Sung Hee, Jang Hak C, Bae Jee Cheol, Won Jong Cheol, Kim Sung-Hoon, Kim Jong-Il, Kwak Soo Heon, Park Kyong S |
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Survival Following Chemotherapy in Ovarian Clear Cell Carcinoma is Not Associated with Pathological Misclassification of Tumor Histotype.
Clinical cancer research : an official journal of the American Association for Cancer Research 2019 Apr . Takenaka Masataka, Köbel Martin, Garsed Dale W, Fereday Sian, Pandey Ahwan, Etemadmoghadam Dariush, Hendley Joy, Kawabata Ayako, Noguchi Daito, Yanaihara Nozomu, Takahashi Hiroyuki, Kiyokawa Takako, Ikegami Masahiro, Takano Hirokuni, Isonishi Seiji, Ochiai Kazuhiko, Traficante Nadia, Gadipally Sreeja R, Semple Timothy, Vassiliadis Dane, Amarasinghe Kaushalya Christmalee, Li Jason, Mir Arnau Gisela, Okamoto Aikou, Friedlander Michael, Bowtell David D |
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Genetic polymorphisms of diabetes-related genes, their interaction with diabetes status, and breast cancer incidence and mortality: The Long Island Breast Cancer Study Project.
Molecular carcinogenesis 2019 03 58 (3): 436-446. Parada Humberto, Cleveland Rebecca J, North Kari E, Stevens June, Teitelbaum Susan L, Neugut Alfred I, Santella Regina M, Martinez Maria E, Gammon Marilie |
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Cumulative evidence for relationships between multiple variants of HNF1B and the risk of prostate and endometrial cancers.
BMC medical genetics 2018 Jul 19 (1): 128. Tong Yu, Qu Yi, Li Shiping, Zhao Fengyan, Wang Yibin, Mu Dez |
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Genetic factors influencing prostate cancer risk in Norwegian men.
The Prostate 2017 Nov . Chen Haitao, Ewing Charles M, Zheng Sigun, Grindedaal Eli M, Cooney Kathleen A, Wiley Kathleen, Djurovic Srdjan, Andreassen Ole A, Axcrona Karol, Mills Ian G, Xu Jianfeng, Maehle Lovise, Fosså Sophie D, Isaacs William |
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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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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 |
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Identification of 8 Novel Mutations in Nephrogenesis-Related Genes in Chinese Han Patients with Unilateral Renal Agenesis.
American journal of nephrology 2017 Jun 46 (1): 55-63. Wu Hangdi, Xu Qian, Xie Jingyuan, Ma Jun, Qiao Panpan, Zhang Wen, Yu Haijin, Wang Weiming, Qian Ying, Zhang Qianying, Guo Yiqing, Tang Yonghua, Chen Xiao-Nong, Wang Zhaohui, Chen N |
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Variants in MODY genes associated with maternal lipids profiles in second trimester of pregnancy.
The journal of gene medicine 2017 Jun . Wang Xiaojing, Li Wei, Ma Liangkun, Ping Fan, Liu Juntao, Wu Xueyan, Mao Jiangfeng, Wang Xi, Nie M |
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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 |
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Genetic risk factors for ovarian cancer and their role for endometriosis risk.
Gynecologic oncology 2017 Feb . Burghaus Stefanie, Fasching Peter A, Häberle Lothar, Rübner Matthias, Büchner Kathrin, Blum Simon, Engel Anne, Ekici Arif B, Hartmann Arndt, Hein Alexander, Beckmann Matthias W, Renner Stefan |
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Genetic variants of increased waist circumference in psychosis.
Psychiatric genetics 2017 12 27 (6): 210-218. Hukic Dzana S, Ösby Urban, Olsson Eric, Hilding Agneta, Östenson Claes-Göran, Gu Harvest F, Ehrenborg Ewa, Edman Gunnar, Schalling Martin, Lavebratt Catharina, Frisén Loui |
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HNF1B variants associate with promoter methylation and regulate gene networks activated in prostate and ovarian cancer.
Oncotarget 2016 Oct . Ross-Adams Helen, Ball Stephen, Lawrenson Kate, Halim Silvia, Russell Roslin, Wells Claire, Strand Siri H, Ørntoft Torben F, Larson Melissa, Armasu Sebastian, Massie Charles E, Asim Mohammad, Mortensen Martin M, Borre Michael, Woodfine Kathryn, Warren Anne Y, Lamb Alastair D, Kay Jonathan, Whitaker Hayley, Ramos-Montoya Antonio, Murrell Adele, Sørensen Karina D, Fridley Brooke L, Goode Ellen L, Gayther Simon A, Masters John, Neal David E, Mills Ian |
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Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.
Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep . Bekheirnia Mir Reza, Bekheirnia Nasim, Bainbridge Matthew N, Gu Shen, Coban Akdemir Zeynep Hande, Gambin Tomek, Janzen Nicolette K, Jhangiani Shalini N, Muzny Donna M, Michael Mini, Brewer Eileen D, Elenberg Ewa, Kale Arundhati S, Riley Alyssa A, Swartz Sarah J, Scott Daryl A, Yang Yaping, Srivaths Poyyapakkam R, Wenderfer Scott E, Bodurtha Joann, Applegate Carolyn D, Velinov Milen, Myers Angela, Borovik Lior, Craigen William J, Hanchard Neil A, Rosenfeld Jill A, Lewis Richard Alan, Gonzales Edmond T, Gibbs Richard A, Belmont John W, Roth David R, Eng Christine, Braun Michael C, Lupski James R, Lamb Dolores |
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Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states.
Schizophrenia research 2016 Apr . González-Peñas Javier, Amigo Jorge, Santomé Luis, Sobrino Beatriz, Brenlla Julio, Agra Santiago, Paz Eduardo, Páramo Mario, Carracedo Ángel, Arrojo Manuel, Costas Javi |
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Systematic meta-analyses of gene-specific genetic association studies in prostate cancer.
Oncotarget 2016 Mar . Hao Qiang, Wei Dong, Zhang Yaoguang, Chen Xin, Yang Fan, Yang Ze, Zhu Xiaoquan, Wang Jian |
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A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysis.
Oncotarget 2016 09 7 (37): 59029-59048. Ríos-Tamayo Rafael, Lupiañez Carmen Belén, Campa Daniele, Hielscher Thomas, Weinhold Niels, Martínez-López Joaquin, Jerez Andrés, Landi Stefano, Jamroziak Krzysztof, Dumontet Charles, Watek Marzena, Lesueur Fabienne, Reis Rui Manuel, Marques Herlander, Jurczyszyn Artur, Vogel Ulla, Buda Gabriele, García-Sanz Ramón, Orciuolo Enrico, Petrini Mario, Vangsted Annette J, Gemignani Federica, Försti Asta, Goldschmidt Hartmut, Hemminki Kari, Canzian Federico, Jurado Manuel, Sainz Ju |
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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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Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT.
Kidney international 2015 Oct . Nicolaou Nayia, Pulit Sara L, Nijman Isaac J, Monroe Glen R, Feitz Wout F J, Schreuder Michiel F, van Eerde Albertien M, de Jong Tom P V M, Giltay Jacques C, van der Zwaag Bert, Havenith Marlies R, Zwakenberg Susan, van der Zanden Loes F M, Poelmans Geert, Cornelissen Elisabeth A M, Lilien Marc R, Franke Barbara, Roeleveld Nel, van Rooij Iris A L M, Cuppen Edwin, Bongers Ernie M H F, Giles Rachel H, Knoers Nine V A M, Renkema Kirsten |
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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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Meta-analysis of the association between the HNF1B rs4430796 (A>G) polymorphism and risk of prostate cancer based on case-control studies.
Genetics and molecular research : GMR 2015 14 (3): 7426-35. Zhao Y, Liang J, Qi J G, Yang N, Wu G, Lin Y L, Cao J Y, Wang Q, Wang Q |
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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 |
- Page last reviewed:Oct 1, 2020
- Page last updated:May 05, 2021
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