Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: RFX6[original query] |
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Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population.
Nature genetics 2010 Sep 42 (9): 751-4. Takata Ryo, Akamatsu Shusuke, Kubo Michiaki, Takahashi Atsushi, Hosono Naoya, Kawaguchi Takahisa, Tsunoda Tatsuhiko, Inazawa Johji, Kamatani Naoyuki, Ogawa Osamu, Fujioka Tomoaki, Nakamura Yusuke, Nakagawa Hidewa |
Replication and fine mapping for association of the C2orf43, FOXP4, GPRC6A and RFX6 genes with prostate cancer in the Chinese population. PloS one 2012 7 (5): e37866. Long Qing-Zhi, Du Yue-Feng, Ding Xiao-Ying, Li Xiang, Song Wen-Bin, Yang Yong, Zhang Peng, Zhou Jian-Ping, Liu Xiao-Ga |
Susceptibility loci associations with prostate cancer risk in northern Chinese men. Asian Pacific journal of cancer prevention : APJCP 2013 14 (5): 3075-8. Wang Na-Na, Xu Yong, Yang Kuo, Wei Dong, Zhang Yao-Guang, Liu Ming, Shi Xiao-Hong, Liang Si-Ying, Sun Liang, Zhu Xiao-Quan, Yang Yi-Ge, Tang Lei, Zhao Cheng-Xiao, Wang Xin, Chen Xin, Hui Juan, Zhang Yu-Hong, Zhu Ling, Yang Fan, Zhang Yu-Rong, Yang Ze, Wang Jian- |
Genetic variants in 2q31 and 5p15 are associated with aggressive benign prostatic hyperplasia in a Chinese population. The Prostate 2013 Aug 73 (11): 1182-90. Qi Jun, Tian Lu, Chen Zhuo, Wang Li, Tao Sha, Gu Xin, Na Rong, Jiao Yang, Kang Jian, Zheng Siqun, Xu Jianfeng, Sun Jiel |
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 |
Association of THADA, FOXP4, GPRC6A/RFX6 genes and 8q24 risk alleles with prostate cancer in Northern Chinese men. Journal of B.U.ON. : official journal of the Balkan Union of Oncology 0 20 (5): 1223-8. Li Xing-Hui, Xu Yong, Yang Kuo, Shi Jian-Jian, Zhang Xiao, Yang Fang, Yuan Huiping, Zhu Xiaoquan, Zhang Yu-Hong, Wang Jian-Ye, Yang |
A three-step programmed method for the identification of causative gene mutations of maturity onset diabetes of the young (MODY). Gene 2016 May . Li Qian, Cao Xi, Qiu Hai-Yan, Lu Jing, Gao Rui, Liu Chao, Yuan Ming-Xia, Yang Guang-Ran, Yang Jin-K |
Clinical, Genetic, and Biochemical Characteristics of Early-Onset Diabetes in the Finnish Population. The Journal of clinical endocrinology and metabolism 2016 May jc20154296. Hanna Huopio, Päivi Miettinen, Jorma Ilonen, Päivi Nykänen, Riitta Veijola, Päivi Keskinen, Kirsti Näntö-Salonen, Jagadish Vangipurapu, Joose Raivo, Alena Stan?áková, Jonna Männistö, Teemu Kuulasmaa, Mikael Knip, Timo Otonkoski, Markku Laak |
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 |
Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance. Nature communications 2017 10 8 (1): 888. Patel Kashyap A, Kettunen Jarno, Laakso Markku, Stan?áková Alena, Laver Thomas W, Colclough Kevin, Johnson Matthew B, Abramowicz Marc, Groop Leif, Miettinen Päivi J, Shepherd Maggie H, Flanagan Sarah E, Ellard Sian, Inagaki Nobuya, Hattersley Andrew T, Tuomi Tiinamaija, Cnop Miriam, Weedon Michael |
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 |
Screening the RFX6-DNA binding domain for potential genetic variants in patients with type 2 diabetes. World journal of diabetes 2019 Mar 10 (3): 181-188. Mahmoud Ismail Sami, Homsi Ayat, Al-Ameer Hamzeh J, Alzyoud Jihad, Darras Mais, Shhab Mohammad Al, Zihlif Malek, Hatmal Ma'mon M, Alshaer Walh |
Identification and Validation of Prognostically Relevant Gene Signature in Melanoma. BioMed research international 2020 2020 5323614. Gao Yali, Li Yaling, Niu Xueli, Wu Yutong, Guan Xiuhao, Hong Yuxiao, Chen Hongduo, Song Bi |
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 |
Exome sequencing in children with clinically suspected maturity-onset diabetes of the young. Pediatric diabetes 2021 8 22 (7): 960-968. Tosur Mustafa, Soler-Alfonso Claudia, Chan Katie M, Khayat Michael M, Jhangiani Shalini N, Meng Qingchang, Refaey Ahmad, Muzny Donna, Gibbs Richard A, Murdock David R, Posey Jennifer E, Balasubramanyam Ashok, Redondo Maria J, Sabo Ani |
A novel RFX6 heterozygous mutation (p.R652X) in maturity-onset diabetes mellitus: A case report. Journal of diabetes investigation 2021 3 12 (10): 1914-1918. Imaki Sakiho, Iizuka Katsumi, Horikawa Yukio, Yasuda Megumi, Kubota Sodai, Kato Takehiro, Liu Yanyan, Takao Ken, Mizuno Masami, Hirota Takuo, Suwa Tetsuya, Hosomichi Kazuyoshi, Tajima Atsushi, Fujiwara Yuuka, Yamazaki Yuji, Kuwata Hitoshi, Seino Yutaka, Yabe Daisu |
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 |
Neonatal and early-onset diabetes in Ukraine: Atypical features and mortality. Diabetic medicine : a journal of the British Diabetic Association 2022 11 e15013. Globa Evgenia, Zelinska Nataliya, Johnson Matthew B, Flanagan Sarah E, De Franco Eli |
Statistical evidence for high-penetrance MODY-causing genes in a large population-based cohort. Endocrinology, diabetes & metabolism 2022 Oct e372. Billings Liana K, Shi Zhuqing, Resurreccion W Kyle, Wang Chi-Hsiung, Wei Jun, Pollin Toni I, Udler Miriam S, Xu Jianfe |
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 |
Prostate cancer genetic risk and associated aggressive disease in men of African ancestry. Nature communications 2023 12 14 (1): 8037. Pamela X Y Soh, Naledi Mmekwa, Desiree C Petersen, Kazzem Gheybi, Smit van Zyl, Jue Jiang, Sean M Patrick, Raymond Campbell, Weerachai Jaratlerdseri, Shingai B A Mutambirwa, M S Riana Bornman, Vanessa M Hay |
The Genetic Spectrum of Maturity-Onset Diabetes of the Young (MODY) in Qatar, a Population-Based Study. International journal of molecular sciences 2023 1 24 (1): . Elashi Asma A, Toor Salman M, Diboun Ilhame, Al-Sarraj Yasser, Taheri Shahrad, Suhre Karsten, Abou-Samra Abdul Badi, Albagha Omar M |
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