Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: TNRC6B[original query] |
---|
Sequence variants at 22q13 are associated with prostate cancer risk.
Cancer research 2009 Jan 69 (1): 10-5. Sun Jielin, Zheng Siqun Lilly, Wiklund Fredrik, Isaacs Sarah D, Li Ge, Wiley Kathleen E, Kim Seong-Tae, Zhu Yi, Zhang Zheng, Hsu Fang-Chi, Turner Aubrey R, Stattin Pär, Liu Wennuan, Kim Jin Woo, Duggan David, Carpten John, Isaacs William, Grönberg Henrik, Xu Jianfeng, Chang Bao- |
A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants.
Carcinogenesis 2012 Mar 33 (3): 598-603. Tao Sha, Wang Zhong, Feng Junjie, Hsu Fang-Chi, Jin Guangfu, Kim Seong-Tae, Zhang Zheng, Gronberg Henrik, Zheng Lilly S, Isaacs William B, Xu Jianfeng, Sun Jiel |
Variants in BET1L and TNRC6B associate with increasing fibroid volume and fibroid type among European Americans. Human genetics 2013 Dec 132 (12): 1361-9. Edwards Todd L, Hartmann Katherine E, Velez Edwards Digna |
BET1L and TNRC6B associate with uterine fibroid risk among European Americans. Human genetics 2013 Aug 132 (8): 943-53. Edwards Todd L, Michels Kara A, Hartmann Katherine E, Velez Edwards Digna |
Single nucleotide polymorphisms of microRNA processing machinery genes and outcome of hepatocellular carcinoma. PloS one 2014 9 (3): e92791. Liu Shuang, An Jie, Lin Jianhong, Liu Yanli, Bao Lidao, Zhang Wen, Zhao Jian-J |
Noncoding RNA-related polymorphisms in pediatric acute lymphoblastic leukemia susceptibility. Pediatric research 2014 Jun 75 (6): 767-73. Gutierrez-Camino Angela, Lopez-Lopez Elixabet, Martin-Guerrero Idoia, Piñan Maria A, Garcia-Miguel Purificacion, Sanchez-Toledo Jose, Carbone Bañeres Ana, Uriz Javier, Navajas Aurora, Garcia-Orad Afri |
Evaluation of GWAS candidate susceptibility loci for uterine leiomyoma in the multi-ethnic NIEHS uterine fibroid study. Frontiers in genetics 2015 6 241. Aissani Brahim, Zhang Kui, Wiener Howa |
Single nucleotide polymorphisms of microRNA processing genes and outcome of non-Hodgkin's lymphoma. OncoTargets and therapy 2015 8 1735-41. Gao Yuhuan, Diao Lanping, Li Huan, Guo Zhanj |
Genetic variants in miRNA processing genes and pre-miRNAs are associated with the risk of chronic lymphocytic leukemia. PloS one 2015 10 (3): e0118905. Martin-Guerrero Idoia, Gutierrez-Camino Angela, Lopez-Lopez Elixabet, Bilbao-Aldaiturriaga Nerea, Pombar-Gomez Maria, Ardanaz Maite, Garcia-Orad Afri |
Single-nucleotide polymorphisms of microRNA processing machinery genes are associated with risk for gastric cancer. OncoTargets and therapy 2015 8 567-71. Xie Ying, Wang Yingnan, Zhao Yuefei, Guo Zhanj |
Single-nucleotide polymorphisms of microRNA processing machinery genes and risk of colorectal cancer. OncoTargets and therapy 2015 8 421-5. Zhao Yufei, Du Yanming, Zhao Shengnan, Guo Zhanj |
Replication of GWAS loci revealed the moderate effect of TNRC6B locus on susceptibility of Saudi women to develop uterine leiomyomas. The journal of obstetrics and gynaecology research 2016 Dec . Bondagji Nabeel Saleem, Morad Fatima Amanullah, Al-Nefaei Afnan Abed Abdullah, Khan Imran Ali, Elango Ramu, Abdullah Layla Saleh, M Al-Mansouri Nisma, Sabir Jamal, Banaganapalli Babajan, Edris Sherif, Shaik Noor Ahm |
Genetic polymorphisms of microRNA machinery genes predict overall survival of esophageal squamous carcinoma. Journal of clinical laboratory analysis 2017 Dec . Wang Cuiju, Dong Hailing, Fan Haiyan, Wu Jianhua, Wang Guiyi |
Association of BET1L and TNRC6B with uterine leiomyoma risk and its relevant clinical features in Han Chinese population. Scientific reports 2018 May 8 (1): 7401. Liu Bailing, Wang Tao, Jiang Jue, Li Miao, Ma Wenqi, Wu Haibin, Zhou |
A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.
Frontiers in genetics 2019 10 511. Edwards Todd L, Giri Ayush, Hellwege Jacklyn N, Hartmann Katherine E, Stewart Elizabeth A, Jeff Janina M, Bray Michael J, Pendergrass Sarah A, Torstenson Eric S, Keaton Jacob M, Jones Sarah H, Gogoi Radhika P, Kuivaniemi Helena, Jackson Kathryn L, Kho Abel N, Kullo Iftikhar J, McCarty Catherine A, Im Hae Kyung, Pacheco Jennifer A, Pathak Jyotishman, Williams Marc S, Tromp Gerard, Kenny Eimear E, Peissig Peggy L, Denny Joshua C, Roden Dan M, Velez Edwards Digna |
Disentangling the genetics of lean mass. The American journal of clinical nutrition 2019 Feb . Karasik David, Zillikens M Carola, Hsu Yi-Hsiang, Aghdassi Ali, Akesson Kristina, Amin Najaf, Barroso Inês, Bennett David A, Bertram Lars, Bochud Murielle, Borecki Ingrid B, Broer Linda, Buchman Aron S, Byberg Liisa, Campbell Harry, Campos-Obando Natalia, Cauley Jane A, Cawthon Peggy M, Chambers John C, Chen Zhao, Cho Nam H, Choi Hyung Jin, Chou Wen-Chi, Cummings Steven R, de Groot Lisette C P G M, De Jager Phillip L, Demuth Ilja, Diatchenko Luda, Econs Michael J, Eiriksdottir Gudny, Enneman Anke W, Eriksson Joel, Eriksson Johan G, Estrada Karol, Evans Daniel S, Feitosa Mary F, Fu Mao, Gieger Christian, Grallert Harald, Gudnason Vilmundur, Lenore Launer J, Hayward Caroline, Hofman Albert, Homuth Georg, Huffman Kim M, Husted Lise B, Illig Thomas, Ingelsson Erik, Ittermann Till, Jansson John-Olov, Johnson Toby, Biffar Reiner, Jordan Joanne M, Jula Antti, Karlsson Magnus, Khaw Kay-Tee, Kilpeläinen Tuomas O, Klopp Norman, Kloth Jacqueline S L, Koller Daniel L, Kooner Jaspal S, Kraus William E, Kritchevsky Stephen, Kutalik Zoltán, Kuulasmaa Teemu, Kuusisto Johanna, Laakso Markku, Lahti Jari, Lang Thomas, Langdahl Bente L, Lerch Markus M, Lewis Joshua R, Lill Christina, Lind Lars, Lindgren Cecilia, Liu Yongmei, Livshits Gregory, Ljunggren Östen, Loos Ruth J F, Lorentzon Mattias, Luan Jian'an, Luben Robert N, Malkin Ida, McGuigan Fiona E, Medina-Gomez Carolina, Meitinger Thomas, Melhus Håkan, Mellström Dan, Michaëlsson Karl, Mitchell Braxton D, Morris Andrew P, Mosekilde Leif, Nethander Maria, Newman Anne B, O'Connell Jeffery R, Oostra Ben A, Orwoll Eric S, Palotie Aarno, Peacock Munro, Perola Markus, Peters Annette, Prince Richard L, Psaty Bruce M, Räikkönen Katri, Ralston Stuart H, Ripatti Samuli, Rivadeneira Fernando, Robbins John A, Rotter Jerome I, Rudan Igor, Salomaa Veikko, Satterfield Suzanne, Schipf Sabine, Shin Chan Soo, Smith Albert V, Smith Shad B, Soranzo Nicole, Spector Timothy D, Stancáková Alena, Stefansson Kari, Steinhagen-Thiessen Elisabeth, Stolk Lisette, Streeten Elizabeth A, Styrkarsdottir Unnur, Swart Karin M A, Thompson Patricia, Thomson Cynthia A, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Tikkanen Emmi, Tranah Gregory J, Uitterlinden André G, van Duijn Cornelia M, van Schoor Natasja M, Vandenput Liesbeth, Vollenweider Peter, Völzke Henry, Wactawski-Wende Jean, Walker Mark, J Wareham Nicholas, Waterworth Dawn, Weedon Michael N, Wichmann H-Erich, Widen Elisabeth, Williams Frances M K, Wilson James F, Wright Nicole C, Yerges-Armstrong Laura M, Yu Lei, Zhang Weihua, Zhao Jing Hua, Zhou Yanhua, Nielson Carrie M, Harris Tamara B, Demissie Serkalem, Kiel Douglas P, Ohlsson Cla |
The rs12532734 Polymorphism Near the Solute Carrier 26A3 Gene Locus Is Associated With Gallstone Disease in Children. Journal of pediatric gastroenterology and nutrition 2022 Sep . Krawczyk Marcin, Niewiadomska Olga, Jankowska Irena, Jankowski Krzysztof, ?widerska Jolanta, Lebensztejn Dariusz, Wi?cek Sabina, Gozdowska Jolanta, Ku?aga Zbigniew, Weber Susanne N, Lammert Frank, Socha Pio |
A minority of somatically mutated genes in pre-existing fatty liver disease have prognostic importance in the development of NAFLD. Liver international : official journal of the International Association for the Study of the Liver 2022 4 42 (8): 1823-1835. Mann Jake P, Hoare Matth |
Exome-wide screening identifies novel rare risk variants for major depression disorder. Molecular psychiatry 2022 4 27 (7): 3069-3074. Cheng Shiqiang, Cheng Bolun, Liu Li, Yang Xuena, Meng Peilin, Yao Yao, Pan Chuyu, Zhang Jingxi, Li Chun'e, Zhang Huijie, Chen Yujing, Zhang Zhen, Wen Yan, Jia Yumeng, Zhang Fe |
Single nucleotide variants in microRNA biosynthesis genes in Mexican individuals. Frontiers in genetics 2023 3 14 1022912. Juárez-Luis Jesús, Canseco-Ocaña Moisés, Cid-Soto Miguel Angel, Castro-Martínez Xochitl H, Martínez-Hernández Angélica, Orozco Lorena, Hernández-Zavala Araceli, Córdova Emilio |
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder. Human genetics 2024 2 . Ashraf Yahia, Danyang Li, Sanna Lejerkrans, Shyam Rajagopalan, Nelli Kalnak, Kristiina Tammimi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: