Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and HSD17B12[original query] |
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| The impact of common genetic variations in genes of the sex hormone metabolic pathways on steroid hormone levels and prostate cancer aggressiveness. Cancer prevention research (Philadelphia, Pa.) 2011 Dec 4 (12): 2044-50. Sun Tong, Oh William K, Jacobus Susanna, Regan Meredith, Pomerantz Mark, Freedman Matthew L, Lee Gwo-Shu Mary, Kantoff Philip |
| Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci. PLoS genetics 2011 Mar 7 (3): e1002026. Nguyen Le B, Diskin Sharon J, Capasso Mario, Wang Kai, Diamond Maura A, Glessner Joseph, Kim Cecilia, Attiyeh Edward F, Mosse Yael P, Cole Kristina, Iolascon Achille, Devoto Marcella, Hakonarson Hakon, Li Hongzhe K, Maris John |
| Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility. Carcinogenesis 2013 Mar 34 (3): 605-11. Capasso Mario, Diskin Sharon J, Totaro Francesca, Longo Luca, De Mariano Marilena, Russo Roberta, Cimmino Flora, Hakonarson Hakon, Tonini Gian Paolo, Devoto Marcella, Maris John M, Iolascon Achil |
| Molecular markers in key steroidogenic pathways, circulating steroid levels, and prostate cancer progression. Clinical cancer research : an official journal of the American Association for Cancer Research 2013 Feb 19 (3): 699-709. Lévesque Éric, Huang Shu-Pin, Audet-Walsh Étienne, Lacombe Louis, Bao Bo-Ying, Fradet Yves, Laverdière Isabelle, Rouleau Mélanie, Huang Chao-Yuan, Yu Chia-Cheng, Caron Patrick, Guillemette Chant |
| The impact of germline genetic variations in hydroxysteroid (17-beta) dehydrogenases on prostate cancer outcomes after prostatectomy. European urology 2012 Jul 62 (1): 88-96. Audet-Walsh Étienne, Bellemare Judith, Lacombe Louis, Fradet Yves, Fradet Vincent, Douville Pierre, Guillemette Chantal, Lévesque Ér |
Genome-wide association analysis identifies six new loci associated with forced vital capacity.
Nature genetics 2014 Jul 46 (7): 669-77. Loth Daan W, Artigas María Soler, Gharib Sina A, Wain Louise V, Franceschini Nora, Koch Beate, Pottinger Tess D, Smith Albert Vernon, Duan Qing, Oldmeadow Chris, Lee Mi Kyeong, Strachan David P, James Alan L, Huffman Jennifer E, Vitart Veronique, Ramasamy Adaikalavan, Wareham Nicholas J, Kaprio Jaakko, Wang Xin-Qun, Trochet Holly, Kähönen Mika, Flexeder Claudia, Albrecht Eva, Lopez Lorna M, de Jong Kim, Thyagarajan Bharat, Alves Alexessander Couto, Enroth Stefan, Omenaas Ernst, Joshi Peter K, Fall Tove, Viñuela Ana, Launer Lenore J, Loehr Laura R, Fornage Myriam, Li Guo, Wilk Jemma B, Tang Wenbo, Manichaikul Ani, Lahousse Lies, Harris Tamara B, North Kari E, Rudnicka Alicja R, Hui Jennie, Gu Xiangjun, Lumley Thomas, Wright Alan F, Hastie Nicholas D, Campbell Susan, Kumar Rajesh, Pin Isabelle, Scott Robert A, Pietiläinen Kirsi H, Surakka Ida, Liu Yongmei, Holliday Elizabeth G, Schulz Holger, Heinrich Joachim, Davies Gail, Vonk Judith M, Wojczynski Mary, Pouta Anneli, Johansson Asa, Wild Sarah H, Ingelsson Erik, Rivadeneira Fernando, Völzke Henry, Hysi Pirro G, Eiriksdottir Gudny, Morrison Alanna C, Rotter Jerome I, Gao Wei, Postma Dirkje S, White Wendy B, Rich Stephen S, Hofman Albert, Aspelund Thor, Couper David, Smith Lewis J, Psaty Bruce M, Lohman Kurt, Burchard Esteban G, Uitterlinden André G, Garcia Melissa, Joubert Bonnie R, McArdle Wendy L, Musk A Bill, Hansel Nadia, Heckbert Susan R, Zgaga Lina, van Meurs Joyce B J, Navarro Pau, Rudan Igor, Oh Yeon-Mok, Redline Susan, Jarvis Deborah L, Zhao Jing Hua, Rantanen Taina, O'Connor George T, Ripatti Samuli, Scott Rodney J, Karrasch Stefan, Grallert Harald, Gaddis Nathan C, Starr John M, Wijmenga Cisca, Minster Ryan L, Lederer David J, Pekkanen Juha, Gyllensten Ulf, Campbell Harry, Morris Andrew P, Gläser Sven, Hammond Christopher J, Burkart Kristin M, Beilby John, Kritchevsky Stephen B, Gudnason Vilmundur, Hancock Dana B, Williams O Dale, Polasek Ozren, Zemunik Tatijana, Kolcic Ivana, Petrini Marcy F, Wjst Matthias, Kim Woo Jin, Porteous David J, Scotland Generation, Smith Blair H, Viljanen Anne, Heliövaara Markku, Attia John R, Sayers Ian, Hampel Regina, Gieger Christian, Deary Ian J, Boezen H Marike, Newman Anne, Jarvelin Marjo-Riitta, Wilson James F, Lind Lars, Stricker Bruno H, Teumer Alexander, Spector Timothy D, Melén Erik, Peters Marjolein J, Lange Leslie A, Barr R Graham, Bracke Ken R, Verhamme Fien M, Sung Joohon, Hiemstra Pieter S, Cassano Patricia A, Sood Akshay, Hayward Caroline, Dupuis Josée, Hall Ian P, Brusselle Guy G, Tobin Martin D, London Stephanie |
| Common genetic variants in NEFL influence gene expression and neuroblastoma risk. Cancer research 2014 Dec 74 (23): 6913-24. Capasso Mario, Diskin Sharon, Cimmino Flora, Acierno Giovanni, Totaro Francesca, Petrosino Giuseppe, Pezone Lucia, Diamond Maura, McDaniel Lee, Hakonarson Hakon, Iolascon Achille, Devoto Marcella, Maris John |
| Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease.
The Journal of clinical endocrinology and metabolism 2019 Nov 104 (11): 5008-5023. Pott Janne, Bae Yoon Ju, Horn Katrin, Teren Andrej, Kühnapfel Andreas, Kirsten Holger, Ceglarek Uta, Loeffler Markus, Thiery Joachim, Kratzsch Jürgen, Scholz Mark |
| Genetic variants in ELOVL2 and HSD17B12 predict melanoma-specific survival. International journal of cancer 2019 Feb . Dai Wei, Liu Hongliang, Xu Xinyuan, Ge Jie, Luo Sheng, Zhu Dakai, Amos Christopher I, Fang Shenying, Lee Jeffrey E, Li Xin, Nan Hongmei, Li Chunying, Wei Qing |
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