Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: HSD17B4[original query] |
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Association between single-nucleotide polymorphisms in hormone metabolism and DNA repair genes and epithelial ovarian cancer: results from two Australian studies and an additional validation set. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007 Dec 16 (12): 2557-65. Beesley Jonathan, Jordan Susan J, Spurdle Amanda B, Song Honglin, Ramus Susan J, Kjaer Suzanne Kruger, Hogdall Estrid, DiCioccio Richard A, McGuire Valerie, Whittemore Alice S, Gayther Simon A, Pharoah Paul D P, Webb Penelope M, Chenevix-Trench Georgia, , , |
Genetic variation in hormone metabolizing genes and risk of testicular germ cell tumors. Cancer causes & control : CCC 2008 Nov 19 (9): 917-29. Figueroa Jonine D, Sakoda Lori C, Graubard Barry I, Chanock Stephen, Rubertone Mark V, Erickson R Loren, McGlynn Katherine |
Inherited variation in the androgen pathway is associated with the efficacy of androgen-deprivation therapy in men with prostate cancer. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2008 Feb 26 (6): 842-7. Ross Robert W, Oh William K, Xie Wanling, Pomerantz Mark, Nakabayashi Mari, Sartor Oliver, Taplin Mary-Ellen, Regan Meredith M, Kantoff Philip W, Freedman Matth |
Association of testicular germ cell tumor with polymorphisms in estrogen receptor and steroid metabolism genes. Endocrine-related cancer 2010 Mar 17 (1): 17-25. Ferlin Alberto, Ganz Francesco, Pengo Manuel, Selice Riccardo, Frigo Anna Chiara, Foresta Car |
Effect modification of endocrine disruptors and testicular germ cell tumour risk by hormone-metabolizing genes. International journal of andrology 2010 Aug 33 (4): 588-96. Chia V M, Li Y, Quraishi S M, Graubard B I, Figueroa J D, Weber J-P, Chanock S J, Rubertone M V, Erickson R L, McGlynn K |
Polymorphisms in genes hydroxysteroid-dehydrogenase-17b type 2 and type 4 and endometrial cancer risk. Gynecologic oncology 2011 Apr 121 (1): 54-8. Karageorgi Stalo, McGrath Monica, Lee I-Min, Buring Julie, Kraft Peter, De Vivo Immacula |
Estrogen and progesterone-related gene variants and colorectal cancer risk in women. BMC medical genetics 2011 12 (1): 78. Lin Jennifer H, Manson JoAnn E, Kraft Peter, Cochrane Barbara B, Gunter Marc J, Chlebowski Rowan T, Zhang Shumin |
Androgen metabolism and JAK/STAT pathway genes and prostate cancer risk. Cancer epidemiology 2012 Aug 36 (4): 347-53. Kwon Erika M, Holt Sarah K, Fu Rong, Kolb Suzanne, Williams Gabrielle, Stanford Janet L, Ostrander Elaine |
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 |
Epistasis between the HSD17B4 and TG polymorphisms is associated with premature ovarian failure. Fertility and sterility 2012 Apr 97 (4): 968-73. Pyun Jung-A, Kim Sunshin, Cha Dong Hyun, Ko Jeong-Jae, Kwack KyuB |
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.
PLoS genetics 2013 Jun 9 (6): e1003500. Randall Joshua C, Winkler Thomas W, Kutalik Zoltán, Berndt Sonja I, Jackson Anne U, Monda Keri L, Kilpeläinen Tuomas O, Esko Tõnu, Mägi Reedik, Li Shengxu, Workalemahu Tsegaselassie, Feitosa Mary F, Croteau-Chonka Damien C, Day Felix R, Fall Tove, Ferreira Teresa, Gustafsson Stefan, Locke Adam E, Mathieson Iain, Scherag Andre, Vedantam Sailaja, Wood Andrew R, Liang Liming, Steinthorsdottir Valgerdur, Thorleifsson Gudmar, Dermitzakis Emmanouil T, Dimas Antigone S, Karpe Fredrik, Min Josine L, Nicholson George, Clegg Deborah J, Person Thomas, Krohn Jon P, Bauer Sabrina, Buechler Christa, Eisinger Kristina, , Bonnefond Amélie, Froguel Philippe, , Hottenga Jouke-Jan, Prokopenko Inga, Waite Lindsay L, Harris Tamara B, Smith Albert Vernon, Shuldiner Alan R, McArdle Wendy L, Caulfield Mark J, Munroe Patricia B, Grönberg Henrik, Chen Yii-Der Ida, Li Guo, Beckmann Jacques S, Johnson Toby, Thorsteinsdottir Unnur, Teder-Laving Maris, Khaw Kay-Tee, Wareham Nicholas J, Zhao Jing Hua, Amin Najaf, Oostra Ben A, Kraja Aldi T, Province Michael A, Cupples L Adrienne, Heard-Costa Nancy L, Kaprio Jaakko, Ripatti Samuli, Surakka Ida, Collins Francis S, Saramies Jouko, Tuomilehto Jaakko, Jula Antti, Salomaa Veikko, Erdmann Jeanette, Hengstenberg Christian, Loley Christina, Schunkert Heribert, Lamina Claudia, Wichmann H Erich, Albrecht Eva, Gieger Christian, Hicks Andrew A, Johansson Asa, Pramstaller Peter P, Kathiresan Sekar, Speliotes Elizabeth K, Penninx Brenda, Hartikainen Anna-Liisa, Jarvelin Marjo-Riitta, Gyllensten Ulf, Boomsma Dorret I, Campbell Harry, Wilson James F, Chanock Stephen J, Farrall Martin, Goel Anuj, Medina-Gomez Carolina, Rivadeneira Fernando, Estrada Karol, Uitterlinden André G, Hofman Albert, Zillikens M Carola, den Heijer Martin, Kiemeney Lambertus A, Maschio Andrea, Hall Per, Tyrer Jonathan, Teumer Alexander, Völzke Henry, Kovacs Peter, Tönjes Anke, Mangino Massimo, Spector Tim D, Hayward Caroline, Rudan Igor, Hall Alistair S, Samani Nilesh J, Attwood Antony Paul, Sambrook Jennifer G, Hung Joseph, Palmer Lyle J, Lokki Marja-Liisa, Sinisalo Juha, Boucher Gabrielle, Huikuri Heikki, Lorentzon Mattias, Ohlsson Claes, Eklund Niina, Eriksson Johan G, Barlassina Cristina, Rivolta Carlo, Nolte Ilja M, Snieder Harold, Van der Klauw Melanie M, Van Vliet-Ostaptchouk Jana V, Gejman Pablo V, Shi Jianxin, Jacobs Kevin B, Wang Zhaoming, Bakker Stephan J L, Mateo Leach Irene, Navis Gerjan, van der Harst Pim, Martin Nicholas G, Medland Sarah E, Montgomery Grant W, Yang Jian, Chasman Daniel I, Ridker Paul M, Rose Lynda M, Lehtimäki Terho, Raitakari Olli, Absher Devin, Iribarren Carlos, Basart Hanneke, Hovingh Kees G, Hyppönen Elina, Power Chris, Anderson Denise, Beilby John P, Hui Jennie, Jolley Jennifer, Sager Hendrik, Bornstein Stefan R, Schwarz Peter E H, Kristiansson Kati, Perola Markus, Lindström Jaana, Swift Amy J, Uusitupa Matti, Atalay Mustafa, Lakka Timo A, Rauramaa Rainer, Bolton Jennifer L, Fowkes Gerry, Fraser Ross M, Price Jackie F, Fischer Krista, Krjutå Kov Kaarel, Metspalu Andres, Mihailov Evelin, Langenberg Claudia, Luan Jian'an, Ong Ken K, Chines Peter S, Keinanen-Kiukaanniemi Sirkka M, Saaristo Timo E, Edkins Sarah, Franks Paul W, Hallmans Göran, Shungin Dmitry, Morris Andrew David, Palmer Colin N A, Erbel Raimund, Moebus Susanne, Nöthen Markus M, Pechlivanis Sonali, Hveem Kristian, Narisu Narisu, Hamsten Anders, Humphries Steve E, Strawbridge Rona J, Tremoli Elena, Grallert Harald, Thorand Barbara, Illig Thomas, Koenig Wolfgang, Müller-Nurasyid Martina, Peters Annette, Boehm Bernhard O, Kleber Marcus E, März Winfried, Winkelmann Bernhard R, Kuusisto Johanna, Laakso Markku, Arveiler Dominique, Cesana Giancarlo, Kuulasmaa Kari, Virtamo Jarmo, Yarnell John W G, Kuh Diana, Wong Andrew, Lind Lars, de Faire Ulf, Gigante Bruna, Magnusson Patrik K E, Pedersen Nancy L, Dedoussis George, Dimitriou Maria, Kolovou Genovefa, Kanoni Stavroula, Stirrups Kathleen, Bonnycastle Lori L, Njølstad Inger, Wilsgaard Tom, Ganna Andrea, Rehnberg Emil, Hingorani Aroon, Kivimaki Mika, Kumari Meena, Assimes Themistocles L, Barroso Inês, Boehnke Michael, Borecki Ingrid B, Deloukas Panos, Fox Caroline S, Frayling Timothy, Groop Leif C, Haritunians Talin, Hunter David, Ingelsson Erik, Kaplan Robert, Mohlke Karen L, O'Connell Jeffrey R, Schlessinger David, Strachan David P, Stefansson Kari, van Duijn Cornelia M, Abecasis Gonçalo R, McCarthy Mark I, Hirschhorn Joel N, Qi Lu, Loos Ruth J F, Lindgren Cecilia M, North Kari E, Heid Iris |
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family. Journal of clinical research in pediatric endocrinology 2016 Apr . Dursun Fatma, Mohamoud Hussein Sheikh Ali, Karim Noreen, Naeem Muhammad, Jelani Musharraf, K?rm?z?bekmez Hev |
Polymorphisms in androgen metabolism genes with serum testosterone levels and prognosis in androgen-deprivation therapy. Urologic oncology 2020 7 38 (11): 849.e11-849.e18. Shiota Masaki, Endo Satoshi, Fujimoto Naohiro, Tsukahara Shigehiro, Ushijima Miho, Kashiwagi Eiji, Takeuchi Ario, Inokuchi Junichi, Uchiumi Takeshi, Eto Masatos |
Examining the role of mitochondrial genetic variation in nicotine dependence. Psychiatry research 2022 3 310 114452. Giannoulis Stavroula V, Chenoweth Meghan J, Saquilayan Paulo, Tyndale Rachel F, Lerman Caryn, Kennedy James L, Zawertailo Laurie, Gonçalves Vanes |
Whole-Exome Sequencing identified Olfactory Receptor genes as a key contributor to extreme obesity with progression to nonalcoholic steatohepatitis in Mexican patients: Olfactory receptor genes in obese NASH patients. Annals of hepatology 2022 10 27 (6): 100767. Torres-Reyes L A, Gonzalez-Aldaco K, Panduro A, Jose-Abrego A, Roman |
Susceptibility to Colorectal Cancer Based on HSD17B4 rs721673 and rs721675 Polymorphisms and Alcohol Intake among Taiwan Biobank Participants: A Retrospective Case Control Study Using the Nationwide Claims Data. Journal of personalized medicine 2023 4 13 (4): . Tzu-Chiao Lin, Min-Hua Chuang, Chia-Ni Hsiung, Pi-Kai Chang, Chien-An Sun, Tsan Yang, Yu-Ching Chou, Je-Ming Hu, Chih-Hsiung H |
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