Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: TTC39B[original query] |
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Common variants at 30 loci contribute to polygenic dyslipidemia.
Nature genetics 2009 Jan 41 (1): 56-65. Kathiresan Sekar, Willer Cristen J, Peloso Gina M, Demissie Serkalem, Musunuru Kiran, Schadt Eric E, Kaplan Lee, Bennett Derrick, Li Yun, Tanaka Toshiko, Voight Benjamin F, Bonnycastle Lori L, Jackson Anne U, Crawford Gabriel, Surti Aarti, Guiducci Candace, Burtt Noel P, Parish Sarah, Clarke Robert, Zelenika Diana, Kubalanza Kari A, Morken Mario A, Scott Laura J, Stringham Heather M, Galan Pilar, Swift Amy J, Kuusisto Johanna, Bergman Richard N, Sundvall Jouko, Laakso Markku, Ferrucci Luigi, Scheet Paul, Sanna Serena, Uda Manuela, Yang Qiong, Lunetta Kathryn L, Dupuis Josée, de Bakker Paul I W, O'Donnell Christopher J, Chambers John C, Kooner Jaspal S, Hercberg Serge, Meneton Pierre, Lakatta Edward G, Scuteri Angelo, Schlessinger David, Tuomilehto Jaakko, Collins Francis S, Groop Leif, Altshuler David, Collins Rory, Lathrop G Mark, Melander Olle, Salomaa Veikko, Peltonen Leena, Orho-Melander Marju, Ordovas Jose M, Boehnke Michael, Abecasis Gonçalo R, Mohlke Karen L, Cupples L Adrien |
Biological, clinical and population relevance of 95 loci for blood lipids.
Nature 2010 Aug 466 (7307): 707-13. Teslovich Tanya M, Musunuru Kiran, Smith Albert V, Edmondson Andrew C, Stylianou Ioannis M, Koseki Masahiro, Pirruccello James P, Ripatti Samuli, Chasman Daniel I, Willer Cristen J, Johansen Christopher T, Fouchier Sigrid W, Isaacs Aaron, Peloso Gina M, Barbalic Maja, Ricketts Sally L, Bis Joshua C, Aulchenko Yurii S, Thorleifsson Gudmar, Feitosa Mary F, Chambers John, Orho-Melander Marju, Melander Olle, Johnson Toby, Li Xiaohui, Guo Xiuqing, Li Mingyao, Shin Cho Yoon, Jin Go Min, Jin Kim Young, Lee Jong-Young, Park Taesung, Kim Kyunga, Sim Xueling, Twee-Hee Ong Rick, Croteau-Chonka Damien C, Lange Leslie A, Smith Joshua D, Song Kijoung, Hua Zhao Jing, Yuan Xin, Luan Jian'an, Lamina Claudia, Ziegler Andreas, Zhang Weihua, Zee Robert Y L, Wright Alan F, Witteman Jacqueline C M, Wilson James F, Willemsen Gonneke, Wichmann H-Erich, Whitfield John B, Waterworth Dawn M, Wareham Nicholas J, Waeber Gérard, Vollenweider Peter, Voight Benjamin F, Vitart Veronique, Uitterlinden Andre G, Uda Manuela, Tuomilehto Jaakko, Thompson John R, Tanaka Toshiko, Surakka Ida, Stringham Heather M, Spector Tim D, Soranzo Nicole, Smit Johannes H, Sinisalo Juha, Silander Kaisa, Sijbrands Eric J G, Scuteri Angelo, Scott James, Schlessinger David, Sanna Serena, Salomaa Veikko, Saharinen Juha, Sabatti Chiara, Ruokonen Aimo, Rudan Igor, Rose Lynda M, Roberts Robert, Rieder Mark, Psaty Bruce M, Pramstaller Peter P, Pichler Irene, Perola Markus, Penninx Brenda W J H, Pedersen Nancy L, Pattaro Cristian, Parker Alex N, Pare Guillaume, Oostra Ben A, O'Donnell Christopher J, Nieminen Markku S, Nickerson Deborah A, Montgomery Grant W, Meitinger Thomas, McPherson Ruth, McCarthy Mark I, McArdle Wendy, Masson David, Martin Nicholas G, Marroni Fabio, Mangino Massimo, Magnusson Patrik K E, Lucas Gavin, Luben Robert, Loos Ruth J F, Lokki Marja-Liisa, Lettre Guillaume, Langenberg Claudia, Launer Lenore J, Lakatta Edward G, Laaksonen Reijo, Kyvik Kirsten O, Kronenberg Florian, König Inke R, Khaw Kay-Tee, Kaprio Jaakko, Kaplan Lee M, Johansson Asa, Jarvelin Marjo-Riitta, Janssens A Cecile J W, Ingelsson Erik, Igl Wilmar, Kees Hovingh G, Hottenga Jouke-Jan, Hofman Albert, Hicks Andrew A, Hengstenberg Christian, Heid Iris M, Hayward Caroline, Havulinna Aki S, Hastie Nicholas D, Harris Tamara B, Haritunians Talin, Hall Alistair S, Gyllensten Ulf, Guiducci Candace, Groop Leif C, Gonzalez Elena, Gieger Christian, Freimer Nelson B, Ferrucci Luigi, Erdmann Jeanette, Elliott Paul, Ejebe Kenechi G, Döring Angela, Dominiczak Anna F, Demissie Serkalem, Deloukas Panagiotis, de Geus Eco J C, de Faire Ulf, Crawford Gabriel, Collins Francis S, Chen Yii-der I, Caulfield Mark J, Campbell Harry, Burtt Noel P, Bonnycastle Lori L, Boomsma Dorret I, Boekholdt S Matthijs, Bergman Richard N, Barroso Inês, Bandinelli Stefania, Ballantyne Christie M, Assimes Themistocles L, Quertermous Thomas, Altshuler David, Seielstad Mark, Wong Tien Y, Tai E-Shyong, Feranil Alan B, Kuzawa Christopher W, Adair Linda S, Taylor Herman A, Borecki Ingrid B, Gabriel Stacey B, Wilson James G, Holm Hilma, Thorsteinsdottir Unnur, Gudnason Vilmundur, Krauss Ronald M, Mohlke Karen L, Ordovas Jose M, Munroe Patricia B, Kooner Jaspal S, Tall Alan R, Hegele Robert A, Kastelein John J P, Schadt Eric E, Rotter Jerome I, Boerwinkle Eric, Strachan David P, Mooser Vincent, Stefansson Kari, Reilly Muredach P, Samani Nilesh J, Schunkert Heribert, Cupples L Adrienne, Sandhu Manjinder S, Ridker Paul M, Rader Daniel J, van Duijn Cornelia M, Peltonen Leena, Abecasis Gonçalo R, Boehnke Michael, Kathiresan Sek |
Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study. PLoS genetics 2011 Jun 7 (6): e1002138. Dumitrescu Logan, Carty Cara L, Taylor Kira, Schumacher Fredrick R, Hindorff Lucia A, Ambite José L, Anderson Garnet, Best Lyle G, Brown-Gentry Kristin, B?žková Petra, Carlson Christopher S, Cochran Barbara, Cole Shelley A, Devereux Richard B, Duggan Dave, Eaton Charles B, Fornage Myriam, Franceschini Nora, Haessler Jeff, Howard Barbara V, Johnson Karen C, Laston Sandra, Kolonel Laurence N, Lee Elisa T, MacCluer Jean W, Manolio Teri A, Pendergrass Sarah A, Quibrera Miguel, Shohet Ralph V, Wilkens Lynne R, Haiman Christopher A, Le Marchand Loïc, Buyske Steven, Kooperberg Charles, North Kari E, Crawford Dana |
Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array. European journal of human genetics : EJHG 2015 Apr . Rodriguez Santiago, Gaunt Tom R, Guo Yiran, Zheng Jie, Barnes Michael R, Tang Weihang, Danish Fazal, Johnson Andrew, Castillo Berta A, Li Yun R, Hakonarson Hakon, Buxbaum Sarah G, Palmer Tom, Tsai Michael Y, Lange Leslie A, Ebrahim Shah, Davey Smith George, Lawlor Debbie A, Folsom Aaron R, Hoogeveen Ron, Reiner Alex, Keating Brendan, Day Ian |
Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis. Nature communications 2016 7 12350. Steinthorsdottir Valgerdur, Thorleifsson Gudmar, Aradottir Kristrun, Feenstra Bjarke, Sigurdsson Asgeir, Stefansdottir Lilja, Kristinsdottir Anna M, Zink Florian, Halldorsson Gisli H, Munk Nielsen Nete, Geller Frank, Melbye Mads, Gudbjartsson Daniel F, Geirsson Reynir T, Thorsteinsdottir Unnur, Stefansson Ka |
Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer. Oncotarget 2016 Jan . French Juliet D, Johnatty Sharon E, Lu Yi, Beesley Jonathan, Gao Bo, Kalimutho Murugan, Henderson Michelle J, Russell Amanda J, Kar Siddhartha, Chen Xiaoqing, Hillman Kristine M, Kaufmann Susanne, Sivakumaran Haran, O'Reilly Martin, Wang Chen, Korbie Darren J, Study Group Australian Ovarian Cancer, Study Australian Cancer, Lambrechts Diether, Despierre Evelyn, Nieuwenhuysen Els Van, Lambrechts Sandrina, Vergote Ignace, Karlan Beth, Lester Jenny, Orsulic Sandra, Walsh Christine, Fasching Peter A, Beckmann Matthias W, Ekici Arif B, Hein Alexander, Matsuo Keitaro, Hosono Satoyo, Pisterer Jacobus, Hillemanns Peter, Nakanishi Toru, Yatabe Yasushi, Goodman Marc T, Lurie Galina, Matsuno Rayna K, Thompson Pamela J, Pejovic Tanja, Bean Yukie, Heitz Florian, Harter Philipp, du Bois Andreas, Schwaab Ira, Hogdall Estrid, Kjaer Susanne K, Jensen Allan, Hogdall Claus, Lundvall Lene, Engelholm Svend Aage, Brown Bob, Flanagan James M, Metcalf Michelle D, Siddiqui Nadeem, Sellers Thomas, Fridley Brooke, Cunningham Julie, Schildkraut Joellen M, Iversen Ed, Weber Rachel Palmieri, Brennan Donal, Berchuck Andrew, Pharoah Paul, Harnett Paul, Norris Murray D, Haber Michelle, Goode Ellen L, Lee Jason S, Khanna Kum Kum, Meyer Kerstin B, Chenevix-Trench Georgia, deFazio Anna, Edwards Stacey L, MacGregor Stuart, Association Consortium On Behalf Of The Ovarian Canc |
BRCA2 loss-of-function germline mutations are associated with esophageal squamous cell carcinoma risk in Chinese. International journal of cancer 2019 Aug . Ko Josephine Mun-Yee, Ning Lvwen, Zhao Xue-Ke, Chai Annie Wai Yeeng, Lei Lisa Chan, Choi Sheyne Sta Ana, Tao Lihua, Law Simon, Kwong Ava, Lee Nikki Pui-Yue, Chan Kin-Tak, Lo Anthony, Song Xin, Chen Pei-Nan, Chang Yun-Li, Wang Li Dong, Lung Maria |
Association of the TTC39B rs581080 SNP and serum lipid levels and the risk of coronary artery disease and ischemic stroke. International journal of clinical and experimental pathology 2020 1 10 (11): 11195-11205. Huang Jian-Hua, Yin Rui-Xing, Li Wei-Jun, Huang Feng, Chen Wu-Xian, Cao Xiao-Li, Chen Yu-Mi |
TTC39B rs1407977 SNP is associated with the risk of coronary heart disease and ischemic stroke. International journal of clinical and experimental pathology 2020 1 11 (10): 5044-5053. Li Hui, Yin Rui-Xing, Huang Jian-Hua, Huang Feng, Chen Wu-Xian, Cao Xiao- |
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