Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: STAB1[original query] |
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Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
Nature genetics 2010 Oct . Heid IM, Jackson AU, Randall JC, Winkler TW, Qi L, Steinthorsdottir V, Thorleifsson G, Zillikens MC, Speliotes EK, Mägi R, Workalemahu T, White CC, Bouatia-Naji N, Harris TB, Berndt SI, Ingelsson E, Willer CJ, Weedon MN, Luan J, Vedantam S, Esko T, Kilpeläinen TO, Kutalik Z, Li S, Monda KL, Dixon AL, Holmes CC, Kaplan LM, Liang L, Min JL, Moffatt MF, Molony C, Nicholson G, Schadt EE, Zondervan KT, Feitosa MF, Ferreira T, Allen HL, Weyant RJ, Wheeler E, Wood AR, Estrada K, Goddard ME, Lettre G, Mangino M, Nyholt DR, Purcell S, Smith AV, Visscher PM, Yang J, McCarroll SA, Nemesh J, Voight BF, Absher D, Amin N, Aspelund T, Coin L, Glazer NL, Hayward C, Heard-Costa NL, Hottenga JJ, Johansson A, Johnson T, Kaakinen M, Kapur K, Ketkar S, Knowles JW, Kraft P, Kraja AT, Lamina C, Leitzmann MF, McKnight B, Morris AP, Ong KK, Perry JR, Peters MJ, Polasek O, Prokopenko I, Rayner NW, Ripatti S, Rivadeneira F, Robertson NR, Sanna S, Sovio U, Surakka I, Teumer A, van Wingerden S, Vitart V, Zhao JH, Cavalcanti-Proença C, Chines PS, Fisher E, Kulzer JR, Lecoeur C, Narisu N, Sandholt C, Scott LJ, Silander K, Stark K, Tammesoo ML, Teslovich TM, Timpson NJ, Watanabe RM, Welch R, Chasman DI, Cooper MN, Jansson JO, Kettunen J, Lawrence RW, Pellikka N, Perola M, Vandenput L, Alavere H, Almgren P, Atwood LD, Bennett AJ, Biffar R, Bonnycastle LL, Bornstein SR, Buchanan TA, Campbell H, Day IN, Dei M, Dörr M, Elliott P, Erdos MR, Eriksson JG, Freimer NB, Fu M, Gaget S, Geus EJ, Gjesing AP, Grallert H, Gräßler J, Groves CJ, Guiducci C, Hartikainen AL, Hassanali N, Havulinna AS, Herzig KH, Hicks AA, Hui J, Igl W, Jousilahti P, Jula A, Kajantie E, Kinnunen L, Kolcic I, Koskinen S, Kovacs P, Kroemer HK, Krzelj V, Kuusisto J, Kvaloy K, Laitinen J, Lantieri O, Lathrop GM, Lokki ML, Luben RN, Ludwig B, McArdle WL, McCarthy A, Morken MA, Nelis M, Neville MJ, Paré G, Parker AN, Peden JF, Pichler I, Pietiläinen KH, Platou CG, Pouta A, Ridderstråle M, Samani NJ, Saramies J, Sinisalo J, Smit JH, Strawbridge RJ, Stringham HM, Swift AJ, Teder-Laving M, Thomson B, Usala G, van Meurs JB, van Ommen GJ, Vatin V, Volpato CB, Wallaschofski H, Walters GB, Widen E, Wild SH, Willemsen G, Witte DR, Zgaga L, Zitting P, Beilby JP, James AL, Kähönen M, Lehtimäki T, Nieminen MS, Ohlsson C, Palmer LJ, Raitakari O, Ridker PM, Stumvoll M, Tönjes A, Viikari J, Balkau B, Ben-Shlomo Y, Bergman RN, Boeing H, Smith GD, Ebrahim S, Froguel P, Hansen T, Hengstenberg C, Hveem K, Isomaa B, Jørgensen T, Karpe F, Khaw KT, Laakso M, Lawlor DA, Marre M, Meitinger T, Metspalu A, Midthjell K, Pedersen O, Salomaa V, Schwarz PE, Tuomi T, Tuomilehto J, Valle TT, Wareham NJ, Arnold AM, Beckmann JS, Bergmann S, Boerwinkle E, Boomsma DI, Caulfield MJ, Collins FS, Eiriksdottir G, Gudnason V, Gyllensten U, Hamsten A, Hattersley AT, Hofman A, Hu FB, Illig T, Iribarren C, Jarvelin MR, Kao WH, Kaprio J, Launer LJ, Munroe PB, Oostra B, Penninx BW, Pramstaller PP, Psaty BM, Quertermous T, Rissanen A, Rudan I, Shuldiner AR, Soranzo N, Spector TD, Syvanen AC, Uda M, Uitterlinden A, Völzke H, Vollenweider P, Wilson JF, Witteman JC, Wright AF, Abecasis GR, Boehnke M, Borecki IB, Deloukas P, Frayling TM, Groop LC, Haritunians T, Hunter DJ, Kaplan RC, North KE, O'Connell JR, Peltonen L, Schlessinger D, Strachan DP, Hirschhorn JN, Assimes TL, Wichmann HE, Thorsteinsdottir U, van Duijn CM, Stefansson K, Cupples LA, Loos RJ, Barroso I, McCarthy MI, Fox CS, Mohlke KL, Lindgren CM |
Obesity susceptibility loci and dietary intake in the Look AHEAD Trial. The American journal of clinical nutrition 2012 Jun 95 (6): 1477-86. McCaffery Jeanne M, Papandonatos George D, Peter Inga, Huggins Gordon S, Raynor Hollie A, Delahanty Linda M, Cheskin Lawrence J, Balasubramanyam Ashok, Wagenknecht Lynne E, Wing Rena R, , |
Pathway analysis of a genome-wide association study in schizophrenia. Gene 2013 Aug 525 (1): 107-15. Lee Young Ho, Kim Jae-Hoon, Song Gwan G |
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.
Nature communications 2016 7 10572. Kristjansson Ragnar P, Oddsson Asmundur, Helgason Hannes, Sveinbjornsson Gardar, Arnadottir Gudny A, Jensson Brynjar O, Jonasdottir Aslaug, Jonasdottir Adalbjorg, Bragi Walters G, Sulem Gerald, Oskarsdottir Arna, Benonisdottir Stefania, Davidsson Olafur B, Masson Gisli, Th Magnusson Olafur, Holm Hilma, Sigurdardottir Olof, Jonsdottir Ingileif, Eyjolfsson Gudmundur I, Olafsson Isleifur, Gudbjartsson Daniel F, Thorsteinsdottir Unnur, Sulem Patrick, Stefansson Ka |
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475?000 Individuals. Circulation. Cardiovascular genetics 2017 Oct 10 (5): . Kraja Aldi T, Cook James P, Warren Helen R, Surendran Praveen, Liu Chunyu, Evangelou Evangelos, Manning Alisa K, Grarup Niels, Drenos Fotios, Sim Xueling, Smith Albert Vernon, Amin Najaf, Blakemore Alexandra I F, Bork-Jensen Jette, Brandslund Ivan, Farmaki Aliki-Eleni, Fava Cristiano, Ferreira Teresa, Herzig Karl-Heinz, Giri Ayush, Giulianini Franco, Grove Megan L, Guo Xiuqing, Harris Sarah E, Have Christian T, Havulinna Aki S, Zhang He, Jørgensen Marit E, Käräjämäki AnneMari, Kooperberg Charles, Linneberg Allan, Little Louis, Liu Yongmei, Bonnycastle Lori L, Lu Yingchang, Mägi Reedik, Mahajan Anubha, Malerba Giovanni, Marioni Riccardo E, Mei Hao, Menni Cristina, Morrison Alanna C, Padmanabhan Sandosh, Palmas Walter, Poveda Alaitz, Rauramaa Rainer, Rayner Nigel William, Riaz Muhammad, Rice Ken, Richard Melissa A, Smith Jennifer A, Southam Lorraine, Stan?áková Alena, Stirrups Kathleen E, Tragante Vinicius, Tuomi Tiinamaija, Tzoulaki Ioanna, Varga Tibor V, Weiss Stefan, Yiorkas Andrianos M, Young Robin, Zhang Weihua, Barnes Michael R, Cabrera Claudia P, Gao He, Boehnke Michael, Boerwinkle Eric, Chambers John C, Connell John M, Christensen Cramer K, de Boer Rudolf A, Deary Ian J, Dedoussis George, Deloukas Panos, Dominiczak Anna F, Dörr Marcus, Joehanes Roby, Edwards Todd L, Esko Tõnu, Fornage Myriam, Franceschini Nora, Franks Paul W, Gambaro Giovanni, Groop Leif, Hallmans Göran, Hansen Torben, Hayward Caroline, Heikki Oksa, Ingelsson Erik, Tuomilehto Jaakko, Jarvelin Marjo-Riitta, Kardia Sharon L R, Karpe Fredrik, Kooner Jaspal S, Lakka Timo A, Langenberg Claudia, Lind Lars, Loos Ruth J F, Laakso Markku, McCarthy Mark I, Melander Olle, Mohlke Karen L, Morris Andrew P, Palmer Colin N A, Pedersen Oluf, Polasek Ozren, Poulter Neil R, Province Michael A, Psaty Bruce M, Ridker Paul M, Rotter Jerome I, Rudan Igor, Salomaa Veikko, Samani Nilesh J, Sever Peter J, Skaaby Tea, Stafford Jeanette M, Starr John M, van der Harst Pim, van der Meer Peter, , van Duijn Cornelia M, Vergnaud Anne-Claire, Gudnason Vilmundur, Wareham Nicholas J, Wilson James G, Willer Cristen J, Witte Daniel R, Zeggini Eleftheria, Saleheen Danish, Butterworth Adam S, Danesh John, Asselbergs Folkert W, Wain Louise V, Ehret Georg B, Chasman Daniel I, Caulfield Mark J, Elliott Paul, Lindgren Cecilia M, Levy Daniel, Newton-Cheh Christopher, Munroe Patricia B, Howson Joanna M M, |
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia. PloS one 2020 6 15 (6): e0234246. Zhang Rong, Gehlen Jan, Kawalia Amit, Melissari Maria-Theodora, Dakal Tikam Chand, Menon Athira M, Höfele Julia, Riedhammer Korbinian, Waffenschmidt Lea, Fabian Julia, Breuer Katinka, Kalanithy Jeshurun, Hilger Alina Christine, Sharma Amit, Hölscher Alice, Boemers Thomas M, Pauly Markus, Leutner Andreas, Fuchs Jörg, Seitz Guido, Ludwikowski Barbara M, Gomez Barbara, Hubertus Jochen, Heydweiller Andreas, Kurz Ralf, Leonhardt Johannes, Kosch Ferdinand, Holland-Cunz Stefan, Münsterer Oliver, Ure Beno, Schmiedeke Eberhard, Neser Jörg, Degenhardt Petra, Märzheuser Stefanie, Kleine Katharina, Schäfer Mattias, Spychalski Nicole, Deffaa Oliver J, Gosemann Jan-Hendrik, Lacher Martin, Heilmann-Heimbach Stefanie, Zwink Nadine, Jenetzky Ekkehart, Ludwig Michael, Grote Phillip, Schumacher Johannes, Thiele Holger, Reutter Hei |
Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients. Translational psychiatry 2020 Jan 10 (1): 5. Li Mo, Shen Lu, Chen Luan, Huai Cong, Huang Hailiang, Wu Xi, Yang Chao, Ma Jingsong, Zhou Wei, Du Huihui, Fan Lingzi, He Lin, Wan Chunling, Qin Shengyi |
The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci. Frontiers in neurology 2020 1 10 1284. Germer Elisabeth Luisa, Imhoff Sophie, Vilariño-Güell Carles, Kasten Meike, Seibler Philip, Brüggemann Norbert, , Klein Christine, Trinh Joan |
Functional multigenic variations associated with hodgkin lymphoma.
International journal of laboratory hematology 2021 Jul . Osman Yasser, Elsharkawy Tarek, Hashim Tariq Mohammad, Alratroot Jumana Abdulwahab, Alsuwat Hind Saleh, Otaibi Waad Mohammed Al, Hegazi Fatma Mohammed, AbdulAzeez Sayed, Borgio J Franc |
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia. Journal of lipid research 2022 4 63 (6): 100209. Dong Weilai, Wong Karen H Y, Liu Youbin, Levy-Sakin Michal, Hung Wei-Chien, Li Mo, Li Boyang, Jin Sheng Chih, Choi Jungmin, Lopez-Giraldez Francesc, Vaka Dedeepya, Poon Annie, Chu Catherine, Lao Richard, Balamir Melek, Movsesyan Irina, Malloy Mary J, Zhao Hongyu, Kwok Pui-Yan, Kane John P, Lifton Richard P, Pullinger Clive |
Rare variant associations with plasma protein levels in the UK Biobank. Nature 2023 10 622 (7982): 339-347. Ryan S Dhindsa, Oliver S Burren, Benjamin B Sun, Bram P Prins, Dorota Matelska, Eleanor Wheeler, Jonathan Mitchell, Erin Oerton, Ventzislava A Hristova, Katherine R Smith, Keren Carss, Sebastian Wasilewski, Andrew R Harper, Dirk S Paul, Margarete A Fabre, Heiko Runz, Coralie Viollet, Benjamin Challis, Adam Platt, , Dimitrios Vitsios, Euan A Ashley, Christopher D Whelan, Menelas N Pangalos, Quanli Wang, Slavé Petrovs |
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