HLBS-PopOmics
Query Trace: HLBSGenome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction. BMC genomics 2017 Sep 18 (1): 740. Qian David C, Molfese David L, Jin Jennifer L, Titus Alexander J, He Yixuan, Li Yafang, Vaissié Maxime, Viswanath Humsini, Baldwin Philip R, Krahe Ralf, Salas Ramiro, Amos Christopher |
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. PloS one 2017 12 (7): e0182115. Yeo Astrid, Li Li, Warren Liling, Aponte Jennifer, Fraser Dana, King Karen, Johansson Kelley, Barnes Allison, MacPhee Colin, Davies Richard, Chissoe Stephanie, Tarka Elizabeth, O'Donoghue Michelle L, White Harvey D, Wallentin Lars, Waterworth Da |
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nature communications 2017 Oct 8 (1): 910. Joshi Peter K, Pirastu Nicola, Kentistou Katherine A, Fischer Krista, Hofer Edith, Schraut Katharina E, Clark David W, Nutile Teresa, Barnes Catriona L K, Timmers Paul R H J, Shen Xia, Gandin Ilaria, McDaid Aaron F, Hansen Thomas Folkmann, Gordon Scott D, Giulianini Franco, Boutin Thibaud S, Abdellaoui Abdel, Zhao Wei, Medina-Gomez Carolina, Bartz Traci M, Trompet Stella, Lange Leslie A, Raffield Laura, van der Spek Ashley, Galesloot Tessel E, Proitsi Petroula, Yanek Lisa R, Bielak Lawrence F, Payton Antony, Murgia Federico, Concas Maria Pina, Biino Ginevra, Tajuddin Salman M, Seppälä Ilkka, Amin Najaf, Boerwinkle Eric, Børglum Anders D, Campbell Archie, Demerath Ellen W, Demuth Ilja, Faul Jessica D, Ford Ian, Gialluisi Alessandro, Gögele Martin, Graff MariaElisa, Hingorani Aroon, Hottenga Jouke-Jan, Hougaard David M, Hurme Mikko A, Ikram M Arfan, Jylhä Marja, Kuh Diana, Ligthart Lannie, Lill Christina M, Lindenberger Ulman, Lumley Thomas, Mägi Reedik, Marques-Vidal Pedro, Medland Sarah E, Milani Lili, Nagy Reka, Ollier William E R, Peyser Patricia A, Pramstaller Peter P, Ridker Paul M, Rivadeneira Fernando, Ruggiero Daniela, Saba Yasaman, Schmidt Reinhold, Schmidt Helena, Slagboom P Eline, Smith Blair H, Smith Jennifer A, Sotoodehnia Nona, Steinhagen-Thiessen Elisabeth, van Rooij Frank J A, Verbeek André L, Vermeulen Sita H, Vollenweider Peter, Wang Yunpeng, Werge Thomas, Whitfield John B, Zonderman Alan B, Lehtimäki Terho, Evans Michele K, Pirastu Mario, Fuchsberger Christian, Bertram Lars, Pendleton Neil, Kardia Sharon L R, Ciullo Marina, Becker Diane M, Wong Andrew, Psaty Bruce M, van Duijn Cornelia M, Wilson James G, Jukema J Wouter, Kiemeney Lambertus, Uitterlinden André G, Franceschini Nora, North Kari E, Weir David R, Metspalu Andres, Boomsma Dorret I, Hayward Caroline, Chasman Daniel, Martin Nicholas G, Sattar Naveed, Campbell Harry, Esko T?nu, Kutalik Zoltán, Wilson James |
Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. The Lancet. Respiratory medicine 2017 Nov 5 (11): 869-880. Allen Richard J, Porte Joanne, Braybrooke Rebecca, Flores Carlos, Fingerlin Tasha E, Oldham Justin M, Guillen-Guio Beatriz, Ma Shwu-Fan, Okamoto Tsukasa, John Alison E, Obeidat Ma'en, Yang Ivana V, Henry Amanda, Hubbard Richard B, Navaratnam Vidya, Saini Gauri, Thompson Norma, Booth Helen L, Hart Simon P, Hill Mike R, Hirani Nik, Maher Toby M, McAnulty Robin J, Millar Ann B, Molyneaux Philip L, Parfrey Helen, Rassl Doris M, Whyte Moira K B, Fahy William A, Marshall Richard P, Oballa Eunice, Bossé Yohan, Nickle David C, Sin Don D, Timens Wim, Shrine Nick, Sayers Ian, Hall Ian P, Noth Imre, Schwartz David A, Tobin Martin D, Wain Louise V, Jenkins R Gis |
Genome-wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry. Addiction biology 2017 Oct . Sanchez-Roige Sandra, Fontanillas Pierre, Elson Sarah L, , Gray Joshua C, de Wit Harriet, Davis Lea K, MacKillop James, Palmer Abraham |
Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Nature communications 2017 09 8 (1): 599. Tian Chao, Hromatka Bethann S, Kiefer Amy K, Eriksson Nicholas, Noble Suzanne M, Tung Joyce Y, Hinds David |
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. The Lancet. Neurology 2017 Nov 16 (11): 898-907. Schormair Barbara, Zhao Chen, Bell Steven, Tilch Erik, Salminen Aaro V, Pütz Benno, Dauvilliers Yves, Stefani Ambra, Högl Birgit, Poewe Werner, Kemlink David, Sonka Karel, Bachmann Cornelius G, Paulus Walter, Trenkwalder Claudia, Oertel Wolfgang H, Hornyak Magdolna, Teder-Laving Maris, Metspalu Andres, Hadjigeorgiou Georgios M, Polo Olli, Fietze Ingo, Ross Owen A, Wszolek Zbigniew, Butterworth Adam S, Soranzo Nicole, Ouwehand Willem H, Roberts David J, Danesh John, Allen Richard P, Earley Christopher J, Ondo William G, Xiong Lan, Montplaisir Jacques, Gan-Or Ziv, Perola Markus, Vodicka Pavel, Dina Christian, Franke Andre, Tittmann Lukas, Stewart Alexandre F R, Shah Svati H, Gieger Christian, Peters Annette, Rouleau Guy A, Berger Klaus, Oexle Konrad, Di Angelantonio Emanuele, Hinds David A, Müller-Myhsok Bertram, Winkelmann Juliane, , |
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Nature genetics 2017 Dec 49 (12): 1752-1757. Ferreira Manuel A, Vonk Judith M, Baurecht Hansjörg, Marenholz Ingo, Tian Chao, Hoffman Joshua D, Helmer Quinta, Tillander Annika, Ullemar Vilhelmina, van Dongen Jenny, Lu Yi, Rüschendorf Franz, Esparza-Gordillo Jorge, Medway Chris W, Mountjoy Edward, Burrows Kimberley, Hummel Oliver, Grosche Sarah, Brumpton Ben M, Witte John S, Hottenga Jouke-Jan, Willemsen Gonneke, Zheng Jie, Rodríguez Elke, Hotze Melanie, Franke Andre, Revez Joana A, Beesley Jonathan, Matheson Melanie C, Dharmage Shyamali C, Bain Lisa M, Fritsche Lars G, Gabrielsen Maiken E, Balliu Brunilda, , , , , Nielsen Jonas B, Zhou Wei, Hveem Kristian, Langhammer Arnulf, Holmen Oddgeir L, Løset Mari, Abecasis Gonçalo R, Willer Cristen J, Arnold Andreas, Homuth Georg, Schmidt Carsten O, Thompson Philip J, Martin Nicholas G, Duffy David L, Novak Natalija, Schulz Holger, Karrasch Stefan, Gieger Christian, Strauch Konstantin, Melles Ronald B, Hinds David A, Hübner Norbert, Weidinger Stephan, Magnusson Patrik K E, Jansen Rick, Jorgenson Eric, Lee Young-Ae, Boomsma Dorret I, Almqvist Catarina, Karlsson Robert, Koppelman Gerard H, Paternoster Lavin |
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux. Scientific reports 2017 Nov 7 (1): 14595. Darlow John M, Darlay Rebecca, Dobson Mark G, Stewart Aisling, Charoen Pimphen, Southgate Jennifer, Baker Simon C, Xu Yaobo, Hunziker Manuela, Lambert Heather J, Green Andrew J, Santibanez-Koref Mauro, Sayer John A, Goodship Timothy H J, Puri Prem, Woolf Adrian S, Kenda Rajko B, Barton David E, Cordell Heather |
A genome-wide association study links small-vessel ischemic stroke to autophagy. Scientific reports 2017 Nov 7 (1): 15229. Lee Tsong-Hai, Ko Tai-Ming, Chen Chien-Hsiun, Chang Yeu-Jhy, Lu Liang-Suei, Chang Chien-Hung, Huang Kuo-Lun, Chang Ting-Yu, Lee Jiann-Der, Chang Ku-Chou, Yang Jen-Tsung, Wen Ming-Shien, Wang Chao-Yung, Chen Ying-Ting, Chen Tsai-Chuan, Chou Shu-Yu, Lee Ming-Ta Michael, Chen Yuan-Tsong, Wu Jer-Yua |
Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans. Obesity (Silver Spring, Md.) 2017 Nov . Gao Chuan, Langefeld Carl D, Ziegler Julie T, Taylor Kent D, Norris Jill M, Chen Yii-Der I, Hellwege Jacklyn N, Guo Xiuqing, Allison Matthew A, Speliotes Elizabeth K, Rotter Jerome I, Bowden Donald W, Wagenknecht Lynne E, Palmer Nicholette |
A genome-wide association analysis identifies PDE1A|DNAJC10 locus on chromosome 2 associated with idiopathic pulmonary arterial hypertension in a Japanese population. Oncotarget 2017 Sep 8 (43): 74917-74926. Kimura Mai, Tamura Yuichi, Guignabert Christophe, Takei Makoto, Kosaki Kenjiro, Tanabe Nobuhiro, Tatsumi Koichiro, Saji Tsutomu, Satoh Toru, Kataoka Masaharu, Kamitsuji Shigeo, Kamatani Naoyuki, Thuillet Raphaël, Tu Ly, Humbert Marc, Fukuda Keiichi, Sano Motoa |
Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men. American journal of respiratory cell and molecular biology 2017 Oct . Chen Han, Cade Brian E, Gleason Kevin J, Bjonnes Andrew C, Stilp Adrienne M, Sofer Tamar, Conomos Matthew P, Ancoli-Israel Sonia, Arens Raanan, Azarbarzin Ali, Bell Graeme I, Below Jennifer E, Chun Sung, Evans Daniel S, Ewert Ralf, Frazier-Wood Alexis C, Gharib Sina A, Haba-Rubio José, Hagen Erika W, Heinzer Raphael, Hillman David R, Johnson W Craig, Kutalik Zoltan, Lane Jacqueline M, Larkin Emma K, Lee Seung Ku, Liang Jingjing, Loredo Jose S, Mukherjee Sutapa, Palmer Lyle J, Papanicolaou George J, Penzel Thomas, Peppard Paul E, Post Wendy S, Ramos Alberto R, Rice Ken, Rotter Jerome I, Sands Scott A, Shah Neomi A, Shin Chol, Stone Katie L, Stubbe Beate, Sul Jae-Hoon, Tafti Mehdi, Taylor Kent D, Teumer Alexander, Thornton Timothy A, Tranah Gregory J, Wang Chaolong, Wang Heming, Warby Simon C, Wellman D Andrew, Zee Phyllis C, Hanis Craig L, Laurie Cathy C, Gottlieb Daniel J, Patel Sanjay R, Zhu Xiaofeng, Sunyaev Shamil R, Saxena Richa, Lin Xihong, Redline Sus |
A molecular pathway analysis informs the genetic risk for arrhythmias during antipsychotic treatment. International clinical psychopharmacology 2017 Oct . Kure Fischer Ellen, Drago Anton |
Association analyses based on false discovery rate implicate new loci for coronary artery disease. Nature genetics 2017 Sep 49 (9): 1385-1391. Nelson Christopher P, Goel Anuj, Butterworth Adam S, Kanoni Stavroula, Webb Tom R, Marouli Eirini, Zeng Lingyao, Ntalla Ioanna, Lai Florence Y, Hopewell Jemma C, Giannakopoulou Olga, Jiang Tao, Hamby Stephen E, Di Angelantonio Emanuele, Assimes Themistocles L, Bottinger Erwin P, Chambers John C, Clarke Robert, Palmer Colin N A, Cubbon Richard M, Ellinor Patrick, Ermel Raili, Evangelou Evangelos, Franks Paul W, Grace Christopher, Gu Dongfeng, Hingorani Aroon D, Howson Joanna M M, Ingelsson Erik, Kastrati Adnan, Kessler Thorsten, Kyriakou Theodosios, Lehtimäki Terho, Lu Xiangfeng, Lu Yingchang, März Winfried, McPherson Ruth, Metspalu Andres, Pujades-Rodriguez Mar, Ruusalepp Arno, Schadt Eric E, Schmidt Amand F, Sweeting Michael J, Zalloua Pierre A, AlGhalayini Kamal, Keavney Bernard D, Kooner Jaspal S, Loos Ruth J F, Patel Riyaz S, Rutter Martin K, Tomaszewski Maciej, Tzoulaki Ioanna, Zeggini Eleftheria, Erdmann Jeanette, Dedoussis George, Björkegren Johan L M, , , , Schunkert Heribert, Farrall Martin, Danesh John, Samani Nilesh J, Watkins Hugh, Deloukas Pan |
Fifteen Genetic Loci Associated With the Electrocardiographic P Wave. Circulation. Cardiovascular genetics 2017 Aug 10 (4): . Christophersen Ingrid E, Magnani Jared W, Yin Xiaoyan, Barnard John, Weng Lu-Chen, Arking Dan E, Niemeijer Maartje N, Lubitz Steven A, Avery Christy L, Duan Qing, Felix Stephan B, Bis Joshua C, Kerr Kathleen F, Isaacs Aaron, Müller-Nurasyid Martina, Müller Christian, North Kari E, Reiner Alex P, Tinker Lesley F, Kors Jan A, Teumer Alexander, Petersmann Astrid, Sinner Moritz F, Buzkova Petra, Smith Jonathan D, Van Wagoner David R, Völker Uwe, Waldenberger Melanie, Peters Annette, Meitinger Thomas, Limacher Marian C, Wilhelmsen Kirk C, Psaty Bruce M, Hofman Albert, Uitterlinden Andre, Krijthe Bouwe P, Zhang Zhu-Ming, Schnabel Renate B, Kääb Stefan, van Duijn Cornelia, Rotter Jerome I, Sotoodehnia Nona, Dörr Marcus, Li Yun, Chung Mina K, Soliman Elsayed Z, Alonso Alvaro, Whitsel Eric A, Stricker Bruno H, Benjamin Emelia J, Heckbert Susan R, Ellinor Patrick |
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Nature genetics 2017 Jun . Hammerschlag Anke R, Stringer Sven, de Leeuw Christiaan A, Sniekers Suzanne, Taskesen Erdogan, Watanabe Kyoko, Blanken Tessa F, Dekker Kim, Te Lindert Bart H W, Wassing Rick, Jonsdottir Ingileif, Thorleifsson Gudmar, Stefansson Hreinn, Gislason Thorarinn, Berger Klaus, Schormair Barbara, Wellmann Juergen, Winkelmann Juliane, Stefansson Kari, Oexle Konrad, Van Someren Eus J W, Posthuma Daniel |
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Hypertension (Dallas, Tex. : 1979) 2017 Jul . Wain Louise V, Vaez Ahmad, Jansen Rick, Joehanes Roby, van der Most Peter J, Erzurumluoglu A Mesut, O'Reilly Paul F, Cabrera Claudia P, Warren Helen R, Rose Lynda M, Verwoert Germaine C, Hottenga Jouke-Jan, Strawbridge Rona J, Esko Tonu, Arking Dan E, Hwang Shih-Jen, Guo Xiuqing, Kutalik Zoltan, Trompet Stella, Shrine Nick, Teumer Alexander, Ried Janina S, Bis Joshua C, Smith Albert V, Amin Najaf, Nolte Ilja M, Lyytikäinen Leo-Pekka, Mahajan Anubha, Wareham Nicholas J, Hofer Edith, Joshi Peter K, Kristiansson Kati, Traglia Michela, Havulinna Aki S, Goel Anuj, Nalls Mike A, Sõber Siim, Vuckovic Dragana, Luan Jian'an, Del Greco M Fabiola, Ayers Kristin L, Marrugat Jaume, Ruggiero Daniela, Lopez Lorna M, Niiranen Teemu, Enroth Stefan, Jackson Anne U, Nelson Christopher P, Huffman Jennifer E, Zhang Weihua, Marten Jonathan, Gandin Ilaria, Harris Sarah E, Zemunik Tatijana, Lu Yingchang, Evangelou Evangelos, Shah Nabi, de Borst Martin H, Mangino Massimo, Prins Bram P, Campbell Archie, Li-Gao Ruifang, Chauhan Ganesh, Oldmeadow Christopher, Abecasis Gonçalo, Abedi Maryam, Barbieri Caterina M, Barnes Michael R, Batini Chiara, Beilby John, Blake Tineka, Boehnke Michael, Bottinger Erwin P, Braund Peter S, Brown Morris, Brumat Marco, Campbell Harry, Chambers John C, Cocca Massimiliano, Collins Francis, Connell John, Cordell Heather J, Damman Jeffrey J, Davies Gail, de Geus Eco J, de Mutsert Renée, Deelen Joris, Demirkale Yusuf, Doney Alex S F, Dörr Marcus, Farrall Martin, Ferreira Teresa, Frånberg Mattias, Gao He, Giedraitis Vilmantas, Gieger Christian, Giulianini Franco, Gow Alan J, Hamsten Anders, Harris Tamara B, Hofman Albert, Holliday Elizabeth G, Hui Jennie, Jarvelin Marjo-Riitta, Johansson Åsa, Johnson Andrew D, Jousilahti Pekka, Jula Antti, Kähönen Mika, Kathiresan Sekar, Khaw Kay-Tee, Kolcic Ivana, Koskinen Seppo, Langenberg Claudia, Larson Marty, Launer Lenore J, Lehne Benjamin, Liewald David C M, Lin Li, Lind Lars, Mach François, Mamasoula Chrysovalanto, Menni Cristina, Mifsud Borbala, Milaneschi Yuri, Morgan Anna, Morris Andrew D, Morrison Alanna C, Munson Peter J, Nandakumar Priyanka, Nguyen Quang Tri, Nutile Teresa, Oldehinkel Albertine J, Oostra Ben A, Org Elin, Padmanabhan Sandosh, Palotie Aarno, Paré Guillaume, Pattie Alison, Penninx Brenda W J H, Poulter Neil, Pramstaller Peter P, Raitakari Olli T, Ren Meixia, Rice Kenneth, Ridker Paul M, Riese Harriëtte, Ripatti Samuli, Robino Antonietta, Rotter Jerome I, Rudan Igor, Saba Yasaman, Saint Pierre Aude, Sala Cinzia F, Sarin Antti-Pekka, Schmidt Reinhold, Scott Rodney, Seelen Marc A, Shields Denis C, Siscovick David, Sorice Rossella, Stanton Alice, Stott David J, Sundström Johan, Swertz Morris, Taylor Kent D, Thom Simon, Tzoulaki Ioanna, Tzourio Christophe, Uitterlinden André G, Völker Uwe, Vollenweider Peter, Wild Sarah, Willemsen Gonneke, Wright Alan F, Yao Jie, Thériault Sébastien, Conen David, Attia John, Sever Peter, Debette Stéphanie, Mook-Kanamori Dennis O, Zeggini Eleftheria, Spector Tim D, van der Harst Pim, Palmer Colin N A, Vergnaud Anne-Claire, Loos Ruth J F, Polasek Ozren, Starr John M, Girotto Giorgia, Hayward Caroline, Kooner Jaspal S, Lindgren Cecila M, Vitart Veronique, Samani Nilesh J, Tuomilehto Jaakko, Gyllensten Ulf, Knekt Paul, Deary Ian J, Ciullo Marina, Elosua Roberto, Keavney Bernard D, Hicks Andrew A, Scott Robert A, Gasparini Paolo, Laan Maris, Liu YongMei, Watkins Hugh, Hartman Catharina A, Salomaa Veikko, Toniolo Daniela, Perola Markus, Wilson James F, Schmidt Helena, Zhao Jing Hua, Lehtimäki Terho, van Duijn Cornelia M, Gudnason Vilmundur, Psaty Bruce M, Peters Annette, Rettig Rainer, James Alan, Jukema J Wouter, Strachan David P, Palmas Walter, Metspalu Andres, Ingelsson Erik, Boomsma Dorret I, Franco Oscar H, Bochud Murielle, Newton-Cheh Christopher, Munroe Patricia B, Elliott Paul, Chasman Daniel I, Chakravarti Aravinda, Knight Joanne, Morris Andrew P, Levy Daniel, Tobin Martin D, Snieder Harold, Caulfield Mark J, Ehret Georg |
Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112?117). Molecular psychiatry 2017 Oct 22 (10): 1376-1384. Clarke T-K, Adams M J, Davies G, Howard D M, Hall L S, Padmanabhan S, Murray A D, Smith B H, Campbell A, Hayward C, Porteous D J, Deary I J, McIntosh A |
Genome-wide association study of a nicotine metabolism biomarker in African American smokers: impact of chromosome 19 genetic influences. Addiction (Abingdon, England) 2017 Sep . Chenoweth Meghan J, Ware Jennifer J, Zhu Andy Z X, Cole Christopher B, Cox Lisa Sanderson, Nollen Nikki, Ahluwalia Jasjit S, Benowitz Neal L, Schnoll Robert A, Hawk Larry W, Cinciripini Paul M, George Tony P, Lerman Caryn, Knight Joanne, Tyndale Rachel F, |
Genome-wide association study of subclinical interstitial lung disease in MESA. Respiratory research 2017 May 18 (1): 97. Manichaikul Ani, Wang Xin-Qun, Sun Li, Dupuis Josée, Borczuk Alain C, Nguyen Jennifer N, Raghu Ganesh, Hoffman Eric A, Onengut-Gumuscu Suna, Farber Emily A, Kaufman Joel D, Rabinowitz Dan, Stukovsky Karen D Hinckley, Kawut Steven M, Hunninghake Gary M, Washko George R, O'Connor George T, Rich Stephen S, Barr R Graham, Lederer David |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Cell 2016 11 167 (5): 1415-1429.e19. Astle William J, Elding Heather, Jiang Tao, Allen Dave, Ruklisa Dace, Mann Alice L, Mead Daniel, Bouman Heleen, Riveros-Mckay Fernando, Kostadima Myrto A, Lambourne John J, Sivapalaratnam Suthesh, Downes Kate, Kundu Kousik, Bomba Lorenzo, Berentsen Kim, Bradley John R, Daugherty Louise C, Delaneau Olivier, Freson Kathleen, Garner Stephen F, Grassi Luigi, Guerrero Jose, Haimel Matthias, Janssen-Megens Eva M, Kaan Anita, Kamat Mihir, Kim Bowon, Mandoli Amit, Marchini Jonathan, Martens Joost H A, Meacham Stuart, Megy Karyn, O'Connell Jared, Petersen Romina, Sharifi Nilofar, Sheard Simon M, Staley James R, Tuna Salih, van der Ent Martijn, Walter Klaudia, Wang Shuang-Yin, Wheeler Eleanor, Wilder Steven P, Iotchkova Valentina, Moore Carmel, Sambrook Jennifer, Stunnenberg Hendrik G, Di Angelantonio Emanuele, Kaptoge Stephen, Kuijpers Taco W, Carrillo-de-Santa-Pau Enrique, Juan David, Rico Daniel, Valencia Alfonso, Chen Lu, Ge Bing, Vasquez Louella, Kwan Tony, Garrido-Martín Diego, Watt Stephen, Yang Ying, Guigo Roderic, Beck Stephan, Paul Dirk S, Pastinen Tomi, Bujold David, Bourque Guillaume, Frontini Mattia, Danesh John, Roberts David J, Ouwehand Willem H, Butterworth Adam S, Soranzo Nico |
Genetic Drivers of von Willebrand Factor Levels in an Ischemic Stroke Population and Association With Risk for Recurrent Stroke. Stroke 2017 Jun 48 (6): 1444-1450. Williams Stephen R, Hsu Fang-Chi, Keene Keith L, Chen Wei-Min, Dzhivhuho Godfrey, Rowles Joe L, Southerland Andrew M, Furie Karen L, Rich Stephen S, Worrall Bradford B, Sale Michèle M, |
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. The Journal of clinical investigation 2017 May 127 (5): 1798-1812. Wild Philipp S, Felix Janine F, Schillert Arne, Teumer Alexander, Chen Ming-Huei, Leening Maarten J G, Völker Uwe, Großmann Vera, Brody Jennifer A, Irvin Marguerite R, Shah Sanjiv J, Pramana Setia, Lieb Wolfgang, Schmidt Reinhold, Stanton Alice V, Malzahn Dörthe, Smith Albert Vernon, Sundström Johan, Minelli Cosetta, Ruggiero Daniela, Lyytikäinen Leo-Pekka, Tiller Daniel, Smith J Gustav, Monnereau Claire, Di Tullio Marco R, Musani Solomon K, Morrison Alanna C, Pers Tune H, Morley Michael, Kleber Marcus E, Aragam Jayashri, Benjamin Emelia J, Bis Joshua C, Bisping Egbert, Broeckel Ulrich, Cheng Susan, Deckers Jaap W, Del Greco M Fabiola, Edelmann Frank, Fornage Myriam, Franke Lude, Friedrich Nele, Harris Tamara B, Hofer Edith, Hofman Albert, Huang Jie, Hughes Alun D, Kähönen Mika, Investigators Knhi, Kruppa Jochen, Lackner Karl J, Lannfelt Lars, Laskowski Rafael, Launer Lenore J, Leosdottir Margrét, Lin Honghuang, Lindgren Cecilia M, Loley Christina, MacRae Calum A, Mascalzoni Deborah, Mayet Jamil, Medenwald Daniel, Morris Andrew P, Müller Christian, Müller-Nurasyid Martina, Nappo Stefania, Nilsson Peter M, Nuding Sebastian, Nutile Teresa, Peters Annette, Pfeufer Arne, Pietzner Diana, Pramstaller Peter P, Raitakari Olli T, Rice Kenneth M, Rivadeneira Fernando, Rotter Jerome I, Ruohonen Saku T, Sacco Ralph L, Samdarshi Tandaw E, Schmidt Helena, Sharp Andrew S P, Shields Denis C, Sorice Rossella, Sotoodehnia Nona, Stricker Bruno H, Surendran Praveen, Thom Simon, Töglhofer Anna M, Uitterlinden André G, Wachter Rolf, Völzke Henry, Ziegler Andreas, Münzel Thomas, März Winfried, Cappola Thomas P, Hirschhorn Joel N, Mitchell Gary F, Smith Nicholas L, Fox Ervin R, Dueker Nicole D, Jaddoe Vincent W V, Melander Olle, Russ Martin, Lehtimäki Terho, Ciullo Marina, Hicks Andrew A, Lind Lars, Gudnason Vilmundur, Pieske Burkert, Barron Anthony J, Zweiker Robert, Schunkert Heribert, Ingelsson Erik, Liu Kiang, Arnett Donna K, Psaty Bruce M, Blankenberg Stefan, Larson Martin G, Felix Stephan B, Franco Oscar H, Zeller Tanja, Vasan Ramachandran S, Dörr Marc |
Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Scientific reports 2017 Sep 7 (1): 11008. Prins Bram P, Kuchenbaecker Karoline B, Bao Yanchun, Smart Melissa, Zabaneh Delilah, Fatemifar Ghazaleh, Luan Jian'an, Wareham Nick J, Scott Robert A, Perry John R B, Langenberg Claudia, Benzeval Michaela, Kumari Meena, Zeggini Elefther |
Male-specific association of the FCGR2A His167Arg polymorphism with Kawasaki disease. PloS one 2017 12 (9): e0184248. Kwon Young-Chang, Kim Jae-Jung, Yun Sin Weon, Yu Jeong Jin, Yoon Kyung Lim, Lee Kyung-Yil, Kil Hong-Ryang, Kim Gi Beom, Han Myung-Ki, Song Min Seob, Lee Hyoung Doo, Ha Kee-Soo, Sohn Sejung, Ebata Ryota, Hamada Hiromichi, Suzuki Hiroyuki, Ito Kaoru, Onouchi Yoshihiro, Hong Young Mi, Jang Gi Young, Lee Jong-Keuk, |
Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos. Scientific reports 2017 Sep 7 (1): 10348. Sofer Tamar, Wong Quenna, Hartwig Fernando P, Taylor Kent, Warren Helen R, Evangelou Evangelos, Cabrera Claudia P, Levy Daniel, Kramer Holly, Lange Leslie A, Horta Bernardo L, , Kerr Kathleen F, Reiner Alex P, Franceschini No |
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. Nature genetics 2017 Sep . Zhao Wei, Rasheed Asif, Tikkanen Emmi, Lee Jung-Jin, Butterworth Adam S, Howson Joanna M M, Assimes Themistocles L, Chowdhury Rajiv, Orho-Melander Marju, Damrauer Scott, Small Aeron, Asma Senay, Imamura Minako, Yamauch Toshimasa, Chambers John C, Chen Peng, Sapkota Bishwa R, Shah Nabi, Jabeen Sehrish, Surendran Praveen, Lu Yingchang, Zhang Weihua, Imran Atif, Abbas Shahid, Majeed Faisal, Trindade Kevin, Qamar Nadeem, Mallick Nadeem Hayyat, Yaqoob Zia, Saghir Tahir, Rizvi Syed Nadeem Hasan, Memon Anis, Rasheed Syed Zahed, Memon Fazal-Ur-Rehman, Mehmood Khalid, Ahmed Naveeduddin, Qureshi Irshad Hussain, Tanveer-Us-Salam , Iqbal Wasim, Malik Uzma, Mehra Narinder, Kuo Jane Z, Sheu Wayne H-H, Guo Xiuqing, Hsiung Chao A, Juang Jyh-Ming J, Taylor Kent D, Hung Yi-Jen, Lee Wen-Jane, Quertermous Thomas, Lee I-Te, Hsu Chih-Cheng, Bottinger Erwin P, Ralhan Sarju, Teo Yik Ying, Wang Tzung-Dau, Alam Dewan S, Di Angelantonio Emanuele, Epstein Steve, Nielsen Sune F, Nordestgaard Børge G, Tybjaerg-Hansen Anne, Young Robin, , Benn Marianne, Frikke-Schmidt Ruth, Kamstrup Pia R, , , , Jukema J Wouter, Sattar Naveed, Smit Roelof, Chung Ren-Hua, Liang Kae-Woei, Anand Sonia, Sanghera Dharambir K, Ripatti Samuli, Loos Ruth J F, Kooner Jaspal S, Tai E Shyong, Rotter Jerome I, Chen Yii-Der Ida, Frossard Philippe, Maeda Shiro, Kadowaki Takashi, Reilly Muredach, Pare Guillaume, Melander Olle, Salomaa Veikko, Rader Daniel J, Danesh John, Voight Benjamin F, Saleheen Dani |
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Genetic variants in RBFOX3 are associated with sleep latency. European journal of human genetics : EJHG 2016 Oct 24 (10): 1488-95. Amin Najaf, Allebrandt Karla V, van der Spek Ashley, Müller-Myhsok Bertram, Hek Karin, Teder-Laving Maris, Hayward Caroline, Esko Tõnu, van Mill Josine G, Mbarek Hamdi, Watson Nathaniel F, Melville Scott A, Del Greco Fabiola M, Byrne Enda M, Oole Edwin, Kolcic Ivana, Chen Ting-Hsu, Evans Daniel S, Coresh Josef, Vogelzangs Nicole, Karjalainen Juha, Willemsen Gonneke, Gharib Sina A, Zgaga Lina, Mihailov Evelin, Stone Katie L, Campbell Harry, Brouwer Rutger Ww, Demirkan Ayse, Isaacs Aaron, Dogas Zoran, Marciante Kristin D, Campbell Susan, Borovecki Fran, Luik Annemarie I, Li Man, Hottenga Jouke Jan, Huffman Jennifer E, van den Hout Mirjam Cgn, Cummings Steven R, Aulchenko Yurii S, Gehrman Philip R, Uitterlinden André G, Wichmann Heinz-Erich, Müller-Nurasyid Martina, Fehrmann Rudolf Sn, Montgomery Grant W, Hofman Albert, Kao Wen Hong Linda, Oostra Ben A, Wright Alan F, Vink Jacqueline M, Wilson James F, Pramstaller Peter P, Hicks Andrew A, Polasek Ozren, Punjabi Naresh M, Redline Susan, Psaty Bruce M, Heath Andrew C, Merrow Martha, Tranah Gregory J, Gottlieb Daniel J, Boomsma Dorret I, Martin Nicholas G, Rudan Igor, Tiemeier Henning, van IJcken Wilfred Fj, Penninx Brenda W, Metspalu Andres, Meitinger Thomas, Franke Lude, Roenneberg Till, van Duijn Cornelia |
Novel genetic risk factors for asthma in African American children: Precision Medicine and the SAGE II Study. Immunogenetics 2016 Jul 68 (6-7): 391-400. White Marquitta J, Risse-Adams O, Goddard P, Contreras M G, Adams J, Hu D, Eng C, Oh S S, Davis A, Meade K, Brigino-Buenaventura E, LeNoir M A, Bibbins-Domingo K, Pino-Yanes M, Burchard E |
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies. The Lancet. Neurology 2016 06 15 (7): 695-707. Authors are not available |
Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans. American journal of respiratory and critical care medicine 2016 Oct 194 (7): 886-897. Cade Brian E, Chen Han, Stilp Adrienne M, Gleason Kevin J, Sofer Tamar, Ancoli-Israel Sonia, Arens Raanan, Bell Graeme I, Below Jennifer E, Bjonnes Andrew C, Chun Sung, Conomos Matthew P, Evans Daniel S, Johnson W Craig, Frazier-Wood Alexis C, Lane Jacqueline M, Larkin Emma K, Loredo Jose S, Post Wendy S, Ramos Alberto R, Rice Ken, Rotter Jerome I, Shah Neomi A, Stone Katie L, Taylor Kent D, Thornton Timothy A, Tranah Gregory J, Wang Chaolong, Zee Phyllis C, Hanis Craig L, Sunyaev Shamil R, Patel Sanjay R, Laurie Cathy C, Zhu Xiaofeng, Saxena Richa, Lin Xihong, Redline Sus |
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Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome. Human molecular genetics 2016 Apr 25 (7): 1447-56. Johansson Åsa, Eriksson Niclas, Lindholm Daniel, Varenhorst Christoph, James Stefan, Syvänen Ann-Christine, Axelsson Tomas, Siegbahn Agneta, Barratt Bryan J, Becker Richard C, Himmelmann Anders, Katus Hugo A, Steg Philippe Gabriel, Storey Robert F, Wallentin Lars, |
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis. Human molecular genetics 2016 May 25 (9): 1867-74. Hinds David A, Buil Alfonso, Ziemek Daniel, Martinez-Perez Angel, Malik Rainer, Folkersen Lasse, Germain Marine, Mälarstig Anders, Brown Andrew, Soria Jose Manuel, Dichgans Martin, Bing Nan, Franco-Cereceda Anders, Souto Juan Carlos, Dermitzakis Emmanouil T, Hamsten Anders, Worrall Bradford B, Tung Joyce Y, , Sabater-Lleal Mar |
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person. Nature communications 2016 Feb 7 10448. Hu Youna, Shmygelska Alena, Tran David, Eriksson Nicholas, Tung Joyce Y, Hinds David |
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Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease. Nature communications 2016 Jan 7 10558. Hartiala Jaana A, Tang W H Wilson, Wang Zeneng, Crow Amanda L, Stewart Alexandre F R, Roberts Robert, McPherson Ruth, Erdmann Jeanette, Willenborg Christina, Hazen Stanley L, Allayee Hoom |
A genome-wide association study of pulmonary tuberculosis in Morocco. Human genetics 2016 Mar 135 (3): 299-307. Grant A V, Sabri A, Abid A, Abderrahmani Rhorfi I, Benkirane M, Souhi H, Naji Amrani H, Alaoui-Tahiri K, Gharbaoui Y, Lazrak F, Sentissi I, Manessouri M, Belkheiri S, Zaid S, Bouraqadi A, El Amraoui N, Hakam M, Belkadi A, Orlova M, Boland A, Deswarte C, Amar L, Bustamante J, Boisson-Dupuis S, Casanova J L, Schurr E, El Baghdadi J, Abel |
A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction. Scientific reports 2016 Jan 6 18812. Taylor Jacquelyn Y, Schwander Karen, Kardia Sharon L R, Arnett Donna, Liang Jingjing, Hunt Steven C, Rao D C, Sun Yan |
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study. The Lancet. Neurology 2016 Feb 15 (2): 174-184. , |
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. BMC genetics 2015 Dec 16 138. Lutz Sharon M, Cho Michael H, Young Kendra, Hersh Craig P, Castaldi Peter J, McDonald Merry-Lynn, Regan Elizabeth, Mattheisen Manuel, DeMeo Dawn L, Parker Margaret, Foreman Marilyn, Make Barry J, Jensen Robert L, Casaburi Richard, Lomas David A, Bhatt Surya P, Bakke Per, Gulsvik Amund, Crapo James D, Beaty Terri H, Laird Nan M, Lange Christoph, Hokanson John E, Silverman Edwin K, , |
Genome-wide Meta-analysis on the Sense of Smell Among US Older Adults. Medicine 2015 Nov 94 (47): e1892. Dong Jing, Yang Jingyun, Tranah Greg, Franceschini Nora, Parimi Neeta, Alkorta-Aranburu Gorka, Xu Zongli, Alonso Alvaro, Cummings Steven R, Fornage Myriam, Huang Xuemei, Kritchevsky Stephen, Liu Yongmei, London Stephanie, Niu Liang, Wilson Robert S, De Jager Philip L, Yu Lei, Singleton Andrew B, Harris Tamara, Mosley Thomas H, Pinto Jayant M, Bennett David A, Chen Hongl |
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis. Nature communications 2015 Sep 6 8382. Corvol Harriet, Blackman Scott M, Boëlle Pierre-Yves, Gallins Paul J, Pace Rhonda G, Stonebraker Jaclyn R, Accurso Frank J, Clement Annick, Collaco Joseph M, Dang Hong, Dang Anthony T, Franca Arianna, Gong Jiafen, Guillot Loic, Keenan Katherine, Li Weili, Lin Fan, Patrone Michael V, Raraigh Karen S, Sun Lei, Zhou Yi-Hui, O'Neal Wanda K, Sontag Marci K, Levy Hara, Durie Peter R, Rommens Johanna M, Drumm Mitchell L, Wright Fred A, Strug Lisa J, Cutting Garry R, Knowles Michael |
Genome-wide association study of new-onset atrial fibrillation after coronary artery bypass grafting surgery. American heart journal 2015 Sep 170 (3): 580-90.e28. Kertai Miklos D, Li Yi-Ju, Ji Yunqi, Qi Wenjing, Lombard Frederick W, Shah Svati H, Kraus William E, Stafford-Smith Mark, Newman Mark F, Milano Carmelo A, Waldron Nathan, Podgoreanu Mihai V, Mathew Joseph P, |
Genome-wide association study on progression of carotid artery intima media thickness over 10 years in a Chinese cohort. Atherosclerosis 2015 Nov 243 (1): 30-7. Xie Gaoqiang, Myint Phyo Kyaw, Voora Deepak, Laskowitz Daniel T, Shi Ping, Ren Fuxiu, Wang Hao, Yang Ying, Huo Yong, Gao Wei, Wu Yangfe |
Genetic association analyses highlight biological pathways underlying mitral valve prolapse. Nature genetics 2015 Oct 47 (10): 1206-11. Dina Christian, Bouatia-Naji Nabila, Tucker Nathan, Delling Francesca N, Toomer Katelynn, Durst Ronen, Perrocheau Maelle, Fernandez-Friera Leticia, Solis Jorge, , Le Tourneau Thierry, Chen Ming-Huei, Probst Vincent, Bosse Yohan, Pibarot Philippe, Zelenika Diana, Lathrop Mark, Hercberg Serge, Roussel Ronan, Benjamin Emelia J, Bonnet Fabrice, Lo Su Hao, Dolmatova Elena, Simonet Floriane, Lecointe Simon, Kyndt Florence, Redon Richard, Le Marec Hervé, Froguel Philippe, Ellinor Patrick T, Vasan Ramachandran S, Bruneval Patrick, Markwald Roger R, Norris Russell A, Milan David J, Slaugenhaupt Susan A, Levine Robert A, Schott Jean-Jacques, Hagege Albert A, , Jeunemaitre Xavier, |
New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Sep 168 (6): 459-470. Alemany Silvia, Ribasés Marta, Vilor-Tejedor Natàlia, Bustamante Mariona, Sánchez-Mora Cristina, Bosch Rosa, Richarte Vanesa, Cormand Bru, Casas Miguel, Ramos-Quiroga Josep A, Sunyer Jor |
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. The pharmacogenomics journal 2016 06 16 (3): 231-7. Mosley J D, Shaffer C M, Van Driest S L, Weeke P E, Wells Q S, Karnes J H, Velez Edwards D R, Wei W-Q, Teixeira P L, Bastarache L, Crawford D C, Li R, Manolio T A, Bottinger E P, McCarty C A, Linneman J G, Brilliant M H, Pacheco J A, Thompson W, Chisholm R L, Jarvik G P, Crosslin D R, Carrell D S, Baldwin E, Ralston J, Larson E B, Grafton J, Scrol A, Jouni H, Kullo I J, Tromp G, Borthwick K M, Kuivaniemi H, Carey D J, Ritchie M D, Bradford Y, Verma S S, Chute C G, Veluchamy A, Siddiqui M K, Palmer C N A, Doney A, MahmoudPour S H, Maitland-van der Zee A H, Morris A D, Denny J C, Roden D |
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Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study. BMC genetics 2015 May 16 56. Tin Adrienne, Köttgen Anna, Folsom Aaron R, Maruthur Nisa M, Tajuddin Salman M, Nalls Mike A, Evans Michele K, Zonderman Alan B, Friedrich Christopher A, Boerwinkle Eric, Coresh Josef, Kao Wen Hong Lin |
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Genome-wide association study of recalcitrant atopic dermatitis in Korean children. The Journal of allergy and clinical immunology 2015 Sep 136 (3): 678-684.e4. Kim Kyung Won, Myers Rachel A, Lee Ji Hyun, Igartua Catherine, Lee Kyung Eun, Kim Yoon Hee, Kim Eun-Jin, Yoon Dankyu, Lee Joo-Shil, Hirota Tomomitsu, Tamari Mayumi, Takahashi Atsushi, Kubo Michiaki, Choi Je-Min, Kim Kyu-Earn, Nicolae Dan L, Ober Carole, Sohn Myung Hy |
Genetics of aging, health, and survival: dynamic regulation of human longevity related traits. Frontiers in genetics 2015 6 122. Yashin Anatoliy I, Wu Deqing, Arbeeva Liubov S, Arbeev Konstantin G, Kulminski Alexander M, Akushevich Igor, Kovtun Mikhail, Culminskaya Irina, Stallard Eric, Li Miaozhu, Ukraintseva Svetlana |
Identification of a Novel Mucin Gene HCG22 Associated With Steroid-Induced Ocular Hypertension. Investigative ophthalmology & visual science 2015 Apr 56 (4): 2737-48. Jeong Shinwu, Patel Nitin, Edlund Christopher K, Hartiala Jaana, Hazelett Dennis J, Itakura Tatsuo, Wu Pei-Chang, Avery Robert L, Davis Janet L, Flynn Harry W, Lalwani Geeta, Puliafito Carmen A, Wafapoor Hussein, Hijikata Minako, Keicho Naoto, Gao Xiaoyi, Argüeso Pablo, Allayee Hooman, Coetzee Gerhard A, Pletcher Mathew T, Conti David V, Schwartz Stephen G, Eaton Alexander M, Fini M Elizabe |
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