Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 31 Records) |
Query Trace: Venous thromboembolism[original query] |
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Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.
Blood 2010 Dec 116 (23): 5032-6. Tang Weihong, Basu Saonli, Kong Xiaoxiao, Pankow James S, Aleksic Nena, Tan Adrian, Cushman Mary, Boerwinkle Eric, Folsom Aaron |
Human metabolic individuality in biomedical and pharmaceutical research.
Nature 2011 Sep 477 (7362): 54-60. Suhre Karsten, Shin So-Youn, Petersen Ann-Kristin, Mohney Robert P, Meredith David, Wägele Brigitte, Altmaier Elisabeth, , Deloukas Panos, Erdmann Jeanette, Grundberg Elin, Hammond Christopher J, de Angelis Martin Hrabé, Kastenmüller Gabi, Köttgen Anna, Kronenberg Florian, Mangino Massimo, Meisinger Christa, Meitinger Thomas, Mewes Hans-Werner, Milburn Michael V, Prehn Cornelia, Raffler Johannes, Ried Janina S, Römisch-Margl Werner, Samani Nilesh J, Small Kerrin S, Wichmann H-Erich, Zhai Guangju, Illig Thomas, Spector Tim D, Adamski Jerzy, Soranzo Nicole, Gieger Christi |
A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.
Journal of thrombosis and haemostasis : JTH 2012 Aug 10 (8): 1521-31. Heit J A, Armasu S M, Asmann Y W, Cunningham J M, Matsumoto M E, Petterson T M, De Andrade |
A genome-wide association study of the Protein C anticoagulant pathway.
PloS one 2011 6 (12): e29168. Athanasiadis Georgios, Buil Alfonso, Souto Juan Carlos, Borrell Montserrat, López Sonia, Martinez-Perez Angel, Lathrop Mark, Fontcuberta Jordi, Almasy Laura, Soria José Manu |
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
Circulation 2013 Sep 128 (12): 1310-24. Sabater-Lleal Maria, Huang Jie, Chasman Daniel, Naitza Silvia, Dehghan Abbas, Johnson Andrew D, Teumer Alexander, Reiner Alex P, Folkersen Lasse, Basu Saonli, Rudnicka Alicja R, Trompet Stella, Mälarstig Anders, Baumert Jens, Bis Joshua C, Guo Xiuqing, Hottenga Jouke J, Shin So-Youn, Lopez Lorna M, Lahti Jari, Tanaka Toshiko, Yanek Lisa R, Oudot-Mellakh Tiphaine, Wilson James F, Navarro Pau, Huffman Jennifer E, Zemunik Tatijana, Redline Susan, Mehra Reena, Pulanic Drazen, Rudan Igor, Wright Alan F, Kolcic Ivana, Polasek Ozren, Wild Sarah H, Campbell Harry, Curb J David, Wallace Robert, Liu Simin, Eaton Charles B, Becker Diane M, Becker Lewis C, Bandinelli Stefania, Räikkönen Katri, Widen Elisabeth, Palotie Aarno, Fornage Myriam, Green David, Gross Myron, Davies Gail, Harris Sarah E, Liewald David C, Starr John M, Williams Frances M K, Grant Peter J, Spector Timothy D, Strawbridge Rona J, Silveira Angela, Sennblad Bengt, Rivadeneira Fernando, Uitterlinden Andre G, Franco Oscar H, Hofman Albert, van Dongen Jenny, Willemsen Gonneke, Boomsma Dorret I, Yao Jie, Swords Jenny Nancy, Haritunians Talin, McKnight Barbara, Lumley Thomas, Taylor Kent D, Rotter Jerome I, Psaty Bruce M, Peters Annette, Gieger Christian, Illig Thomas, Grotevendt Anne, Homuth Georg, Völzke Henry, Kocher Thomas, Goel Anuj, Franzosi Maria Grazia, Seedorf Udo, Clarke Robert, Steri Maristella, Tarasov Kirill V, Sanna Serena, Schlessinger David, Stott David J, Sattar Naveed, Buckley Brendan M, Rumley Ann, Lowe Gordon D, McArdle Wendy L, Chen Ming-Huei, Tofler Geoffrey H, Song Jaejoon, Boerwinkle Eric, Folsom Aaron R, Rose Lynda M, Franco-Cereceda Anders, Teichert Martina, Ikram M Arfan, Mosley Thomas H, Bevan Steve, Dichgans Martin, Rothwell Peter M, Sudlow Cathie L M, Hopewell Jemma C, Chambers John C, Saleheen Danish, Kooner Jaspal S, Danesh John, Nelson Christopher P, Erdmann Jeanette, Reilly Muredach P, Kathiresan Sekar, Schunkert Heribert, Morange Pierre-Emmanuel, Ferrucci Luigi, Eriksson Johan G, Jacobs David, Deary Ian J, Soranzo Nicole, Witteman Jacqueline C M, de Geus Eco J C, Tracy Russell P, Hayward Caroline, Koenig Wolfgang, Cucca Francesco, Jukema J Wouter, Eriksson Per, Seshadri Sudha, Markus Hugh S, Watkins Hugh, Samani Nilesh J, , , , , , Wallaschofski Henri, Smith Nicholas L, Tregouet David, Ridker Paul M, Tang Weihong, Strachan David P, Hamsten Anders, O'Donnell Christopher |
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Genetic epidemiology 2013 Jul 37 (5): 512-21. Tang Weihong, Teichert Martina, Chasman Daniel I, Heit John A, Morange Pierre-Emmanuel, Li Guo, Pankratz Nathan, Leebeek Frank W, Paré Guillaume, de Andrade Mariza, Tzourio Christophe, Psaty Bruce M, Basu Saonli, Ruiter Rikje, Rose Lynda, Armasu Sebastian M, Lumley Thomas, Heckbert Susan R, Uitterlinden André G, Lathrop Mark, Rice Kenneth M, Cushman Mary, Hofman Albert, Lambert Jean-Charles, Glazer Nicole L, Pankow James S, Witteman Jacqueline C, Amouyel Philippe, Bis Joshua C, Bovill Edwin G, Kong Xiaoxiao, Tracy Russell P, Boerwinkle Eric, Rotter Jerome I, Trégouët David-Alexandre, Loth Daan W, Stricker Bruno H Ch, Ridker Paul M, Folsom Aaron R, Smith Nicholas |
Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism.
American journal of human genetics 2015 Apr 96 (4): 532-42. Germain Marine, Chasman Daniel I, de Haan Hugoline, Tang Weihong, Lindström Sara, Weng Lu-Chen, de Andrade Mariza, de Visser Marieke C H, Wiggins Kerri L, Suchon Pierre, Saut Noémie, Smadja David M, Le Gal Grégoire, van Hylckama Vlieg Astrid, Di Narzo Antonio, Hao Ke, Nelson Christopher P, Rocanin-Arjo Ares, Folkersen Lasse, Monajemi Ramin, Rose Lynda M, Brody Jennifer A, Slagboom Eline, Aïssi Dylan, Gagnon France, Deleuze Jean-Francois, Deloukas Panos, Tzourio Christophe, Dartigues Jean-Francois, Berr Claudine, Taylor Kent D, Civelek Mete, Eriksson Per, , Psaty Bruce M, Houwing-Duitermaat Jeanine, Goodall Alison H, Cambien François, Kraft Peter, Amouyel Philippe, Samani Nilesh J, Basu Saonli, Ridker Paul M, Rosendaal Frits R, Kabrhel Christopher, Folsom Aaron R, Heit John, Reitsma Pieter H, Trégouët David-Alexandre, Smith Nicholas L, Morange Pierre-Emmanu |
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 |
Novel genetic predictors of venous thromboembolism risk in African Americans.
Blood 2016 Feb . Hernandez Wenndy, Gamazon Eric R, Smithberger Erin, O'Brien Travis J, Harralson Arthur F, Tuck Matthew, Barbour April, Kittles Rick A, Cavallari Larisa H, Perera Minoli |
Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism.
Blood 2016 Dec . Rühle Frank, Witten Anika, Barysenka Andrei, Huge Andreas, Arning Astrid, Heller Christine, Krümpel Anne, Mesters Rolf, Franke Andre, Lieb Wolfgang, Riemenschneider Mona, Hiersche Milan, Limperger Verena, Nowak-Göttl Ulrike, Stoll Moni |
Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor.
Circulation. Cardiovascular genetics 2017 Apr 10 (2): . Klarin Derek, Emdin Connor A, Natarajan Pradeep, Conrad Mark F, , Kathiresan Sek |
Identification of unique venous thromboembolism-susceptibility variants in African-Americans.
Thrombosis and haemostasis 2017 Feb . Heit John A, Armasu Sebastian M, McCauley Bryan M, Kullo Iftikhar J, Sicotte Hugues, Pathak Jyotishman, Chute Christopher G, Gottesman Omri, Bottinger Erwin P, Denny Joshua C, Roden Dan M, Li Rongling, Ritchie Marylyn D, de Andrade Mari |
Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels.
Human molecular genetics 2017 Feb 26 (3): 637-649. Sennblad Bengt, Basu Saonli, Mazur Johanna, Suchon Pierre, Martinez-Perez Angel, van Hylckama Vlieg Astrid, Truong Vinh, Li Yuhuang, Gådin Jesper R, Tang Weihong, Grossman Vera, de Haan Hugoline G, Handin Niklas, Silveira Angela, Souto Juan Carlos, Franco-Cereceda Anders, Morange Pierre-Emmanuel, Gagnon France, Soria Jose Manuel, Eriksson Per, Hamsten Anders, Maegdefessel Lars, Rosendaal Frits R, Wild Philipp, Folsom Aaron R, Trégouët David-Alexandre, Sabater-Lleal Mar |
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
Nature genetics 2018 04 50 (4): 524-537. Malik Rainer, Chauhan Ganesh, Traylor Matthew, Sargurupremraj Muralidharan, Okada Yukinori, Mishra Aniket, Rutten-Jacobs Loes, Giese Anne-Katrin, van der Laan Sander W, Gretarsdottir Solveig, Anderson Christopher D, Chong Michael, Adams Hieab H H, Ago Tetsuro, Almgren Peter, Amouyel Philippe, Ay Hakan, Bartz Traci M, Benavente Oscar R, Bevan Steve, Boncoraglio Giorgio B, Brown Robert D, Butterworth Adam S, Carrera Caty, Carty Cara L, Chasman Daniel I, Chen Wei-Min, Cole John W, Correa Adolfo, Cotlarciuc Ioana, Cruchaga Carlos, Danesh John, de Bakker Paul I W, DeStefano Anita L, den Hoed Marcel, Duan Qing, Engelter Stefan T, Falcone Guido J, Gottesman Rebecca F, Grewal Raji P, Gudnason Vilmundur, Gustafsson Stefan, Haessler Jeffrey, Harris Tamara B, Hassan Ahamad, Havulinna Aki S, Heckbert Susan R, Holliday Elizabeth G, Howard George, Hsu Fang-Chi, Hyacinth Hyacinth I, Ikram M Arfan, Ingelsson Erik, Irvin Marguerite R, Jian Xueqiu, Jiménez-Conde Jordi, Johnson Julie A, Jukema J Wouter, Kanai Masahiro, Keene Keith L, Kissela Brett M, Kleindorfer Dawn O, Kooperberg Charles, Kubo Michiaki, Lange Leslie A, Langefeld Carl D, Langenberg Claudia, Launer Lenore J, Lee Jin-Moo, Lemmens Robin, Leys Didier, Lewis Cathryn M, Lin Wei-Yu, Lindgren Arne G, Lorentzen Erik, Magnusson Patrik K, Maguire Jane, Manichaikul Ani, McArdle Patrick F, Meschia James F, Mitchell Braxton D, Mosley Thomas H, Nalls Michael A, Ninomiya Toshiharu, O'Donnell Martin J, Psaty Bruce M, Pulit Sara L, Rannikmäe Kristiina, Reiner Alexander P, Rexrode Kathryn M, Rice Kenneth, Rich Stephen S, Ridker Paul M, Rost Natalia S, Rothwell Peter M, Rotter Jerome I, Rundek Tatjana, Sacco Ralph L, Sakaue Saori, Sale Michele M, Salomaa Veikko, Sapkota Bishwa R, Schmidt Reinhold, Schmidt Carsten O, Schminke Ulf, Sharma Pankaj, Slowik Agnieszka, Sudlow Cathie L M, Tanislav Christian, Tatlisumak Turgut, Taylor Kent D, Thijs Vincent N S, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Tiedt Steffen, Trompet Stella, Tzourio Christophe, van Duijn Cornelia M, Walters Matthew, Wareham Nicholas J, Wassertheil-Smoller Sylvia, Wilson James G, Wiggins Kerri L, Yang Qiong, Yusuf Salim, , , , , , Bis Joshua C, Pastinen Tomi, Ruusalepp Arno, Schadt Eric E, Koplev Simon, Björkegren Johan L M, Codoni Veronica, Civelek Mete, Smith Nicholas L, Trégouët David A, Christophersen Ingrid E, Roselli Carolina, Lubitz Steven A, Ellinor Patrick T, Tai E Shyong, Kooner Jaspal S, Kato Norihiro, He Jiang, van der Harst Pim, Elliott Paul, Chambers John C, Takeuchi Fumihiko, Johnson Andrew D, , , , , , , , , , , Sanghera Dharambir K, Melander Olle, Jern Christina, Strbian Daniel, Fernandez-Cadenas Israel, Longstreth W T, Rolfs Arndt, Hata Jun, Woo Daniel, Rosand Jonathan, Pare Guillaume, Hopewell Jemma C, Saleheen Danish, Stefansson Kari, Worrall Bradford B, Kittner Steven J, Seshadri Sudha, Fornage Myriam, Markus Hugh S, Howson Joanna M M, Kamatani Yoichiro, Debette Stephanie, Dichgans Mart |
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.
Blood 2019 Aug . Lindstrom Sara, Wang Lu, Smith Erin N, Gordon William, van Hylckama Vlieg Astrid, de Andrade Mariza, Brody Jennifer A, Pattee Jack W, Haessler Jeffrey, Brumpton Ben M, Chasman Daniel I, Suchon Pierre, Chen Ming-Huei, Turman Constance, Germain Marine, Wiggins Kerri L, MacDonald James, Braekkan Sigrid K, Armasu Sebastian M, Pankratz Nathan, Jackson Rebecca D, Nielsen Jonas B, Giulianini Franco, Puurunen Marja K, Ibrahim Manal, Heckbert Susan R, Damrauer Scott M, Natarajan Pradeep, Klarin Derek, de Vries Paul S, Sabater-Lleal Maria, Huffman Jennifer E, Bammler Theo K, Frazer Kelly A, McCauley Bryan M, Taylor Kent, Pankow James S, Reiner Alexander P, Gabrielsen Maiken E, Deleuze Jean-François, O'Donnell Chris J, Kim Jihye, McKnight Barbara, Kraft Peter, Hansen John-Bjarne, Rosendaal Frits R, Heit John A, Psaty Bruce M, Tang Weihong, Kooperberg Charles, Hveem Kristian, Ridker Paul M, Morange Pierre-Emmanuel, Johnson Andrew D, Kabrhel Christopher, Trégouët David-Alexandre, Smith Nicholas |
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease.
Nature genetics 2019 11 51 (11): 1574-1579. Klarin Derek, Busenkell Emma, Judy Renae, Lynch Julie, Levin Michael, Haessler Jeffery, Aragam Krishna, Chaffin Mark, Haas Mary, Lindström Sara, Assimes Themistocles L, Huang Jie, Min Lee Kyung, Shao Qing, Huffman Jennifer E, Kabrhel Christopher, Huang Yunfeng, Sun Yan V, Vujkovic Marijana, Saleheen Danish, Miller Donald R, Reaven Peter, DuVall Scott, Boden William E, Pyarajan Saiju, Reiner Alex P, Trégouët David-Alexandre, Henke Peter, Kooperberg Charles, Gaziano J Michael, Concato John, Rader Daniel J, Cho Kelly, Chang Kyong-Mi, Wilson Peter W F, Smith Nicholas L, O'Donnell Christopher J, Tsao Philip S, Kathiresan Sekar, Obi Andrea, Damrauer Scott M, Natarajan Pradeep, , |
A large-scale exome array analysis of venous thromboembolism.
Genetic epidemiology 2019 Jan . Lindström Sara, Brody Jennifer A, Turman Constance, Germain Marine, Bartz Traci M, Smith Erin N, Chen Ming-Huei, Puurunen Marja, Chasman Daniel, Hassler Jeffrey, Pankratz Nathan, Basu Saonli, Guan Weihua, Gyorgy Beata, Ibrahim Manal, Empana Jean-Philippe, Olaso Robert, Jackson Rebecca, Braekkan Sigrid K, McKnight Barbara, Deleuze Jean-Francois, O'Donnell Cristopher J, Jouven Xavier, Frazer Kelly A, Psaty Bruce M, Wiggins Kerri L, Taylor Kent, Reiner Alexander P, Heckbert Susan R, Kooperberg Charles, Ridker Paul, Hansen John-Bjarne, Tang Weihong, Johnson Andrew D, Morange Pierre-Emmanuel, Trégouët David A, Kraft Peter, Smith Nicholas L, Kabrhel Christopher, |
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology.
Blood 2019 Feb 133 (9): 967-977. de Vries Paul S, Sabater-Lleal Maria, Huffman Jennifer E, Marten Jonathan, Song Ci, Pankratz Nathan, Bartz Traci M, de Haan Hugoline G, Delgado Graciela E, Eicher John D, Martinez-Perez Angel, Ward-Caviness Cavin K, Brody Jennifer A, Chen Ming-Huei, de Maat Moniek P M, Frånberg Mattias, Gill Dipender, Kleber Marcus E, Rivadeneira Fernando, Soria José Manuel, Tang Weihong, Tofler Geoffrey H, Uitterlinden André G, van Hylckama Vlieg Astrid, Seshadri Sudha, Boerwinkle Eric, Davies Neil M, Giese Anne-Katrin, Ikram M Kamran, Kittner Steven J, McKnight Barbara, Psaty Bruce M, Reiner Alex P, Sargurupremraj Muralidharan, Taylor Kent D, , , Fornage Myriam, Hamsten Anders, März Winfried, Rosendaal Frits R, Souto Juan Carlos, Dehghan Abbas, Johnson Andrew D, Morrison Alanna C, O'Donnell Christopher J, Smith Nicholas |
Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study.
EBioMedicine 2020 Sep 59 102956. Yuan Shuai, Carter Paul, Bruzelius Maria, Vithayathil Mathew, Kar Siddhartha, Mason Amy M, Lin Ang, Burgess Stephen, Larsson Susanna |
A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling.
American journal of human genetics 2020 Jul . Rodriguez Benjamin A T, Bhan Arunoday, Beswick Andrew, Elwood Peter C, Niiranen Teemu J, Salomaa Veikko, , Trégouët David-Alexandre, Morange Pierre-Emmanuel, Civelek Mete, Ben-Shlomo Yoav, Schlaeger Thorsten, Chen Ming-Huei, Johnson Andrew |
Genome-Wide Association Meta-Analysis of Single-Nucleotide Polymorphisms and Symptomatic Venous Thromboembolism during Therapy for Acute Lymphoblastic Leukemia and Lymphoma in Caucasian Children.
Cancers 2020 May 12 (5): . Mateos Marion K, Tulstrup Morten, Quinn Michael Cj, Tuckuviene Ruta, Marshall Glenn M, Gupta Ramneek, Mayoh Chelsea, Wolthers Benjamin O, Barbaro Pasquale M, Ruud Ellen, Sutton Rosemary, Huttunen Pasi, Revesz Tamas, Trakymiene Sonata S, Barbaric Draga, Tedgård Ulf, Giles Jodie E, Alvaro Frank, Jonsson Olafur G, Mechinaud Françoise, Saks Kadri, Catchpoole Daniel, Kotecha Rishi S, Dalla-Pozza Luciano, Chenevix-Trench Georgia, Trahair Toby N, MacGregor Stuart, Schmiegelow Kje |
Kallikrein augments the anticoagulant function of the protein C system in thrombin generation.
Journal of thrombosis and haemostasis : JTH 2021 9 . Wan Jun, Vadaq Nadira, Konings Joke, Jaeger Martin, Kumar Vinod, de Laat Bas, Joosten Leo, Netea Mihai G, van der Ven Andre J, de Groot Philip G, de Mast Quirijn, Roest Ma |
Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism.
Thrombosis and haemostasis 2021 Feb . Herrera-Rivero Marisol, Stoll Monika, Hegenbarth Jana-Charlotte, Rühle Frank, Limperger Verena, Junker Ralf, Franke André, Hoffmann Per, Shneyder Maria, Stach Michael, Nowak-Göttl Ulri |
An assessment of the effect of the genotype on postoperative venous thromboembolism risk in 140,831 surgical patients.
Annals of medicine and surgery (2012) 2021 Nov 71 102938. A Christensen Mathias, Bonde Alexander, Sillesen Mart |
Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.
Journal of the American Heart Association 2021 Oct e022482. Leskelä Jaakko, Toppila Iiro, Härma Mari-Anne, Palviainen Teemu, Salminen Aino, Sandholm Niina, Pietiäinen Milla, Kopra Elisa, Pais de Barros Jean-Paul, , Lassenius Mariann I, Kumar Anmol, Harjutsalo Valma, Roslund Kajsa, Forsblom Carol, Loukola Anu, Havulinna Aki S, Lagrost Laurent, Salomaa Veikko, Groop Per-Henrik, Perola Markus, Kaprio Jaakko, Lehto Markku, Pussinen Pirkko |
Whole-exome sequencing of 14?389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Human molecular genetics 2022 May . Pankratz Nathan, Wei Peng, Brody Jennifer A, Chen Ming-Huei, de Vries Paul S, Huffman Jennifer E, Stimson Mary Rachel, Auer Paul L, Boerwinkle Eric, Cushman Mary, de Maat Moniek P M, Folsom Aaron R, Franco Oscar H, Gibbs Richard A, Haagenson Kelly K, Hofman Albert, Johnsen Jill M, Kovar Christie L, Kraaij Robert, McKnight Barbara, Metcalf Ginger A, Muzny Donna, Psaty Bruce M, Tang Weihong, Uitterlinden André G, van Rooij Jeroen G J, Dehghan Abbas, O'Donnell Christopher J, Reiner Alex P, Morrison Alanna C, Smith Nicholas |
Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations.
Journal of thrombosis and haemostasis : JTH 2022 3 20 (6): 1331-1349. Temprano-Sagrera Gerard, Sitlani Colleen M, Bone William P, Martin-Bornez Miguel, Voight Benjamin F, Morrison Alanna C, Damrauer Scott M, de Vries Paul S, Smith Nicholas L, Sabater-Lleal Mar |
Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke.
Neurology 2022 Aug . Jaworek Thomas, Xu Huichun, Gaynor Brady J, Cole John W, Rannikmae Kristiina, Stanne Tara M, Tomppo Liisa, Abedi Vida, Amouyel Philippe, Armstrong Nicole D, Attia John, Bell Steven, Benavente Oscar R, Boncoraglio Giorgio B, Butterworth Adam, , Carcel-Marquez Jara, Chen Zhengming, Chong Michael, Cruchaga Carlos, Cushman Mary, Danesh John, Debette Stephanie, Duggan David J, Durda Jon Peter, Engstrom Gunnar, Enzinger Chris, Faul Jessica D, Fecteau Natalie S, Fernandez-Cadenas Israel, Gieger Christian, Giese Anne-Katrin, Grewal Raji P, Grittner Ulrike, Havulinna Aki S, Heitsch Laura, Hochberg Marc C, Holliday Elizabeth, Hu Jie, Ilinca Andreea, , Irvin Marguerite R, Jackson Rebecca D, Jacob Mina A, Janssen Raquel Rabionet, Jimenez-Conde Jordi, Johnson Julie A, Kamatani Yoichiro, Kardia Sharon L, Koido Masaru, Kubo Michiaki, Lange Leslie, Lee Jin-Moo, Lemmens Robin, Levi Christopher R, Li Jiang, Li Liming, Lin Kuang, Lopez Haley, Luke Sothear, Maguire Jane, McArdle Patrick F, McDonough Caitrin W, Meschia James F, Metso Tiina, Muller-Nurasyid Martina, O'Connor Timothy D, O'Donnell Martin, Peddareddygari Leema R, Pera Joanna, Perry James A, Peters Annette, Putaala Jukka, Ray Debashree, Rexrode Kathryn, Ribases Marta, Rosand Jonathan, Rothwell Peter M, Rundek Tatjana, Ryan Kathleen A, Sacco Ralph L, Salomaa Veikko, Sanchez-Mora Cristina, Schmidt Reinhold, Sharma Pankaj, Slowik Agnieszka, Smith Jennifer A, Smith Nicholas L, Wassertheil-Smoller Sylvia, Soederholm Martin, Stine O C, Strbian Daniel, Sudlow Cathie L, Tatlisumak Turgut, Terao Chikashi, Thijs Vincent, Torres-Aguila Nuria P, Tregouet David-Alexandre, Tuladhar Anil M, Veldink Jan H, Walters Robin G, Weir David R, Woo Daniel, Worrall Bradford B, Hong Charles C, Ross Owen, Zand Ramin, Leeuw Frank-Erik de, Lindgren Arne G, Pare Guillaume, Anderson Christopher D, Markus Hugh S, Jern Christina, Malik Rainer, Dichgans Martin, Mitchell Braxton D, Kittner Steven J, |
Whole exome sequencing identifies genetic variants in Chinese Han pregnant women with venous thromboembolism.
Thrombosis research 2022 Mar 211 49-55. Shen Yupei, Zhang Yan, Xiong Ying, Zhang Zhiping, Zhang Baohua, Li Aihong, Zhang Zhaofeng, Ding Jing, Du Jing, Che Y |
Role of circulating polyunsaturated fatty acids on cardiovascular diseases risk: analysis using Mendelian randomization and fatty acid genetic association data from over 114,000 UK Biobank participants.
BMC medicine 2022 6 20 (1): 210. Borges Maria Carolina, Haycock Philip C, Zheng Jie, Hemani Gibran, Holmes Michael V, Davey Smith George, Hingorani Aroon D, Lawlor Deborah |
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