X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (467) 467
Publication (35) 35
Book Chapter (4) 4
Newspaper Article (4) 4
Patent (3) 3
Book / eBook (2) 2
Dissertation (2) 2
Magazine Article (2) 2
Book Review (1) 1
Conference Proceeding (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (229) 229
female (160) 160
male (139) 139
middle aged (102) 102
genetics (91) 91
risk factors (91) 91
adult (90) 90
genetics & heredity (89) 89
aged (87) 87
genome-wide association study (85) 85
medical and health sciences (70) 70
medicin och hälsovetenskap (69) 69
polymorphism, single nucleotide (69) 69
genome-wide association (65) 65
research (61) 61
genomes (60) 60
genetic aspects (59) 59
metaanalysis (54) 54
disease (53) 53
epidemiology (53) 53
genotype (52) 52
phenotype (51) 51
risk (50) 50
african americans - genetics (44) 44
loci (44) 44
genomics (43) 43
studies (43) 43
analysis (42) 42
mortality (42) 42
young adult (42) 42
abridged index medicus (41) 41
aged, 80 and over (38) 38
genetic predisposition to disease (38) 38
adolescent (37) 37
cardiovascular disease (37) 37
genetic variation (35) 35
medical genetics (35) 35
medicinsk genetik (35) 35
african americans (34) 34
alleles (34) 34
basic medicine (33) 33
health aspects (33) 33
klinisk medicin (33) 33
medicinska och farmaceutiska grundvetenskaper (33) 33
biochemistry & molecular biology (32) 32
clinical medicine (32) 32
population (32) 32
european continental ancestry group - genetics (31) 31
genome-wide association studies (31) 31
public health (31) 31
animals (30) 30
cohort studies (30) 30
association (29) 29
genes (29) 29
multidisciplinary sciences (29) 29
gene frequency (28) 28
genetic loci (28) 28
lipids (28) 28
polymorphism, single nucleotide - genetics (28) 28
atherosclerosis (27) 27
body mass index (27) 27
cholesterol (27) 27
health sciences (27) 27
meta-analysis (27) 27
cardiovascular diseases (26) 26
age (25) 25
gene expression (25) 25
medicine, general & internal (25) 25
case-control studies (24) 24
prevalence (24) 24
medical research (23) 23
variants (23) 23
genetic research (22) 22
hematology (22) 22
quantitative trait loci (22) 22
cardiovascular diseases - genetics (21) 21
coronary-heart-disease (21) 21
diabetes (21) 21
inflammation (21) 21
prospective studies (21) 21
cancer (20) 20
child (20) 20
medicine (20) 20
usage (20) 20
association studies (19) 19
cardiac & cardiovascular systems (19) 19
expression (19) 19
health (19) 19
mutation (19) 19
blood pressure (18) 18
coronary artery disease (18) 18
coronary heart disease (18) 18
design (18) 18
genome-wide association study - methods (18) 18
health risks (18) 18
proteins (18) 18
peripheral vascular disease (17) 17
risk-factors (17) 17
stroke (17) 17
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The New England journal of medicine, ISSN 1533-4406, 2016, Volume 374, Issue 12, pp. 1134 - 1144
Journal Article
by Holmes, Michael V and Dale, Caroline E and Zuccolo, Luisa and Silverwood, Richard J and Guo, Yiran and Ye, Zheng and Prieto-Merino, David and Dehghan, Abbas and Trompet, Stella and Wong, Andrew and Cavadino, Alana and Drogan, Dagmar and Padmanabhan, Sandosh and Li, Shanshan and Yesupriya, Ajay and Leusink, Maarten and Sundstrom, Johan and Hubacek, Jaroslav A and Pikhart, Hynek and Swerdlow, Daniel I and Panayiotou, Andrie G and Borinskaya, Svetlana A and Finan, Chris and Shah, Sonia and Kuchenbaecker, Karoline B and Shah, Tina and Engmann, Jorgen and Folkersen, Lasse and Eriksson, Per and Ricceri, Fulvio and Melander, Olle and Sacerdote, Carlotta and Gamble, Dale M and Rayaprolu, Sruti and Ross, Owen A and McLachlan, Stela and Vikhireva, Olga and Sluijs, Ivonne and Scott, Robert A and Adamkova, Vera and Flicker, Leon and Bockxmeer, Frank M van and Power, Christine and Marques-Vidal, Pedro and Meade, Tom and Marmot, Michael G and Ferro, Jose M and Paulos-Pinheiro, Sofia and Humphries, Steve E and Talmud, Philippa J and Leach, Irene Mateo and Verweij, Niek and Linneberg, Allan and Skaaby, Tea and Doevendans, Pieter A and Cramer, Maarten J and Harst, Pim van der and Klungel, Olaf H and Dowling, Nicole F and Dominiczak, Anna F and Kumari, Meena and Nicolaides, Andrew N and Weikert, Cornelia and Boeing, Heiner and Ebrahim, Shah and Gaunt, Tom R and Price, Jackie F and Lannfelt, Lars and Peasey, Anne and Kubinova, Ruzena and Pajak, Andrzej and Malyutina, Sofia and Voevoda, Mikhail I and Tamosiunas, Abdonas and Maitland-van der Zee, Anke H and Norman, Paul E and Hankey, Graeme J and Bergmann, Manuela M and Hofman, Albert and Franco, Oscar H and Cooper, Jackie and Palmen, Jutta and Spiering, Wilko and Jong, Pim A de and Kuh, Diana and Hardy, Rebecca and Uitterlinden, Andre G and Ikram, M Arfan and Ford, Ian and Hyppönen, Elina and Almeida, Osvaldo P and Wareham, Nicholas J and Khaw, Kay-Tee and Hamsten, Anders and Husemoen, Lise Lotte N and Tjønneland, Anne and Tolstrup, Janne S and Rimm, Eric and Beulens, Joline W J and Verschuren, W M Monique and ... and on behalf of The InterAct Consortium and InterAct Consortium and IMPROVE Study Grp
BMJ : British Medical Journal, ISSN 1756-1833, 7/2014, Volume 349, Issue jul10 6, pp. g4164 - g4164
Journal Article
by Webb, Thomas R and Erdmann, Jeanette and Stirrups, Kathleen E and Stitziel, Nathan O and Masca, Nicholas G.D and Jansen, Henning and Kanoni, Stavroula and Nelson, Christopher P and Ferrario, Paola G and König, Inke R and Eicher, John D and Johnson, Andrew D and Hamby, Stephen E and Betsholtz, Christer and Ruusalepp, Arno and Franzén, Oscar and Schadt, Eric E and Björkegren, Johan L.M and Weeke, Peter E and Auer, Paul L and Schick, Ursula M and Lu, Yingchang and Zhang, He and Dube, Marie-Pierre and Goel, Anuj and Farrall, Martin and Peloso, Gina M and Won, Hong-Hee and Do, Ron and van Iperen, Erik and Kruppa, Jochen and Mahajan, Anubha and Scott, Robert A and Willenborg, Christina and Braund, Peter S and van Capelleveen, Julian C and Doney, Alex S.F and Donnelly, Louise A and Asselta, Rosanna and Merlini, Pier A and Duga, Stefano and Marziliano, Nicola and Denny, Josh C and Shaffer, Christian and El-Mokhtari, Nour Eddine and Franke, Andre and Heilmann, Stefanie and Hengstenberg, Christian and Hoffmann, Per and Holmen, Oddgeir L and Hveem, Kristian and Jansson, Jan-Håkan and Jöckel, Karl-Heinz and Kessler, Thorsten and Kriebel, Jennifer and Laugwitz, Karl L and Marouli, Eirini and Martinelli, Nicola and McCarthy, Mark I and Van Zuydam, Natalie R and Meisinger, Christa and Esko, Tõnu and Mihailov, Evelin and Escher, Stefan A and Alver, Maris and Moebus, Susanne and Morris, Andrew D and Virtamo, Jarma and Nikpay, Majid and Olivieri, Oliviero and Provost, Sylvie and AlQarawi, Alaa and Robertson, Neil R and Akinsansya, Karen O and Reilly, Dermot F and Vogt, Thomas F and Yin, Wu and Asselbergs, Folkert W and Kooperberg, Charles and Jackson, Rebecca D and Stahl, Eli and Müller-Nurasyid, Martina and Strauch, Konstantin and Varga, Tibor V and Waldenberger, Melanie and Zeng, Lingyao and Chowdhury, Rajiv and Salomaa, Veikko and Ford, Ian and Jukema, J. Wouter and Amouyel, Philippe and Kontto, Jukka and Nordestgaard, Børge G and Ferrières, Jean and Saleheen, Danish and Sattar, Naveed and Surendran, Praveen and Wagner, Aline and Young, Robin and Howson, Joanna M.M and ... and Wellcome Trust Case Control Consortium and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators and MORGAM Investigators and Wellcome Trust Case Control and Myocardial Infarction Genetics
Journal of the American College of Cardiology, ISSN 0735-1097, 2017, Volume 69, Issue 7, pp. 823 - 836
...Over the past decade, genome-wide association studies (GWAS) have identified several thousand robust associations (p < 5 × 10−8 ) for a range of human traits... 
Cardiovascular | Internal Medicine | expression quantitative trait loci | genetics | genome-wide association | single nucleotide polymorphism | cholesteryl ester transfer protein | SR-BI | CARDIAC & CARDIOVASCULAR SYSTEMS | METAANALYSIS | CETP MASS | SUSCEPTIBILITY | RISK | PHOSPHOLIPASE A | VARIANT | SCAVENGER RECEPTOR | ABDOMINAL AORTIC-ANEURYSM | Genome-Wide Association Study | Gene Frequency | Humans | Coronary Artery Disease - genetics | Female | Male | Coronary Artery Disease - epidemiology | Genetic Pleiotropy | Polymorphism, Single Nucleotide | Genetic Loci | Odds Ratio | Case-Control Studies | Coronary heart disease | Analysis | Genealogy | Cardiovascular disease | Genomes | Metabolism | Gene expression | Blood | Risk factors | Studies | Celiac disease | Lipoproteins | Coronary vessels | Rheumatoid arthritis | Quality control | Calcification | Diabetes | Bioinformatics | LD, linkage disequilibrium | CETP, cholesteryl ester transfer protein | eQTL, expression quantitative trait locus | CAD, coronary artery disease | GWAS, genome-wide association study | BMI, body mass index | SNP, single nucleotide polymorphism | HDL, high-density lipoprotein | LDL, low-density lipoprotein | Original Investigation | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
Journal Article
by Tragante, Vinicius and Barnes, Michael R and Ganesh, Santhi K and Lanktree, Matthew B and Guo, Wei and Franceschini, Nora and Smith, Erin N and Johnson, Toby and Holmes, Michael V and Padmanabhan, Sandosh and Karczewski, Konrad J and Almoguera, Berta and Barnard, John and Baumert, Jens and Chang, Yen-Pei Christy and Elbers, Clara C and Farrall, Martin and Fischer, Mary E and Gaunt, Tom R and Gho, Johannes M.I.H and Gieger, Christian and Goel, Anuj and Gong, Yan and Isaacs, Aaron and Kleber, Marcus E and Leach, Irene Mateo and McDonough, Caitrin W and Meijs, Matthijs F.L and Melander, Olle and Nelson, Christopher P and Nolte, Ilja M and Pankratz, Nathan and Price, Tom S and Shaffer, Jonathan and Shah, Sonia and Tomaszewski, Maciej and van der Most, Peter J and Van Iperen, Erik P.A and Vonk, Judith M and Witkowska, Kate and Wong, Caroline O.L and Zhang, Li and Beitelshees, Amber L and Berenson, Gerald S and Bhatt, Deepak L and Brown, Morris and Burt, Amber and Cooper-DeHoff, Rhonda M and Connell, John M and Cruickshanks, Karen J and Curtis, Sean P and Davey-Smith, George and Delles, Christian and Gansevoort, Ron T and Guo, Xiuqing and Haiqing, Shen and Hastie, Claire E and Hofker, Marten H and Hovingh, G. Kees and Kim, Daniel S and Kirkland, Susan A and Klein, Barbara E and Klein, Ronald and Li, Yun R and Maiwald, Steffi and Newton-Cheh, Christopher and O’Brien, Eoin T and Onland-Moret, N. Charlotte and Palmas, Walter and Parsa, Afshin and Penninx, Brenda W and Pettinger, Mary and Vasan, Ramachandran S and Ranchalis, Jane E and M Ridker, Paul and Rose, Lynda M and Sever, Peter and Shimbo, Daichi and Steele, Laura and Stolk, Ronald P and Thorand, Barbara and Trip, Mieke D and van Duijn, Cornelia M and Verschuren, W. Monique and Wijmenga, Cisca and Wyatt, Sharon and Young, J. Hunter and Zwinderman, Aeilko H and Bezzina, Connie R and Boerwinkle, Eric and Casas, Juan P and Caulfield, Mark J and Chakravarti, Aravinda and Chasman, Daniel I and Davidson, Karina W and Doevendans, Pieter A and Dominiczak, Anna F and FitzGerald, Garret A and Gums, John G and Fornage, Myriam and ...
American journal of human genetics, ISSN 0002-9297, 2014, Volume 94, Issue 3, pp. 349 - 360
Journal Article
by Asselbergs, Folkert W and Guo, Yiran and van Iperen, Erik P.A and Sivapalaratnam, Suthesh and Tragante, Vinicius and Lanktree, Matthew B and Lange, Leslie A and Almoguera, Berta and Appelman, Yolande E and Barnard, John and Baumert, Jens and Beitelshees, Amber L and Bhangale, Tushar R and Chen, Yii-Der Ida and Gaunt, Tom R and Gong, Yan and Hopewell, Jemma C and Johnson, Toby and Kleber, Marcus E and Langaee, Taimour Y and Li, Mingyao and Li, Yun R and Liu, Kiang and McDonough, Caitrin W and Meijs, Matthijs F.L and Middelberg, Rita P.S and Musunuru, Kiran and Nelson, Christopher P and O’Connell, Jeffery R and Padmanabhan, Sandosh and Pankow, James S and Pankratz, Nathan and Rafelt, Suzanne and Rajagopalan, Ramakrishnan and Romaine, Simon P.R and Schork, Nicholas J and Shaffer, Jonathan and Shen, Haiqing and Smith, Erin N and Tischfield, Sam E and van der Most, Peter J and van Vliet-Ostaptchouk, Jana V and Verweij, Niek and Volcik, Kelly A and Zhang, Li and Bailey, Kent R and Bailey, Kristian M and Bauer, Florianne and Boer, Jolanda M.A and Braund, Peter S and Burt, Amber and Burton, Paul R and Buxbaum, Sarah G and Chen, Wei and Cooper-DeHoff, Rhonda M and Cupples, L. Adrienne and deJong, Jonas S and Delles, Christian and Duggan, David and Fornage, Myriam and Furlong, Clement E and Glazer, Nicole and Gums, John G and Hastie, Claire and Holmes, Michael V and Illig, Thomas and Kirkland, Susan A and Kivimaki, Mika and Klein, Ronald and Klein, Barbara E and Kooperberg, Charles and Kottke-Marchant, Kandice and Kumari, Meena and LaCroix, Andrea Z and Mallela, Laya and Murugesan, Gurunathan and Ordovas, Jose and Ouwehand, Willem H and Post, Wendy S and Saxena, Richa and Scharnagl, Hubert and Schreiner, Pamela J and Shah, Tina and Shields, Denis C and Shimbo, Daichi and Srinivasan, Sathanur R and Stolk, Ronald P and Swerdlow, Daniel I and Taylor, Herman A and Topol, Eric J and Toskala, Elina and van Pelt, Joost L and van Setten, Jessica and Yusuf, Salim and Whittaker, John C and Zwinderman, A.H and Anand, Sonia S and Balmforth, Anthony J and Berenson, Gerald S and Bezzina, Connie R and ... and LifeLines Cohort Study
American journal of human genetics, ISSN 0002-9297, 2012, Volume 91, Issue 5, pp. 823 - 838
Journal Article
by Crosby, Jacy and Peloso, Gina M and Auer, Paul L and Crosslin, David R and Stitziel, Nathan O and Lange, Leslie A and Lu, Yingchang and Tang, Zheng-Zheng and Zhang, He and Hindy, George and Masca, Nicholas and Stirrups, Kathleen and Kanoni, Stavroula and Do, Ron and Jun, Goo and Hu, Youna and Kang, Hyun Min and Xue, Chenyi and Goel, Anuj and Farrall, Martin and Duga, Stefano and Merlini, Pier Angelica and Asselta, Rosanna and Girelli, Domenico and Olivieri, Oliviero and Martinelli, Nicola and Yin, Wu and Reilly, Dermot and Speliotes, Elizabeth and Fox, Caroline S and Hveem, Kristian and Holmen, Oddgeir L and Nikpay, Majid and Farlow, Deborah N and Assimes, Themistocles L and Franceschini, Nora and Robinson, Jennifer and North, Kari E and Martin, Lisa W and DePristo, Mark and Gupta, Namrata and Escher, Stefan A and Jansson, Jan-Håkan and Van Zuydam, Natalie and Palmer, Colin N. A and Wareham, Nicholas and Koch, Werner and Meitinger, Thomas and Peters, Annette and Lieb, Wolfgang and Erbel, Raimund and Konig, Inke R and Kruppa, Jochen and Degenhardt, Franziska and Gottesman, Omri and Bottinger, Erwin P and O'Donnell, Christopher J and Psaty, Bruce M and Ballantyne, Christie M and Abecasis, Goncalo and Ordovas, Jose M and Melander, Olle and Watkins, Hugh and Orho-Melander, Marju and Ardissino, Diego and Loos, Ruth J. F and McPherson, Ruth and Willer, Cristen J and Erdmann, Jeanette and Hall, Alistair S and Samani, Nilesh J and Deloukas, Panos and Schunkert, Heribert and Wilson, James G and Kooperberg, Charles and Rich, Stephen S and Tracy, Russell P and Lin, Dan-Yu and Altshuler, David and Gabriel, Stacey and Nickerson, Deborah A and Jarvik, Gail P and Cupples, L. Adrienne and Reiner, Alex P and Boerwinkle, Eric and Kathiresan, Sekar and The TG and HDL Working Group of the Exome Sequencing Project, National Heart, Lung, and Blood Institute and Natl Heart Lung Blood Inst and Exome Sequencing Project and TG and HDL Working Group of the Exome Sequencing Project, National Heart, Lung, and Blood Institute
The New England journal of medicine, ISSN 1533-4406, 2014, Volume 371, Issue 1, pp. 22 - 31
Journal Article
Nature communications, ISSN 2041-1723, 2018, Volume 9, Issue 1, pp. 1 - 13
Journal Article