X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (67) 67
index medicus (66) 66
female (52) 52
male (41) 41
aged (34) 34
middle aged (33) 33
risk factors (33) 33
polymorphism, single nucleotide (30) 30
genome-wide association study (26) 26
african americans (21) 21
epidemiology (21) 21
genetics & heredity (21) 21
genetics (19) 19
risk (19) 19
african americans - genetics (18) 18
genomes (17) 17
genomics (17) 17
metaanalysis (17) 17
research (17) 17
cardiovascular-disease (16) 16
genetic predisposition to disease (16) 16
genome-wide association (16) 16
loci (15) 15
population (15) 15
adult (14) 14
analysis (13) 13
cholesterol (13) 13
genetic aspects (13) 13
medical research (13) 13
cohort studies (12) 12
disease (12) 12
genetic variation (12) 12
abridged index medicus (11) 11
genetic association studies (11) 11
haplotypes (11) 11
mortality (11) 11
stroke (11) 11
aged, 80 and over (10) 10
atherosclerosis (10) 10
design (10) 10
european continental ancestry group - genetics (10) 10
genome-wide association studies (10) 10
public, environmental & occupational health (10) 10
cardiovascular disease (9) 9
cardiovascular diseases (9) 9
clinical neurology (9) 9
gene frequency (9) 9
genetic loci (9) 9
health aspects (9) 9
human genetics (9) 9
linkage disequilibrium (9) 9
medical and health sciences (9) 9
peripheral vascular disease (9) 9
population genetics (9) 9
research article (9) 9
association (8) 8
cardiovascular diseases - genetics (8) 8
common variants (8) 8
coronary-heart-disease (8) 8
genotype (8) 8
health (8) 8
multidisciplinary sciences (8) 8
stroke - genetics (8) 8
studies (8) 8
wide association (8) 8
womens health (8) 8
biochemistry & molecular biology (7) 7
body mass index (7) 7
cancer (7) 7
coronary-artery-disease (7) 7
european continental ancestry group (7) 7
genetic research (7) 7
inflammation (7) 7
lipids (7) 7
lipoproteins (7) 7
medicin och hälsovetenskap (7) 7
meta-analysis (7) 7
physiological aspects (7) 7
quantitative trait loci (7) 7
science (7) 7
single nucleotide polymorphisms (7) 7
single-nucleotide polymorphism (7) 7
variants (7) 7
women (7) 7
adolescent (6) 6
alleles (6) 6
atherosclerosis risk (6) 6
biology (6) 6
c-reactive protein (6) 6
cholesterol, ldl - blood (6) 6
complex traits (6) 6
computational biology (6) 6
gene expression (6) 6
hematology (6) 6
hispanic americans - genetics (6) 6
ischemic-stroke (6) 6
medicine (6) 6
minority & ethnic groups (6) 6
myocardial-infarction (6) 6
neurology (6) 6
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


PLoS genetics, ISSN 1553-7404, 2011, Volume 7, Issue 6, p. e1002138
Journal Article
Aging (Albany, NY.), ISSN 1945-4589, 2016, Volume 8, Issue 9, pp. 1844 - 1865
textabstractEstimates of biological age based on DNA methylation patterns, often referred to as "epigenetic age", "DNAm age", have been shown to be robust... 
DNA methylation | Epigenetics | All-cause mortality | Epigenetic clock | Lifespan | Mortality | lifespan | CANCER | epigenetics | CELL BIOLOGY | all-cause mortality | DISEASE | mortality | COHORT | EPIDEMIOLOGY | BRAIN | epigenetic clock | BLOOD | LIFE
Journal Article
PloS one, ISSN 1932-6203, 2016, Volume 11, Issue 3, p. e0144997
Journal Article
by Wu, Ying and Waite, Lindsay L and Jackson, Anne U and Sheu, Wayne H-H and Buyske, Steven and Absher, Devin and Arnett, Donna K and Boerwinkle, Eric and Bonnycastle, Lori L and Carty, Cara L and Cheng, Iona and Cochran, Barbara and Croteau-Chonka, Damien C and Dumitrescu, Logan and Eaton, Charles B and Franceschini, Nora and Guo, Xiuqing and Henderson, Brian E and Hindorff, Lucia A and Kim, Eric and Kinnunen, Leena and Komulainen, Pirjo and Lee, Wen-Jane and Le Marchand, Loic and Lin, Yi and Lindström, Jaana and Lingaas-Holmen, Oddgeir and Mitchell, Sabrina L and Narisu, Narisu and Robinson, Jennifer G and Schumacher, Fred and Stančáková, Alena and Sundvall, Jouko and Sung, Yun-Ju and Swift, Amy J and Wang, Wen-Chang and Wilkens, Lynne and Wilsgaard, Tom and Young, Alicia M and Adair, Linda S and Ballantyne, Christie M and Bůžková, Petra and Chakravarti, Aravinda and Collins, Francis S and Duggan, David and Feranil, Alan B and Ho, Low-Tone and Hung, Yi-Jen and Hunt, Steven C and Hveem, Kristian and Juang, Jyh-Ming J and Kesäniemi, Antero Y and Kuusisto, Johanna and Laakso, Markku and Lakka, Timo A and Lee, I-Te and Leppert, Mark F and Matise, Tara C and Moilanen, Leena and Njølstad, Inger and Peters, Ulrike and Quertermous, Thomas and Rauramaa, Rainer and Rotter, Jerome I and Saramies, Jouko and Tuomilehto, Jaakko and Uusitupa, Matti and Wang, Tzung-Dau and Boehnke, Michael and Haiman, Christopher A and Chen, Yii-Der I and Kooperberg, Charles and Assimes, Themistocles L and Crawford, Dana C and Hsiung, Chao A and North, Kari E and Mohlke, Karen L
PLoS genetics, ISSN 1553-7404, 2013, Volume 9, Issue 3, p. e1003379
Genome-wide association studies (GWAS) have identified similar to 100 loci associated with blood lipid levels, but much of the trait heritability remains... 
COMMON VARIANTS | DENSITY-LIPOPROTEIN CHOLESTEROL | FUNCTIONAL POLYMORPHISM | GENE | GENOTYPE IMPUTATION | GENETICS & HEREDITY | RISK | LIPASE | COMPLEX TRAITS | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Apolipoprotein A-V | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Apolipoproteins A - genetics | Lipoproteins, HDL - genetics | Lipoproteins, HDL - blood | Humans | African Americans - genetics | Cholesterol, HDL - genetics | Lipoproteins, LDL - genetics | Proprotein Convertases - genetics | Cholesterol, LDL - genetics | Serine Endopeptidases - genetics | Triglycerides - blood | Cholesterol, HDL - blood | Cholesterol, LDL - blood | Triglycerides - genetics | Lipoproteins, LDL - blood | Proprotein Convertase 9 | Quantitative genetics | Genetic variation | Physiological aspects | Cholesterol, LDL | Genetic aspects | Research | Population genetics | Health aspects | Medisinsk genetikk: 714 | VDP | Basic medical, dental and veterinary science disciplines: 710 | Medical molecular biology: 711 | Medical genetics: 714 | Medisinske Fag: 700 | Medisinsk molekylærbiologi: 711 | Medical disciplines: 700 | Basale medisinske, odontologiske og veterinærmedisinske fag: 710 | Medical research | Genealogy | Womens health | African Americans | Population | Genomes | Gene loci | Gene expression | Epidemiology | Cholesterol
Journal Article
by Howson, Joanna M M and Zhao, Wei and Barnes, Daniel R and Ho, Weang-Kee and Young, Robin and Paul, Dirk S and Waite, Lindsay L and Freitag, Daniel F and Fauman, Eric B and Salfati, Elias L and Sun, Benjamin B and Eicher, John D and Johnson, Andrew D and Sheu, Wayne H H and Nielsen, Sune F and Lin, Wei-Yu and Surendran, Praveen and Malarstig, Anders and Wilk, Jemma B and Tybjærg-Hansen, Anne and Rasmussen, Katrine L and Kamstrup, Pia R and Deloukas, Panos and Erdmann, Jeanette and Kathiresan, Sekar and Samani, Nilesh J and Schunkert, Heribert and Watkins, Hugh and Do, Ron and Rader, Daniel J and Johnson, Julie A and Hazen, Stanley L and Quyyumi, Arshed A and Spertus, John A and Pepine, Carl J and Franceschini, Nora and Justice, Anne and Reiner, Alex P and Buyske, Steven and Hindorff, Lucia A and Carty, Cara L and North, Kari E and Kooperberg, Charles and Boerwinkle, Eric and Young, Kristin and Graff, Mariaelisa and Peters, Ulrike and Absher, Devin and Hsiung, Chao A and Lee, Wen-Jane and Taylor, Kent D and Chen, Ying-Hsiang and Lee, I-Te and Guo, Xiuqing and Chung, Ren-Hua and Hung, Yi-Jen and Rotter, Jerome I and Juang, Jyh-Ming J and Quertermous, Thomas and Wang, Tzung-Dau and Rasheed, Asif and Frossard, Philippe and Alam, Dewan S and Majumder, Abdulla al Shafi and Di Angelantonio, Emanuele and Chowdhury, Rajiv and Chen, Yii-Der Ida and Nordestgaard, Børge G and Assimes, Themistocles L and Danesh, John and Butterworth, Adam S and Saleheen, Danish and EPIC-CVD and CARDIoGRAMplusC4D
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 7, pp. 1113 - 1119
Journal Article
by Traylor, Matthew and Farrall, Martin and Holliday, Elizabeth G and Sudlow, Cathie and Hopewell, Jemma C and Cheng, Yu-Ching and Fornage, Myriam and Ikram, M Arfan and Malik, Rainer and Bevan, Steve and Thorsteinsdottir, Unnur and Nalls, Mike A and Longstreth, WT and Wiggins, Kerri L and Yadav, Sunaina and Parati, Eugenio A and DeStefano, Anita L and Worrall, Bradford B and Kittner, Steven J and Khan, Muhammad Saleem and Reiner, Alex P and Helgadottir, Anna and Achterberg, Sefanja and Fernandez-Cadenas, Israel and Abboud, Sherine and Schmidt, Reinhold and Walters, Matthew and Chen, Wei-Min and Ringelstein, E Bernd and O'Donnell, Martin and Ho, Weang Kee and Pera, Joanna and Lemmens, Robin and Norrving, Bo and Higgins, Peter and Benn, Marianne and Sale, Michele and Kuhlenbäumer, Gregor and Doney, Alexander S F and Vicente, Astrid M and Delavaran, Hossein and Algra, Ale and Davies, Gail and Oliveira, Sofia A and Palmer, Colin N A and Deary, Ian and Schmidt, Helena and Pandolfo, Massimo and Montaner, Joan and Carty, Cara and de Bakker, Paul I W and Kostulas, Konstantinos and Ferro, Jose M and van Zuydam, Natalie R and Valdimarsson, Einar and Nordestgaard, Børge G and Lindgren, Arne and Thijs, Vincent and Slowik, Agnieszka and Saleheen, Danish and Paré, Guillaume and Berger, Klaus and Thorleifsson, Gudmar and Hofman, Albert and Mosley, Thomas H and Mitchell, Braxton D and Furie, Karen and Clarke, Robert and Levi, Christopher and Seshadri, Sudha and Gschwendtner, Andreas and Boncoraglio, Giorgio B and Sharma, Pankaj and Bis, Joshua C and Gretarsdottir, Solveig and Psaty, Bruce M and Rothwell, Peter M and Rosand, Jonathan and Meschia, James F and Stefansson, Kari and Dichgans, Martin and Markus, Hugh S and The Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) and on behalf of the International Stroke Genetics Consortium and WTCCC 2 and Australian Stroke Genetics Collabo and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2)
Lancet neurology, ISSN 1474-4422, 2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
PloS one, ISSN 1932-6203, 2016, Volume 11, Issue 10, p. e0164132
Journal Article
PLoS Biology, ISSN 1544-9173, 09/2013, Volume 11, Issue 9, p. e1001661
Journal Article