X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (23) 23
index medicus (19) 19
genetics & heredity (17) 17
female (13) 13
male (13) 13
research (13) 13
aged (11) 11
genetic predisposition to disease (11) 11
genome-wide association (11) 11
middle aged (11) 11
polymorphism, single nucleotide (11) 11
article (9) 9
genetic aspects (9) 9
genome-wide association study (9) 9
risk (9) 9
risk factors (9) 9
disease (8) 8
genetic variation (8) 8
adult (7) 7
aged, 80 and over (7) 7
cancer (7) 7
expression (7) 7
genetics (7) 7
immunology (7) 7
iceland (6) 6
physiological aspects (6) 6
case-control studies (5) 5
diagnosis (5) 5
genotype (5) 5
medical research (5) 5
single nucleotide polymorphisms (5) 5
biochemistry & molecular biology (4) 4
common variants (4) 4
confessions (4) 4
gene expression (4) 4
genes (4) 4
genomes (4) 4
health aspects (4) 4
identification (4) 4
original research (4) 4
psoriasis (4) 4
tumors (4) 4
usage (4) 4
alleles (3) 3
analysis (3) 3
apoptosis (3) 3
association studies (3) 3
base sequence (3) 3
breast cancer (3) 3
breast neoplasms - genetics (3) 3
breast neoplasms - metabolism (3) 3
carcinoma, basal cell - genetics (3) 3
cells (3) 3
criminal psychology (3) 3
disease susceptibility (3) 3
european continental ancestry group - genetics (3) 3
false confessions (3) 3
genetic markers (3) 3
immunologic diseases. allergy (3) 3
imputation (3) 3
loci (3) 3
melanoma (3) 3
men (3) 3
molecular sequence data (3) 3
multidisciplinary sciences (3) 3
mutation (3) 3
odds ratio (3) 3
police (3) 3
polymorphism, single nucleotide - genetics (3) 3
population (3) 3
prostatic neoplasms - genetics (3) 3
questioning (3) 3
receptor (3) 3
rna-seq (3) 3
sample size (3) 3
skin (3) 3
skin neoplasms - genetics (3) 3
studies (3) 3
susceptibility loci (3) 3
transcriptome (3) 3
urinary bladder neoplasms - genetics (3) 3
urothelial cell-carcinoma (3) 3
adenocarcinoma - genetics (2) 2
admission of guilt (2) 2
antibodies (2) 2
association studies articles (2) 2
autoimmunity (2) 2
b-cells (2) 2
basal-cell carcinoma (2) 2
behavior (2) 2
biomarkers (2) 2
bladder cancer (2) 2
breast neoplasms - pathology (2) 2
breast-cancer (2) 2
cardiovascular disease (2) 2
care and treatment (2) 2
cell biology (2) 2
cell line (2) 2
cells, cultured (2) 2
chromosomes (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Genetics, ISSN 1061-4036, 2007, Volume 39, Issue 7, pp. 865 - 869
Journal Article
Nature Genetics, ISSN 1061-4036, 2008, Volume 40, Issue 6, pp. 703 - 706
We carried out a genome-wide association study of breast cancer predisposition with replication and refinement studies involving 6,145 cases and 33,016... 
RISK | TUMORS | FGFR2 | GENETICS & HEREDITY | GENOME-WIDE ASSOCIATION | Carcinoma, Ductal, Breast - genetics | Carcinoma, Lobular - pathology | Receptors, Estrogen - metabolism | Adenocarcinoma - pathology | Prognosis | Receptor, Fibroblast Growth Factor, Type 2 - metabolism | Humans | Middle Aged | Carcinoma, Intraductal, Noninfiltrating - metabolism | Carcinoma, Medullary - metabolism | Male | Carcinoma, Intraductal, Noninfiltrating - genetics | Case-Control Studies | Breast Neoplasms - metabolism | Ribosomal Proteins - metabolism | Genetic Variation | Adenocarcinoma - metabolism | Carcinoma, Lobular - genetics | Aged, 80 and over | Adult | Carcinoma, Ductal, Breast - pathology | Female | Adenocarcinoma - genetics | Carcinoma, Ductal, Breast - metabolism | Chromosomes, Human, Pair 5 - genetics | Genetic Predisposition to Disease | Carcinoma, Medullary - genetics | Ribosomal Proteins - genetics | Carcinoma, Medullary - pathology | Breast Neoplasms - genetics | Carcinoma, Intraductal, Noninfiltrating - pathology | International Agencies | Breast Neoplasms - pathology | Aged | Carcinoma, Lobular - metabolism | Polymorphism, Single Nucleotide | Receptor, Fibroblast Growth Factor, Type 2 - genetics | Apoptosis | Cohort Studies | Receptors | Estrogen | Physiological aspects | Breast cancer | Genetic aspects | Single nucleotide polymorphisms | Research | Diagnosis | Risk factors | Genetic markers | Progesterone | Multivariate analysis | Gene expression | Chromosomes
Journal Article
Nature Genetics, ISSN 1061-4036, 2012, Volume 44, Issue 12, pp. 1326 - 1329
Journal Article
Nature Genetics, ISSN 1061-4036, 2008, Volume 40, Issue 11, pp. 1307 - 1312
Journal Article
Nature Genetics, ISSN 1061-4036, 2009, Volume 41, Issue 8, pp. 909 - 914
Journal Article
by Stacey, S.N and Sulem, P and Jonasdottir, A and Masson, G and Gudmundsson, J and Gudbjartsson, D.F and Magnusson, O.T and Gudjonsson, S.A and Sigurgeirsson, B and Thorisdottir, K and Ragnarsson, R and Benediktsdottir, K.R and Nexo, B.A and Tjonneland, A and Overvad, K and Rudnai, P and Gurzau, E and Koppova, K and Hemminki, K and Corredera, C and Fuentelsaz, V and Grasa, P and Navarrete, S and Fuertes, F and Garcia-Prats, M.D and Sanambrosio, E and Panadero, A and Juan, A. de and Garcia, A and Rivera, F and Planelles, D and Soriano, V and Requena, C and Aben, K.K.H and Rossum, M.M. van and Cremers, R.G.H.M and Oort, I.M. van and Spronsen, D.J. van and Schalken, J.A and Peters, W.H.M and Helfand, B.T and Donovan, J.L and Hamdy, F.C and Badescu, D and Coeanu, O and Jinga, M and Csiki, I.E and Constantinescu, V and Badea, P and Mates, I.N and Dinu, D.E and Constantin, A and Mates, D and Kristjansdottir, S and Agnarsson, B.A and Jonsson, E and Barkardottir, R.B and Einarsson, G.V and Sigurdsson, F and Moller, P.H and Stefansson, T and Valdimarsson, T and Johannsson, O.T and Sigurdsson, H and Jonsson, T and Jonasson, J.G and Tryggvadottir, L and Rice, T and Hansen, H.M and Xiao, Y and Lachance, D.H and Kosel, M.L and Decker, P.A and Thorleifsson, G and Johannsdottir, H and Helgadottir, H.T and Sigurdsson, A and Steinthorsdottir, V and Lindblom, A and Sandler, R.S and Keku, T.O and Banasik, K and Jorgensen, T and Witte, D.R and Hansen, T and Pedersen, O and Jinga, V and Neal, D.E and Catalona, W.J and Wrensch, M and Wiencke, J and Jenkins, R.B and Nagore, E and Vogel, U and Kiemeney, L.A.L.M and Kumar, R and Mayordomo, J.I and Olafsson, J.H and et al and Swedish Low-Risk Colorectal Canc and Swedish Low-risk Colorectal Cancer Study Group and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm and Centrum för klinisk forskning, Västerås
Nature Genetics, ISSN 1061-4036, 2011, Volume 43, Issue 11, pp. 1098 - 1103
Journal Article
Nature Genetics, ISSN 1061-4036, 2011, Volume 43, Issue 11, pp. 1127 - 1130
We tested 16 million SNPs, identified through whole-genome sequencing of 457 Icelanders, for association with gout and serum uric acid levels. Genotypes were... 
GENOTYPES | SLC2A9 | URATE | IMPUTATION | METABOLISM | GENETICS & HEREDITY | CARDIOVASCULAR-DISEASE | RISK | CANCER | GENOME-WIDE ASSOCIATION | FAMILY | Gout - genetics | Polymorphism, Single Nucleotide | Uric Acid - blood | Mutation, Missense | Humans | Iceland | Urine | Genes | Genomes
Journal Article
Nature Communications, ISSN 2041-1723, 2017, Volume 8, Issue 1, p. 14517
Journal Article
Science Translational Medicine, ISSN 1946-6234, 2010, Volume 2, Issue 62, pp. 62ra92 - 62ra92
Journal Article