X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (135) 135
index medicus (135) 135
genetics & heredity (91) 91
genomes (74) 74
research (70) 70
genome-wide association (62) 62
genetics (59) 59
polymorphism, single nucleotide (55) 55
article (53) 53
genetic variation (48) 48
genome-wide association study (47) 47
studies (46) 46
genomics (44) 44
methods (44) 44
models, genetic (43) 43
genetic aspects (41) 41
genotype (40) 40
female (38) 38
population genetics (35) 35
male (33) 33
phenotype (33) 33
heritability (32) 32
schizophrenia (32) 32
gene expression (30) 30
genome-wide association study - methods (30) 30
genetic predisposition to disease (29) 29
polymorphism, single nucleotide - genetics (29) 29
disease (28) 28
genealogy (28) 28
genetic research (28) 28
case-control studies (27) 27
genetics, population (27) 27
variants (27) 27
linkage disequilibrium (26) 26
multidisciplinary sciences (26) 26
usage (26) 26
risk (25) 25
statistics (25) 25
genome, human (24) 24
single nucleotide polymorphisms (24) 24
genome-wide association studies (23) 23
genotype & phenotype (23) 23
alleles (22) 22
gene frequency (22) 22
haplotypes (22) 22
loci (21) 21
population (21) 21
risk factors (20) 20
algorithms (19) 19
complex traits (19) 19
european continental ancestry group - genetics (18) 18
computer simulation (17) 17
genes (17) 17
quantitative trait loci (17) 17
consortia (16) 16
estimates (15) 15
research article (15) 15
schizophrenia - genetics (15) 15
software (15) 15
susceptibility loci (15) 15
traits (15) 15
african americans (14) 14
analysis (14) 14
human genome (14) 14
identification and classification (14) 14
architecture (13) 13
body-mass index (13) 13
genetic diversity (13) 13
health aspects (13) 13
medical and health sciences (13) 13
medicin och hälsovetenskap (13) 13
metaanalysis (13) 13
adult (12) 12
body mass index (12) 12
chromosome mapping (12) 12
cohort studies (12) 12
common snps (12) 12
diseases (12) 12
genetic loci (12) 12
gwas (12) 12
human genetics (12) 12
middle aged (12) 12
partitioning heritability (12) 12
evolution, molecular (11) 11
genetics and genomics (11) 11
mental disorders (11) 11
biotechnology & applied microbiology (10) 10
common (10) 10
epidemiology (10) 10
gene (10) 10
genetic markers (10) 10
genetic predisposition to disease - genetics (10) 10
genetic variation - genetics (10) 10
human height (10) 10
inference (10) 10
mathematical & computational biology (10) 10
missing heritability (10) 10
principal component analysis (10) 10
selection, genetic (10) 10
single-nucleotide polymorphism (10) 10
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, 08/2019, Volume 51, Issue 8, pp. 1202 - 1204
[...]we analyzed genotypes imputed with the Haplotype Reference Consortium (HRC), a more comprehensive SNP set that produced higher likelihoods for each model... 
HERITABILITY | GENETICS & HEREDITY | Enrichment | Computer simulation | Bias | Single-nucleotide polymorphism | Epidemiology | Estimates | Population genetics | Empirical analysis | Consortia | Genetics | Software | Heritability | Public health | Genotypes | Methods | Index Medicus
Journal Article
Nature genetics, ISSN 1061-4036, 12/2018, Volume 50, Issue 12, pp. 1753 - 1753
In the version of this article originally published, there were errors in equations. In the HTML and PDF, the initial term of equation 10 was estimated GCP but... 
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2019, Volume 105, Issue 3, pp. 456 - 476
Complex traits and common diseases are extremely polygenic, their heritability spread across thousands of loci. One possible explanation is that thousands of... 
SLD4M | GWAS | negative selection | polygenicity | heritability | Index Medicus
Journal Article
Journal Article
Nature genetics, ISSN 1061-4036, 7/2018, Volume 50, Issue 7, pp. 906 - 908
Biobank-based genome-wide association studies are enabling exciting insights in complex trait genetics, but much uncertainty remains over best practices for... 
Journal Article
Genetic epidemiology, ISSN 0741-0395, 12/2017, Volume 41, Issue 8, pp. 811 - 823
Methods for genetic risk prediction have been widely investigated in recent years. However, most available training data involves European samples, and it is... 
type 2 diabetes | genome-wide association study | polygenic prediction | height
Journal Article
Nature genetics, ISSN 1061-4036, 11/2018, Volume 50, Issue 11, pp. 1600 - 1607
Common variant heritability has been widely reported to be concentrated in variants within cell-type-specific noncoding functional annotations, but little is... 
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2019, Volume 104, Issue 4, pp. 611 - 624
Regulatory elements, e.g., enhancers and promoters, have been widely reported to be enriched for disease and complex trait heritability. We investigated how... 
genetic architecture | enhancer | regulatory elements | promoter | heritability | ORIGIN | EVOLUTION | VARIANTS | GENE | ANNOTATION | GENETICS & HEREDITY | ARCHITECTURE | MISSING HERITABILITY | GENOME-WIDE ASSOCIATION | COMPLEX TRAIT | Usage | Promoters (Genetics) | Research | Nucleotide sequencing | Genetic regulation | DNA sequencing
Journal Article
Nature, ISSN 0028-0836, 7/2018, Volume 559, Issue 7714, pp. 350 - 355
The selective pressures that shape clonal evolution in healthy individuals are largely unknown. Here we investigate 8,342 mosaic chromosomal alterations (mCAs)... 
Journal Article
Proceedings: Biological Sciences, ISSN 0962-8452, 12/2015, Volume 282, Issue 1821, pp. 1 - 10
Susceptibility to common human diseases is influenced by both genetic and environmental factors. The explosive growth of genetic data, and the knowledge that... 
Review
Journal Article
Genetic Epidemiology, ISSN 0741-0395, 03/2019, Volume 43, Issue 2, pp. 180 - 188
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 01/2017, Volume 100, Issue 1, p. 31
Journal Article
Genetics, 07/2014, Volume 197, Issue 3, p. 1045
Using a reduced subset of SNPs in a linear mixed model can improve power for genome-wide association studies, yet this can result in insufficient correction... 
Genetics, Population | Genome-Wide Association Study | Confounding Factors (Epidemiology) | Humans | Polymorphism, Single Nucleotide - genetics | Linear Models | Multiple Sclerosis - genetics | Models, Genetic | Principal Component Analysis
Journal Article
PLoS Genetics, ISSN 1553-7390, 05/2013, Volume 9, Issue 5, pp. e1003520 - e1003520
Important knowledge about the determinants of complex human phenotypes can be obtained from the estimation of heritability, the fraction of phenotypic... 
HEART | GENETIC-VARIATION | HUMAN HEIGHT | DISEASES | VARIANTS | COMMON SNPS | GENETICS & HEREDITY | MISSING HERITABILITY | DESCENT | GENOME-WIDE ASSOCIATION | AGE | Quantitative genetics | Epigenetic inheritance | Phenotype | Genealogy | Research | Index Medicus | Studies | Genotype & phenotype | Liability | Genetics | Cardiovascular disease | Genomes | Estimates | Methods | Siblings
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 11/2016, Volume 99, Issue 5, p. 1130
Journal Article
20.