X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1103) 1103
rare variants (1096) 1096
humans (1016) 1016
genetics & heredity (625) 625
genome-wide association (461) 461
genetics (374) 374
genomics (372) 372
genetic variation (360) 360
female (357) 357
article (356) 356
male (335) 335
genome-wide association study (332) 332
genetic predisposition to disease (304) 304
genes (303) 303
polymorphism, single nucleotide (301) 301
genomes (299) 299
genotype (278) 278
analysis (274) 274
models, genetic (253) 253
genetic aspects (241) 241
phenotype (240) 240
mutation (237) 237
research (227) 227
gene frequency (225) 225
rare variant (207) 207
disease (203) 203
association (197) 197
risk (193) 193
genetic research (187) 187
computer simulation (178) 178
middle aged (169) 169
alleles (168) 168
adult (167) 167
mathematical & computational biology (167) 167
risk factors (167) 167
mutations (166) 166
case-control studies (165) 165
studies (155) 155
genetic association studies (145) 145
susceptibility (139) 139
biochemistry & molecular biology (134) 134
population (134) 134
common diseases (132) 132
neurosciences (129) 129
aged (127) 127
algorithms (127) 127
loci (122) 122
missing heritability (117) 117
sequence analysis, dna (115) 115
software (112) 112
common variants (111) 111
linkage disequilibrium (109) 109
polymorphism, single nucleotide - genetics (107) 107
genome, human (106) 106
gene (104) 104
schizophrenia (104) 104
haplotypes (103) 103
exome (102) 102
dna sequencing (96) 96
nucleotide sequencing (96) 96
multidisciplinary sciences (95) 95
pedigree (95) 95
research article (94) 94
animals (92) 92
biotechnology & applied microbiology (91) 91
heritability (91) 91
methods (91) 91
genome-wide association studies (89) 89
genome-wide association study - methods (89) 89
psychiatry (89) 89
single nucleotide polymorphisms (89) 89
medical research (88) 88
sequence analysis, dna - methods (88) 88
complex traits (87) 87
genetic predisposition to disease - genetics (86) 86
gwas (85) 85
high-throughput nucleotide sequencing (85) 85
usage (83) 83
common (82) 82
gene expression (82) 82
genetic variation - genetics (81) 81
next-generation sequencing (81) 81
genotype & phenotype (79) 79
phenotypes (78) 78
polymorphism (78) 78
identification (76) 76
population genetics (76) 76
susceptibility loci (75) 75
metaanalysis (74) 74
public, environmental & occupational health (74) 74
statistics (74) 74
human genetics (70) 70
diseases (69) 69
medicine (69) 69
quantitative trait loci (69) 69
genetic association (68) 68
medicine, experimental (68) 68
biology (67) 67
exome sequencing (67) 67
genetic variance (66) 66
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Genetic Epidemiology, ISSN 0741-0395, 10/2019, Volume 43, Issue 7, pp. 800 - 814
The power of genetic association analyses can be increased by jointly meta‐analyzing multiple correlated phenotypes. Here, we develop a meta‐analysis... 
kernel‐regression | multiple‐phenotypes | meta‐analysis | rare‐variant | region‐based | Phenotypes | Statistical analysis | Genotypes | Genetic analysis
Journal Article
Journal Article
Journal of Proteome Research, ISSN 1535-3893, 02/2017, Volume 16, Issue 2, pp. 999 - 1013
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 03/2019, Volume 104, Issue 3, pp. 410 - 421
Set-based analysis that jointly tests the association of variants in a group has emerged as a popular tool for analyzing rare and low-frequency variants in... 
variant set test | omnibus test | rare-variant analysis | whole-genome sequencing | TESTS | LIPOPROTEIN | GENETICS & HEREDITY | MISSING HERITABILITY | ASSOCIATION | GENOME | HIGHER CRITICISM | Genetic variation | Atherosclerosis | Physiological aspects | Genetic aspects | Research | Nucleotide sequencing | Risk factors | Methods | DNA sequencing
Journal Article