| CommonMind Consortium |
cohort |
6 |
3 |
CMC, CMC dataset, CommonMind, CommonMind Consortium9 |
| common variants |
cohort |
75 |
62 |
543 common SNPs (MAF ≥ 0.05), Common variants, Illumina markers, MAF ≥1% variants, SNP, SNPs, all common SNPs, common SNP, common SNPs, common SNPs of small effect, common alleles, common disease associated variant, common gene variant, common genetic variants, common genetic variation, common loci, common single nucleotide polymorphism, common single nucleotide polymorphisms, common variant, common variant association, common variants, common variants (MAF >5%), common variation, common variations, common, genome-wide SNPs, common-disease/common-variant, genome-wide SNPs, high-frequency variant, highly common variants, individual common variants, single nucleotide polymorphisms |
| communication |
phenotype |
4 |
2 |
|
| community |
cohort |
8 |
5 |
Community family, Community group, community samples, community sources |
| Community comparison families |
cohort |
5 |
4 |
community comparison families |
| community residents |
cohort |
2 |
— |
|
| community sample |
cohort |
7 |
4 |
CON subjects, community, community sample |
| comorbid alcoholism and depression |
phenotype |
2 |
2 |
|
| comorbidity |
phenotype |
16 |
9 |
comorbid conditions, comorbid psychopathology, indices of comorbid psychopathology |
| comparison group |
cohort |
8 |
— |
low genetic, low environmental risk group, untreated group |
| comparison subjects |
cohort |
2 |
2 |
comparison sample, control subjects, population-based comparison sample |
| complement system |
drug |
2 |
1 |
complement pathway |
| complex behavioral outcomes |
phenotype |
4 |
1 |
|
| complex diseases |
phenotype |
38 |
25 |
common complex diseases, common disease, common diseases, common variant common disease scenario, complex disease, complex disease liability loci, complex diseases, complex disorders |
| complex disorders |
phenotype |
9 |
6 |
complex disorders, complex traits, disease, multifactorial disorders, multigenic disorders |
| complex traits |
phenotype |
41 |
20 |
complex trait, complex traits, complex traits (including disease), complex traits of interest, polygenic trait |
| compound |
drug |
3 |
1 |
drug, treatment compound |
| compulsive behavior |
phenotype |
4 |
2 |
compulsive, compulsive behavior, compulsivity |
| compulsivity |
phenotype |
6 |
2 |
|
| COMT |
gene |
30 |
23 |
COMT, COMT Val158Met, COMT gene, COMT genotype, Catechol-O-Methyltransferase, Catechol-O-methyl transferase, Catechol-O-methyltransferase, Catechol-o-methyltransferase, catechol-O-methyl transferase, catechol-O-methyl-transferase, catechol-O-methyltransferase, catechol-o-methyltransferase |
