|
asian continental ancestry group - genetics |
27 |
|
single nucleotide polymorphism |
24 |
|
genome-wide association study |
23 |
|
female |
21 |
|
genotype |
21 |
|
male |
21 |
|
genetic association |
19 |
|
genetic predisposition to disease |
19 |
|
controlled study |
17 |
|
copy number variation |
15 |
|
gene identification |
15 |
|
gene locus |
15 |
|
human |
15 |
|
major clinical study |
15 |
|
neuregulin-1 - genetics |
15 |
|
asian |
14 |
|
association |
14 |
|
polymorphism, single nucleotide |
14 |
|
bile duct atresia |
13 |
|
chinese |
13 |
|
chromosome 10q |
13 |
|
gene frequency |
13 |
|
gene function |
13 |
|
genetic susceptibility |
13 |
|
hirschsprung disease |
13 |
|
hirschsprung disease - genetics |
13 |
|
humans |
13 |
|
priority journal |
13 |
|
risk factor |
13 |
|
risk factors |
13 |
|
adult |
12 |
|
animal tissue |
12 |
|
anorectal malformation |
12 |
|
chromosome aberration |
12 |
|
ephrin-a2 - genetics |
12 |
|
gwa |
12 |
|
lupus erythematosus, systemic - genetics |
12 |
|
middle aged |
12 |
|
ret |
12 |
|
sle |
12 |
|
uhrf1bp1 |
12 |
|
wnt signaling pathway |
12 |
|
aged |
11 |
|
antigens, cd3 - genetics |
11 |
|
case-control studies |
11 |
|
cd247 |
11 |
|
cos cells |
11 |
|
epidemiology |
11 |
|
ethnic group |
11 |
|
gene expression |
11 |
|
gene mapping |
11 |
|
gene mutation |
11 |
|
genetic predisposition |
11 |
|
genetics |
11 |
|
gwas |
11 |
|
human tissue |
11 |
|
kw034 - copy number/structural variation |
11 |
|
lupus erythematosus, systemic - genetics - immunology |
11 |
|
mutation - genetics |
11 |
|
nucleotide sequence |
11 |
|
systemic lupus erythematosus |
11 |
|
whole exome sequencing |
11 |
|
polymorphism, single nucleotide - genetics |
10 |
|
rare complex disease |
10 |
|
young adult |
10 |
|
amino acid substitution |
9 |
|
asian-specific |
9 |
|
exome-chip association analysis |
9 |
|
expression quantitative trait loci |
9 |
|
natural selection |
9 |
|
pax4 |
9 |
|
type 2 diabetes |
9 |
|
adiponectin - blood - genetics |
8 |
|
blood pressure - genetics |
8 |
|
body mass index |
8 |
|
cell differentiation - physiology |
8 |
|
cyclin a2 |
8 |
|
degeneration |
8 |
|
development |
8 |
|
disc |
8 |
|
gene deletion |
8 |
|
gene duplication |
8 |
|
gene expression regulation |
8 |
|
hbv integration |
8 |
|
hedgehog proteins - genetics - metabolism |
8 |
|
hepatocellular carcinoma |
8 |
|
hirschsprung disease - genetics - physiopathology |
8 |
|
hypertension - blood - genetics |
8 |
|
intervertebral |
8 |
|
kw080 - genome-wide association |
8 |
|
lumbar |
8 |
|
mri |
8 |
|
neuroglia - cytology - physiology |
8 |
|
receptors, notch - genetics - metabolism |
8 |
|
splicing |
8 |
|
amino acid substitution - genetics |
7 |
|
animals |
7 |
|
c-reactive protein |
7 |
|
cardiovascular diseases |
7 |
|
col4a5 |
7 |
|
col4a6 |
7 |
|
complex traits and polygenic disorders |
7 |
|
de novo mutations |
7 |
|
ens |
7 |
|
gene |
7 |
|
gonosomal mosaicism |
7 |
|
hong kong |
7 |
|
isolated diffuse oesophageal leiomyomatosis |
7 |
|
kw040 - development |
7 |
|
kw065 - gastrointestinal system |
7 |
|
kw099 - malformation |
7 |
|
multivariate analysis |
7 |
|
mutations |
7 |
|
neural crest |
7 |
|
neuregulin 1 |
7 |
|
rare variants |
7 |
|
schizophrenia |
7 |
|
schizophrenia - genetics |
7 |
|
single-nucleotide polymorphism |
7 |
|
v266l |
7 |
|
5' untranslated region |
6 |
|
adolescent |
6 |
|
adrenomedullin |
6 |
|
age factors |
6 |
|
aged, 80 and over |
6 |
|
alanine |
6 |
|
anorectal malformations |
6 |
|
arhgap4 |
6 |
|
asian continental ancestry group |
6 |
|
biological markers |
6 |
|
biological markers - blood - metabolism |
6 |
|
blood pressure |
6 |
|
carcinoma, papillary - genetics - metabolism - pathology |
6 |
|
cell adhesion molecules - blood |
6 |
|
cell proliferation |
6 |
|
cell transformation, neoplastic - genetics - metabolism |
6 |
|
chemicals and cas registry numbers |
6 |
|
child |
6 |
|
choledochal cyst |
6 |
|
cross-sectional studies |
6 |
|
de novo |
6 |
|
dysglycemia |
6 |
|
electrophoretic mobility shift assay |
6 |
|
exome |
6 |
|
exon |
6 |
|
fibrinogen |
6 |
|
fibrinogen - genetics - metabolism |
6 |
|
gamma-glutamyltransferase - blood - metabolism |
6 |
|
gene cluster |
6 |
|
gene expression regulation, neoplastic |
6 |
|
germ-line mutation |
6 |
|
ggt |
6 |
|
gli3 |
6 |
|
goiter, nodular - genetics - metabolism - pathology |
6 |
|
han chinese |
6 |
|
haplotype |
6 |
|
haplotypes |
6 |
|
hong kong - epidemiology |
6 |
|
hong kong - epidemiology - ethnology |
6 |
|
hypertension |
6 |
|
hypertension - blood - enzymology - epidemiology |
6 |
|
hypertension - blood - epidemiology - genetics |
6 |
|
hypertension - blood - ethnology - genetics - physiopathology |
6 |
|
immunoblotting |
6 |
|
insulin resistance - genetics |
6 |
|
interleukin-6 |
6 |
|
interleukin-6 - blood - genetics |
6 |
|
lipocalin-2 |
6 |
|
liver function test |
6 |
|
luciferases - diagnostic use |
6 |
|
mecp2 |
6 |
|
medical sciences |
6 |
|
neoplasm staging |
6 |
|
nuclear proteins - genetics - metabolism |
6 |
|
pharmacy and pharmacology environmental studies |
6 |
|
polymorphism |
6 |
|
predictive value of tests |
6 |
|
prevalence |
6 |
|
questionnaires |
6 |
|
rare variants association |
6 |
|
rats |
6 |
|
receptors, cell surface - blood |
6 |
|
regression analysis |
6 |
|
renbp |
6 |
|
reverse transcriptase polymerase chain reaction |
6 |
|
sex factors |
6 |
|
shh |
6 |
|
signal transduction - genetics |
6 |
|
single nucleotide |
6 |
|
single nucleotide polymorphisms |
6 |
|
thyroid gland - cytology - metabolism |
6 |
|
thyroid neoplasms - genetics - metabolism - pathology |
6 |
|
toxicology and environmental safety |
6 |
|
transcription factors - genetics - metabolism |
6 |
|
transcription, genetic |
6 |
|
up-regulation |
6 |
|
valine |
6 |
|
γ-glutamyl transaminase |
6 |
|
age distribution |
5 |
|
blood glucose - metabolism |
5 |
|
carrier proteins - genetics |
5 |
|
cds |
5 |
|
cell adhesion molecules |
5 |
|
cell adhesion molecules - genetics |
5 |
|
cholesterol |
5 |
|
chromosomes, human, pair 9 |
5 |
|
cohort studies |
5 |
|
complex traits: theory and methods |
5 |
|
copy number variant |
5 |
|
cytoskeletal proteins - genetics |
5 |
|
diabetes mellitus |
5 |
|
diabetes mellitus - blood - drug therapy - epidemiology |
5 |
|
endocrinology |
5 |
|
epilepsy - genetics |
5 |
|
f11 receptor |
5 |
|
gastrointestinal system |
5 |
|
gene polymorphism |
5 |
|
genetic mapping |
5 |
|
genome sequencing |
5 |
|
genome-wide association |
5 |
|
genotype-phenotype correlation |
5 |
|
glycosylated hemoglobin a |
5 |
|
hemoglobin a, glycosylated - metabolism |
5 |
|
hscr |
5 |
|
hypertension - ethnology - genetics |
5 |
|
hypertension - genetics - physiopathology |
5 |
|
hypoglycemic agents - therapeutic use |
5 |
|
insulin - blood |
5 |
|
kw020 - characterization of disorders |
5 |
|
kw024 - chromosomal deletions |
5 |
|
kw039 - delineation of diseases |
5 |
|
kw078 - genome scan |
5 |
|
models, genetic |
5 |
|
network |
5 |
|
neurogenetics |
5 |
|
nuclear proteins - genetics |
5 |
|
obesity |
5 |
|
obesity - ethnology - genetics |
5 |
|
physical chromosome mapping - methods |
5 |
|
prognosis |
5 |
|
proto-oncogene proteins c-ret - genetics |
5 |
|
raindance |
5 |
|
rare variant |
5 |
|
receptors, cell surface - genetics |
5 |
|
retrospective studies |
5 |
|
sex distribution |
5 |
|
snp |
5 |
|
targeted resequencing |
5 |
|
united states - epidemiology |
5 |
|
wga |
5 |
|
whole genome association |
5 |
|
ace |
4 |
|
alzheimer disease - genetics |
4 |
|
alzheimer's disease |
4 |
|
apoe |
4 |
|
binding sites |
4 |
|
blood pressure measurement |
4 |
|
bone density - genetics |
4 |
|
calcium-binding proteins - genetics |
4 |
|
caudal regression |
4 |
|
chromosome 1q |
4 |
|
chromosome 2q |
4 |
|
chromosome 5q |
4 |
|
cognitive decline |
4 |
|
computational biology - methods |
4 |
|
copy-number variation |
4 |
|
founder mutation |
4 |
|
fractures, bone - complications - genetics - physiopathology |
4 |
|
gene-environment interaction |
4 |
|
genomics |
4 |
|
homozygosity mapping |
4 |
|
intercellular signaling peptides and proteins - genetics |
4 |
|
joint effect |
4 |
|
kw117 - mutation detection |
4 |
|
kw139 - polymorphism |
4 |
|
population-based linkage |
4 |
|
psychosis |
4 |
|
quantitative trait, heritable |
4 |
|
recessive mutation |
4 |
|
sacral agenesis |
4 |
|
sample selection |
4 |
|
algorithms |
3 |
|
alleles |
3 |
|
biomedicine |
3 |
|
chromosome mapping - methods |
3 |
|
cognition |
3 |
|
cognition disorders - diagnosis - genetics |
3 |
|
colorectal cancer |
3 |
|
colorectal neoplasms - genetics |
3 |
|
cspg5 |
3 |
|
depression |
3 |
|
endophenotypes |
3 |
|
environment |
3 |
|
erbb4 |
3 |
|
european continental ancestry group - genetics |
3 |
|
gene sequence |
3 |
|
genetic |
3 |
|
genetic epidemiology |
3 |
|
high-throughput assay |
3 |
|
human genetics |
3 |
|
interaction |
3 |
|
intermediate phenotypes |
3 |
|
internal medicine |
3 |
|
kw008 - bioinformatics |
3 |
|
linkage disequilibrium analysis |
3 |
|
memory disorders - diagnosis - genetics |
3 |
|
memory impairment |
3 |
|
mental retardation - diagnosis - genetics |
3 |
|
metabolic diseases |
3 |
|
molecular medicine |
3 |
|
neuregulin-1 |
3 |
|
pedigree |
3 |
|
personality inventory |
3 |
|
polygenic risk scores |
3 |
|
protein ret |
3 |
|
quantitative trait association |
3 |
|
quantitative trait loci |
3 |
|
rare disease |
3 |
|
replication |
3 |
|
sampling studies |
3 |
|
schizophrenia - diagnosis - genetics |
3 |
|
schizophrenic psychology |
3 |
|
sleep |
3 |
|
sleep duration |
3 |
|
statistical genetics |
3 |
|
study design |
3 |
|
wes |
3 |
|
wgs |
3 |
|
adh2 |
2 |
|
admixture |
2 |
|
aggression |
2 |
|
alcohol consumption |
2 |
|
allele |
2 |
|
analysis of variance |
2 |
|
anxiety |
2 |
|
anxiety - diagnosis - epidemiology - genetics - psychology |
2 |
|
ap3s1 gene |
2 |
|
association study |
2 |
|
asthma |
2 |
|
bdnf |
2 |
|
biology |
2 |
|
breast neoplasms - diagnosis - genetics |
2 |
|
cardiovascular disease |
2 |
|
case control study |
2 |
|
chromosomal mapping |
2 |
|
chromosome mapping - statistics & numerical data |
2 |
|
classification |
2 |
|
coalescence |
2 |
|
commd7 gene |
2 |
|
comorbidity |
2 |
|
computer simulation |
2 |
|
csf1 gene |
2 |
|
databases, factual |
2 |
|
depression - diagnosis - epidemiology - genetics - psychology |
2 |
|
dna pooling |
2 |
|
early detection of cancer |
2 |
|
endophenotype |
2 |
|
epilepsy |
2 |
|
epilepsygene expression |
2 |
|
experimental errors |
2 |
|
extended pedigree |
2 |
|
factor analysis, statistical |
2 |
|
family |
2 |
|
genetic architecture |
2 |
|
genetic association studies |
2 |
|
genetic sharing |
2 |
|
genetic variation |
2 |
|
genome scan |
2 |
|
genome-wide |
2 |
|
genome-wide association study - statistics and numerical data |
2 |
|
genotype error |
2 |
|
great britain - epidemiology |
2 |
|
haplotype estimation |
2 |
|
heritability |
2 |
|
identical by descent (ibd) |
2 |
|
identity-by-descent (ibd) |
2 |
|
kw052 - epilepsy |
2 |
|
kw080 - genome sequencing |
2 |
|
kw101 - mapping complex traits |
2 |
|
kw118 - mutation detection |
2 |
|
kw124 - neurogenetics |
2 |
|
liability threshold model |
2 |
|
linkage |
2 |
|
linkage disequilibrium |
2 |
|
longitudinal |
2 |
|
markov chain monte carlo |
2 |
|
methodology |
2 |
|
model-fitting |
2 |
|
mx |
2 |
|
neurogenetics and neurodegeneration |
2 |
|
neuroticism |
2 |
|
pedigree error |
2 |
|
personality - genetics |
2 |
|
polygenic risk score |
2 |
|
population stratification |
2 |
|
population surveillance |
2 |
|
prostatic neoplasms - diagnosis - genetics |
2 |
|
psychiatric disorders |
2 |
|
psychiatric genetics |
2 |
|
psychiatric status rating scales |
2 |
|
psychopathology |
2 |
|
qtl |
2 |
|
qtl association analyses |
2 |
|
quantitative genetics |
2 |
|
regulation |
2 |
|
selection |
2 |
|
severity of illness index |
2 |
|
sibs |
2 |
|
sibships |
2 |
|
single nucleotide polymorphisms (snp) |
2 |
|
snps |
2 |
|
socioeconomic factors |
2 |
|
software |
2 |
|
stability |
2 |
|
statistical model |
2 |
|
statistics, nonparametric |
2 |
|
susceptibility |
2 |
|
tdt |
2 |
|
twins |
2 |
|
variance components |
2 |
|
variance explained |
2 |
|
vulnerability |
2 |
|
addiction |
1 |
|
adolescence |
1 |
|
adoption |
1 |
|
adoption - psychology |
1 |
|
age of onset |
1 |
|
alcohol abuse |
1 |
|
antisocial behavior |
1 |
|
aptitude |
1 |
|
association analysis |
1 |
|
atherosclerosis |
1 |
|
attitude |
1 |
|
bmi |
1 |
|
cannabis |
1 |
|
change |
1 |
|
child behavior checklist for ages 2-3 |
1 |
|
child development |
1 |
|
child, preschool |
1 |
|
childhood |
1 |
|
chromosome mapping |
1 |
|
chromosomes, human, pair 3 - genetics |
1 |
|
chromosomes, human, pair 9 - genetics |
1 |
|
cognitive ability |
1 |
|
colorado |
1 |
|
conditioning |
1 |
|
continuity |
1 |
|
diabetes |
1 |
|
diallel cross |
1 |
|
differential heritability |
1 |
|
differential shared environmentality |
1 |
|
east asians |
1 |
|
empirical p-value |
1 |
|
environment influences |
1 |
|
externalizing |
1 |
|
family study |
1 |
|
gabrg2 |
1 |
|
general cognitive ability |
1 |
|
genes |
1 |
|
genetic counseling |
1 |
|
genetic influences |
1 |
|
genetic linkage |
1 |
|
genetic linkage - genetics |
1 |
|
genetic variation - genetics |
1 |
|
genome |
1 |
|
genome, human - genetics |
1 |
|
genomewide |
1 |
|
genomewide association |
1 |
|
glyca |
1 |
|
height |
1 |
|
hla-dr antigens - genetics |
1 |
|
huntington disease - epidemiology - etiology - genetics |
1 |
|
huntington disease - epidemiology - genetics |
1 |
|
huntington's disease |
1 |
|
hutterite |
1 |
|
identical by descent |
1 |
|
inbred strains |
1 |
|
incomplete diallel |
1 |
|
infant |
1 |
|
infant twins |
1 |
|
inflammation |
1 |
|
intelligence |
1 |
|
intelligence - genetics |
1 |
|
internalizing |
1 |
|
interval mapping |
1 |
|
large pedigrees |
1 |
|
likelihood functions |
1 |
|
linkage analysis |
1 |
|
linkage methods |
1 |
|
linkage study |
1 |
|
lipid factors |
1 |
|
lipids - blood - genetics |
1 |
|
lipoproteins - blood - genetics |
1 |
|
longitudinal studies |
1 |
|
marijuana abuse - genetics |
1 |
|
marker alleles |
1 |
|
maximum likelihood |
1 |
|
mhc |
1 |
|
model fitting |
1 |
|
modifier genes |
1 |
|
multiple linear regression |
1 |
|
multiple regression |
1 |
|
multiple sclerosis |
1 |
|
multiple sclerosis - epidemiology - genetics |
1 |
|
multipoint sib-pair analysis |
1 |
|
multivariate analyses |
1 |
|
normality |
1 |
|
observer variation |
1 |
|
parents - psychology |
1 |
|
phenotype |
1 |
|
pleiotropy |
1 |
|
population group |
1 |
|
power simulations |
1 |
|
qtls |
1 |
|
quantitative trait loci (qtl) |
1 |
|
quantitative traits |
1 |
|
rater bias |
1 |
|
receptors, n-methyl-d-aspartate - genetics |
1 |
|
rheumatoid arthritis |
1 |
|
shyness |
1 |
|
sib pairs |
1 |
|
siblings - psychology |
1 |
|
social environment |
1 |
|
statistical power |
1 |
|
statistics as topic |
1 |
|
temperament |
1 |
|
trans-activators - genetics |
1 |
|
trinucleotide repeat |
1 |
|
trinucleotide repeat expansion |
1 |
|
twin analysis |
1 |
|
twins - blood - genetics |
1 |
|
twins, dizygotic - blood - genetics |
1 |
|
twins, dizygotic - genetics - psychology |
1 |
|
twins, monozygotic - blood - genetics |
1 |
|
twins, monozygotic - genetics - psychology |
1 |
|
ubiquitin thiolesterase - genetics |
1 |
|
venezuela - epidemiology |
1 |
|
weight |
1 |
|
whole genome scan |
1 |
