|
risk factor |
22 |
|
vitamin d |
21 |
|
single nucleotide polymorphism |
20 |
|
hirschsprung disease |
18 |
|
genotype |
17 |
|
controlled study |
15 |
|
copy number variation |
15 |
|
coronary artery disease |
15 |
|
gene identification |
15 |
|
gene locus |
15 |
|
genetic association |
15 |
|
human |
15 |
|
major clinical study |
15 |
|
neuregulin-1 - genetics |
15 |
|
bile duct atresia |
13 |
|
cancer susceptibility genes |
13 |
|
chromosome 10q |
13 |
|
early-age onset |
13 |
|
female |
13 |
|
gene function |
13 |
|
genetic predisposition |
13 |
|
genetic susceptibility |
13 |
|
hirschsprung disease - genetics |
13 |
|
male |
13 |
|
mst1r |
13 |
|
nasopharyngeal carcinoma |
13 |
|
priority journal |
13 |
|
whole-exome sequencing |
13 |
|
animal tissue |
12 |
|
anorectal malformation |
12 |
|
chinese |
12 |
|
chromosome aberration |
12 |
|
epidemiology |
12 |
|
gwa |
12 |
|
ischemic stroke |
12 |
|
myocardial infarction |
12 |
|
recurrence |
12 |
|
ret |
12 |
|
secondary prevention |
12 |
|
wnt signaling pathway |
12 |
|
cos cells |
11 |
|
ethnic group |
11 |
|
gene expression |
11 |
|
gene mapping |
11 |
|
gene mutation |
11 |
|
human tissue |
11 |
|
kw034 - copy number/structural variation |
11 |
|
mutation - genetics |
11 |
|
nucleotide sequence |
11 |
|
adipocyte |
10 |
|
b-type natriuretic peptide |
10 |
|
cardiac troponin |
10 |
|
fibroblast growth factor |
10 |
|
lipocalin-2 |
10 |
|
mutations |
10 |
|
risk prediction |
10 |
|
type 2 diabetes mellitus |
10 |
|
asian continental ancestry group - genetics |
9 |
|
asian-specific |
9 |
|
atrial fibrillation |
9 |
|
exome-chip association analysis |
9 |
|
expression quantitative trait loci |
9 |
|
genes |
9 |
|
mendelian randomization |
9 |
|
natural selection |
9 |
|
pax4 |
9 |
|
rare complex disease |
9 |
|
sex disparity |
9 |
|
type 2 diabetes |
9 |
|
young-onset ischemic stroke |
9 |
|
biliary atresia |
8 |
|
gene deletion |
8 |
|
gene duplication |
8 |
|
gene expression regulation |
8 |
|
gene frequency |
8 |
|
amino acid substitution - genetics |
7 |
|
col4a5 |
7 |
|
col4a6 |
7 |
|
complex traits and polygenic disorders |
7 |
|
de novo mutations |
7 |
|
ens |
7 |
|
enteric nervous system |
7 |
|
gonosomal mosaicism |
7 |
|
isolated diffuse oesophageal leiomyomatosis |
7 |
|
kw040 - development |
7 |
|
kw065 - gastrointestinal system |
7 |
|
kw080 - genome-wide association |
7 |
|
kw099 - malformation |
7 |
|
neural crest |
7 |
|
neuregulin 1 |
7 |
|
polymorphism, single nucleotide - genetics |
7 |
|
rare variants |
7 |
|
schizophrenia - genetics |
7 |
|
v266l |
7 |
|
whole exome sequencing |
7 |
|
adolescents |
6 |
|
bioinformatics |
6 |
|
bnt162b2 vaccine |
6 |
|
choledochal cyst |
6 |
|
clustering |
6 |
|
de novo |
6 |
|
drug-target mendelian randomization |
6 |
|
exome |
6 |
|
genetic risk predisposition |
6 |
|
hmgcr inhibitors |
6 |
|
liver fibrosis |
6 |
|
organoid |
6 |
|
pcsk9 inhibitors |
6 |
|
rare variants association |
6 |
|
safety |
6 |
|
steroid |
6 |
|
vaccine side effect |
6 |
|
vaccine-induced myocarditis |
6 |
|
accessory tragus |
5 |
|
ankyloglossia |
5 |
|
carrier proteins - genetics |
5 |
|
cds |
5 |
|
chromosomes, human, pair 9 |
5 |
|
complex traits: theory and methods |
5 |
|
consanguinity |
5 |
|
cytoskeletal proteins - genetics |
5 |
|
epilepsy - genetics |
5 |
|
gastrointestinal system |
5 |
|
genetic mapping |
5 |
|
genetic predisposition to disease |
5 |
|
genome sequencing |
5 |
|
hscr |
5 |
|
identification of disease genes |
5 |
|
kw020 - characterization of disorders |
5 |
|
kw024 - chromosomal deletions |
5 |
|
kw039 - delineation of diseases |
5 |
|
kw078 - genome scan |
5 |
|
neurogenetics |
5 |
|
physical chromosome mapping - methods |
5 |
|
polymorphism, single nucleotide |
5 |
|
proto-oncogene proteins c-ret - genetics |
5 |
|
raindance |
5 |
|
rare variant |
5 |
|
targeted resequencing |
5 |
|
blood pressure measurement |
4 |
|
chromosome 1q |
4 |
|
chromosome 2q |
4 |
|
chromosome 5q |
4 |
|
complex traits |
4 |
|
copy number/structural variation |
4 |
|
exome sequencing |
4 |
|
genome-wide association |
4 |
|
genotype-phenotype correlations |
4 |
|
ikbkap |
4 |
|
kasai portoenterostomy |
4 |
|
liver organoids |
4 |
|
massively parallel sequencing |
4 |
|
morpholinos |
4 |
|
mutation detection |
4 |
|
prognosis |
4 |
|
zebrafish |
4 |
|
cardiac enhancers |
3 |
|
common variants |
3 |
|
copy number variants |
3 |
|
genetics |
3 |
|
intrinsic cardiac abnormality |
3 |
|
mecp2 mutation |
3 |
|
noncoding variants |
3 |
|
notch signaling pathway |
3 |
|
rett syndrome |
3 |
|
tetralogy of fallot |
3 |
|
wnt/β-catenin signaling pathway |
3 |
|
aganglionosis |
2 |
|
artificial intelligence |
2 |
|
base composition |
2 |
|
biliary atresia (ba) |
2 |
|
comparative genomics |
2 |
|
congenital surgical diseases |
2 |
|
cpg islands - genetics |
2 |
|
cpg suppression |
2 |
|
dna - methylation. |
2 |
|
dna transposable elements - genetics |
2 |
|
enteric neural crest cells |
2 |
|
evolution, molecular |
2 |
|
evolutionary genetics. |
2 |
|
extra-cellular matrix |
2 |
|
fibrosis |
2 |
|
genetic |
2 |
|
genetic architecture |
2 |
|
genome, human |
2 |
|
hirschsprung's disease - genetic aspects. |
2 |
|
introns. |
2 |
|
liver |
2 |
|
molecular evolution |
2 |
|
neural stem cell niche |
2 |
|
pathogenesis |
2 |
|
pathology |
2 |
|
variant detection |
2 |
|
variant prioritization |
2 |
|
amyloid beta |
1 |
|
annotation |
1 |
|
atopy |
1 |
|
bivariate |
1 |
|
crispr/cas9 |
1 |
|
enrichment |
1 |
|
gene |
1 |
|
genetic correlation |
1 |
|
method |
1 |
|
rhinitis |
1 |
|
selection |
1 |
