|
asian continental ancestry group - genetics |
18 |
|
genetic predisposition to disease |
18 |
|
systemic lupus erythematosus |
18 |
|
genome-wide association study |
17 |
|
sle |
16 |
|
asian |
14 |
|
association |
14 |
|
chinese |
13 |
|
hong kong |
13 |
|
lupus erythematosus, systemic - genetics |
13 |
|
animal tissue |
12 |
|
anorectal malformation |
12 |
|
chromosome aberration |
12 |
|
ephrin-a2 - genetics |
12 |
|
single nucleotide polymorphism |
12 |
|
uhrf1bp1 |
12 |
|
wnt signaling pathway |
12 |
|
antigens, cd3 - genetics |
11 |
|
cd247 |
11 |
|
gwas |
11 |
|
lupus erythematosus, systemic - genetics - immunology |
11 |
|
intracellular signaling peptides and proteins - genetics |
10 |
|
lupus erythematosus, systemic - enzymology - genetics |
10 |
|
chemicals and cas registry numbers |
8 |
|
cyclin a2 |
8 |
|
hbv integration |
8 |
|
hepatocellular carcinoma |
8 |
|
humans |
8 |
|
lupus nephritis |
8 |
|
model |
8 |
|
phenotyping |
8 |
|
prediction |
8 |
|
prenatal exome |
8 |
|
risk assessment |
8 |
|
splicing |
8 |
|
variants of unknown clinical significance |
8 |
|
adult |
7 |
|
antibodies, antinuclear - blood |
7 |
|
antigens, cd11b - genetics |
7 |
|
asian continental ancestry group - ethnology - genetics |
7 |
|
autoantibodies |
7 |
|
autoantibodies - blood |
7 |
|
cluster analysis |
7 |
|
disease susceptibility |
7 |
|
epidemiology |
7 |
|
epistasis |
7 |
|
ets1 |
7 |
|
female |
7 |
|
hong kong - epidemiology |
7 |
|
il-17 |
7 |
|
lupus erythematosus |
7 |
|
lupus erythematosus, systemic - ethnology - genetics |
7 |
|
lupus erythematosus, systemic - ethnology - immunology |
7 |
|
male |
7 |
|
middle aged |
7 |
|
multivariate analysis |
7 |
|
nephritis - ethnology - genetics |
7 |
|
prevalence |
7 |
|
protein-serine-threonine kinases - genetics |
7 |
|
systemic |
7 |
|
autoimmunity |
6 |
|
blood |
6 |
|
bnt162b2 vaccine |
6 |
|
cell composition |
6 |
|
cell lineage-specific |
6 |
|
clustering |
6 |
|
dna methylation |
6 |
|
founder mutation |
6 |
|
genetic risk predisposition |
6 |
|
genotype |
6 |
|
linkage disequilibrium |
6 |
|
lupus |
6 |
|
methylationepic |
6 |
|
nerve tissue proteins - genetics |
6 |
|
paediatric-onset |
6 |
|
polymorphism, single nucleotide - genetics |
6 |
|
stat4 transcription factor - genetics |
6 |
|
vaccine side effect |
6 |
|
vaccine-induced myocarditis |
6 |
|
aim2 |
5 |
|
alps-like disease |
5 |
|
bronchiectasis |
5 |
|
china |
5 |
|
crohn disease |
5 |
|
cystic fibrosis |
5 |
|
cytoskeletal proteins - genetics |
5 |
|
ebv‐encoded small rna |
5 |
|
epilepsy - genetics |
5 |
|
epstein–barr virus |
5 |
|
exome |
5 |
|
exome sequencing |
5 |
|
gene sequence |
5 |
|
genetic defect |
5 |
|
genome‐wide analysis |
5 |
|
heterozygosity |
5 |
|
ifi16 |
5 |
|
immune dysregulation |
5 |
|
immunodeficiency |
5 |
|
inflammasome |
5 |
|
interleukin 10 receptor |
5 |
|
mendelian disease |
5 |
|
molecular sequence data |
5 |
|
nasopharyngeal carcinoma |
5 |
|
polymorphism, single nucleotide |
5 |
|
quality control |
5 |
|
rasgrp1 |
5 |
|
sequencing |
5 |
|
t-cell receptor signaling |
5 |
|
trafficking defects |
5 |
|
transcript isoform |
5 |
|
variant annotation |
5 |
|
variant prioritization |
5 |
|
alleles |
4 |
|
apoe ɛ4-negative |
4 |
|
base sequence |
4 |
|
blood smear |
4 |
|
bone marrow examination |
4 |
|
case report |
4 |
|
case-control studies |
4 |
|
child |
4 |
|
child, preschool |
4 |
|
clinical article |
4 |
|
dna mutational analysis |
4 |
|
filipino (citizen) |
4 |
|
frequency haplotypes |
4 |
|
gene frequency |
4 |
|
haplotype frequency |
4 |
|
haplotypes |
4 |
|
hla |
4 |
|
hla antigens |
4 |
|
homozygosity mapping |
4 |
|
interferon regulatory factors - genetics |
4 |
|
kw075 - genetic mapping |
4 |
|
kw078 – genome scan |
4 |
|
kw083 - genotype-phenotype correlations |
4 |
|
kw086 – identification of disease genes |
4 |
|
kw087 - immune system |
4 |
|
late-onset alzheimer's disease |
4 |
|
major histocompatibility complex (mhc) |
4 |
|
matching probability |
4 |
|
mlkl |
4 |
|
molecular basis of mendelian disorders |
4 |
|
population-based linkage |
4 |
|
rare variants |
4 |
|
recessive mutation |
4 |
|
registry/registry analysis |
4 |
|
stem cell |
4 |
|
whole exome sequencing |
4 |
|
5' untranslated regions - genetics |
3 |
|
adolescent |
3 |
|
agammaglobulinemia |
3 |
|
age of onset |
3 |
|
algorithms |
3 |
|
alternative splicing |
3 |
|
alternative splicing - genetics |
3 |
|
alternative splicing pattern |
3 |
|
amino acid conservation |
3 |
|
amino acid sequence |
3 |
|
animals |
3 |
|
autism spectrum disorder |
3 |
|
brcc3 |
3 |
|
btk mutations |
3 |
|
carrier proteins - genetics |
3 |
|
cd40l |
3 |
|
clec16a |
3 |
|
coding mutation |
3 |
|
cohort studies |
3 |
|
conserved sequence |
3 |
|
cord blood |
3 |
|
deubiquitinase |
3 |
|
developmental delay |
3 |
|
disease progression |
3 |
|
dna, complementary - genetics |
3 |
|
ests |
3 |
|
evolutionary distance |
3 |
|
exons |
3 |
|
exons - genetics |
3 |
|
expressed sequence tags |
3 |
|
expressed sequences |
3 |
|
fbn1 |
3 |
|
flow cytometry |
3 |
|
functional impact |
3 |
|
functional polymorphism |
3 |
|
gene expression - genetics |
3 |
|
gene expression regulation |
3 |
|
genetic association studies |
3 |
|
genetic diseases, x-linked - genetics |
3 |
|
genetic testing |
3 |
|
genetics |
3 |
|
genome, human |
3 |
|
genotype-phenotype correlation |
3 |
|
hla gene frequency |
3 |
|
hla haplotype frequency |
3 |
|
infant |
3 |
|
infection - diagnosis - epidemiology - genetics - physiopathology |
3 |
|
interferon |
3 |
|
introns - genetics |
3 |
|
josd2 |
3 |
|
macrocephaly |
3 |
|
marfan syndrome |
3 |
|
marfan syndrome - genetics |
3 |
|
megalencephaly |
3 |
|
mice |
3 |
|
mice, inbred c57bl |
3 |
|
microfilament proteins - genetics |
3 |
|
mtor |
3 |
|
multiple intestinal atresias (mia) |
3 |
|
mutation - genetics |
3 |
|
mutation screening |
3 |
|
mutation, missense |
3 |
|
nlrp3 |
3 |
|
nssnp |
3 |
|
phenotype |
3 |
|
phylogeny |
3 |
|
pik3ca |
3 |
|
polymorphism, genetic |
3 |
|
ppp2r5d |
3 |
|
promoter regions, genetic |
3 |
|
protein-tyrosine kinases - genetics - immunology |
3 |
|
pten |
3 |
|
receptors, transforming growth factor beta - genetics |
3 |
|
registry |
3 |
|
rna - genetics |
3 |
|
rna splice sites - genetics |
3 |
|
rna-binding proteins - genetics |
3 |
|
sequence alignment |
3 |
|
sequence analysis, dna |
3 |
|
sequence analysis, dna - methods |
3 |
|
sequence homology, amino acid |
3 |
|
severe combined immunodeficiency (scid) |
3 |
|
sex factors |
3 |
|
somatic mosaicism |
3 |
|
spliced variants |
3 |
|
stat1 |
3 |
|
synteny |
3 |
|
taloromyces marneffei |
3 |
|
tgfbr2 |
3 |
|
toll-like receptor 7 - genetics |
3 |
|
ttc7a |
3 |
|
type i |
3 |
|
veoibd |
3 |
|
whole exome sequencing (wes) |
3 |
|
x-linked agammaglobulinemia |
3 |
|
x-linked combined immunodeficiency diseases - diagnosis - epidemiology - genetics - physiopathology |
3 |
|
x-linked hyper-igm syndrome |
3 |
|
xla |
3 |
|
young adult |
3 |
|
zebrafish - genetics |
3 |
|
african continental ancestry group - genetics |
2 |
|
antigen-antibody complex - genetics - immunology |
2 |
|
association studies |
2 |
|
autoimmune diseases |
2 |
|
bacterial septicaemia |
2 |
|
biomarker |
2 |
|
calculated panel reactive antibody |
2 |
|
canakinumab |
2 |
|
ccl2 |
2 |
|
cdna sequencing |
2 |
|
complex diseases |
2 |
|
cryopyrin-associated periodic syndrome |
2 |
|
east asian |
2 |
|
expressed sequence tag |
2 |
|
gene dosage |
2 |
|
gene dosage - genetics - immunology |
2 |
|
gene expression |
2 |
|
gene expression regulation - genetics |
2 |
|
gene expression regulation - genetics - immunology |
2 |
|
genetic association study |
2 |
|
genetic predisposition to disease - ethnology - genetics |
2 |
|
genetic predisposition to disease - genetics |
2 |
|
genetic susceptibility |
2 |
|
genetic variation - immunology |
2 |
|
genome scan |
2 |
|
genome sequencing |
2 |
|
genotype and phenotype correlation |
2 |
|
genotype-phenotype correlations |
2 |
|
iga nephropathy |
2 |
|
immune system |
2 |
|
infectious disease |
2 |
|
integrative analysis |
2 |
|
irf3 |
2 |
|
lupus erythematosus, systemic - genetics - metabolism |
2 |
|
mbl |
2 |
|
micrornas - genetics - metabolism |
2 |
|
missing heritability |
2 |
|
mutation detection |
2 |
|
ngs |
2 |
|
novel mutation |
2 |
|
organ allocation |
2 |
|
pleiotropy |
2 |
|
polymorphism |
2 |
|
population differences |
2 |
|
population genetics |
2 |
|
population structure |
2 |
|
promoter regions, genetic - genetics |
2 |
|
protein-protein interactions |
2 |
|
receptors, igg - genetics |
2 |
|
renal transplantation |
2 |
|
replication |
2 |
|
selection |
2 |
|
sensitization |
2 |
|
sequence-specific subtraction |
2 |
|
sequencing depth |
2 |
|
severe acute respiratory syndrome |
2 |
|
shared genes |
2 |
|
short inversion detection |
2 |
|
single-nucleotide polymorphisms |
2 |
|
somatic mosaicism mutation |
2 |
|
split reads method |
2 |
|
structural variations |
2 |
|
susceptibility |
2 |
|
transcription factor |
2 |
|
unacceptable antigen |
2 |
|
virtual cross-match |
2 |
|
x chromosome |
2 |
|
african americans - genetics |
1 |
|
allele |
1 |
|
als |
1 |
|
alzheimer's disease |
1 |
|
analgesics, opioid - toxicity |
1 |
|
ankrd11 gene |
1 |
|
apoe ε4 |
1 |
|
apoe ε4 carriers and non-carriers |
1 |
|
association study |
1 |
|
autophagy |
1 |
|
bayes theorem |
1 |
|
bioinformatics |
1 |
|
charcot-marie-tooth disease |
1 |
|
charcot-marie-tooth disease - genetics - physiopathology |
1 |
|
chromosome mapping |
1 |
|
chromosome y |
1 |
|
classification |
1 |
|
classification factors |
1 |
|
clinical phenotypes |
1 |
|
connexins - genetics |
1 |
|
cytokines |
1 |
|
development and evaluation (grade) |
1 |
|
dimerization |
1 |
|
diprenorphine - metabolism |
1 |
|
dirichlet distribution |
1 |
|
dna - genetics |
1 |
|
down-regulation |
1 |
|
electromyography |
1 |
|
enkephalin, ala(2)-mephe(4)-gly(5)- |
1 |
|
enkephalin, d-penicillamine (2,5)- |
1 |
|
enkephalins - pharmacology |
1 |
|
epilepsy |
1 |
|
escherichia coli proteins - genetics |
1 |
|
european continental ancestry group - genetics |
1 |
|
frameshift mutation |
1 |
|
frameshift variant |
1 |
|
frequency |
1 |
|
functional assays |
1 |
|
g protein |
1 |
|
gamma |
1 |
|
gene |
1 |
|
gene expression profiling - methods |
1 |
|
gene fusion |
1 |
|
gene locus |
1 |
|
gene structure |
1 |
|
gene-targeting |
1 |
|
genetic |
1 |
|
genetic algorithm |
1 |
|
genetic correlation |
1 |
|
genetic defects |
1 |
|
genetic diseases, x-linked - genetics - physiopathology |
1 |
|
genetic linkage |
1 |
|
genome |
1 |
|
genomics |
1 |
|
gge |
1 |
|
ghrh gene |
1 |
|
gjb1 (connexin32) |
1 |
|
gnas |
1 |
|
grading of recommendations assessment |
1 |
|
gtp-binding protein alpha subunits, gs - genetics |
1 |
|
gtp-binding protein beta subunits - chemistry |
1 |
|
gtp-binding protein gamma subunits - chemistry - genetics - metabolism |
1 |
|
gtp-binding proteins - physiology |
1 |
|
guideline |
1 |
|
han |
1 |
|
haploinsufficiency |
1 |
|
haplotype |
1 |
|
hsp40 heat-shock proteins - genetics |
1 |
|
hub gene cluster |
1 |
|
imputation |
1 |
|
in vitro functional assays |
1 |
|
inborn errors of immunity |
1 |
|
intracellular signaling peptides and proteins - genetics - metabolism |
1 |
|
introns |
1 |
|
isolated growth hormone deficiency |
1 |
|
kbg syndrome |
1 |
|
kidney diseases |
1 |
|
lethal dose 50 |
1 |
|
ligands |
1 |
|
linkage analysis |
1 |
|
literature review |
1 |
|
long non-coding rna |
1 |
|
long noncoding rna |
1 |
|
loss of function mutation |
1 |
|
mhc |
1 |
|
mice, knockout |
1 |
|
mir-20a-5p |
1 |
|
mixture distributions |
1 |
|
models, statistical |
1 |
|
molecular diagnosis |
1 |
|
morphine - toxicity |
1 |
|
morphine analgesia |
1 |
|
morphine derivatives - toxicity |
1 |
|
morphine lethality |
1 |
|
multinomial distribution |
1 |
|
multiplex pcr |
1 |
|
mutant chimeric proteins - genetics - metabolism |
1 |
|
mutation |
1 |
|
neat1 |
1 |
|
next-generation sequencing |
1 |
|
oligopeptides - toxicity |
1 |
|
osteoarthritis (oa) |
1 |
|
pancreatic ductal adenocarcinoma |
1 |
|
pedigree |
1 |
|
pertussis toxin |
1 |
|
protein structure |
1 |
|
pvt1 |
1 |
|
pyridoxine |
1 |
|
quantitative trait loci |
1 |
|
receptors, opioid, delta - analysis |
1 |
|
receptors, opioid, mu - analysis |
1 |
|
receptors, opioid, mu - genetics |
1 |
|
recombinant human growth hormone |
1 |
|
recombination, genetic |
1 |
|
reverse transcriptase polymerase chain reaction |
1 |
|
rna 3' polyadenylation signals |
1 |
|
sequence deletion |
1 |
|
short stature |
1 |
|
shrinkage estimators |
1 |
|
single nucleotide polymorphisms |
1 |
|
snp |
1 |
|
software |
1 |
|
spats2l |
1 |
|
survey |
1 |
|
tlr4 |
1 |
|
transcription initiation site |
1 |
|
truncated transcript |
1 |
|
tumor cells, cultured |
1 |
|
turner syndrome |
1 |
|
type i interferon |
1 |
|
ulk1 |
1 |
|
virulence factors, bordetella - pharmacology |
1 |
|
weighted gene co-expression network analysis (wgcna) |
1 |
|
whole-exome sequencing |
1 |
|
x-linked |
1 |
|
μ opioid receptor |
1 |
