about
A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levelsRefined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genesHereditary lung cancer syndrome targets never smokers with germline EGFR gene T790M mutationsGenetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer.Linkage studies of catechol-O-methyltransferase (COMT) and dopamine-beta-hydroxylase (DBH) cDNA expression levels.Comparison of missing data approaches in linkage analysisComparison of microsatellites, single-nucleotide polymorphisms (SNPs) and composite markers derived from SNPs in linkage analysisLinkage analysis of alcohol dependence using both affected and discordant sib pairs.A logistic mixture model for a family-based association study.Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population.Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X.Power of selective genotyping in genome-wide association studies of quantitative traits.Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations.Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans.Genome-wide association analysis of radiation resistance in Drosophila melanogaster.Genetics and bitter taste responses to goitrin, a plant toxin found in vegetables.PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome.Eating disorder predisposition is associated with ESRRA and HDAC4 mutationsA novel germline mutation in BAP1 predisposes to familial clear-cell renal cell carcinoma.Transethnic replication of association of CTG18.1 repeat expansion of TCF4 gene with Fuchs' corneal dystrophy in Chinese implies common causal variantGenetic variant I148M in PNPLA3 is associated with the ultrasonography-determined steatosis degree in a Chinese populationDNA polymerase-α regulates the activation of type I interferons through cytosolic RNA:DNA synthesisDistribution of model-based multipoint heterogeneity lod scores.The affected-/discordant-sib-pair design can guarantee validity of multipoint model-free linkage analysis of incomplete pedigrees when there is marker-marker disequilibrium.Subclinical lung disease, macrocytosis, and premature graying in kindreds with telomerase (TERT) mutations.TCF4 Triplet Repeat Expansion and Nuclear RNA Foci in Fuchs' Endothelial Corneal Dystrophy.Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.Genetic variant in PNPLA3 is associated with nonalcoholic fatty liver disease in ChinaAdult-onset pulmonary fibrosis caused by mutations in telomeraseGender and telomere length: systematic review and meta-analysisSRC-2-mediated coactivation of anti-tumorigenic target genes suppresses MYC-induced liver cancer.Adult-onset liver disease and hepatocellular carcinoma in S-adenosylhomocysteine hydrolase deficiencyTelomere shortening in familial and sporadic pulmonary fibrosisEpigenetic inheritance of telomere length obscures identification of causative PARN locus.Whole-exome sequencing identifies ADRA2A mutation in atypical familial partial lipodystrophyHomozygosity mapping identifies a bile acid biosynthetic defect in an adult with cirrhosis of unknown etiology.Association and familial segregation of CTG18.1 trinucleotide repeat expansion of TCF4 gene in Fuchs' endothelial corneal dystrophy.A novel de novo KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Möbius syndromeEnhancing the power to detect low-frequency variants in genome-wide screens.Minimum Information about a Genotyping Experiment (MIGEN).
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Chao Xing
@ast
Chao Xing
@en
Chao Xing
@es
Chao Xing
@nl
Chao Xing
@sl
type
label
Chao Xing
@ast
Chao Xing
@en
Chao Xing
@es
Chao Xing
@nl
Chao Xing
@sl
prefLabel
Chao Xing
@ast
Chao Xing
@en
Chao Xing
@es
Chao Xing
@nl
Chao Xing
@sl
P106
P2002
BioinfoMcDermot
P2798
P31
P496
0000-0002-1838-0502