Author details

Full Name

Xiayi Ke

Affiliation

ORCID

Career Start Year

2001

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
29334797	Association of functional MMP-2 gene variant with intracranial aneurysms: case-control genetic association study and meta-analysis.	Br J Neurosurg	2018
29526602	Epigenome-wide study for the offspring exposed to maternal HBV infection during pregnancy, a pilot study.	Gene	2018
29551577	Association of prenatal organochlorine pesticide-dichlorodiphenyltrichloroethane exposure with fetal genome-wide DNA methylation.	Life Sciences	2018
28550290	Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects.	Scientific Reports	2017
26833012	[Levels of phthalate internal exposure levels in pregnant women and influencing factors].	Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]	2015
23207651	A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing.	Mol Psychiatry	2014
24395926	Analysis of circulating cholesterol levels as a mediator of an association between ABO blood group and coronary heart disease.	Circulation: Cardiovascular Genetics	2014
24480391	Interaction of benzo[a]pyrene with other risk factors in hepatocellular carcinoma: a case-control study in Xiamen, China.	Annals of Epidemiology	2014
24071862	Integrated analysis of genome-wide genetic and epigenetic association data for identification of disease mechanisms.	Epigenetics	2013
22045296	Evolutionary conserved longevity genes and human cognitive abilities in elderly cohorts.	European Journal of Human Genetics	2012
22628180	Genome-wide association uncovers shared genetic effects among personality traits and mood states.	Am J Med Genet B Neuropsychiatr Genet	2012
22770979	Presence of multiple independent effects in risk loci of common complex human diseases.	American Journal of Human Genetics	2012
23300510	Genetic copy number variation and general cognitive ability.	PLoS ONE	2012
21826061	Genome-wide association studies establish that human intelligence is highly heritable and polygenic.	Mol Psychiatry	2011
21070295	Assessment of the functionality of genome-wide canine SNP arrays and implications for canine disease association studies.	Animal Genetics	2011
21293383	HLA-DPB1-COL11A2 and three additional xMHC loci are independently associated with RA in a UK cohort.	Genes and Immunity	2011
21370227	Examining the overlap between genome-wide rare variant association signals and linkage peaks in rheumatoid arthritis.		2011
20453842	Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.	Nat Genet	2010
19435719	Association of CD40 with rheumatoid arthritis confirmed in a large UK case-control study.	Annals of the Rheumatic Diseases	2010
19674979	Overlap of disease susceptibility loci for rheumatoid arthritis and juvenile idiopathic arthritis.	Annals of the Rheumatic Diseases	2010
20852893	Rare variation at the TNFAIP3 locus and susceptibility to rheumatoid arthritis.	Hum Genet	2010
20072139	Association of the AFF3 gene and IL2/IL21 gene region with juvenile idiopathic arthritis.	Genes and Immunity	2010
19825187	Observational study on variability between biobanks in the estimation of DNA concentration.	BMC Res Notes	2009
19741008	Investigating the viability of genetic screening/testing for RA susceptibility using combinations of five confirmed risk loci.	Rheumatology	2009
19359276	Identification of AF4/FMR2 family, member 3 (AFF3) as a novel rheumatoid arthritis susceptibility locus and confirmation of two further pan-autoimmune susceptibility genes.	Human Molecular Genetics	2009
19116933	Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis.	Arthritis Rheum	2009
19116909	Association of the IL2RA/CD25 gene with juvenile idiopathic arthritis.	Arthritis Rheum	2009
19605748	A re-evaluation of three putative functional single nucleotide polymorphisms in rheumatoid arthritis.	Annals of the Rheumatic Diseases	2009
19417005	Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23.	Human Molecular Genetics	2009
19898481	Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk.	Nat Genet	2009
19838693	Genome-wide association analysis of canine atopic dermatitis and identification of disease related SNPs.	Immunogenetics	2009
18445023	Genetic susceptibility to keloid scarring: SMAD gene SNP frequencies in Afro-Caribbeans.	Exp Dermatol	2008
18034172	Polymorphisms in the IL-12beta and IL-23R genes are associated with psoriasis of early onset in a UK cohort.		2008
18434327	Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility.	Human Molecular Genetics	2008
18341666	Polymorphisms in the PTPN22 region are associated with psoriasis of early onset.	British Journal of Dermatology	2008
18197193	Singleton SNPs in the human genome and implications for genome-wide association studies.	Eur J Hum Genet	2008
18794857	Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13.	Nature Genetics	2008
17687331	An IRF8-binding promoter variant and AIRE control CHRNA1 promiscuous expression in thymus.	Nature	2007
17982455	Rheumatoid arthritis association at 6q23.	Nature Genetics	2007
16532062	An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population.	PLoS Genet	2006
16467560	The portability of tagSNPs across populations: a worldwide survey.	Genome Res	2006
16702437	Fine-scale map of encyclopedia of DNA elements regions in the Korean population.	Genetics	2006
17006452	Functional epistasis on a common MHC haplotype associated with multiple sclerosis.	Nature	2006
16998491	A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.	Nat Genet	2006
16251460	Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants.	Genome Res	2005
16103130	A comparison of tagging methods and their tagging space.	Hum Mol Genet	2005
15747258	A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.	Am J Hum Genet	2005
14734624	The impact of SNP density on fine-scale patterns of linkage disequilibrium.	Hum Mol Genet	2004
15367493	Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.	Hum Mol Genet	2004
12914576	CpG islands in human X-inactivation.	Annals of Human Genetics	2003