X. Liang

发表

KIAA1462, A Coronary Artery Disease Associated Gene, Is a Candidate Gene for Late Onset Alzheimer Disease in APOE Carriers

J. Gilbert, J. Haines, M. Pericak-Vance, 2013, PloS one.

Genetic variants in DNA repair genes and the risk of cutaneous malignant melanoma in melanoma‐prone families with/without CDKN2A mutations

S. Chanock, M. Yeager, M. Tucker, 2012, International journal of cancer.

ASSOCIATION OF HUMAN LEUKOCYTE ANTIGENS (HLA) WITH NASOPHARYNGEAL CARCINOMA (NPC) IN HIGH-RISK MULTIPLEX FAMILIES IN TAIWAN

M. Carrington, Chien-Jen Chen, A. Goldstein, 2009 .

Exploring biomarkers for ischemic stroke through integrated microarray data analysis

Jialei Yang, L. Su, J. Long, 2022, Brain Research.

Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations

S. Chanock, M. Yeager, M. Tucker, 2010, Familial Cancer.

Super-Enhancer–Associated nine-gene prognostic score model for prediction of survival in chronic lymphocytic leukemia patients

Linhui Hu, L. Pu, Z. Zhai, 2021, Frontiers in Genetics.

Familial aggregation of acute myeloid leukemia and myelodysplastic syndromes.

M. Björkholm, S. Kristinsson, L. Goldin, 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families

S. Chanock, M. Yeager, M. Tucker, 2013, The Journal of investigative dermatology.

Whole-Genome Amplification of Oral Rinse Self-Collected DNA in a Population-Based Case-Control Study of Breast Cancer

J. Haines, R. Welch, A. Hutchinson, 2007, Cancer Epidemiology Biomarkers & Prevention.

Common genetic variants in candidate genes and risk of familial lymphoid malignancies

S. Chanock, M. Yeager, N. Caporaso, 2009, British journal of haematology.

Identifying rheumatoid arthritis susceptibility genes using high-dimensional methods

T. Lam, A. Goldstein, Qizhai Li, 2009, BMC proceedings.

Effect of heterogeneity on the chromosome 10 risk in late‐onset Alzheimer disease

J. Gilbert, J. Haines, M. Pericak-Vance, 2007, Human mutation.

Genomic convergence to identify candidate genes for Alzheimer Disease on chromosome 10

Stephan Züchner, J. Gilbert, J. Haines, 2009, Human mutation.

Association Analysis of Genetic Polymorphisms in the CDC2 Gene with Late-Onset Alzheimer Disease

J. Gilbert, J. Haines, M. Pericak-Vance, 2006, Dementia and Geriatric Cognitive Disorders.

Association of human leukocyte antigens with nasopharyngeal carcinoma in high-risk multiplex families in Taiwan.

M. Carrington, Chien-Jen Chen, A. Goldstein, 2009, Human immunology.

Exploring biomarkers and therapeutic targets for ischemic stroke through integrated microarray data analysis

Jialei Yang, L. Su, J. Long, 2021, SSRN Electronic Journal.

Robust Tests for Single‐marker Analysis in Case‐Control Genetic Association Studies

G. Zheng, Kai Yu, Qizhai Li, 2009, Annals of human genetics.

The challenge of detecting epistasis (G×G Interactions): Genetic Analysis Workshop 16

P. Chanda, G. Clarke, M. Province, 2009, Genetic epidemiology.

No Association between SNP rs498055 on Chromosome 10 and Late‐Onset Alzheimer Disease in Multiple Datasets

J. Gilbert, J. Haines, M. Pericak-Vance, 2007, Annals of Human Genetics.

A regulatory variant at 19p13.3 is associated with primary biliary cholangitis risk and ARID3A expression

M. Seldin, Xiangdong Liu, M. Gershwin, 2023, Nature Communications.

Familial aggregation of acute myeloid leukemia and myelodysplastic syndromes.

M. Björkholm, S. Kristinsson, L. Goldin, 2012, Journal of Clinical Oncology.

KIAA1462, A Coronary Artery Disease Associated Gene, Is a Candidate Gene for Late Onset Alzheimer Disease in APOE Carriers

M. Pericak-Vance, G. Small, N. Schnetz-Boutaud, 2013, PloS one.