Z. Zhao

发表

A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation

F. Hu, S. Chanock, R. Hoover, 2008, PLoS genetics.

IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

David C. Wilson, Judy H. Cho, C. Gieger, 2018, Nature Communications.

Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays

P. Visscher, Z. Zhao, G. Montgomery, 2008, Nucleic acids research.

Common sequence variants on 20q11.22 confer melanoma susceptibility

Nils Homer, S. Puig, E. Gillanders, 2008, Nature Genetics.

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3

Jeffrey E. Lee, S. Puig, K. Brown, 2011, Nature Genetics.

Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma

D. Duffy, N. Martin, Z. Zhao, 2009, Melanoma research.

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

Tariq Ahmad, Katherine I. Morley, Vibeke Andersen, 2011, Nature Genetics.

Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

P. Visscher, A. Morris, N. Martin, 2010, Nature Genetics.

Polymorphisms in MGMT and DNA repair genes and the risk of esophageal adenocarcinoma

David C Whiteman, James Doecke, Shahram Sadeghi, 2008, International journal of cancer.

Genetic Susceptibility in IBD: Overlap Between Ulcerative Colitis and Crohn's Disease

Z. Zhao, G. Montgomery, J. Andrews, 2013, Inflammatory bowel diseases.

Oncogenic PIK3CA mutations in colorectal cancers and polyps

N. Matsubara, Z. Zhao, G. Montgomery, 2012, International journal of cancer.

Erratum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 (Nature Genetics (2011) 43 (246-252))

Judy H. Cho, M. Daly, R. Ophoff, 2011 .

Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.

Nicole Soranzo, Manuel A. R. Ferreira, Sarah E Medland, 2010, American journal of human genetics.

Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi

T. Spector, P. Deloukas, J. Barrett, 2009, Nature Genetics.

Susceptibility variants for male-pattern baldness on chromosome 20p11

Thomas W. Mühleisen, S. Cichon, T. Mühleisen, 2008, Nature Genetics.

A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color.

Nicholas G Martin, David L Duffy, D. Duffy, 2008, American journal of human genetics.

A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation.

Wei Chen, Nicholas G Martin, David L Duffy, 2007, American journal of human genetics.

Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.

D. Duffy, N. Martin, Z. Zhao, 2010, The Journal of investigative dermatology.

Dizygotic twinning.

N. Martin, G. Willemsen, Z. Zhao, 2008, Human reproduction update.

High density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis

Hailiang Huang, Stephan Ripke, Andre Franke, 2014, Nature Genetics.

The search for genes contributing to endometriosis risk.

Z. Zhao, G. Montgomery, D. Nyholt, 2008, Human reproduction update.

A study of the TNF/LTA/LTB locus and susceptibility to severe malaria in highland papuan children and adults

R. Price, Z. Zhao, G. Montgomery, 2010, Malaria Journal.

Single Nucleotide Polymorphisms in Obesity-Related Genes and the Risk of Esophageal Cancers

Z. Zhao, G. Montgomery, N. Hayward, 2008, Cancer Epidemiology Biomarkers & Prevention.

High prevalence of sessile serrated adenomas with BRAF mutations: a prospective study of patients undergoing colonoscopy.

Rozemary Karamatic, Mark Appleyard, Kazutomo Togashi, 2006, Gastroenterology.

Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning.

D. Duffy, N. Martin, Z. Zhao, 2008, Human reproduction.

Novel variants in growth differentiation factor 9 in mothers of dizygotic twins.

D. Duffy, N. Martin, Z. Zhao, 2006, The Journal of clinical endocrinology and metabolism.

Linkage and association analysis of spectrophotometrically quantified hair color in Australian adolescents: the effect of OCA2 and HERC2.

D. Duffy, N. Martin, Z. Zhao, 2008, The Journal of investigative dermatology.

Smoking behaviour modifies IL23r‐associated disease risk in patients with Crohn's disease

T. Merriman, Z. Zhao, G. Montgomery, 2015, Journal of gastroenterology and hepatology.

Functional evaluation of genetic variants associated with endometriosis near GREB1.

Z. Zhao, G. Montgomery, D. Nyholt, 2015, Human reproduction.

Evaluation of polymorphisms in predicted target sites for micro RNAs differentially expressed in endometriosis.

Z. Zhao, G. Montgomery, D. Nyholt, 2011, Molecular human reproduction.

A deletion mutation in GDF9 in sisters with spontaneous DZ twins.

D. Duffy, N. Martin, Z. Zhao, 2004, Twin research : the official journal of the International Society for Twin Studies.

Genetic variation in tumour necrosis factor and lymphotoxin is not associated with endometriosis in an Australian sample.

Z. Zhao, G. Montgomery, D. Nyholt, 2007, Human reproduction.

Association between polymorphisms in the progesterone receptor gene and endometriosis.

D. O'Connor, D. Duffy, N. Martin, 2005, Molecular human reproduction.

Analysis of the 5q31–33 Locus Shows an Association between Single Nucleotide Polymorphism Variants in the IL-5 Gene and Symptomatic Infection with the Human Blood Fluke, Schistosoma japonicum1

Z. Zhao, G. Montgomery, Yuesheng Li, 2007, The Journal of Immunology.

Symptomatic Infection with the Human Gene and IL-5 Polymorphism Variants in the Association between Single Nucleotide 33 Locus Shows an − Analysis of the 5 q 31

Z. Zhao, G. Montgomery, Yuesheng Li, 2007 .

KCNN4 Gene Variant Is Associated With Ileal Crohn's Disease in the Australian and New Zealand Population

T. Merriman, Z. Zhao, G. Montgomery, 2010, The American Journal of Gastroenterology.

Polymorphisms in Nevus-Associated Genes MTAP, PLA2G6, and IRF4 and the Risk of Invasive Cutaneous Melanoma

Nicholas G Martin, David C Whiteman, David L Duffy, 2011, Twin Research and Human Genetics.

Genetic and gene expression analyses of the polycystic ovary syndrome candidate gene fibrillin-3 and other fibrillin family members in human ovaries

Z. Zhao, G. Montgomery, T. Hickey, 2009, Molecular human reproduction.

Association of Helicobacter pylori infection with reduced risk for esophageal cancer is independent of environmental and genetic modifiers.

Z. Zhao, G. Montgomery, N. Hayward, 2010, Gastroenterology.

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

Nicole Soranzo, Johan Hansson, Nicholas G Martin, 2010, American journal of human genetics.

High intake of folate from food sources is associated with reduced risk of esophageal cancer in an Australian population.

Z. Zhao, G. Montgomery, D. Whiteman, 2011, The Journal of nutrition.

KRAS variation and risk of endometriosis.

N. Martin, Z. Zhao, G. Montgomery, 2006, Molecular human reproduction.

Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk.

P. Pollock, Z. Zhao, G. Montgomery, 2008, Human reproduction.

Association Study of Common Mitochondrial Variants and Cognitive Ability

P. Visscher, A. McRae, D. Duffy, 2009, Behavior genetics.

Power and SNP tagging in whole mitochondrial genome association studies.

P. Visscher, A. McRae, Z. Zhao, 2008, Genome research.

A Comparison of DNA Pools Constructed Following Whole Genome Amplification for Two-Stage SNP Genotyping Designs

Z. Zhao, G. Montgomery, D. Nyholt, 2005, Twin Research and Human Genetics.

A comparison of DNA pools constructed following whole genome amplification for two-stage SNP genotyping designs.

Z. Zhao, G. Montgomery, D. Nyholt, 2005, Twin research and human genetics : the official journal of the International Society for Twin Studies.

Polymorphisms in the vascular endothelial growth factor gene and the risk of familial endometriosis.

Z. Zhao, G. Montgomery, D. Nyholt, 2008, Molecular human reproduction.

Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis.

N. Martin, Z. Zhao, G. Montgomery, 2014, Fertility and sterility.

ATG16L1 T300A Shows Strong Associations With Disease Subgroups in a Large Australian IBD Population: Further Support for Significant Disease Heterogeneity

Z. Zhao, G. Montgomery, N. Hayward, 2008, The American Journal of Gastroenterology.

Functional evaluationof genetic variants associated with endometriosis near GREB 1

Z. Zhao, G. Montgomery, D. Nyholt, 2015 .

Assessment of PALB2 as a Candidate Melanoma Susceptibility Gene

K. Brown, J. Trent, N. Martin, 2014, PloS one.

R. Price, Z. Zhao, G. Montgomery, 2010, The Journal of infectious diseases.

Common Variation in the CYP17A1 and IFIT1 Genes on Chromosome 10 Does Not Contribute to the Risk of Endometriosis.

Z. Zhao, G. Montgomery, D. Nyholt, 2008, The open reproductive science journal.

High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19.

Nicholas G Martin, Andrew Morris, Susan A Treloar, 2011, Fertility and sterility.

Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes.

D. Duffy, N. Martin, Z. Zhao, 2003, Human reproduction.

Variants in EMX2 and PTEN do not contribute to risk of endometriosis.

N. Martin, Z. Zhao, G. Montgomery, 2007, Molecular human reproduction.

The use of common mitochondrial variants to detect and characterise population structure in the Australian population: implications for genome-wide association studies

P. Visscher, A. McRae, Z. Zhao, 2008, European Journal of Human Genetics.

High intake of folate from food sources is associated with reduced risk of esophageal cancer in an Australian population.

Z. Zhao, G. Montgomery, D. Whiteman, 2011, The Journal of nutrition.

Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents

P. Visscher, A. McRae, D. Duffy, 2009, Diabetologia.