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Increased DNA Methylation at the AXIN1 Gene in a Monozygotic Twin from a Pair Discordant for a Caudal Duplication Anomaly

American journal of human genetics, 2006-07, Vol.79 (1), p.155-162

2006

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High naevus count and MC1R red hair alleles contribute synergistically to increased melanoma risk

British journal of dermatology (1951), 2019-11, Vol.181 (5), p.1009-1016

2019

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High naevus count and MC 1R red hair alleles contribute synergistically to increased melanoma risk

British journal of dermatology (1951), 2019-11, Vol.181 (5), p.1009-1016

2019

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The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls

British journal of dermatology (1951), 2020-08, Vol.183 (2), p.357-366

2020

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虹膜色素病变作为皮肤黑色素瘤风险的标志物:澳大利亚病例对照研究

British journal of dermatology (1951), 2018-05, Vol.178 (5), p.e391-e391

2018

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Iris pigmented lesions as a marker of cutaneous melanoma risk: an Australian case–control study

British journal of dermatology (1951), 2018-05, Vol.178 (5), p.1119-1127

2018

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痣数和 MC1R R 等位基因对黑色素瘤风险有一定贡献

British journal of dermatology (1951), 2019-11, Vol.181 (5), p.e131-e131

2019

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Phenotypic and genotypic analysis of amelanotic and hypomelanotic melanoma patients

Journal of the European Academy of Dermatology and Venereology, 2019-06, Vol.33 (6), p.1076-1083

2019

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Naevus count and MC1R R alleles contribute to melanoma risk

British journal of dermatology (1951), 2019-11, Vol.181 (5), p.e119-e119

2019

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CDKN2A testing threshold in a high‐risk Australian melanoma cohort: number of primaries, family history and young age of onset impact risk

Journal of the European Academy of Dermatology and Venereology, 2020-12, Vol.34 (12), p.e797-e798

2020

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Iris pigmented lesions as a marker of cutaneous melanoma risk: an Australian case–control study

British journal of dermatology (1951), 2018-05, Vol.178 (5), p.e372-e372

2018

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虹膜色素病变作为皮肤黑色素瘤风险的标志物:澳大利亚病例对照研究

British journal of dermatology (1951), 2018-05, Vol.178 (5), p.e391-e391

2018

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Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: a cross-sectional study

British journal of dermatology (1951), 2016-02, Vol.174 (2), p.356-363

2016

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Noncoding Variations in the Gene Encoding Ceramide Synthase 6 are Associated with Type 2 Diabetes in a Large Indigenous Australian Pedigree

Twin research and human genetics, 2019-04, Vol.22 (2), p.79-87

2019

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Risk of asthma in adult twins with type 2 diabetes and increased body mass index

Allergy (Copenhagen), 2011-04, Vol.66 (4), p.562-568

2011

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Effects of early rearing environment on behavioral development of guide dogs

Journal of veterinary behavior, 2009-11, Vol.4 (6), p.240-241

2009

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Effects of HFE C282Y and H63D Polymorphisms and Polygenic Background on Iron Stores in a Large Community Sample of Twins

American journal of human genetics, 2000-04, Vol.66 (4), p.1246-1258

2000

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Haplotype sharing excludes canine orthologous Filaggrin locus in atopy in West Highland White Terriers

Animal genetics, 2009-10, Vol.40 (5), p.793-794

2009

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Characterization of the methylation patterns of MS4A2 in atopic cases and controls

Allergy (Copenhagen), 2010-03, Vol.65 (3), p.333-337

2010

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Association and interaction analyses of eight genes under asthma linkage peaks

Allergy (Copenhagen), 2009-11, Vol.64 (11), p.1623-1628

2009

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Psoriasis in Australian twins

Journal of the American Academy of Dermatology, 1993-09, Vol.29 (3), p.428-434

1993

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Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-01, Vol.144B (1), p.95-100

2007

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Cleft lip with or without cleft palate : associations with transforming growth factor alpha and retinoic acid receptor loci

American journal of human genetics, 1992-12, Vol.51 (6), p.1377-1385

1992

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Validation of a new antiserum directed towards the synthetic c-terminus of the FOS protein in avian species: immunological, physiological and behavioral evidence

Journal of neuroscience methods, 1999-09, Vol.91 (1), p.31-45

1999

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No common major gene for apolipoprotein A-I and HDL3-C levels: Evidence from bivariate segregation analysis

Genetic epidemiology, 1999, Vol.16 (1), p.54-68

1999

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Increased DNA Methylation at the AXIN1 Gene in a Monozygotic Twin from a Pair Discordant for a Caudal Duplication Anomaly

High naevus count and MC1R red hair alleles contribute synergistically to increased melanoma risk

High naevus count and MC 1R red hair alleles contribute synergistically to increased melanoma risk

The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls

虹膜色素病变作为皮肤黑色素瘤风险的标志物:澳大利亚病例对照研究

Iris pigmented lesions as a marker of cutaneous melanoma risk: an Australian case–control study

痣数和 MC1R R 等位基因对黑色素瘤风险有一定贡献

Phenotypic and genotypic analysis of amelanotic and hypomelanotic melanoma patients

Naevus count and MC1R R alleles contribute to melanoma risk

CDKN2A testing threshold in a high‐risk Australian melanoma cohort: number of primaries, family history and young age of onset impact risk

Iris pigmented lesions as a marker of cutaneous melanoma risk: an Australian case–control study

虹膜色素病变作为皮肤黑色素瘤风险的标志物:澳大利亚病例对照研究

Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: a cross-sectional study

Noncoding Variations in the Gene Encoding Ceramide Synthase 6 are Associated with Type 2 Diabetes in a Large Indigenous Australian Pedigree

Risk of asthma in adult twins with type 2 diabetes and increased body mass index

Effects of early rearing environment on behavioral development of guide dogs

Effects of HFE C282Y and H63D Polymorphisms and Polygenic Background on Iron Stores in a Large Community Sample of Twins

Haplotype sharing excludes canine orthologous Filaggrin locus in atopy in West Highland White Terriers

Characterization of the methylation patterns of MS4A2 in atopic cases and controls

Association and interaction analyses of eight genes under asthma linkage peaks

Psoriasis in Australian twins

Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins

Cleft lip with or without cleft palate : associations with transforming growth factor alpha and retinoic acid receptor loci

Validation of a new antiserum directed towards the synthetic c-terminus of the FOS protein in avian species: immunological, physiological and behavioral evidence

No common major gene for apolipoprotein A-I and HDL3-C levels: Evidence from bivariate segregation analysis

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