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Lista de obras de David L. Duffy

'Mind your Moles' study: protocol of a prospective cohort study of melanocytic naevi

scientific article published on 19 September 2018

4th Pediatric Allergy and Asthma Meeting (PAAM)

artículo científico publicado en 2016

A Deletion Mutation in GDF9 in Sisters with Spontaneous DZ Twins

article by Grant W. Montgomery et al published 1 December 2004 in CrossRef Listing of Deleted DOIs

A Genome Scan for Epidermal Skin Pattern in Adolescent Twins Reveals Suggestive Linkage on 12p13.31

A Population-based Study of Bronchial Asthma in Adult Twin Pairs ⬇️

artículo científico publicado el 1 de agosto de 1992

A comprehensive analysis of complex traits in problem 2A.

artículo científico publicado en 1997

A factor analysis of associations among self–reported immune related symptoms in a large twin sample

artículo científico publicado en 1998

A functional polymorphism in the promoter region of the cyclooxygenase-2 gene is not associated with asthma and atopy in an Australian population

artículo científico publicado en 2004

A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q.

artículo científico publicado en 2004

A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins

artículo científico publicado en 2010

A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation

artículo científico publicado en 2008

A genome-wide association study to identify genetic markers associated with endometrial cancer grade

artículo científico publicado en 2012

A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions

article published in 2006

A genomewide search for type 2 diabetes-susceptibility genes in indigenous Australians

artículo científico publicado en 2001

A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability

artículo científico publicado en 2007

A major quantitative trait locus for CD4–CD8 ratio is located on chromosome 11

article

A method for meta-analysis of molecular association studies

artículo científico publicado en 2005

A methodological appraisal of the impact of different classification procedures used in three different phases of the australian rheumatoid arthritis twin survey.

artículo científico publicado en 1998

A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk.

artículo científico publicado en 2013

A non-synonymous mutation in the canine Pkd1 gene is associated with autosomal dominant polycystic kidney disease in Bull Terriers

artículo científico publicado en 2011

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

artículo científico publicado en 2011

A polymorphism in the promoter region of the human interleukin-16 gene is not associated with asthma or atopy in an Australian population.

artículo científico publicado en 2005

A population-based study of Australian twins with melanoma suggests a strong genetic contribution to liability

artículo científico publicado en 2009

A psychometric evaluation of the Short Interpersonal Reactions Inventory (SIRI) in an Australian twin sample

article

A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits

artículo científico publicado en 2006

A simulation study concerning the effect of varying the residual phenotypic correlation on the power of bivariate quantitative trait loci linkage analysis

artículo científico publicado en 2004

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

artículo científico publicado en 2008

A study of diabetes mellitus within a large sample of Australian twins

artículo científico publicado en 2008

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

artículo científico publicado en 2007

ADAM33 haplotypes are associated with asthma in a large Australian population

artículo científico publicado en 2006

Accuracy of Inferred APOE Genotypes for a Range of Genotyping Arrays and Imputation Reference Panels

Acquired melanocytic naevus phenotypes and MC1R genotypes in Han Chinese: a cross-sectional study.

artículo científico publicado en 2017

Allergens, IgE, mediators, inflammatory mechanisms

artículo científico publicado en 1998

An Integrated Genetic Map for Linkage Analysis

article

Analysis of Quantitative Trait Loci

artículo científico publicado en 2017

Analysis of cultured human melanocytes based on polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P loci

artículo científico publicado en 2009

Application of transmission disequilibrium tests to nonsyndromic oral clefts: Including candidate genes and environmental exposures in the models

artículo científico publicado en 1997

Applying statistical approaches in the dissection of genes versus environment for asthma and allergic disease.

artículo científico publicado en 2001

Association and interaction analyses of eight genes under asthma linkage peaks

article

Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

artículo científico publicado en 2010

Association between polymorphisms in the progesterone receptor gene and endometriosis

artículo científico publicado en 2005

Association study of common mitochondrial variants and cognitive ability

artículo científico publicado en 2009

Atopic Disease and Immunologic Response

artículo científico publicado en 1997

Atopic dermatitis in West Highland white terriers is associated with a 1.3-Mb region on CFA 17

article by Joana B. Roque et al published 12 October 2011 in Immunogenetics

Atopy in Australia

article

Attention deficit hyperactivity disorder in Australian adults: prevalence, persistence, conduct problems and disadvantage

artículo científico publicado en 2012

BRAF polymorphisms and risk of melanocytic neoplasia

artículo científico publicado en 2005

Biometrical genetic analysis of the cotwin control design

artículo científico publicado en 1994

CCR5-Delta32 mutation is strongly associated with primary sclerosing cholangitis.

artículo científico publicado en 2004

CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma

artículo científico publicado en 1999

Candidate Glycoprotein Biomarkers for Canine Visceral Hemangiosarcoma and Validation Using Semi-Quantitative Lectin/Immunohistochemical Assays

artículo científico publicado en 2021

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

artículo científico publicado en 2009

Classifying dermoscopic patterns of naevi in a case-control study of melanoma

artículo científico publicado en 2017

Common sequence variants on 20q11.22 confer melanoma susceptibility

artículo científico publicado en 2008

Common variants in the trichohyalin gene are associated with straight hair in Europeans

artículo científico publicado en 2009

Contrast effects and sex influence maternal and self-report dimensional measures of attention-deficit hyperactivity disorder

artículo científico publicado en 2014

Cyclooxygenase-1 gene polymorphisms in patients with different asthma phenotypes and atopy

artículo científico publicado en 2005

Cyclooxygenase-2 gene polymorphisms in an Australian population: association of the -1195G > A promoter polymorphism with mild asthma

artículo científico publicado en 2008

Cysteinyl Leukotrienes Pathway Genes, Atopic Asthma and Drug Response: From Population Isolates to Large Genome-Wide Association Studies

artículo científico publicado en 2016

Dense mapping of chromosome 12q13.12-q23.3 and linkage to asthma and atopy☆☆☆★★★

artículo científico publicado en 1999

Digital quantification of human eye color highlights genetic association of three new loci

artículo científico publicado en 2010

Direction of causation: Reply to commentaries

Distribution analyses of acquired melanocytic naevi on the trunk

artículo científico publicado en 2014

Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes

artículo científico publicado en 2003

Dizygotic twinning is not linked to variation at the alpha-inhibin locus on human chromosome 2

artículo científico publicado en 2000

Early life environmental predictors of asthma age-of-onset

artículo científico publicado en 2014

Effect of the BDNF V166M polymorphism on working memory in healthy adolescents

artículo científico publicado en 2006

Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins

artículo científico publicado en 2000

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

scientific article published on 01 January 2007

Epidermal growth factor gene (EGF) polymorphism and risk of melanocytic neoplasia

artículo científico publicado en 2004

Erratum: Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

article

Estimation of variance components for age at menarche in twin families

artículo científico publicado en 2007

Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot"

artículo científico publicado en 2010

Evidence for Linkage of Chromosome 12q15–q24.1 Markers to High Total Serum IgE Concentrations in Children of the German Multicenter Allergy Study

article

Evidence for the genetic control of immunoglobulin E reactivity to the allergens of Alternaria alternata

artículo científico publicado en 2002

Evidence of genetic effects on blood lead concentration

artículo científico publicado en 2007

Examination of chromosome 7p22 candidate genes RBaK, PMS2 and GNA12 in familial hyperaldosteronism type II.

artículo científico publicado en 2008

Exploring the association between severe respiratory syncytial virus infection and asthma: a registry-based twin study

artículo científico publicado en 2009

Familial aggregation of albuminuria and arterial hypertension in an Aboriginal Australian community and the contribution of variants in ACE and TP53.

artículo científico publicado en 2016

Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity

artículo científico publicado en 2005

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

artículo científico publicado en 2009

First all-in-one diagnostic tool for DNA intelligence: genome-wide inference of biogeographic ancestry, appearance, relatedness, and sex with the Identitas v1 Forensic Chip

artículo científico publicado en 2012

From GWAS to genome sequencing: complementary approaches to identify melanoma predisposition genes

artículo científico publicado en 2012

GSTP1 does not modify MC1R effects on melanoma risk

scientific article published on 23 March 2017

GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development

artículo científico publicado en 2011

Genes Determining Nevus Count and Dermoscopic Appearance in Australian Melanoma Cases and Controls

artículo científico publicado en 2019

Genetic Epidemiology of Asthma ⬇️

artículo científico publicado el 1 de enero de 1997

Genetic Factors Explain Variation in the Age at Onset of Psoriasis: A Population-based Twin Study.

artículo científico publicado en 2015

Genetic analysis of the age at menopause by using estimating equations and Bayesian random effects models

artículo científico publicado en 2000

Genetic and Environmental Influences on Skin Pattern Deterioration

Genetic and Environmental Risk Factors for Asthma

artículo científico publicado en 1998

Genetic control of the renal clearance of urate: a study of twins ⬇️

artículo científico publicado el 1 de marzo de 1992

Genetic determinants of diabetes are similarly associated with other immune-mediated diseases

artículo científico publicado en 2007

Genetic influence on the age at onset of asthma: a twin study

artículo científico publicado en 2010

Genetic influences of chromosomes 5q31-q33 and 11q13 on specific IgE responsiveness to common inhaled allergens among African American families. Collaborative Study on the Genetics of Asthma (CSGA).

artículo científico publicado en 1998

Genetic influences on handedness: data from 25,732 Australian and Dutch twin families

artículo científico publicado en 2009

Genetic regulation of Dermatophagoides pteronyssinus–specific IgE responsiveness: A genome-wide multipoint linkage analysis in families recruited through 2 asthmatic sibs

article

Genetic studies on atopy and helminthiasis

artículo científico publicado en 1999

Genetic time-series analysis identifies a major QTL for in vivo alcohol metabolism not predicted by in vitro studies of structural protein polymorphism at the ADH1B or ADH1C loci

artículo científico publicado en 2005

Genetics of asthma and hay fever in Australian twins.

artículo científico publicado en 1990

Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up

artículo científico publicado en 2015

Genome-Wide Association Shows that Pigmentation Genes Play a Role in Skin Aging

artículo científico publicado en 2017

Genome-Wide Association Studies Identify Multiple Genetic Loci Influencing Eyebrow Color Variation in Europeans

artículo científico publicado en 2019

Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype

artículo científico publicado en 2014

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

artículo científico publicado en 2020

Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

artículo científico publicado en 2018

Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA.

artículo científico publicado en 2012

Genome-wide association study identifies 48 common genetic variants associated with handedness

artículo científico publicado en 2020

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

scientific journal article

Genome-wide association study identifies novel loci predisposing to cutaneous melanoma

artículo científico publicado en 2011

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

artículo científico publicado en 2009

Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. ⬇️

artículo científico publicado en 2018

Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits

artículo científico publicado en 2013

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma ⬇️

artículo científico publicado en 2015

Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q.

artículo científico publicado en 2005

Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26.

artículo científico publicado en 2005

Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants

scientific article published on 23 September 2020

HLA and genomewide allele sharing in dizygotic twins

artículo científico publicado en 2006

Handedness in twins: joint analysis of data from 35 samples

artículo científico publicado en 2006

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

artículo científico publicado en 2009

Haplotype sharing excludes orthologousCOL4A3,COL4A4orMYH9loci in hereditary nephritis in bull terriers

artículo científico publicado en 2009

Head Motion and Inattention/Hyperactivity Share Common Genetic Influences: Implications for fMRI Studies of ADHD.

artículo científico publicado en 2016

Heritability and linkage analysis of appendicitis utilizing age at onset

artículo científico publicado en 2009

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

artículo científico publicado en 2016

Heterogeneity of melanoma risk in families of melanoma patients.

artículo científico publicado en 1994

High allergen‐specific serum immunoglobulin E levels in nonatopic West Highland white terriers ⬇️

artículo científico publicado el 26 de enero de 2011

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

scientific article published on 17 July 2019

Human pigmentation genes under environmental selection ⬇️

artículo científico publicado el 26 de septiembre de 2012

Human twinning is not linked to the region of chromosome 4 syntenic with the sheep twinning geneFecB

article

IBD sharing around the PPARG locus is not increased in dizygotic twins or their mothers

artículo científico publicado en 2001

IRF4 rs12203592*T/T genotype is associated with nodular melanoma

artículo científico publicado en 2019

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

artículo científico publicado en 2010

Identification of IL6R and chromosome 11q13.5 as risk loci for asthma

artículo científico publicado en 2011

Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees

artículo científico publicado en 2004

Identification of a melanoma susceptibility locus and somatic mutation in TET2.

artículo científico publicado en 2014

Identification of families with cortical Lewy body disease.

artículo científico publicado en 2004

IgE Responsiveness to Dermatophagoides farinae in West Highland White Terrier Dogs Is Associated with Region on CFA35

scientific article published on 01 September 2011

Increased DNA methylation at the AXIN1 gene in a monozygotic twin from a pair discordant for a caudal duplication anomaly

artículo científico publicado en 2006

Increasing the Response Rate to a Mailed Questionnaire by Including more Stamps on the Return Envelope: A Cotwin Control Study

article

Informativeness of twin-nuclear family and nuclear family designs for segregation analysis

artículo científico publicado en 1991

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes

artículo científico publicado en 2004

Investigation of diabetes mellitus in Burmese cats as an inherited trait: a preliminary study

artículo científico publicado en 2013

Investigation of the relationship between smoking and appendicitis in Australian twins

artículo científico publicado en 2008

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

artículo científico publicado en 2018

Is fragile X syndrome a risk factor for dizygotic twinning?

artículo científico publicado en 1997

Is the genetics of moliness simply the genetics of sun exposure? A path analysis of nevus counts and risk factors in British twins

artículo científico publicado en 1992

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities

article

Limited genetic control of specific IgE responses to rye grass pollen allergens in Australian twins

article

Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task

artículo científico publicado en 2005

Linkage analysis excludes the involvement of the canine PKD2 homologue in bull terrier polycystic kidney disease

artículo científico publicado en 2006

Linkage analysis of Dermatophagoides pteronyssinus–specific IgE responsiveness with polymorphic markers on chromosome 6p21 (HLA-D region) in Caucasian families by the transmission/disequilibrium test

article

Linkage and Association Analysis of Spectrophotometrically Quantified Hair Color in Australian Adolescents: the Effect of OCA2 and HERC2

article

Linkage and association analysis of radiation damage repair genes XRCC3 and XRCC5 with nevus density in adolescent twins

artículo científico publicado en 2003

Linkage confirms canine pkd1 orthologue as a candidate for bull terrier polycystic kidney disease

artículo científico publicado en 2009

Linkage of Asthma and Total Serum IgE Concentration to Markers on Chromosome 12q: Evidence from Afro-Caribbean and Caucasian Populations

article

Linkage of Paget disease of bone to a novel region on human chromosome 18q23.

artículo científico publicado en 2001

MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations

artículo científico publicado en 2001

Major quantitative trait locus for eosinophil count is located on chromosome 2q

artículo científico publicado en 2004

Maternal Cigarette Smoking and Oral Clefts: A Meta-analysis

artículo científico publicado en 1997

Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?

artículo científico publicado en 2000

Meta-analysis identifies seven susceptibility loci involved in the atopic march

artículo científico publicado en 2015

Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy

artículo científico publicado en 2010

Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization

artículo científico publicado en 2013

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

artículo científico publicado en 2012

Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits

artículo científico publicado en 2014

Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma

artículo científico publicado en 2021

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

artículo científico publicado en 2009

Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q

article

Mutations atKCNQ1and an unknown locus cause long QT syndrome in a large Australian family: Implications for genetic testing

article

Mutations in the follicle-stimulating hormone receptor and familial dizygotic twinning

artículo científico publicado en 2001

NATURAL SELECTION AND QUANTITATIVE GENETICS OF LIFE-HISTORY TRAITS IN WESTERN WOMEN: A TWIN STUDY

article

Natural selection and quantitative genetics of life-history traits in Western women: a twin study

artículo científico publicado en 2001

New Concepts for Distinguishing the Hidden Patterns of Linkage Disequilibrium Which Underlie Association Between Genotypes and Complex Phenotypes

No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2008

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

artículo científico publicado en 2019

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways ⬇️

artículo científico publicado en 2018

Novel susceptibility gene for late-onset NIDDM is localized to human chromosome 12q

article

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

artículo científico publicado en 2006

Ocular melanoma is not associated with CDKN2A or MC1R variants--a population-based study

artículo científico publicado en 2003

Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females

artículo científico publicado en 2005

Osteoporosis in rheumatoid arthritis

scientific article published on 01 June 1995

PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers

artículo científico publicado en 2011

Phenotypic and genotypic analysis of amelanotic and hypomelanotic melanoma patients

artículo científico publicado en 2019

Phenotypic characterization of nevus and tumor patterns in MITF E318K mutation carrier melanoma patients

artículo científico publicado en 2013

Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma

artículo científico publicado en 2011

Polymorphisms in the 5-lipoxygenase activating protein (ALOX5AP) gene are not associated with asthma in an Australian population

article

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

artículo científico publicado en 2009

Potential Modifying Loci Associated With Primary Lens Luxation, Pedal Hyperkeratosis, and Ocular Phenotypes in Miniature Bull Terriers

artículo científico publicado en 2015

Progesterone receptor polymorphisms and risk of breast cancer: results from two Australian breast cancer studies

article

Psoriasis in Australian twins.

artículo científico publicado en 1993

Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways ⬇️

artículo científico publicado en 2019

Rapid screening of 4000 individuals for germ-line variations in the BRAF gene

artículo científico publicado en 2006

Real-time PCR quantification of the canine filaggrin orthologue in the skin of atopic and non-atopic dogs: a pilot study

artículo científico publicado en 2011

Recent human effective population size estimated from linkage disequilibrium

artículo científico publicado en 2007

Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles

artículo científico publicado en 2007

Red hair is the null phenotype of MC1R.

artículo científico publicado en 2008

Report of Endometrial Cancer in Australian BRCA1 and BRCA2 mutation-positive Families.

artículo científico publicado en 2011

Respiratory symptoms in Queensland schoolchildren: an association between month of birth and respiratory illness

artículo científico publicado en 1991

Risk factors for asthma in young adults: a co-twin control study.

artículo científico publicado en 2006

Risk factors for atherosclerosis in twins

scientific article published on 01 January 1993

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

artículo científico publicado en 2010

Robust estimation of experimentwise P values applied to a genome scan of multiple asthma traits identifies a new region of significant linkage on chromosome 20q13.

artículo científico publicado en 2005

Screening a 2 cM genetic map for allelic association: A simulated oligogenic trait

article by David Duffy published 1995 in Genetic Epidemiology

Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families

artículo científico publicado en 2005

Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

artículo científico publicado en 2017

Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1.

artículo científico publicado en 2008

Special twin environments, genetic influences and their effects on the handedness of twins and their siblings

artículo científico publicado en 2003

Spectrophotometric methods for quantifying pigmentation in human hair-influence of MC1R genotype and environment

artículo científico publicado en 2008

Systematic review and meta-analysis of the association between {beta}2-adrenoceptor polymorphisms and asthma: a HuGE review.

artículo científico publicado en 2005

The CD14 C-159T polymorphism is not associated with asthma or asthma severity in an Australian adult population.

artículo científico publicado en 2005

The EPAS1 gene influences the aerobic-anaerobic contribution in elite endurance athletes

artículo científico publicado en 2005

The Genetics of Renal Excretion of Urate in Man ⬇️

artículo científico publicado el 1 de enero de 1991

The Korean Twin Registry--methods, current stage, and interim results.

artículo científico publicado en 2002

The Queensland Study of Melanoma: environmental and genetic associations (Q-MEGA); study design, baseline characteristics, and repeatability of phenotype and sun exposure measures

artículo científico publicado en 2008

The Relationship Between Personality and Somatic and Psychological Distress: A Comparison of Chinese and Australian Adolescents

article

The androgen receptor CAG repeat polymorphism and modification of breast cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2005

The inheritance of extra-hepatic portosystemic shunts and elevated bile acid concentrations in Maltese dogs

artículo científico publicado en 2013

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

artículo científico publicado en 2019

The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes.

artículo científico publicado en 2003

The standard error of Cohen's kappa by J. Barry Garner, Statistics in Medicine, 10, 767-775 (1991)

artículo científico publicado el 1 de agosto de 1992

The value of relatives with phenotypes but missing genotypes in association studies for quantitative traits

article published in 2005

Toward the full spectrum of genes for human skin colour

artículo científico publicado en 2018

Type A personality in Australian twins

article

Unexpectedly severe acute radiotherapy side effects are associated with single nucleotide polymorphisms of the melanocortin-1 receptor

artículo científico publicado en 2009

Variance components analyses of multiple asthma traits in a large sample of Australian families ascertained through a twin proband.

artículo científico publicado en 2006

Variation at DENND1B and Asthma on the Island of Tristan da Cunha

scientific article published on 14 October 2019

Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning

artículo científico

Variation in Latent Classes of Adult Attention-Deficit Hyperactivity Disorder by Sex and Environmental Adversity

artículo científico publicado en 2013

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

artículo científico publicado en 2008

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