J. Ellis

R. Saffery, K. Allen, J. Koplin, 2014, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Androgenic correlates of genetic variation in the gene encoding 5α-reductase type 1

G. Jerums, S. Harrap, S. Panagiotopoulos, 2005, Journal of Human Genetics.

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Constantin Polychronakos, Yiran Guo, Dong Li, 2016 .

Significant population variation in adult male height associated with the Y chromosome and the aromatase gene.

S. Harrap, J. Ellis, M. Stebbing, 2001, The Journal of clinical endocrinology and metabolism.

Association of the Human Y Chromosome With High Blood Pressure in the General Population

S. Harrap, J. Ellis, M. Stebbing, 2000, Hypertension.

Sex-dependent association of blood pressure with oestrogen receptor genes ERα and ERβ

S. Harrap, J. Ellis, Tania Infantino, 2004 .

Sex-dependent association of blood pressure with oestrogen receptor genes ERalpha and ERbeta.

S. Harrap, J. Ellis, Tania Infantino, 2004, Journal of hypertension.

Sex, Genes And Blood Pressure

S. Harrap, J. Ellis, M. Stebbing, 2001, Clinical and experimental pharmacology & physiology.

Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene

S. Harrap, K. Scurrah, J. Ellis, 2010, Experimental dermatology.

Non‐proportional odds multivariate logistic regression of ordinal family data

L. Gurrin, S. Harrap, K. Scurrah, 2015, Biometrical journal. Biometrische Zeitschrift.

Evidence of increased DNA methylation of the androgen receptor gene in occipital hair follicles from men with androgenetic alopecia

S. Harrap, N. Wong, R. Sinclair, 2011, The British journal of dermatology.

Male pattern baldness: current treatments, future prospects.

R. Sinclair, J. Ellis, 2008, Drug discovery today.

Gene‐wide association study between the aromatase gene (CYP19A1) and female pattern hair loss

G. Giles, G. Severi, S. Harrap, 2009, The British journal of dermatology.

Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia

S. Harrap, K. Scurrah, J. Ellis, 2007, Human Genetics.

Polymorphism of the androgen receptor gene is associated with male pattern baldness.

S. Harrap, J. Ellis, M. Stebbing, 2001, The Journal of investigative dermatology.

Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male‐pattern baldness

R Erbel, M. Nöthen, T. Becker, 2011, The British journal of dermatology.

Sex bias in paediatric autoimmune disease - Not just about sex hormones?

J. Munro, R. Chiaroni-Clarke, J. Ellis, 2016, Journal of autoimmunity.

SEARCHING FOR FUNCTIONAL GENETIC VARIANTS IN NON‐CODING DNA

S. Petrou, S. Harrap, J. Ellis, 2008, Clinical and experimental pharmacology & physiology.

Androgen Receptor Copy Number Variation and Androgenetic Alopecia: A Case-Control Study

S. White, S. Harrap, J. Ellis, 2009, PloS one.

A Loss-of-Function Polymorphism in the Human P2X4 Receptor Is Associated With Increased Pulse Pressure

S. Harrap, B. Cromer, L. Stokes, 2011, Hypertension.

The MassARRAY® System for Targeted SNP Genotyping.

J. Ellis, Benjamin Ong, 2017, Methods in molecular biology.

Genomewide association study of peanut allergy reproduces association with amino acid polymorphisms in HLA‐DRB1

A Motyer, Damjan Vukcevic, A. Motyer, 2017, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Future Directions: Gene Polymorphism Diagnostics Relevant to Hair

J. Ellis, 2010 .

The role of genetics and environment in the rise of childhood food allergy

R. Saffery, K. Allen, J. Ellis, 2012, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

A convergent model for placental dysfunction encompassing combined sub-optimal one-carbon donor and vitamin D bioavailability.

R. Saffery, R. Morley, J. Ellis, 2009, Medical hypotheses.

Genetic sharing and heritability of paediatric age of onset autoimmune diseases

Hongzhe Li, Constantin Polychronakos, Yiran Guo, 2015, Nature Communications.

Sibling Exposure and Risk of Juvenile Idiopathic Arthritis

A. Pezic, A. Ponsonby, A. Kemp, 2015, Arthritis & rheumatology.

Fc-gamma receptor polymorphisms differentially influence susceptibility to systemic lupus erythematosus and lupus nephritis.

T. Kuijpers, M. Bijl, M. Tanck, 2016, Rheumatology.

Gene–environment interaction in autoimmune disease

A. Ponsonby, A. Kemp, J. Ellis, 2014, Expert Reviews in Molecular Medicine.

5th Pediatric Allergy and Asthma Meeting (PAAM)

A. Ponsonby, M. Wake, A. Lowe, 2018, Clinical and Translational Allergy.

Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes

S. Harrap, J. Ellis, M. Stebbing, 1998 .

Epigenetic dysregulation of naive CD4+ T-cell activation genes in childhood food allergy

M. Tang, R. Saffery, P. Vuillermin, 2018, Nature Communications.

Epistasis amongst PTPN2 and genes of the vitamin D pathway contributes to risk of juvenile idiopathic arthritis

H. Hakonarson, T. Dwyer, B. Lie, 2015, The Journal of Steroid Biochemistry and Molecular Biology.

Genomewide Association Study Using a High-Density Single Nucleotide Polymorphism Array and Case-Control Design Identifies a Novel Essential Hypertension Susceptibility Locus in the Promoter Region of Endothelial NO Synthase

C. Hoggart, J. Beckmann, Z. Kutalik, 2012, Hypertension.

CD226 (DNAM-1) is associated with susceptibility to juvenile idiopathic arthritis

A. Hinks, J. Houwing-Duistermaat, M. Schilham, 2014, Annals of the rheumatic diseases.

Interaction of Crohn's Disease Susceptibility Genes in an Australian Paediatric Cohort

A. Catto-Smith, D. Cameron, J. Ellis, 2010, PloS one.

Variation in associations between allelic variants of the vitamin D receptor gene and onset of type 1 diabetes mellitus by ambient winter ultraviolet radiation levels: a meta-regression analysis.

J. Carlin, T. Dwyer, A. Pezic, 2008, American journal of epidemiology.

Association of Increased Sun Exposure Over the Life‐course with a Reduced Risk of Juvenile Idiopathic Arthritis

T. Dwyer, A. Pezic, A. Ponsonby, 2018, Photochemistry and photobiology.

Polymorphisms affecting vitamin D-binding protein modify the relationship between serum vitamin D (25[OH]D3) and food allergy.

T. Dwyer, J. Hopper, A. Ponsonby, 2016, The Journal of allergy and clinical immunology.

In vitro exposure of human blood mononuclear cells to active vitamin D does not induce substantial change to DNA methylation on a genome-scale

R. Saffery, D. Martino, J. Ellis, 2014, The Journal of Steroid Biochemistry and Molecular Biology.

Stress-sensitive neurosignalling in depression: an integrated network biology approach to candidate gene selection for genetic association analysis

C. Pennell, J. V. Van eekelen, R. Saffery, 2012, Mental illness.

The genetics of androgenetic alopecia.

S. Harrap, J. Ellis, J. A. Ellis, 2001, Clinics in dermatology.

Effects of NRG1 and DAOA genetic variation on transition to psychosis in individuals at ultra-high risk for psychosis

C. Pantelis, I. Everall, D. Velakoulis, 2013, Translational Psychiatry.

Adiposity Gain During Childhood, ACE I/D Polymorphisms and Metabolic Outcomes

T. Dwyer, J. Dickinson, A. Pezic, 2008, Obesity.

Genetic determinants of paediatric food allergy: A systematic review

K. Allen, J. Koplin, D. Martino, 2019, Allergy.

APOE Genotype and Cardio-Respiratory Fitness Interact to Determine Adiposity in 8-Year-Old Children from the Tasmanian Infant Health Survey

T. Dwyer, J. Dickinson, A. Pezic, 2011, PloS one.

The Epithelial Sodium Channel &ggr;-Subunit Gene and Blood Pressure: Family Based Association, Renal Gene Expression, and Physiological Analyses

N. Samani, P. Braund, S. Hunt, 2011, Hypertension.

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

Joseph T. Glessner, Debra K. Shivers, J. Glessner, 2016, BMC Medical Genetics.

Gene–environment interaction in problematic substance use: interaction between DRD4 and insecure attachments

T. Dwyer, G. Patton, E. Williamson, 2013, Addiction biology.

Possible environmental determinants of juvenile idiopathic arthritis.

A. Ponsonby, J. Munro, J. Ellis, 2010, Rheumatology.

CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY

A. Pezic, A. Ponsonby, R. Chavez, 2012, Pediatric Rheumatology.

A role for the DRD4 exon III VNTR in modifying the association between nicotine dependence and neuroticism.

G. Patton, M. O. van de Ven, C. Olsson, 2011, Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco.

The skin barrier function gene SPINK5 is associated with challenge‐proven IgE‐mediated food allergy in infants

A. Ponsonby, A. Lowe, L. Gurrin, 2017, Allergy.

Children with East Asian-Born Parents Have an Increased Risk of Allergy but May Not Have More Asthma in Early Childhood.

A. Ponsonby, A. Lowe, L. Gurrin, 2019, The journal of allergy and clinical immunology. In practice.

Higher parental occupational social contact is associated with a reduced risk of incident pediatric type 1 diabetes: Mediation through molecular enteroviral indices

J. Carlin, T. Dwyer, A. Pezic, 2018, PloS one.

Insulin gene polymorphism and premature male pattern baldness in the general population.

S. Harrap, J. Ellis, M. Stebbing, 1999, Clinical science.

Genetic variation at the Th2 immune gene IL13 is associated with IgE‐mediated paediatric food allergy

A. Ponsonby, A. Lowe, M. Tang, 2017, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

The DNA methylation landscape of CD4+ T cells in oligoarticular juvenile idiopathic arthritis.

A. Ponsonby, R. Saffery, J. Craig, 2018, Journal of autoimmunity.

Association of juvenile idiopathic arthritis with PTPN22 rs2476601 is specific to females in a Greek population

M. Zervou, G. Goulielmos, R. Chiaroni-Clarke, 2016, Pediatric Rheumatology.

A survey of national and multi-national registries and cohort studies in juvenile idiopathic arthritis: challenges and opportunities

W. Thomson, K. Minden, N. Wulffraat, 2017, Pediatric Rheumatology.

Genes controlling postural changes in blood pressure: comprehensive association analysis of ATP-sensitive potassium channel genes KCNJ8 and ABCC9.

C. Nichols, S. Harrap, K. Scurrah, 2010, Physiological genomics.

Genetic linkage of β and γ subunits of epithelial sodium channel to systolic blood pressure

S. Harrap, J. Ellis, A. Lamantia, 1999, The Lancet.

Selective Genotyping Reveals Association Between the Epithelial Sodium Channel γ-Subunit and Systolic Blood Pressure

S. Harrap, K. Scurrah, J. Ellis, 2007, Hypertension.

Identification and genetic determination of an early life risk disposition for depressive disorder: Atypical stress‐related behaviour in early childhood

S. Zubrick, C. Pennell, J. V. Van eekelen, 2011 .

Genome-scale case-control analysis of CD4+ T-cell DNA methylation in juvenile idiopathic arthritis reveals potential targets involved in disease

A. Ponsonby, L. Gordon, R. Saffery, 2012, Clinical Epigenetics.

Constitutive and Relative Facultative Skin Pigmentation among Victorian Children Including Comparison of Two Visual Skin Charts for Determining Constitutive Melanin Density

T. Dwyer, A. Pezic, A. Ponsonby, 2013, Photochemistry and photobiology.

Insulin gene polymorphism and premature male pattern baldness in the general population

S. Harrap, J. Ellis, M. Stebbing, 1999 .

Synthase Hypertension Susceptibility Locus in the Promoter Region of Endothelial NO Polymorphism Array and Case-Control Design Identifies a Novel Essential Genomewide Association Study Using a High-Density Single Nucleotide

C. Hoggart, J. Beckmann, Z. Kutalik, 2011 .

MicroRNAs in CD4(+) T cell subsets are markers of disease risk and T cell dysfunction in individuals at risk for type 1 diabetes.

James M. Wettenhall, T. Speed, A. Ponsonby, 2016, Journal of autoimmunity.

Comprehensive multi-stage linkage analyses identify a locus for adult height on chromosome 3p in a healthy Caucasian population

G. Byrnes, S. Harrap, K. Scurrah, 2007, Human Genetics.

Phenotypic and environmental factors associated with elevated autoantibodies at clinical onset of paediatric type 1 diabetes mellitus.

J. Carlin, T. Dwyer, A. Pezic, 2012, Results in immunology.

Microbial exposure, interferon gamma gene demethylation in naïve T‐cells, and the risk of allergic disease

A. Ponsonby, P. Sly, R. Saffery, 2009, Allergy.

Beta2-adrenergic receptor polymorphisms are associated with asthma and COPD in adults.

D. Johns, M. Abramson, E. Walters, 2006, Journal of human genetics.

Genetic analysis of male pattern baldness and the 5alpha-reductase genes.

S. Harrap, J. Ellis, M. Stebbing, 1998, The Journal of investigative dermatology.