Author

Juleen A. Cavanaugh

Observed names: Cavanaugh, Juleen Ann, J CAVANAUGH, J Cavanaugh, J. A. CAVANAUGH, J. A. Cavanaugh, J.A. Cavanaugh, JULEEN A CAVANAUGH, Juleen A Cavanaugh, Juleen Cavanaugh

Institution: Australian National University

Observed institutions: Australian National University, Commonwealth Scientific and Industrial Research Organisation, The University of Sydney, Government of South Australia, Canberra Hospital, University of Chicago, St Vincent's Hospital Sydney

OpenAlex ID: A5031776615

Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19

2004 · Heng F Seow, Stefan Bröer, et al. · Nature Genetics · 270

Molecular Cloning of Mouse Amino Acid Transport System B0, a Neutral Amino Acid Transporter Related to Hartnup Disorder

2004 · Angelika Bröer, Karin Klingel, et al. · Journal of Biological Chemistry · 247

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Screening for Hemochromatosis in Asymptomatic Subjects With or Without a Family History

2006 · Lawrie W. Powell, Jeannette L. Dixon, et al. · Archives of Internal Medicine · 199

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Prevalence of CARD15/NOD2 Mutations in Caucasian Healthy People

2007 · Jean-Pierre Hugot, Isabelle Zaccaria, et al. · The American Journal of Gastroenterology · 198

International Collaboration Provides Convincing Linkage Replication in Complex Disease through Analysis of a Large Pooled Data Set: Crohn Disease and Chromosome 16

2001 · Juleen Cavanaugh · The American Journal of Human Genetics · 197

Characterization of the monomethylarsonate reductase and dehydroascorbate reductase activities of Omega class glutathione transferase variants: implications for arsenic metabolism and the age-at-onset of Alzheimer's and Parkinson's diseases

2005 · Erica M. Schmuck, Philip G. Board, et al. · Pharmacogenetics and Genomics · 168

The Clinical Relevance of Compound Heterozygosity for the C282Y and H63D Substitutions in Hemochromatosis

2006 · Alissa Walsh, Jeannette L. Dixon, et al. · Clinical Gastroenterology and Hepatology · 113

Characterisation of a highly sensitive troponin I assay and its application to a cardio-healthy population

2012 · Gus Koerbin, Jill Tate, et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 111

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

2008 · Stefan Bröer, Charles G. Bailey, et al. · Journal of Clinical Investigation · 111

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Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16

1998 · J. A. CAVANAUGH, D. F. CALLEN, et al. · Annals of Human Genetics · 108

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CARD15/NOD2 Risk Alleles in the Development of Crohn's Disease in the Australian Population

2003 · J. A. Cavanaugh, K. E. Adams, et al. · Annals of Human Genetics · 94

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

2008 · Elizabeth V. Fowler, James Doecke, et al. · The American Journal of Gastroenterology · 90

The IBD International Genetics Consortium Provides Further Evidence for Linkage to IBD4 and Shows Gene-Environment Interaction

2005 · Marie Pierik, Huiying Yang, et al. · Inflammatory Bowel Diseases · 71

Deleterious GRM1 Mutations in Schizophrenia

2012 · Mohammed Akli Ayoub, Dora Angelicheva, et al. · PLoS ONE · 70

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

2010 · Lisa A Simms, James D Doecke, et al. · The American Journal of Gastroenterology · 65

The molecular basis of neutral aminoacidurias

2005 · Angelika Bröer, Juleen A. Cavanaugh, et al. · Pflügers Archiv - European Journal of Physiology · 60

NOD2: Ethnic and geographic differences

2006 · Juleen Cavanaugh · World Journal of Gastroenterology · 56

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Neutral amino acid transport in epithelial cells and its malfunction in Hartnup disorder

2005 · S. Bröer, J.A. Cavanaugh, et al. · Biochemical Society Transactions · 49

Further evidence for allelic heterogeneity in Hartnup disorder

2008 · Dimitar N. Azmanov, Sonja Kowalczuk, et al. · Human Mutation · 35

Choice of Statistical Tools for Outlier Removal Causes Substantial Changes in Analyte Reference Intervals in Healthy Populations

2020 · Peter E Hickman, Gus Koerbin, et al. · Clinical Chemistry · 27

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‘Aussie normals’: an a priori study to develop clinical chemistry reference intervals in a healthy Australian population

2014 · G. Koerbin, J.A. Cavanaugh, et al. · Pathology · 26

Deletion of Glu155 causes a deficiency of glutathione transferase Omega 1-1 but does not alter sensitivity to arsenic trioxide and other cytotoxic drugs

2008 · Erica Schmuck, Jean Cappello, et al. · The International Journal of Biochemistry & Cell Biology · 26

Persistence of the Common Hartnup Disease D173N Allele in Populations of European Origin

2007 · Dimitar N. Azmanov, Helen Rodgers, et al. · Annals of Human Genetics · 16

Using a thyroid disease-free population to define the reference interval for TSH and free T4 on the Abbott Architect analyser

2016 · Peter E. Hickman, Gus Koerbin, et al. · Clinical Endocrinology · 13

Lack of association of theCD14promoter polymorphism −159C/T with Caucasian inflammatory bowel disease

2005 · Kirsten E. Peters, Nathan J. O'Callaghan, et al. · Scandinavian Journal of Gastroenterology · 12

Works count: 51

Citation count: 2,531

H-index: 22

I10-index: 26