Author

Tracy E Dudding

Observed names: Dudding, Tracy, Dudding, Tracy E, Dudding, Tracy E., T Dudding, T. DUDDING, T. Dudding, T. E. Dudding, Tracy Dudding, Tracy E. Dudding, ˙ Tracy E. Dudding

Institution: Hunter Genetics

Observed institutions: Edith Cowan University, The University of Sydney, The University of Queensland, Princess Margaret Hospital for Children, Women's and Children's Hospital, Children's Hospital at Westmead, UNSW Sydney, Hunter Medical Research Institute, Hunter Genetics, John Hunter Children's Hospital, Hunter New England Local Health District, Imperial College London, The University of Adelaide, University of Newcastle Australia, Newcastle University

ORCID: 0000-0002-9551-1107

Observed ORCID: 0000-0002-9551-1107

OpenAlex ID: A5110118883

Genome-wide association study identifies novel breast cancer susceptibility loci

2007 · Douglas F. Easton, Karen A. Pooley, et al. · Nature · 2,322

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Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

2012 · Lijia Huang, Jodi Warman-Chardon, et al. · Orphanet Journal of Rare Diseases · 159

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The association between adverse pregnancy outcomes and maternal factor V Leiden genotype: a meta-analysis

2004 · John Attia, Tracy Dudding · Thrombosis and Haemostasis · 122

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants

2021 · Adam M. Bournazos, Lisa G. Riley, et al. · Genetics in Medicine · 97

Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus

2004 · T. E. Dudding, K. Friend, et al. · Neurology · 97

Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes

2015 · Renske Oegema, Thomas D. Cushion, et al. · Human Molecular Genetics · 92

A randomized controlled trial of a decision aid for women considering genetic testing for breast and ovarian cancer risk

2007 · Claire E. Wakefield, Bettina Meiser, et al. · Breast Cancer Research and Treatment · 77

Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis

2008 · T. DUDDING, J. HERON, et al. · Journal of Thrombosis and Haemostasis · 64

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Homologous recombination DNA repair defects in PALB2-associated breast cancers

2019 · Anqi Li, Felipe C. Geyer, et al. · npj Breast Cancer · 56

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Lessons from the skin—cutaneous features of familial cancer

2008 · Ingrid M Winship, Tracy E Dudding · The Lancet Oncology · 54

Risk perceptions and knowledge of breast cancer genetics in women at increased risk of developing hereditary breast cancer

2001 · Bettina Meiser, Phyllis Butow, et al. · Psychology and Health · 51

Reproductive decisions after neonatal screening identifies cystic fibrosis

2000 · Tracy Dudding, Bridget Wilcken, et al. · Archives of Disease in Childhood Fetal & Neonatal · 51

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The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

2019 · Gisella Figlioli, Massimo Bogliolo, et al. · npj Breast Cancer · 43

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Risk-reducing surgery in women with familial susceptibility for breast and/or ovarian cancer

2006 · Yoland Antill, John Reynolds, et al. · European Journal of Cancer · 41

Frameshift mutation hotspot identified in Smith-Magenis syndrome: case report and review of literature

2010 · Hoa T Truong, Tracy Dudding, et al. · BMC Medical Genetics · 40

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Screening behavior in women at increased familial risk for breast cancer

2006 · Yoland C. Antill, John Reynolds, et al. · Familial Cancer · 40

A Randomized Controlled Trial of a Decision Aid for Women at Increased Risk of Ovarian Cancer

2006 · K. Tiller, B. Meiser, et al. · Medical Decision Making · 37

Development of a Communication Aid to Facilitate Risk Communication in Consultations with Unaffected Women from High Risk Breast Cancer Families: A Pilot Study

2006 · E. A. Lobb, P. N. Butow, et al. · Journal of Genetic Counseling · 34

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Knowledge of risk management strategies, and information and risk management preferences of women at increased risk for ovarian cancer

2004 · K. Tiller, B. Meiser, et al. · Psycho-Oncology · 32

Differential regulation of twoFLNAtranscripts explains some of the phenotypic heterogeneity in the loss-of-function filaminopathies

2017 · Zandra A Jenkins, Alison Macharg, et al. · Human Mutation · 31

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Development and validation of a targeted gene sequencing panel for application to disparate cancers

2019 · Mark J. McCabe, Marie-Emilie A. Gauthier, et al. · Scientific Reports · 27

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Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure

2010 · T. E. Dudding, O. Lawrence, et al. · Human Reproduction · 20

Neonatal screening for cystic fibrosis

2000 · T Dudding, B Wilcken, et al. · The Lancet · 16

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Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA

2015 · Margriet van Kogelenberg, Alice R. Clark, et al. · Journal of Molecular Medicine · 13

Nevoid hypertrichosis with multiple patches of hair that underwent almost complete spontaneous resolution

1998 · Tracy E. Dudding, Maureen Rogers, et al. · American Journal of Medical Genetics · 13

Works count: 49

Citation count: 3,686

H-index: 21

I10-index: 27