Tracy Dudding

3.7k total citations
24 papers, 752 citations indexed

About

Tracy Dudding is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tracy Dudding has authored 24 papers receiving a total of 752 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tracy Dudding's work include BRCA gene mutations in cancer (8 papers), Mitochondrial Function and Pathology (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Tracy Dudding is often cited by papers focused on BRCA gene mutations in cancer (8 papers), Mitochondrial Function and Pathology (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Tracy Dudding collaborates with scholars based in Australia, United Kingdom and United States. Tracy Dudding's co-authors include John Attia, Kathy Tucker, Peter W. Schofield, K. Friend, Judy Kirk, Bettina Meiser, Ingrid Winship, Clara Gaff, Robert I. Richards and Kelly‐Anne Phillips and has published in prestigious journals such as The Lancet, Neurology and The Lancet Oncology.

In The Last Decade

Tracy Dudding

23 papers receiving 739 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tracy Dudding Australia 16 276 239 148 122 115 24 752
Myra Wick United States 16 299 1.1× 397 1.7× 170 1.1× 131 1.1× 58 0.5× 55 1.1k
Solaf M. Elsayed Egypt 15 471 1.7× 548 2.3× 109 0.7× 50 0.4× 100 0.9× 63 1.1k
Isabelle Pellegrini France 19 305 1.1× 529 2.2× 73 0.5× 62 0.5× 23 0.2× 35 1.7k
Richard H. Scott United Kingdom 21 676 2.4× 760 3.2× 363 2.5× 57 0.5× 62 0.5× 42 1.5k
Maureen Byrne United States 11 57 0.2× 130 0.5× 94 0.6× 30 0.2× 44 0.4× 31 817
Marja Hietala Finland 17 245 0.9× 485 2.0× 71 0.5× 180 1.5× 9 0.1× 37 918
Merel C. van Maarle Netherlands 16 199 0.7× 135 0.6× 309 2.1× 37 0.3× 15 0.1× 29 788
Matias Wagner Germany 16 225 0.8× 447 1.9× 73 0.5× 96 0.8× 9 0.1× 83 792
Dawna Gilchrist Canada 15 552 2.0× 221 0.9× 59 0.4× 33 0.3× 24 0.2× 31 1.0k
Christina Evers Germany 16 274 1.0× 293 1.2× 53 0.4× 27 0.2× 71 0.6× 33 743

Countries citing papers authored by Tracy Dudding

Since Specialization
Citations

This map shows the geographic impact of Tracy Dudding's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Tracy Dudding with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tracy Dudding more than expected).

Fields of papers citing papers by Tracy Dudding

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tracy Dudding. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Tracy Dudding. The network helps show where Tracy Dudding may publish in the future.

Co-authorship network of co-authors of Tracy Dudding

This figure shows the co-authorship network connecting the top 25 collaborators of Tracy Dudding. A scholar is included among the top collaborators of Tracy Dudding based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Tracy Dudding. Tracy Dudding is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Dudding, Tracy, Marta Arpone, David Francis, et al.. (2016). Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia. Genes. 7(9). 68–68. 6 indexed citations
2.
Oegema, Renske, Thomas D. Cushion, Ian G. Phelps, et al.. (2015). Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes. Human Molecular Genetics. 24(18). 5313–5325. 61 indexed citations
3.
Kogelenberg, Margriet van, Alice R. Clark, Zandra A. Jenkins, et al.. (2015). Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA. Journal of Molecular Medicine. 93(7). 773–782. 9 indexed citations
4.
Huang, Lijia, Jodi Warman‐Chardon, Melissa T. Carter, et al.. (2012). Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia. Orphanet Journal of Rare Diseases. 7(1). 67–67. 104 indexed citations
5.
Dudding, Tracy & John Attia. (2012). Maternal factor V Leiden and adverse pregnancy outcome: deciding whether or not to test. The Journal of Maternal-Fetal & Neonatal Medicine. 25(7). 889–894. 5 indexed citations
6.
Dudding, Tracy, Cliff Meldrum, AD Spigelman, et al.. (2010). Can a familial gastrointestinal tumour syndrome be allelic with Waardenburg syndrome?. Clinical Genetics. 79(6). 554–560. 10 indexed citations
7.
Truong, Hoa T., Tracy Dudding, Christopher Blanchard, & Sarah H. Elsea. (2010). Frameshift mutation hotspot identified in Smith-Magenis syndrome: case report and review of literature. BMC Medical Genetics. 11(1). 142–142. 27 indexed citations
8.
Winship, Ingrid & Tracy Dudding. (2008). Lessons from the skin - cutaneous features of familial cancer. The Lancet. 9(5).
9.
Dudding, Tracy, Jon Heron, Eha Nurk, et al.. (2008). Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis. Journal of Thrombosis and Haemostasis. 6(11). 1868–1875. 42 indexed citations
10.
Winship, Ingrid & Tracy Dudding. (2008). Lessons from the skin—cutaneous features of familial cancer. The Lancet Oncology. 9(5). 462–472. 28 indexed citations
11.
Wakefield, Claire E., Bettina Meiser, Judi Homewood, et al.. (2007). A randomized controlled trial of a decision aid for women considering genetic testing for breast and ovarian cancer risk. Breast Cancer Research and Treatment. 107(2). 289–301. 65 indexed citations
12.
Ronan, Anne, Karin Buiting, & Tracy Dudding. (2007). Atypical Angelman syndrome with macrocephaly due to a familial imprinting center deletion. American Journal of Medical Genetics Part A. 146A(1). 78–82. 6 indexed citations
13.
Antill, Yoland, John Reynolds, Mary‐Anne Young, et al.. (2006). Risk-reducing surgery in women with familial susceptibility for breast and/or ovarian cancer. European Journal of Cancer. 42(5). 621–628. 34 indexed citations
14.
Reynolds, John, Mary Young, Judy Kirk, et al.. (2006). Screening behavior in women at increased familial risk for breast cancer. Familial Cancer. 5(4). 359–368. 35 indexed citations
15.
Lobb, Elizabeth, Phyllis Butow, Alison Moore, et al.. (2006). Development of a Communication Aid to Facilitate Risk Communication in Consultations with Unaffected Women from High Risk Breast Cancer Families: A Pilot Study. Australasian Journal of Paramedicine. 15(5). 393–405. 22 indexed citations
16.
Attia, John & Tracy Dudding. (2004). The association between adverse pregnancy outcomes and maternal factor V Leiden genotype: a meta-analysis. Thrombosis and Haemostasis. 91(4). 700–711. 85 indexed citations
17.
Meiser, Bettina, Leroy C. Gould, Kathy Tucker, et al.. (2004). Knowledge of risk management strategies, and information and risk management preferences of women at increased risk for ovarian cancer. Psycho-Oncology. 14(4). 249–261. 22 indexed citations
18.
Dudding, Tracy, et al.. (2004). Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus. Neurology. 63(12). 2288–2292. 58 indexed citations
19.
Dudding, Tracy, et al.. (2000). Reproductive decisions after neonatal screening identifies cystic fibrosis. Archives of Disease in Childhood Fetal & Neonatal. 82(2). F124–F127. 40 indexed citations
20.
Dudding, Tracy, et al.. (1998). Nevoid hypertrichosis with multiple patches of hair that underwent almost complete spontaneous resolution. American Journal of Medical Genetics. 79(3). 195–196. 6 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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