Tracy Dudding‐Byth

1.0k total citations
18 papers, 272 citations indexed

About

Tracy Dudding‐Byth is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tracy Dudding‐Byth has authored 18 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 10 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tracy Dudding‐Byth's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Tracy Dudding‐Byth is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Tracy Dudding‐Byth collaborates with scholars based in Australia, United Kingdom and United States. Tracy Dudding‐Byth's co-authors include Cheryl Shoubridge, Victoria L. Harvey, Benjamin Kamien, Anna Hackett, Rodney J. Scott, Michelle C. Ward, Gemma Poke, Michael Field, William T. Gibson and Kathryn Friend and has published in prestigious journals such as International Journal of Molecular Sciences, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

Tracy Dudding‐Byth

17 papers receiving 270 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‐Byth Australia 10 147 146 37 24 24 18 272
Frédérique Sloan‐Béna Switzerland 9 123 0.8× 87 0.6× 30 0.8× 24 1.0× 12 0.5× 23 263
Konstantina Kosma Greece 10 130 0.9× 137 0.9× 37 1.0× 21 0.9× 8 0.3× 30 288
Christopher Stoddard United States 7 167 1.1× 91 0.6× 27 0.7× 8 0.3× 41 1.7× 11 258
Mathilde Nizon France 13 239 1.6× 153 1.0× 41 1.1× 11 0.5× 26 1.1× 26 387
Dhanya Lakshmi Narayanan India 10 135 0.9× 88 0.6× 22 0.6× 8 0.3× 19 0.8× 42 261
Amal Hashem Saudi Arabia 9 236 1.6× 138 0.9× 46 1.2× 8 0.3× 54 2.3× 11 354
Irén Haltrich Hungary 9 103 0.7× 93 0.6× 22 0.6× 33 1.4× 15 0.6× 33 239
Nathalie Marle France 11 170 1.2× 237 1.6× 56 1.5× 16 0.7× 42 1.8× 23 373
Mahmoud Taleb Al‐Ali United Arab Emirates 10 174 1.2× 150 1.0× 44 1.2× 6 0.3× 38 1.6× 34 312
Gabriela Stangoni Italy 9 122 0.8× 166 1.1× 35 0.9× 16 0.7× 18 0.8× 24 257

Countries citing papers authored by Tracy Dudding‐Byth

Since Specialization
Citations

This map shows the geographic impact of Tracy Dudding‐Byth'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‐Byth 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‐Byth more than expected).

Fields of papers citing papers by Tracy Dudding‐Byth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tracy Dudding‐Byth. 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‐Byth. The network helps show where Tracy Dudding‐Byth may publish in the future.

Co-authorship network of co-authors of Tracy Dudding‐Byth

This figure shows the co-authorship network connecting the top 25 collaborators of Tracy Dudding‐Byth. A scholar is included among the top collaborators of Tracy Dudding‐Byth 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‐Byth. Tracy Dudding‐Byth is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Dudding‐Byth, Tracy, et al.. (2025). Updated penetrance estimates for recurrent copy number variants – an improved definition and formula. European Journal of Human Genetics. 34(1). 119–127.
2.
Dudding‐Byth, Tracy, et al.. (2024). A systematic review and pooled analysis of penetrance estimates of copy-number variants associated with neurodevelopment. Genetics in Medicine. 27(1). 101227–101227. 6 indexed citations
3.
Leffler, Melanie, Louise Christie, Anna Hackett, et al.. (2023). Further delineation of dosage‐sensitive K/L mediated Xq28 duplication syndrome includes incomplete penetrance. Clinical Genetics. 103(6). 681–687. 1 indexed citations
4.
Ashton, Katie A., Ying Zhu, Futao Zhang, et al.. (2023). Integration of EpiSign, facial phenotyping, and likelihood ratio interpretation of clinical abnormalities in the re‐classification of an ARID1B missense variant. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 193(3). e32056–e32056. 3 indexed citations
5.
Shoubridge, Cheryl, et al.. (2022). IQSEC2 ‐related encephalopathy in males due to missense variants in the pleckstrin homology domain. Clinical Genetics. 102(1). 72–77. 4 indexed citations
6.
Baker, Emma K., et al.. (2022). Methylation analysis and developmental profile of two individuals with Angelman syndrome due to mosaic imprinting defects. European Journal of Medical Genetics. 65(4). 104456–104456. 3 indexed citations
7.
Bruinsma, Fiona, Susan J. Jordan, Julie K. Bassett, et al.. (2021). Analgesic use and the risk of renal cell carcinoma – Findings from the Consortium for the Investigation of Renal Malignancies (CONFIRM) study. Cancer Epidemiology. 75. 102036–102036. 6 indexed citations
8.
Dudding‐Byth, Tracy, et al.. (2021). Experiences of non‐invasive prenatal screening: A survey study. Australian and New Zealand Journal of Obstetrics and Gynaecology. 62(2). 241–249. 10 indexed citations
9.
Field, Michael, Tracy Dudding‐Byth, Marta Arpone, et al.. (2019). Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing. International Journal of Molecular Sciences. 20(16). 3907–3907. 13 indexed citations
10.
Kamien, Benjamin, Anne Ronan, Gemma Poke, et al.. (2018). A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing. Molecular Syndromology. 9(2). 70–82. 32 indexed citations
11.
Hackett, Anna, Marie Shaw, Alina Ilie, et al.. (2018). A recurrent missense variant inSLC9A7causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylation. Human Molecular Genetics. 28(4). 598–614. 21 indexed citations
12.
Shoubridge, Cheryl, Victoria L. Harvey, & Tracy Dudding‐Byth. (2018). IQSEC2mutation update and review of the female-specific phenotype spectrum including intellectual disability and epilepsy. Human Mutation. 40(1). 5–24. 35 indexed citations
13.
Beygo, Jasmin, Benjamin Kamien, Jill Clayton‐Smith, et al.. (2017). Atypical Angelman syndrome due to a mosaic imprinting defect: Case reports and review of the literature. American Journal of Medical Genetics Part A. 173(3). 753–757. 18 indexed citations
14.
Dudding‐Byth, Tracy, Elizabeth Holliday, Anna Hackett, et al.. (2017). Computer face-matching technology using two-dimensional photographs accurately matches the facial gestalt of unrelated individuals with the same syndromic form of intellectual disability. BMC Biotechnology. 17(1). 90–90. 24 indexed citations
15.
McInerney‐Leo, Aideen, Jessica Harris, Michael Gattas, et al.. (2016). Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate Families. Human Mutation. 37(7). 695–702. 33 indexed citations
16.
Kamien, Benjamin, M. Cristina Digilio, Antonio Novelli, et al.. (2015). Narrowing the critical region for overgrowth within 13q14.2-q14.3 microdeletions. European Journal of Medical Genetics. 58(11). 629–633. 6 indexed citations
17.
Dudding‐Byth, Tracy. (2015). A powerful team: the family physician advocating for patients with a rare disease.. PubMed. 44(9). 634–8. 17 indexed citations
18.
Corbett, Mark, Tracy Dudding‐Byth, Patricia Crock, et al.. (2015). A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A. Journal of Medical Genetics. 52(4). 269–274. 40 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Frédérique Sloan‐Béna Breakdown of academic impact, for papers by Konstantina Kosma Breakdown of academic impact, for papers by Christopher Stoddard Breakdown of academic impact, for papers by Mathilde Nizon Breakdown of academic impact, for papers by Dhanya Lakshmi Narayanan Breakdown of academic impact, for papers by Amal Hashem Breakdown of academic impact, for papers by Irén Haltrich Breakdown of academic impact, for papers by Nathalie Marle Breakdown of academic impact, for papers by Mahmoud Taleb Al‐Ali Breakdown of academic impact, for papers by Gabriela Stangoni
Rankless by CCL
2026