Tracy Dudding‐Byth

4.8k citations

70 papers · 3.7k · 1 hit paper · h-index 28

Impact in

Genetics top 1%
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Cancer Research top 5%
- Cancer Genomics and Diagnostics

Papers in

Genetics 41
- Genetics and Neurodevelopmental Disorders 15
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 11
- BRCA gene mutations in cancer 10
- Genetic Syndromes and Imprinting 5
Hematology 7
- Blood Coagulation and Thrombosis Mechanisms 4

Co-authors: John Attia (5 shared papers)Katherine Mary Tucker (7 shared papers)Kathie L. Friend (2 shared papers)Peter William Schofield (2 shared papers)Judy Kirk (5 shared papers)Ingrid Winship (4 shared papers)Bettina Meiser (4 shared papers)Cheryl Shoubridge (2 shared papers)
Journals: Clinical Genetics (5 papers)Human Mutation (5 papers)Genetics in Medicine (4 papers)The American Journal of Human Genetics (4 papers)European Journal of Human Genetics (2 papers)
Partner nations: Australia United States United Kingdom

In The Last Decade

Tracy Dudding‐Byth

65 papers receiving 3.6k citations

Tracy Dudding‐Byth's Hit Papers

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Genome-wide association study identifies novel breast cancer susceptibility loci 2007 · 1.9k citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2007 Nature

Peers

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-authors

The 25 scholars most cited alongside Tracy Dudding‐Byth, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Tracy Dudding‐Byth Line = papers co-authored together Tracy Dudding‐Byth links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 70 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Genome-wide association study identifies novel breast cancer susceptibility loci Nature ·Douglas F. Easton, Karen A. Pooley, Alison Margaret Dunning, Paul D.P. Pharoah, Deborah J. Thompson, Dennis G. Ballinger, Jeffery P. Struewing, Jonathan James Morrison Hit paper breakdown →	2007	1916
2	Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia Orphanet Journal of Rare Diseases ·Lijia Huang, Jodi Warman‐Chardon, Melissa T. Carter, Kathie L. Friend, Tracy Dudding‐Byth, Jeremy Schwartzentruber, Ruobing Zou, Peter William Schofield	2012	122
3	The association between adverse pregnancy outcomes and maternal factor V Leiden genotype: a meta-analysis Thrombosis and Haemostasis ·John Attia, Tracy Dudding‐Byth	2004	94
4	The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome Genetics in Medicine ·Pleuntje J. van der Sluijs, Sandra Jansen, Samantha A. Schrier Vergano, Miho Adachi-Fukuda, Yasemin Alanay, Adila Al‐Kindy, Anwar Baban, Allan Bayat	2018	93
5	Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures The American Journal of Human Genetics ·Slavé Petrovski, Sébastien Küry, Candace T. Myers, Kwame Anyane‐Yeboa, Benjamin Cognè, Martin G. Bialer, Fan Xia, Parisa Hemati	2016	92
6	Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus Neurology ·Tracy Dudding‐Byth, Kathie L. Friend, Peter William Schofield, S. Lee, Ingrid Wilkinson, Robert I. Richards	2004	77
7	Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes Human Molecular Genetics ·Renske Oegema, Thomas David Cushion, Ian G. Phelps, Seo‐Kyung Chung, Jennifer C. Dempsey, Sarah Collins, Jonathan G.L. Mullins, Tracy Dudding‐Byth	2015	73
8	Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants Genetics in Medicine ·Adam Bournazos, Lisa G. Riley, Shobhana Bommireddipalli, Lesley C. Adès, Lauren S. Akesson, Mohammad Al-Shinnag, Stephen I. Alexander, Alison Dalton Archibald	2021	66
9	A randomized controlled trial of a decision aid for women considering genetic testing for breast and ovarian cancer risk Breast Cancer Research and Treatment ·Claire Elizabeth Wakefield, Bettina Meiser, Judi Homewood, Michelle Peate, Alan Taylor, Elizabeth Anne Lobb, Judy Kirk, Young Mary-Anne	2007	65
10	The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients Modern Pathology ·Ngoc Minh Nguyen, Yassemine Khawajkie, Nawel Mechtouf, Maryam Rezaei, Magali Bréguet, Elvira Kurvinen, Sujatha M. Jagadeesh, Aslı Ece Solmaz	2018	64
11	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 ·Tracy Dudding‐Byth, Jon Heron, Amarin Thakkinstian, Eha Nurk, Jean Golding, Marcus E. Pembrey, Susan M. Ring, John Attia	2008	50
12	A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A Journal of Medical Genetics ·Mark A Corbett, Tracy Dudding‐Byth, Patricia Crock, Elena Botta, Louise Christie, Tiziana Nardò, Giuseppina Caligiuri, Lynne Hobson	2015	48
13	Spinocerebellar ataxia type 29 due to mutations in ITPR1: a case series and review of this emerging congenital ataxia Orphanet Journal of Rare Diseases ·Jessica L. Zambonin, Allison Bellomo, Hilla Ben‐Pazi, David B. Everman, Lee M. Frazer, Michael T. Geraghty, Amy D. Harper, Julie R. Jones	2017	46
14	Homologous recombination DNA repair defects in PALB2-associated breast cancers npj Breast Cancer ·Anqi Li, Felipe Correa Geyer, Pedro Blecua, Ju Youn Lee, Pier Selenica, David N. Brown, Fresia G. Pareja, Simon Lee	2019	46
15	Reproductive decisions after neonatal screening identifies cystic fibrosis Archives of Disease in Childhood Fetal & Neonatal ·Tracy Dudding‐Byth +4 others	2000	45
16	Risk perceptions and knowledge of breast cancer genetics in women at increased risk of developing hereditary breast cancer Psychology and Health ·Bettina Meiser, Phyllis Noemi Butow, Alexandra L Barratt, Michael R. Gattas, Clara Gaff, Eric Haan, Margaret A. Gleeson, Tracy Dudding‐Byth	2001	45
17	IQSEC2mutation update and review of the female-specific phenotype spectrum including intellectual disability and epilepsy Human Mutation ·Cheryl Shoubridge, Tracy Dudding‐Byth +1 other	2018	41
18	Risk-reducing surgery in women with familial susceptibility for breast and/or ovarian cancer European Journal of Cancer ·Yoland Catherine Antill, John Reynolds, Young Mary-Anne, Judy Kirk, Katherine Mary Tucker, Tarli L. Bogtstra, Shirley Wong, Tracy Dudding‐Byth	2006	39
19	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 ·Tracy Dudding‐Byth, Anne Baxter, Elizabeth G. Holliday, Anna Hackett, Sheridan O’Donnell, Susan M. White, John Attia, Han G. Brunner	2017	38
20	Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate Families Human Mutation ·Aideen M McInerney-Leo, Jessica Harris, Michael R. Gattas, Elizabeth Peach, Stephen Sinnott, Tracy Dudding‐Byth, Sulekha Rajagopalan, Christopher Barnett	2016	38

About Tracy Dudding‐Byth

Tracy Dudding‐Byth is a scholar working on Genetics, Hematology, Molecular Biology, Pediatrics, Perinatology and Child Health and Oncology, having authored 70 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (15 papers), Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (11 papers), BRCA gene mutations in cancer (10 papers), Epigenetics and DNA Methylation (6 papers), Prenatal Screening and Diagnostics (5 papers), Genetic Syndromes and Imprinting (5 papers) and Blood Coagulation and Thrombosis Mechanisms (4 papers). The work is most often cited by research in Genetics (1.8k citations), Cancer Research (436 citations), Molecular Biology (1.6k citations), Pathology and Forensic Medicine (295 citations) and Oncology (400 citations). Tracy Dudding‐Byth has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include John Attia, Katherine Mary Tucker, Kathie L. Friend, Peter William Schofield, Judy Kirk, Ingrid Winship, Bettina Meiser, Cheryl Shoubridge, Rodney J. Scott and Robert I. Richards. Their work appears in journals such as Clinical Genetics, Human Mutation, Genetics in Medicine, The American Journal of Human Genetics and European Journal of Human Genetics.

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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In The Last Decade

Tracy Dudding‐Byth

Tracy Dudding‐Byth's Hit Papers

Peers

Countries citing papers authored by Tracy Dudding‐Byth

Fields of papers citing papers by Tracy Dudding‐Byth

All Works

About Tracy Dudding‐Byth

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