Bronwyn Kerr

10.7k total citations
67 papers, 3.2k citations indexed

About

Bronwyn Kerr is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Bronwyn Kerr has authored 67 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Genetics, 31 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Bronwyn Kerr's work include Protein Tyrosine Phosphatases (12 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomic variations and chromosomal abnormalities (8 papers). Bronwyn Kerr is often cited by papers focused on Protein Tyrosine Phosphatases (12 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomic variations and chromosomal abnormalities (8 papers). Bronwyn Kerr collaborates with scholars based in United Kingdom, United States and Australia. Bronwyn Kerr's co-authors include Joseph H. Hersh, Michael L. Cunningham, John King, Gail Williams, Mark Stephan, Dian Donnai, Meredith Wilson, Jill Clayton‐Smith, Gillian Turner and David Mowat and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Cancer.

In The Last Decade

Bronwyn Kerr

65 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bronwyn Kerr United Kingdom 32 1.6k 1.3k 480 436 399 67 3.2k
Richard J. Sinke Netherlands 39 2.2k 1.4× 1.2k 0.9× 491 1.0× 231 0.5× 286 0.7× 119 4.4k
Arthur S. Aylsworth United States 32 1.8k 1.1× 1.9k 1.4× 575 1.2× 290 0.7× 596 1.5× 93 3.8k
Lina Basel‐Vanagaite Israel 32 1.9k 1.2× 1.4k 1.1× 233 0.5× 245 0.6× 497 1.2× 111 3.6k
Damien Sanlaville France 33 1.6k 1.0× 2.2k 1.7× 356 0.7× 305 0.7× 585 1.5× 189 3.7k
Alan Fryer United Kingdom 33 1.5k 0.9× 1.4k 1.1× 338 0.7× 279 0.6× 581 1.5× 103 4.5k
Patrick Edery France 33 2.4k 1.5× 1.6k 1.2× 1.2k 2.6× 171 0.4× 250 0.6× 117 4.5k
Angelo Selicorni Italy 29 2.5k 1.6× 1.8k 1.4× 206 0.4× 237 0.5× 553 1.4× 176 3.8k
Lynne M. Bird United States 29 1.5k 1.0× 1.8k 1.4× 258 0.5× 256 0.6× 476 1.2× 101 3.2k
Nathaniel H. Robin United States 32 2.0k 1.3× 2.4k 1.9× 523 1.1× 295 0.7× 672 1.7× 151 4.2k
R. Ellen Magenis United States 32 2.0k 1.3× 2.0k 1.5× 299 0.6× 205 0.5× 538 1.3× 71 3.7k

Countries citing papers authored by Bronwyn Kerr

Since Specialization
Citations

This map shows the geographic impact of Bronwyn Kerr'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 Bronwyn Kerr with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bronwyn Kerr more than expected).

Fields of papers citing papers by Bronwyn Kerr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bronwyn Kerr. 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 Bronwyn Kerr. The network helps show where Bronwyn Kerr may publish in the future.

Co-authorship network of co-authors of Bronwyn Kerr

This figure shows the co-authorship network connecting the top 25 collaborators of Bronwyn Kerr. A scholar is included among the top collaborators of Bronwyn Kerr 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 Bronwyn Kerr. Bronwyn Kerr 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.
Ellingford, Jamie M., Nick Telford, Jill Urquhart, et al.. (2021). High penetrance of myeloid neoplasia with diverse clinical and cytogenetic features in three siblings with a familial GATA2 deficiency. Cancer Genetics. 256-257. 77–80. 1 indexed citations
2.
Gripp, Karen W., Marni E. Axelrad, Kathryn C. Chatfield, et al.. (2019). Costello syndrome: Clinical phenotype, genotype, and management guidelines. American Journal of Medical Genetics Part A. 179(9). 1725–1744. 72 indexed citations
3.
Lennon, Rachel, Helen M. Stuart, Agnieszka Bierżyńska, et al.. (2015). Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease. Pediatric Nephrology. 30(9). 1459–1465. 33 indexed citations
4.
Banka, Siddharth, Damien Lederer, Valérie Benoît, et al.. (2014). Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2). Clinical Genetics. 87(3). 252–258. 91 indexed citations
5.
Rauen, Katherine A., Susan Huson, Emma Burkitt‐Wright, et al.. (2014). Recent developments in neurofibromatoses and RASopathies: Management, diagnosis and current and future therapeutic avenues. American Journal of Medical Genetics Part A. 167(1). 1–10. 36 indexed citations
6.
Giannoulatou, Eleni, Gil McVean, Indira B. Taylor, et al.. (2013). Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline. Proceedings of the National Academy of Sciences. 110(50). 20152–20157. 58 indexed citations
7.
8.
Dauwerse, Johannes G., Jill Dixon, Saskia Seland, et al.. (2010). Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome. Nature Genetics. 43(1). 20–22. 243 indexed citations
9.
O’Connor, Rory V., et al.. (2009). Radial aplasia in CHARGE syndrome: A new association. European Journal of Medical Genetics. 52(4). 239–241. 7 indexed citations
10.
Kerr, Bronwyn, Judith Allanson, Karen W. Gripp, et al.. (2008). The diagnosis of Costello syndrome: Nomenclature in Ras/MAPK pathway disorders. American Journal of Medical Genetics Part A. 146A(9). 1218–1220. 16 indexed citations
11.
Day, Richard O., Dian Donnai, Alan Fryer, et al.. (2008). A clinical and genetic study of the Say/Barber/Biesecker/Young‐Simpson type of Ohdo syndrome. Clinical Genetics. 74(5). 434–444. 17 indexed citations
12.
Lehmann, Katarina, Petra Seemann, Fatma Sılan, et al.. (2007). A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN. The American Journal of Human Genetics. 81(2). 388–396. 84 indexed citations
13.
Ghasemlou, Nader, et al.. (2005). Tissue displacement and impact force are important contributors to outcome after spinal cord contusion injury. Experimental Neurology. 196(1). 9–17. 74 indexed citations
14.
White, Susan M., J. M. Graham, Bronwyn Kerr, et al.. (2005). The adult phenotype in Costello syndrome. American Journal of Medical Genetics Part A. 136A(2). 128–135. 60 indexed citations
15.
Prescott, Katrina, Kathryn Woodfine, Maurice Super, et al.. (2004). A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome. Human Genetics. 116(1-2). 83–90. 22 indexed citations
16.
Cleary, Maureen, J H Walter, Bronwyn Kerr, & J. E. Wraith. (2002). Facial appearance in glycogen storage disease type III. Clinical Dysmorphology. 11(2). 117–120. 5 indexed citations
17.
Blair, Edward, Charles Redwood, Houman Ashrafian, et al.. (2001). Mutations in the gamma2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis.. Journal of Medical Genetics. 38. 115 indexed citations
18.
Wilson, Laura C., et al.. (1998). Choanal atresia and hypothelia following methimazole exposure in utero: A second report. American Journal of Medical Genetics. 75(2). 220–222. 52 indexed citations
19.
Kerr, Bronwyn, William D. Foulkes, David Cade, et al.. (1998). False family history of breast cancer in the family cancer clinic. European Journal of Surgical Oncology. 24(4). 275–279. 15 indexed citations
20.
Kerr, Bronwyn, Ági K. Gedeon, John C. Mulley, & Gillian Turner. (1992). Localization of non‐specific X‐linked mental retardation genes. American Journal of Medical Genetics. 43(1-2). 392–401. 39 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 Richard J. Sinke Breakdown of academic impact, for papers by Arthur S. Aylsworth Breakdown of academic impact, for papers by Lina Basel‐Vanagaite Breakdown of academic impact, for papers by Damien Sanlaville Breakdown of academic impact, for papers by Alan Fryer Breakdown of academic impact, for papers by Patrick Edery Breakdown of academic impact, for papers by Angelo Selicorni Breakdown of academic impact, for papers by Lynne M. Bird Breakdown of academic impact, for papers by Nathaniel H. Robin Breakdown of academic impact, for papers by R. Ellen Magenis
Rankless by CCL
2026