Julian Barwell

8.0k total citations
33 papers, 749 citations indexed

About

Julian Barwell is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, Julian Barwell has authored 33 papers receiving a total of 749 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 11 papers in Cancer Research and 10 papers in Molecular Biology. Recurrent topics in Julian Barwell's work include BRCA gene mutations in cancer (12 papers), Genetic factors in colorectal cancer (7 papers) and Cancer Genomics and Diagnostics (7 papers). Julian Barwell is often cited by papers focused on BRCA gene mutations in cancer (12 papers), Genetic factors in colorectal cancer (7 papers) and Cancer Genomics and Diagnostics (7 papers). Julian Barwell collaborates with scholars based in United Kingdom, United States and Australia. Julian Barwell's co-authors include Katie Snape, Nadeem Qureshi, Joe Kai, Chris Jacobs, Louise Izatt, Amanda Collins, Diana Eccles, Andrew Cuthbert, Anthony Howell and Angela F. Brady and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Human Molecular Genetics.

In The Last Decade

Julian Barwell

31 papers receiving 735 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julian Barwell United Kingdom 14 337 213 174 121 118 33 749
Lisa Shah United States 15 198 0.6× 146 0.7× 260 1.5× 195 1.6× 70 0.6× 45 899
Shanna Gustafson United States 12 290 0.9× 173 0.8× 95 0.5× 79 0.7× 122 1.0× 16 636
Isabelle Coupier France 14 274 0.8× 275 1.3× 255 1.5× 96 0.8× 275 2.3× 35 834
Holly J. Pederson United States 11 215 0.6× 107 0.5× 249 1.4× 127 1.0× 51 0.4× 34 611
Geraldine R. Vink Netherlands 17 237 0.7× 172 0.8× 202 1.2× 405 3.3× 96 0.8× 82 995
Anne‐Bine Skytte Denmark 14 243 0.7× 109 0.5× 154 0.9× 94 0.8× 44 0.4× 40 506
Stanley Hooker United States 16 310 0.9× 118 0.6× 187 1.1× 129 1.1× 40 0.3× 26 735
Jessica N. Everett United States 16 316 0.9× 397 1.9× 149 0.9× 312 2.6× 253 2.1× 30 985
Philippe Vennin France 17 495 1.5× 182 0.9× 231 1.3× 310 2.6× 78 0.7× 56 1.1k
Sarah Scollon United States 17 473 1.4× 158 0.7× 199 1.1× 116 1.0× 65 0.6× 47 991

Countries citing papers authored by Julian Barwell

Since Specialization
Citations

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

Fields of papers citing papers by Julian Barwell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julian Barwell

This figure shows the co-authorship network connecting the top 25 collaborators of Julian Barwell. A scholar is included among the top collaborators of Julian Barwell 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 Julian Barwell. Julian Barwell 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.
Watkins, Lance, et al.. (2024). Pharmacological management of fragile X syndrome: a systematic review and narrative summary of the current evidence. Expert Opinion on Pharmacotherapy. 25(3). 301–313. 3 indexed citations
2.
Barwell, Julian, et al.. (2023). Monozygotic twins and cholesteatomas: nature or nuture?. European Archives of Oto-Rhino-Laryngology. 280(12). 5649–5654.
3.
Garrido-Navas, M. Carmen, et al.. (2022). Identification of hereditary breast and ovarian cancer germline variants in Granada (Spain): NGS perspective. Molecular Genetics and Genomics. 297(3). 859–871. 3 indexed citations
4.
Guy, Alyson, Lu Liu, Mathieu Quinodoz, et al.. (2021). Mutations in the ribosome biogenesis factor gene LTV1 are linked to LIPHAK syndrome, a novel poikiloderma-like disorder. Human Molecular Genetics. 31(12). 1970–1978. 2 indexed citations
5.
Barwell, Julian, Marc Tischkowitz, Ian Kesterton, et al.. (2021). Assessing BRCA1 activity in DNA damage repair using human induced pluripotent stem cells as an approach to assist classification of BRCA1 variants of uncertain significance. PLoS ONE. 16(12). e0260852–e0260852. 1 indexed citations
6.
Snape, Katie, et al.. (2019). The new genomic medicine service and implications for patients. Clinical Medicine. 19(4). 273–277. 53 indexed citations
7.
Barwell, Julian, et al.. (2017). Inclusion of diverse populations in genomic research and health services: Genomix workshop report. Journal of Community Genetics. 8(4). 267–273. 27 indexed citations
8.
Watson, Wendy, et al.. (2015). Supporting families with Cancer: A patient centred survivorship model of care. Familial Cancer. 14(4). 637–640. 2 indexed citations
9.
Iwuji, Chinenye, Lynne Howells, Sarah Thomasset, et al.. (2014). Cancer chemoprevention. European Journal of Cancer Prevention. 23(6). 594–601. 2 indexed citations
10.
Qureshi, Nadeem, et al.. (2013). What hinders minority ethnic access to cancer genetics services and what may help?. European Journal of Human Genetics. 22(7). 866–874. 61 indexed citations
11.
Tanteles, George A., Robert Murray, Jamie Mills, et al.. (2012). Variation in Telangiectasia Predisposing Genes Is Associated With Overall Radiation Toxicity. International Journal of Radiation Oncology*Biology*Physics. 84(4). 1031–1036. 19 indexed citations
12.
Murray, Robert, George A. Tanteles, Jamie Mills, et al.. (2011). Association between single nucleotide polymorphisms in the DNA repair gene LIG3 and acute adverse skin reactions following radiotherapy. Radiotherapy and Oncology. 99(2). 231–234. 14 indexed citations
13.
Bancroft, Elizabeth, Imogen Locke, Audrey Ardern‐Jones, et al.. (2010). The carrier clinic: an evaluation of a novel clinic dedicated to the follow-up of BRCA1 and BRCA2 carriers—implications for oncogenetics practice. Journal of Medical Genetics. 47(7). 486–491. 11 indexed citations
14.
Barwell, Julian, Lyndon Walker, S. Sharif, & Greg J. Evans. (2009). Should women with Neurofibromatosis type 1 be offered breast screening between the ages of 40 and 50? Planning national recruitment to a prospective study. European Journal of Surgical Oncology. 35(11). 1207–1207. 1 indexed citations
15.
Barwell, Julian, Laurent Pangon, Zoe Docherty, et al.. (2007). Is telomere length in peripheral blood lymphocytes correlated with cancer susceptibility or radiosensitivity?. British Journal of Cancer. 97(12). 1696–1700. 37 indexed citations
16.
Barwell, Julian, Laurent Pangon, Shirley Hodgson, et al.. (2007). Biallelic mutation of MSH2 in primary human cells is associated with sensitivity to irradiation and altered RAD51 foci kinetics. Journal of Medical Genetics. 44(8). 516–520. 15 indexed citations
17.
Pollard, Patrick J., Mona El‐Bahrawy, Richard Poulsom, et al.. (2006). Expression of HIF-1α, HIF-2α (EPAS1), and Their Target Genes in Paraganglioma and Pheochromocytoma with VHL and SDH Mutations. The Journal of Clinical Endocrinology & Metabolism. 91(11). 4593–4598. 109 indexed citations
18.
Geary, Johanne, Huw Thomas, James Mackay, et al.. (2006). The management of families affected by hereditary non-polyposis colorectal cancer (HNPCC). Familial Cancer. 6(1). 13–19. 8 indexed citations
19.
Docherty, Zoe, Caroline Langman, Ian Kesterton, et al.. (2006). Is chromosome radiosensitivity and apoptotic response to irradiation correlated with cancer susceptibility?. International Journal of Radiation Biology. 83(1). 1–12. 19 indexed citations
20.
Barwell, Julian, Grenville Fox, Jonathan Round, & Jonathan Berg. (2002). Choanal atresia: The result of maternal thyrotoxicosis or fetal carbimazole?. American Journal of Medical Genetics. 111(1). 55–56. 25 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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