Philip Smith

632 total citations
14 papers, 235 citations indexed

About

Philip Smith is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Philip Smith has authored 14 papers receiving a total of 235 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Neurology. Recurrent topics in Philip Smith's work include Neurofibromatosis and Schwannoma Cases (5 papers), BRCA gene mutations in cancer (4 papers) and RNA modifications and cancer (3 papers). Philip Smith is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (5 papers), BRCA gene mutations in cancer (4 papers) and RNA modifications and cancer (3 papers). Philip Smith collaborates with scholars based in United Kingdom, Netherlands and United States. Philip Smith's co-authors include Craig G. Simpson, John W. Brown, Gillian P. Clark, Diane Davidson, John W. Brown, Andrew J. Wallace, D. Gareth Evans, Naomi L. Bowers, Fiona Lalloo and Helen Byers and has published in prestigious journals such as The Plant Journal, British Journal of Cancer and European Journal of Cancer.

In The Last Decade

Philip Smith

14 papers receiving 226 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Philip Smith United Kingdom	6	161	92	37	24	17	14	235
Alejandro Correa-Sáez Spain	8	135 0.8×	57 0.6×	14 0.4×	14 0.6×	31 1.8×	10	205
J. Imamura Japan	11	298 1.9×	233 2.5×	31 0.8×	63 2.6×	46 2.7×	15	373
Weiguo Li China	6	292 1.8×	23 0.3×	15 0.4×	12 0.5×	14 0.8×	17	351
Juntao Ma China	9	155 1.0×	62 0.7×	15 0.4×	5 0.2×	32 1.9×	21	259
Adele Loidl Austria	8	382 2.4×	185 2.0×	15 0.4×	25 1.0×	39 2.3×	9	419
Akil Hamza Canada	8	360 2.2×	55 0.6×	30 0.8×	6 0.3×	17 1.0×	10	400
Andrew Bottley United Kingdom	9	239 1.5×	206 2.2×	39 1.1×	3 0.1×	16 0.9×	13	377
Sarit Farage-Barhom Israel	6	355 2.2×	290 3.2×	55 1.5×	3 0.1×	40 2.4×	7	489
L. Panzeri Italy	8	265 1.6×	139 1.5×	19 0.5×	17 0.7×	16 0.9×	13	317

Countries citing papers authored by Philip Smith

Since Specialization

Citations

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

Fields of papers citing papers by Philip Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philip Smith

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

All Works

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14 of 14 papers shown

Smith, Miriam J., George J. Burghel, Sarah Waller, et al.. (2024). Genetic findings in people with schwannomas who do not meet clinical diagnostic criteria for NF2-related schwannomatosis. Journal of Medical Genetics. 61(11). 1011–1015. 2 indexed citations

Morgan, Robert D., George J. Burghel, Michael Bulman, et al.. (2023). Is Reflex Germline BRCA1/2 Testing Necessary in Women Diagnosed with Non-Mucinous High-Grade Epithelial Ovarian Cancer Aged 80 Years or Older?. Cancers. 15(3). 730–730. 2 indexed citations

Morgan, Robert D., George J. Burghel, Michael Bulman, et al.. (2022). Predicting the likelihood of a BRCA1/2 pathogenic variant being somatic by testing only tumour DNA in non-mucinous high-grade epithelial ovarian cancer. Journal of Clinical Pathology. 76(10). 684–689. 3 indexed citations

Rowlands, Charlie F, Philip Smith, Claire Hartley, et al.. (2022). Re‐evaluation of missense variant classifications in NF2. Human Mutation. 43(5). 643–654. 5 indexed citations

Wallace, Andrew J., Hélene Schlecht, Naomi L. Bowers, et al.. (2022). Screening of potential novel candidate genes in schwannomatosis patients. Human Mutation. 43(10). 1368–1376. 6 indexed citations

Morgan, Robert D., George J. Burghel, Michael Bulman, et al.. (2022). BRCA1/2 in non-mucinous epithelial ovarian cancer: tumour with or without germline testing?. British Journal of Cancer. 127(1). 163–167. 4 indexed citations

Bowers, Naomi L., Claire Hartley, Philip Smith, et al.. (2020). Sporadic vestibular schwannoma: a molecular testing summary. Journal of Medical Genetics. 58(4). 227–233. 13 indexed citations

Smith, Philip, et al.. (2020). Neurofibromatosis type 2 discordance in monozygous twins. Familial Cancer. 19(1). 37–40. 2 indexed citations

Byers, Helen, Yvonne Wallis, Elke M. van Veen, et al.. (2016). Sensitivity of BRCA1/2 testing in high-risk breast/ovarian/male breast cancer families: little contribution of comprehensive RNA/NGS panel testing. European Journal of Human Genetics. 24(11). 1591–1597. 24 indexed citations

10.

Buonamici, Silvia, Kevin Lim, Jacob Feala, et al.. (2014). 456 SF3B1 mutations induce disease relevant aberrant mRNA splicing in cancer and confer sensitivity to spliceosome inhibition. European Journal of Cancer. 50. 149–149. 2 indexed citations

11.

Stewart, Helen, et al.. (2001). De novo deletion of chromosome 18q in a baby with Harlequin ichthyosis. American Journal of Medical Genetics. 102(4). 342–345. 5 indexed citations

12.

Simpson, Craig G., Gillian P. Clark, Diane Davidson, Philip Smith, & John W. Brown. (1996). Mutation of putative branchpoint consensus sequences in plant introns reduces splicing efficiency. The Plant Journal. 9(3). 369–380. 52 indexed citations

13.

Brown, John W., Philip Smith, & Craig G. Simpson. (1996). Arabidopsis consensus intron sequences. Plant Molecular Biology. 32(3). 531–535. 113 indexed citations

14.

Smith, Philip. (1969). Coding strategies in language. Information and Control. 14(1). 72–97. 2 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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