Val Davison

690 total citations
10 papers, 368 citations indexed

About

Val Davison is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Val Davison has authored 10 papers receiving a total of 368 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Neurology. Recurrent topics in Val Davison's work include Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (2 papers) and Renal and related cancers (2 papers). Val Davison is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (2 papers) and Renal and related cancers (2 papers). Val Davison collaborates with scholars based in United Kingdom, United States and Germany. Val Davison's co-authors include Sara Dyer, Dominic McMullan, Richard G. Grundy, David W. Ellison, Pramila Ramani, Paul Davies, Lisa Cooper‐Charles, Jenny Morton, Chirag Patel and Farida Latif and has published in prestigious journals such as American Journal Of Pathology, Genome biology and European Journal of Cancer.

In The Last Decade

Val Davison

10 papers receiving 350 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Val Davison United Kingdom	7	199	120	98	53	40	10	368
Devin McQuaid United States	10	312 1.6×	337 2.8×	56 0.6×	123 2.3×	17 0.4×	12	562
Gordana Raca United States	12	421 2.1×	235 2.0×	77 0.8×	61 1.2×	21 0.5×	28	667
Sanja Rogić Canada	12	496 2.5×	104 0.9×	148 1.5×	95 1.8×	35 0.9×	21	802
Catherine Taylor United Kingdom	8	325 1.6×	272 2.3×	22 0.2×	37 0.7×	46 1.1×	8	444
R.K. Track	4	145 0.7×	121 1.0×	24 0.2×	22 0.4×	21 0.5×	6	263
Fernando Santos‐Simarro Spain	14	262 1.3×	234 1.9×	42 0.4×	9 0.2×	22 0.6×	50	470
Sophia Kitsiou‐Tzeli Greece	16	422 2.1×	407 3.4×	25 0.3×	15 0.3×	26 0.7×	39	656
Erica H. Gerkes Netherlands	10	221 1.1×	203 1.7×	43 0.4×	14 0.3×	15 0.4×	14	386
Nicole Maas Belgium	7	191 1.0×	351 2.9×	36 0.4×	21 0.4×	15 0.4×	13	455
Kathrin Schramm Germany	7	221 1.1×	56 0.5×	52 0.5×	43 0.8×	13 0.3×	15	309

Countries citing papers authored by Val Davison

Since Specialization

Citations

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

Fields of papers citing papers by Val Davison

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Val Davison

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

All Works

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10 of 10 papers shown

Patel, Chirag, et al.. (2011). Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome. European Journal of Human Genetics. 19(6). 634–639. 59 indexed citations

McRonald, Fiona E., John A. Halsall, Robert S. Illingworth, et al.. (2010). Immunostaining of modified histones defines high-level features of the human metaphase epigenome. Genome biology. 11(11). R110–R110. 56 indexed citations

Shuib, Salwati, Dominic McMullan, Eleanor Rattenberry, et al.. (2009). Microarray based analysis of 3p25‐p26 deletions (3p‐ syndrome). American Journal of Medical Genetics Part A. 149A(10). 2099–2105. 76 indexed citations

Abdulrahman, Mahera, Mark R. Morris, Elena Prigmore, et al.. (2007). Characterization of a 3;6 translocation associated with renal cell carcinoma. Genes Chromosomes and Cancer. 46(4). 311–317. 26 indexed citations

Ng, Shu‐Kay, Tim Cole, Val Davison, et al.. (2007). Congenital abnormalities and clinical features associated with Wilms’ tumour: A comprehensive study from a centre serving a large population. European Journal of Cancer. 43(9). 1422–1429. 11 indexed citations

Wordsworth, Sarah, James Buchanan, Regina Regan, et al.. (2007). Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom. PubMed. 1(1-2). 35–45. 27 indexed citations

Chughtai, Shaheen, Pramila Ramani, Sara Dyer, et al.. (2006). Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastoma. European Journal of Cancer. 42(12). 1826–1834. 3 indexed citations

Dyer, Sara, Val Davison, Paul Davies, et al.. (2002). Genomic Imbalances in Pediatric Intracranial Ependymomas Define Clinically Relevant Groups. American Journal Of Pathology. 161(6). 2133–2141. 105 indexed citations

Martin, William L., S. Pretlove, Andrew A. Mercer, et al.. (2001). Duplication of chromosome 2 in association with ventriculomegaly — a case report. Prenatal Diagnosis. 21(13). 1169–1170. 1 indexed citations

10.

Bullock, Sarah, et al.. (1996). Detection of germinal mosaicism in a DMD family. Biochemical Society Transactions. 24(2). 273S–273S. 4 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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