R Wadey

1.4k total citations
14 papers, 1.1k citations indexed

About

R Wadey is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, R Wadey has authored 14 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in R Wadey's work include Congenital heart defects research (6 papers), Renal and related cancers (5 papers) and Renal cell carcinoma treatment (2 papers). R Wadey is often cited by papers focused on Congenital heart defects research (6 papers), Renal and related cancers (5 papers) and Renal cell carcinoma treatment (2 papers). R Wadey collaborates with scholars based in United Kingdom, India and United States. R Wadey's co-authors include Peter Scambler, Judith Goodship, John Burn, David I. Wilson, John K. Cowell, Jon Pritchard, G I Bell, M. E. Robertson, Timothy J. Knott and L B Rall and has published in prestigious journals such as Nature, Nucleic Acids Research and The American Journal of Human Genetics.

In The Last Decade

R Wadey

14 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R Wadey United Kingdom	9	943	417	281	273	163	14	1.1k
John N. Wylie Canada	11	1.3k 1.4×	282 0.7×	129 0.5×	239 0.9×	129 0.8×	16	1.4k
Francesca Romana Lepri Italy	18	608 0.6×	429 1.0×	85 0.3×	165 0.6×	74 0.5×	62	972
Rossella Capolino Italy	18	449 0.5×	369 0.9×	84 0.3×	146 0.5×	92 0.6×	56	825
Alexa Kidd New Zealand	14	663 0.7×	327 0.8×	68 0.2×	75 0.3×	58 0.4×	24	1.1k
Rodger Palmer United Kingdom	13	397 0.4×	494 1.2×	105 0.4×	37 0.1×	76 0.5×	20	915
Irene Bottillo Italy	18	531 0.6×	253 0.6×	179 0.6×	110 0.4×	86 0.5×	65	1.1k
Carel Meijers Netherlands	17	649 0.7×	469 1.1×	193 0.7×	65 0.2×	480 2.9×	22	1.4k
Yao‐Shan Fan United States	18	346 0.4×	432 1.0×	56 0.2×	54 0.2×	202 1.2×	39	913
Georg Klaus Hinkel Germany	17	498 0.5×	528 1.3×	82 0.3×	36 0.1×	90 0.6×	41	933
A. Al Saadi United States	12	201 0.2×	160 0.4×	46 0.2×	203 0.7×	132 0.8×	16	726

Countries citing papers authored by R Wadey

Since Specialization

Citations

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

Fields of papers citing papers by R Wadey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R Wadey

This figure shows the co-authorship network connecting the top 25 collaborators of R Wadey. A scholar is included among the top collaborators of R Wadey 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 R Wadey. R Wadey 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

Carlson, Christine, Howard I. Sirotkin, Raj K. Pandita, et al.. (1997). Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients. The American Journal of Human Genetics. 61(3). 620–629. 274 indexed citations

Taylor, Christina, R Wadey, Hilary O‘Donnell, et al.. (1997). Cloning and mapping of murine Idd: conserved synteny of the DiGeorge syndrome critical region. UCL Discovery (University College London). 1 indexed citations

Sutherland, Helen, R Wadey, Judith M. McKie, et al.. (1996). Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.. PubMed. 59(1). 23–31. 83 indexed citations

Halford, Stephanie, R Wadey, Jenny Whiting, et al.. (1995). CATCH-22 - CAN MOLECULAR GENETICS EXPLAIN THE PHENOTYPE. UCL Discovery (University College London). 577–580. 1 indexed citations

Wadey, R, S. C. M. Daw, A.R. Wickremasinghe, et al.. (1993). Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134).. Journal of Medical Genetics. 30(10). 818–821. 21 indexed citations

Burn, John, Atsuyoshi Takao, David I. Wilson, et al.. (1993). Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.. Journal of Medical Genetics. 30(10). 822–824. 204 indexed citations

Kelly, David A., Stephanie Halford, R Wadey, et al.. (1992). Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome.. PubMed. 51(5). 964–70. 124 indexed citations

Scambler, Peter, Stephanie Halford, R Wadey, et al.. (1991). MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES. UCL Discovery (University College London). 4 indexed citations

Jadresić, Lyda, et al.. (1991). Molecular analysis of chromosome region 11p13 in patients with Drash syndrome. Human Genetics. 86(5). 497–501. 12 indexed citations

10.

Baird, Paul N., R Wadey, & John K. Cowell. (1991). Loss of heterozygosity for chromosome region 11p15 in Wilms' tumours is not related to HRAS gene transforming mutations.. PubMed. 6(7). 1147–9. 4 indexed citations

11.

Wadey, R, Peter Little, Jon Pritchard, & John K. Cowell. (1990). Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid library. Human Genetics. 84(5). 417–23. 11 indexed citations

12.

Wadey, R & John K. Cowell. (1989). A MspI RFLP associated with the human catatase gene. Nucleic Acids Research. 17(8). 3332–3332. 2 indexed citations

13.

Boehm, Thomas, Isabelle Lavenir, A. Förster, et al.. (1988). The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locus.. PubMed. 3(6). 691–5. 16 indexed citations

14.

Scott, Jenny, John K. Cowell, M. E. Robertson, et al.. (1985). Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues. Nature. 317(6034). 260–262. 336 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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