R Wadey

1.4k citations
14 papers · 1.1k · h-index 9

Impact in

  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Congenital heart defects research
    • Renal and related cancers
    • RNA modifications and cancer

Papers in

    • Congenital heart defects research 6
    • Renal and related cancers 5
    • CRISPR and Genetic Engineering 2
    • Molecular Biology Techniques and Applications 1
    • Genomic variations and chromosomal abnormalities 2
    • Congenital Ear and Nasal Anomalies 2

R Wadey

14 papers receiving 1.1k citations

Peers

R Wadey
Comparison fields: 5 of 54
  • Genetics 377
  • Molecular Biology 921
  • Endocrinology, Diabetes and Metabolism 124
  • Pulmonary and Respiratory Medicine 221
  • Cancer Research 101
Replace Ryuji Fukuzawa with:
Ryuji Fukuzawa Japan
John N. Wylie Canada
Jacqueline Siegel‐Bartelt Canada
Rodger Palmer United Kingdom
Michael S. Rutenberg United States
Carel Meijers Netherlands
Olaug K. Rødningen Norway
Viviana Cordeddu Italy
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Citations per field
00.5×2.6×
Ryuji Fukuzawa · 1×
Citations per year

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-authors

The 25 scholars most cited alongside R Wadey, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with R Wadey Line = papers co-authored together R Wadey links everyone, so they are left out of the graph.

All Works

14 of 14 papers shown
#Work
1 1985335
2 1997274
3 1993204
4
Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome.
1992124
5
Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.
199683
6 199321
7
The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locus.
198816
8 199112
9 199011
10
MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES
19914
11
Loss of heterozygosity for chromosome region 11p15 in Wilms' tumours is not related to HRAS gene transforming mutations.
19914
12 19892
13
CATCH-22 - CAN MOLECULAR GENETICS EXPLAIN THE PHENOTYPE
19951
14
Cloning and mapping of murine Idd: conserved synteny of the DiGeorge syndrome critical region
19971

About R Wadey

R Wadey is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Genetics and Public Health, Environmental and Occupational Health, having authored 14 papers that have together received 1.1k indexed citations. Recurring topics across this work include Congenital heart defects research (6 papers), Renal and related cancers (5 papers), Renal cell carcinoma treatment (2 papers), Genomic variations and chromosomal abnormalities (2 papers), CRISPR and Genetic Engineering (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Multiple and Secondary Primary Cancers (1 paper) and Molecular Biology Techniques and Applications (1 paper). The work is most often cited by research in Genetics (377 citations), Molecular Biology (921 citations), Endocrinology, Diabetes and Metabolism (124 citations), Pulmonary and Respiratory Medicine (221 citations) and Cancer Research (101 citations). R Wadey has collaborated with scholars based in United Kingdom, India and United States. Frequent co-authors include Peter Scambler, Judith Goodship, John Burn, David I. Wilson, John K. Cowell, Jon Pritchard, Christopher F. Graham, Jenny Scott, L. Priestley and Timothy J. Knott. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Nucleic Acids Research, Nature and The American Journal of Human Genetics.

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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