David Tegay

694 total citations
18 papers, 236 citations indexed

About

David Tegay is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, David Tegay has authored 18 papers receiving a total of 236 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pathology and Forensic Medicine. Recurrent topics in David Tegay's work include Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (4 papers) and Genetic factors in colorectal cancer (4 papers). David Tegay is often cited by papers focused on Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (4 papers) and Genetic factors in colorectal cancer (4 papers). David Tegay collaborates with scholars based in United States, Italy and United Kingdom. David Tegay's co-authors include Eli Hatchwell, Andrew Lane, Jasmin Roohi, Sandra Burkett, Roscoe Stanyon, Gary Stone, Richard J. Scriven, Wim Brussel, Stephen R. Williams and Louise Brueton and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bone and Journal of Medical Genetics.

In The Last Decade

David Tegay

17 papers receiving 229 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Tegay United States 10 133 112 58 33 23 18 236
Ewelina Bukowska‐Olech Poland 11 157 1.2× 147 1.3× 22 0.4× 25 0.8× 18 0.8× 41 273
Irén Haltrich Hungary 9 103 0.8× 93 0.8× 25 0.4× 25 0.8× 11 0.5× 33 239
Mary Haddadin United States 6 210 1.6× 103 0.9× 60 1.0× 38 1.2× 11 0.5× 7 343
María Ceballos-Chávez Spain 10 309 2.3× 107 1.0× 42 0.7× 47 1.4× 21 0.9× 13 385
Wim Brussel Netherlands 6 241 1.8× 115 1.0× 71 1.2× 26 0.8× 8 0.3× 8 363
Sheetal Shetty United States 9 143 1.1× 62 0.6× 60 1.0× 30 0.9× 66 2.9× 20 298
Annabella Marozza Italy 9 163 1.2× 108 1.0× 69 1.2× 20 0.6× 16 0.7× 11 287
Sergi Villatoro Spain 11 162 1.2× 185 1.7× 35 0.6× 62 1.9× 38 1.7× 19 358
Ana Medeira Portugal 10 176 1.3× 159 1.4× 29 0.5× 13 0.4× 20 0.9× 17 300
Magdalena Socha Poland 10 143 1.1× 113 1.0× 43 0.7× 17 0.5× 39 1.7× 24 260

Countries citing papers authored by David Tegay

Since Specialization
Citations

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

Fields of papers citing papers by David Tegay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Tegay

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

All Works

18 of 18 papers shown
1.
Loke, Johnny, Ishraq Alim, Susan Klugman, et al.. (2022). Prediction of breast cancer risk based on flow variant analysis of circulating peripheral blood mononuclear cells. Human Genetics and Genomics Advances. 3(2). 100085–100085. 2 indexed citations
2.
Tegay, David, et al.. (2019). Precision oncology: lessons learned and challenges for the future. SHILAP Revista de lepidopterología.
3.
Yang, Hsih‐Te, Ronak Shah, David Tegay, & Kenan Onel. (2019). <p>Precision oncology: lessons learned and challenges for the future</p>. Cancer Management and Research. Volume 11. 7525–7536. 9 indexed citations
4.
Cohn, Jason E., et al.. (2017). Video Education on Hereditary Breast and Ovarian Cancer (HBOC) for Physicians: an Interventional Study. Journal of Cancer Education. 33(6). 1213–1221. 5 indexed citations
5.
Tegay, David, Kenneth Ward, Lesa Nelson, et al.. (2016). KBG syndrome involving a single-nucleotide duplication in ANKRD11. Molecular Case Studies. 2(6). a001131–a001131. 12 indexed citations
6.
Tegay, David, Kenneth Ward, Justine Coppinger, et al.. (2016). SCN8A mutation in a child presenting with seizures and developmental delays. Molecular Case Studies. 2(6). a001073–a001073. 11 indexed citations
7.
Chan, Vivian, et al.. (2016). Acceptance of technology-based tools in a sample of Parkinson’s patients. Chronic Illness. 13(1). 3–13. 7 indexed citations
8.
Cohn, Jason E., et al.. (2014). Physician Risk Assessment Knowledge Regarding BRCA Genetics Testing. Journal of Cancer Education. 30(3). 573–579. 13 indexed citations
9.
Chan, Vivian, et al.. (2014). Impact of Academic Affiliation and Training on Knowledge of Hereditary Colorectal Cancer. Public Health Genomics. 17(2). 76–83. 4 indexed citations
10.
Boudin, Eveline, Karen Jennes, Fenna de Freitas, et al.. (2013). No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disorders. Bone. 55(1). 52–56. 8 indexed citations
11.
Levy, Brynn, David Tegay, Peter Papenhausen, et al.. (2012). Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?. Genetics in Medicine. 14(9). 811–818. 4 indexed citations
12.
Ott, Claus‐Eric, Gundula Leschik, Louise Brueton, et al.. (2010). Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Human Mutation. 31(8). E1587–E1593. 58 indexed citations
13.
Williams, Stephen R., Santhosh Girirajan, David Tegay, et al.. (2009). Array comparative genomic hybridisation of 52 subjects with a Smith–Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delay. Journal of Medical Genetics. 47(4). 223–229. 19 indexed citations
14.
Tegay, David, et al.. (2009). Toriello–Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2. Clinical Genetics. 75(3). 259–264. 23 indexed citations
15.
Roohi, Jasmin, David Tegay, John Pomeroy, et al.. (2008). A de novo apparently balanced translocation [46,XY,t(2;9)(p13;p24)] interrupting RAB11FIP5 identifies a potential candidate gene for autism spectrum disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(4). 411–417. 14 indexed citations
16.
Tegay, David, et al.. (2008). Bronchial anomalies in VACTERL association. Pediatric Pulmonology. 43(9). 930–932. 11 indexed citations
17.
Shah, Shetal, et al.. (2007). Trisomy 2 mosaicism in hypomelanosis of Ito. American Journal of Medical Genetics Part A. 143A(20). 2466–2468. 18 indexed citations
18.
Tegay, David, Andrew Lane, Jasmin Roohi, & Eli Hatchwell. (2007). Contiguous gene deletion involving L1CAM and AVPR2 causes X‐linked hydrocephalus with nephrogenic diabetes insipidus. American Journal of Medical Genetics Part A. 143A(6). 594–598. 18 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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