Virginia K. Proud

2.3k total citations
32 papers, 1.1k citations indexed

About

Virginia K. Proud is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Virginia K. Proud has authored 32 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Surgery. Recurrent topics in Virginia K. Proud's work include Genomics and Rare Diseases (4 papers), Connective tissue disorders research (4 papers) and Congenital limb and hand anomalies (4 papers). Virginia K. Proud is often cited by papers focused on Genomics and Rare Diseases (4 papers), Connective tissue disorders research (4 papers) and Congenital limb and hand anomalies (4 papers). Virginia K. Proud collaborates with scholars based in United States, Canada and Netherlands. Virginia K. Proud's co-authors include Alan K. Percy, Stephen G. Kaler, Yvonne Mark, Courtney Holmes, Neil A. Segal, William A. Gahl, David S. Goldstein, Donald L. Nuss, Robert E. Kelly and Michael J. Goretsky and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and Annals of Neurology.

In The Last Decade

Virginia K. Proud

32 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Virginia K. Proud United States 17 549 320 251 184 122 32 1.1k
Sarah Dyack Canada 15 440 0.8× 319 1.0× 74 0.3× 214 1.2× 102 0.8× 37 1.2k
Callum Wilson New Zealand 21 956 1.7× 241 0.8× 93 0.4× 96 0.5× 104 0.9× 58 1.6k
Nadia Sakati Saudi Arabia 22 819 1.5× 546 1.7× 215 0.9× 55 0.3× 160 1.3× 78 1.7k
Tony Roscioli Australia 24 877 1.6× 769 2.4× 144 0.6× 67 0.4× 109 0.9× 85 1.7k
Solaf M. Elsayed Egypt 15 548 1.0× 471 1.5× 72 0.3× 96 0.5× 109 0.9× 63 1.1k
Jung Min Ko South Korea 22 767 1.4× 677 2.1× 167 0.7× 29 0.2× 184 1.5× 156 1.6k
Ivo Kremensky Bulgaria 18 753 1.4× 295 0.9× 104 0.4× 32 0.2× 84 0.7× 75 1.4k
Barbara Illi Italy 23 1.2k 2.2× 150 0.5× 155 0.6× 45 0.2× 43 0.4× 42 1.6k
Vito Guarnieri Italy 23 617 1.1× 456 1.4× 198 0.8× 102 0.6× 36 0.3× 78 1.8k
Mary Ann Mitnick United States 18 1.3k 2.3× 472 1.5× 115 0.5× 86 0.5× 88 0.7× 26 2.1k

Countries citing papers authored by Virginia K. Proud

Since Specialization
Citations

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

Fields of papers citing papers by Virginia K. Proud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Virginia K. Proud. 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 Virginia K. Proud. The network helps show where Virginia K. Proud may publish in the future.

Co-authorship network of co-authors of Virginia K. Proud

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

All Works

20 of 20 papers shown
1.
Risheg, Hiba, Romela Pasion, Virginia K. Proud, et al.. (2013). Clinical Comparison of Overlapping Deletions of 19p13.3. American Journal of Medical Genetics Part A. 161(5). 1110–1116. 9 indexed citations
2.
Hu, Ping, Daniel Pineda‐Alvarez, Benjamin D. Solomon, et al.. (2010). Minimal evidence for a direct involvement of twisted gastrulation homolog 1 (TWSG1) gene in human holoprosencephaly☆. Molecular Genetics and Metabolism. 102(4). 470–480. 10 indexed citations
3.
Tompson, Stuart W., Carlos A. Bacino, Nicole P. Safina, et al.. (2010). Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene. The American Journal of Human Genetics. 87(5). 708–712. 54 indexed citations
4.
Smith, Laura P., et al.. (2009). Polyhydramnios, fetal overgrowth, and macrocephaly: Prenatal ultrasound findings of Costello syndrome. American Journal of Medical Genetics Part A. 149A(4). 779–784. 31 indexed citations
5.
Tifft, Cynthia J., et al.. (2009). Enzyme Replacement Therapy in the Home Setting for Mucopolysaccharidosis VI. Journal of Infusion Nursing. 32(1). 45–52. 5 indexed citations
6.
Poley, J. Rainer & Virginia K. Proud. (2008). Hardikar syndrome: New features. American Journal of Medical Genetics Part A. 146A(19). 2473–2479. 7 indexed citations
7.
Nuss, Donald L., Michael J. Goretsky, Virginia K. Proud, et al.. (2006). Classification of the dysmorphology of pectus excavatum. Journal of Pediatric Surgery. 41(9). 1573–1581. 80 indexed citations
8.
Toydemir, Reha M., Harold Chen, Virginia K. Proud, et al.. (2006). Trismus‐pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8. American Journal of Medical Genetics Part A. 140A(22). 2387–2393. 51 indexed citations
9.
Stacey, Michael W., Robert E. Kelly, Donald L. Nuss, et al.. (2006). Family study of the inheritance of pectus excavatum. Journal of Pediatric Surgery. 41(10). 1699–1703. 91 indexed citations
10.
Garcia-Barceló, Mercè, Zhengwei Yuan, Vincent Chi‐Hang Lui, et al.. (2005). Population Differences in the Polyalanine Domain and 6 New Mutations in HLXB9 in Patients with Currarino Syndrome. Clinical Chemistry. 52(1). 46–52. 20 indexed citations
11.
Saul, Robert A., Virginia K. Proud, Harold A. Taylor, Jules G. Leroy, & Jürgen W. Spranger. (2005). Prenatal mucolipidosis type II (I‐cell disease) can present as Pacman dysplasia. American Journal of Medical Genetics Part A. 135A(3). 328–332. 15 indexed citations
12.
Alford, Raye Lynn, Thomas B. Friedman, Bronya J.B. Keats, et al.. (2003). Early childhood hearing loss: Clinical and molecular genetics. An educational slide set of the American College of Medical Genetics. Genetics in Medicine. 5(4). 338–341. 4 indexed citations
13.
Nakabayashi, Kazuhiko, Bridget A. Fernandez, Ikuko Teshima, et al.. (2002). Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome. Genomics. 79(2). 186–196. 25 indexed citations
14.
Lin, Angela E., Paul Grossfeld, Robert M. Hamilton, et al.. (2002). Further delineation of cardiac abnormalities in Costello syndrome. American Journal of Medical Genetics. 111(2). 115–129. 78 indexed citations
15.
Monk, David, Emma Wakeling, Virginia K. Proud, et al.. (2000). Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome. The American Journal of Human Genetics. 66(1). 36–46. 107 indexed citations
16.
McClay, John E., Brian J. Wiatrak, & Virginia K. Proud. (1997). Bifid Epiglottis and Polydactyly: A New Genetic Syndrome. Otolaryngology. 116(1). 129–133. 11 indexed citations
17.
Finley, Sara, et al.. (1997). CNS malformation in a child with Kabuki (Niikawa-Kuroki) syndrome: Report and review. American Journal of Medical Genetics. 72(2). 205–209. 27 indexed citations
18.
Kaler, Stephen G., Virginia K. Proud, Alan K. Percy, et al.. (1994). Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus. Nature Genetics. 8(2). 195–202. 186 indexed citations
19.
Proud, Virginia K., Clive Levine, & Nancy J. Carpenter. (1992). New X‐linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum. American Journal of Medical Genetics. 43(1-2). 458–466. 35 indexed citations
20.
Proud, Virginia K., et al.. (1976). Biochemical changes in temperature‐activated statoblasts of an ectoproct bryozoan. Journal of Experimental Zoology. 197(1). 141–147. 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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