V. Proud

449 total citations
10 papers, 312 citations indexed

About

V. Proud is a scholar working on Molecular Biology, Genetics and General Health Professions. According to data from OpenAlex, V. Proud has authored 10 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 4 papers in General Health Professions. Recurrent topics in V. Proud's work include Health Sciences Research and Education (3 papers), BRCA gene mutations in cancer (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). V. Proud is often cited by papers focused on Health Sciences Research and Education (3 papers), BRCA gene mutations in cancer (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). V. Proud collaborates with scholars based in United States, France and Mexico. V. Proud's co-authors include E. Diane Johnson, Thomas Scholl, Amie M. Deffenbaugh, Khédoudja Nafa, Kenneth Offit, Helmut Hanenberg, Larry Norton, Roberta A. Diotti, Sat Dev Batish and Brendan Mullaney and has published in prestigious journals such as JNCI Journal of the National Cancer Institute, Human Molecular Genetics and Mayo Clinic Proceedings.

In The Last Decade

V. Proud

10 papers receiving 307 citations

Peers

Countries citing papers authored by V. Proud

Since Specialization

Citations

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

Fields of papers citing papers by V. Proud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. Proud

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

#	Work	Indexed citations
1	Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies 2007 ·Human Genetics ·Lisenka E.L.M. Vissers, Paweł Stankiewicz, Svetlana A. Yatsenko, (unknown), (unknown), V. Proud, Bert B.A. de Vries, Rolph Pfundt, Carlo Marcelis, Joleen L. Zackowski, Weimin Bi, Ad Geurts van Kessel, James R. Lupski, Joris A. Veltman	24
2	Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia 2003 ·JNCI Journal of the National Cancer Institute ·Kenneth Offit, Orna Levran, Brendan Mullaney, Kandice Mah, Khédoudja Nafa, Sat Dev Batish, Roberta A. Diotti, (unknown), Amie M. Deffenbaugh, Thomas Scholl, V. Proud, Mark E. Robson, Larry Norton, Nathan A. Ellis, Helmut Hanenberg, Arleen D. Auerbach	122
3	Unique family with Townes-Brocks syndrome,SALL1 mutation, and cardiac defects 2001 ·American Journal of Medical Genetics ·(unknown), (unknown), Cindy Neunert, Daniel Schneider, V. Proud	31
4	A Novel Phenotypic Pattern in X-Linked Inheritance: Craniofrontonasal Syndrome Maps to Xp22 1997 ·Human Molecular Genetics ·George Feldman, (unknown), (unknown), Dolores Saavedra, Nathaniel H. Robin, V. Proud, Laura Robb, V Der Kaloustian, J. Christopher Carey, M. Michael Cohen, Valérie Cormier‐Daire, Arnold Munnich, Elaine H. Zackai, Andrew O.M. Wilkie, R. Arlen Price, Maximilian Muenke	28
5	Determination of the Genomic Structure of the XNP/ATRX Gene Encoding a Potential Zinc Finger Helicase 1997 ·Genomics ·Laurent Villard, Anne-Marie Lossi, Carlos Cardoso, V. Proud, (unknown), Laurence Colleaux, (unknown), (unknown)	50
6	Students online: learning medical genetics. 1993 ·PubMed ·V. Proud, E. Diane Johnson, J. A. Mitchell	6
7	Medical students using Grateful Med: Analysis of failed searches and a six-month follow-up study 1992 ·Computers and Biomedical Research ·(unknown), E. Diane Johnson, John E. Hewett, V. Proud	16
8	Hemoglobin Columbia Missouri or α2[88 (F9) Ala→Val]β2: A New High-Oxygen-Affinity Hemoglobin That Causes Erythrocytosis 1991 ·Mayo Clinic Proceedings ·Michael C. Perry, Charlotte Head, (unknown), Richard T. Jones, Henry Taylor, V. Proud	12
9	New thoughts about medical students as effective searchers of MEDLINE 1990 ·Academic Medicine ·Joshua A. Mitchell, E. Diane Johnson, V. Proud	12
10	Teaching human genetics in biochemistry by computer literature searching. 1989 ·PubMed ·V. Proud, F J Schmidt, E. Diane Johnson, J. A. Mitchell	11

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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