Nancy E. Simpson

2.7k total citations
83 papers, 2.0k citations indexed

About

Nancy E. Simpson is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Nancy E. Simpson has authored 83 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 22 papers in Genetics and 14 papers in Epidemiology. Recurrent topics in Nancy E. Simpson's work include Neuroendocrine Tumor Research Advances (13 papers), Lung Cancer Research Studies (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Nancy E. Simpson is often cited by papers focused on Neuroendocrine Tumor Research Advances (13 papers), Lung Cancer Research Studies (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Nancy E. Simpson collaborates with scholars based in Canada, United States and Australia. Nancy E. Simpson's co-authors include Henry B. Lowman, Steven Bass, James A. Wells, Bradley N. White, M. W. Partington, Kenneth K. Kídd, Paul J. Goodfellow, Jeanette J. A. Holden, Shirley M. Myers and W. Kalow and has published in prestigious journals such as Nature, Science and Nucleic Acids Research.

In The Last Decade

Nancy E. Simpson

83 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nancy E. Simpson Canada 24 810 591 298 262 261 83 2.0k
Patricia Tippett United Kingdom 32 993 1.2× 1.1k 1.9× 202 0.7× 103 0.4× 190 0.7× 187 3.6k
Walter W. Noll United States 21 770 1.0× 507 0.9× 236 0.8× 213 0.8× 354 1.4× 43 2.0k
Digamber S. Borgaonkar United States 20 1.1k 1.4× 955 1.6× 260 0.9× 192 0.7× 73 0.3× 66 2.4k
Jean‐Michel Bidart France 37 1.3k 1.6× 423 0.7× 398 1.3× 814 3.1× 237 0.9× 100 3.6k
Hiroki Utsunomiya Japan 29 510 0.6× 940 1.6× 274 0.9× 197 0.8× 273 1.0× 91 3.1k
Laurent Essioux Switzerland 18 600 0.7× 672 1.1× 86 0.3× 249 1.0× 101 0.4× 32 1.7k
Jan D. Marshall United States 29 1.2k 1.5× 1.8k 3.1× 337 1.1× 105 0.4× 213 0.8× 78 3.1k
R.T. Taggart United States 26 1.3k 1.6× 413 0.7× 236 0.8× 85 0.3× 160 0.6× 53 2.0k
Michael F. Seldin United States 21 1.0k 1.3× 482 0.8× 82 0.3× 161 0.6× 123 0.5× 39 2.3k
Athena Milatovich United States 19 1.1k 1.3× 442 0.7× 65 0.2× 246 0.9× 94 0.4× 32 2.3k

Countries citing papers authored by Nancy E. Simpson

Since Specialization
Citations

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

Fields of papers citing papers by Nancy E. Simpson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nancy E. Simpson. 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 Nancy E. Simpson. The network helps show where Nancy E. Simpson may publish in the future.

Co-authorship network of co-authors of Nancy E. Simpson

This figure shows the co-authorship network connecting the top 25 collaborators of Nancy E. Simpson. A scholar is included among the top collaborators of Nancy E. Simpson 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 Nancy E. Simpson. Nancy E. Simpson 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.
Simpson, Nancy E.. (1994). Clinical Signs and Procedures in Dermatology. BMJ. 308(6934). 988.1–988.1. 3 indexed citations
2.
Lowman, Henry B., Steven Bass, Nancy E. Simpson, & James A. Wells. (1991). Selecting high-affinity binding proteins by monovalent phage display. Biochemistry. 30(45). 10832–10838. 243 indexed citations
3.
Carson, Nancy & Nancy E. Simpson. (1991). A physical map of human chromosome 10 and a comparison with an existing genetic map. Genomics. 11(2). 379–388. 11 indexed citations
4.
Brooks‐Wilson, Angela, et al.. (1990). Two polymorphisms at the D10S94 locus. Nucleic Acids Research. 18(16). 4959–4959. 2 indexed citations
5.
Myers, Shirley M., Nancy Carson, Judith R. Kidd, et al.. (1990). A refined linkage map for DNA markers around the pericentromeric region of chromosome 10. Genomics. 8(3). 461–468. 14 indexed citations
6.
Kídd, Kenneth K. & Nancy E. Simpson. (1990). Search for the Gene for Multiple Endocrine Neoplasia Type 2A. Elsevier eBooks. 46. 305–343. 1 indexed citations
7.
Gagel, Robert F., Charles E. Jackson, Bruce A.J. Ponder, et al.. (1989). Multiple Endocrine Neoplasia Type 2 Syndromes: Nomenclature Recommendations from the Workshop Organizing Committee. 37(3). 99. 4 indexed citations
8.
Wu, Jia Qian, Vijaya Ramesh, J.R. Kidd, et al.. (1988). The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10. Cytogenetic and Genome Research. 48(2). 126–127. 9 indexed citations
9.
Waters, Brent, et al.. (1988). A Linkage Study of Primary Affective Disorder. The British Journal of Psychiatry. 152(4). 560–562. 5 indexed citations
10.
Simpson, Nancy E.. (1988). The map of chromosome 20.. Journal of Medical Genetics. 25(12). 794–804. 7 indexed citations
11.
Keats, Bronya J.B., Mei Lü, Cynthia Forster‐Gibson, et al.. (1987). Linkage studies of Friedreich ataxia by means of blood-group and protein markers. PubMed Central. 2 indexed citations
12.
Farrer, Lindsay A., Paul J. Goodfellow, Shirley M. Myers, et al.. (1987). An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.. Europe PMC (PubMed Central). 40(4). 329–37. 10 indexed citations
13.
Goodfellow, Paul J., Alessandra M.V. Duncan, Lindsay A. Farrer, et al.. (1987). Localization and linkage of three polymorphic DNA sequences on human chromosome 20. Cytogenetic and Genome Research. 44(2-3). 112–117. 18 indexed citations
14.
Riddell, D. Christie, J. B. Beckett, Arthur K. Chan, et al.. (1986). Regional localization of 18 human X-linked DNA sequences. Cytogenetic and Genome Research. 42(3). 123–128. 26 indexed citations
15.
Walsh, Linda, Robert Ehrlich, Judy A. Falk, & Nancy E. Simpson. (1983). HLA Haplotype Segregation in Families of Type 1 Diabetics. Human Heredity. 33(4). 253–260. 1 indexed citations
16.
Simpson, Nancy E., Louis Dallaire, James R. Miller, et al.. (1979). Antenatal diagnosis of neural tube defects in Canada: extension of a collaborative study.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 120(6). 653–7. 4 indexed citations
17.
Cox, Diane W., et al.. (1978). Group-Specific Component, Alphai-Antitrypsin and Esterase D in Canadian Eskimos. Human Heredity. 28(5). 341–350. 13 indexed citations
18.
Simpson, Nancy E., et al.. (1976). Prenatal diagnosis of genetic disease in Canada: report of a collaborative study.. PubMed. 115(8). 739–48. 158 indexed citations
19.
McAlpine, P.J., et al.. (1974). Genetic Markers in Blood in a Canadian Eskimo Population with a Comparison of Allele Frequencies in Circumpolar Populations. Human Heredity. 24(2). 114–143. 35 indexed citations
20.
Weitkamp, L.R., et al.. (1969). An Electrophoretic Comparison of Human Serum Albumin Variants: Eight Distinguishable Types. Human Heredity. 19(2). 159–169. 37 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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