Nancy E. Simpson
Impact in
- Developmental Biology top 5%
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
Papers in
-
- Glycosylation and Glycoproteins Research 4
- Genetics 22
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 4
- Co-authors
- James A. Wells (1 shared paper)Henry B. Lowman (1 shared paper)Steven Bass (1 shared paper)Bradley N. White (10 shared papers)M. W. Partington (7 shared papers)Kenneth K. Kídd (12 shared papers)Paul J. Goodfellow (13 shared papers)W. Kalow (4 shared papers)
- Journals
- Nucleic Acids Research (6 papers)Human Genetics (5 papers)Journal of Medical Genetics (4 papers)Human Heredity (4 papers)Genomics (4 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Nancy E. Simpson
79 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 112
- Developmental Biology 94
- Genetics 534
- Endocrinology, Diabetes and Metabolism 249
- Pediatrics, Perinatology and Child Health 188
- Radiology, Nuclear Medicine and Imaging 226
Countries citing papers authored by Nancy E. Simpson
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
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-authors
The 25 scholars most cited alongside Nancy E. Simpson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 82 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1987 | 340 | |
| 2 | 1991 | 244 | |
| 3 | Prenatal diagnosis of genetic disease in Canada: report of a collaborative study. | 1976 | 158 |
| 4 | 1964 | 70 | |
| 5 | 1968 | 58 | |
| 6 | Diabetes in the families of diabetics. | 1968 | 46 |
| 7 | 1962 | 42 | |
| 8 | Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3. | 1985 | 42 |
| 9 | 1986 | 40 | |
| 10 | 1969 | 37 | |
| 11 | 1969 | 37 | |
| 12 | 1974 | 35 | |
| 13 | 1981 | 34 | |
| 14 | 1962 | 33 | |
| 15 | THE "SILENT" GENE FOR SERUM CHOLINESTERASE. | 1964 | 33 |
| 16 | C5 types of serum cholinesterase in a Brazilian population. | 1966 | 33 |
| 17 | 1972 | 29 | |
| 18 | 1980 | 23 | |
| 19 | 1989 | 23 | |
| 20 | COMPARISONS OF TWO METHODS FOR TYPING OF SERUM CHOLINESTERASE AND PREVALENCE OF ITS VARIANTS IN A BRAZILIAN POPULATION. | 1965 | 23 |
About Nancy E. Simpson
Nancy E. Simpson is a scholar working on Molecular Biology, Genetics, Epidemiology, Surgery and Oncology, having authored 82 papers that have together received 1.8k indexed citations. Recurring topics across this work include Neuroendocrine Tumor Research Advances (13 papers), Lung Cancer Research Studies (8 papers), Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (7 papers), Pancreatic function and diabetes (6 papers), Congenital limb and hand anomalies (5 papers), Glycosylation and Glycoproteins Research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Developmental Biology (94 citations), Genetics (534 citations), Endocrinology, Diabetes and Metabolism (249 citations), Pediatrics, Perinatology and Child Health (188 citations) and Radiology, Nuclear Medicine and Imaging (226 citations). Nancy E. Simpson has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include James A. Wells, Henry B. Lowman, Steven Bass, Bradley N. White, M. W. Partington, Kenneth K. Kídd, Paul J. Goodfellow, W. Kalow, Jeanette J. A. Holden and Shirley M. Myers. Their work appears in journals such as Nucleic Acids Research, Human Genetics, Journal of Medical Genetics, Human Heredity and Genomics.
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.