Sherry Taylor
Impact in
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- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Genetic Neurodegenerative Diseases
Papers in
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- Epigenetics and DNA Methylation 1
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- Hemophilia Treatment and Research 2
- Iron Metabolism and Disorders 2
- Blood Coagulation and Thrombosis Mechanisms 2
- Co-authors
- Richard H. Myers (1 shared paper)M. Yat Tse (1 shared paper)John J. Wasmuth (1 shared paper)Will D. King (1 shared paper)Gillian P. Bates (1 shared paper)Marina Frontali (1 shared paper)Michael R. Altherr (1 shared paper)Nora Zwingerman (1 shared paper)
- Journals
- Neurosurgery (2 papers)Blood (2 papers)Prenatal Diagnosis (1 paper)Canadian Family Physician (1 paper)Journal of Anatomy (1 paper)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Sherry Taylor
15 papers receiving 317 citations
Peers
Comparison fields: 5 of 65
- Genetics 132
- Cellular and Molecular Neuroscience 70
- Molecular Biology 143
- Neurology 28
- Hematology 19
Countries citing papers authored by Sherry Taylor
This map shows the geographic impact of Sherry Taylor'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 Sherry Taylor with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sherry Taylor more than expected).
Fields of papers citing papers by Sherry Taylor
This network shows the impact of papers produced by Sherry Taylor. 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 Sherry Taylor. The network helps show where Sherry Taylor may publish in the future.
Co-authors
The 25 scholars most cited alongside Sherry Taylor, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 118 | |
| 2 | Genetic education for primary care providers: improving attitudes, knowledge, and confidence. | 2009 | 76 |
| 3 | 2011 | 46 | |
| 4 | 1992 | 18 | |
| 5 | 2016 | 18 | |
| 6 | 2016 | 14 | |
| 7 | 1998 | 8 | |
| 8 | 1998 | 8 | |
| 9 | Genetic education for primary care providers | 2009 | 6 |
| 10 | 2020 | 5 | |
| 11 | Maternal age-based prenatal screening for chromosomal disorders: attitudes of women and health care providers toward changes. | 2013 | 4 |
| 12 | 2017 | 1 | |
| 13 | 2024 | 1 | |
| 14 | 2018 | 1 | |
| 15 | 1976 | 1 |
About Sherry Taylor
Sherry Taylor is a scholar working on Molecular Biology, Hematology, Pediatrics, Perinatology and Child Health, Genetics and Economics and Econometrics, having authored 15 papers that have together received 325 indexed citations. Recurring topics across this work include Hemophilia Treatment and Research (2 papers), BRCA gene mutations in cancer (2 papers), Iron Metabolism and Disorders (2 papers), Blood Coagulation and Thrombosis Mechanisms (2 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Rare Diseases (1 paper), Epigenetics and DNA Methylation (1 paper) and Pharmaceutical industry and healthcare (1 paper). The work is most often cited by research in Genetics (132 citations), Cellular and Molecular Neuroscience (70 citations), Molecular Biology (143 citations), Neurology (28 citations) and Hematology (19 citations). Sherry Taylor has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Richard H. Myers, M. Yat Tse, John J. Wasmuth, Will D. King, Gillian P. Bates, Marina Frontali, Michael R. Altherr, Nora Zwingerman, Andrea Novelletto and Carol Sze Ki Lin. Their work appears in journals such as Neurosurgery, Blood, Prenatal Diagnosis, Canadian Family Physician and Journal of Anatomy.
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.