Sarah Reid
- Genetics top 2%
- BRCA gene mutations in cancer 3
- Genomic variations and chromosomal abnormalities 2
- Craniofacial Disorders and Treatments 1
- Cancer Research top 5%
- Cell Biology top 5%
- Molecular Biology top 10%
- DNA Repair Mechanisms 3
- CRISPR and Genetic Engineering 2
- Fibroblast Growth Factor Research 1
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- Neonatal Respiratory Health Research 2
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- Cardiac, Anesthesia and Surgical Outcomes 1
- Co-authors
- Nazneen RahmanSandra HanksPatrick KellySheila SealHiran JayatilakeAnthony RenwickDeborah J. ThompsonMichael R. Stratton
- Cited by
- GeneticsCancer ResearchCell Biology
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
Sarah Reid
10 papers receiving 1.7k citations
Hit Papers
Peers
Comparison fields: 5 of 73
- Genetics 929
- Cancer Research 447
- Cell Biology 335
- Molecular Biology 1.2k
- Pathology and Forensic Medicine 269
Countries citing papers authored by Sarah Reid
This map shows the geographic impact of Sarah Reid'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 Sarah Reid with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah Reid more than expected).
Fields of papers citing papers by Sarah Reid
This network shows the impact of papers produced by Sarah Reid. 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 Sarah Reid. The network helps show where Sarah Reid may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Sarah Reid, 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 | 2013 | 8 | |
| 2 | Biallelic mutations in PALB2 cause Fanconi anemia and predispose to childhood cancer | 2007 | 1 |
| 3 | PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility genebreakdown → | 2006 | 689 |
| 4 | 2006 | 43 | |
| 5 | 2006 | 453 | |
| 6 | 2004 | 444 | |
| 7 | 2003 | 26 | |
| 8 | 2002 | 32 | |
| 9 | 2001 | 3 | |
| 10 | Molecular genetics of ulcerative colitis-associated colon cancer in the interleukin 2- and beta(2)-microglobulin-deficient mouse. | 2001 | 31 |
About Sarah Reid
Sarah Reid is a scholar working on Genetics, Pharmacy and Endocrine and Autonomic Systems, having authored 10 papers that have together received 1.7k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (3 papers), BRCA gene mutations in cancer (3 papers), CRISPR and Genetic Engineering (2 papers), Neonatal Respiratory Health Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Cardiac, Anesthesia and Surgical Outcomes (1 paper), Craniofacial Disorders and Treatments (1 paper) and Fibroblast Growth Factor Research (1 paper). The work is most often cited by research in Genetics (929 citations), Cancer Research (447 citations) and Cell Biology (335 citations). Sarah Reid has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Nazneen Rahman, Sandra Hanks, Patrick Kelly, Sheila Seal, Hiran Jayatilake, Anthony Renwick, Deborah J. Thompson, Michael R. Stratton, D. Gareth Evans and Rita Barfoot. Their work appears in journals such as Nature Genetics, Developmental Brain Research, Genetics, British Journal of Urology and Gastroenterology.
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.