M. S. Pembrey
- Genetics top 10%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 10%
- Cell Biology
- Surgery
- Co-authors
- Ségolène AyméMartin BobrowSandy RaeburnPeter FarndonBéatrice GodardJean‐Jacques CassimanGerry Evers‐KieboomsUlf Kristoffersson
- Topics
- BRCA gene mutations in cancer (2 papers)Child and Adolescent Health (1 paper)Genetic Syndromes and Imprinting (1 paper)
- Cited by
- GeneticsCell Biology
- Partner nations
- United KingdomFrance
In The Last Decade
M. S. Pembrey
7 papers receiving 620 citations
Hit Papers
Peers
Comparison fields: 5 of 101
- Genetics 264
- Molecular Biology 216
- Pediatrics, Perinatology and Child Health 97
- Cell Biology 82
- Surgery 81
Countries citing papers authored by M. S. Pembrey
This map shows the geographic impact of M. S. Pembrey'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 M. S. Pembrey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. S. Pembrey more than expected).
Fields of papers citing papers by M. S. Pembrey
This network shows the impact of papers produced by M. S. Pembrey. 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 M. S. Pembrey. The network helps show where M. S. Pembrey may publish in the future.
Co-authorship network of co-authors of M. S. Pembrey
This figure shows the co-authorship network connecting the top 25 collaborators of M. S. Pembrey. A scholar is included among the top collaborators of M. S. Pembrey 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 M. S. Pembrey. M. S. Pembrey is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 62 | |
| 2 | Population genetic screening programmes. Proposed recommendations of the European Society of Human Genetics (vol 8, pg 998, 2000) | 1 |
| 3 | 1 | |
| 4 | 3 | |
| 5 | 5 | |
| 6 | Principles and Practice of Medical Geneticsbreakdown → | 572 |
| 7 | 20 |
About M. S. Pembrey
M. S. Pembrey is a scholar working on Genetics, Cognitive Neuroscience and Clinical Psychology, having authored 7 papers that have together received 664 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (2 papers), Child and Adolescent Health (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (264 citations), Genetics (57 citations) and Cell Biology (82 citations). M. S. Pembrey has collaborated with scholars based in United Kingdom and France. Frequent co-authors include Ségolène Aymé, Martin Bobrow, Sandy Raeburn, Peter Farndon, Béatrice Godard, Jean‐Jacques Cassiman, Gerry Evers‐Kiebooms, Ulf Kristoffersson, Jörg Schmidtke and Lisbeth Tranebjærg. Their work appears in journals such as The Lancet, Archives of Disease in Childhood and Journal of Medical Genetics.
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.