M Pembrey
Impact in
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- Congenital Heart Disease Studies
- Obstetrics and Gynecology top 10%
- Pregnancy and preeclampsia studies
Papers in
- Genetics 10
- Craniofacial Disorders and Treatments 3
- Cleft Lip and Palate Research 2
- BRCA gene mutations in cancer 2
- Genetic and rare skin diseases. 2
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- Birth, Development, and Health 2
- Co-authors
- Rebecca Coffey (4 shared papers)J L Wilkinson (1 shared paper)Jane Somerville (1 shared paper)Ori Scott (1 shared paper)Paul Brennan (1 shared paper)Julian Little (1 shared paper)John Burn (1 shared paper)B Keeton (1 shared paper)
- Journals
- Journal of Medical Genetics (4 papers)Acta Oto-Laryngologica (2 papers)The Lancet (2 papers)Journal of Thrombosis and Haemostasis (1 paper)European Journal of Endocrinology (1 paper)
- Partner nations
- United KingdomIndiaAustralia
In The Last Decade
M Pembrey
20 papers receiving 479 citations
Peers
Comparison fields: 5 of 67
- Epidemiology 205
- Obstetrics and Gynecology 44
- Genetics 145
- Cardiology and Cardiovascular Medicine 116
- Developmental Biology 10
Countries citing papers authored by M Pembrey
This map shows the geographic impact of M 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 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 Pembrey more than expected).
Fields of papers citing papers by M Pembrey
This network shows the impact of papers produced by M 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 Pembrey. The network helps show where M Pembrey may publish in the future.
Co-authors
The 25 scholars most cited alongside M Pembrey, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 251 | |
| 2 | 2008 | 42 | |
| 3 | 1970 | 41 | |
| 4 | 1992 | 29 | |
| 5 | 2004 | 29 | |
| 6 | 1988 | 27 | |
| 7 | 1989 | 27 | |
| 8 | 1991 | 13 | |
| 9 | 1985 | 13 | |
| 10 | 1987 | 8 | |
| 11 | Okihiro syndrome: thenar hypoplasia and Duane anomaly in three generations. | 1993 | 8 |
| 12 | 1971 | 7 | |
| 13 | 1996 | 6 | |
| 14 | Discordant identical twins. VI. Psoriasis and migraine. | 1972 | 4 |
| 15 | Discordant identical twins. II. Parkinsonism. | 1972 | 4 |
| 16 | Discordant identical twins. V. Neural tube defects. | 1972 | 3 |
| 17 | The Gly972Arg variant in insulin receptor substrate-1 is not associated with birthweight in contemporary English children | 2000 | 2 |
| 18 | 1997 | 1 | |
| 19 | Clinical application of recombinant DNA techniques in families with genetic disease. | 1983 | 1 |
| 20 | 1979 | 1 |
About M Pembrey
M Pembrey is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Pulmonary and Respiratory Medicine and Developmental Biology, having authored 21 papers that have together received 518 indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (3 papers), Cleft Lip and Palate Research (2 papers), Birth, Development, and Health (2 papers), BRCA gene mutations in cancer (2 papers), Congenital limb and hand anomalies (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers), Genetic and rare skin diseases. (2 papers) and Kruppel-like factors research (1 paper). The work is most often cited by research in Epidemiology (205 citations), Obstetrics and Gynecology (44 citations), Genetics (145 citations), Cardiology and Cardiovascular Medicine (116 citations) and Developmental Biology (10 citations). M Pembrey has collaborated with scholars based in United Kingdom, India and Australia. Frequent co-authors include Rebecca Coffey, J L Wilkinson, Jane Somerville, Ori Scott, Paul Brennan, Julian Little, John Burn, B Keeton, E D Silove and L. D. Allan. Their work appears in journals such as Journal of Medical Genetics, Acta Oto-Laryngologica, The Lancet, Journal of Thrombosis and Haemostasis and European Journal of Endocrinology.
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.