Michael Baraitser
Impact in
- Developmental Biology top 1%
- Genetics top 0.5%
- Craniofacial Disorders and Treatments
- Genetics and Neurodevelopmental Disorders
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Genetic and Kidney Cyst Diseases
Papers in
- Genetics 93
- Connective tissue disorders research 23
- Neurogenetic and Muscular Disorders Research 19
- Craniofacial Disorders and Treatments 18
- Genetics and Neurodevelopmental Disorders 13
- Cleft Lip and Palate Research 12
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- Congenital limb and hand anomalies 17
- Co-authors
- R M Winter (25 shared papers)Jorge Manuel Saraiva (1 shared paper)Jane A. Hurst (10 shared papers)John Burn (13 shared papers)M A Patton (12 shared papers)I. Karen Temple (16 shared papers)E M Brett (12 shared papers)William Reardon (18 shared papers)
- Journals
- Journal of Medical Genetics (81 papers)Clinical Genetics (17 papers)Journal of Neurology Neurosurgery & Psychiatry (8 papers)Neuropediatrics (7 papers)Archives of Disease in Childhood (5 papers)
- Partner nations
- United KingdomCanadaIndia
In The Last Decade
Michael Baraitser
209 papers receiving 5.7k citations
Peers
Comparison fields: 5 of 141
- Developmental Biology 253
- Genetics 3.0k
- Genetics 667
- Pediatrics, Perinatology and Child Health 788
- Molecular Biology 2.5k
Countries citing papers authored by Michael Baraitser
This map shows the geographic impact of Michael Baraitser'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 Michael Baraitser with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael Baraitser more than expected).
Fields of papers citing papers by Michael Baraitser
This network shows the impact of papers produced by Michael Baraitser. 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 Michael Baraitser. The network helps show where Michael Baraitser may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael Baraitser, 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 220 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 390 | |
| 2 | 1990 | 264 | |
| 3 | 1992 | 241 | |
| 4 | 1982 | 200 | |
| 5 | 1982 | 160 | |
| 6 | 1987 | 135 | |
| 7 | 1988 | 106 | |
| 8 | 1980 | 105 | |
| 9 | 1987 | 102 | |
| 10 | 1990 | 101 | |
| 11 | 1988 | 87 | |
| 12 | 1984 | 78 | |
| 13 | 1982 | 75 | |
| 14 | 1987 | 75 | |
| 15 | 1977 | 73 | |
| 16 | 1975 | 72 | |
| 17 | 1988 | 69 | |
| 18 | 1993 | 65 | |
| 19 | 1980 | 64 | |
| 20 | 1989 | 61 |
About Michael Baraitser
Michael Baraitser is a scholar working on Genetics, Genetics, Developmental Biology, Molecular Biology and Surgery, having authored 220 papers that have together received 6.2k indexed citations. Recurring topics across this work include Connective tissue disorders research (23 papers), Neurogenetic and Muscular Disorders Research (19 papers), Craniofacial Disorders and Treatments (18 papers), Congenital limb and hand anomalies (17 papers), Genetic Neurodegenerative Diseases (14 papers), Genetics and Neurodevelopmental Disorders (13 papers), Fetal and Pediatric Neurological Disorders (12 papers) and Cleft Lip and Palate Research (12 papers). The work is most often cited by research in Developmental Biology (253 citations), Genetics (3.0k citations), Genetics (667 citations), Pediatrics, Perinatology and Child Health (788 citations) and Molecular Biology (2.5k citations). Michael Baraitser has collaborated with scholars based in United Kingdom, Canada and India. Frequent co-authors include R M Winter, Jorge Manuel Saraiva, Jane A. Hurst, John Burn, M A Patton, I. Karen Temple, E M Brett, William Reardon, Robin M. Winter and Christine Oley. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Journal of Neurology Neurosurgery & Psychiatry, Neuropediatrics and Archives of Disease in Childhood.
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.