M A Patton
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Genetics top 2%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Craniofacial Disorders and Treatments
Papers in
-
- Protein Tyrosine Phosphatases 9
- RNA modifications and cancer 6
- Genetics 18
- Genetic Syndromes and Imprinting 5
- Neurogenetic and Muscular Disorders Research 4
- Craniofacial Disorders and Treatments 4
- Co-authors
- Andrew H. Crosby (11 shared papers)M Baraitser (11 shared papers)A. Harden (1 shared paper)Stewart Boyd (1 shared paper)Kamini Kalidas (4 shared papers)Adam Shaw (1 shared paper)Steven Jeffery (1 shared paper)Mike Sharland (6 shared papers)
- Journals
- Journal of Medical Genetics (22 papers)Clinical Genetics (5 papers)European Journal of Pediatrics (3 papers)Heart (2 papers)Human Genetics (2 papers)
- Partner nations
- United KingdomOmanUnited States
In The Last Decade
M A Patton
62 papers receiving 2.1k citations
Peers
Comparison fields: 5 of 96
- Developmental Biology 135
- Genetics 861
- Genetics 165
- Molecular Biology 1.1k
- Pediatrics, Perinatology and Child Health 258
Countries citing papers authored by M A Patton
This map shows the geographic impact of M A Patton'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 A Patton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M A Patton more than expected).
Fields of papers citing papers by M A Patton
This network shows the impact of papers produced by M A Patton. 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 A Patton. The network helps show where M A Patton may publish in the future.
Co-authors
The 25 scholars most cited alongside M A Patton, 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 63 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 198 | |
| 2 | 1988 | 192 | |
| 3 | 1997 | 107 | |
| 4 | 2002 | 97 | |
| 5 | Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1. | 1994 | 91 |
| 6 | 2008 | 80 | |
| 7 | 1998 | 75 | |
| 8 | 1987 | 72 | |
| 9 | 2001 | 68 | |
| 10 | 1996 | 66 | |
| 11 | 1988 | 64 | |
| 12 | 2008 | 58 | |
| 13 | 2007 | 57 | |
| 14 | 1992 | 55 | |
| 15 | 1994 | 54 | |
| 16 | 1988 | 47 | |
| 17 | 1989 | 43 | |
| 18 | 2008 | 40 | |
| 19 | 1987 | 39 | |
| 20 | 1996 | 36 |
About M A Patton
M A Patton is a scholar working on Molecular Biology, Genetics, Surgery, Cellular and Molecular Neuroscience and Developmental Biology, having authored 63 papers that have together received 2.2k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (9 papers), Congenital limb and hand anomalies (6 papers), RNA modifications and cancer (6 papers), Congenital Anomalies and Fetal Surgery (5 papers), Genetic Syndromes and Imprinting (5 papers), Neurogenetic and Muscular Disorders Research (4 papers), Orthopedic Surgery and Rehabilitation (4 papers) and Craniofacial Disorders and Treatments (4 papers). The work is most often cited by research in Developmental Biology (135 citations), Genetics (861 citations), Genetics (165 citations), Molecular Biology (1.1k citations) and Pediatrics, Perinatology and Child Health (258 citations). M A Patton has collaborated with scholars based in United Kingdom, Oman and United States. Frequent co-authors include Andrew H. Crosby, M Baraitser, A. Harden, Stewart Boyd, Kamini Kalidas, Adam Shaw, Steven Jeffery, Mike Sharland, William J. McKenna and Michael A. Simpson. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, European Journal of Pediatrics, Heart and Human 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.