Michael A. Patton
Impact in
- Immunology top 2%
- Galectins and Cancer Biology
- Molecular Biology top 1%
- Protein Tyrosine Phosphatases
- RNA modifications and cancer
- Congenital heart defects research
Papers in
- Genetics 32
- Genomic variations and chromosomal abnormalities 8
- Craniofacial Disorders and Treatments 8
- Genetics and Neurodevelopmental Disorders 8
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- Protein Tyrosine Phosphatases 19
- RNA modifications and cancer 12
- Co-authors
- Andrew H. Crosby (20 shared papers)Steve Jeffery (12 shared papers)Marco Tartaglia (6 shared papers)Kamini Kalidas (6 shared papers)Han G. Brunner (3 shared papers)Bruce D. Gelb (4 shared papers)Raju Kucherlapati (2 shared papers)Hannie Kremer (2 shared papers)
- Journals
- Nature Genetics (10 papers)The American Journal of Human Genetics (9 papers)Clinical Infectious Diseases (4 papers)Brain (3 papers)Vaccine (3 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Michael A. Patton
101 papers receiving 8.9k citations
Michael A. Patton's Hit Papers
Peers
Comparison fields: 5 of 151
- Immunology 1.6k
- Molecular Biology 5.2k
- Genetics 1.8k
- Neurology 489
- Developmental Biology 118
Countries citing papers authored by Michael A. Patton
This map shows the geographic impact of Michael 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 Michael 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 Michael A. Patton more than expected).
Fields of papers citing papers by Michael A. Patton
This network shows the impact of papers produced by Michael 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 Michael A. Patton. The network helps show where Michael A. Patton may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael 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 101 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome Hit paper breakdown → | 2001 | 1367 |
| 2 | Polysaccharide Conjugate Vaccine against Pneumococcal Pneumonia in Adults Hit paper breakdown → | 2015 | 980 |
| 3 | 2002 | 623 | |
| 4 | 2004 | 339 | |
| 5 | 1999 | 281 | |
| 6 | 2009 | 256 | |
| 7 | 2000 | 251 | |
| 8 | 1994 | 232 | |
| 9 | 2001 | 221 | |
| 10 | 2002 | 212 | |
| 11 | 2014 | 209 | |
| 12 | 2004 | 202 | |
| 13 | 1997 | 198 | |
| 14 | 1993 | 180 | |
| 15 | 2010 | 169 | |
| 16 | 1993 | 162 | |
| 17 | 2008 | 149 | |
| 18 | 2003 | 144 | |
| 19 | 2011 | 133 | |
| 20 | 2005 | 129 |
About Michael A. Patton
Michael A. Patton is a scholar working on Genetics, Molecular Biology, Genetics, Cellular and Molecular Neuroscience and Epidemiology, having authored 101 papers that have together received 9.3k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (19 papers), RNA modifications and cancer (12 papers), Galectins and Cancer Biology (11 papers), Hereditary Neurological Disorders (9 papers), Genomic variations and chromosomal abnormalities (8 papers), Craniofacial Disorders and Treatments (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Respiratory viral infections research (7 papers). The work is most often cited by research in Immunology (1.6k citations), Molecular Biology (5.2k citations), Genetics (1.8k citations), Neurology (489 citations) and Developmental Biology (118 citations). Michael A. Patton has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Andrew H. Crosby, Steve Jeffery, Marco Tartaglia, Kamini Kalidas, Han G. Brunner, Bruce D. Gelb, Raju Kucherlapati, Hannie Kremer, Giuseppe Zampino and Rosalie B. Goldberg. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics, Clinical Infectious Diseases, Brain and Vaccine.
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.