Michael S. Watson
Impact in
- Genetics top 0.1%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Papers in
-
- Metabolism and Genetic Disorders 15
- Genetics 56
- Genomics and Rare Diseases 29
- BRCA gene mutations in cancer 17
- Genomic variations and chromosomal abnormalities 17
- Genetics and Neurodevelopmental Disorders 12
- Co-authors
- Christa Lese MartinWayne W. GrodyMichele A. Lloyd-PuryearBruce R. KorfRobert L. NussbaumKelly E. OrmondSarah S. KaliaJonathan S. Berg
- Journals
- Genetics in Medicine (40 papers)PEDIATRICS (3 papers)Science (2 papers)Mental Retardation and Developmental Disabilities Research Reviews (2 papers)International Journal of Neonatal Screening (2 papers)
- Partner nations
- United StatesUnited KingdomAustralia
In The Last Decade
Michael S. Watson
109 papers receiving 9.4k citations
Hit Papers
Peers
Comparison fields: 5 of 164
- Genetics 5.2k
- Clinical Biochemistry 856
- Pediatrics, Perinatology and Child Health 1.9k
- Cancer Research 1.2k
- Rheumatology 817
Countries citing papers authored by Michael S. Watson
This map shows the geographic impact of Michael S. Watson'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 S. Watson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael S. Watson more than expected).
Fields of papers citing papers by Michael S. Watson
This network shows the impact of papers produced by Michael S. Watson. 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 S. Watson. The network helps show where Michael S. Watson may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Michael S. Watson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 0 | |
| 2 | 2021 | 142 | |
| 3 | 2019 | 104 | |
| 4 | 2018 | 19 | |
| 5 | 2018 | 16 | |
| 6 | 2017 | 11 | |
| 7 | Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics Hit paper breakdown → | 2016 | 1023 |
| 8 | 2014 | 39 | |
| 9 | ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing Hit paper breakdown → | 2013 | 1643 |
| 10 | 2010 | 64 | |
| 11 | 2010 | 7 | |
| 12 | 2009 | 7 | |
| 13 | 2008 | 157 | |
| 14 | 2008 | 18 | |
| 15 | 2006 | 366 | |
| 16 | 2004 | 40 | |
| 17 | 2001 | 326 | |
| 18 | 2001 | 16 | |
| 19 | 1999 | 1 | |
| 20 | 1991 | 30 |
About Michael S. Watson
Michael S. Watson is a scholar working on Clinical Biochemistry, Genetics, Pediatrics, Perinatology and Child Health, Developmental Biology and Genetics, having authored 115 papers that have together received 9.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (29 papers), BRCA gene mutations in cancer (17 papers), Genomic variations and chromosomal abnormalities (17 papers), Metabolism and Genetic Disorders (15 papers), Prenatal Screening and Diagnostics (14 papers), Genetics and Neurodevelopmental Disorders (12 papers), Congenital heart defects research (10 papers) and Genetic factors in colorectal cancer (8 papers). The work is most often cited by research in Genetics (5.2k citations), Clinical Biochemistry (856 citations), Pediatrics, Perinatology and Child Health (1.9k citations), Cancer Research (1.2k citations) and Rheumatology (817 citations). Michael S. Watson has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Christa Lese Martin, Wayne W. Grody, Michele A. Lloyd-Puryear, Bruce R. Korf, Robert L. Nussbaum, Kelly E. Ormond, Sarah S. Kalia, Jonathan S. Berg, Heidi L. Rehm and R. Rodney Howell. Their work appears in journals such as Genetics in Medicine, PEDIATRICS, Science, Mental Retardation and Developmental Disabilities Research Reviews and International Journal of Neonatal Screening.
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.