M. Watson
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
-
- Shoulder and Clavicle Injuries 6
- Co-authors
- Lipmann Kessel (1 shared paper)George R. Sutherland (1 shared paper)Newton E. Morton (1 shared paper)P. A. Jacobs (1 shared paper)GILLIAN M. TURNER (1 shared paper)M. W. Partington (1 shared paper)U. Froster‐Iskenius (1 shared paper)Patricia N. Howard‐Peebles (1 shared paper)
- Journals
- Genetics in Medicine (3 papers)Proceedings of the National Academy of Sciences (2 papers)Journal of Medical Genetics (2 papers)Human Genetics (1 paper)The Journal of Pediatrics (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
M. Watson
24 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 75
- Genetics 596
- Pediatrics, Perinatology and Child Health 286
- Surgery 432
- Cognitive Neuroscience 182
- Epidemiology 269
Countries citing papers authored by M. Watson
This map shows the geographic impact of M. 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 M. Watson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Watson more than expected).
Fields of papers citing papers by M. Watson
This network shows the impact of papers produced by M. 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 M. Watson. The network helps show where M. Watson may publish in the future.
Co-authors
The 25 scholars most cited alongside M. 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
Showing the 20 most-cited of 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1985 | 423 | |
| 2 | 1977 | 229 | |
| 3 | 2013 | 228 | |
| 4 | 1985 | 104 | |
| 5 | Promoting safe and effective genetic testing in the United States. Final report of the Task Force on Genetic Testing. | 2000 | 52 |
| 6 | 1984 | 49 | |
| 7 | 1991 | 45 | |
| 8 | 1978 | 30 | |
| 9 | 1987 | 27 | |
| 10 | 1989 | 27 | |
| 11 | 1997 | 25 | |
| 12 | 1989 | 24 | |
| 13 | A method of processing first-trimester chorionic villous biopsies for cytogenetic analysis. | 1984 | 23 |
| 14 | Linkage disequilibrium study of RFLPs detected at the human muscle nicotinic acetylcholine receptor subunit genes. | 1989 | 20 |
| 15 | 1985 | 19 | |
| 16 | 1996 | 15 | |
| 17 | 1996 | 11 | |
| 18 | Translocations involving chromosome 12p11-13, methotrexate metabolism, and outcome in childhood B-progenitor cell acute lymphoblastic leukemia: a Pediatric Oncology Group study. | 1998 | 11 |
| 19 | Bipolar salvage shoulder arthroplasty. Follow-up in 14 patients. | 1996 | 9 |
| 20 | 2021 | 7 |
About M. Watson
M. Watson is a scholar working on Genetics, Epidemiology, Surgery, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 27 papers that have together received 1.4k indexed citations. Recurring topics across this work include Shoulder Injury and Treatment (7 papers), Shoulder and Clavicle Injuries (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Prenatal Screening and Diagnostics (3 papers), Congenital heart defects research (3 papers), Chronic Myeloid Leukemia Treatments (2 papers) and Autism Spectrum Disorder Research (2 papers). The work is most often cited by research in Genetics (596 citations), Pediatrics, Perinatology and Child Health (286 citations), Surgery (432 citations), Cognitive Neuroscience (182 citations) and Epidemiology (269 citations). M. Watson has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Lipmann Kessel, George R. Sutherland, Newton E. Morton, P. A. Jacobs, GILLIAN M. TURNER, M. W. Partington, U. Froster‐Iskenius, Patricia N. Howard‐Peebles, Stephanie L. Sherman and Brian G. Skotko. Their work appears in journals such as Genetics in Medicine, Proceedings of the National Academy of Sciences, Journal of Medical Genetics, Human Genetics and The Journal of Pediatrics.
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.