Leonard Prouty
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Genomics and Chromatin Dynamics 2
- Retinoids in leukemia and cellular processes 2
- Co-authors
- Mark A. Dayton (2 shared papers)Kerry Blanchard (2 shared papers)Briana J. Williams (2 shared papers)Jian Liang (2 shared papers)Alan R. Mootnick (2 shared papers)Philip D. Buchanan (2 shared papers)William S. Pollitzer (2 shared papers)Sushil K. Jain (2 shared papers)
- Journals
- Clinical Genetics (2 papers)Blood (2 papers)Journal of Cellular Biochemistry (1 paper)BMC Medicine (1 paper)Cytokine (1 paper)
- Partner nations
- United States
In The Last Decade
Leonard Prouty
17 papers receiving 380 citations
Peers
Comparison fields: 5 of 80
- Developmental Biology 13
- Genetics 157
- Hematology 48
- Molecular Biology 191
- Cognitive Neuroscience 46
Countries citing papers authored by Leonard Prouty
This map shows the geographic impact of Leonard Prouty'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 Leonard Prouty with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Leonard Prouty more than expected).
Fields of papers citing papers by Leonard Prouty
This network shows the impact of papers produced by Leonard Prouty. 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 Leonard Prouty. The network helps show where Leonard Prouty may publish in the future.
Co-authors
The 25 scholars most cited alongside Leonard Prouty, 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 | 1998 | 116 | |
| 2 | 1988 | 50 | |
| 3 | 1983 | 41 | |
| 4 | 2004 | 31 | |
| 5 | 1983 | 27 | |
| 6 | 2004 | 22 | |
| 7 | 1994 | 20 | |
| 8 | 2013 | 18 | |
| 9 | 1988 | 17 | |
| 10 | 1999 | 17 | |
| 11 | 1998 | 14 | |
| 12 | 1988 | 9 | |
| 13 | 1989 | 6 | |
| 14 | 1987 | 5 | |
| 15 | Oligohydramnios sequence (Potter's syndrome): case clustering in northeastern Tennessee. | 1987 | 4 |
| 16 | 1998 | 2 | |
| 17 | 2017 | 2 |
About Leonard Prouty
Leonard Prouty is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 17 papers that have together received 401 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Acute Myeloid Leukemia Research (2 papers), Genomics and Chromatin Dynamics (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Prenatal Screening and Diagnostics (2 papers), Acute Lymphoblastic Leukemia research (2 papers) and Retinoids in leukemia and cellular processes (2 papers). The work is most often cited by research in Developmental Biology (13 citations), Genetics (157 citations), Hematology (48 citations), Molecular Biology (191 citations) and Cognitive Neuroscience (46 citations). Leonard Prouty has collaborated with scholars based in United States. Frequent co-authors include Mark A. Dayton, Kerry Blanchard, Briana J. Williams, Jian Liang, Alan R. Mootnick, Philip D. Buchanan, William S. Pollitzer, Sushil K. Jain, Roger E. Stevenson and Charles E. Schwartz. Their work appears in journals such as Clinical Genetics, Blood, Journal of Cellular Biochemistry, BMC Medicine and Cytokine.
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.