Robert E. Pyatt
Impact in
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
- Mesenchymal stem cell research
- Hematology top 5%
- Hematopoietic Stem Cell Transplantation
Papers in
- Genetics 24
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 6
- Neurogenetic and Muscular Disorders Research 5
- Virus-based gene therapy research 4
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- Congenital heart defects research 4
- Muscle Physiology and Disorders 4
- Co-authors
- Thomas W. Prior (9 shared papers)Jon McMahel (5 shared papers)Edward F. Srour (6 shared papers)André Gothot (5 shared papers)Susan Rice (5 shared papers)Sayaka Hashimoto (11 shared papers)David Mihal (3 shared papers)Caroline Astbury (15 shared papers)
- Journals
- Blood (5 papers)European Journal of Medical Genetics (4 papers)Journal of Molecular Diagnostics (2 papers)Journal of Health Communication (1 paper)Cytogenetic and Genome Research (1 paper)
- Partner nations
- United StatesNigeriaSouth Sudan
In The Last Decade
Robert E. Pyatt
40 papers receiving 992 citations
Peers
Comparison fields: 5 of 84
- Genetics 315
- Hematology 189
- Genetics 204
- Pathology and Forensic Medicine 118
- Molecular Biology 433
Countries citing papers authored by Robert E. Pyatt
This map shows the geographic impact of Robert E. Pyatt'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 Robert E. Pyatt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert E. Pyatt more than expected).
Fields of papers citing papers by Robert E. Pyatt
This network shows the impact of papers produced by Robert E. Pyatt. 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 Robert E. Pyatt. The network helps show where Robert E. Pyatt may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert E. Pyatt, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 207 | |
| 2 | 1997 | 174 | |
| 3 | 1999 | 83 | |
| 4 | 1997 | 82 | |
| 5 | 2010 | 66 | |
| 6 | Assessment of proliferative and colony-forming capacity after successive in vitro divisions of single human CD34+ cells initially isolated in G0. | 1998 | 46 |
| 7 | 2014 | 41 | |
| 8 | 2006 | 31 | |
| 9 | 2006 | 27 | |
| 10 | 2007 | 24 | |
| 11 | 2011 | 19 | |
| 12 | 2012 | 18 | |
| 13 | 2012 | 18 | |
| 14 | Case report on hereditary non-polyposis colon cancer (HNPCC) in Nigeria. | 2000 | 18 |
| 15 | 2013 | 17 | |
| 16 | 2013 | 16 | |
| 17 | 2020 | 14 | |
| 18 | 2004 | 14 | |
| 19 | 2019 | 13 | |
| 20 | FIRST: A Model for Developing New Science Faculty. | 2005 | 12 |
About Robert E. Pyatt
Robert E. Pyatt is a scholar working on Genetics, Molecular Biology, Hematology, Pediatrics, Perinatology and Child Health and Genetics, having authored 40 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Hematopoietic Stem Cell Transplantation (6 papers), Genomics and Rare Diseases (6 papers), Prenatal Screening and Diagnostics (6 papers), Neurogenetic and Muscular Disorders Research (5 papers), Virus-based gene therapy research (4 papers), Congenital heart defects research (4 papers) and Muscle Physiology and Disorders (4 papers). The work is most often cited by research in Genetics (315 citations), Hematology (189 citations), Genetics (204 citations), Pathology and Forensic Medicine (118 citations) and Molecular Biology (433 citations). Robert E. Pyatt has collaborated with scholars based in United States, Nigeria and South Sudan. Frequent co-authors include Thomas W. Prior, Jon McMahel, Edward F. Srour, André Gothot, Susan Rice, Sayaka Hashimoto, David Mihal, Caroline Astbury, Julie M. Gastier‐Foster and Shalini C. Reshmi. Their work appears in journals such as Blood, European Journal of Medical Genetics, Journal of Molecular Diagnostics, Journal of Health Communication and Cytogenetic and Genome Research.
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.