David R. Witt
Impact in
-
- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
- Genetics top 5%
- Genomics and Rare Diseases
Papers in
-
- Biochemical and Molecular Research 4
- Surgery 5
- Congenital Anomalies and Fetal Surgery 3
- Co-authors
- K. Klinger (2 shared papers)Anthony P. Shuber (2 shared papers)Judith G. Hall (5 shared papers)Garry R. Cutting (2 shared papers)Brenda Richards (1 shared paper)Henry L. Dorkin (1 shared paper)Rosemary Balfour (1 shared paper)Robert C. Stern (1 shared paper)
- Journals
- Genetics in Medicine (2 papers)Human Genetics (2 papers)Clinical Genetics (2 papers)Nature Genetics (1 paper)Journal of Inherited Metabolic Disease (1 paper)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
David R. Witt
22 papers receiving 1.9k citations
Peers
Comparison fields: 5 of 101
- Pulmonary and Respiratory Medicine 619
- Genetics 187
- Genetics 444
- Cellular and Molecular Neuroscience 282
- Neurology 107
Countries citing papers authored by David R. Witt
This map shows the geographic impact of David R. Witt'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 David R. Witt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David R. Witt more than expected).
Fields of papers citing papers by David R. Witt
This network shows the impact of papers produced by David R. Witt. 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 David R. Witt. The network helps show where David R. Witt may publish in the future.
Co-authors
The 25 scholars most cited alongside David R. Witt, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 343 | |
| 2 | 1993 | 335 | |
| 3 | 2004 | 315 | |
| 4 | 1996 | 288 | |
| 5 | 1987 | 105 | |
| 6 | 1986 | 77 | |
| 7 | 1986 | 71 | |
| 8 | 2003 | 66 | |
| 9 | Cystic fibrosis heterozygote screening in 5,161 pregnant women. | 1996 | 65 |
| 10 | 1988 | 55 | |
| 11 | 1996 | 43 | |
| 12 | 1987 | 37 | |
| 13 | 1994 | 30 | |
| 14 | 2005 | 20 | |
| 15 | 1985 | 18 | |
| 16 | 2004 | 17 | |
| 17 | 2011 | 16 | |
| 18 | 2008 | 12 | |
| 19 | 2000 | 8 | |
| 20 | Approach to multiple congenital anomaly syndromes. | 1985 | 2 |
About David R. Witt
David R. Witt is a scholar working on Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Genetics, having authored 23 papers that have together received 1.9k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (4 papers), Biochemical and Molecular Research (4 papers), Metabolism and Genetic Disorders (3 papers), Skin and Cellular Biology Research (3 papers), Prenatal Screening and Diagnostics (3 papers), Tracheal and airway disorders (3 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (619 citations), Genetics (187 citations), Genetics (444 citations), Cellular and Molecular Neuroscience (282 citations) and Neurology (107 citations). David R. Witt has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include K. Klinger, Anthony P. Shuber, Judith G. Hall, Garry R. Cutting, Brenda Richards, Henry L. Dorkin, Rosemary Balfour, Robert C. Stern, Richard B. Parad and Joel Skoletsky. Their work appears in journals such as Genetics in Medicine, Human Genetics, Clinical Genetics, Nature Genetics and Journal of Inherited Metabolic Disease.
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.