David P. Witte
Impact in
- Hematology top 0.5%
- Blood Coagulation and Thrombosis Mechanisms
- Nephrology top 0.5%
- Renal Diseases and Glomerulopathies
Papers in
-
- Glycosylation and Glycoproteins Research 13
- Congenital heart defects research 11
- Physiology 41
- Lysosomal Storage Disorders Research 28
- Co-authors
- S. Steven Potter (13 shared papers)Gregory A. Grabowski (31 shared papers)Jay L. Degen (18 shared papers)Bruce J. Aronow (24 shared papers)Dorothy M. Supp (4 shared papers)Hsiu Mei Hsieh‐Li (4 shared papers)Martina Brueckner (2 shared papers)Matthew J. Flick (10 shared papers)
- Journals
- Journal of Clinical Investigation (10 papers)Blood (8 papers)Proceedings of the National Academy of Sciences (8 papers)American Journal Of Pathology (6 papers)Human Molecular Genetics (6 papers)
- Partner nations
- United StatesAustraliaGermany
In The Last Decade
David P. Witte
239 papers receiving 13.6k citations
David P. Witte's Hit Papers
Peers
Comparison fields: 5 of 152
- Hematology 1.3k
- Nephrology 725
- Immunology 2.0k
- Molecular Biology 5.8k
- Immunology and Allergy 469
Countries citing papers authored by David P. Witte
This map shows the geographic impact of David P. Witte'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 P. Witte with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David P. Witte more than expected).
Fields of papers citing papers by David P. Witte
This network shows the impact of papers produced by David P. Witte. 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 P. Witte. The network helps show where David P. Witte may publish in the future.
Co-authors
The 25 scholars most cited alongside David P. Witte, 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 241 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Absence of radius and ulna in mice lacking hoxa-11 andhoxd-11 Hit paper breakdown → | 1995 | 509 |
| 2 | 1997 | 455 | |
| 3 | 1997 | 429 | |
| 4 | 2003 | 410 | |
| 5 | 2004 | 361 | |
| 6 | 1995 | 346 | |
| 7 | 1996 | 287 | |
| 8 | 1987 | 239 | |
| 9 | 1998 | 203 | |
| 10 | 2006 | 197 | |
| 11 | 1999 | 189 | |
| 12 | 2000 | 187 | |
| 13 | 1989 | 186 | |
| 14 | 1997 | 186 | |
| 15 | 1993 | 178 | |
| 16 | 2008 | 175 | |
| 17 | 2001 | 156 | |
| 18 | 2017 | 155 | |
| 19 | 1996 | 154 | |
| 20 | 2003 | 148 |
About David P. Witte
David P. Witte is a scholar working on Molecular Biology, Physiology, Oncology, Pulmonary and Respiratory Medicine and Hematology, having authored 241 papers that have together received 14.0k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (28 papers), Cellular transport and secretion (15 papers), Glycosylation and Glycoproteins Research (13 papers), Congenital heart defects research (11 papers), Platelet Disorders and Treatments (11 papers), Renal Diseases and Glomerulopathies (11 papers), Blood Coagulation and Thrombosis Mechanisms (11 papers) and Systemic Lupus Erythematosus Research (10 papers). The work is most often cited by research in Hematology (1.3k citations), Nephrology (725 citations), Immunology (2.0k citations), Molecular Biology (5.8k citations) and Immunology and Allergy (469 citations). David P. Witte has collaborated with scholars based in United States, Australia and Germany. Frequent co-authors include S. Steven Potter, Gregory A. Grabowski, Jay L. Degen, Bruce J. Aronow, Dorothy M. Supp, Hsiu Mei Hsieh‐Li, Martina Brueckner, Matthew J. Flick, Judith A.K. Harmony and Mario R. Capecchi. Their work appears in journals such as Journal of Clinical Investigation, Blood, Proceedings of the National Academy of Sciences, American Journal Of Pathology and Human Molecular Genetics.
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.