David P. Witte

17.2k citations
241 papers · 14.3k · h-index 66

Impact in

  • Hematology top 0.5%
    • Blood Coagulation and Thrombosis Mechanisms
  • Nephrology top 1%
    • Renal Diseases and Glomerulopathies

Papers in

    • Platelet Disorders and Treatments 11
    • Blood Coagulation and Thrombosis Mechanisms 11
    • Glycosylation and Glycoproteins Research 13
    • Congenital heart defects research 11

David P. Witte

240 papers receiving 13.9k citations

Peers

David P. Witte
Comparison fields: 5 of 154
  • Hematology 1.3k
  • Nephrology 747
  • Immunology 2.0k
  • Molecular Biology 5.8k
  • Genetics 861
Replace Thomas L. Saunders with:
Thomas L. Saunders United States
Magnus Nordenskjöld Sweden
William C. Aird United States
Pierre J. Courtoy Belgium
Stephen E. Harris United States
Natalie A. Sims Australia
Søren K. Moestrup Denmark
Aris N. Economides United States
Jeffrey L. Platt United States
Kathleen Corey Flanders United States
David P. Witte relative to Thomas L. Saunders United States Thomas L. Saunders's profile →
Citations per field
00.5×1.5×
Thomas L. Saunders · 1×
Citations per year

Countries citing papers authored by David P. Witte

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with David P. Witte Line = papers co-authored together David P. Witte links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 241 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1995504
2 1997451
3 1997432
4 2003413
5 2004383
6 1995338
7 1996284
8 1987241
9 1998203
10 2006200
11 2000190
12 1989189
13 1997187
14 1999185
15 2008185
16 1993181
17 2017163
18 2016162
19 2001160
20 1996155

About David P. Witte

David P. Witte is a scholar working on Hematology, Molecular Biology, Physiology, Immunology and Oncology, having authored 241 papers that have together received 14.3k 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), Renal Diseases and Glomerulopathies (13 papers), Platelet Disorders and Treatments (11 papers), Blood Coagulation and Thrombosis Mechanisms (11 papers), Congenital heart defects research (11 papers) and Systemic Lupus Erythematosus Research (10 papers). The work is most often cited by research in Hematology (1.3k citations), Nephrology (747 citations), Immunology (2.0k citations), Molecular Biology (5.8k citations) and Genetics (861 citations). David P. Witte has collaborated with scholars based in United States, Australia and Germany. Frequent co-authors include S. Steven Potter, Gregory Alex Grabowski, Jay L. Degen, Bruce J. Aronow, Dorothy M. Supp, Hsiu Mei Hsieh‐Li, Martina K. Brueckner, Matthew J. Flick, Judith A.K. Harmony and Brian Quinn. 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.

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