David C. Ward
Impact in
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities
- Virus-based gene therapy research
- Molecular Biology top 0.1%
- Advanced biosensing and bioanalysis techniques
- Genomics and Chromatin Dynamics
- DNA Repair Mechanisms
- DNA and Nucleic Acid Chemistry
- RNA and protein synthesis mechanisms
Papers in
-
- Advanced biosensing and bioanalysis techniques 34
- RNA and protein synthesis mechanisms 29
- DNA and Nucleic Acid Chemistry 27
- Genomics and Chromatin Dynamics 25
- CRISPR and Genetic Engineering 25
- Genetics 96
- Genomic variations and chromosomal abnormalities 35
- Virus-based gene therapy research 30
- Co-authors
- Peter Lichter (13 shared papers)E. Reich (11 shared papers)Laura Manuelidis (7 shared papers)Stephen Gwyn Ballard (6 shared papers)Jeffry J. Leary (4 shared papers)Michael R. Speicher (6 shared papers)David J. Brigati (3 shared papers)Patricia Bray‐Ward (18 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (37 papers)Genomics (35 papers)Journal of Virology (13 papers)Fertility and Sterility (9 papers)Journal of Biological Chemistry (9 papers)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
David C. Ward
297 papers receiving 26.3k citations
David C. Ward's Hit Papers
Peers
Comparison fields: 5 of 190
- Genetics 7.9k
- Molecular Biology 17.2k
- Cancer Research 2.4k
- Plant Science 4.8k
- Pathology and Forensic Medicine 2.0k
Countries citing papers authored by David C. Ward
This map shows the geographic impact of David C. Ward'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 C. Ward with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David C. Ward more than expected).
Fields of papers citing papers by David C. Ward
This network shows the impact of papers produced by David C. Ward. 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 C. Ward. The network helps show where David C. Ward may publish in the future.
Co-authors
The 25 scholars most cited alongside David C. Ward, 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 315 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer Hit paper breakdown → | 1994 | 1700 |
| 2 | Mutation detection and single-molecule counting using isothermal rolling-circle amplification Hit paper breakdown → | 1998 | 1207 |
| 3 | High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones Hit paper breakdown → | 1990 | 1186 |
| 4 | Karyotyping human chromosomes by combinatorial multi-fluor FISH Hit paper breakdown → | 1996 | 1015 |
| 5 | Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries Hit paper breakdown → | 1988 | 1008 |
| 6 | Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes. Hit paper breakdown → | 1981 | 980 |
| 7 | Rapid and sensitive colorimetric method for visualizing biotin-labeled DNA probes hybridized to DNA or RNA immobilized on nitrocellulose: Bio-blots. Hit paper breakdown → | 1983 | 970 |
| 8 | Immunological method for mapping genes on Drosophila polytene chromosomes. Hit paper breakdown → | 1982 | 648 |
| 9 | Detection of viral genomes in cultured cells and paraffin-embedded tissue sections using biotin-labeled hybridization probes Hit paper breakdown → | 1983 | 617 |
| 10 | Fluorescence Studies of Nucleotides and Polynucleotides Hit paper breakdown → | 1969 | 562 |
| 11 | Immunoassays with rolling circle DNA amplification: A versatile platform for ultrasensitive antigen detection Hit paper breakdown → | 2000 | 511 |
| 12 | 1995 | 497 | |
| 13 | 1988 | 462 | |
| 14 | Base Specificity in the Interaction of Polynucleotides with Antibiotic Drugs Hit paper breakdown → | 1965 | 456 |
| 15 | 2003 | 391 | |
| 16 | 2005 | 377 | |
| 17 | 1995 | 372 | |
| 18 | 1984 | 353 | |
| 19 | 1992 | 334 | |
| 20 | 2008 | 332 |
About David C. Ward
David C. Ward is a scholar working on Molecular Biology, Genetics, Plant Science, Infectious Diseases and Animal Science and Zoology, having authored 315 papers that have together received 28.3k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (50 papers), Genomic variations and chromosomal abnormalities (35 papers), Advanced biosensing and bioanalysis techniques (34 papers), Virus-based gene therapy research (30 papers), RNA and protein synthesis mechanisms (29 papers), DNA and Nucleic Acid Chemistry (27 papers), Genomics and Chromatin Dynamics (25 papers) and CRISPR and Genetic Engineering (25 papers). The work is most often cited by research in Genetics (7.9k citations), Molecular Biology (17.2k citations), Cancer Research (2.4k citations), Plant Science (4.8k citations) and Pathology and Forensic Medicine (2.0k citations). David C. Ward has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Peter Lichter, E. Reich, Laura Manuelidis, Stephen Gwyn Ballard, Jeffry J. Leary, Michael R. Speicher, David J. Brigati, Patricia Bray‐Ward, Peter Tattersall and Thomas Haaf. Their work appears in journals such as Proceedings of the National Academy of Sciences, Genomics, Journal of Virology, Fertility and Sterility and Journal of Biological Chemistry.
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.