David Frederick Callen
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- BRCA gene mutations in cancer
- Genetic diversity and population structure
- Cancer Research top 1%
- MicroRNA in disease regulation
Papers in
- Genetics 82
- Genomic variations and chromosomal abnormalities 60
- Genetics and Neurodevelopmental Disorders 5
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- Carcinogens and Genotoxicity Assessment 8
- Co-authors
- George R. Sutherland (35 shared papers)Elizabeth G. Baker (35 shared papers)Paul Matthew Neilsen (27 shared papers)Helen J. Eyre (23 shared papers)Robert I. Richards (19 shared papers)Grant R. Sutherland (20 shared papers)Scott A. Whitmore (24 shared papers)Hilary A. Phillips (10 shared papers)
- Journals
- Genomics (36 papers)Human Genetics (16 papers)Journal of Medical Genetics (9 papers)Clinical Genetics (7 papers)Nucleic Acids Research (7 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
David Frederick Callen
272 papers receiving 13.0k citations
David Frederick Callen's Hit Papers
Peers
Comparison fields: 5 of 115
- Genetics 3.5k
- Cancer Research 734
- Pathology and Forensic Medicine 650
- Oncology 781
- Molecular Biology 1.8k
Countries citing papers authored by David Frederick Callen
This map shows the geographic impact of David Frederick Callen'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 Frederick Callen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Frederick Callen more than expected).
Fields of papers citing papers by David Frederick Callen
This network shows the impact of papers produced by David Frederick Callen. 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 Frederick Callen. The network helps show where David Frederick Callen may publish in the future.
Co-authors
The 25 scholars most cited alongside David Frederick Callen, 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 281 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genome-wide association study identifies novel breast cancer susceptibility loci Hit paper breakdown → | 2007 | 1919 |
| 2 | Incidence and origin of "null" alleles in the (AC)n microsatellite markers. Hit paper breakdown → | 1993 | 568 |
| 3 | 1998 | 503 | |
| 4 | 2010 | 483 | |
| 5 | 1996 | 354 | |
| 6 | 2010 | 302 | |
| 7 | 2012 | 264 | |
| 8 | 1996 | 248 | |
| 9 | 2001 | 240 | |
| 10 | 2015 | 201 | |
| 11 | 1987 | 154 | |
| 12 | 2012 | 153 | |
| 13 | 2014 | 148 | |
| 14 | 2014 | 142 | |
| 15 | 2004 | 141 | |
| 16 | 1992 | 138 | |
| 17 | Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics. | 1991 | 128 |
| 18 | 1994 | 126 | |
| 19 | 1995 | 124 | |
| 20 | 2004 | 124 |
About David Frederick Callen
David Frederick Callen is a scholar working on Genetics, Cancer Research, Oncology, Physiology and Molecular Biology, having authored 281 papers that have together received 13.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (60 papers), Lysosomal Storage Disorders Research (18 papers), Cancer-related Molecular Pathways (9 papers), Vitamin D Research Studies (8 papers), Carcinogens and Genotoxicity Assessment (8 papers), Ubiquitin and proteasome pathways (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and DNA Repair Mechanisms (5 papers). The work is most often cited by research in Genetics (3.5k citations), Cancer Research (734 citations), Pathology and Forensic Medicine (650 citations), Oncology (781 citations) and Molecular Biology (1.8k citations). David Frederick Callen has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include George R. Sutherland, Elizabeth G. Baker, Paul Matthew Neilsen, Helen J. Eyre, Robert I. Richards, Grant R. Sutherland, Scott A. Whitmore, Hilary A. Phillips, Rachel J. Suetani and J.C. Mulley. Their work appears in journals such as Genomics, Human Genetics, Journal of Medical Genetics, Clinical Genetics and Nucleic Acids 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.