Karin M. Dent
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 16
- Genomics and Rare Diseases 11
- BRCA gene mutations in cancer 9
- Co-authors
- Michael J. Bamshad (6 shared papers)Holly K. Tabor (5 shared papers)Jay Shendure (2 shared papers)Chad D. Huff (1 shared paper)Paul Shannon (1 shared paper)Choli Lee (1 shared paper)Deborah A. Nickerson (1 shared paper)Kati J. Buckingham (1 shared paper)
- Journals
- American Journal of Medical Genetics Part C Seminars in Medical Genetics (3 papers)Clinical Cancer Research (1 paper)Nature Genetics (1 paper)Biological Psychiatry (1 paper)Molecular Psychiatry (1 paper)
- Partner nations
- United StatesCanadaNetherlands
In The Last Decade
Karin M. Dent
26 papers receiving 2.1k citations
Karin M. Dent's Hit Papers
Peers
Comparison fields: 5 of 116
- Genetics 1.1k
- Cancer Research 264
- Molecular Biology 950
- Cellular and Molecular Neuroscience 231
- Biological Psychiatry 28
Countries citing papers authored by Karin M. Dent
This map shows the geographic impact of Karin M. Dent'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 Karin M. Dent with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin M. Dent more than expected).
Fields of papers citing papers by Karin M. Dent
This network shows the impact of papers produced by Karin M. Dent. 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 Karin M. Dent. The network helps show where Karin M. Dent may publish in the future.
Co-authors
The 25 scholars most cited alongside Karin M. Dent, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Exome sequencing identifies the cause of a mendelian disorder Hit paper breakdown → | 2009 | 1303 |
| 2 | 1999 | 207 | |
| 3 | 2005 | 117 | |
| 4 | 1999 | 110 | |
| 5 | 2012 | 89 | |
| 6 | 2013 | 55 | |
| 7 | 2017 | 34 | |
| 8 | 2006 | 31 | |
| 9 | 2016 | 25 | |
| 10 | 2004 | 24 | |
| 11 | 2004 | 22 | |
| 12 | 2015 | 17 | |
| 13 | 2018 | 17 | |
| 14 | 2018 | 16 | |
| 15 | 2001 | 14 | |
| 16 | 2006 | 11 | |
| 17 | 2020 | 10 | |
| 18 | 2018 | 9 | |
| 19 | 2014 | 8 | |
| 20 | 2020 | 8 |
About Karin M. Dent
Karin M. Dent is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Pediatrics, Perinatology and Child Health and Clinical Psychology, having authored 29 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (11 papers), BRCA gene mutations in cancer (9 papers), Family and Disability Support Research (4 papers), Prenatal Screening and Diagnostics (3 papers), Ethics in Clinical Research (3 papers), Patient-Provider Communication in Healthcare (2 papers), Autism Spectrum Disorder Research (2 papers) and Counseling Practices and Supervision (2 papers). The work is most often cited by research in Genetics (1.1k citations), Cancer Research (264 citations), Molecular Biology (950 citations), Cellular and Molecular Neuroscience (231 citations) and Biological Psychiatry (28 citations). Karin M. Dent has collaborated with scholars based in United States, Canada and Netherlands. Frequent co-authors include Michael J. Bamshad, Holly K. Tabor, Jay Shendure, Chad D. Huff, Paul Shannon, Choli Lee, Deborah A. Nickerson, Kati J. Buckingham, Ethylin Wang Jabs and Abigail W. Bigham. Their work appears in journals such as American Journal of Medical Genetics Part C Seminars in Medical Genetics, Clinical Cancer Research, Nature Genetics, Biological Psychiatry and Molecular Psychiatry.
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.