David Dimmock
Impact in
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
- Genetics top 1%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Mitochondrial Function and Pathology 25
- Genetics 46
- Genomics and Rare Diseases 33
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 7
- BRCA gene mutations in cancer 7
- Co-authors
- Stephen F. Kingsmore (28 shared papers)Michelle M. Clark (8 shared papers)David Bick (9 shared papers)Lauge Farnaes (14 shared papers)Daniel Helbling (14 shared papers)Susan M. White (1 shared paper)Tiong Yang Tan (1 shared paper)Zornitza Stark (1 shared paper)
- Journals
- Molecular Case Studies (10 papers)npj Genomic Medicine (8 papers)Molecular Genetics and Metabolism (7 papers)Genetics in Medicine (5 papers)Journal of Pediatric Gastroenterology and Nutrition (4 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
David Dimmock
114 papers receiving 4.0k citations
David Dimmock's Hit Papers
Peers
Comparison fields: 5 of 114
- Clinical Biochemistry 880
- Genetics 1.6k
- Cancer Research 410
- Molecular Biology 1.5k
- Pediatrics, Perinatology and Child Health 361
Countries citing papers authored by David Dimmock
This map shows the geographic impact of David Dimmock'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 Dimmock with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Dimmock more than expected).
Fields of papers citing papers by David Dimmock
This network shows the impact of papers produced by David Dimmock. 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 Dimmock. The network helps show where David Dimmock may publish in the future.
Co-authors
The 25 scholars most cited alongside David Dimmock, 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 116 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases Hit paper breakdown → | 2018 | 349 |
| 2 | Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization Hit paper breakdown → | 2018 | 284 |
| 3 | 2015 | 269 | |
| 4 | 2012 | 169 | |
| 5 | 2018 | 142 | |
| 6 | 2018 | 138 | |
| 7 | 2008 | 123 | |
| 8 | 2012 | 116 | |
| 9 | 2011 | 111 | |
| 10 | 2011 | 108 | |
| 11 | 2010 | 102 | |
| 12 | 2019 | 91 | |
| 13 | 2020 | 89 | |
| 14 | 2008 | 77 | |
| 15 | 2007 | 74 | |
| 16 | 2008 | 69 | |
| 17 | 2020 | 69 | |
| 18 | 2015 | 67 | |
| 19 | 2018 | 65 | |
| 20 | 2012 | 64 |
About David Dimmock
David Dimmock is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health, having authored 116 papers that have together received 4.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (33 papers), Metabolism and Genetic Disorders (30 papers), Mitochondrial Function and Pathology (25 papers), Genomic variations and chromosomal abnormalities (11 papers), Genetic factors in colorectal cancer (8 papers), Neonatal Health and Biochemistry (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and BRCA gene mutations in cancer (7 papers). The work is most often cited by research in Clinical Biochemistry (880 citations), Genetics (1.6k citations), Cancer Research (410 citations), Molecular Biology (1.5k citations) and Pediatrics, Perinatology and Child Health (361 citations). David Dimmock has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Stephen F. Kingsmore, Michelle M. Clark, David Bick, Lauge Farnaes, Daniel Helbling, Susan M. White, Tiong Yang Tan, Zornitza Stark, Lee‐Jun C. Wong and Shimul Chowdhury. Their work appears in journals such as Molecular Case Studies, npj Genomic Medicine, Molecular Genetics and Metabolism, Genetics in Medicine and Journal of Pediatric Gastroenterology and Nutrition.
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.