David Dimmock
Impact in
- Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
- Genetics top 0.5%
- Genomics and Rare Diseases
Papers in
-
- Metabolism and Genetic Disorders 35
- Genetics 69
- Genomics and Rare Diseases 60
- Genetics and Neurodevelopmental Disorders 4
- Co-authors
- Stephen F. Kingsmore (20 shared papers)Michelle M. Clark (8 shared papers)David P Bick (11 shared papers)Lauge Farnaes (10 shared papers)Zornitza Stark (1 shared paper)Susan M. White (1 shared paper)Tiong Yang Tan (1 shared paper)Daniel C. Helbling (13 shared papers)
- Journals
- Genetics in Medicine (12 papers)Molecular Genetics and Metabolism (9 papers)The American Journal of Human Genetics (8 papers)npj Genomic Medicine (8 papers)The Journal of Pediatrics (5 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
David Dimmock
149 papers receiving 10.3k citations
David Dimmock's Hit Papers
Peers
Comparison fields: 5 of 148
- Clinical Biochemistry 1.2k
- Genetics 4.3k
- Health Informatics 109
- Cancer Research 503
- Molecular Biology 2k
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 150 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Guidelines for investigating causality of sequence variants in human disease Hit paper breakdown → | 2014 | 970 |
| 2 | Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma Hit paper breakdown → | 2017 | 613 |
| 3 | 2010 | 576 | |
| 4 | 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 | 449 |
| 5 | 2012 | 381 | |
| 6 | Wastewater sequencing reveals early cryptic SARS-CoV-2 variant transmission Hit paper breakdown → | 2022 | 345 |
| 7 | Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization Hit paper breakdown → | 2018 | 342 |
| 8 | 2016 | 310 | |
| 9 | 2015 | 308 | |
| 10 | A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants Hit paper breakdown → | 2019 | 276 |
| 11 | 2018 | 239 | |
| 12 | 2017 | 229 | |
| 13 | 2019 | 219 | |
| 14 | Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children’s hospitals demonstrates improved clinical outcomes and reduced costs of care Hit paper breakdown → | 2021 | 195 |
| 15 | 2018 | 187 | |
| 16 | 2012 | 184 | |
| 17 | 2018 | 154 | |
| 18 | 2020 | 149 | |
| 19 | 2008 | 144 | |
| 20 | 2012 | 132 |
About David Dimmock
David Dimmock is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Health Information Management and Public Health, Environmental and Occupational Health, having authored 150 papers that have together received 10.6k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (60 papers), Metabolism and Genetic Disorders (35 papers), Mitochondrial Function and Pathology (23 papers), Immunodeficiency and Autoimmune Disorders (6 papers), Lysosomal Storage Disorders Research (5 papers), Electronic Health Records Systems (5 papers), Medical and Health Sciences Research (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Clinical Biochemistry (1.2k citations), Genetics (4.3k citations), Health Informatics (109 citations), Cancer Research (503 citations) and Molecular Biology (2k 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 P Bick, Lauge Farnaes, Zornitza Stark, Susan M. White, Tiong Yang Tan, Daniel C. Helbling, Lee‐Jun C. Wong and Julie A. Cakici. Their work appears in journals such as Genetics in Medicine, Molecular Genetics and Metabolism, The American Journal of Human Genetics, npj Genomic Medicine and The Journal of Pediatrics.
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.