David T. Miller
Impact in
- Genetics top 0.2%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 46
- Genomics and Rare Diseases 26
- Genomic variations and chromosomal abnormalities 24
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- Nuclear physics research studies 12
- Co-authors
- Christa Lese Martin (13 shared papers)Wendy K. Chung (9 shared papers)M. Abramovici (9 shared papers)Teri E. Klein (5 shared papers)C. Sue Richards (6 shared papers)Prem R. Menon (4 shared papers)Kent D. McKelvey (3 shared papers)Gail E. Herman (3 shared papers)
- Journals
- Genetics in Medicine (27 papers)Physical Review C (7 papers)Clinical Chemistry (4 papers)The American Journal of Human Genetics (3 papers)Human Mutation (3 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
David T. Miller
134 papers receiving 11.2k citations
David T. Miller's Hit Papers
Peers
Comparison fields: 5 of 169
- Genetics 5.6k
- Pediatrics, Perinatology and Child Health 1.2k
- Hardware and Architecture 451
- Cognitive Neuroscience 1.0k
- Ophthalmology 433
Countries citing papers authored by David T. Miller
This map shows the geographic impact of David T. Miller'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 T. Miller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David T. Miller more than expected).
Fields of papers citing papers by David T. Miller
This network shows the impact of papers produced by David T. Miller. 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 T. Miller. The network helps show where David T. Miller may publish in the future.
Co-authors
The 25 scholars most cited alongside David T. Miller, 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 138 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies Hit paper breakdown → | 2010 | 2162 |
| 2 | Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics Hit paper breakdown → | 2016 | 1305 |
| 3 | Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders Hit paper breakdown → | 2019 | 477 |
| 4 | Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration Hit paper breakdown → | 2010 | 452 |
| 5 | ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG) Hit paper breakdown → | 2021 | 399 |
| 6 | 2008 | 316 | |
| 7 | 2010 | 313 | |
| 8 | 2012 | 300 | |
| 9 | 2010 | 250 | |
| 10 | ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG) Hit paper breakdown → | 2023 | 245 |
| 11 | ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG) Hit paper breakdown → | 2022 | 200 |
| 12 | 2005 | 197 | |
| 13 | 2021 | 191 | |
| 14 | 2008 | 180 | |
| 15 | 1998 | 163 | |
| 16 | 2017 | 163 | |
| 17 | 2007 | 159 | |
| 18 | 2007 | 158 | |
| 19 | 1984 | 151 | |
| 20 | 1997 | 148 |
About David T. Miller
David T. Miller is a scholar working on Genetics, Nuclear and High Energy Physics, Hardware and Architecture, Neurology and Molecular Biology, having authored 138 papers that have together received 11.6k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (26 papers), Genomic variations and chromosomal abnormalities (24 papers), Nuclear physics research studies (12 papers), Congenital heart defects research (12 papers), Neurofibromatosis and Schwannoma Cases (8 papers), VLSI and Analog Circuit Testing (7 papers), Prenatal Screening and Diagnostics (7 papers) and Integrated Circuits and Semiconductor Failure Analysis (6 papers). The work is most often cited by research in Genetics (5.6k citations), Pediatrics, Perinatology and Child Health (1.2k citations), Hardware and Architecture (451 citations), Cognitive Neuroscience (1.0k citations) and Ophthalmology (433 citations). David T. Miller has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Christa Lese Martin, Wendy K. Chung, M. Abramovici, Teri E. Klein, C. Sue Richards, Prem R. Menon, Kent D. McKelvey, Gail E. Herman, Christopher N. Vlangos and Sherri J. Bale. Their work appears in journals such as Genetics in Medicine, Physical Review C, Clinical Chemistry, The American Journal of Human Genetics and Human Mutation.
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.