David T. Miller
Impact in
- Genetics top 0.5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
- Hardware and Architecture top 2%
- VLSI and Analog Circuit Testing
Papers in
- Genetics 35
- Genomic variations and chromosomal abnormalities 22
- Genomics and Rare Diseases 20
-
- Congenital heart defects research 8
- Co-authors
- M. Abramovici (9 shared papers)Christa Lese Martin (11 shared papers)Wendy K. Chung (9 shared papers)P.R. Menon (4 shared papers)Ross Cagan (3 shared papers)C. Sue Richards (6 shared papers)Teri E. Klein (4 shared papers)Gail E. Herman (3 shared papers)
- Journals
- Genetics in Medicine (17 papers)Clinical Chemistry (3 papers)Annals of Human Genetics (2 papers)Clinical Biochemistry (2 papers)Physical review. C (2 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
David T. Miller
94 papers receiving 5.1k citations
David T. Miller's Hit Papers
Peers
Comparison fields: 5 of 158
- Genetics 2.6k
- Hardware and Architecture 435
- Cancer Research 505
- Pediatrics, Perinatology and Child Health 585
- Pathology and Forensic Medicine 456
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 96 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 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 | 1023 |
| 2 | Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders Hit paper breakdown → | 2019 | 367 |
| 3 | 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 | 302 |
| 4 | 2005 | 183 | |
| 5 | 1998 | 157 | |
| 6 | 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 | 157 |
| 7 | 1984 | 143 | |
| 8 | 2021 | 142 | |
| 9 | 2007 | 140 | |
| 10 | 2008 | 139 | |
| 11 | 1997 | 130 | |
| 12 | 2019 | 117 | |
| 13 | 2012 | 116 | |
| 14 | 2011 | 108 | |
| 15 | 2020 | 97 | |
| 16 | 1983 | 89 | |
| 17 | 2018 | 85 | |
| 18 | 2011 | 84 | |
| 19 | 1998 | 81 | |
| 20 | 1983 | 81 |
About David T. Miller
David T. Miller is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Electrical and Electronic Engineering, having authored 96 papers that have together received 5.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Genomics and Rare Diseases (20 papers), Prenatal Screening and Diagnostics (11 papers), Congenital heart defects research (8 papers), VLSI and Analog Circuit Testing (7 papers), Genetic factors in colorectal cancer (6 papers), Integrated Circuits and Semiconductor Failure Analysis (6 papers) and Cancer Genomics and Diagnostics (6 papers). The work is most often cited by research in Genetics (2.6k citations), Hardware and Architecture (435 citations), Cancer Research (505 citations), Pediatrics, Perinatology and Child Health (585 citations) and Pathology and Forensic Medicine (456 citations). David T. Miller has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include M. Abramovici, Christa Lese Martin, Wendy K. Chung, P.R. Menon, Ross Cagan, C. Sue Richards, Teri E. Klein, Gail E. Herman, Kent D. McKelvey and Michael S. Watson. Their work appears in journals such as Genetics in Medicine, Clinical Chemistry, Annals of Human Genetics, Clinical Biochemistry and Physical review. C.
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.