David B. Flannery
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic and rare skin diseases.
- BRCA gene mutations in cancer
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- Pharmacological Effects and Toxicity Studies
- Prenatal Screening and Diagnostics
Papers in
- Genetics 27
- Genomic variations and chromosomal abnormalities 9
- BRCA gene mutations in cancer 6
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- Prenatal Screening and Diagnostics 9
- Co-authors
- Barry Wolf (5 shared papers)Megan Lyon (2 shared papers)Deborah R. Maiese (1 shared paper)Michael S. Watson (1 shared paper)James O’D. McGee (1 shared paper)John M. Burns (1 shared paper)Janet G. Graham (1 shared paper)Jaime L. Frías (1 shared paper)
- Journals
- Genetics in Medicine (7 papers)The Journal of Pediatrics (5 papers)Clinical Genetics (5 papers)Prenatal Diagnosis (2 papers)Neurology (2 papers)
- Partner nations
- United StatesAustraliaUnited Kingdom
In The Last Decade
David B. Flannery
58 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 128
- Genetics 801
- Pediatrics, Perinatology and Child Health 400
- Developmental Biology 43
- Clinical Biochemistry 108
- Molecular Biology 568
Countries citing papers authored by David B. Flannery
This map shows the geographic impact of David B. Flannery'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 B. Flannery with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David B. Flannery more than expected).
Fields of papers citing papers by David B. Flannery
This network shows the impact of papers produced by David B. Flannery. 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 B. Flannery. The network helps show where David B. Flannery may publish in the future.
Co-authors
The 25 scholars most cited alongside David B. Flannery, 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 60 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1988 | 261 | |
| 2 | 2005 | 220 | |
| 3 | Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism. | 1989 | 131 |
| 4 | 2019 | 123 | |
| 5 | 2018 | 110 | |
| 6 | 1988 | 99 | |
| 7 | 1982 | 68 | |
| 8 | 1986 | 56 | |
| 9 | 1990 | 47 | |
| 10 | 2011 | 43 | |
| 11 | 2002 | 39 | |
| 12 | Nucleolar organizer region variants as a risk factor for Down syndrome. | 1985 | 35 |
| 13 | 1999 | 35 | |
| 14 | 1990 | 34 | |
| 15 | 2018 | 29 | |
| 16 | 1983 | 25 | |
| 17 | 1984 | 21 | |
| 18 | 1985 | 21 | |
| 19 | 1986 | 21 | |
| 20 | 1988 | 21 |
About David B. Flannery
David B. Flannery is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Clinical Biochemistry, Pharmacy and Molecular Biology, having authored 60 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (9 papers), BRCA gene mutations in cancer (6 papers), Metabolism and Genetic Disorders (5 papers), Congenital heart defects research (5 papers), Oral and gingival health research (4 papers), Telemedicine and Telehealth Implementation (4 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Genetics (801 citations), Pediatrics, Perinatology and Child Health (400 citations), Developmental Biology (43 citations), Clinical Biochemistry (108 citations) and Molecular Biology (568 citations). David B. Flannery has collaborated with scholars based in United States, Australia and United Kingdom. Frequent co-authors include Barry Wolf, Megan Lyon, Deborah R. Maiese, Michael S. Watson, James O’D. McGee, John M. Burns, Janet G. Graham, Jaime L. Frías, E S Cantú and I. T. Thomas. Their work appears in journals such as Genetics in Medicine, The Journal of Pediatrics, Clinical Genetics, Prenatal Diagnosis and Neurology.
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.