David B. Flannery

2.0k total citations
45 papers, 1.2k citations indexed

About

David B. Flannery is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, David B. Flannery has authored 45 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 14 papers in Pediatrics, Perinatology and Child Health and 13 papers in Molecular Biology. Recurrent topics in David B. Flannery's work include BRCA gene mutations in cancer (7 papers), Prenatal Screening and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). David B. Flannery is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Prenatal Screening and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). David B. Flannery collaborates with scholars based in United States, United Kingdom and Switzerland. David B. Flannery's co-authors include Barry Wolf, John M. Burns, James O’D. McGee, Deborah Maiese, Michael S. Watson, Jaime L. Frías, Janet G. Graham, E S Cantú, I. T. Thomas and John M. Pellock and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Hepatology.

In The Last Decade

David B. Flannery

45 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
David B. Flannery United States 18 599 381 337 197 102 45 1.2k
M O Rethoré France 21 754 1.3× 599 1.6× 395 1.2× 310 1.6× 48 0.5× 62 1.5k
Orit Reish Israel 25 516 0.9× 880 2.3× 425 1.3× 144 0.7× 165 1.6× 72 1.8k
Margaret H. MacGillivray United States 28 517 0.9× 531 1.4× 324 1.0× 73 0.4× 64 0.6× 83 1.8k
K. H. Gustavson Sweden 20 627 1.0× 391 1.0× 240 0.7× 90 0.5× 24 0.2× 65 1.2k
Stephen R. Braddock United States 25 538 0.9× 525 1.4× 296 0.9× 302 1.5× 44 0.4× 71 1.7k
Lars Hagenäs Sweden 29 918 1.5× 680 1.8× 450 1.3× 197 1.0× 52 0.5× 87 2.2k
M Gautier France 16 498 0.8× 396 1.0× 237 0.7× 236 1.2× 46 0.5× 60 1.7k
Florence Fellmann Switzerland 18 691 1.2× 417 1.1× 188 0.6× 227 1.2× 53 0.5× 54 1.4k
Sandra Janssens Belgium 20 430 0.7× 483 1.3× 293 0.9× 74 0.4× 21 0.2× 66 1.5k
Bruce A. Buehler United States 18 228 0.4× 281 0.7× 277 0.8× 84 0.4× 28 0.3× 37 786

Countries citing papers authored by David B. Flannery

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of David B. Flannery

This figure shows the co-authorship network connecting the top 25 collaborators of David B. Flannery. A scholar is included among the top collaborators of David B. Flannery based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with David B. Flannery. David B. Flannery is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Liu, Joseph N., et al.. (2023). The cost of ‘free’: Advising patients about sponsored genetic testing. Cleveland Clinic Journal of Medicine. 90(3). 161–164. 2 indexed citations
2.
Noss, Ryan, et al.. (2022). Rapid implementation of telegenetic services during the COVID-19 pandemic allowed continuing patient access, but not equally for all. Health and Technology. 12(4). 839–844. 2 indexed citations
3.
Maiese, Deborah, et al.. (2019). Current conditions in medical genetics practice. Genetics in Medicine. 21(8). 1874–1877. 104 indexed citations
4.
David, Karen L., Robert G. Best, Joshua L. Deignan, et al.. (2018). Patient re-contact after revision of genomic test results: points to consider—a statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 21(4). 769–771. 85 indexed citations
5.
Flannery, David B.. (2018). Challenges and opportunities for effective delivery of clinical genetic services in the U.S. healthcare system. Current Opinion in Pediatrics. 30(6). 740–745. 9 indexed citations
6.
Condit, Celeste M., et al.. (2008). Depiction of gene-environment relationships in online medical recommendations. Genetics in Medicine. 10(6). 450–456. 5 indexed citations
7.
Kulharya, Anita S., et al.. (2008). Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features. American Journal of Medical Genetics Part A. 146A(17). 2234–2241. 13 indexed citations
8.
9.
Kulharya, Anita S., et al.. (2001). Packed red cell transfusion does not compromise chromosome analysis in newborns. Genetics in Medicine. 3(4). 314–317. 5 indexed citations
10.
Reddy, Kavita S., et al.. (1999). Microdeletion of chromosome sub-band 2q37.3 in two patients with abnormal situs viscerum. American Journal of Medical Genetics. 84(5). 460–468. 32 indexed citations
11.
Kulharya, Anita S., Jaime Garcia‐Heras, Heather B. Radtke, et al.. (1998). Prenatal diagnosis of a trisomy 17p derived from a de novo non‐mosaic satellited marker. Clinical Genetics. 54(5). 421–425. 14 indexed citations
12.
Monaghan, Bruce A., Frederick S. Kaplan, Charles S. August, Michael D. Fallon, & David B. Flannery. (1991). Transient infantile osteopetrosis. The Journal of Pediatrics. 118(2). 252–256. 13 indexed citations
13.
Figueroa, Ramón, et al.. (1991). Frontofacionasal dysplasia. American Journal of Medical Genetics. 40(3). 338–340. 7 indexed citations
14.
Flannery, David B.. (1990). Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicism. American Journal of Medical Genetics. 35(1). 18–21. 41 indexed citations
15.
Flannery, David B., et al.. (1990). Partial calcanectomy for the treatment of osteomyelitis of the os calcis.. PubMed. 29(3). 226–30. 7 indexed citations
16.
Flannery, David B., John M. Opitz, & James F. Reynolds. (1989). Syndrome of imperforate oropharynx with costovertebral and auricular anomalies. American Journal of Medical Genetics. 32(2). 189–191. 8 indexed citations
17.
Ardinger, Holly H, Joan Atkin, R. Dwain Blackston, et al.. (1988). Verification of the fetal valproate syndrome phenotype. American Journal of Medical Genetics. 29(1). 171–185. 217 indexed citations
18.
Burns, John M., et al.. (1988). Direct visualization of single copy genes on banded metaphase chromosomes by nonisotopicin situhybridization. Nucleic Acids Research. 16(9). 3951–3961. 89 indexed citations
19.
Fischer, Asma Q., et al.. (1988). Joubert Syndrome: Early Diagnosis by Recognition of the Behavioral Phenotype and Confirmation by Cranial Sonography. Journal of Child Neurology. 3(4). 247–249. 9 indexed citations
20.
Flannery, David B., et al.. (1983). Dietary management of phenylketonuria from birth using a phenylalanine-free product. The Journal of Pediatrics. 103(2). 247–249. 6 indexed citations

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.

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