Bryan D. Hall
Impact in
- Genetics top 1%
- Congenital Ear and Nasal Anomalies
- Connective tissue disorders research
- Craniofacial Disorders and Treatments
- Developmental Biology top 2%
Papers in
- Genetics 56
- Connective tissue disorders research 16
- Craniofacial Disorders and Treatments 9
- Congenital Ear and Nasal Anomalies 8
- Genetic and rare skin diseases. 8
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- Hedgehog Signaling Pathway Studies 8
- Co-authors
- David W. Smith (7 shared papers)Kenneth Lyons Jones (4 shared papers)David W. Smith (5 shared papers)John M. Graham (6 shared papers)Mahin Golabi (10 shared papers)Marilyn C. Higginbottom (1 shared paper)Maimon M. Cohen (3 shared papers)Jacqueline A. Noonan (2 shared papers)
- Journals
- The Journal of Pediatrics (16 papers)American Journal of Medical Genetics (32 papers)New England Journal of Medicine (3 papers)PEDIATRICS (3 papers)Radiology (2 papers)
- Partner nations
- United StatesCanadaSpain
In The Last Decade
Bryan D. Hall
117 papers receiving 5.0k citations
Peers
Comparison fields: 5 of 116
- Genetics 858
- Genetics 2.2k
- Developmental Biology 180
- Urology 438
- Pediatrics, Perinatology and Child Health 834
Countries citing papers authored by Bryan D. Hall
This map shows the geographic impact of Bryan D. Hall'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 Bryan D. Hall with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bryan D. Hall more than expected).
Fields of papers citing papers by Bryan D. Hall
This network shows the impact of papers produced by Bryan D. Hall. 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 Bryan D. Hall. The network helps show where Bryan D. Hall may publish in the future.
Co-authors
The 25 scholars most cited alongside Bryan D. Hall, 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 120 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 438 | |
| 2 | 1998 | 347 | |
| 3 | 1979 | 314 | |
| 4 | 1979 | 266 | |
| 5 | 1979 | 207 | |
| 6 | 1987 | 203 | |
| 7 | 1973 | 201 | |
| 8 | 1975 | 197 | |
| 9 | 1972 | 172 | |
| 10 | The OEIS complex (omphalocele, exstrophy, imperforate anus, spinal defects). | 1978 | 168 |
| 11 | 1996 | 160 | |
| 12 | 1991 | 146 | |
| 13 | 1990 | 140 | |
| 14 | 1997 | 107 | |
| 15 | 1974 | 104 | |
| 16 | 2003 | 90 | |
| 17 | 1975 | 75 | |
| 18 | 1998 | 73 | |
| 19 | 1979 | 69 | |
| 20 | 1980 | 66 |
About Bryan D. Hall
Bryan D. Hall is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, having authored 120 papers that have together received 5.5k indexed citations. Recurring topics across this work include Connective tissue disorders research (16 papers), Prenatal Screening and Diagnostics (10 papers), Craniofacial Disorders and Treatments (9 papers), Tumors and Oncological Cases (8 papers), Congenital Ear and Nasal Anomalies (8 papers), Hedgehog Signaling Pathway Studies (8 papers), Genetic and rare skin diseases. (8 papers) and Vascular Malformations and Hemangiomas (7 papers). The work is most often cited by research in Genetics (858 citations), Genetics (2.2k citations), Developmental Biology (180 citations), Urology (438 citations) and Pediatrics, Perinatology and Child Health (834 citations). Bryan D. Hall has collaborated with scholars based in United States, Canada and Spain. Frequent co-authors include David W. Smith, Kenneth Lyons Jones, David W. Smith, John M. Graham, Mahin Golabi, Marilyn C. Higginbottom, Maimon M. Cohen, Jacqueline A. Noonan, Angela E. Lin and John M. Opitz. Their work appears in journals such as The Journal of Pediatrics, American Journal of Medical Genetics, New England Journal of Medicine, PEDIATRICS and Radiology.
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.