Gary A. Bellus
Impact in
- Genetics top 1%
- Connective tissue disorders research
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Papers in
-
- Fibroblast Growth Factor Research 9
- Ubiquitin and proteasome pathways 2
- Genetics 18
- Connective tissue disorders research 12
- Craniofacial Disorders and Treatments 4
- Genetics and Neurodevelopmental Disorders 2
- Cleft Lip and Palate Research 2
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Clair A. Francomano (8 shared papers)Iain McIntosh (5 shared papers)Ilkka Kaitila (4 shared papers)Jacqueline T. Hecht (3 shared papers)William A. Horton (2 shared papers)Timothy Hefferon (2 shared papers)Rosa Isela Ortiz De Luna (2 shared papers)Arthur S. Aylsworth (2 shared papers)
- Journals
- Pediatric Dermatology (3 papers)The American Journal of Human Genetics (3 papers)Nature Genetics (2 papers)Molecular Case Studies (1 paper)The Journal of Pediatrics (1 paper)
- Partner nations
- United StatesFinlandCanada
In The Last Decade
Gary A. Bellus
30 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 85
- Genetics 1.3k
- Clinical Biochemistry 120
- Molecular Biology 1.2k
- Developmental Biology 29
- Dermatology 83
Countries citing papers authored by Gary A. Bellus
This map shows the geographic impact of Gary A. Bellus'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 Gary A. Bellus with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gary A. Bellus more than expected).
Fields of papers citing papers by Gary A. Bellus
This network shows the impact of papers produced by Gary A. Bellus. 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 Gary A. Bellus. The network helps show where Gary A. Bellus may publish in the future.
Co-authors
The 25 scholars most cited alongside Gary A. Bellus, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Achondroplasia is defined by recurrent G380R mutations of FGFR3. | 1995 | 356 |
| 2 | 1995 | 346 | |
| 3 | 1996 | 245 | |
| 4 | 1998 | 160 | |
| 5 | 2000 | 130 | |
| 6 | 1999 | 124 | |
| 7 | 2002 | 106 | |
| 8 | 1999 | 82 | |
| 9 | 1990 | 80 | |
| 10 | 1998 | 63 | |
| 11 | 2000 | 58 | |
| 12 | 1994 | 53 | |
| 13 | 2011 | 39 | |
| 14 | 2010 | 22 | |
| 15 | 2011 | 21 | |
| 16 | 2011 | 21 | |
| 17 | 1996 | 20 | |
| 18 | 2014 | 19 | |
| 19 | 2007 | 19 | |
| 20 | 1996 | 11 |
About Gary A. Bellus
Gary A. Bellus is a scholar working on Molecular Biology, Genetics, Surgery, Oncology and Pathology and Forensic Medicine, having authored 30 papers that have together received 2.0k indexed citations. Recurring topics across this work include Connective tissue disorders research (12 papers), Fibroblast Growth Factor Research (9 papers), Craniofacial Disorders and Treatments (4 papers), Genetics and Neurodevelopmental Disorders (2 papers), Ubiquitin and proteasome pathways (2 papers), Metabolism and Genetic Disorders (2 papers), Cleft Lip and Palate Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (1.3k citations), Clinical Biochemistry (120 citations), Molecular Biology (1.2k citations), Developmental Biology (29 citations) and Dermatology (83 citations). Gary A. Bellus has collaborated with scholars based in United States, Finland and Canada. Frequent co-authors include Clair A. Francomano, Iain McIntosh, Ilkka Kaitila, Jacqueline T. Hecht, William A. Horton, Timothy Hefferon, Rosa Isela Ortiz De Luna, Arthur S. Aylsworth, Mirta A. Machado and Elizabeth A. Smith. Their work appears in journals such as Pediatric Dermatology, The American Journal of Human Genetics, Nature Genetics, Molecular Case Studies and The Journal of Pediatrics.
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.