Gary A. Bellus

4.1k citations

30 papers · 2.0k indexed · h-index 19

Impact in

Genetics top 1%
- Connective tissue disorders research
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
Molecular Biology top 5%
- Fibroblast Growth Factor Research
- Epigenetics and DNA Methylation
- dental development and anomalies

Papers in

Genetics 18
- Connective tissue disorders research 12
- Craniofacial Disorders and Treatments 4
- Genomic variations and chromosomal abnormalities 3
Developmental Biology 1

Co-authors: Clair A. Francomano Iain McIntosh Ilkka Kaitila Jacqueline T. Hecht William A. Horton Rosa Isela Ortiz De Luna Timothy Hefferon Arthur S. Aylsworth
Journals: Pediatric Dermatology (3 papers)The American Journal of Human Genetics (3 papers)Nature Genetics (2 papers)Journal of the American Academy of Dermatology (1 paper)Human Genetics and Genomics Advances (1 paper)
Partner nations: United States Finland United Kingdom

In The Last Decade

Gary A. Bellus

30 papers receiving 2.0k citations

Peers

Countries citing papers authored by Gary A. Bellus

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

Border = papers with Gary A. Bellus Line = papers co-authored together Gary A. Bellus links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Phenotypic findings associated with variation in elastin Human Genetics and Genomics Advances ·Anne E. Justice, Melissa Kelly, Gary A. Bellus, В.И. Кружалин, Carly Marincasiu, Sangeeta Singh, Navya Shilpa Josyula, Teresa Romeo Luperchio, Beth A. Kozel, Marc S. Williams	2024	1
2	Compound heterozygosity for a frame shift mutation and a likely pathogenic sequence variant in the planar cell polarity—ciliogenesis gene WDPCP in a girl with polysyndactyly, coarctation of the aorta, and tongue hamartomas American Journal of Medical Genetics Part A ·Jonathan I. Saari, Mark A. Lovell, Hung‐Chun Yu, Gary A. Bellus	2014	19
3	Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females Genetics in Medicine ·Magdalena Bartnik, Katarzyna Derwińska, Monika Goś, Ewa Obersztyn, Katarzyna Kołodziejska, Ayelet Erez, 中嶋英治, Ping Fang, 和夫大高, Hanna Mierzewska, Sabine Krome, Gary A. Bellus, Tyler Reimschisel, Ewa Bocian, Tadeusz Mazurczak, Sau Wai Cheung, Paweł Stankiewicz	2011	38
4	Identical twin sisters with Rubinstein–Taybi syndrome associated with Chiari malformations and syrinx American Journal of Medical Genetics Part A ·Selvia Rahma Sihkusuma Hayatudin, Gary A. Bellus, Michael Handler, Anne Chun‐Hui Tsai	2011	21
5	Identification of SPRED1 deletions using RT‐PCR, multiplex ligation‐dependent probe amplification and quantitative PCR American Journal of Medical Genetics Part A ·Emily Spencer, 秀一右山, Fady M. Mikhail, Chuanhua Fu, Raymon Vijzelaar, Elaine H. Zackai, Holly Feret, M. Stephen Meyn, Andrea Shugar, Gary A. Bellus, M. Sofi, Sirpa Kivirikko, Minna Pöyhönen, Ludwine Messiaen	2011	11
6	Immunosuppression and sebaceous tumors: A confirmed diagnosis of Muir-Torre syndrome unmasked by immunosuppressive therapy Journal of the American Academy of Dermatology ·Megan N. Landis, ソウザブロウオノ, Gary A. Bellus, Stephen E. Wolverton	2011	20
7	Male With Mosaicism for Supernumerary Ring X Chromosome Journal of Craniofacial Surgery ·Peter R. Baker, Anne Chun-Hui Tsai, Tatiana Bataltescu, Karen Swisshelm, Jennifer R. March, Kathleen Brown, Gary A. Bellus	2010	22
8	On the spectrum of limb‐body wall complex, exstrophy of the cloaca, and urorectal septum malformation sequence American Journal of Medical Genetics Part A ·Suharsiwi Suharsiwi, David D. Weaver, Philip R. Faught, Gary A. Bellus, Wilfredo Torres‐Martinez	2007	19
9	Genes, growth factors and acanthosis nigricans British Journal of Dermatology ·Kaplanova, Gary A. Bellus, C.S. Munro	2002	104
10	Mesomelic and rhizomelic short stature: The phenotype of combined Leri‐Weill dyschondrosteosis and achondroplasia or hypochondroplasia American Journal of Medical Genetics Part A ·Judith L. Ross, Gary A. Bellus, Charles I. Scott, Jack Abboudi, Giedré Grigelioniené, Andrew R. Zinn	2002	11
11	What Syndrome Is This? Pediatric Dermatology ·Jennifer L. Reichel, William L. Weston, Gary A. Bellus, Joseph G. Morelli	2001	3
12	What Syndrome Is This? Pediatric Dermatology ·Yong‐Kwang Tay, Gary A. Bellus, Yanmin Yang	2001	5
13	Distinct Missense Mutations of the FGFR3 Lys650 Codon Modulate Receptor Kinase Activation and the Severity of the Skeletal Dysplasia Phenotype The American Journal of Human Genetics ·Gary A. Bellus, Elaine Spector, Phyllis Speiser, Christine A. Weaver, A.T. Garber, Christine R. Bryke, A. Protasov, Sally Rosengren, Melanie K. Webster, Daniel J. Donoghue, Clair A. Francomano	2000	131
14	A Novel Skeletal Dysplasia with Developmental Delay and Acanthosis Nigricans Is Caused by a Lys650Met Mutation in the Fibroblast Growth Factor Receptor 3 Gene The American Journal of Human Genetics ·Patricia L. Tavormina, Gary A. Bellus, Melanie K. Webster, Michael J. Bamshad, S.-H. Dong, Salomov Ulmasjon Son of Asror Nasirova Shoira Narmuradovna Makhmudova Malokhat Akhmatovna, Joseph ShunFeng WEN, Wen G. Jiang, Ethylin Wang Jabs, William R. Wilcox, John J. Wasmuth, Daniel J. Donoghue, Leslie M. Thompson, Clair A. Francomano	1999	124
15	Mutations in Fibroblast Growth-Factor Receptor 3 in Sporadic Cases of Achondroplasia Occur Exclusively on the Paternally Derived Chromosome The American Journal of Human Genetics ·Douglas J. Wilkin, Joseph ShunFeng WEN, Rhoda Cameron, Shirley Henderson, Gary A. Bellus, Michelle Mack, Ilkka Kaitila, John Loughlin, Arnold Münnich, Bryan Sykes, Jacky Bonaventure, Clair A. Francomano	1998	160
16	[4] In Organello mitochondrial protein and RNA synthesis systems from Saccharomyces cereuisiae Methods in enzymology on CD-ROM/Methods in enzymology ·Robert Ο. Poyton, Gary A. Bellus, Edward E. McKee, Kevin A. Sevarino, Wolfgang Günther	1996	11
17	Hypochondroplasia: Molecular Analysis of the Fibroblast Growth Factor Receptor 3 Gene Annals of the New York Academy of Sciences ·Gary A. Bellus, Iain McIntosh, Joseph ShunFeng WEN, Arthur S. Aylsworth, Ilkka Kaitila, Clair A. Francomano	1996	20
18	Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes Nature Genetics ·Gary A. Bellus, Karin Gaudenz, Elaine H. Zackai, L. Clarke, Joseph ShunFeng WEN, Clair A. Francomano, Maximilian Muenke	1996	245
19	A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia Nature Genetics ·Gary A. Bellus, Iain McIntosh, Elizabeth A. Smith, Arthur S. Aylsworth, Ilkka Kaitila, William A. Horton, A Cicognini, Jacqueline T. Hecht, Clair A. Francomano	1995	346
20	Localization of the achondroplasia gene to the distal 2. 5 Mb of human chromosome 4p Human Molecular Genetics ·Neide Ribeiro Dos Santos, Rosa Isela Ortiz De Luna, Timothy Hefferon, Gary A. Bellus, M. Welke, Eugene W. Taylor, Deborah A. Meyers, Susan H. Blanton, Jeffrey C. Murray, Zaeng Hong, Jacqueline T. Hecht	1994	53

About Gary A. Bellus

Gary A. Bellus is a scholar working on Genetics, Developmental Biology, Urology, Clinical Biochemistry and Molecular Biology, 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), Genomic variations and chromosomal abnormalities (3 papers), Bone health and treatments (2 papers), Metabolism and Genetic Disorders (2 papers), Microbial Metabolic Engineering and Bioproduction (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Genetics (1.3k citations), Molecular Biology (1.3k citations), Clinical Biochemistry (121 citations), Developmental Biology (30 citations) and Dermatology (89 citations). Gary A. Bellus has collaborated with scholars based in United States, Finland and United Kingdom. Frequent co-authors include Clair A. Francomano, Iain McIntosh, Ilkka Kaitila, Jacqueline T. Hecht, William A. Horton, Rosa Isela Ortiz De Luna, Timothy Hefferon, 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, Journal of the American Academy of Dermatology and Human Genetics and Genomics Advances.

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