Roberta A Pagon

7.0k total citations · 1 hit paper
97 papers, 4.5k citations indexed

About

Roberta A Pagon is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Roberta A Pagon has authored 97 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Genetics, 37 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Roberta A Pagon's work include BRCA gene mutations in cancer (16 papers), Genomics and Rare Diseases (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers). Roberta A Pagon is often cited by papers focused on BRCA gene mutations in cancer (16 papers), Genomics and Rare Diseases (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers). Roberta A Pagon collaborates with scholars based in United States, Canada and United Kingdom. Roberta A Pagon's co-authors include John M. Graham, Jonathan Zonana, Siu‐Li Yong, Cary O. Harding, Thomas H. Shepard, Bryan D. Hall, Sandra L. H. Davenport, David W. Smith, Marc S. Williams and Sterling K. Clarren and has published in prestigious journals such as Gastroenterology, The Journal of Clinical Endocrinology & Metabolism and PEDIATRICS.

In The Last Decade

Roberta A Pagon

92 papers receiving 4.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association

1981 610 citations Roberta A Pagon, John M. Graham et al. The Journal of Pediatrics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Roberta A Pagon United States	35	1.9k	1.6k	1.0k	923	861	97	4.5k
Bernard L. Maria United States	33	1.4k 0.7×	1.1k 0.7×	794 0.8×	760 0.8×	604 0.7×	104	4.3k
Lies H. Hoefsloot Netherlands	45	3.7k 1.9×	1.7k 1.1×	1.1k 1.1×	772 0.8×	1.0k 1.2×	136	6.6k
Mireille Claustres France	46	4.3k 2.2×	1.8k 1.1×	722 0.7×	427 0.5×	1.7k 2.0×	221	8.2k
Bryan D. Hall United States	37	1.8k 0.9×	2.1k 1.3×	820 0.8×	1.5k 1.6×	835 1.0×	120	5.0k
Alain Verloès France	46	4.4k 2.3×	3.8k 2.3×	1.1k 1.0×	1.1k 1.1×	1.0k 1.2×	314	8.7k
Joël Zlotogora Israel	35	1.9k 1.0×	2.0k 1.2×	400 0.4×	381 0.4×	306 0.4×	170	5.0k
Laurence Faivre France	40	2.6k 1.4×	3.3k 2.1×	344 0.3×	841 0.9×	1.4k 1.6×	215	6.3k
M. Leppert United States	40	2.8k 1.4×	1.4k 0.8×	602 0.6×	658 0.7×	516 0.6×	169	6.1k
Thomy de Ravel Belgium	38	2.0k 1.1×	1.9k 1.2×	387 0.4×	382 0.4×	475 0.6×	112	4.2k
Susan Huson United Kingdom	42	1.5k 0.8×	968 0.6×	386 0.4×	943 1.0×	864 1.0×	110	7.1k

Countries citing papers authored by Roberta A Pagon

Since Specialization

Citations

This map shows the geographic impact of Roberta A Pagon'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 Roberta A Pagon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roberta A Pagon more than expected).

Fields of papers citing papers by Roberta A Pagon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roberta A Pagon. 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 Roberta A Pagon. The network helps show where Roberta A Pagon may publish in the future.

Co-authorship network of co-authors of Roberta A Pagon

This figure shows the co-authorship network connecting the top 25 collaborators of Roberta A Pagon. A scholar is included among the top collaborators of Roberta A Pagon 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 Roberta A Pagon. Roberta A Pagon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lubin, Ira M., Margaret M. McGovern, Susan J. Gross, et al.. (2009). Clinician Perspectives about Molecular Genetic Testing for Heritable Conditions and Development of a Clinician-Friendly Laboratory Report. Journal of Molecular Diagnostics. 11(2). 162–171. 41 indexed citations

Faucett, W. Andrew, et al.. (2008). A model program to increase translation of rare disease genetic tests: collaboration, education, and test translation program. Genetics in Medicine. 10(5). 343–348. 14 indexed citations

Pagon, Roberta A. (2007). GeneTests: Integrating Genetic Services into Patient Care. The American Journal of Human Genetics. 81(4). 658–659. 5 indexed citations

Parisi, Melissa A., Linda Ramsdell, Mark W. Burns, et al.. (2007). A Gender Assessment Team: experience with 250 patients over a period of 25 years. Genetics in Medicine. 9(6). 348–357. 50 indexed citations

Pagon, Roberta A. (2002). Genetic testing for disease susceptibilities: consequences for genetic counseling. Trends in Molecular Medicine. 8(6). 306–307. 12 indexed citations

Pagon, Roberta A, Peter Tarczy‐Hornoch, Thomas D. Bird, et al.. (2002). GeneTests-GeneClinics: Genetic testing information for a growing audience. Human Mutation. 19(5). 501–509. 57 indexed citations

Tarczy‐Hornoch, Peter, et al.. (2000). GeneClinics: A Hybrid Text/Data Electronic Publishing Model Using XML Applied to Clinical Genetic Testing. Journal of the American Medical Informatics Association. 7(3). 267–276. 18 indexed citations

Kawame, Hiroshi, Mark Hannibal, Louanne Hudgins, & Roberta A Pagon. (1999). Phenotypic spectrum and management issues in Kabuki syndrome. The Journal of Pediatrics. 134(4). 480–485. 123 indexed citations

Malzac, Perrine, Hayley Webber, A. Moncla, et al.. (1998). Mutation Analysis of UBE3A in Angelman Syndrome Patients. The American Journal of Human Genetics. 62(6). 1353–1360. 121 indexed citations

10.

Schowalter, David B., Roberta A Pagon, Robert E. Kalina, & Ruth A. McDonald. (1997). Facio-oculo-acoustico-renal (FOAR) syndrome: Case report and review. American Journal of Medical Genetics. 69(1). 45–49. 13 indexed citations

11.

Cantrell, Michael A., Jonathan S. Bogan, Elizabeth Simpson, et al.. (1992). Deletion mapping of H-Y antigen to the long arm of the human Y chromosome. Genomics. 13(4). 1255–1260. 17 indexed citations

12.

Harding, Cary O. & Roberta A Pagon. (1990). Incidence of tuberous sclerosis in patients with cardiac rhabdomyoma. American Journal of Medical Genetics. 37(4). 443–446. 124 indexed citations

13.

Pagon, Roberta A. (1988). Retinitis pigmentosa. Survey of Ophthalmology. 33(3). 137–177. 204 indexed citations

14.

Drummond‐Borg, Margaret, et al.. (1988). Nonfluorescent dicentric Y in males with hypospadias. The Journal of Pediatrics. 113(3). 469–473. 4 indexed citations

15.

Pagon, Roberta A, et al.. (1984). Müllerian anomalies and renal agenesis:Autosomal dominant urogenital adysplasia. The Journal of Pediatrics. 104(6). 861–864. 28 indexed citations

16.

Cassidy, Suzanne B., Roberta A Pagon, Melanie Pepin, & Joel D. Blumhagen. (1983). Family studies in tuberous sclerosis. evaluation of apparently unaffected parents.. PubMed. 249(10). 1302–4. 31 indexed citations

17.

Pagon, Roberta A, et al.. (1983). Autosomal recessive eye and brain anomalies: Warburg syndrome. The Journal of Pediatrics. 102(4). 542–546. 50 indexed citations

18.

Bunt-Milam, Ann H., Robert E. Kalina, & Roberta A Pagon. (1983). Clinical-ultrastructural study of a retinal dystrophy.. PubMed. 24(4). 458–69. 47 indexed citations

19.

Pagon, Roberta A, John M. Graham, Jonathan Zonana, & Siu‐Li Yong. (1981). Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association. The Journal of Pediatrics. 99(2). 223–227. 610 indexed citations breakdown →

20.

Pagon, Roberta A, David W. Smith, & Thomas H. Shepard. (1979). Urethral obstruction malformation complex: A cause of abdominal muscle deficiency and the “prune belly”. The Journal of Pediatrics. 94(6). 900–906. 143 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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