Vincent M. Riccardi

14.7k total citations · 4 hit papers
180 papers, 9.3k citations indexed

About

Vincent M. Riccardi is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Vincent M. Riccardi has authored 180 papers receiving a total of 9.3k indexed citations (citations by other indexed papers that have themselves been cited), including 101 papers in Neurology, 44 papers in Molecular Biology and 39 papers in Genetics. Recurrent topics in Vincent M. Riccardi's work include Neurofibromatosis and Schwannoma Cases (100 papers), Neuroblastoma Research and Treatments (28 papers) and Meningioma and schwannoma management (27 papers). Vincent M. Riccardi is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (100 papers), Neuroblastoma Research and Treatments (28 papers) and Meningioma and schwannoma management (27 papers). Vincent M. Riccardi collaborates with scholars based in United States, Canada and Brazil. Vincent M. Riccardi's co-authors include James G. Smirniotopoulos, Uta Francke, David H. Ledbetter, Richard A. Lewis, Eva Sujansky, Ann C. M. Smith, Susan Airhart, Lewis B. Holmes, Robert E. Ferrell and Louise C. Strong and has published in prestigious journals such as Science, New England Journal of Medicine and Cell.

In The Last Decade

Vincent M. Riccardi

177 papers receiving 8.8k 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.

Von Recklinghausen Neurofibromatosis

1981 995 citations Vincent M. Riccardi profile →
Neurofibromatosis, Phenotype, Natural History, and Pathogenesis

1992 591 citations Vincent M. Riccardi et al. profile →
Chromosomal Imbalance in the Aniridia-Wilms' Tumor Association: 11p Interstitial Deletion

1978 557 citations Vincent M. Riccardi, Uta Francke et al. PEDIATRICS profile →
Deletions of Chromosome 15 as a Cause of the Prader–Willi Syndrome

1981 454 citations David H. Ledbetter, Vincent M. Riccardi et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vincent M. Riccardi United States	45	4.9k	2.8k	2.2k	2.0k	1.6k	180	9.3k
David Viskochil United States	48	5.0k 1.0×	2.6k 0.9×	1.2k 0.6×	1.6k 0.8×	1.6k 1.0×	159	8.6k
Susan Huson United Kingdom	42	4.7k 1.0×	1.5k 0.5×	968 0.4×	2.2k 1.1×	1.3k 0.8×	110	7.1k
Meena Upadhyaya United Kingdom	44	3.7k 0.8×	2.5k 0.9×	837 0.4×	934 0.5×	1.2k 0.8×	166	6.7k
Kyu‐Chang Wang South Korea	44	2.2k 0.5×	1.4k 0.5×	446 0.2×	819 0.4×	1.7k 1.1×	335	7.2k
Jeffrey H. Wisoff United States	53	3.3k 0.7×	1.4k 0.5×	837 0.4×	1.6k 0.8×	162 0.1×	156	8.5k
Hildegard Kehrer‐Sawatzki Germany	37	1.6k 0.3×	2.3k 0.8×	1.9k 0.8×	345 0.2×	630 0.4×	126	4.6k
Rosalie E. Ferner United Kingdom	41	5.3k 1.1×	633 0.2×	222 0.1×	2.4k 1.2×	1.2k 0.8×	90	6.1k
M. Leppert United States	40	590 0.1×	2.8k 1.0×	1.4k 0.6×	343 0.2×	286 0.2×	169	6.1k
Takanori Hirose Japan	41	2.0k 0.4×	1.2k 0.4×	131 0.1×	973 0.5×	1.4k 0.9×	246	6.1k
Sigrid Tinschert Germany	31	860 0.2×	1.3k 0.5×	985 0.4×	351 0.2×	596 0.4×	94	3.1k

Countries citing papers authored by Vincent M. Riccardi

Since Specialization

Citations

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

Fields of papers citing papers by Vincent M. Riccardi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vincent M. Riccardi. 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 Vincent M. Riccardi. The network helps show where Vincent M. Riccardi may publish in the future.

Co-authorship network of co-authors of Vincent M. Riccardi

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Riccardi, Vincent M., et al.. (2022). Head circumference and anthropometric changes and their relation to plexiform and skin neurofibromas in sporadic and familial neurofibromatosis 1 Brazilian adults: a cross-sectional study. Orphanet Journal of Rare Diseases. 17(1). 341–341. 2 indexed citations

Riccardi, Vincent M., et al.. (2018). Prevalence and clinicopathological characteristics of lipomatous neurofibromas in neurofibromatosis 1: An investigation of 229 cutaneous neurofibromas and a systematic review of the literature. Journal of Cutaneous Pathology. 45(10). 743–753. 6 indexed citations

Riccardi, Vincent M.. (2017). The Praxitype and Phenotype Hierarchies Exemplified by NF1. 2(1). 1–3.

Rauen, Katherine A., Susan Huson, Emma Burkitt‐Wright, et al.. (2014). Recent developments in neurofibromatoses and RASopathies: Management, diagnosis and current and future therapeutic avenues. American Journal of Medical Genetics Part A. 167(1). 1–10. 36 indexed citations

Sbidian, É., S. Hadj‐Rabia, Vincent M. Riccardi, et al.. (2012). Clinical characteristics predicting internal neurofibromas in 357 children with neurofibromatosis-1: results from a cross-selectional study. Orphanet Journal of Rare Diseases. 7(1). 62–62. 12 indexed citations

Tucker, Tracy, Vincent M. Riccardi, Carolyn J. Brown, et al.. (2011). S100B and neurofibromin immunostaining and X‐inactivation patterns of laser‐microdissected cells indicate a multicellular origin of some NF1‐associated neurofibromas. Journal of Neuroscience Research. 89(9). 1451–1460. 5 indexed citations

Riccardi, Vincent M., et al.. (1987). Discounting an Adverse Maternal Effect on Severity of Neurofibromatosis. PEDIATRICS. 79(3). 386–393. 15 indexed citations

Darby, John, Vincent M. Riccardi, Susan Huson, et al.. (1986). Linkage Analysis between the β‐Nerve Growth Factor Gene and Other Chromosome lp Markers and Disseminated Neurofibromatosisa. Annals of the New York Academy of Sciences. 486(1). 311–326. 3 indexed citations

Riccardi, Vincent M., Helen Mintz Hittner, Louise C. Strong, et al.. (1982). Wilms tumor with aniridia/iris dysplasia and apparently normal chromosomes. The Journal of Pediatrics. 100(4). 574–577. 25 indexed citations

10.

Riccardi, Vincent M.. (1982). Clinical genetics and genetic counseling.. The American Journal of Human Genetics. 34(1). 150–151. 2 indexed citations

11.

Riccardi, Vincent M., John J. Mulvihill, Michael M. Paparella, et al.. (1982). Books Received. The Laryngoscope. 92(2). 218–218. 1 indexed citations

12.

Cleaver, James E., A.E. Greene, L.L. Coriell, & Vincent M. Riccardi. (1981). An autosomal dominant inheritance for multiple sunlight-induced malignancy in a patient without abnormalities in DNA repair or replication. Cytogenetic and Genome Research. 29(2). 122–124. 10 indexed citations

13.

Riccardi, Vincent M., et al.. (1981). Neurofibromatosis (von Recklinghausen disease) : genetics, cell biology, and biochemistry. Raven Press eBooks.

14.

Ferrell, R E & Vincent M. Riccardi. (1981). Catalase levels in patients with aniridia and/or Wilms’ tumor: utility and limitations. Cytogenetic and Genome Research. 31(2). 120–123. 19 indexed citations

15.

Ledbetter, David H., et al.. (1980). Ring chromosome 15: phenotype, Ag-NOR analysis, secondary aneuploidy, and associated chromosome instability. Cytogenetic and Genome Research. 27(2-3). 111–122. 36 indexed citations

16.

Francke, Uta, Lewis B. Holmes, L. Atkins, & Vincent M. Riccardi. (1979). Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13. Cytogenetic and Genome Research. 24(3). 185–192. 321 indexed citations

17.

Riccardi, Vincent M.. (1977). Trisomy 8: an international study of 70 patients.. PubMed. 13(3C). 171–84. 93 indexed citations

18.

Francke, Uta, et al.. (1977). Gene dose effect: intraband mapping of the <i>LDH A </i>locus using cells from four individuals with different interstitial deletions of 11p. Cytogenetic and Genome Research. 19(4). 197–207. 58 indexed citations

19.

Riccardi, Vincent M. & Lewis B. Holmes. (1974). Brachydactyly, Type E: Hereditary shortening of digits, metacarpals, metatarsals, and long bones. The Journal of Pediatrics. 84(2). 251–254. 15 indexed citations

20.

Riccardi, Vincent M., Leonard Atkins, & Lewis B. Holmes. (1970). Absent patellae, mild mental retardation, skeletal and genitourinary anomalies, and C group autosomal mosaicism. The Journal of Pediatrics. 77(4). 664–672. 23 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.

Explore authors with similar magnitude of impact