Vincent M. Riccardi - Concepedia

Author

Vincent M. Riccardi

Also Known As

Daniel Hale, Luíza Rodrigues, Min Kyu Kim, V M Riccardi, V Riccardi, V. M. Riccardi, V. Riccardi, V.M. Riccardi, VINCENT M. RICCARDI, Vincent M Riccardi

244

Publications

14.6K

Citations

H-Index

183

Concepts

All Affiliations

Baylor College of Medicine Massachusetts General Hospital Texas Medical Center Johns Hopkins University University of British Columbia

About

Vincent M. Riccardi is an author at Baylor College of Medicine specializing in medicine, pathology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	69	6.2K
2	Health Sciences	8	8	394
3	Public Health	8	8	1.5K
4	Social Sciences	5	5	185
5	Natural Sciences	1	1	33

Vincent M. Riccardi

127

Publications

11.1K

Citations

H-Index

Page 1

	Year	Citations
Neurofibromatosis, Phenotype, Natural History, and Pathogenesis Vincent M. Riccardi, James G. Smirniotopoulos Journal of Neuropathology & Experimental Neurology Tumor InnervationPathologyTumor BiologyNeuro-oncologySurgical Pathology	1992	795
Chromosomal Imbalance in the Aniridia-Wilms' Tumor Association: 11p Interstitial Deletion Vincent M. Riccardi, Eva Sujansky, Ann C. M. Smith, PEDIATRICS Agr TriadCytogeneticsGeneticsGenetic EpidemiologyPathology	1978	729
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation Eric Legius, Ludwine Messiaen, P. Wolkenstein, Genetics in Medicine	2021	687
Deletions of Chromosome 15 as a Cause of the Prader–Willi Syndrome David H. Ledbetter, Vincent M. Riccardi, Susan Airhart, New England Journal of Medicine GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification	1981	622
Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13 Uta Francke, Lewis B. Holmes, L. Atkins, Cytogenetic and Genome Research	1979	400
Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis. Anil G. Menon, K M Anderson, Vincent M. Riccardi, Proceedings of the National Academy of Sciences Neuro-oncologyNf1 RegionTumoral PathologySomatic VariantGenetic Disorder	1990	399
Distinctive Cancer Associations in Patients With Neurofibromatosis Type 1 Elina Uusitalo, Matti Rantanen, Roope A. Kallionpää, Journal of Clinical Oncology	2016	386
An Absence of Cutaneous Neurofibromas Associated with a 3-bp Inframe Deletion in Exon 17 of the NF1 Gene (c.2970-2972 delAAT): Evidence of a Clinically Significant NF1 Genotype-Phenotype Correlation Meena Upadhyaya, Susan Huson, D. M. Davies, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGenetic EpidemiologyNf1 GenePathology	2006	360
Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. Martin Ruttledge, Anne Andermann, Catherine M. Phelan, PubMed	1996	259
Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation Scott R. Plotkin, Ludwine Messiaen, Eric Legius, Genetics in Medicine	2022	247

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