Maurizio Genuardi - Concepedia

Author

Maurizio Genuardi

Università Cattolica del Sacro Cuore ORCID

Also Known As

A.P. Fidalgo, Andrea Bartuli, Carmen Tartari, Finlay Macrae, Genuardi M., Genuardi Maurizio, M Genuardi, M. GENUARDI, M. Genuardi, MAURIZIO GENUARDI

343

Publications

12K

Citations

H-Index

184

Concepts

All Affiliations

Università Cattolica del Sacro Cuore University of Florence Istituti di Ricovero e Cura a Carattere Scientifico Agostino Gemelli University Polyclinic Centro di Riferimento Oncologico

About

Maurizio Genuardi is an author at Università Cattolica del Sacro Cuore specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	38	77	4.8K
2	Health Sciences	5	5	137
3	Natural Sciences	3	3	414
4	Arts	2	2	56
5	Engineering	2	2	37

Maurizio Genuardi

160

Publications

9.9K

Citations

H-Index

Page 1

	Year	Citations
Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results Sharon E. Plon, Diana Eccles, Douglas F. Easton, Human Mutation Genetic TestingCancer PathologySequence Variant ClassificationGeneticsGenetic Epidemiology	2008	897
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts Hans F. A. Vasen, Ignacio Blanco, Katja Aktan–Collan, Gut	2013	722
Cancer risk and survival in <i>path_MMR</i> carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database Pål Møller, Toni T. Seppälä, Inge Bernstein, Gut	2017	544
Association of Type and Location of<i>BRCA1</i>and<i>BRCA2</i>Mutations With Risk of Breast and Ovarian Cancer Timothy R. Rebbeck, Nandita Mitra, Fei Wan, JAMA	2015	484
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance Yvonne Hendriks, Anja Wagner, Hans Morreau, Gastroenterology Somatic VariantCancer EpidemiologyCancer RiskMedicineGenetic Epidemiology	2004	427
MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1 Alfonso Bellacosa, Lucia Cicchillitti, Filippo Schepis, Proceedings of the National Academy of Sciences ChromatinGenome InstabilityNatural SciencesGeneticsEpigenetic Change	1999	264
A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer Alessandra Viel, Alessandro Bruselles, Ettore Meccia, EBioMedicine	2017	223
Evidence of a four-hit mechanism involving<i>SMARCB1</i>and<i>NF2</i>in schwannomatosis-associated schwannomas Roberta Sestini, Costanza Bacci, Aldesia Provenzano, Human Mutation Neuro-oncologySomatic VariantMendelian DisorderGenetic DisorderMedicine	2007	179
Biphasic Kinetics of the Human DNA Repair Protein MED1 (MBD4), a Mismatch-specific DNA N-Glycosylase Fiorella Petronzelli, Antonio Riccio, George D. Markham, Journal of Biological Chemistry	2000	178
Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database Pål Møller, Toni T. Seppälä, Inge Bernstein, Gut	2016	164

Page 1