M. Riboni

Most-cited papers

1. Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT

   L. Feliubadaló, M. Font, J. Purroy, F. Rousaud +35 more

   1999Nature Genetics334 citations

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2. SLC7A7, encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance

   G. Borsani, M. Bassi, M. P. Sperandeo, A. De Grandi +8 more

   1999Nature Genetics247 citations

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3. Identification and characterisation of human xCT that co-expresses, with 4F2 heavy chain, the amino acid transport activity system xc–

   M. Bassi, Emma Gasol, M. Manzoni, M. Pineda +5 more

   2001Pflügers Archiv172 citations

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4. Identification and expression of NEU3, a novel human sialidase associated to the plasma membrane.

   E. Monti, M. Bassi, N. Papini, M. Riboni +7 more

   2000Biochemical Journal168 citations Open access

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5. Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria.

   M. Font, L. Feliubadaló, X. Estivill, V. Nunes +18 more

   2001Human Molecular Genetics142 citations Open access

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6. Molecular cloning and characterization of NEU4, the fourth member of the human sialidase gene family.

   E. Monti, M. Bassi, R. Bresciani, S. Civini +9 more

   2004Genomics119 citations

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7. X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats.

   M. Bassi, R. Ramesar, Barbara Caciotti, I. Winship +6 more

   1999American Journal of Human Genetics110 citations Open access

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8. Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility

   Irene Catucci, A. Osorio, B. Arver, Guido Neidhardt +24 more

   2017Genetics in Medicine89 citations Open access

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9. Structure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance.

   M. P. Sperandeo, M. T. Bassi, M. Riboni, Giancarlo Parenti +14 more

   2000American Journal of Human Genetics75 citations Open access

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10. PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer

    P. Peterlongo, Irene Catucci, G. Pasquini, P. Verderio +7 more

    2011Breast Cancer Research and Treatment46 citations

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11. Dietary intake of cyanidin-3-glucoside induces a long-lasting cardioprotection from ischemia/reperfusion injury by altering the microbiota.

    M. Trinei, A. Carpi, R. Menabò, M. Storto +9 more

    2021Journal of Nutritional Biochemistry31 citations

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12. SLC7A8, a gene mapping within the lysinuric protein intolerance critical region, encodes a new member of the glycoprotein-associated amino acid transporter family.

    M. T. Bassi, M. P. Sperandeo, B. Incerti, A. Bulfone +11 more

    1999Genomics25 citations

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13. The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers

    Irene Catucci, P. Verderio, S. Pizzamiglio, S. Manoukian +15 more

    2011Breast Cancer Research and Treatment18 citations Open access

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14. Genomic characterization of asymptomatic CT-detected lung cancers

    E. Belloni, G. Veronesi, C. Micucci, S. Javan +12 more

    2011Oncogene8 citations Open access

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15. is mutated in patients with lysinuric protein intolerance

    G. Borsani, M. Bassi, M. P. Sperandeo, A. De Grandi +8 more

    19993 citations

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