Paola Riva

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 20

Top Venues

Human genetics

International journal of molecular sciences

Cancers

European journal of human genetics : EJHG

Università degli Studi di Milano

Università degli Studi di Milano (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Università degli Studi di Milano Jul 01 2015

Italy

Full Professor :: Medical Biotechnology and Translational Medicine

Università degli Studi di Milano

Italy

Associate Professor :: Medical Biotechnology and Translational Medicine

Univerità degli Studi di Milano

Italy

University Researcher/Assistant Professor :: Biology and Genetics for Medical Sciences

Education History

Università degli Studi di Milano

Italy

PHD :: Biology and Genetics for Medical Sciences

Publications

Viviana Tritto, Paola Bettinaglio, Eleonora Mangano, Claudia Cesaretti, Federica Marasca, Chiara Castronovo, Roberta Bordoni, Cristina Battaglia, Veronica Saletti, Valeria Ranzani, Beatrice Bodega, Marica Eoli, Federica Natacci, Paola Riva
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes. Human genetics 143 (6) (2024)
Viviana Tritto, Paola Bettinaglio, Eleonora Mangano, Claudia Cesaretti, Federica Marasca, Chiara Castronovo, Roberta Bordoni, Cristina Battaglia, Veronica Saletti, Valeria Ranzani, Beatrice Bodega, Marica Eoli, Federica Natacci, Paola Riva
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes. Human genetics (2024)
Viviana Tritto, Paola Bettinaglio, Eleonora Mangano, Claudia Cesaretti, Federica Marasca, Chiara Castronovo, Roberta Bordoni, Cristina Battaglia, Veronica Saletti, Valeria Ranzani, Beatrice Bodega, Marica Eoli, Federica Natacci, Paola Riva
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes. Human genetics 143 (6) (2024)
Viviana Tritto, Paola Bettinaglio, Eleonora Mangano, Claudia Cesaretti, Federica Marasca, Chiara Castronovo, Roberta Bordoni, Cristina Battaglia, Veronica Saletti, Valeria Ranzani, Beatrice Bodega, Marica Eoli, Federica Natacci, Paola Riva
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes. Human genetics 143 (6) (2024)
Viviana Tritto, Paola Bettinaglio, Eleonora Mangano, Claudia Cesaretti, Federica Marasca, Chiara Castronovo, Roberta Bordoni, Cristina Battaglia, Veronica Saletti, Valeria Ranzani, Beatrice Bodega, Marica Eoli, Federica Natacci, Paola Riva
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes. Human genetics 143 (6) (2024)
Viviana Tritto, Federico Grilli, Donatella Milani, Paola Riva
Deregulated expression of polycomb repressive complex 2 target genes in a NF1 patient with microdeletion generating the RNF135-SUZ12 chimeric gene. Neurogenetics (2023)
Viviana Tritto, Daniele Capitanio, Cecilia Gelfi, Paola Riva
Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes. International journal of molecular sciences 24 (4) (2023)
Viviana Tritto, Daniele Capitanio, Cecilia Gelfi, Paola Riva
Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes. International journal of molecular sciences 24 (4) (2023)
Paola Bettinaglio, Viviana Tritto, Rosina Paterra, Marica Eoli, Paola Riva
Expression analysis of NF1-mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR. Annals of human genetics (2023)
Viviana Tritto, Daniele Capitanio, Cecilia Gelfi, Paola Riva
Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes. International journal of molecular sciences 24 (4) (2023)
Paola Bettinaglio, Eleonora Mangano, Viviana Tritto, Roberta Bordoni, Rosina Paterra, Arianna Borghi, Marinella Volontè, Cristina Battaglia, Veronica Saletti, Claudia Cesaretti, Federica Natacci, Mariarosa Anna Beatrice Melone, Marica Eoli, Paola Riva
New insights into the molecular basis of spinal neurofibromatosis type 1. European journal of human genetics : EJHG (2023)
Rosina Paterra, Paola Bettinaglio, Arianna Borghi, Eleonora Mangano, Viviana Tritto, Claudia Cesaretti, Carla Schettino, Roberta Bordoni, Claudia Santoro, Sabrina Avignone, Marco Moscatelli, Mariarosa Anna Beatrice Melone, Veronica Saletti, Giulio Piluso, Federica Natacci, Paola Riva, Marica Eoli
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort. Cancers 15 (1) (2022)
Rosina Paterra, Paola Bettinaglio, Arianna Borghi, Eleonora Mangano, Viviana Tritto, Claudia Cesaretti, Carla Schettino, Roberta Bordoni, Claudia Santoro, Sabrina Avignone, Marco Moscatelli, Mariarosa Anna Beatrice Melone, Veronica Saletti, Giulio Piluso, Federica Natacci, Paola Riva, Marica Eoli
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort. Cancers 15 (1) (2022)
Rosina Paterra, Paola Bettinaglio, Arianna Borghi, Eleonora Mangano, Viviana Tritto, Claudia Cesaretti, Carla Schettino, Roberta Bordoni, Claudia Santoro, Sabrina Avignone, Marco Moscatelli, Mariarosa Anna Beatrice Melone, Veronica Saletti, Giulio Piluso, Federica Natacci, Paola Riva, Marica Eoli
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort. Cancers 15 (1) (2022)
Rosina Paterra, Paola Bettinaglio, Arianna Borghi, Eleonora Mangano, Viviana Tritto, Claudia Cesaretti, Carla Schettino, Roberta Bordoni, Claudia Santoro, Sabrina Avignone, Marco Moscatelli, Mariarosa Anna Beatrice Melone, Veronica Saletti, Giulio Piluso, Federica Natacci, Paola Riva, Marica Eoli
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort. Cancers 15 (1) (2022)
Viviana Tritto, Marica Eoli, Rosina Paterra, Serena Redaelli, Marco E M Moscatelli, Francesco Rusconi, Paola Riva
Characterization of 22q12 Microdeletions Causing Position Effect in Rare NF2 Patients with Complex Phenotypes. International journal of molecular sciences 23 (17) (2022)
Nicoletta Villa, Serena Redaelli, Elena Sala, Donatella Conconi, Lorenza Romitti, Emanuela Manfredini, Francesca Crosti, Gaia Roversi, Maria Luisa Lavitrano, Ornella Rodeschini, Maria Paola Recalcati, Rocco Giovanni Piazza, Leda Dalprà, Paola Riva, Angela Bentivegna
Human Chromosome 18 and Acrocentrics: A Dangerous Liaison. International journal of molecular sciences 22 (11) (2021)
Luca Ferrari, Eleonora Mangano, Maria Teresa Bonati, Ilaria Monterosso, Daniele Capitanio, Federica Chiappori, Ilaria Brambilla, Cecilia Gelfi, Cristina Battaglia, Roberta Bordoni, Paola Riva
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model? European journal of human genetics : EJHG 28 (10) (2020)
Viviana Tritto, Luca Ferrari, Silvia Esposito, Paola Zuccotti, Donatella Bianchessi, Federica Natacci, Veronica Saletti, Marica Eoli, Paola Riva
Non-Coding RNA and Tumor Development in Neurofibromatosis Type 1: ANRIL Rs2151280 Is Associated with Optic Glioma Development and a Mild Phenotype in Neurofibromatosis Type 1 Patients. Genes 10 (11) (2019)
Luca Ferrari, Giulietta Scuvera, Arianna Tucci, Donatella Bianchessi, Francesco Rusconi, Francesca Menni, Elena Battaglioli, Donatella Milani, Paola Riva
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth. Human genetics 136 (10) (2017)
Silvia Moncini, Paola Castronovo, Alessandra Murgia, Silvia Russo, Maria Francesca Bedeschi, Marta Lunghi, Angelo Selicorni, Maria Teresa Bonati, Paola Riva, Marco Venturin
Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability. Journal of human genetics 61 (4) (2015)

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Publication Activity (10 Years)

Top Topics

Top Venues

Paola Riva