Valentina Massa

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 18

Top Topics

Bioinformatics Analysis

Cognitive Impairment

Top Venues

Birth defects research

International journal of molecular sciences

American journal of medical genetics. Part A

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

Publications

Laura Avagliano, Silvia Castiglioni, Antonella Lettieri, Chiara Parodi, Elisabetta Di Fede, Esi Taci, Paolo Grazioli, Elisa Adele Colombo, Cristina Gervasini, Valentina Massa
Intrauterine growth in chromatinopathies: A long road for better understanding and for improving clinical management. Birth defects research 116 (7) (2024)
Elisabetta Gibellato, Paola Cianci, Milena Mariani, Barbara Parma, Sylvia Huisman, Robert Śmigiel, Anne-Marie Bisgaard, Valentina Massa, Cristina Gervasini, Alex Moretti, Alessandro Cattoni, Andrea Biondi, Angelo Selicorni
SMC1A epilepsy syndrome: clinical data from a large international cohort. American journal of medical genetics. Part A 194 (7) (2024)
Elisabetta Gibellato, Paola Cianci, Milena Mariani, Barbara Parma, Sylvia Huisman, Robert Śmigiel, Anne-Marie Bisgaard, Valentina Massa, Cristina Gervasini, Alex Moretti, Alessandro Cattoni, Andrea Biondi, Angelo Selicorni
SMC1A epilepsy syndrome: clinical data from a large international cohort. American journal of medical genetics. Part A 194 (7) (2024)
Elisabetta Gibellato, Paola Cianci, Milena Mariani, Barbara Parma, Sylvia Huisman, Robert Śmigiel, Anne-Marie Bisgaard, Valentina Massa, Cristina Gervasini, Alex Moretti, Alessandro Cattoni, Andrea Biondi, Angelo Selicorni
SMC1A epilepsy syndrome: clinical data from a large international cohort. American journal of medical genetics. Part A (2024)
Roberto Oleari, Antonella Lettieri, Stefano Manzini, Alyssa J J Paganoni, Valentina André, Paolo Grazioli, Marco Busnelli, Paolo Duminuco, Antonio Vitobello, Christophe Philippe, Varoona Bizaoui, Helen L Storr, Federica Amoruso, Fani Memi, Valeria Vezzoli, Valentina Massa, Peter Scheiffele, Sasha Rose Howard, Alessia Caramello
Combined omic analyses reveal autism-linked NLGN3 gene as a key developmental regulator of GnRH neuron biology and disease. Disease models & mechanisms (2023)
Chiara Chiereghin, Michela Robusto, Valentina Massa, Pierangela Castorina, Umberto Ambrosetti, Rosanna Asselta, Giulia Soldà
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss. Cells 11 (11) (2022)
Silvia Castiglioni, Elisabetta Di Fede, Clara Bernardelli, Antonella Lettieri, Chiara Parodi, Paolo Grazioli, Elisa Adele Colombo, Silvia Ancona, Donatella Milani, Emerenziana Ottaviano, Elisa Borghi, Valentina Massa, Filippo Ghelma, Aglaia Vignoli, Elena Lesma, Cristina Gervasini
KMT2A : Umbrella Gene for Multiple Diseases. Genes 13 (3) (2022)
Clara Bernardelli, Silvia Ancona, Melania Lazzari, Antonella Lettieri, Piera Selvaggio, Valentina Massa, Cristina Gervasini, Federico Raimondi, Raffaella Chiaramonte, Elena Lesma
LAM Cells as Potential Drivers of Senescence in Lymphangioleiomyomatosis Microenvironment. International journal of molecular sciences 23 (13) (2022)
Angelo Selicorni, Milena Mariani, Antonella Lettieri, Valentina Massa
Cornelia de Lange Syndrome: From a Disease to a Broader Spectrum. Genes 12 (7) (2021)
Roberto Oleari, Valentina Massa, Alessia Caramello, Antonella Lettieri
The Differential Roles for Neurodevelopmental and Neuroendocrine Genes in Shaping GnRH Neuron Physiology and Deficiency. International journal of molecular sciences 22 (17) (2021)
Elisabetta Di Fede, Emerenziana Ottaviano, Paolo Grazioli, Camilla Ceccarani, Antonio Galeone, Chiara Parodi, Elisa Adele Colombo, Giulia Bassanini, Grazia Fazio, Marco Severgnini, Donatella Milani, Elvira Verduci, Thomas Vaccari, Valentina Massa, Elisa Borghi, Cristina Gervasini
Insights into the Role of the Microbiota and of Short-Chain Fatty Acids in Rubinstein-Taybi Syndrome. International journal of molecular sciences 22 (7) (2021)
Valentina Massa, Laura Avagliano, Paolo Grazioli, Sandra C P De Castro, Chiara Parodi, Dawn Savery, Patrizia Vergani, Serena Cuttin, Patrizia Doi, Gaetano Bulfamante, Andrew J Copp, Nicholas D E Greene
Dynamic acetylation profile during mammalian neurulation. Birth defects research 112 (2) (2019)
Grazia Fazio, Valentina Massa, Andrea Grioni, Vojtech Bystry, Silvia Rigamonti, Claudia Saitta, Marta Galbiati, Carmelo Rizzari, Caterina Consarino, Andrea Biondi, Angelo Selicorni, Giovanni Cazzaniga
First evidence of a paediatric patient with Cornelia de Lange syndrome with acute lymphoblastic leukaemia. Journal of clinical pathology 72 (8) (2019)
Laura Avagliano, Valentina Massa, Timothy M George, Sarah Qureshy, Gaetano Pietro Bulfamante, Richard H Finnell
Overview on neural tube defects: From development to physical characteristics. Birth defects research 111 (19) (2018)
Laura Rachele Bettini, Federica Graziola, Grazia Fazio, Paolo Grazioli, Valeria Scagliotti, Mariavittoria Pasquini, Giovanni Cazzaniga, Andrea Biondi, Lidia Larizza, Angelo Selicorni, Carles Gaston-Massuet, Valentina Massa
Rings and Bricks: Expression of Cohesin Components is Dynamic during Development and Adult Life. International journal of molecular sciences 19 (2) (2018)
Grazia Fazio, Laura Rachele Bettini, Silvia Rigamonti, Dorela Meta, Andrea Biondi, Giovanni Cazzaniga, Angelo Selicorni, Valentina Massa
Impairment of Retinoic Acid Signaling in Cornelia de Lange Syndrome Fibroblasts. Birth defects research 109 (16) (2017)
Laura Avagliano, Paolo Grazioli, Milena Mariani, Gaetano P Bulfamante, Angelo Selicorni, Valentina Massa
Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome. Orphanet journal of rare diseases 12 (1) (2017)
Laura Avagliano, Gaetano Pietro Bulfamante, Valentina Massa
Cornelia de Lange syndrome: To diagnose or not to diagnose in utero? Birth defects research 109 (10) (2017)