Eva Trevisson

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 30

Top Venues

European journal of human genetics : EJHG

Cancers

Journal of clinical immunology

Journal of clinical medicine

University of Padova

Università degli Studi di Padova (PHD)

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

Affiliation History

University of Padova Mar 31 2011

Italy

MD PhD :: Dept of Women's and Children's Health

Education History

Università degli Studi di Padova - Mar 17 2008

Italy

PHD :: Pediatrics

Università degli Studi di Padova Scuola di Medicina e Chirurgia - Jul 26 2004

Italy

PHD

Publications

Linda Rossini, Claudia Maria Bonardi, Silvia Bresolin, Eva Trevisson, Antonio Marzollo
Severe Herpes Simplex Encephalitis: an Unusual Presentation of IPEX. Journal of clinical immunology 44 (4) (2024)
Tito Brambullo, Alberto De Lazzari, Arianna Franchi, Eva Trevisson, Maria Luisa Garau, Federico Scarmozzino, Vincenzo Vindigni, Franco Bassetto
A Misdiagnosed Familiar Brooke-Spiegler Syndrome: Case Report and Review of the Literature. Journal of clinical medicine 13 (8) (2024)
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, Cecilia Mancini, Manuela Priolo, Adeline Alice Bonnard, Camilla Cappelletti, Chiara Leoni, Andrea Ciolfi, Simone Pizzi, Viviana Cordeddu, Cesare Rossi, Marco Ferilli, Mafalda Mucciolo, Vito Luigi Colona, Christine Fauth, Melissa Bellini, Giacomo Biasucci, Lorenzo Sinibaldi, Silvana Briuglia, Andrea Gazzin, Diana Carli, Luigi Memo, Eva Trevisson, Concetta Schiavariello, Maria Luca, Antonio Novelli, Caroline Michot, Anne Sweertvaegher, David Germanaud, Emanuela Scarano, Alessandro De Luca, Giuseppe Zampino, Martin Zenker, Alessandro Mussa, Bruno Dallapiccola, Hélène Cave, Maria Cristina Digilio, Tartaglia Marco
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis. European journal of human genetics : EJHG 32 (8) (2024)
Cristina Calderan, Ugo Sorrentino, Luca Persano, Eva Trevisson, Geppo Sartori, Leonardo Salviati, Maria Andrea Desbats
A yeast based assay establishes the pathogenicity of novel missense ACTA2 variants associated with aortic aneurysms. European journal of human genetics : EJHG (2024)
Cristina Calderan, Ugo Sorrentino, Luca Persano, Eva Trevisson, Geppo Sartori, Leonardo Salviati, Maria Andrea Desbats
A yeast based assay establishes the pathogenicity of novel missense ACTA2 variants associated with aortic aneurysms. European journal of human genetics : EJHG 32 (7) (2024)
Linda Rossini, Claudia Maria Bonardi, Silvia Bresolin, Eva Trevisson, Antonio Marzollo
Severe Herpes Simplex Encephalitis: an Unusual Presentation of IPEX. Journal of clinical immunology 44 (4) (2024)
Cristina Calderan, Ugo Sorrentino, Luca Persano, Eva Trevisson, Geppo Sartori, Leonardo Salviati, Maria Andrea Desbats
A yeast based assay establishes the pathogenicity of novel missense ACTA2 variants associated with aortic aneurysms. European journal of human genetics : EJHG 32 (7) (2024)
Linda Rossini, Claudia Maria Bonardi, Silvia Bresolin, Eva Trevisson, Antonio Marzollo
Severe Herpes Simplex Encephalitis: an Unusual Presentation of IPEX. Journal of clinical immunology 44 (4) (2024)
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, Cecilia Mancini, Manuela Priolo, Adeline Alice Bonnard, Camilla Cappelletti, Chiara Leoni, Andrea Ciolfi, Simone Pizzi, Viviana Cordeddu, Cesare Rossi, Marco Ferilli, Mafalda Mucciolo, Vito Luigi Colona, Christine Fauth, Melissa Bellini, Giacomo Biasucci, Lorenzo Sinibaldi, Silvana Briuglia, Andrea Gazzin, Diana Carli, Luigi Memo, Eva Trevisson, Concetta Schiavariello, Maria Luca, Antonio Novelli, Caroline Michot, Anne Sweertvaegher, David Germanaud, Emanuela Scarano, Alessandro De Luca, Giuseppe Zampino, Martin Zenker, Alessandro Mussa, Bruno Dallapiccola, Hélène Cave, Maria Cristina Digilio, Tartaglia Marco
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis. European journal of human genetics : EJHG 32 (8) (2024)
Cristina Calderan, Ugo Sorrentino, Luca Persano, Eva Trevisson, Geppo Sartori, Leonardo Salviati, Maria Andrea Desbats
A yeast based assay establishes the pathogenicity of novel missense ACTA2 variants associated with aortic aneurysms. European journal of human genetics : EJHG 32 (7) (2024)
Tito Brambullo, Alberto De Lazzari, Arianna Franchi, Eva Trevisson, Maria Luisa Garau, Federico Scarmozzino, Vincenzo Vindigni, Franco Bassetto
A Misdiagnosed Familiar Brooke-Spiegler Syndrome: Case Report and Review of the Literature. Journal of clinical medicine 13 (8) (2024)
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, Cecilia Mancini, Manuela Priolo, Adeline Alice Bonnard, Camilla Cappelletti, Chiara Leoni, Andrea Ciolfi, Simone Pizzi, Viviana Cordeddu, Cesare Rossi, Marco Ferilli, Mafalda Mucciolo, Vito Luigi Colona, Christine Fauth, Melissa Bellini, Giacomo Biasucci, Lorenzo Sinibaldi, Silvana Briuglia, Andrea Gazzin, Diana Carli, Luigi Memo, Eva Trevisson, Concetta Schiavariello, Maria Luca, Antonio Novelli, Caroline Michot, Anne Sweertvaegher, David Germanaud, Emanuela Scarano, Alessandro De Luca, Giuseppe Zampino, Martin Zenker, Alessandro Mussa, Bruno Dallapiccola, Hélène Cave, Maria Cristina Digilio, Tartaglia Marco
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis. European journal of human genetics : EJHG 32 (8) (2024)
Cristina Calderan, Ugo Sorrentino, Luca Persano, Eva Trevisson, Geppo Sartori, Leonardo Salviati, Maria Andrea Desbats
A yeast based assay establishes the pathogenicity of novel missense ACTA2 variants associated with aortic aneurysms. European journal of human genetics : EJHG 32 (7) (2024)
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, Cecilia Mancini, Manuela Priolo, Adeline Alice Bonnard, Camilla Cappelletti, Chiara Leoni, Andrea Ciolfi, Simone Pizzi, Viviana Cordeddu, Cesare Rossi, Marco Ferilli, Mafalda Mucciolo, Vito Luigi Colona, Christine Fauth, Melissa Bellini, Giacomo Biasucci, Lorenzo Sinibaldi, Silvana Briuglia, Andrea Gazzin, Diana Carli, Luigi Memo, Eva Trevisson, Concetta Schiavariello, Maria Luca, Antonio Novelli, Caroline Michot, Anne Sweertvaegher, David Germanaud, Emanuela Scarano, Alessandro De Luca, Giuseppe Zampino, Martin Zenker, Alessandro Mussa, Bruno Dallapiccola, Hélène Cave, Maria Cristina Digilio, Tartaglia Marco
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis. European journal of human genetics : EJHG (2024)
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, Cecilia Mancini, Manuela Priolo, Adeline Alice Bonnard, Camilla Cappelletti, Chiara Leoni, Andrea Ciolfi, Simone Pizzi, Viviana Cordeddu, Cesare Rossi, Marco Ferilli, Mafalda Mucciolo, Vito Luigi Colona, Christine Fauth, Melissa Bellini, Giacomo Biasucci, Lorenzo Sinibaldi, Silvana Briuglia, Andrea Gazzin, Diana Carli, Luigi Memo, Eva Trevisson, Concetta Schiavariello, Maria Luca, Antonio Novelli, Caroline Michot, Anne Sweertvaegher, David Germanaud, Emanuela Scarano, Alessandro De Luca, Giuseppe Zampino, Martin Zenker, Alessandro Mussa, Bruno Dallapiccola, Hélène Cave, Maria Cristina Digilio, Tartaglia Marco
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis. European journal of human genetics : EJHG 32 (8) (2024)
Denis Vecellio Reane, Cristina Cerqua, Sabrina Sacconi, Leonardo Salviati, Eva Trevisson, Anna Raffaello
The Splicing of the Mitochondrial Calcium Uniporter Genuine Activator MICU1 Is Driven by RBFOX2 Splicing Factor during Myogenic Differentiation. International journal of molecular sciences 23 (5) (2022)
Eleonora Cosmo, Luisa Frizziero, Giacomo Miglionico, Chiara Sofia De Biasi, Marisa Bruno, Eva Trevisson, Ilaria Gabbiato, Giulia Midena, Raffaele Parrozzani
Choroidal Abnormalities in Pediatric NF1: A Cohort Natural History Study. Cancers 14 (6) (2022)
Ugo Sorrentino, Chiara Piccolo, Chiara Rigon, Valeria Brasson, Eva Trevisson, Francesca Boaretto, Alessandro Martini, Matteo Cassina
DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature. Audiology research 11 (4) (2021)
Ugo Sorrentino, Silvia Bellonzi, Chiara Mozzato, Valeria Brasson, Irene Toldo, Raffaele Parrozzani, Maurizio Clementi, Matteo Cassina, Eva Trevisson
Epilepsy in NF1: Epidemiologic, Genetic, and Clinical Features. A Monocentric Retrospective Study in a Cohort of 784 Patients. Cancers 13 (24) (2021)
Diana Corallo, Carlo Zanon, Marcella Pantile, Gian Paolo Tonini, Angelica Zin, Samuela Francescato, Bartolomeo Rossi, Eva Trevisson, Claudia Pinato, Ezequiel Monferrer, Rosa Noguera, Salvador F Aliño, Maria José Herrero, Alessandra Biffi, Elisabetta Viscardi, Sanja Aveic
Integrated CGH/WES Analyses Advance Understanding of Aggressive Neuroblastoma Evolution: A Case Study. Cells 10 (10) (2021)
Valeria Morbidoni, Elisa Baschiera, Monica Forzan, Valentina Fumini, Dario Seif Ali, Gianpietro Giorgi, Lisa Buson, Maria Andrea Desbats, Matteo Cassina, Maurizio Clementi, Leonardo Salviati, Eva Trevisson
Hybrid Minigene Assay: An Efficient Tool to Characterize mRNA Splicing Profiles of NF1 Variants. Cancers 13 (5) (2021)
Valeria Morbidoni, Emanuele Agolini, Kevin C Slep, Luca Pannone, Daniela Zuccarello, Matteo Cassina, Enrico Grosso, Giorgia Gai, Leonardo Salviati, Bruno Dallapiccola, Antonio Novelli, Simone Martinelli, Eva Trevisson
Biallelic mutations in the TOGARAM1 gene cause a novel primary ciliopathy. Journal of medical genetics 58 (8) (2020)
Alicia Bach, Jingyi Mi, Matthew Hunter, Benjamin J Halliday, Sixto García-Miñaúr, Francesca Sperotto, Eva Trevisson, David M Markie, Ian M Morison, Marwan S Shinawi, Daniel N Willis, Stephen P Robertson
Wilms tumor in patients with osteopathia striata with cranial sclerosis. European journal of human genetics : EJHG 29 (3) (2020)
D Gareth R Evans, Roope A Kallionpää, Maurizio Clementi, Eva Trevisson, Victor-Felix Mautner, Sacha J Howell, Lauren Lewis, Ouidad Zehou, Sirkku Peltonen, Antonella Brunello, Elaine F Harkness, Pierre Wolkenstein, Juha Peltonen
Breast cancer in neurofibromatosis 1: survival and risk of contralateral breast cancer in a five country cohort study. Genetics in medicine : official journal of the American College of Medical Genetics 22 (2) (2019)
Matteo Cassina, Luisa Frizziero, Enrico Opocher, Raffaele Parrozzani, Ugo Sorrentino, Elisabetta Viscardi, Giacomo Miglionico, Edoardo Midena, Maurizio Clementi, Eva Trevisson
Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment Recommendations. Cancers 11 (11) (2019)
Cristina Cerqua, Alberto Casarin, Fabien Pierrel, Luis Vazquez Fonseca, Giampietro Viola, Leonardo Salviati, Eva Trevisson
Vitamin K2 cannot substitute Coenzyme Q10 as electron carrier in the mitochondrial respiratory chain of mammalian cells. Scientific reports 9 (1) (2019)
Eva Trevisson, Valeria Morbidoni, Monica Forzan, Cecilia Daolio, Valentina Fumini, Raffaele Parrozzani, Matteo Cassina, Edoardo Midena, Leonardo Salviati, Maurizio Clementi
The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromas. Molecular genetics & genomic medicine 7 (5) (2019)
Magdalena Koczkowska, Tom Callens, Yunjia Chen, Alicia Gomes, Alesha D Hicks, Angela Sharp, Eric Johns, Kim Armfield Uhas, Linlea Armstrong, Katherine Armstrong Bosanko, Dusica Babovic-Vuksanovic, Laura Baker, Donald G Basel, Mario Bengala, James T Bennett, Chelsea Chambers, Lola K Clarkson, Maurizio Clementi, Fanny M Cortés, Mitch Cunningham, M Daniela D'Agostino, Martin B Delatycki, Maria C Digilio, Laura Dosa, Silvia Esposito, Stephanie Fox, Mary-Louise Freckmann, Christine Fauth, Teresa Giugliano, Sandra Giustini, Allison Goetsch, Yael Goldberg, Robert S Greenwood, Cristin Griffis, Karen W Gripp, Punita Gupta, Eric Haan, Rachel K Hachen, Tamara L Haygarth, Concepción Hernández-Chico, Katelyn Hodge, Robert J Hopkin, Louanne Hudgins, Sandra Janssens, Kory Keller, Geraldine Kelly-Mancuso, Aaina Kochhar, Bruce R Korf, Andrea M Lewis, Jan Liebelt, Angie Lichty, Robert H Listernick, Michael J Lyons, Isabelle Maystadt, Mayra Martinez Ojeda, Carey McDougall, Lesley K McGregor, Daniela Melis, Nancy Mendelsohn, Malgorzata J M Nowaczyk, June Ortenberg, Karin Panzer, John G Pappas, Mary Ella Pierpont, Giulio Piluso, Valentina Pinna, Eniko K Pivnick, Dinel A Pond, Cynthia M Powell, Caleb Rogers, Noa Ruhrman Shahar, S Lane Rutledge, Veronica Saletti, Sarah A Sandaradura, Claudia Santoro, Ulrich A Schatz, Allison Schreiber, Daryl A Scott, Elizabeth A Sellars, Ruth Sheffer, Elizabeth Siqveland, John M Slopis, Rosemarie Smith, Alberto Spalice, David W Stockton, Haley Streff, Amy Theos, Gail E Tomlinson, Grace Tran, Pamela L Trapane, Eva Trevisson, Nicole J Ullrich, Jenneke Van den Ende, Samantha A Schrier Vergano, Stephanie E Wallace, Michael F Wangler, David D Weaver, Kaleb H Yohay, Elaine Zackai, Jonathan Zonana, Vickie Zurcher, Kathleen B M Claes, Marica Eoli, Yolanda Martin, Katharina Wimmer, Alessandro De Luca, Eric Legius, Ludwine M Messiaen
Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype-phenotype study in neurofibromatosis type 1. Human mutation 41 (1) (2019)
Eva Trevisson, Matteo Cassina, Enrico Opocher, Virginia Vicenzi, Marta Lucchetta, Raffaele Parrozzani, Giacomo Miglionico, Rodica Mardari, Elisabetta Viscardi, Edoardo Midena, Maurizio Clementi
Natural history of optic pathway gliomas in a cohort of unselected patients affected by Neurofibromatosis 1. Journal of neuro-oncology 134 (2) (2017)
Eva Trevisson, Maurizio Clementi, Leonardo Salviati
Is there a link between COQ6 and schwannomatosis? Genetics in medicine : official journal of the American College of Medical Genetics 17 (4) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Eva Trevisson