All papers authored by Giuseppe Merla
Refreshing results…
2023
Alessandra Romagnoli 
,
Martina Di Rienzo,
Elisa Petruccioli,
Carmela Fusco,
Ivana Palucci ,
Lucia Micale,
Tommaso Mazza ,
Giovanni Delogu ,
Giuseppe Merla ,
Delia Goletti ,
Mauro Piacentini ,
Gian Maria Fimia
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,
Martina Di Rienzo,
Elisa Petruccioli,
Carmela Fusco,
Ivana Palucci ,
Lucia Micale,
Tommaso Mazza ,
Giovanni Delogu ,
Giuseppe Merla ,
Delia Goletti ,
Mauro Piacentini ,
Gian Maria Fimia
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2022
Allan Bayat ,
Guillem de Valles‐Ibáñez ,
Manuela Pendziwiat,
Alexej Knaus,
Kerstin Alt,
Elisa Biamino,
Annette Bley,
Sophie Calvert,
Patrick Carney,
Alfonso Caro‐Llopis,
Berten Ceulemans,
Janice Cousin,
Suzanne Davis,
Vincent des Portes,
Patrick Edery
and 54 other authors
,
Guillem de Valles‐Ibáñez ,
Manuela Pendziwiat,
Alexej Knaus,
Kerstin Alt,
Elisa Biamino,
Annette Bley,
Sophie Calvert,
Patrick Carney,
Alfonso Caro‐Llopis,
Berten Ceulemans,
Janice Cousin,
Suzanne Davis,
Vincent des Portes,
Patrick Edery
and 54 other authors
PIGNencephalopathy: Characterizing the epileptology
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Aidin Foroutan ,
Sadegheh Haghshenas ,
Pratibha Bhai,
Michael A. Levy,
Jennifer Kerkhof ,
Haley McConkey,
Marcello Niceta ,
Andrea Ciolfi,
Lucia Pedace,
Evelina Miele ,
David Genevieve,
Solveig Heide,
Mariëlle Alders,
Giuseppe Zampino,
Giuseppe Merla
and 16 other authors
,
Sadegheh Haghshenas ,
Pratibha Bhai,
Michael A. Levy,
Jennifer Kerkhof ,
Haley McConkey,
Marcello Niceta ,
Andrea Ciolfi,
Lucia Pedace,
Evelina Miele ,
David Genevieve,
Solveig Heide,
Mariëlle Alders,
Giuseppe Zampino,
Giuseppe Merla
and 16 other authors
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome
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2021
Elisabetta Flex ,
Valentina Imperatore ,
Giovanna Carpentieri,
Alessandro Bruselles ,
Andrea Ciolfi,
Simone Pizzi,
Maria Giovanna Tedesco,
Daniela Rogaia,
Amedea Mencarelli,
Giuseppe Di Cara,
Alberto Verrotti,
Stefania Troiani,
Giuseppe Merla ,
Marco Tartaglia ,
Paolo Prontera
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,
Valentina Imperatore ,
Giovanna Carpentieri,
Alessandro Bruselles ,
Andrea Ciolfi,
Simone Pizzi,
Maria Giovanna Tedesco,
Daniela Rogaia,
Amedea Mencarelli,
Giuseppe Di Cara,
Alberto Verrotti,
Stefania Troiani,
Giuseppe Merla ,
Marco Tartaglia ,
Paolo Prontera
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Kathleen Rooney ,
Michael A. Levy,
Sadegheh Haghshenas,
Jennifer Kerkhof ,
Daniela Rogaia,
Maria Giovanna Tedesco,
Valentina Imperatore ,
Amedea Mencarelli,
Gabriella Maria Squeo,
Eleonora Di Venere,
Giuseppe Di Cara,
Alberto Verrotti,
Giuseppe Merla ,
Matthew L. Tedder ,
Barbara R. DuPont
and 2 other authors
,
Michael A. Levy,
Sadegheh Haghshenas,
Jennifer Kerkhof ,
Daniela Rogaia,
Maria Giovanna Tedesco,
Valentina Imperatore ,
Amedea Mencarelli,
Gabriella Maria Squeo,
Eleonora Di Venere,
Giuseppe Di Cara,
Alberto Verrotti,
Giuseppe Merla ,
Matthew L. Tedder ,
Barbara R. DuPont
and 2 other authors
Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome
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2020
Elisabetta Di Fede,
Valentina Massa,
Bartolomeo Augello,
Gabriella Squeo,
Emanuela Scarano,
Anna Maria Perri,
Rita Fischetto,
Francesco Andrea Causio,
Giuseppe Zampino,
Maria Piccione ,
Elena Curridori,
Tommaso Mazza,
Stefano Castellana,
Lidia Larizza,
Filippo Ghelma
and 6 other authors
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,
Elena Curridori,
Tommaso Mazza,
Stefano Castellana,
Lidia Larizza,
Filippo Ghelma
and 6 other authors
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Flavia Cerrato ,
Angela Sparago ,
Francesca Ariani,
Fulvia Brugnoletti,
Luciano Calzari ,
Fabio Coppedè,
Alessandro De Luca ,
Cristina Gervasini ,
Emiliano Giardina,
Fiorella Gurrieri ,
Cristiana Lo Nigro,
Giuseppe Merla ,
Monica Miozzo,
Silvia Russo ,
Eugenio Sangiorgi
and 8 other authors
,
Angela Sparago ,
Francesca Ariani,
Fulvia Brugnoletti,
Luciano Calzari ,
Fabio Coppedè,
Alessandro De Luca ,
Cristina Gervasini ,
Emiliano Giardina,
Fiorella Gurrieri ,
Cristiana Lo Nigro,
Giuseppe Merla ,
Monica Miozzo,
Silvia Russo ,
Eugenio Sangiorgi
and 8 other authors
DNA Methylation in the Diagnosis of Monogenic Diseases
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Gabriella Maria Squeo,
Bartolomeo Augello,
Valentina Massa,
Donatella Milani,
Elisa Adele Colombo,
Tommaso Mazza,
Stefano Castellana,
Maria Piccione ,
Silvia Maitz,
Antonio Petracca,
Paolo Prontera,
Maria Accadia,
Matteo Della Monica,
Marilena Carmela Di Giacomo,
Daniela Melis
and 9 other authors
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,
Silvia Maitz,
Antonio Petracca,
Paolo Prontera,
Maria Accadia,
Matteo Della Monica,
Marilena Carmela Di Giacomo,
Daniela Melis
and 9 other authors
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2019
Paolo Prontera,
Daniela Rogaia,
Ester Sallicandro,
Amedea Mencarelli,
Valentina Imperatore,
Gabriella Maria Squeo,
Giuseppe Merla ,
Sandro Elisei,
Danilo Moretti-Ferreira ,
Susanna Esposito,
Gabriela Stangoni
,
Sandro Elisei,
Danilo Moretti-Ferreira ,
Susanna Esposito,
Gabriela Stangoni
Schilbach–Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene
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