Carla Lintas (C Lintas)

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 31

Top Topics

Endometrial Cancer

Dna Methylation

Autism Spectrum Disorder

Top Venues

International journal of molecular sciences

Clinical genetics

Molecular genetics & genomic medicine

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

Publications

Carla Lintas, Benedetta Canalis, Alessia Azzarà, Giovanna Sabarese, Giuseppe Perrone, Fiorella Gurrieri
Exploring the Role of the MUTYH Gene in Breast, Ovarian and Endometrial Cancer. Genes 15 (5) (2024)
Carla Lintas, Benedetta Canalis, Alessia Azzarà, Giovanna Sabarese, Giuseppe Perrone, Fiorella Gurrieri
Exploring the Role of the MUTYH Gene in Breast, Ovarian and Endometrial Cancer. Genes 15 (5) (2024)
Carla Lintas, Benedetta Canalis, Alessia Azzarà, Giovanna Sabarese, Giuseppe Perrone, Fiorella Gurrieri
Exploring the Role of the MUTYH Gene in Breast, Ovarian and Endometrial Cancer. Genes 15 (5) (2024)
Carla Lintas, Benedetta Canalis, Alessia Azzarà, Giovanna Sabarese, Giuseppe Perrone, Fiorella Gurrieri
Exploring the Role of the MUTYH Gene in Breast, Ovarian and Endometrial Cancer. Genes 15 (5) (2024)
Claudio Tabolacci, Daniela De Vita, Antonio Facchiano, Giuseppina Bozzuto, Simone Beninati, Cristina Maria Failla, Marta Di Martile, Carla Lintas, Carlo Mischiati, Annarita Stringaro, Donatella Del Bufalo, Francesco Facchiano
Phytochemicals as Immunomodulatory Agents in Melanoma. International journal of molecular sciences 24 (3) (2023)
Alessia Azzarà, Ilaria Cassano, Carla Lintas, Fabio Pilato, Fioravante Capone, Vincenzo Di Lazzaro, Fiorella Gurrieri
Melkersson-Rosenthal Syndrome and Migraine: A New Phenotype Associated with SCN1A Variants? Genes 14 (7) (2023)
Claudio Tabolacci, Daniela De Vita, Antonio Facchiano, Giuseppina Bozzuto, Simone Beninati, Cristina Maria Failla, Marta Di Martile, Carla Lintas, Carlo Mischiati, Annarita Stringaro, Donatella Del Bufalo, Francesco Facchiano
Phytochemicals as Immunomodulatory Agents in Melanoma. International journal of molecular sciences 24 (3) (2023)
Carla Lintas, Ilaria Cassano, Alessia Azzarà, Maria Grazia Stigliano, Chiara Gregorj, Roberto Sacco, Andrea Stoccoro, Fabio Coppedè, Fiorella Gurrieri
Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental Disorders. Genes 14 (3) (2023)
Claudio Tabolacci, Daniela De Vita, Antonio Facchiano, Giuseppina Bozzuto, Simone Beninati, Cristina Maria Failla, Marta Di Martile, Carla Lintas, Carlo Mischiati, Annarita Stringaro, Donatella Del Bufalo, Francesco Facchiano
Phytochemicals as Immunomodulatory Agents in Melanoma. International journal of molecular sciences 24 (3) (2023)
Francesca Cucinotta, Carla Lintas, Pasquale Tomaiuolo, Marco Baccarin, Chiara Picinelli, Paola Castronovo, Roberto Sacco, Ignazio Stefano Piras, Laura Turriziani, Arianna Ricciardello, Scattoni Maria Luisa, Antonio M Persico
Diagnostic yield and clinical impact of chromosomal microarray analysis in autism spectrum disorder. Molecular genetics & genomic medicine (2023)
Carla Lintas, Ilaria Cassano, Alessia Azzarà, Maria Grazia Stigliano, Chiara Gregorj, Roberto Sacco, Andrea Stoccoro, Fabio Coppedè, Fiorella Gurrieri
Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental Disorders. Genes 14 (3) (2023)
Carla Lintas, Ilaria Cassano, Alessia Azzarà, Maria Grazia Stigliano, Chiara Gregorj, Roberto Sacco, Andrea Stoccoro, Fabio Coppedè, Fiorella Gurrieri
Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental Disorders. Genes 14 (3) (2023)
Carla Lintas, Angelo Facchiano, Alessia Azzarà, Ilaria Cassano, Claudio Tabolacci, Cinzia Galasso, Fiorella Gurrieri
Deletion of a Single Lysine Residue at Position 292 of CAMK2A Disrupts Protein Function, Causing Severe Epileptic Encephalopathy and Intellectual Disability. Genes 14 (7) (2023)
Alessia Azzarà, Ilaria Cassano, Carla Lintas, Laura Bernardini, Fabio Pilato, Fioravante Capone, Vincenzo Di Lazzaro, Fiorella Gurrieri
A new gene for autosomal dominant facial palsy/migraine identified in a family by whole exome sequencing. European journal of neurology (2023)
Carla Lintas, Irene Bottillo, Roberto Sacco, Alessia Azzarà, Ilaria Cassano, Maria Pia Ciccone, Paola Grammatico, Fiorella Gurrieri
Expanding the Spectrum of KDM5C Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype Correlations. Genes 13 (12) (2022)
Carla Lintas, Irene Bottillo, Roberto Sacco, Alessia Azzarà, Ilaria Cassano, Maria Pia Ciccone, Paola Grammatico, Fiorella Gurrieri
Expanding the Spectrum of KDM5C Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype Correlations. Genes 13 (12) (2022)
Alessia Azzarà, Laura Risi Ambrogioni, Ilaria Cassano, Carla Lintas, Umile Giuseppe Longo, Vincenzo Denaro, Fiorella Gurrieri
Genetic Characterization in Familial Rotator Cuff Tear: An Exome Sequencing Study. Biology 11 (11) (2022)
Carla Lintas, Irene Bottillo, Roberto Sacco, Alessia Azzarà, Ilaria Cassano, Maria Pia Ciccone, Paola Grammatico, Fiorella Gurrieri
Expanding the Spectrum of KDM5C Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype Correlations. Genes 13 (12) (2022)
Carla Lintas, Roberto Sacco, Alessia Azzarà, Ilaria Cassano, Luigi Laino, Paola Grammatico, Fiorella Gurrieri
Genetic Dysruption of the Histaminergic Pathways: A Novel Deletion at the 15q21.2 <i>locus</i> Associated with Variable Expressivity of Neuropsychiatric Disorders. Genes 13 (10) (2022)
Carla Lintas, Irene Bottillo, Roberto Sacco, Alessia Azzarà, Ilaria Cassano, Maria Pia Ciccone, Paola Grammatico, Fiorella Gurrieri
Expanding the Spectrum of KDM5C Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype Correlations. Genes 13 (12) (2022)
Carla Lintas, Irene Bottillo, Roberto Sacco, Alessia Azzarà, Ilaria Cassano, Maria Pia Ciccone, Paola Grammatico, Fiorella Gurrieri
Expanding the Spectrum of KDM5C Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype Correlations. Genes 13 (12) (2022)
Claudio Tabolacci, Martina Cordella, Sabrina Mariotti, Stefania Rossi, Cinzia Senatore, Carla Lintas, Lauretta Levati, Daniela D'Arcangelo, Antonio Facchiano, Stefania D'Atri, Roberto Nisini, Francesco Facchiano
Melanoma Cell Resistance to Vemurafenib Modifies Inter-Cellular Communication Signals. Biomedicines 9 (1) (2021)
Ignazio S Piras, Filippo Manti, Anna Costa, Valentina Carone, Bruna Scalese, Joshua S Talboom, Christian Veronesi, Claudio Tabolacci, Antonio M Persico, Matthew J Huentelman, Roberto Sacco, Carla Lintas
Molecular biomarkers to track clinical improvement following an integrative treatment model in autistic toddlers. Acta neuropsychiatrica 33 (5) (2021)
Ignazio Stefano Piras, Stefano Gabriele, Laura Altieri, Federica Lombardi, Roberto Sacco, Carla Lintas, Barbara Manzi, Paolo Curatolo, Maria Nobile, Catia Rigoletto, Massimo Molteni, Antonio M Persico
Reevaluation of Serum Arylesterase Activity in Neurodevelopmental Disorders. Antioxidants (Basel, Switzerland) 10 (2) (2021)
Carla Lintas, Roberto Sacco, Alessia Azzarà, Ilaria Cassano, Fiorella Gurrieri
Genotype-Phenotype Correlations in Relation to Newly Emerging Monogenic Forms of Autism Spectrum Disorder and Associated Neurodevelopmental Disorders: The Importance of Phenotype Reevaluation after Pangenomic Results. Journal of clinical medicine 10 (21) (2021)
Marco Baccarin, Chiara Picinelli, Pasquale Tomaiuolo, Paola Castronovo, Anna Costa, Magda Verdecchia, Chiara Cannizzaro, Giusi Barbieri, Roberto Sacco, Antonio M Persico, Carla Lintas
Appropriateness of array-CGH in the ADHD clinics: A comparative study. Genes, brain, and behavior 19 (6) (2020)
Ignazio Stefano Piras, Anna Costa, Maria Cristina Tirindelli, Andrea Stoccoro, Matthew J Huentelman, Roberto Sacco, Fabio Coppedè, Carla Lintas
Genetic and epigenetic MTHFR gene variants in the mothers of attention-deficit/hyperactivity disorder affected children as possible risk factors for neurodevelopmental disorders. Epigenomics 12 (10) (2020)
Francesca Cucinotta, Arianna Ricciardello, Laura Turriziani, Giorgia Calabrese, Marilena Briguglio, Maria Boncoddo, Fabiana Bellomo, Pasquale Tomaiuolo, Silvia Martines, Marianna Bruschetta, Francesca La Fauci Belponer, Tiziana Di Bella, Costanza Colombi, Marco Baccarin, Chiara Picinelli, Paola Castronovo, Carla Lintas, Roberto Sacco, Thomas Biederer, Barbara Kellam, Stephen W Scherer, Antonio M Persico
FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family. Molecular genetics & genomic medicine 8 (9) (2020)
Paola Castronovo, Marco Baccarin, Arianna Ricciardello, Chiara Picinelli, Pasquale Tomaiuolo, Francesca Cucinotta, Myriam Frittoli, Carla Lintas, Roberto Sacco, Antonio M Persico
Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review. Clinical genetics 97 (1) (2019)
Carla Lintas
Linking genetics to epigenetics: The role of folate and folate-related pathways in neurodevelopmental disorders. Clinical genetics 95 (2) (2018)
Carla Lintas, A M Persico
Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes. Clinical genetics 94 (3-4) (2017)