Fiorella Gurrieri

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Topics

Infectious Diseases

Intellectual Disability

Top Venues

Journal of nephrology

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

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

Publications

Maria Vittoria Ristori, Valerio Guarrasi, Paolo Soda, Nicola Petrosillo, Fiorella Gurrieri, Umile Giuseppe Longo, Massimo Ciccozzi, Elisabetta Riva, Silvia Angeletti
Emerging Microorganisms and Infectious Diseases: One Health Approach for Health Shared Vision. Genes 15 (7) (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)
Maria Vittoria Ristori, Valerio Guarrasi, Paolo Soda, Nicola Petrosillo, Fiorella Gurrieri, Umile Giuseppe Longo, Massimo Ciccozzi, Elisabetta Riva, Silvia Angeletti
Emerging Microorganisms and Infectious Diseases: One Health Approach for Health Shared Vision. Genes 15 (7) (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)
Maria Vittoria Ristori, Valerio Guarrasi, Paolo Soda, Nicola Petrosillo, Fiorella Gurrieri, Umile Giuseppe Longo, Massimo Ciccozzi, Elisabetta Riva, Silvia Angeletti
Emerging Microorganisms and Infectious Diseases: One Health Approach for Health Shared Vision. Genes 15 (7) (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)
Eugenio Sangiorgi, Alessia Azzarà, Roberto Rumore, Ilaria Cassano, Elena Verecchia, Luciano Giacò, Maria Alessandra Tullio, Fiorella Gurrieri, Raffaele Manna
Identification by Exome Sequencing of Predisposing Variants in Familial Cases of Autoinflammatory Recurrent Fevers. Genes 14 (7) (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)
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, 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, Claudia Rendeli, Anna Maria Crivello, Fulvia Brugnoletti, Roberto Rumore, Emanuele Ausili, Eugenio Sangiorgi, Fiorella Gurrieri
Identification of new candidate genes for spina bifida through exome sequencing. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 37 (8) (2021)
Annamaria Milillo, Clelia Molinario, Stefano Costanzi, Gisella Vischini, Francesca La Carpia, Francesco La Greca, Donato Rigante, Giovanni Gambaro, Fiorella Gurrieri, Eugenio Sangiorgi
Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura. Journal of nephrology 31 (5) (2018)