Mara Giordano

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 21

Top Topics

Atrial Fibrillation

Venous Thromboembolism

Intellectual Disability

Dna Methylation

Top Venues

International journal of molecular sciences

Journal of clinical medicine

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

Publications

Luca Cumitini, Giulia Renda, Mara Giordano, Roberta Rolla, Tarek Shail, Sara Sacchetti, Lorena Iezzi, Luca Giacomini, Valentina Zanotti, Raffaella Auciello, Ilaria Angilletta, Melissa Foglietta, Mirco Zucchelli, Ivana Antonucci, Liborio Stuppia, Sabina Gallina, Umberto Dianzani, Giuseppe Patti
Role of CES1 and ABCB1 Genetic Polymorphisms on Functional Response to Dabigatran in Patients with Atrial Fibrillation. Journal of clinical medicine 13 (9) (2024)
Sara Sacchetti, Chiara Puricelli, Marco Mennuni, Valentina Zanotti, Luca Giacomini, Mara Giordano, Umberto Dianzani, Giuseppe Patti, Roberta Rolla
Research into New Molecular Mechanisms in Thrombotic Diseases Paves the Way for Innovative Therapeutic Approaches. International journal of molecular sciences 25 (5) (2024)
Luca Cumitini, Giulia Renda, Mara Giordano, Roberta Rolla, Tarek Shail, Sara Sacchetti, Lorena Iezzi, Luca Giacomini, Valentina Zanotti, Raffaella Auciello, Ilaria Angilletta, Melissa Foglietta, Mirco Zucchelli, Ivana Antonucci, Liborio Stuppia, Sabina Gallina, Umberto Dianzani, Giuseppe Patti
Role of CES1 and ABCB1 Genetic Polymorphisms on Functional Response to Dabigatran in Patients with Atrial Fibrillation. Journal of clinical medicine 13 (9) (2024)
Sara Sacchetti, Chiara Puricelli, Marco Mennuni, Valentina Zanotti, Luca Giacomini, Mara Giordano, Umberto Dianzani, Giuseppe Patti, Roberta Rolla
Research into New Molecular Mechanisms in Thrombotic Diseases Paves the Way for Innovative Therapeutic Approaches. International journal of molecular sciences 25 (5) (2024)
Sara Sacchetti, Chiara Puricelli, Marco Mennuni, Valentina Zanotti, Luca Giacomini, Mara Giordano, Umberto Dianzani, Giuseppe Patti, Roberta Rolla
Research into New Molecular Mechanisms in Thrombotic Diseases Paves the Way for Innovative Therapeutic Approaches. International journal of molecular sciences 25 (5) (2024)
Chiara Puricelli, Elena Boggio, Casimiro Luca Gigliotti, Ian Stoppa, Salvatore Sutti, Mara Giordano, Umberto Dianzani, Roberta Rolla
Platelets, Protean Cells with All-Around Functions and Multifaceted Pharmacological Applications. International journal of molecular sciences 24 (5) (2023)
Federica Costa, Eleonora Beltrami, Simona Mellone, Sara Sacchetti, Elena Boggio, Casimiro Luca Gigliotti, Ian Stoppa, Umberto Dianzani, Roberta Rolla, Mara Giordano
Genes and Microbiota Interaction in Monogenic Autoimmune Disorders. Biomedicines 11 (4) (2023)
Federica Costa, Eleonora Beltrami, Simona Mellone, Sara Sacchetti, Elena Boggio, Casimiro Luca Gigliotti, Ian Stoppa, Umberto Dianzani, Roberta Rolla, Mara Giordano
Genes and Microbiota Interaction in Monogenic Autoimmune Disorders. Biomedicines 11 (4) (2023)
Chiara Puricelli, Elena Boggio, Casimiro Luca Gigliotti, Ian Stoppa, Salvatore Sutti, Mara Giordano, Umberto Dianzani, Roberta Rolla
Platelets, Protean Cells with All-Around Functions and Multifaceted Pharmacological Applications. International journal of molecular sciences 24 (5) (2023)
Daria Apostolo, Davide D'Onghia, Stelvio Tonello, Rosalba Minisini, Alessio Baricich, Carla Gramaglia, Filippo Patrucco, Patrizia Zeppegno, Antonio Acquaviva, Piero Emilio Balbo, Luigi Mario Castello, Annalisa Chiocchetti, Annalisa Chiocchetti, Chiara Gerevini, Mara Giordano, Fatiha Laaguid, Marcello Manfredi, Davide Raineri, Cristina Rigamonti, Roberta Rolla, Valentina Romano, Marco Confalonieri, Paola Savoia, Elisa Zavattaro, Mario Pirisi, Barbara Ruaro, Pier Paolo Sainaghi, Mattia Bellan, null null
Decreased Gas6 and sAxl Plasma Levels Are Associated with Hair Loss in COVID-19 Survivors. International journal of molecular sciences 24 (7) (2023)
Chiara Puricelli, Elena Boggio, Casimiro Luca Gigliotti, Ian Stoppa, Salvatore Sutti, Mara Giordano, Umberto Dianzani, Roberta Rolla
Platelets, Protean Cells with All-Around Functions and Multifaceted Pharmacological Applications. International journal of molecular sciences 24 (5) (2023)
Simona Mellone, Enrica Bertelli, Barbara Roviglione, Denise Vurchio, Sara Ronzani, Andrea Secco, Enrico Felici, Mariachiara Martina Strozzi, Federico Schena, Mara Giordano
Co-Occurrence of a Pathogenic HSD3B2 Variant and a Duplication on 10q22.3-q23.2 Detected in Newborn Twins with Salt-Wasting Congenital Adrenal Hyperplasia. Genes 13 (12) (2022)
Simona Mellone, Enrica Bertelli, Barbara Roviglione, Denise Vurchio, Sara Ronzani, Andrea Secco, Enrico Felici, Mariachiara Martina Strozzi, Federico Schena, Mara Giordano
Co-Occurrence of a Pathogenic HSD3B2 Variant and a Duplication on 10q22.3-q23.2 Detected in Newborn Twins with Salt-Wasting Congenital Adrenal Hyperplasia. Genes 13 (12) (2022)
Simona Mellone, Enrica Bertelli, Barbara Roviglione, Denise Vurchio, Sara Ronzani, Andrea Secco, Enrico Felici, Mariachiara Martina Strozzi, Federico Schena, Mara Giordano
Co-Occurrence of a Pathogenic HSD3B2 Variant and a Duplication on 10q22.3-q23.2 Detected in Newborn Twins with Salt-Wasting Congenital Adrenal Hyperplasia. Genes 13 (12) (2022)
Simona Mellone, Enrica Bertelli, Barbara Roviglione, Denise Vurchio, Sara Ronzani, Andrea Secco, Enrico Felici, Mariachiara Martina Strozzi, Federico Schena, Mara Giordano
Co-Occurrence of a Pathogenic HSD3B2 Variant and a Duplication on 10q22.3-q23.2 Detected in Newborn Twins with Salt-Wasting Congenital Adrenal Hyperplasia. Genes 13 (12) (2022)
Simona Mellone, Enrica Bertelli, Barbara Roviglione, Denise Vurchio, Sara Ronzani, Andrea Secco, Enrico Felici, Mariachiara Martina Strozzi, Federico Schena, Mara Giordano
Co-Occurrence of a Pathogenic HSD3B2 Variant and a Duplication on 10q22.3-q23.2 Detected in Newborn Twins with Salt-Wasting Congenital Adrenal Hyperplasia. Genes 13 (12) (2022)
Roberta Degrandi, Flavia Prodam, Giulia Genoni, Giorgio Bellomo, Gianni Bona, Mara Giordano, Simonetta Bellone, Alice Monzani
The Prevalence of Thyroid Autoimmunity in Children with Developmental Dyslexia. BioMed research international 2021 (2021)
Antonella Fanelli, Silvia Vannelli, Deepak Babu, Simona Mellone, Alessia Cucci, Alice Monzani, Wael Al Essa, Andrea Secco, Antonia Follenzi, Simonetta Bellone, Flavia Prodam, Mara Giordano
Copy number variations residing outside the SHOX enhancer region are involved in Short Stature and Léri-Weill dyschondrosteosis. Molecular genetics & genomic medicine (2021)
Roberta Rolla, Giulia Paglino, Chiara Puricelli, Simona Mellone, Maurizio Sciancalepore, Eleonora Beltrami, Chiara Cerutti, Selena Piccotti, Stefania Tota, Annamaria Scotta, Patrizia Pergolini, Umberto Dianzani, Mara Giordano
Screening for haemoglobin disorders: The experience of the piedmont north-eastern quadrant. International journal of laboratory hematology 43 (2) (2020)
Deepak Babu, Silvia Vannelli, Antonella Fanelli, Simona Mellone, Ave Maria Baffico, Lucia Corrado, Wael Al Essa, Anna Grandone, Simonetta Bellone, Alice Monzani, Giulia Vinci, Luisa De Sanctis, Liborio Stuppia, Flavia Prodam, Mara Giordano
Variants in the 5'UTR reduce SHOX expression and contribute to SHOX haploinsufficiency. European journal of human genetics : EJHG 29 (1) (2020)
Alice Monzani, Deepak Babu, Simona Mellone, Giulia Genoni, Antonella Fanelli, Flavia Prodam, Simonetta Bellone, Mara Giordano
Co-occurrence of genomic imbalances on Xp22.1 in the SHOX region and 15q25.2 in a girl with short stature, precocious puberty, urogenital malformations and bone anomalies. BMC medical genomics 12 (1) (2019)