Giovanbattista Giovanni Battista Ferrero (G B Ferrero, Giovanni Battista Ferrero)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

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

Top Topics

Sickle Cell Disease

Pulmonary Arterial Hypertension

Top Venues

European journal of human genetics : EJHG

Annals of hematology

American journal of medical genetics. Part A

British journal of haematology

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

Publications

Andrea Gazzin, Federico Fornari, Marcello Niceta, Chiara Leoni, Maria Lisa Dentici, Diana Carli, Anna Maria Villar, Giulio Calcagni, Elena Banaudi, Stefania Massuras, Simona Cardaropoli, Elena Airulo, Paola Daniele, Emanuele Monda, Giuseppe Limongelli, Chiara Riggi, Giuseppe Zampino, Maria Cristina Digilio, Alessandro De Luca, Tartaglia Marco, Giovanbattista Giovanni Battista Ferrero, Alessandro Mussa
Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant. European journal of human genetics : EJHG 32 (8) (2024)
Andrea Piolatto, Carmen Maria Gaglioti, Nicolò Tesio, Maria Grazia Clemente, Martina Culcasi, Alessio Matrone, Maria Paola Pila, Angela Sambataro, Filomena Longo, Raffaella Origa, Giovanbattista Giovanni Battista Ferrero
Deferasirox film-coated tablet-associated ulcerative colitis: An emerging pattern in thalassemia patients? British journal of haematology (2024)
Khaled M Musallam, Susanna Barella, Raffaella Origa, Giovanbattista Giovanni Battista Ferrero, Roberto Lisi, Annamaria Pasanisi, Filomena Longo, Barbara Gianesin, Gian Luca Forni, null null
Revisiting iron overload status and change thresholds as predictors of mortality in transfusion-dependent β-thalassemia: a 10-year cohort study. Annals of hematology 103 (7) (2024)
Andrea Gazzin, Federico Fornari, Marcello Niceta, Chiara Leoni, Maria Lisa Dentici, Diana Carli, Anna Maria Villar, Giulio Calcagni, Elena Banaudi, Stefania Massuras, Simona Cardaropoli, Elena Airulo, Paola Daniele, Emanuele Monda, Giuseppe Limongelli, Chiara Riggi, Giuseppe Zampino, Maria Cristina Digilio, Alessandro De Luca, Tartaglia Marco, Giovanbattista Giovanni Battista Ferrero, Alessandro Mussa
Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant. European journal of human genetics : EJHG (2024)
Andrea Gazzin, Federico Fornari, Marcello Niceta, Chiara Leoni, Maria Lisa Dentici, Diana Carli, Anna Maria Villar, Giulio Calcagni, Elena Banaudi, Stefania Massuras, Simona Cardaropoli, Elena Airulo, Paola Daniele, Emanuele Monda, Giuseppe Limongelli, Chiara Riggi, Giuseppe Zampino, Maria Cristina Digilio, Alessandro De Luca, Tartaglia Marco, Giovanbattista Giovanni Battista Ferrero, Alessandro Mussa
Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant. European journal of human genetics : EJHG 32 (8) (2024)
Andrea Gazzin, Federico Fornari, Marcello Niceta, Chiara Leoni, Maria Lisa Dentici, Diana Carli, Anna Maria Villar, Giulio Calcagni, Elena Banaudi, Stefania Massuras, Simona Cardaropoli, Elena Airulo, Paola Daniele, Emanuele Monda, Giuseppe Limongelli, Chiara Riggi, Giuseppe Zampino, Maria Cristina Digilio, Alessandro De Luca, Tartaglia Marco, Giovanbattista Giovanni Battista Ferrero, Alessandro Mussa
Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant. European journal of human genetics : EJHG 32 (8) (2024)
Andrea Gazzin, Federico Fornari, Marcello Niceta, Chiara Leoni, Maria Lisa Dentici, Diana Carli, Anna Maria Villar, Giulio Calcagni, Elena Banaudi, Stefania Massuras, Simona Cardaropoli, Elena Airulo, Paola Daniele, Emanuele Monda, Giuseppe Limongelli, Chiara Riggi, Giuseppe Zampino, Maria Cristina Digilio, Alessandro De Luca, Tartaglia Marco, Giovanbattista Giovanni Battista Ferrero, Alessandro Mussa
Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant. European journal of human genetics : EJHG 32 (8) (2024)
Andrea Piolatto, Carmen Maria Gaglioti, Nicolò Tesio, Maria Grazia Clemente, Martina Culcasi, Alessio Matrone, Maria Paola Pila, Angela Sambataro, Filomena Longo, Raffaella Origa, Giovanbattista Giovanni Battista Ferrero
Deferasirox film-coated tablet-associated ulcerative colitis: An emerging pattern in thalassemia patients? British journal of haematology 205 (2) (2024)
Khaled M Musallam, Susanna Barella, Raffaella Origa, Giovanbattista Giovanni Battista Ferrero, Roberto Lisi, Annamaria Pasanisi, Filomena Longo, Barbara Gianesin, Gian Luca Forni, null null
Revisiting iron overload status and change thresholds as predictors of mortality in transfusion-dependent β-thalassemia: a 10-year cohort study. Annals of hematology (2024)
Khaled M Musallam, Susanna Barella, Raffaella Origa, Giovanbattista Giovanni Battista Ferrero, Roberto Lisi, Annamaria Pasanisi, Filomena Longo, Barbara Gianesin, Gian Luca Forni, null null
Revisiting iron overload status and change thresholds as predictors of mortality in transfusion-dependent β-thalassemia: a 10-year cohort study. Annals of hematology 103 (7) (2024)
Khaled M Musallam, Susanna Barella, Raffaella Origa, Giovanbattista Giovanni Battista Ferrero, Roberto Lisi, Annamaria Pasanisi, Filomena Longo, Barbara Gianesin, Gian Luca Forni
Pretransfusion hemoglobin level and mortality in adults with transfusion-dependent β-thalassemia. Blood (2023)
Patrick R Blackburn, Frédéric Ebstein, Tzung-Chien Hsieh, Marialetizia Motta, Francesca Clementina Radio, Johanna C Herkert, Tuula Rinne, Isabelle Thiffault, Michele Rapp, Mariel Alders, Saskia Maas, Bénédicte Gerard, Thomas Smol, Catherine Vincent-Delorme, Benjamin Cogné, Bertrand Isidor, Marie Vincent, Ruxandra Bachmann-Gagescu, Anita Rauch, Pascal Joset, Giovanbattista Giovanni Battista Ferrero, Andrea Ciolfi, Thomas Husson, Anne-Marie Guerrot, Carlos A Bacino, Colleen Macmurdo, Stephanie S Thompson, Jill Anne Rosenfeld, Laurence Olivier-Faivre, Frédéric Tran Mau Them, Wallid Deb, Virginie Vignard, Pankaj B Agrawal, Jill A Madden, Alice Goldenberg, François Lecoquierre, Michael Zech, Holger Prokisch, Ján Necpál, Robert Jech, Juliane Winkelmann, Monika Turčanová Koprušáková, Vassiliki Konstantopoulou, John R Younce, Marwan Shinawi, Chloe Mighton, Charlotte Fung, Chantal Morel, Jordan Lerner- Ellis, Stephanie DiTroia, Magalie Barth, Dominique Bonneau, Ingrid Krapels, Sander Stegmann, Vyne van der Schoot, Theresa Brunet, Cornelia Bußmann, Cyril Mignot, Thomas Courtin, Claudia Ravelli, Boris Keren, Alban Ziegler, Linda Hasadsri, Pavel N Pichurin, Eric W Klee, Katheryn Grand, Pedro A Sanchez-Lara, Elke Krüger, Stéphane Bézieau, Hannah Klinkhammer, Peter Michael Krawitz, Evan E Eichler, Tartaglia Marco, Sébastien Küry, Tianyun Wang
Loss-of-function variants in CUL3 cause a syndromic neurodevelopmental disorder. medRxiv : the preprint server for health sciences (2023)
Diana Carli, Nicoletta Resta, Giovanbattista Giovanni Battista Ferrero, Martino Ruggieri, Alessandro Mussa
Mosaic RASopathies: A review of disorders caused by somatic pathogenic variants in the genes of the RAS/MAPK pathway. American journal of medical genetics. Part C, Seminars in medical genetics (2022)
César Augusto Pinheiro Ferreira Alves, O Sherbini, F D'Arco, Dora Batia Dyne Steel, Manju A Kurian, F C Radio, Giovanbattista Giovanni Battista Ferrero, Diana Carli, Tartaglia Marco, Tuğçe B Balcı, N N Powell-Hamilton, S A Schrier Vergano, H Reutter, Julia Hoefele, R Günthner, Elizabeth R Roeder, R O Littlejohn, Davor Lessel, Sabine Peters, C Kentros, Kwame Anyane-Yeboa, Claudia B Catarino, Saadet Mercimek-Mahmutoglu, J Denecke, Michael J Lyons, Florentine Radelfahr, Elizabeth Joyce Bhoj, Laura Bryant, Adeline Vanderver
Brain Abnormalities in Patients with Germline Variants in H3F3 : Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors. AJNR. American journal of neuroradiology 43 (7) (2022)
Diana Carli, Giovanbattista Giovanni Battista Ferrero, Anna Fusillo, Paola Coppo, Roberta La Selva, Federica Zinali, Simona Cardaropoli, Carlotta Ranieri, Matteo Iacoviello, Nicoletta Resta, Alessandro Mussa
A new case of Smith-Kingsmore syndrome with somatic MTOR pathogenic variant expands the phenotypic spectrum to lateralized overgrowth. Clinical genetics 99 (5) (2021)
Filomena Longo, Andrea Piolatto, Giovanbattista Giovanni Battista Ferrero, Antonio Piga
Ineffective Erythropoiesis in β-Thalassaemia: Key Steps and Therapeutic Options by Drugs. International journal of molecular sciences 22 (13) (2021)
Lisa Pavinato, Slavica Trajkova, Enrico Grosso, Elisa Giorgio, Alessandro Bruselles, Francesca Clementina Radio, Tommaso Pippucci, Paola Dimartino, Tartaglia Marco, Aleksandar Petlichkovski, Silvia De Rubeis, Joseph D Buxbaum, Giovanbattista Giovanni Battista Ferrero, Roberto Keller, Alfredo Brusco
Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature review. American journal of medical genetics. Part A 185 (6) (2021)
Diana Carli, Andrea Gazzin, Maria Roberta Bongioanni, Mauro Bergui, Alessandro Mussa, Giovanbattista Giovanni Battista Ferrero
Chronic subdural hematoma: A previously unreported life-threatening complication in adult with Sotos syndrome. American journal of medical genetics. Part A 182 (12) (2020)
Giovanni Innella, Donatella Greco, Diana Carli, Pamela Magini, Elisa Giorgio, Ornella Galesi, Giovanbattista Giovanni Battista Ferrero, Corrado Romano, Alfredo Brusco, Claudio Graziano
Clinical spectrum and follow-up in six individuals with Lamb-Shaffer syndrome (SOX5). American journal of medical genetics. Part A 185 (2) (2020)
Alessandro Mussa, Kelly A Duffy, Diana Carli, Jessica R Griff, Riccardo Fagiano, Jonida Kupa, Garrett M Brodeur, Giovanbattista Giovanni Battista Ferrero, Jennifer M Kalish
The effectiveness of Wilms tumor screening in Beckwith-Wiedemann spectrum. Journal of cancer research and clinical oncology 145 (12) (2019)
Diana Carli, Evelise Riberi, Giovanbattista Giovanni Battista Ferrero, Alessandro Mussa
Syndromic Disorders Caused by Disturbed Human Imprinting Journal of clinical research in pediatric endocrinology 12 (1) (2019)