Stefano Paolacci

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 10

Top Topics

Autism Spectrum Disorder

Anorexia Nervosa

Top Venues

Journal of clinical medicine

Molecular genetics & genomic medicine

Congenital anomalies

Journal of personalized medicine

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

Publications

Gabriele Bonetti, Stefano Paolacci, Michele Samaja, Paolo Enrico Maltese, Sandro Michelini, Serena Michelini, Silvia Michelini, Maurizio Ricci, Marina Cestari, Astrit Dautaj, Maria Chiara Medori, Matteo Bertelli
Low Efficacy of Genetic Tests for the Diagnosis of Primary Lymphedema Prompts Novel Insights into the Underlying Molecular Pathways. International journal of molecular sciences 23 (13) (2022)
Sandro Michelini, Karen L Herbst, Vincenza Precone, Elena Manara, Giuseppe Marceddu, Astrit Dautaj, Paolo Enrico Maltese, Stefano Paolacci, Maria Rachele Ceccarini, Tommaso Beccari, Elisa Sorrentino, Barbara Aquilanti, Valeria Velluti, Giuseppina Matera, Lucilla Gagliardi, Giacinto Abele Donato Miggiano, Matteo Bertelli
A Multi-Gene Panel to Identify Lipedema-Predisposing Genetic Variants by a Next-Generation Sequencing Strategy. Journal of personalized medicine 12 (2) (2022)
Francesca Cristofoli, Elisa Sorrentino, Giulia Guerri, Roberta Miotto, Roberta Romanelli, Alessandra Zulian, Stefano Cecchin, Stefano Paolacci, Jan Miertus, Matteo Bertelli, Paolo Enrico Maltese, Pietro Chiurazzi, Liborio Stuppia, Marco Castori, Giuseppe Marceddu
Variant Selection and Interpretation: An Example of Modified VarSome Classifier of ACMG Guidelines in the Diagnostic Setting. Genes 12 (12) (2021)
Manuela Baronio, Hajra Sadia, Stefano Paolacci, Domenico Prestamburgo, Danilo Miotti, Vittorio A Guardamagna, Giuseppe Natalini, Stephanie G B Sullivan, Matteo Bertelli
Molecular Aspects of Regional Pain Syndrome. Pain research & management 2020 (2020)
Sehime Gulsun Temel, Mahmut Çerkez Ergoren, Elena Manara, Stefano Paolacci, Gulten Tuncel, Şeref Gül, Matteo Bertelli
Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome. European journal of human genetics : EJHG 28 (12) (2020)
Stefano Paolacci, Aysha Karim Kiani, Elena Manara, Tommaso Beccari, Maria Rachele Ceccarini, Liborio Stuppia, Pietro Chiurazzi, Laura Dalla Ragione, Matteo Bertelli
Genetic contributions to the etiology of anorexia nervosa: New perspectives in molecular diagnosis and treatment. Molecular genetics & genomic medicine 8 (7) (2020)
Lorenzo Lorusso, Vincenza Precone, Daniela Ferrari, Gaelle K Ngonga, Antonio Giampiero Russo, Stefano Paolacci, Matteo Bertelli
Paraneoplastic Neurological Syndromes: Study of Prevalence in a Province of the Lombardy Region, Italy. Journal of clinical medicine 9 (10) (2020)
Stefano Paolacci, Raul Ettore Mattassi, Giuseppe Marceddu, Elena Manara, Alessandra Zulian, Giulia Guerri, Luca De Antoni, Carlo Arduino, Daniela Cavalca, Matteo Bertelli
Somatic Variant Analysis Identifies Targets for Tailored Therapies in Patients with Vascular Malformations. Journal of clinical medicine 9 (11) (2020)
Stefano Paolacci, Flavio Faletra, Paolo Enrico Maltese, Mariachiara Quadrifoglio, Matteo Bertelli
A next generation sequencing custom gene panel designed to distinguish isolated polydactyly from syndromic polydactyly during prenatal diagnosis. Congenital anomalies 59 (6) (2019)
Sandro Michelini, Stefano Paolacci, Elena Manara, Costantino Eretta, Raul Mattassi, Byung-Boong Lee, Matteo Bertelli
Genetic tests in lymphatic vascular malformations and lymphedema. Journal of medical genetics 55 (4) (2018)