Fortunato Lonardo (F Lonardo)

Loop profile Scopus Author ID ISNI ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 5

Top Topics

Intellectual Disability

Top Venues

Clinical genetics

Children (Basel, Switzerland)

International journal of molecular sciences

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

Publications

Flaviana Marzano, Matteo Chiara, Arianna Consiglio, Gabriele D'Amato, Mattia Gentile, Valentina Mirabelli, Maria Piane, Camilla Savio, Marco Fabiani, Domenica D'Elia, Elisabetta Sbisà, Gioacchino Scarano, Fortunato Lonardo, Apollonia Tullo, Graziano Pesole, Maria Felicia Faienza
Whole-Exome and Transcriptome Sequencing Expands the Genotype of Majewski Osteodysplastic Primordial Dwarfism Type II. International journal of molecular sciences 24 (15) (2023)
Paolo Fontana, Alberto Budillon, Domenico Simeone, Francesca Del Vecchio Blanco, Martina Caiazza, Alessandra D'Amico, Fortunato Lonardo, Vincenzo Nigro, Giuseppe Limongelli, Gioacchino Scarano
A Novel Homozygous GPAA1 Variant in a Patient with a Glycosylphosphatidylinositol Biosynthesis Defect. Genes 14 (7) (2023)
Giovanna Tritto, Ivana Ricca, Marco Turi, Andrea Gemma, Filippo Muratori, Gioacchino Scarano, Fortunato Lonardo
Clinical Characterization of a 6-Year-Old Patient with Autism and Two Adjacent Duplications on 10q11.22q11.23. A Case Report. Children (Basel, Switzerland) 8 (6) (2021)
Fortunato Lonardo, M S Lonardo, F Acquaviva, M Della Monica, F Scarano, G Scarano
Say-Barber-Biesecker-Young-Simpson syndrome and Genitopatellar syndrome: Lumping or splitting? Clinical genetics 95 (2) (2018)
Paolo Fontana, M Grasso, F Acquaviva, E Gennaro, M L Galli, M Falco, F Scarano, G Scarano, Fortunato Lonardo
SNORD116 deletions cause Prader-Willi syndrome with a mild phenotype and macrocephaly. Clinical genetics 92 (4) (2017)