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Dario Cocciadiferro
84
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Online (84)
Mediatypes
Articles (Online) (31)
OpenAccess-fulltext (53)
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1
Exploiting in silico structural analysis to introduce emerg..:
Cocciadiferro, Dario
;
Mazza, Tommaso
;
Vecchio, Davide
...
Frontiers in Genetics. 14 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
2
Clinical variability in DYNC2H1-related skeletal ciliopathi..:
Piceci-Sparascio, Francesca
;
Micale, Lucia
;
Torres, Barbara
...
European Journal of Human Genetics. 31 (2023) 4 - p. 479-484 , 2023
Link:
https://doi.org/10.1038/..
?
3
Duplication at 19q13.32q13.33 Segregating with Neuropsychia..:
Guadagnolo, Daniele
;
Mastromoro, Gioia
;
Torres, Barbara
...
Genes. 14 (2023) 12 - p. 2157 , 2023
Link:
https://doi.org/10.3390/..
?
4
Clinical and functional characterization of COL2A1 p.Gly444..:
Marchionni, Enrica
;
D'Apice, Maria Rosaria
;
Lupo, Viviana
...
Bone Reports. 19 (2023) - p. 101728 , 2023
Link:
https://doi.org/10.1016/..
?
5
Early prenatal diagnosis of a recurrent case of short-rib t..:
Fontana, Paolo
;
Agolini, Emanuele
;
Cocciadiferro, Dario
...
The Journal of Maternal-Fetal & Neonatal Medicine. 36 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1080/..
?
6
COVID-19: S-Peptide RBD 484–508 Induces IFN-γ T-Cell Respon..:
Murdocca, Michela
;
Citro, Gennaro
;
Centanini, Eleonora
...
Viruses. 15 (2023) 7 - p. 1417 , 2023
Link:
https://doi.org/10.3390/..
?
7
Whole Exome Sequencing in 16p13.11 Microdeletion Patients R..:
Granata, Paola
;
Cocciadiferro, Dario
;
Zito, Alessandra
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
8
De Novo Mutation in KMT2C Manifesting as Kleefstra Syndrome..:
Siano, Maria Anna
;
De Maggio, Ilaria
;
Petillo, Roberta
...
Pediatric Reports. 14 (2022) 1 - p. 131-139 , 2022
Link:
https://doi.org/10.3390/..
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9
Delineation of the clinical profile of CNOT2 haploinsuffici..:
Niceta, Marcello
;
Pizzi, Simone
;
Inzana, Francesca
...
Clinical Genetics. 103 (2022) 2 - p. 156-166 , 2022
Link:
https://doi.org/10.1111/..
?
10
Expanding the novel MAPKAPK5–related developmental disorder..:
Vecchio, Davide
;
Cocciadiferro, Dario
;
Macchiaiolo, Marina
...
Clinical Genetics. 102 (2022) 2 - p. 142-148 , 2022
Link:
https://doi.org/10.1111/..
?
11
Expression analysis of miRNA hsa‐let7b‐5p in naso‐oropharyn..:
Latini, Andrea
;
Vancheri, Chiara
;
Amati, Francesca
...
Journal of Cellular and Molecular Medicine. 26 (2022) 19 - p. 4940-4948 , 2022
Link:
https://doi.org/10.1111/..
?
12
Gene Set Enrichment Analysis of Interaction Networks Weight..:
Zito, Alessandra
;
Lualdi, Marta
;
Granata, Paola
...
Frontiers in Genetics. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
13
Copy number variation analysis implicates novel pathways in..:
Guida, Valentina
;
Sparascio, Francesca Piceci
;
Bernardini, Laura
...
Clinical Genetics. 100 (2021) 3 - p. 268-279 , 2021
Link:
https://doi.org/10.1111/..
?
14
TSPEAR variants are primarily associated with ectodermal dy..:
Bowles, Bradley
;
Ferrer, Alejandro
;
Nishimura, Carla J.
...
American Journal of Medical Genetics Part A. 185 (2021) 8 - p. 2417-2433 , 2021
Link:
https://doi.org/10.1002/..
?
15
A case report of isoniazid adverse drug reaction in a pedia..:
Cocciadiferro, Dario
;
Cursi, Laura
;
Cairoli, Sara
...
Medicine: Case Reports and Study Protocols. 2 (2021) 2 - p. e0043 , 2021
Link:
https://doi.org/10.1097/..
1-15