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Petracca, Antonio
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1

Biallelic LZTR1 variants in a 49‐year‐old woman with hypert..:

Di Stolfo, Giuseppe ; Petracca, Antonio ; Bevere, Ester Maria Lucia...
American Journal of Medical Genetics Part A.  194 (2023)  5 - p. , 2023
Link: https://doi.org/10.1002/..
 
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2

Towards a Long-Read Sequencing Approach for the Molecular D..:

Bonetti, Gabriele ; Cozza, William ; Bernini, Andrea...
International Journal of Molecular Sciences.  24 (2023)  23 - p. 16881 , 2023
Link: https://doi.org/10.3390/..
 
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3

Transcriptome Analysis Reveals Altered Expression of Genes ..:

Fusco, Carmela ; Nardella, Grazia ; Di Filippo, Lucio...
Genes.  13 (2022)  6 - p. 961 , 2022
Link: https://doi.org/10.3390/..
 
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4

The Interplay between PARP Inhibitors and Immunotherapy in ..:

Maiorano, Brigida Anna ; Lorusso, Domenica ; Maiorano, Mauro Francesco Pio...
International Journal of Molecular Sciences.  23 (2022)  7 - p. 3871 , 2022
Link: https://doi.org/10.3390/..
 
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5

Compound Heterozygosity for OTOA Truncating Variant and Gen..:

Ortore, Rocco Pio ; Leone, Maria Pia ; Palumbo, Orazio...
Audiology Research.  11 (2021)  3 - p. 443-451 , 2021
Link: https://doi.org/10.3390/..
 
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6

Improving clinical interpretation of five KRIT1 and PDCD10 ..:

Fusco, Carmela ; Nardella, Grazia ; Petracca, Antonio...
Clinical Genetics.  99 (2021)  6 - p. 829-835 , 2021
Link: https://doi.org/10.1111/..
 
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7

Phenotypic Variability of a Pathogenic PKP2 Mutation in an ..:

Leone, Maria Pia ; Palumbo, Pietro ; Saenen, Johan...
Frontiers in Cardiovascular Medicine.  8 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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8

Propranolol for familial cerebral cavernous malformation (T..:

the Treat-CCM Investigators ; Lanfranconi, Silvia ; Scola, Elisa...
Trials.  21 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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9

A Private 16q24.2q24.3 Microduplication in a Boy with Intel..:

Palumbo, Orazio ; Palumbo, Pietro ; Di Muro, Ester...
Genes.  11 (2020)  6 - p. 707 , 2020
Link: https://doi.org/10.3390/..
 
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10

Mutational spectrum and clinical signatures in 114 families..:

Fusco, Carmela ; Nardella, Grazia ; Fischetto, Rita...
Human Molecular Genetics.  28 (2019)  13 - p. 2133-2142 , 2019
Link: https://doi.org/10.1093/..
 
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11

A novel dominant-negative FGFR1 variant causes Hartsfield s..:

Palumbo, Pietro ; Petracca, Antonio ; Maggi, Roberto...
European Journal of Human Genetics.  27 (2019)  7 - p. 1113-1120 , 2019
Link: https://doi.org/10.1038/..
 
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12

A new case of de novo 6q24.2-q25.2 deletion on paternal chr..:

Stagi, Stefano ; Lapi, Elisabetta ; Pantaleo, Marilena...
BMC Medical Genetics.  16 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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13

Characterization of the rs2802292 SNP identifies FOXO3Aas a..:

Forte, Giovanna ; Grossi, Valentina ; Celestini, Valentina...
BMC Cancer.  14 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
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14

Towards a Long-Read Sequencing Approach for the Molecular D..:

Bonetti, Gabriele ; Cozza, William ; Bernini, Andrea...
info:eu-repo/semantics/altIdentifier/pmid/38069202.  , 2023
Link: https://hdl.handle.net/2..
 
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15

Towards a Long-Read Sequencing Approach for the Molecular D..:

Bonetti, Gabriele ; Cozza, William ; Bernini, Andrea...
info:eu-repo/semantics/altIdentifier/pmid/38069202.  , 2023
Link: https://hdl.handle.net/1..
 
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