• 41 Citations
  • 5 h-Index
20132016
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Fingerprint Dive into the research topics where Laura Ciocca is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 18 Similar Profiles
Hypoplastic Left Heart Syndrome Medicine & Life Sciences
Telomere Shortening Medicine & Life Sciences
Chromosomes, Human, Pair 14 Medicine & Life Sciences
Genetic Heterogeneity Medicine & Life Sciences
Retinoblastoma Medicine & Life Sciences
Telomere Medicine & Life Sciences
Chronic Pancreatitis Medicine & Life Sciences
Phenotype Medicine & Life Sciences

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Research Output 2013 2016

  • 41 Citations
  • 5 h-Index
  • 6 Article
10 Citations (Scopus)

Extensive molecular analysis suggested the strong genetic heterogeneity of idiopathic chronic pancreatitis

Sofia, V. M., Da Sacco, L., Surace, C., Tomaiuolo, A. C., Genovese, S., Grotta, S., Gnazzo, M., Petrocchi, S., Ciocca, L., Alghisi, F., Montemitro, E., Martemucci, L., Elce, A., Lucidi, V., Castaldo, G. & Angioni, A., 2016, In : Molecular Medicine. 22, p. 300-309 10 p.

Research output: Contribution to journalArticle

Genetic Heterogeneity
Chronic Pancreatitis
Mutation
Genes
Trypsinogen
5 Citations (Scopus)

Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma

Grotta, S., D'Elia, G., Scavelli, R., Genovese, S., Surace, C., Sirleto, P., Cozza, R., Romanzo, A., De Ioris, M. A., Valente, P., Tomaiuolo, A. C., Lepri, F. R., Franchin, T., Ciocca, L., Russo, S., Locatelli, F. & Angioni, A., Nov 4 2015, In : BMC Cancer. 15, 1, 841.

Research output: Contribution to journalArticle

Retinoblastoma
Mosaicism
Comparative Genomic Hybridization
Multiplex Polymerase Chain Reaction
Point Mutation
5 Citations (Scopus)

Hypoplastic left heart syndrome and 21q22.3 deletion

Ciocca, L., Digilio, M. C., Lombardo, A., D'Elia, G., Baban, A., Capolino, R., Petrocchi, S., Russo, S., Sirleto, P., Roberti, M. C., Marino, B., Angioni, A. & Dallapiccola, B., Mar 1 2015, In : American Journal of Medical Genetics, Part A. 167, 3, p. 579-586 8 p.

Research output: Contribution to journalArticle

Hypoplastic Left Heart Syndrome
Aortic Coarctation
Congenital Heart Defects
Aortic Valve Stenosis
Fluorescence In Situ Hybridization
9 Citations (Scopus)

Epilepsy in patients with duplications of chromosome 14 harboring FOXG1

Pontrelli, G., Cappelletti, S., Claps, D., Sirleto, P., Ciocca, L., Petrocchi, S., Terracciano, A., Serino, D., Fusco, L., Vigevano, F. & Specchio, N., 2014, In : Pediatric Neurology. 50, 5, p. 530-535 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 14
Epilepsy
Seizures
Spasm
Forkhead Transcription Factors
6 Citations (Scopus)

Telomere shortening and telomere position effect in mild ring 17 syndrome

Surace, C., Berardinelli, F., Masotti, A., Roberti, M. C., Da Sacco, L., D'Elia, G., Sirleto, P., Digilio, M. C., Cusmai, R., Grotta, S., Petrocchi, S., Hachem, M. E., Pisaneschi, E., Ciocca, L., Russo, S., Lepri, F. R., Sgura, A. & Angioni, A., Jan 7 2014, In : Epigenetics and Chromatin. 7, 1, 1.

Research output: Contribution to journalArticle

Telomere Shortening
Telomere
Ring Chromosomes
Chromosomes, Human, Pair 17
Reunion