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20182019
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Fingerprint Dive into the research topics where Viola Alesi is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 5 Similar Profiles
Glycogen Storage Disease Type III Medicine & Life Sciences
Uniparental Disomy Medicine & Life Sciences
deletion Physics & Astronomy
Phenotype Medicine & Life Sciences
Chromosomes, Human, Pair 1 Medicine & Life Sciences
Genes Medicine & Life Sciences
Megalencephaly Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences

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Research Output 2018 2019

Intellectual Disability
Siblings
Genes
Chromosome Duplication
Splenomegaly

A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome

Alesi, V., Loddo, S., Calì, F., Orlando, V., Genovese, S., Ferretti, D., Calacci, C., Calvieri, G., Falasca, R., Ulgheri, L., Drago, F., Dallapiccola, B., Baban, A. & Novelli, A., May 30 2019, In : American Journal of Medical Genetics, Part A.

Research output: Contribution to journalArticle

Phenotype
Nose
Language Development Disorders
Haploinsufficiency
Muscle Hypotonia

Copy number variants in autism spectrum disorders

Vicari, S., Napoli, E., Cordeddu, V., Menghini, D., Alesi, V., Loddo, S., Novelli, A. & Tartaglia, M., Feb 20 2019, In : Progress in Neuro-Psychopharmacology and Biological Psychiatry. 92, p. 421-427 7 p.

Research output: Contribution to journalReview article

Genomic Structural Variation
Comparative Genomic Hybridization
Human Genome
Single Nucleotide Polymorphism
Autism Spectrum Disorder

Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome

Davis, K. W., Serrano, M., Loddo, S., Robinson, C., Alesi, V., Dallapiccola, B., Novelli, A. & Butler, M. G., Mar 22 2019, In : International Journal of Molecular Sciences. 20, 6

Research output: Contribution to journalArticle

deletion
Megalencephaly
Mothers
Epilepsy
Phenotype