Galesi, Ornella
I.R.C.C.S. Oasi Maria SS
2 papers on CoChatORCID 0000-0002-7877-938X
Most cited papers
- Verified
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome
Bonaglia, M. C., Giorda, R., Beri, S., De Agostini, C., Novara, F., Fichera, M., Grillo, L., Galesi, O., Vetro, A., Ciccone, R., et al. (2011) · PLoS Genetics
Genomic variations and chromosomal abnormalitiesDNA Repair Mechanisms
Cited by 224
- Verified
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants
Pizzo, L., Jensen, M., Polyak, A., Rosenfeld, J. A., Mannik, K., Krishnan, A., McCready, E., Pichon, O., Le Caignec, C., Van Dijck, A., et al. (2019) · Genetics in Medicine
Genomic variations and chromosomal abnormalitiesGenomics and Rare Diseases
Cited by 193
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