Giulia Arrigo
Azienda Ospedaliera Citta' della Salute e della Scienza di Torino(IT)
Publications by Year
Research Areas
Chromosomal and Genetic Variations, Genomic variations and chromosomal abnormalities, Mesenchymal stem cell research, Acute Myeloid Leukemia Research, Cancer-related molecular mechanisms research
Most-Cited Works
- → Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients(2007)355 cited
- → A Human Homologue of the Drosophila melanogaster diaphanous Gene Is Disrupted in a Patient with Premature Ovarian Failure: Evidence for Conserved Function in Oogenesis and Implications for Human Sterility(1998)258 cited
- → Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome(2011)229 cited
- → 13q Deletion and central nervous system anomalies: further insights from karyotype–phenotype analyses of 14 patients(2007)144 cited
- → Eleven X Chromosome Breakpoints Associated with Premature Ovarian Failure (POF) Map to a 15-Mb YAC Contig Spanning Xq21(1997)130 cited
- → Molecular Cloning, Expression Pattern, and Chromosomal Localization of the Human Na–Cl Thiazide-Sensitive Cotransporter (SLC12A3)(1996)127 cited
- → Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements(2000)87 cited
- → Human NRD Convertase: A Highly Conserved Metalloendopeptidase Expressed at Specific Sites during Development and in Adult Tissues(1998)39 cited
- → Modern Risk Stratification of Acute Myeloid Leukemia in 2023: Integrating Established and Emerging Prognostic Factors(2023)29 cited
- → Comprehensive characterization of mesenchymal stromal cells from patients with Fanconi anaemia(2015)29 cited