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European Journal of Medical Genetics|December 29, 2011
Thrombocytopenia-absent-radius syndrome in a child showing a larger 1q21.1 deletion than the one in his healthy mother, and a significant downregulation of the commonly deleted genesMaria Corsignano Guastadisegni, Roberta Roberto, Alberto L'Abbate, et al.
International Journal of Molecular Sciences|October 16, 2024
Genomic Sequencing to Detect Cross-Breeding Quality in Dogs: An Example Studying Disorders in Sexual DevelopmentLuciana de Gennaro, Matteo Burgio, Giovanni Michele Lacalandra, et al.
Frontiers in Oncology|June 23, 2022
Yeast as a Model to Unravel New BRCA2 Functions in Cell MetabolismAlessandra Costanza, Nicoletta Guaragnella, Antonella Bobba, et al.
International Journal of Molecular Sciences|November 14, 2023
Structural Variation Evolution at the 15q11-q13 Disease-Associated LocusAnnalisa Paparella, Alberto L'Abbate, Donato Palmisano, et al.
Human Cell|August 29, 2020
BL1391: an established cell line from a human malignant peripheral nerve sheath tumor with unique genomic featuresDoron Tolomeo, Antonio Agostini, Gemma Macchia, et al.
BMC Plant Biology|February 5, 2024
Distinct structural variants and repeat landscape shape the genomes of the ancient grapes Aglianico and FalanghinaRiccardo Aversano, Marina Iovene, Salvatore Esposito, et al.
Genes|February 23, 2020
Evolutionary Dynamics of the POTE Gene Family in Human and Nonhuman PrimatesFlavia Angela Maria Maggiolini, Ludovica Mercuri, Francesca Antonacci, et al.
Genome Research|September 30, 2022
A high-resolution map of small-scale inversions in the gibbon genomeLudovica Mercuri, Donato Palmisano, Alberto L'Abbate, et al.
Molecular Cancer|December 17, 2015
t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disordersAlberto L'Abbate, Doron Tolomeo, Francesca De Astis, et al.
Genes|July 29, 2023
Occurrence of L1M Elements in Chromosomal Rearrangements Associated to Chronic Myeloid Leukemia (CML): Insights from Patient-Specific Breakpoints CharacterizationAlberto L'Abbate, Vittoria Moretti, Ester Pungolino, et al.
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