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Genes|November 24, 2022
Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying NSD1 VariantsMarco Ferilli, Andrea Ciolfi, Lucia Pedace, et al.Cancer Letters|February 29, 2024
Clinicopathological and molecular landscape of 5-year IDH-wild-type glioblastoma survivors: A multicentric retrospective studyEvelina Miele, Elena Anghileri, Chiara Calatozzolo, et al.International Journal of Molecular Sciences|February 15, 2022
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related SyndromeAidin Foroutan, Sadegheh Haghshenas, Pratibha Bhai, et al.American Journal of Human Genetics|October 21, 2023
Identification of a robust DNA methylation signature for Fanconi anemiaDaria Pagliara, Andrea Ciolfi, Lucia Pedace, et al.Leukemia|June 20, 2020
Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiencyEmilia J Kozyra, Victor B Pastor, Stylianos Lefkopoulos, et al.American Journal of Human Genetics|August 27, 2019
Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature AgingElisabetta Flex, Simone Martinelli, Anke Van Dijck, et al.American Journal of Human Genetics|February 17, 2021
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in femalesFrancesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, et al.Pageof 5