Searching for New Possible Peripheral Biomarkers of Cognitive Decline in Down Syndrome: The Role of IL-18 Pathway and its Interaction with TGF-β1 and TNF-α - Margherita Grasso; Annamaria Fidilio; Francesca L’Episcopo; Marilena Recupero; Concetta Barone; Marta Lovino; Silvia Alboni; Maria Giulia Bacalini; Giuseppe Caruso; Donatella Greco; Serafino Buono; Rafael De La Torre; et al. (NeuroMolecular Medicine, 2026)

Role of long non-coding RNAs in Down syndrome patients: a transcriptome analysis study - Michele Salemi; Rossella Cannarella; Giovanna Marchese; Maria Grazia Salluzzo; Maria Ravo; Concetta Barone; Mariangela Lo Giudice; Aldo E. Calogero; Corrado Romano (Human Cell, 2021)

CCR3 gene overexpression in patients with Down syndrome - Michele Salemi; Rossella Cannarella; Giovanna Marchese; Maria Grazia Salluzzo; Maria Ravo; Concetta Barone; Angela Cordella; Salvatore Caniglia; Roberto Castiglione; Alda Ragalmuto; Aldo E. Calogero; Corrado Romano (Molecular Biology Reports, 2021)

Study of the MDM2 -410T-G polymorphism (rs2279744) by pyrosequencing in mothers of Down Syndrome subjects - Michele Salemi; Maria Grazia Salluzzo; Concetta Barone; Corrado Romano (Human Cell, 2020)

Expression of miR-132 in Down syndrome subjects - Michele Salemi; Concetta Barone; Maria Grazia Salluzzo; Mariaconcetta Giambirtone; Federico Ridolfo; Corrado Romano (Human Cell, 2018)

Mitochondrial mRNA expression in fibroblasts of Down syndrome subjects - Michele Salemi; Mariaconcetta Giambirtone; Concetta Barone; Maria Grazia Salluzzo; Roberto Russo; Mariangela Lo Giudice; Salvatore Cutuli; Federico Ridolfo; Corrado Romano (Human Cell, 2018)

Gene expression profiling and qRT-PCR expression of RRP1B, PCNT, KIF21A and ADRB2 in leucocytes of Down’s syndrome subjects - MICHELE SALEMI; CONCETTA BARONE; CORRADO ROMANO; FRANCESCA ZOLEZZI; CARMELO ROMANO; CATALDO SCAVUZZO; ROBERTO SALLUZZO; FRANCESCO SCILLATO; MARIA SIGNORELLI; DIMOS KAPETIS; MARIA GRAZIA SALLUZZO; PAOLO BOSCO (Journal of Genetics, 2014)

Marine metagenomics, a valuable tool for enzymes and bioactive compounds discovery - Rosalba Barone; Concetta De Santi; Fortunato Palma Esposito; Pietro Tedesco; Federica Galati; Marco Visone; Alessia Di Scala; Donatella De Pascale (Frontiers in Marine Science, 2014)

The MTRR 66A>G polymorphism and maternal risk of birth of a child with Down syndrome in Caucasian women: a case–control study and a meta-analysis - Fabio Coppedè; Paolo Bosco; Valentina Lorenzoni; Maria Denaro; Guido Anello; Ivana Antonucci; Concetta Barone; Liborio Stuppia; Corrado Romano; Lucia Migliore (Molecular Biology Reports, 2014)

CASP3 protein expression by flow cytometry in Down’s syndrome subjects - Michele Salemi; Rosita A. Condorelli; Corrado Romano; Barone Concetta; Carmelo Romano; Maria Grazia Salluzzo; Paolo Bosco; Aldo E. Calogero (Human Cell, 2014)

The MTR 2756A>G polymorphism and maternal risk of birth of a child with Down syndrome: a case–control study and a meta-analysis - Fabio Coppedè; Paolo Bosco; Valentina Lorenzoni; Francesca Migheli; Concetta Barone; Ivana Antonucci; Liborio Stuppia; Corrado Romano; Lucia Migliore (Molecular Biology Reports, 2013)

Expression of LDOC1 mRNA in leucocytes of patients with Down’s syndrome - MICHELE SALEMI; CONCETTA BARONE; CARMELO ROMANO; FEDERICO RIDOLFO; ROBERTO SALLUZZO; FRANCESCO SCILLATO; CATALDO SCAVUZZO; FILIPPO CARACI; ALDO E. CALOGERO; CORRADO ROMANO; PAOLO BOSCO (Journal of Genetics, 2012)

Differential expression of PARP1 mRNA in leucocytes of patients with Down’s syndrome - MICHELE SALEMI; CONCETTA BARONE; CARMELO ROMANO; FEDERICO RIDOLFO; ELEONORA GULOTTA; CATALDO SCAVUZZO; MARIA GRAZIA SALLUZZO; MARIACONCETTA GIAMBIRTONE; FILIPPO CARACI; CORRADO ROMANO; PAOLO BOSCO (Journal of Genetics, 2011)

SPANX-B and SPANX-C (Xq27 region) gene dosage analysis in Down’s syndrome subjects with undescended testes - Michele Salemi; Corrado Romano; Concetta Barone; Francesco Calí; Filippo Caraci; Carmelo Romano; Cataldo Scavuzzo; Francesco Scillato; Maria Grazia Salluzzo; Maria Piccione; Manuela Martines; Giovanni Corsello; et al. (Journal of Genetics, 2009)