Vincenzo Antona

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags et al. · Human Molecular Genetics · 2013 · 175 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance

Maria Vittoria Cubellis, Laura Pignata, Ankit Verma et al. · Clinical Epigenetics · 2020 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Negative Regulation of β Enolase Gene Transcription in Embryonic Muscle Is Dependent upon a Zinc Finger Factor That Binds to the G-rich Box within the Muscle-specific Enhancer

Rosa Passantino, Vincenzo Antona, Giovanna Barbieri et al. · Journal of Biological Chemistry · 1998 · 63 citations · Full text

Life Sciences, Genetics, Molecular Biology +16

Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 gene

Gregorio Serra, Sofia Felice, Vincenzo Antona et al. · ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics · 2022 · 60 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion

Ingrid Anne Mandy Schierz, Gregorio Serra, Vincenzo Antona et al. · Clinical Dysmorphology · 2020 · 57 citations · Full text

Life Sciences, Developmental Biology, Genetics +9