Giada Ariaudo

Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

Yanick J. Crow, Diana Chase, Johanna L. Schmidt et al. · American Journal of Medical Genetics Part A · 2015 · 613 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling

Gillian Rice, Yoandris del Toro Duany, Emma M. Jenkinson et al. · Nature Genetics · 2014 · 591 citations · Full text

Life Sciences, Genetics, Molecular Biology +16

Depressive symptoms and maternal psychological distress during early infancy: A pilot study in preterm as compared with term mother–infant dyads

Camilla Pisoni, Silvia Spairani, Federica Manzoni et al. · Journal of Affective Disorders · 2019 · 42 citations

Social Sciences, Pediatrics, Psychology +17

Effect of maternal psychopathology on neurodevelopmental outcome and quality of the dyadic relationship in preterm infants: an explorative study

Camilla Pisoni, Silvia Spairani, F Fauci et al. · The Journal of Maternal-Fetal & Neonatal Medicine · 2018 · 32 citations

Social Sciences, Pediatrics, Psychology +17

Outcome of extremely low birth weight infants: What's new in the third millennium? Neuropsychological profiles at four years

Ivana Olivieri, Stefania Maria Bova, Cosimo Urgesi et al. · Early Human Development · 2011 · 28 citations

Public Health, Child Health, Pediatrics +16