Pietropaolo, Susanna

Genetic-background modulation of core and variable autistic-like symptoms in Fmr1 knock-out mice

Pietropaolo, S., Guilleminot, A., Martin, B., D'Amato, F. R., & Crusio, W. E. (2011) · PLoS ONE

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 178

Rescue of fragile X syndrome phenotypes in Fmr1KO mice by a BKCa channel opener molecule

Hébert, B., Pietropaolo, S., Même, S., Laudier, B., Laugeray, A., Doisne, N., Quartier, A., Lefeuvre, S., Got, L., Cahard, D., et al. (2014) · Orphanet Journal of Rare Diseases

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 100

Age-related accumulation of Reelin in amyloid-like deposits

Knuesel, I., Nyffeler, M., Mormède, C., Muhia, M., Meyer, U., Pietropaolo, S., Yee, B. K., Pryce, C. R., LaFerla, F. M., Marighetto, A., et al. (2009) · Neurobiology of Aging

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 94

Dietary supplementation of omega-3 fatty acids rescues fragile X phenotypes in Fmr1-Ko mice

Pietropaolo, S., Goubran, M., Joffre, C., Aubert, A., Lemaire-Mayo, V., Crusio, W. E., & Layé, S. (2014) · Psychoneuroendocrinology

Genetics and Neurodevelopmental DisordersFatty Acid Research and Health

Cited by 63