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Scientific Reports|February 22, 2020
An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArrayElena Bacchelli, Cinzia Cameli, Marta Viggiano, et al.
American Journal of Medical Genetics. Part A|February 7, 2015
Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibilityElena Bacchelli, Agatino Battaglia, Cinzia Cameli, et al.
The Journal of Headache and Pain|December 14, 2016
A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variantsElena Bacchelli, Maria Michela Cainazzo, Cinzia Cameli, et al.
European Journal of Human Genetics : EJHG|August 10, 2018
Genetic variation in CHRNA7 and CHRFAM7A is associated with nicotine dependence and response to varenicline treatmentCinzia Cameli, Elena Bacchelli, Maria De Paola, et al.
Journal of Cellular and Molecular Medicine|December 5, 2019
ELMOD3-SH2D6 gene fusion as a possible co-star actor in autism spectrum disorder scenarioEleonora Loi, Loredana Moi, Sylvain Blois, et al.
Brain Sciences|October 21, 2020
Brain Magnetic Resonance Findings in 117 Children with Autism Spectrum Disorder under 5 Years OldMagali Jane Rochat, Giacomo Distefano, Monica Maffei, et al.
Frontiers in Psychiatry|March 30, 2022
Contribution of CACNA1H Variants in Autism Spectrum Disorder SusceptibilityMarta Viggiano, Tiziano D'Andrea, Cinzia Cameli, et al.
Oncotarget|March 24, 2018
Integrated DNA methylation analysis identifies topographical and tumoral biomarkers in pilocytic astrocytomasManila Antonelli, Antonio Fadda, Eleonora Loi, et al.
Research Square|November 14, 2023
Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum DisorderElena Bacchelli, Marta Viggiano, Fabiola Ceroni, et al.
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