C. Cameli

Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility

E. Bacchelli, E. Maestrini, A. Posar, 2022, Frontiers in Psychiatry.

An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray

E. Bacchelli, A. Battaglia, R. Igliozzi, 2020, Scientific Reports.

Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility

J. Sutcliffe, E. Bacchelli, A. Battaglia, 2015, American journal of medical genetics. Part A.

Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder

E. Bacchelli, A. Battaglia, E. Maestrini, 2022, Frontiers in Genetics.

Analysis of a Sardinian Multiplex Family with Autism Spectrum Disorder Points to Post-Synaptic Density Gene Variants and Identifies CAPG as a Functionally Relevant Candidate Gene

E. Bacchelli, E. Maestrini, E. Bonora, 2019, Journal of clinical medicine.

An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder

E. Bacchelli, E. Maestrini, V. Carelli, 2021, Journal of cellular and molecular medicine.

Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies

H. Mefford, E. Bacchelli, P. Striano, 2019, Annals of clinical and translational neurology.