Fallerini, Chiara

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

Satterstrom, F. K., Kosmicki, J. A., Wang, J., Breen, M. S., De Rubeis, S., An, J.-Y., Peng, M., Collins, R., Grove, J., Klei, L., et al. (2018) · Cell

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 2,323

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Satterstrom, F. K., Kosmicki, J. A., Wang, J., Breen, M. S., De Rubeis, S., An, J.-Y., Peng, M., Collins, R., Grove, J., Klei, L., et al. (2020) · Cell

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 2,321

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Fu, J. M., Satterstrom, F. K., Peng, M., Brand, H., Collins, R. L., Dong, S., Wamsley, B., Klei, L., Wang, L., Hao, S. P., et al. (2022) · Nature Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 640

Human CRY1 variants associate with attention deficit/hyperactivity disorder

Onat, O. E., Kars, M. E., Gül, Ş., Bilguvar, K., Wu, Y., Özhan, A., Aydın, C., Başak, A. N., Trusso, M. A., Goracci, A., et al. (2020) · Journal of Clinical Investigation

Circadian rhythm and melatoninAttention Deficit Hyperactivity Disorder

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Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal Phenotype

Doddato, G., Fabbiani, A., Fallerini, C., Bruttini, M., Hadjistilianou, T., Landi, M., Coradeschi, C., Grosso, S., Tomasini, B., Mencarelli, M. A., et al. (2021) · Frontiers in Genetics

Connective tissue disorders researchProteoglycans and glycosaminoglycans research

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