Dalila C Pinto, PhD
Dr. Pinto is an Assistant Professor of Psychiatry, Genetics and Genomic Sciences, and a faculty member of the Icahn Genomics Insttitute. Dr. Pinto’s laboratory focuses on identifying genes and biological pathways involved in various neurodevelopmental disorders, including autism, intellectual disability, epilepsy, and rett syndrome-like phenotypes. Dr. Pinto integrates various forms of genetic variation (deletions, duplications, indels, single-point mutations), with gene expression, epigenetics and clinical data, using a combination of innovative high-throughput experimental and bioinformatics approaches, that altogether could implicate novel risk factors and provide insights into the mechanisms underlying these disorders. Dr. Pinto’s laboratory also works with worldwide clinical collaborators that are responsible for patients and families recruitment and phenotypic examination.
Autism, Bioinformatics, Chromatin, Computational Biology, Epilepsy, Gene Discovery, Gene Expressions, Gene Regulation, Genetics, Genomics, Mental Retardation, Microarray, Transcription Factors
Multi-Disciplinary Training Areas
Artificial Intelligence and Emerging Technologies in Medicine [AIET], Genetics and Genomic Sciences [GGS], Neuroscience [NEU]