
Dalila C Pinto, PhD
About Me
Dr. Pinto is a tenured Associate Professor of Psychiatry, Genetics and Genomic Sciences, and a faculty member of the Mindich Child Health and Development Institute, the Seaver Autism Center, the Friedman Brain Institute, and the Icahn Genomics Institute. 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.
Language
English
Position
ASSOCIATE PROFESSOR | Psychiatry, ASSOCIATE PROFESSOR | Genetics and Genomic Sciences
Research Topics
Autism, Bioinformatics, Computational Biology, Epilepsy, Gene Expressions, Gene Regulation, Genetics, Genomics, Human Genetics and Genetic Disorders, RNA
Multi-Disciplinary Training Areas
Artificial Intelligence and Emerging Technologies in Medicine [AIET], Genetics and Genomic Sciences [GGS], Neuroscience [NEU]
Education
MSc, MSc, University of Porto
PhD, University of Utrecht
Postdoctoral, Hospital for Sick Children Toronto
Research
Publications
Selected Publications
- Defining suicidality phenotypes for genetic studies: perspectives of the Psychiatric Genomics Consortium Suicide Working Group. Sarah M.C. Colbert, Eric T. Monson, Ole A. Andreassen, Olatunde O. Ayinde, Peter B. Barr, Cosmin A. Bejan, Zuriel Ceja, Hilary Coon, Emily DiBlasi, Howard J. Edenberg, Joel Gelernter, Alexander Hatoum, Anastasia Izotova, Emma C. Johnson, Erin A. Kaufman, Henry R. Kranzler, Maria Koromina, Kelli Lehto, Woojae Myung, John I. Nurnberger, Alessandro Serretti, Jordan W. Smoller, Murray B. Stein, Clement C. Zai, Annette Erlangsen, Marie Gaine, Lourdes Martorell, Reeteka Sud, Claudio Toma, Tim B. Bigdeli, Nathan A. Kimbrel, Douglas Ruderfer, Anna R. Docherty, J. John Mann, Niamh Mullins, Lea Zillich, Zeynep Yilmaz, Naomi R. Wray, D. Blake Woodside, Stephanie H. Witt, Virginia Willour, Leanne M. Williams, David C. Whiteman, Thomas Werge, Frank Wendt, Myrna M. Weissman, Thomas W. Weickert, Dalila Pinto, René S. Kahn, Douglas M. Ruderfer. Molecular Psychiatry
- Impact of common variants on brain gene expression from RNA to protein to schizophrenia risk. Qiuman Liang, Yi Jiang, Annie W. Shieh, Dan Zhou, Rui Chen, Feiran Wang, Meng Xu, Mingming Niu, Xusheng Wang, Dalila Pinto, Yue Wang, Lijun Cheng, Ramu Vadukapuram, Chunling Zhang, Kay Grennan, Gina Giase, Kevin P. White, Junmin Peng, Bingshan Li, Chunyu Liu, Chao Chen, Sidney H. Wang. Nature Communications
- A map of enhancer regions in primary human neural progenitor cells using capture STARR-seq. Sophia C. Gaynor-Gillett, Lijun Cheng, Manman Shi, Jason Liu, Gaoyuan Wang, Megan Spector, Qiuyu Guo, Le Qi, Mary Flaherty, Martha Wall, Ahyeon Hwang, Mengting Gu, Zhanlin Chen, Yuhang Chen, Jennifer R. Moran, Jing Zhang, Donghoon Lee, Mark Gerstein, Daniel H. Geschwind, Kevin P. White, Schahram Akbarian, Alexej Abyzov, Nadav Ahituv, Dhivya Arasappan, Jose Juan Almagro Armenteros, Brian J. Beliveau, Jaroslav Bendl, Sabina Berretta, Rahul A. Bharadwaj, Arjun Bhattacharya, Lucy Bicks, Kristen Brennand, Davide Capauto, Frances A. Champagne, Tanima Chatterjee, Chris Chatzinakos, Andrew Chess, Nikolaos P. Daskalakis, John F. Fullard, Kiran Girdhar, Vahram Haroutunian, Gabriel E. Hoffman, Alex Kozlenkov, Dalila Pinto, Towfique Raj, Panos Roussos, Robert Sebra, Harm van Bakel, Georgios Voloudakis, Biao Zeng. Genome Research