
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
- Genetic regulation of human brain proteome reveals proteins implicated in psychiatric disorders. Jie Luo, Ling Li, Mingming Niu, Dehui Kong, Yi Jiang, Suresh Poudel, Annie W. Shieh, Lijun Cheng, Gina Giase, Kay Grennan, Kevin P. White, Chao Chen, Sidney H. Wang, Dalila Pinto, Yue Wang, Chunyu Liu, Junmin Peng, Xusheng Wang. Molecular Psychiatry
- Enrichment of Rare Variants of Hemophagocytic Lymphohistiocytosis Genes in Systemic Juvenile Idiopathic Arthritis. Mariana Correia Marques, Danielle Rubin, Emily G. Shuldiner, Mallika Datta, Elizabeth Schmitz, Gustavo Gutierrez Cruz, Andrew Patt, Elizabeth Bennett, Alexei Grom, Dirk Foell, Marco Gattorno, John Bohnsack, Rae S.M. Yeung, Sampath Prahalad, Elizabeth Mellins, Jordi Anton, Claudio A. Len, Sheila Oliveira, Patricia Woo, Seza Ozen, Zuoming Deng, Michael J. Ombrello, Jean Paul Achkar, Marta E. Alarcón-Riquelme, Jordi Anton, Victoria L. Arthur, Elizabeth Baskin, John F. Bohnsack, Joanna Cobb, Erkan Demirkaya, Elisa Docampo, Richard H. Duerr, Xavier Estivill, Dirk Foell, Marco Gattorno, Alexei Grom, Ahmet Gül, Maria Odete E. Hilario, Norman T. Ilowite, Johannes Peter Haas, Anne Hinks, M. Ilyas Kamboh, Daniel L. Kastner, Kenneth M. Kaufman, Leah C. Kottyan, Carl D. Langefeld, Claudio Len, Elizabeth D. Mellins, Kirsten Minden, Dalila Pinto. Arthritis and Rheumatology
- Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Samuel F. Berkovic, Benjamin M. Neale, Gábor Zsurka, Milena Zizovic, Fritz Zimprich, Federico Zara, Felix Zahnert, Sara Zagaglia, Emrah Yücesan, Robert Yolken, Uluc Yis, Zuhal Yapıcı, Kazuhiro Yamakawa, David Wu, Randi von Wrede, Isaac Wong, Stefan Wolking, Markus Wolff, Steven M. Wolf, Samuel Wiebe, Peter Widdess-Walsh, Sarah Weckhuysen, Yvonne G. Weber, Nick Watts, Ryan G. Wagner, Sarah von Spiczak, Sophie von Brauchitsch, Markéta Vlčková, Annalisa Vetro, Maria Stella Vari, Andreas van Baalen, Luc Valton, Priya Vaidiswaran, Algirdas Utkus, Sibel Uğur-İşeri, Dilsad Turkdogan, Birute Tumiene, Meng Han Tsai, Pınar Topaloglu, Marian Todaro, Paolo Tinuper, Nicholas John Timpson, Oskari Timonen, George A. Tanteles, Randip S. Taneja, Hillary R. Raynes, Dalila Pinto, Lara Marcuse, Chelsea Lowther, Madeline C. Fields. Nature Neuroscience