# Dalila Pinto

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/dalila-pinto/

## Facts

| Field | Value |
| --- | --- |
| Citations | 37,298 |
| Field | Genomic variations and chromosomal abnormalities |
| h-index | 65 |
| i10-index | 113 |
| Last Known Institution | Allen Institute for Brain Science |
| OpenAlex ID | https://openalex.org/A5088479227 |
| ORCID iD | https://orcid.org/0000-0002-8769-0846 |
| Works | 187 |

## Researcher papers

Showing 12 of 13.

- [Functional impact of global rare copy number variation in autism spectrum disorders](https://scholariq.org/papers/functional-impact-of-global-rare-copy-number-variation-in-autism-spectrum/)
- [Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder](https://scholariq.org/papers/transcriptome-wide-isoform-level-dysregulation-in-asd-schizophrenia-and-bipolar/)
- [Comprehensive functional genomic resource and integrative model for the human brain](https://scholariq.org/papers/comprehensive-functional-genomic-resource-and-integrative-model-for-the-human/)
- [Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders](https://scholariq.org/papers/convergence-of-genes-and-cellular-pathways-dysregulated-in-autism-spectrum/)
- [Integrative functional genomic analysis of human brain development and neuropsychiatric risks](https://scholariq.org/papers/integrative-functional-genomic-analysis-of-human-brain-development-and/)
- [Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments](https://scholariq.org/papers/meta-analysis-of-shank-mutations-in-autism-spectrum-disorders-a-gradient-of/)
- [A genome-wide scan for common alleles affecting risk for autism](https://scholariq.org/papers/a-genome-wide-scan-for-common-alleles-affecting-risk-for-autism/)
- [The PsychENCODE project](https://scholariq.org/papers/the-psychencode-project/)
- [Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders](https://scholariq.org/papers/genetic-and-functional-analyses-of-shank2-mutations-suggest-a-multiple-hit-model/)
- [Individual common variants exert weak effects on the risk for autism spectrum disorders](https://scholariq.org/papers/individual-common-variants-exert-weak-effects-on-the-risk-for-autism-spectrum/)
- [Transcriptome and epigenome landscape of human cortical development modeled in organoids](https://scholariq.org/papers/transcriptome-and-epigenome-landscape-of-human-cortical-development-modeled-in/)
- [Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors](https://scholariq.org/papers/dissecting-the-shared-genetic-architecture-of-suicide-attempt-psychiatric/)

## Researcher topics

- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

- [Allen Institute for Brain Science](https://scholariq.org/institutions/allen-institute-for-brain-science/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.