# Jacob Vorstman

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/jacob-vorstman/

## Facts

| Field | Value |
| --- | --- |
| Citations | 16,736 |
| Field | Congenital heart defects research |
| h-index | 55 |
| i10-index | 124 |
| Last Known Institution | University of Toronto |
| OpenAlex ID | https://openalex.org/A5043050652 |
| ORCID iD | https://orcid.org/0000-0002-1677-3126 |
| Works | 248 |

## Researcher papers

- [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/)
- [Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome](https://scholariq.org/papers/psychiatric-disorders-from-childhood-to-adulthood-in-22q11-2-deletion-syndrome/)
- [Preventive strategies for mental health](https://scholariq.org/papers/preventive-strategies-for-mental-health/)
- [Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome](https://scholariq.org/papers/cognitive-decline-preceding-the-onset-of-psychosis-in-patients-with-22q11-2/)
- [A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder](https://scholariq.org/papers/a-novel-approach-of-homozygous-haplotype-sharing-identifies-candidate-genes-in/)
- [Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion](https://scholariq.org/papers/genetic-contributors-to-risk-of-schizophrenia-in-the-presence-of-a-22q11-2/)

## Researcher topics

- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

- [University of Toronto](https://scholariq.org/institutions/university-of-toronto/)

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