# Stephen W. Scherer

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/stephen-w-scherer/

## Facts

| Field | Value |
| --- | --- |
| Citations | 121,079 |
| Field | Genomic variations and chromosomal abnormalities |
| h-index | 155 |
| i10-index | 626 |
| Last Known Institution | University of Toronto |
| OpenAlex ID | https://openalex.org/A5049296994 |
| ORCID iD | https://orcid.org/0000-0002-8326-1999 |
| Works | 1,043 |

## Researcher papers

Showing 12 of 15.

- [Comprehensive genomic characterization defines human glioblastoma genes and core pathways](https://scholariq.org/papers/comprehensive-genomic-characterization-defines-human-glioblastoma-genes-and-core/)
- [Synaptic, transcriptional and chromatin genes disrupted in autism](https://scholariq.org/papers/synaptic-transcriptional-and-chromatin-genes-disrupted-in-autism/)
- [Detection of large-scale variation in the human genome](https://scholariq.org/papers/detection-of-large-scale-variation-in-the-human-genome/)
- [Mapping autism risk loci using genetic linkage and chromosomal rearrangements](https://scholariq.org/papers/mapping-autism-risk-loci-using-genetic-linkage-and-chromosomal-rearrangements/)
- [Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene](https://scholariq.org/papers/structure-and-chromosomal-localization-of-the-human-constitutive-endothelial/)
- [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/)
- [Rare coding variation provides insight into the genetic architecture and phenotypic context of autism](https://scholariq.org/papers/rare-coding-variation-provides-insight-into-the-genetic-architecture-and/)
- [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/)
- [Single cell-derived clonal analysis of human glioblastoma links functional and genomic heterogeneity](https://scholariq.org/papers/single-cell-derived-clonal-analysis-of-human-glioblastoma-links-functional-and/)
- [Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3](https://scholariq.org/papers/genome-wide-analysis-of-copy-number-variants-in-attention-deficit-hyperactivity/)
- [A role for common fragile site induction in amplification of human oncogenes](https://scholariq.org/papers/a-role-for-common-fragile-site-induction-in-amplification-of-human-oncogenes/)
- [Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence](https://scholariq.org/papers/genome-wide-detection-of-segmental-duplications-and-potential-assembly-errors-in/)

## Researcher topics

- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [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/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)

## Researcher university

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

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