# Nancy J. Minshew

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/nancy-j-minshew/

## Facts

| Field | Value |
| --- | --- |
| Citations | 43,792 |
| Field | Autism Spectrum Disorder Research |
| h-index | 103 |
| i10-index | 219 |
| Last Known Institution | University of Pittsburgh |
| OpenAlex ID | https://openalex.org/A5010132043 |
| ORCID iD | https://orcid.org/0000-0001-7875-1929 |
| Works | 380 |

## Researcher papers

Showing 12 of 13.

- [The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism](https://scholariq.org/papers/the-autism-brain-imaging-data-exchange-towards-a-large-scale-evaluation-of-the/)
- [Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism](https://scholariq.org/papers/large-scale-exome-sequencing-study-implicates-both-developmental-and-functional/)
- [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/)
- [Autism genome-wide copy number variation reveals ubiquitin and neuronal genes](https://scholariq.org/papers/autism-genome-wide-copy-number-variation-reveals-ubiquitin-and-neuronal-genes/)
- [Mapping autism risk loci using genetic linkage and chromosomal rearrangements](https://scholariq.org/papers/mapping-autism-risk-loci-using-genetic-linkage-and-chromosomal-rearrangements/)
- [Practice parameter: Screening and diagnosis of autism](https://scholariq.org/papers/practice-parameter-screening-and-diagnosis-of-autism/)
- [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/)
- [The Screening and Diagnosis of Autistic Spectrum Disorders](https://scholariq.org/papers/the-screening-and-diagnosis-of-autistic-spectrum-disorders/)
- [Common genetic variants on 5p14.1 associate with autism spectrum disorders](https://scholariq.org/papers/common-genetic-variants-on-5p14-1-associate-with-autism-spectrum-disorders/)
- [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/)
- [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/)
- [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/)

## Researcher topics

- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Behavioral and Psychological Studies](https://scholariq.org/topics/behavioral-and-psychological-studies/)
- [Attention Deficit Hyperactivity Disorder](https://scholariq.org/topics/attention-deficit-hyperactivity-disorder/)
- [Obsessive-Compulsive Spectrum Disorders](https://scholariq.org/topics/obsessive-compulsive-spectrum-disorders/)

## Researcher university

- [University of Pittsburgh](https://scholariq.org/institutions/university-of-pittsburgh/)

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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.