# Stanley F. Nelson

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/stanley-f-nelson/

## Facts

| Field | Value |
| --- | --- |
| Citations | 36,614 |
| Field | Genomics and Rare Diseases |
| h-index | 98 |
| i10-index | 237 |
| OpenAlex ID | https://openalex.org/A5073896107 |
| ORCID iD | https://orcid.org/0000-0002-2082-3114 |
| Works | 419 |

## Researcher papers

- [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/)
- [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/)
- [C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy](https://scholariq.org/papers/c-terminal-truncations-in-human-3-5-dna-exonuclease-trex1-cause-autosomal/)
- [Epidermal Growth Factor Receptor Activation in Glioblastoma through Novel Missense Mutations in the Extracellular Domain](https://scholariq.org/papers/epidermal-growth-factor-receptor-activation-in-glioblastoma-through-novel/)
- [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 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/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Muscle Physiology and Disorders](https://scholariq.org/topics/muscle-physiology-and-disorders/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Glioma Diagnosis and Treatment](https://scholariq.org/topics/glioma-diagnosis-and-treatment/)

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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.