# Richard Anney

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/richard-anney/

## Facts

| Field | Value |
| --- | --- |
| Citations | 25,340 |
| Field | Autism Spectrum Disorder Research |
| h-index | 60 |
| i10-index | 123 |
| OpenAlex ID | https://openalex.org/A5023294157 |
| ORCID iD | https://orcid.org/0000-0002-6083-407X |
| Works | 191 |

## Researcher papers

Showing 12 of 18.

- [Identification of common genetic risk variants for autism spectrum disorder](https://scholariq.org/papers/identification-of-common-genetic-risk-variants-for-autism-spectrum-disorder/)
- [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/)
- [Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders](https://scholariq.org/papers/genomic-relationships-novel-loci-and-pleiotropic-mechanisms-across-eight/)
- [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/)
- [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/)
- [Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder](https://scholariq.org/papers/meta-analysis-of-genome-wide-association-studies-of-attention-deficit/)
- [Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder](https://scholariq.org/papers/genome-wide-copy-number-variation-study-associates-metabotropic-glutamate/)
- [Genome‐wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations](https://scholariq.org/papers/genome-wide-association-scan-of-quantitative-traits-for-attention-deficit/)
- [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/)
- [Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence](https://scholariq.org/papers/emotional-lability-in-children-and-adolescents-with-attention-deficit/)
- [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/)

## Researcher topics

- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Attention Deficit Hyperactivity Disorder](https://scholariq.org/topics/attention-deficit-hyperactivity-disorder/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [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/)

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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.