# Timothy W. Yu

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/timothy-w-yu/

## Facts

| Field | Value |
| --- | --- |
| Citations | 24,845 |
| Field | Genomics and Rare Diseases |
| h-index | 58 |
| i10-index | 97 |
| Last Known Institution | Broad Institute |
| OpenAlex ID | https://openalex.org/A5067147799 |
| ORCID iD | https://orcid.org/0000-0003-2988-7701 |
| Works | 179 |

## Researcher papers

- [Synaptic, transcriptional and chromatin genes disrupted in autism](https://scholariq.org/papers/synaptic-transcriptional-and-chromatin-genes-disrupted-in-autism/)
- [Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci](https://scholariq.org/papers/insights-into-autism-spectrum-disorder-genomic-architecture-and-biology-from-71/)
- [Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism](https://scholariq.org/papers/multiple-recurrent-de-novo-cnvs-including-duplications-of-the-7q11-23-williams/)
- [Somatic Mutations in Cerebral Cortical Malformations](https://scholariq.org/papers/somatic-mutations-in-cerebral-cortical-malformations/)

## Researcher topics

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

## Researcher university

- [Broad Institute](https://scholariq.org/institutions/broad-institute/)

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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.