# Wendy K. Chung

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/wendy-k-chung/

## Facts

| Field | Value |
| --- | --- |
| Citations | 75,140 |
| Field | Genomics and Rare Diseases |
| h-index | 127 |
| i10-index | 670 |
| Last Known Institution | Boston Children's Hospital |
| OpenAlex ID | https://openalex.org/A5018722278 |
| ORCID iD | https://orcid.org/0000-0003-3438-5685 |
| Works | 1,255 |

## Researcher papers

Showing 12 of 14.

- [Risks of Breast, Ovarian, and Contralateral Breast Cancer for <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers](https://scholariq.org/papers/risks-of-breast-ovarian-and-contralateral-breast-cancer-for-i-brca1-i-and-i/)
- [Strong Association of De Novo Copy Number Mutations with Autism](https://scholariq.org/papers/strong-association-of-de-novo-copy-number-mutations-with-autism/)
- [Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care](https://scholariq.org/papers/diagnosis-and-management-of-spinal-muscular-atrophy-part-1-recommendations-for/)
- [Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways](https://scholariq.org/papers/exome-sequencing-in-amyotrophic-lateral-sclerosis-identifies-risk-genes-and/)
- [Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses](https://scholariq.org/papers/genome-wide-association-study-identifies-32-novel-breast-cancer-susceptibility/)
- [Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer](https://scholariq.org/papers/identification-of-12-new-susceptibility-loci-for-different-histotypes-of/)
- [Association of Type and Location of<i>BRCA1</i>and<i>BRCA2</i>Mutations With Risk of Breast and Ovarian Cancer](https://scholariq.org/papers/association-of-type-and-location-of-i-brca1-i-and-i-brca2-i-mutations-with-risk/)
- [High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies](https://scholariq.org/papers/high-rate-of-recurrent-de-novo-mutations-in-developmental-and-epileptic/)
- [Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between](https://scholariq.org/papers/return-of-genomic-results-to-research-participants-the-floor-the-ceiling-and-the/)
- [Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease](https://scholariq.org/papers/genes-that-affect-brain-structure-and-function-identified-by-rare-variant/)
- [Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities](https://scholariq.org/papers/defining-the-effect-of-the-16p11-2-duplication-on-cognition-behavior-and-medical/)
- [Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders](https://scholariq.org/papers/large-scale-targeted-sequencing-identifies-risk-genes-for-neurodevelopmental/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [BRCA gene mutations in cancer](https://scholariq.org/topics/brca-gene-mutations-in-cancer/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [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/)

## Researcher university

- [Boston Children's Hospital](https://scholariq.org/institutions/boston-children-s-hospital/)

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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.