# Chad A. Shaw

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/chad-a-shaw/

## Facts

| Field | Value |
| --- | --- |
| Citations | 28,897 |
| Field | Genomic variations and chromosomal abnormalities |
| h-index | 90 |
| i10-index | 215 |
| Last Known Institution | Baylor College of Medicine |
| OpenAlex ID | https://openalex.org/A5072387201 |
| ORCID iD | https://orcid.org/0000-0001-7267-5398 |
| Works | 399 |

## Researcher papers

- [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/)
- [Characterization of Potocki-Lupski Syndrome (dup(17)(p11.2p11.2)) and Delineation of a Dosage-Sensitive Critical Interval That Can Convey an Autism Phenotype](https://scholariq.org/papers/characterization-of-potocki-lupski-syndrome-dup-17-p11-2p11-2-and-delineation-of/)
- [Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases](https://scholariq.org/papers/clinical-use-of-array-comparative-genomic-hybridization-acgh-for-prenatal/)

## Researcher topics

- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Prenatal Screening and Diagnostics](https://scholariq.org/topics/prenatal-screening-and-diagnostics/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [Cancer Cells and Metastasis](https://scholariq.org/topics/cancer-cells-and-metastasis/)

## Researcher university

- [Baylor College of Medicine](https://scholariq.org/institutions/baylor-college-of-medicine/)

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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.