# Arthur L. Beaudet

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/arthur-l-beaudet/

## Facts

| Field | Value |
| --- | --- |
| Citations | 58,676 |
| Field | Genomic variations and chromosomal abnormalities |
| h-index | 124 |
| i10-index | 380 |
| Last Known Institution | Baylor College of Medicine |
| OpenAlex ID | https://openalex.org/A5074963804 |
| ORCID iD | https://orcid.org/0000-0003-2083-3192 |
| Works | 523 |

## Researcher papers

- [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/)
- [Evaluation, Diagnosis, and Treatment of Gastrointestinal Disorders in Individuals With ASDs: A Consensus Report](https://scholariq.org/papers/evaluation-diagnosis-and-treatment-of-gastrointestinal-disorders-in-individuals/)
- [Decreased Resistance to Bacterial Infection and Granulocyte Defects in IAP-Deficient Mice](https://scholariq.org/papers/decreased-resistance-to-bacterial-infection-and-granulocyte-defects-in-iap/)
- [Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes](https://scholariq.org/papers/exome-sequencing-of-457-autism-families-recruited-online-provides-evidence-for/)
- [Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males](https://scholariq.org/papers/increased-mecp2-gene-copy-number-as-the-result-of-genomic-duplication-in/)
- [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/)
- [Derangements of Hippocampal Calcium/Calmodulin-Dependent Protein Kinase II in a Mouse Model for Angelman Mental Retardation Syndrome](https://scholariq.org/papers/derangements-of-hippocampal-calcium-calmodulin-dependent-protein-kinase-ii-in-a/)

## Researcher topics

- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Prenatal Screening and Diagnostics](https://scholariq.org/topics/prenatal-screening-and-diagnostics/)
- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-disorders/)

## 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.