# Andrew O.M. Wilkie

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/andrew-o-m-wilkie/

## Facts

| Field | Value |
| --- | --- |
| Citations | 29,727 |
| Field | Craniofacial Disorders and Treatments |
| h-index | 88 |
| i10-index | 254 |
| Last Known Institution | Nuffield Orthopaedic Centre |
| OpenAlex ID | https://openalex.org/A5015376243 |
| ORCID iD | https://orcid.org/0000-0002-2972-5481 |
| Works | 458 |

## Researcher papers

- [Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2](https://scholariq.org/papers/recessive-robinow-syndrome-allelic-to-dominant-brachydactyly-type-b-is-caused-by/)
- [Germline selection shapes human mitochondrial DNA diversity](https://scholariq.org/papers/germline-selection-shapes-human-mitochondrial-dna-diversity/)
- [Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism](https://scholariq.org/papers/genetic-heterogeneity-in-cornelia-de-lange-syndrome-cdls-and-cdls-like/)

## Researcher topics

- [Craniofacial Disorders and Treatments](https://scholariq.org/topics/craniofacial-disorders-and-treatments/)
- [Cleft Lip and Palate Research](https://scholariq.org/topics/cleft-lip-and-palate-research/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

- [Nuffield Orthopaedic Centre](https://scholariq.org/institutions/nuffield-orthopaedic-centre/)

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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.