# Michael J. Owen

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/michael-j-owen/

## Facts

| Field | Value |
| --- | --- |
| Citations | 124,799 |
| Field | Genetic Associations and Epidemiology |
| h-index | 166 |
| i10-index | 747 |
| Last Known Institution | Genomics (United Kingdom) |
| OpenAlex ID | https://openalex.org/A5026352442 |
| ORCID iD | 0000-0003-4798-0862 |
| Works | 1,216 |

## Researcher papers

Showing 12 of 20.

- [Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease](https://scholariq.org/papers/genome-wide-association-study-identifies-variants-at-clu-and-picalm-associated/)
- [Synaptic, transcriptional and chromatin genes disrupted in autism](https://scholariq.org/papers/synaptic-transcriptional-and-chromatin-genes-disrupted-in-autism/)
- [Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development](https://scholariq.org/papers/cbfa1-a-candidate-gene-for-cleidocranial-dysplasia-syndrome-is-essential-for/)
- [Analysis of shared heritability in common disorders of the brain](https://scholariq.org/papers/analysis-of-shared-heritability-in-common-disorders-of-the-brain/)
- [Schizophrenia](https://scholariq.org/papers/schizophrenia/)
- [Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection](https://scholariq.org/papers/common-schizophrenia-alleles-are-enriched-in-mutation-intolerant-genes-and-in/)
- [Genome-wide association analysis identifies 13 new risk loci for schizophrenia](https://scholariq.org/papers/genome-wide-association-analysis-identifies-13-new-risk-loci-for-schizophrenia/)
- [Integrative functional genomic analysis of human brain development and neuropsychiatric risks](https://scholariq.org/papers/integrative-functional-genomic-analysis-of-human-brain-development-and/)
- [Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome](https://scholariq.org/papers/psychiatric-disorders-from-childhood-to-adulthood-in-22q11-2-deletion-syndrome/)
- [Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease](https://scholariq.org/papers/genetic-evidence-implicates-the-immune-system-and-cholesterol-metabolism-in-the/)
- [Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis](https://scholariq.org/papers/rare-chromosomal-deletions-and-duplications-in-attention-deficit-hyperactivity/)
- [Candidate Single-Nucleotide Polymorphisms From a Genomewide Association Study of Alzheimer Disease](https://scholariq.org/papers/candidate-single-nucleotide-polymorphisms-from-a-genomewide-association-study-of/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)

## Researcher university

- [Genomics (United Kingdom)](https://scholariq.org/institutions/genomics-united-kingdom/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.