# Matthew A. Brown

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/matthew-a-brown/

## Facts

| Field | Value |
| --- | --- |
| Citations | 86,456 |
| Field | Spondyloarthritis Studies and Treatments |
| h-index | 122 |
| i10-index | 529 |
| OpenAlex ID | https://openalex.org/A5006817439 |
| ORCID iD | https://orcid.org/0000-0003-0538-8211 |
| Works | 1,206 |

## Researcher papers

- [Genetics of rheumatoid arthritis contributes to biology and drug discovery](https://scholariq.org/papers/genetics-of-rheumatoid-arthritis-contributes-to-biology-and-drug-discovery/)
- [Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes](https://scholariq.org/papers/genomic-dissection-of-bipolar-disorder-and-schizophrenia-including-28/)
- [Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci](https://scholariq.org/papers/analysis-of-five-chronic-inflammatory-diseases-identifies-27-new-associations/)
- [Whole-genome sequencing of patients with rare diseases in a national health system](https://scholariq.org/papers/whole-genome-sequencing-of-patients-with-rare-diseases-in-a-national-health/)
- [Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease](https://scholariq.org/papers/comprehensive-rare-variant-analysis-via-whole-genome-sequencing-to-determine-the/)
- [Whole-genome sequencing of a sporadic primary immunodeficiency cohort](https://scholariq.org/papers/whole-genome-sequencing-of-a-sporadic-primary-immunodeficiency-cohort/)
- [Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans](https://scholariq.org/papers/loss-of-function-nuclear-factor-b-subunit-1-nfkb1-variants-are-the-most-common/)
- [Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans](https://scholariq.org/papers/defects-in-the-ift-b-component-ift172-cause-jeune-and-mainzer-saldino-syndromes/)
- [Phenotypic Characterization of <i>EIF2AK4</i> Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension](https://scholariq.org/papers/phenotypic-characterization-of-i-eif2ak4-i-mutation-carriers-in-a-large-cohort/)
- [Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations](https://scholariq.org/papers/characterization-of-the-clinical-and-immunologic-phenotype-and-management-of-157/)

## Researcher topics

- [Spondyloarthritis Studies and Treatments](https://scholariq.org/topics/spondyloarthritis-studies-and-treatments/)
- [Rheumatoid Arthritis Research and Therapies](https://scholariq.org/topics/rheumatoid-arthritis-research-and-therapies/)
- [Systemic Lupus Erythematosus Research](https://scholariq.org/topics/systemic-lupus-erythematosus-research/)
- [Psoriasis: Treatment and Pathogenesis](https://scholariq.org/topics/psoriasis-treatment-and-pathogenesis/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)

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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.