# Jan Hillert

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/jan-hillert/

## Facts

| Field | Value |
| --- | --- |
| Citations | 35,180 |
| Field | Multiple Sclerosis Research Studies |
| h-index | 89 |
| i10-index | 360 |
| Last Known Institution | Karolinska Institutet |
| OpenAlex ID | https://openalex.org/A5053300118 |
| ORCID iD | https://orcid.org/0000-0002-7386-6732 |
| Works | 581 |

## Researcher papers

- [Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility](https://scholariq.org/papers/multiple-sclerosis-genomic-map-implicates-peripheral-immune-cells-and-microglia/)
- [Multiple Sclerosis Severity Score](https://scholariq.org/papers/multiple-sclerosis-severity-score/)
- [Variants conferring risk of atrial fibrillation on chromosome 4q25](https://scholariq.org/papers/variants-conferring-risk-of-atrial-fibrillation-on-chromosome-4q25/)
- [The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm](https://scholariq.org/papers/the-same-sequence-variant-on-9p21-associates-with-myocardial-infarction/)
- [Effect of glatiramer acetate on conversion to clinically definite multiple sclerosis in patients with clinically isolated syndrome (PreCISe study): a randomised, double-blind, placebo-controlled trial](https://scholariq.org/papers/effect-of-glatiramer-acetate-on-conversion-to-clinically-definite-multiple/)
- [A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke](https://scholariq.org/papers/a-sequence-variant-in-zfhx3-on-16q22-associates-with-atrial-fibrillation-and/)
- [Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis](https://scholariq.org/papers/variation-in-interleukin-7-receptor-chain-il7r-influences-risk-of-multiple/)
- [Locus for severity implicates CNS resilience in progression of multiple sclerosis](https://scholariq.org/papers/locus-for-severity-implicates-cns-resilience-in-progression-of-multiple/)
- [Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk](https://scholariq.org/papers/low-frequency-and-rare-coding-variation-contributes-to-multiple-sclerosis-risk/)
- [Network-Based Multiple Sclerosis Pathway Analysis with GWAS Data from 15,000 Cases and 30,000 Controls](https://scholariq.org/papers/network-based-multiple-sclerosis-pathway-analysis-with-gwas-data-from-15-000/)

## Researcher topics

- [Multiple Sclerosis Research Studies](https://scholariq.org/topics/multiple-sclerosis-research-studies/)
- [Peripheral Neuropathies and Disorders](https://scholariq.org/topics/peripheral-neuropathies-and-disorders/)
- [Systemic Sclerosis and Related Diseases](https://scholariq.org/topics/systemic-sclerosis-and-related-diseases/)
- [T-cell and B-cell Immunology](https://scholariq.org/topics/t-cell-and-b-cell-immunology/)
- [Immunotherapy and Immune Responses](https://scholariq.org/topics/immunotherapy-and-immune-responses/)

## Researcher university

- [Karolinska Institutet](https://scholariq.org/institutions/karolinska-institutet/)

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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.
