# Jurgen Del‐Favero

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/jurgen-del-favero/

## Facts

| Field | Value |
| --- | --- |
| Citations | 18,297 |
| Field | Genetic Associations and Epidemiology |
| h-index | 63 |
| i10-index | 144 |
| Last Known Institution | Agilent Technologies (Belgium) |
| OpenAlex ID | https://openalex.org/A5040603856 |
| ORCID iD | https://orcid.org/0000-0002-7427-7489 |
| Works | 254 |

## Researcher papers

- [Genome-wide association study identifies 30 loci associated with bipolar disorder](https://scholariq.org/papers/genome-wide-association-study-identifies-30-loci-associated-with-bipolar/)
- [De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy](https://scholariq.org/papers/de-novo-mutations-in-the-sodium-channel-gene-scn1a-cause-severe-myoclonic/)
- [Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects](https://scholariq.org/papers/contribution-of-copy-number-variants-to-schizophrenia-from-a-genome-wide-study/)
- [VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death](https://scholariq.org/papers/vegf-is-a-modifier-of-amyotrophic-lateral-sclerosis-in-mice-and-humans-and/)
- [Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases](https://scholariq.org/papers/partitioning-heritability-of-regulatory-and-cell-type-specific-variants-across/)
- [Mutations in SEPT9 cause hereditary neuralgic amyotrophy](https://scholariq.org/papers/mutations-in-sept9-cause-hereditary-neuralgic-amyotrophy/)
- [A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts](https://scholariq.org/papers/a-comparison-of-ten-polygenic-score-methods-for-psychiatric-disorders-applied/)

## 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/)
- [Bipolar Disorder and Treatment](https://scholariq.org/topics/bipolar-disorder-and-treatment/)

## Researcher university

- [Agilent Technologies (Belgium)](https://scholariq.org/institutions/agilent-technologies-belgium/)

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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.