# Per Hoffmann

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/per-hoffmann/

## Facts

| Field | Value |
| --- | --- |
| Citations | 48,171 |
| Field | Genetic Associations and Epidemiology |
| h-index | 93 |
| i10-index | 321 |
| Last Known Institution | University of Bonn |
| OpenAlex ID | https://openalex.org/A5026517521 |
| ORCID iD | https://orcid.org/0000-0002-6573-983X |
| Works | 702 |

## Researcher papers

Showing 12 of 13.

- [Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression](https://scholariq.org/papers/genome-wide-association-analyses-identify-44-risk-variants-and-refine-the/)
- [Analysis of shared heritability in common disorders of the brain](https://scholariq.org/papers/analysis-of-shared-heritability-in-common-disorders-of-the-brain/)
- [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/)
- [Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology](https://scholariq.org/papers/genome-wide-association-study-of-more-than-40-000-bipolar-disorder-cases/)
- [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/)
- [Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease](https://scholariq.org/papers/rare-coding-variants-in-plcg2-abi3-and-trem2-implicate-microglial-mediated/)
- [Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity](https://scholariq.org/papers/identification-of-15-new-psoriasis-susceptibility-loci-highlights-the-role-of/)
- [The genetic architecture of the human cerebral cortex](https://scholariq.org/papers/the-genetic-architecture-of-the-human-cerebral-cortex/)
- [Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders](https://scholariq.org/papers/transancestral-gwas-of-alcohol-dependence-reveals-common-genetic-underpinnings/)
- [Disruption of the neurexin 1 gene is associated with schizophrenia](https://scholariq.org/papers/disruption-of-the-neurexin-1-gene-is-associated-with-schizophrenia/)
- [Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes](https://scholariq.org/papers/mutations-in-grin2a-cause-idiopathic-focal-epilepsy-with-rolandic-spikes/)
- [Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility](https://scholariq.org/papers/low-frequency-and-rare-exome-chip-variants-associate-with-fasting-glucose-and/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Bipolar Disorder and Treatment](https://scholariq.org/topics/bipolar-disorder-and-treatment/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)

## Researcher university

- [University of Bonn](https://scholariq.org/institutions/university-of-bonn/)

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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.