# Aarno Palotie

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/aarno-palotie/

## Facts

| Field | Value |
| --- | --- |
| Citations | 159,970 |
| Field | Genetic Associations and Epidemiology |
| h-index | 164 |
| i10-index | 714 |
| Last Known Institution | Broad Institute |
| OpenAlex ID | https://openalex.org/A5085708490 |
| ORCID iD | https://orcid.org/0000-0002-2527-5874 |
| Works | 1,224 |

## Researcher papers

Showing 12 of 20.

- [Biological insights from 108 schizophrenia-associated genetic loci](https://scholariq.org/papers/biological-insights-from-108-schizophrenia-associated-genetic-loci/)
- [Synaptic, transcriptional and chromatin genes disrupted in autism](https://scholariq.org/papers/synaptic-transcriptional-and-chromatin-genes-disrupted-in-autism/)
- [Identification of common genetic risk variants for autism spectrum disorder](https://scholariq.org/papers/identification-of-common-genetic-risk-variants-for-autism-spectrum-disorder/)
- [Traumatic brain injury: integrated approaches to improve prevention, clinical care, and research](https://scholariq.org/papers/traumatic-brain-injury-integrated-approaches-to-improve-prevention-clinical-care/)
- [Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism](https://scholariq.org/papers/large-scale-exome-sequencing-study-implicates-both-developmental-and-functional/)
- [A cross-population atlas of genetic associations for 220 human phenotypes](https://scholariq.org/papers/a-cross-population-atlas-of-genetic-associations-for-220-human-phenotypes/)
- [Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence](https://scholariq.org/papers/genome-wide-association-meta-analysis-in-269-867-individuals-identifies-new/)
- [Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls](https://scholariq.org/papers/genome-wide-association-study-of-cnvs-in-16-000-cases-of-eight-common-diseases/)
- [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/)
- [Rare coding variation provides insight into the genetic architecture and phenotypic context of autism](https://scholariq.org/papers/rare-coding-variation-provides-insight-into-the-genetic-architecture-and/)
- [Genome-wide association study identifies multiple loci influencing human serum metabolite levels](https://scholariq.org/papers/genome-wide-association-study-identifies-multiple-loci-influencing-human-serum/)
- [Taurine deficiency as a driver of aging](https://scholariq.org/papers/taurine-deficiency-as-a-driver-of-aging/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [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/)
- [Migraine and Headache Studies](https://scholariq.org/topics/migraine-and-headache-studies/)

## Researcher university

- [Broad Institute](https://scholariq.org/institutions/broad-institute/)

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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.