# Julian Maller

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/julian-maller/

## Facts

| Field | Value |
| --- | --- |
| Citations | 78,882 |
| Field | Genetic Associations and Epidemiology |
| h-index | 37 |
| i10-index | 46 |
| OpenAlex ID | https://openalex.org/A5026130275 |
| ORCID iD | https://orcid.org/0000-0002-1565-9559 |
| Works | 57 |

## Researcher papers

- [The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans](https://scholariq.org/papers/the-genotype-tissue-expression-gtex-pilot-analysis-multitissue-gene-regulation/)
- [A second generation human haplotype map of over 3.1 million SNPs](https://scholariq.org/papers/a-second-generation-human-haplotype-map-of-over-3-1-million-snps/)
- [Identification of common genetic risk variants for autism spectrum disorder](https://scholariq.org/papers/identification-of-common-genetic-risk-variants-for-autism-spectrum-disorder/)
- [Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder](https://scholariq.org/papers/discovery-of-the-first-genome-wide-significant-risk-loci-for-attention-deficit/)
- [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/)
- [Correction: Corrigendum: Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases](https://scholariq.org/papers/correction-corrigendum-synchronized-age-related-gene-expression-changes-across/)
- [Genome‐wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations](https://scholariq.org/papers/genome-wide-association-scan-of-quantitative-traits-for-attention-deficit/)
- [Effect of predicted protein-truncating genetic variants on the human transcriptome](https://scholariq.org/papers/effect-of-predicted-protein-truncating-genetic-variants-on-the-human/)
- [Genome‐wide association scan of attention deficit hyperactivity disorder](https://scholariq.org/papers/genome-wide-association-scan-of-attention-deficit-hyperactivity-disorder/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Attention Deficit Hyperactivity Disorder](https://scholariq.org/topics/attention-deficit-hyperactivity-disorder/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

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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.
