# Michael Gill

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/michael-gill/

## Facts

| Field | Value |
| --- | --- |
| Citations | 106,937 |
| Field | Genetic Associations and Epidemiology |
| h-index | 126 |
| i10-index | 515 |
| OpenAlex ID | https://openalex.org/A5106497970 |
| ORCID iD | https://orcid.org/0000-0003-0206-5337 |
| Works | 840 |

## Researcher papers

Showing 12 of 17.

- [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/)
- [Genome-wide association analysis identifies 13 new risk loci for schizophrenia](https://scholariq.org/papers/genome-wide-association-analysis-identifies-13-new-risk-loci-for-schizophrenia/)
- [Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways](https://scholariq.org/papers/psychiatric-genome-wide-association-study-analyses-implicate-neuronal-immune-and/)
- [Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group](https://scholariq.org/papers/widespread-white-matter-microstructural-differences-in-schizophrenia-across-4322/)
- [Updated European Consensus Statement on diagnosis and treatment of adult ADHD](https://scholariq.org/papers/updated-european-consensus-statement-on-diagnosis-and-treatment-of-adult-adhd/)
- [Identification of common variants associated with human hippocampal and intracranial volumes](https://scholariq.org/papers/identification-of-common-variants-associated-with-human-hippocampal-and/)
- [The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes](https://scholariq.org/papers/the-analysis-of-51-genes-in-dsm-iv-combined-type-attention-deficit-hyperactivity/)
- [Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder](https://scholariq.org/papers/meta-analysis-of-genome-wide-association-studies-of-attention-deficit/)
- [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/)
- [Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence](https://scholariq.org/papers/emotional-lability-in-children-and-adolescents-with-attention-deficit/)
- [Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3](https://scholariq.org/papers/genome-wide-analysis-of-copy-number-variants-in-attention-deficit-hyperactivity/)
- [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/)
- [Attention Deficit Hyperactivity Disorder](https://scholariq.org/topics/attention-deficit-hyperactivity-disorder/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)

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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.