# G. Bragi Walters

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/g-bragi-walters/

## Facts

| Field | Value |
| --- | --- |
| Citations | 39,769 |
| Field | Genetic Associations and Epidemiology |
| h-index | 56 |
| i10-index | 97 |
| Last Known Institution | deCODE Genetics (Iceland) |
| OpenAlex ID | https://openalex.org/A5018138876 |
| ORCID iD | https://orcid.org/0000-0002-5415-6487 |
| Works | 125 |

## Researcher papers

- [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/)
- [Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes](https://scholariq.org/papers/variant-of-transcription-factor-7-like-2-tcf7l2-gene-confers-risk-of-type-2/)
- [Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders](https://scholariq.org/papers/genomic-relationships-novel-loci-and-pleiotropic-mechanisms-across-eight/)
- [Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains](https://scholariq.org/papers/genome-wide-analyses-of-adhd-identify-27-risk-loci-refine-the-genetic/)
- [The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm](https://scholariq.org/papers/the-same-sequence-variant-on-9p21-associates-with-myocardial-infarction/)
- [A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke](https://scholariq.org/papers/a-sequence-variant-in-zfhx3-on-16q22-associates-with-atrial-fibrillation-and/)
- [Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density](https://scholariq.org/papers/sequence-variants-in-the-cldn14-gene-associate-with-kidney-stones-and-bone/)
- [Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm](https://scholariq.org/papers/genome-wide-association-study-identifies-a-sequence-variant-within-the-dab2ip/)

## 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/)
- [Attention Deficit Hyperactivity Disorder](https://scholariq.org/topics/attention-deficit-hyperactivity-disorder/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

- [deCODE Genetics (Iceland)](https://scholariq.org/institutions/decode-genetics-iceland/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.