# John A. Todd

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/john-a-todd/

## Facts

| Field | Value |
| --- | --- |
| Citations | 106,991 |
| Field | Diabetes and associated disorders |
| h-index | 143 |
| i10-index | 584 |
| Last Known Institution | Centre for Human Genetics |
| OpenAlex ID | https://openalex.org/A5001453089 |
| ORCID iD | https://orcid.org/0000-0003-2740-8148 |
| Works | 1,059 |

## Researcher papers

Showing 12 of 16.

- [Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls](https://scholariq.org/papers/genome-wide-association-study-of-14-000-cases-of-seven-common-diseases-and-3-000/)
- [Genomic atlas of the human plasma proteome](https://scholariq.org/papers/genomic-atlas-of-the-human-plasma-proteome/)
- [Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease](https://scholariq.org/papers/association-of-the-t-cell-regulatory-gene-ctla4-with-susceptibility-to/)
- [Common genetic determinants of vitamin D insufficiency: a genome-wide association study](https://scholariq.org/papers/common-genetic-determinants-of-vitamin-d-insufficiency-a-genome-wide-association/)
- [Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes](https://scholariq.org/papers/robust-associations-of-four-new-chromosome-regions-from-genome-wide-analyses-of/)
- [Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants](https://scholariq.org/papers/association-scan-of-14-500-nonsynonymous-snps-in-four-diseases-identifies/)
- [A genome-wide search for human type 1 diabetes susceptibility genes](https://scholariq.org/papers/a-genome-wide-search-for-human-type-1-diabetes-susceptibility-genes/)
- [Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters](https://scholariq.org/papers/lineage-specific-genome-architecture-links-enhancers-and-non-coding-disease/)
- [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/)
- [Maternal Viral Load, Zidovudine Treatment, and the Risk of Transmission of Human Immunodeficiency Virus Type 1 from Mother to Infant](https://scholariq.org/papers/maternal-viral-load-zidovudine-treatment-and-the-risk-of-transmission-of-human/)
- [Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus](https://scholariq.org/papers/susceptibility-to-human-type-1-diabetes-at-iddm2-is-determined-by-tandem-repeat/)
- [A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region](https://scholariq.org/papers/a-genome-wide-association-study-of-nonsynonymous-snps-identifies-a-type-1/)

## Researcher topics

- [Diabetes and associated disorders](https://scholariq.org/topics/diabetes-and-associated-disorders/)
- [Pancreatic function and diabetes](https://scholariq.org/topics/pancreatic-function-and-diabetes/)
- [T-cell and B-cell Immunology](https://scholariq.org/topics/t-cell-and-b-cell-immunology/)
- [Diabetes Management and Research](https://scholariq.org/topics/diabetes-management-and-research/)
- [Immune Cell Function and Interaction](https://scholariq.org/topics/immune-cell-function-and-interaction/)

## Researcher university

- [Centre for Human Genetics](https://scholariq.org/institutions/centre-for-human-genetics/)

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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.