# Cordelia Langford

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/cordelia-langford/

## Facts

| Field | Value |
| --- | --- |
| Citations | 38,187 |
| Field | Genetic Associations and Epidemiology |
| h-index | 68 |
| i10-index | 96 |
| Last Known Institution | Wellcome Sanger Institute |
| OpenAlex ID | https://openalex.org/A5088166261 |
| ORCID iD | https://orcid.org/0000-0002-6940-501X |
| Works | 129 |

## Researcher papers

- [Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis](https://scholariq.org/papers/genetic-risk-and-a-primary-role-for-cell-mediated-immune-mechanisms-in-multiple/)
- [Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis](https://scholariq.org/papers/analysis-of-immune-related-loci-identifies-48-new-susceptibility-variants-for/)
- [The UK10K project identifies rare variants in health and disease](https://scholariq.org/papers/the-uk10k-project-identifies-rare-variants-in-health-and-disease/)
- [A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1](https://scholariq.org/papers/a-genome-wide-association-study-identifies-new-psoriasis-susceptibility-loci-and/)
- [Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity](https://scholariq.org/papers/identification-of-15-new-psoriasis-susceptibility-loci-highlights-the-role-of/)
- [Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease](https://scholariq.org/papers/dense-genotyping-identifies-and-localizes-multiple-common-and-rare-variant/)
- [Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease](https://scholariq.org/papers/excessive-burden-of-lysosomal-storage-disorder-gene-variants-in-parkinson-s/)
- [Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease](https://scholariq.org/papers/unbiased-screen-for-interactors-of-leucine-rich-repeat-kinase-2-supports-a/)
- [Functional epigenetics identifies a protocadherin PCDH10 as a candidate tumor suppressor for nasopharyngeal, esophageal and multiple other carcinomas with frequent methylation](https://scholariq.org/papers/functional-epigenetics-identifies-a-protocadherin-pcdh10-as-a-candidate-tumor/)
- [Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus](https://scholariq.org/papers/common-variants-at-the-mhc-locus-and-at-chromosome-16q24-1-predispose-to-barrett/)

## 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/)
- [SARS-CoV-2 and COVID-19 Research](https://scholariq.org/topics/sars-cov-2-and-covid-19-research/)
- [Genomics and Chromatin Dynamics](https://scholariq.org/topics/genomics-and-chromatin-dynamics/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)

## Researcher university

- [Wellcome Sanger Institute](https://scholariq.org/institutions/wellcome-sanger-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.