World's Best Scientists 2026 revealed!

Overview

Cordelia Langford is affiliated with the Wellcome Sanger Institute in the United Kingdom. Their research primarily spans the fields of Medicine and Biochemistry, Genetics and Molecular Biology, with a focus on Infectious Diseases, Genetics, General Health Professions, Surgery, and Molecular Biology as subfields.

The main topics of their research include:

  • SARS-CoV-2 and COVID-19 Research
  • Geriatric Care and Nursing Homes
  • SARS-CoV-2 detection and testing
  • Evolution and Genetic Dynamics
  • Bacteriophages and microbial interactions
  • Frailty in Older Adults
  • Eosinophilic Esophagitis

Cordelia Langford has coauthored work with the following researchers:

  • Gerry Tonkin-Hill
  • Ian Johnston
  • David K. Jackson
  • Sónia Gonçalves
  • Michael Spencer Chapman

Frequent publication venues include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • UNC Libraries
  • eLife

Selected recent papers authored or coauthored by Cordelia Langford are:

  • Patterns of within-host genetic diversity in SARS-CoV-2, 2020, bioRxiv (Cold Spring Harbor Laboratory)
  • Genomic epidemiology of COVID-19 in care homes in the east of England, 2021, eLife
  • Genomic epidemiology of COVID-19 in care homes in the East of England, 2020, bioRxiv (Cold Spring Harbor Laboratory)
  • Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus, 2020, UNC Libraries
  • Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes, 2020, UNC Libraries

Best Publications

  • Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

    Ewan Birney;John A. Stamatoyannopoulos;Anindya Dutta;Roderic Guigó

  • The ENCODE (ENCyclopedia of DNA elements) Project

    E. A. Feingold;P. J. Good;M. S. Guyer;S. Kamholz

  • Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

    Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer

  • Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

    Andrew P Morris;Benjamin F Voight;Benjamin F Voight;Tanya M Teslovich;Teresa Ferreira

  • Large-scale association analysis identifies new risk loci for coronary artery disease

    Panos Deloukas;Stavroula Kanoni;Christina Willenborg;Martin Farrall

  • The DNA sequence of human chromosome 22

    I. Dunham;N. Shimizu;B. A. Roe;S. Chissoe

  • The UK10K project identifies rare variants in health and disease

    K Walter;J L Min;J Huang

  • The DNA sequence of the human X chromosome

    Mark T Ross;Darren V Grafham;Alison J Coffey;Steven Scherer

  • Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

    Ashley H. Beecham;Nikolaos A. Patsopoulos;Nikolaos A. Patsopoulos;Dionysia K. Xifara;Mary F. Davis

  • Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

    Lam C. Tsoi;Sarah L. Spain;Sarah L. Spain;Jo Knight;Eva Ellinghaus;Eva Ellinghaus

  • A Genome-Wide Association Study Identifies New Psoriasis Susceptibility Loci and an Interaction Between HLA-C and ERAP1

    Amy Strange;Francesca Capon;Chris C A Spencer

  • Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

    D M Evans;Spencer Cca.;J J Pointon;Z Su

  • Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

    Gosia Trynka;Karen A Hunt;Nicholas A Bockett;Jihane Romanos

  • Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.

    Anubha Mahajan;Min Jin Go;Weihua Zhang;Jennifer E. Below

  • Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

    Nick Craddock;Matthew E. Hurles;Niall Cardin;Richard D. Pearson

  • Genome-wide association study identifies five new breast cancer susceptibility loci

    Clare Turnbull;Shahana Ahmed;Jonathan Morrison;David Pernet

  • High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

    Steve Eyre;John Bowes;John Bowes;Dorothée Diogo;Dorothée Diogo;Annette Lee

  • A Novel CpG Island Set Identifies Tissue-Specific Methylation at Developmental Gene Loci

    Robert Illingworth;Alastair Kerr;Dina DeSousa;Helle Jørgensen

  • Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.

    Simon G Gregory;Jessica J Connelly;Aaron J Towers;Jessica Johnson

  • Hospital admission and emergency care attendance risk for SARS-CoV-2 delta (B.1.617.2) compared with alpha (B.1.1.7) variants of concern: a cohort study.

    Katherine A Twohig;Tommy Nyberg;Asad Zaidi;Simon Thelwall

Frequent Co-Authors

Willem H. Ouwehand
Willem H. Ouwehand University of Cambridge
Sarah Hunt
Sarah Hunt European Bioinformatics Institute
Peter Donnelly
Peter Donnelly University of Oxford
Jenefer M. Blackwell
Jenefer M. Blackwell Telethon Kids Institute
Sarah Edkins
Sarah Edkins Cardiff University
Panos Deloukas
Panos Deloukas Queen Mary University of London
Matthew A. Brown
Matthew A. Brown Guy's and St Thomas' NHS Foundation Trust
Christopher G. Mathew
Christopher G. Mathew King's College London
Stephen Sawcer
Stephen Sawcer University of Cambridge
Nilesh J. Samani
Nilesh J. Samani University of Leicester

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