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Chris Wallace

Researcher Next ID · RN-027759

Researcher · Biochemistry, Genetics and Molecular Biology

University of Cambridge

Cambridge, Portugal

Not currently recruitingFunding unknown
Works count
339
Citation count
42,967
H-index
63
i10-index
137

Research interests

Biochemistry, Genetics and Molecular Biology
Immunology and Microbiology
Genetic Associations and Epidemiology
Diabetes and associated disorders
Gene expression and cancer classification
T-cell and B-cell Immunology
Bioinformatics and Genomic Networks

Publications

  • Combining evidence from Mendelian randomization and colocalization: Review and comparison of approaches

    The American Journal of Human Genetics · 2022 · 10.1016/j.ajhg.2022.04.001

  • Mendelian randomization

    Nature Reviews Methods Primers · 2022 · https://doi.org/10.1038/s43586-021-00092-5

  • A more accurate method for colocalisation analysis allowing for multiple causal variants

    PLoS Genetics · 2021 · 10.1371/journal.pgen.1009440

  • Eliciting priors and relaxing the single causal variant assumption in colocalisation analyses

    PLoS Genetics · 2020 · 10.1371/journal.pgen.1008720

  • Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters

    Cell · 2016 · https://doi.org/10.1016/j.cell.2016.09.037

  • Correction: Corrigendum: Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis

    Nature Communications · 2015 · https://doi.org/10.1038/ncomms8741

  • Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers

    Nature Genetics · 2015 · https://doi.org/10.1038/ng.3245

  • Widespread seasonal gene expression reveals annual differences in human immunity and physiology

    Nature Communications · 2015 · 10.1038/ncomms8000

  • Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics

    PLoS Genetics · 2014 · https://doi.org/10.1371/journal.pgen.1004383

  • A Type I Interferon Transcriptional Signature Precedes Autoimmunity in Children Genetically at Risk for Type 1 Diabetes

    Diabetes · 2014 · 10.2337/db13-1777

  • Inherited Variation in Vitamin D Genes Is Associated With Predisposition to Autoimmune Disease Type 1 Diabetes

    Diabetes · 2011 · 10.2337/db10-1656

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

    Nature Genetics · 2011 · 10.1038/ng.998

  • Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

    Nature Genetics · 2011 · 10.1038/ng.970

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

    Nature · 2010 · 10.1038/nature08979

  • A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk

    Nature · 2010 · 10.1038/nature09386

  • Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations

    PLoS Genetics · 2009 · 10.1371/journal.pgen.1000504

  • Genome-wide association study identifies eight loci associated with blood pressure

    Nature Genetics · 2009 · 10.1038/ng.361

  • Vascularized Groin Lymph Node Transfer Using the Wrist as a Recipient Site for Management of Postmastectomy Upper Extremity Lymphedema

    Plastic & Reconstructive Surgery · 2009 · 10.1097/prs.0b013e31819e6529

  • The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes

    Nature Genetics · 2009 · 10.1038/ng.493

  • SLC2A9 Is a High-Capacity Urate Transporter in Humans

    PLoS Medicine · 2008 · 10.1371/journal.pmed.0050197

  • Genome-wide association analysis identifies 20 loci that influence adult height

    Nature Genetics · 2008 · 10.1038/ng.121

  • Common variants near MC4R are associated with fat mass, weight and risk of obesity

    Nature Genetics · 2008 · 10.1038/ng.140

  • Genome-wide Association Study Identifies Genes for Biomarkers of Cardiovascular Disease: Serum Urate and Dyslipidemia

    The American Journal of Human Genetics · 2008 · 10.1016/j.ajhg.2007.11.001

  • Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

    Nature Genetics · 2007 · 10.1038/ng2068

  • Tryptophan depletion impairs stimulus-reward learning while methylphenidate disrupts attentional control in healthy young adults: implications for the monoaminergic basis of impulsive behaviour

    Psychopharmacology · 1999 · 10.1007/pl00005494

Current projects

    No projects listed.