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Publications

Recent publications published by researchers at the MRC WIMM.

Incidence of symptomatic, image-confirmed venous thromboembolism following hospitalization for COVID-19 with 90-day follow-up.

Salisbury R. et al, (2020), Blood Adv, 4, 6230 - 6239

Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome.

Labuhn M. et al, (2019), Cancer Cell, 36, 123 - 138.e10

Variation in PU.1 binding and chromatin looping at neutrophil enhancers influences autoimmune disease susceptibility

Watt S. et al, (2019)

GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals.

Iotchkova V. et al, (2019), Nat Genet, 51, 343 - 353

Low-frequency variation in TP53 has large effects on head circumference and intracranial volume.

Haworth S. et al, (2019), Nat Commun, 10

Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.

Iotchkova V. et al, (2018), Nat Genet, 50

Low frequency genetic variation in the TP53 locus has large effects on head circumference and intracranial volume

St Pourcain B. et al, (2018), BEHAVIOR GENETICS, 48, 514 - 515

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

Astle WJ. et al, (2016), Cell, 167, 1415 - 1429.e19

GARFIELD - GWAS Analysis of Regulatory or Functional Information Enrichment with LD correction

Iotchkova V. et al, (2016)

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.

Iotchkova V. et al, (2016), Nature genetics

Significant impact of miRNA-target gene networks on genetics of human complex traits.

Okada Y. et al, (2016), Sci Rep, 6

The UK10K project identifies rare variants in health and disease.

UK10K Consortium None. et al, (2015), Nature, 526, 82 - 90

MultiMeta: an R package for meta-analyzing multi-phenotype genome-wide association studies.

Vuckovic D. et al, (2015), Bioinformatics, 31, 2754 - 2756

Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.

Timpson NJ. et al, (2015), Nat Commun, 6

Whole-genome sequence-based analysis of thyroid function.

Taylor PN. et al, (2015), Nat Commun, 6

FORGE: A tool to discover cell specific enrichments of GWAS associated SNPs in regulatory regions

Dunham I. et al, (2015)

MultiMeta: An R Package for Meta-Analyzing Multi-Phenotype Genome-Wide Association Studies

Vuckovic D. et al, (2015), HUMAN HEREDITY, 79, 48 - 48

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.

Timpson NJ. et al, (2014), Nat Commun, 5

A multiple phenotype imputation method for genetic studies

Marchini J. and Dahl A., Nature Genetics

eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data.

Breeze CE. et al, Cell Rep, 17, 2137 - 2150

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