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Lista de obras de Valentina Iotchkova

A multiple-phenotype imputation method for genetic studies

artículo científico publicado en 2016

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

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

article

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

artículo científico publicado en 2019

Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

artículo científico publicado en 2016

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

scientific article published on 01 September 2019

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

scientific article published on 11 July 2019

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

artículo científico publicado en 2015

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

The UK10K project identifies rare variants in health and disease

artículo científico publicado en 2015

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

artículo científico publicado en 2017

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

artículo científico publicado en 2016