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Human Molecular Genetics|October 15, 2009
Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencingGraham A Heap, Jennie H M Yang, Kate Downes, et al.The New England Journal of Medicine|December 17, 2008
Shared and distinct genetic variants in type 1 diabetes and celiac diseaseDeborah J Smyth, Vincent Plagnol, Neil M Walker, et al.Nature Genetics|August 25, 2009
Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresourceCalliope A Dendrou, Vincent Plagnol, Erik Fung, et al.Cell Reports|November 17, 2016
Distinct Trends of DNA Methylation Patterning in the Innate and Adaptive Immune SystemsRonald P Schuyler, Angelika Merkel, Emanuele Raineri, et al.Journal of Thrombosis and Haemostasis : JTH|November 28, 2023
Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation frameworkJustyne E Ross, Shruthi Mohan, Jing Zhang, et al.Blood|June 23, 2017
Expanded repertoire of <i>RASGRP2</i> variants responsible for platelet dysfunction and severe bleedingSarah K Westbury, Matthias Canault, Daniel Greene, et al.Haematologica|December 15, 2018
High-throughput elucidation of thrombus formation reveals sources of platelet function variabilityJohanna P van Geffen, Sanne L N Brouns, Joana Batista, et al.Blood Advances|October 4, 2024
The common VTE-protective G haplotype of F5 increases factor V-short, TFPI function, and risk of bleedingMatthew C Sims, Magdalena Gierula, Jonathan C Stephens, et al.Journal of Immunology (Baltimore, Md. : 1950)|February 19, 2013
Postthymic expansion in human CD4 naive T cells defined by expression of functional high-affinity IL-2 receptorsMarcin L Pekalski, Ricardo C Ferreira, Richard M R Coulson, et al.The New England Journal of Medicine|December 16, 2011
A mutation in the thyroid hormone receptor alpha geneElena Bochukova, Nadia Schoenmakers, Maura Agostini, et al.Pageof 9