A functional variant that affects exon-skipping and protein expression ofSP140as genetic mechanism predisposing to multiple sclerosis

The top ten clues to understand the origin of chronic lymphocytic leukemia (CLL)

(2015) Ricardo García-Muñoz et al.   JOURNAL OF AUTOIMMUNITY

The Genetic and Mechanistic Basis for Variation in Gene Regulation

(2015) Athma A. Pai et al.   PLoS Genetics

Determining causality and consequence of expression quantitative trait loci

(2014) A. Battle et al.   HUMAN GENETICS

Structural basis for hijacking CBF-β and CUL5 E3 ligase complex by HIV-1 Vif

(2014) Yingying Guo et al.   NATURE

Genetic and epigenetic fine mapping of causal autoimmune disease variants

(2014) Kyle Kai-How Farh et al.   NATURE

HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV

(2014) Marta García-Montojo et al.   Retrovirology

Heterogeneity of genomic evolution and mutational profiles in multiple myeloma

(2014) Niccolo Bolli et al.   Nature Communications

Structure of human Sp140 PHD finger: an atypical fold interacting with Pin1

(2013) Chiara Zucchelli et al.   FEBS Journal

The CH2 domain of CBP/p300 is a novel zinc finger

(2013) Sangho Park et al.   FEBS LETTERS

A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci

(2013) Jose-Ezequiel Martin et al.   HUMAN MOLECULAR GENETICS

Genetics of rheumatoid arthritis contributes to biology and drug discovery

(2013) Yukinori Okada et al.   NATURE

Transcriptome and genome sequencing uncovers functional variation in humans

(2013) Tuuli Lappalainen et al.   NATURE

A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia

(2013) Helen E Speedy et al.   NATURE GENETICS

Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

(2013) Sonja I Berndt et al.   NATURE GENETICS

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

(2013) Ashley H Beecham et al.   NATURE GENETICS

Genetic insights into common pathways and complex relationships among immune-mediated diseases

(2013) Miles Parkes et al.   NATURE REVIEWS GENETICS

Activation of MSRV-Type Endogenous Retroviruses during Infectious Mononucleosis and Epstein-Barr Virus Latency: The Missing Link with Multiple Sclerosis?

(2013) Giuseppe Mameli et al.   PLoS One

GLiMMPS: Robust statistical model for regulatory variation of alternative splicing using RNA-seq data

(2013) Keyan Zhao et al.   GENOME BIOLOGY

Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy: known and novel aspects of the syndrome

(2012) Kai Kisand et al.   Annals of the New York Academy of Sciences

Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia

(2012) S. L. Slager et al.   BLOOD

Human genetics offers an emerging picture of common pathways and mechanisms in autoimmunity

(2012) Benjamin F Voight et al.   CURRENT OPINION IN IMMUNOLOGY

Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease

(2012) Luke Jostins et al.   NATURE

An integrated map of genetic variation from 1,092 human genomes

(2012)   NATURE

Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population

(2012) Yukinori Okada et al.   NATURE GENETICS

Primer3—new capabilities and interfaces

(2012) Andreas Untergasser et al.   NUCLEIC ACIDS RESEARCH

Post-GWAS Functional Characterization of Susceptibility Variants for Chronic Lymphocytic Leukemia

(2012) Fenna C. M. Sillé et al.   PLoS One

Diagnostic criteria for multiple sclerosis: 2010 Revisions to the McDonald criteria

(2011) Chris H. Polman et al.   ANNALS OF NEUROLOGY

Control of central and peripheral tolerance by Aire

(2011) Todd C. Metzger et al.   IMMUNOLOGICAL REVIEWS

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

(2011) Stephen Sawcer et al.   NATURE

Association of innate immune activation with latent Epstein-Barr virus in active MS lesions

(2011) J. S. Tzartos et al.   NEUROLOGY

High ACSL5 Transcript Levels Associate with Systemic Lupus Erythematosus and Apoptosis in Jurkat T Lymphocytes and Peripheral Blood Cells

(2011) Antonio Catalá-Rabasa et al.   PLoS One

Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL

(2010) S. L. Slager et al.   BLOOD

Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation

(2010) Cole Trapnell et al.   NATURE BIOTECHNOLOGY

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

(2010) Andre Franke et al.   NATURE GENETICS

PML Nuclear Body Component Sp140 Is a Novel Autoantigen in Primary Biliary Cirrhosis

(2009) Alessandro Granito et al.   AMERICAN JOURNAL OF GASTROENTEROLOGY

TopHat: discovering splice junctions with RNA-Seq

(2009) Cole Trapnell et al.   BIOINFORMATICS

Accommodating Linkage Disequilibrium in Genetic-Association Analyses via Ridge Regression

(2008) Nathalie Malo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13

(2008) Vincent Plagnol et al.   BIOSTATISTICS

A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia

(2008) Maria Chiara Di Bernardo et al.   NATURE GENETICS