Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family

Nuclear Receptor NR1H3 in Familial Multiple Sclerosis

(2016) Zhe Wang et al.   NEURON

Publicly Available Data Provide Evidence against NR1H3 R415Q Causing Multiple Sclerosis

(2016) Eric Vallabh Minikel et al.   NEURON

NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk

(2016) Jack Antel et al.   NEURON

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

(2016) A. Dessa Sadovnick et al.   G3-Genes Genomes Genetics

Involvement of FKBP6 in hepatitis C virus replication

(2015) Hirotake Kasai et al.   Scientific Reports

Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits

(2013) Carmela Fusco et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Analysis of CYP27B1 in multiple sclerosis

(2013) Jay P. Ross et al.   JOURNAL OF NEUROIMMUNOLOGY

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

(2013) Ashley H Beecham et al.   NATURE GENETICS

Fine-Mapping the Genetic Association of the Major Histocompatibility Complex in Multiple Sclerosis: HLA and Non-HLA Effects

(2013) Nikolaos A. Patsopoulos et al.   PLoS Genetics

No evidence of association between mutant alleles of theCYP27B1gene and multiple sclerosis

(2012) Maria Ban et al.   ANNALS OF NEUROLOGY

No evidence for a role of rareCYP27B1functional variations in multiple sclerosis

(2012) Nadia Barizzone et al.   ANNALS OF NEUROLOGY

Differential confounding of rare and common variants in spatially structured populations

(2012) Iain Mathieson et al.   NATURE GENETICS

Modelling Genetic Susceptibility to Multiple Sclerosis with Family Data

(2012) Cullen O’Gorman et al.   NEUROEPIDEMIOLOGY

Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene

(2012) D. A. Dyment et al.   NEUROLOGY

Rare variants in the CYP27B1 gene are associated with multiple sclerosis

(2011) Sreeram V. Ramagopalan et al.   ANNALS OF NEUROLOGY

The Rotterdam Study: 2012 objectives and design update

(2011) Albert Hofman et al.   EUROPEAN JOURNAL OF EPIDEMIOLOGY

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

(2011) Stephen Sawcer et al.   NATURE

Aggregation of multiple sclerosis genetic risk variants in multiple and single case families

(2010) Pierre-Antoine Gourraud et al.   ANNALS OF NEUROLOGY

Versatile TPR domains accommodate different modes of target protein recognition and function

(2010) Rudi Kenneth Allan et al.   CELL STRESS & CHAPERONES

Letter to the Editor

(2010) Eleni Papageorgiou et al.   JOURNAL OF PAEDIATRICS AND CHILD HEALTH

Common vs. rare allele hypotheses for complex diseases

(2009) Nicholas J Schork et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

(2009) Melanie Bahlo et al.   NATURE GENETICS

The genomic basis of the Williams – Beuren syndrome

(2008) C. Schubert   CELLULAR AND MOLECULAR LIFE SCIENCES

FKBP36 Is an Inherent Multifunctional Glyceraldehyde-3-phosphate Dehydrogenase Inhibitor

(2008) Franziska Jarczowski et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Common and rare variants in multifactorial susceptibility to common diseases

(2008) Walter Bodmer et al.   NATURE GENETICS

STRING 8--a global view on proteins and their functional interactions in 630 organisms

(2008) L. J. Jensen et al.   NUCLEIC ACIDS RESEARCH

A genome scan in a single pedigree with a high prevalence of multiple sclerosis

(2007) D A Dyment et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY