Breakdown of Multiple Sclerosis Genetics to Identify an Integrated Disease Network and Potential Variant Mechanisms

Mapping the Mouse Cell Atlas by Microwell-Seq

(2018) Xiaoping Han et al.   CELL

Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation

(2018) Eric R. Gamazon et al.   NATURE GENETICS

Genome Sequencing in the Clinic: The Past, Present, and Future of Genomic Medicine

(2018) Jeremy W Prokop et al.   PHYSIOLOGICAL GENOMICS

Interactions between genetic, lifestyle and environmental risk factors for multiple sclerosis

(2016) Tomas Olsson et al.   Nature Reviews Neurology

PROVEAN web server: a tool to predict the functional effect of amino acid substitutions and indels

(2015) Yongwook Choi et al.   BIOINFORMATICS

From cytopenia to leukemia: the role of Gfi1 and Gfi1b in blood formation

(2015) T. Moroy et al.   BLOOD

Systemic Lupus Erythematosus Patients Exhibit Reduced Expression of CLEC16A Isoforms in Peripheral Leukocytes

(2015) Rachel Tam et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

ClinVar: public archive of interpretations of clinically relevant variants

(2015) Melissa J. Landrum et al.   NUCLEIC ACIDS RESEARCH

Gene-Gene Interaction betweenLCEandCLEC16AIncreases the Risk of Psoriasis in a Chinese Population

(2014) Jianbo Wang et al.   Annals of Dermatology

Interaction between adolescent obesity and HLA risk genes in the etiology of multiple sclerosis

(2014) A. K. Hedstrom et al.   NEUROLOGY

Autoimmune disease in people with multiple sclerosis and their relatives: a systematic review and meta-analysis

(2013) Ruth Dobson et al.   JOURNAL OF NEUROLOGY

A Novel Predicted Calcium-Regulated Kinase Family Implicated in Neurological Disorders

(2013) Małgorzata Dudkiewicz et al.   PLoS One

Analysis of PPARGC1B, RUNX3 and TBKBP1 Polymorphisms in Chinese Han Patients with Ankylosing Spondylitis: A Case-Control Study

(2013) Zijian Lian et al.   PLoS One

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

(2011) Nikolaos A. Patsopoulos et al.   ANNALS OF NEUROLOGY

Genome-wide association study of severity in multiple sclerosis

(2011)   GENES AND IMMUNITY

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

(2011) Stephen Sawcer et al.   NATURE

Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data

(2011) Joanne H Wang et al.   Genome Medicine

Association of the AFF3 gene and IL2/IL21 gene region with juvenile idiopathic arthritis

(2010) A Hinks et al.   GENES AND IMMUNITY

Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci

(2010) Eli A Stahl et al.   NATURE GENETICS

I-TASSER: a unified platform for automated protein structure and function prediction

(2010) Ambrish Roy et al.   Nature Protocols

Neuronal Abelson helper integration site-1 (Ahi1) deficiency in mice alters TrkB signaling with a depressive phenotype

(2010) X. Xu et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

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

(2009) Melanie Bahlo et al.   NATURE GENETICS

Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

(2009) Philip L De Jager et al.   NATURE GENETICS

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

(2008) A. D. Johnson et al.   BIOINFORMATICS

ASAP3 Is a Focal Adhesion-associated Arf GAP That Functions in Cell Migration and Invasion

(2008) Vi Luan Ha et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Biological markers for axonal degeneration in CSF and blood of patients with the first event indicative for multiple sclerosis

(2008) Katharina Hein (née Maier) et al.   NEUROSCIENCE LETTERS