A genome-wide association study of brain lesion distribution in multiple sclerosis

Genetic Correlations of Brain Lesion Distribution in Multiple Sclerosis: An Exploratory Study

(2011) M.H. Sombekke et al.   AMERICAN JOURNAL OF NEURORADIOLOGY

Evolution of the blood-brain barrier in newly forming multiple sclerosis lesions

(2011) María I. Gaitán et al.   ANNALS OF NEUROLOGY

A dynamic view of the blood-brain barrier in active multiple sclerosis lesions

(2011) Hans Lassmann   ANNALS OF NEUROLOGY

Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability

(2011) Zoltán Kutalik et al.   GENETIC EPIDEMIOLOGY

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

(2011) Andrew R. Wood et al.   HUMAN MOLECULAR GENETICS

HLA DRB1*1501 is only modestly associated with lesion burden at the first demyelinating event

(2011) Dana Horakova et al.   JOURNAL OF NEUROIMMUNOLOGY

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

(2011) Stephen Sawcer et al.   NATURE

Voxelwise gene-wide association study (vGeneWAS): Multivariate gene-based association testing in 731 elderly subjects

(2011) Derrek P. Hibar et al.   NEUROIMAGE

A Variant in LIN28B Is Associated with 2D:4D Finger-Length Ratio, a Putative Retrospective Biomarker of Prenatal Testosterone Exposure

(2010) Sarah E. Medland et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic Variation and Neuroimaging Measures in Alzheimer Disease

(2010) Alessandro Biffi   ARCHIVES OF NEUROLOGY

Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis

(2010) Sergio E. Baranzini et al.   BRAIN

Biological, clinical and population relevance of 95 loci for blood lipids

(2010) Tanya M. Teslovich et al.   NATURE

Hundreds of variants clustered in genomic loci and biological pathways affect human height

(2010) Hana Lango Allen et al.   NATURE

Direct conversion of fibroblasts to functional neurons by defined factors

(2010) Thomas Vierbuchen et al.   NATURE

LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease

(2010) Carles Vilariño-Güell et al.   NEUROGENETICS

Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

(2010) Li Shen et al.   NEUROIMAGE

Voxelwise genome-wide association study (vGWAS)

(2010) Jason L. Stein et al.   NEUROIMAGE

Phenotypic Complexity, Measurement Bias, and Poor Phenotypic Resolution Contribute to the Missing Heritability Problem in Genetic Association Studies

(2010) Sophie van der Sluis et al.   PLoS One

Web-Based, Participant-Driven Studies Yield Novel Genetic Associations for Common Traits

(2010) Nicholas Eriksson et al.   PLoS Genetics

Combination of Linkage Mapping and Microarray-Expression Analysis Identifies NF-κB Signaling Defect as a Cause of Autosomal-Recessive Mental Retardation

(2009) Orianne Philippe et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal Microcephaly

(2009) Ganeshwaran H. Mochida et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Pathway and network-based analysis of genome-wide association studies in multiple sclerosis

(2009) S. E. Baranzini et al.   HUMAN MOLECULAR GENETICS

Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry

(2009) Hongmei Nan et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Beta amyloid oligomers and fibrils stimulate differential activation of primary microglia

(2009) Cindy M Sondag et al.   Journal of Neuroinflammation

Connecting white matter injury and thalamic atrophy in clinically isolated syndromes

(2009) Roland G. Henry et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Genome-Wide Association Study of Exercise Behavior in Dutch and American Adults

(2009) MARLEEN H.M. DE MOOR et al.   MEDICINE AND SCIENCE IN SPORTS AND EXERCISE

Common variants at ten loci influence QT interval duration in the QTGEN Study

(2009) Christopher Newton-Cheh et al.   NATURE GENETICS

Quality of life in multiple sclerosis is associated with lesion burden and brain volume measures

(2009) E. M. Mowry et al.   NEUROLOGY

Genome-wide strategies for discovering genetic influences on cognition and cognitive disorders: Methodological considerations

(2009) Steven G. Potkin et al.   Cognitive Neuropsychiatry

Genetic Determinants of Circulating Sphingolipid Concentrations in European Populations

(2009) Andrew A. Hicks et al.   PLoS Genetics

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

(2008) Terry Vrijenhoek et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Developmental analysis of Lingo-1/Lern1 protein expression in the mouse brain: Interaction of its intracellular domain with Myt1l

(2008) Franc Llorens et al.   Developmental Neurobiology

Nonrigid registration of multiple sclerosis brain images using lesion inpainting for morphometry or lesion mapping

(2008) Michaël Sdika et al.   HUMAN BRAIN MAPPING

Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis

(2008) Sergio E. Baranzini et al.   HUMAN MOLECULAR GENETICS

A Fast Nonrigid Image Registration With Constraints on the Jacobian Using Large Scale Constrained Optimization

(2008) M. Sdika   IEEE TRANSACTIONS ON MEDICAL IMAGING

Gene discovery through imaging genetics: identification of two novel genes associated with schizophrenia

(2008) S G Potkin et al.   MOLECULAR PSYCHIATRY

Two newly identified genetic determinants of pigmentation in Europeans

(2008) Patrick Sulem et al.   NATURE GENETICS