about
What we truly know about occupation as a risk factor for ALS: A critical and systematic reviewMultiple common variants for celiac disease influencing immune gene expressionNEK1 variants confer susceptibility to amyotrophic lateral sclerosisSystematic identification of trans eQTLs as putative drivers of known disease associationsImpaired structural motor connectome in amyotrophic lateral sclerosisReduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosisITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association studyAge of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.The verbal fluency index: Dutch normative data for cognitive testing in ALS.Markov Models for inferring copy number variations from genotype data on Illumina platformsGene-network analysis identifies susceptibility genes related to glycobiology in autismWeighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patientsA reference panel of 64,976 haplotypes for genotype imputation.Circulating microRNAs in patients with intracranial aneurysmsA blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories.Motor network degeneration in amyotrophic lateral sclerosis: a structural and functional connectivity study.Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studyTrans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLAC9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisUnraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression.Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study.Correlation between structural and functional connectivity impairment in amyotrophic lateral sclerosisCommon inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific mannerGenetic overlap between apparently sporadic motor neuron diseases.Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects.Population genetic differentiation of height and body mass index across Europe.Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq.DeepSAGE reveals genetic variants associated with alternative polyadenylation and expression of coding and non-coding transcripts.Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls.Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.Cell Specific eQTL Analysis without Sorting Cells.Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.The future of motor neuron disease: the challenge is in the genes.Whole Blood Gene Expression Profiles of Patients with a Past Aneurysmal Subarachnoid Hemorrhage.Multicohort genomewide association study reveals a new signal of protection against HIV-1 acquisition.Common variants at VRK2 and TCF4 conferring risk of schizophrenia.
P50
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P50
name
Jan H Veldink
@en
Jan H Veldink
@nl
type
label
Jan H Veldink
@en
Jan H Veldink
@nl
prefLabel
Jan H Veldink
@en
Jan H Veldink
@nl