about
Swedish population substructure revealed by genome-wide single nucleotide polymorphism dataHaploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementiaSplice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intoleranceIncreased functional connectivity common to symptomatic amyotrophic lateral sclerosis and those at genetic riskGenome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern EuropeRare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal PolyneuropathiesOverloading of stable and exclusion of unstable human superoxide dismutase-1 variants in mitochondria of murine amyotrophic lateral sclerosis modelsPyrimethamine decreases levels of SOD1 in leukocytes and cerebrospinal fluid of ALS patients: a phase I pilot studyNEK1 variants confer susceptibility to amyotrophic lateral sclerosisPhysical activity and risk of Amyotrophic Lateral Sclerosis in a prospective cohort studyITPR2 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.Distinct changes in synaptic protein composition at neuromuscular junctions of extraocular muscles versus limb muscles of ALS donors.Changes in the spinal cord proteome of an amyotrophic lateral sclerosis murine model determined by differential in-gel electrophoresis.Development of a Smartphone App for a Genetics Website: The Amyotrophic Lateral Sclerosis Online Genetics Database (ALSoD).Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosisA blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories.Impact of presymptomatic genetic testing for familial amyotrophic lateral sclerosis.Is survival improved by the use of NIV and PEG in amyotrophic lateral sclerosis (ALS)? A post-mortem study of 80 ALS patients.Angiogenin levels and ANG genotypes: dysregulation in amyotrophic lateral sclerosisAnalysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studySystematically perturbed folding patterns of amyotrophic lateral sclerosis (ALS)-associated SOD1 mutantsNovel antibodies reveal inclusions containing non-native SOD1 in sporadic ALS patientsC9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisPolymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisMapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.Genomic landscape of positive natural selection in Northern European populations.PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis.Association study on glutathione S-transferase omega 1 and 2 and familial ALS.Credibility analysis of putative disease-causing genes using bioinformatics.Glial nuclear aggregates of superoxide dismutase-1 are regularly present in patients with amyotrophic lateral sclerosis.Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.Proteins that bind to misfolded mutant superoxide dismutase-1 in spinal cords from transgenic amyotrophic lateral sclerosis (ALS) model mice.Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mappingA yeast functional screen predicts new candidate ALS disease genesChromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.Homozygous SMN2 deletion is a protective factor in the Swedish ALS population.Effects of Cellular Pathway Disturbances on Misfolded Superoxide Dismutase-1 in Fibroblasts Derived from ALS Patients
P50
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P50
name
Peter M Andersen
@en
Peter M Andersen
@nl
type
label
Peter M Andersen
@en
Peter M Andersen
@nl
prefLabel
Peter M Andersen
@en
Peter M Andersen
@nl