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Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS.
Download from doi.orgMethylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease
Download from www.nature.comCross-region reduction in 5-hydroxymethylcytosine in Alzheimer's disease brain
Download from hdl.handle.netEpigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain
Download from www.ncbi.nlm.nih.govMethylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophrenia
Download from dx.doi.orgCompromised paraspeckle formation as a pathogenic factor in FUSopathies
Download from academic.oup.comAnalysis of TDP-43 and its binding partners in neurodegenerative diseases
Download from doi.orgThe genetics and neuropathology of amyotrophic lateral sclerosis
Download from www.researchgate.netThe C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder
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