| scholarly article | Q13442814 |
| P50 | author | Natalie A Twine | Q88688893 |
| Timothy Peters | Q91210729 | ||
| Susan Clark | Q42658558 | ||
| Emily P McCann | Q47502946 | ||
| Beben Benyamin | Q47713406 | ||
| Kelly L Williams | Q48386537 | ||
| Dominic B Rowe | Q50276991 | ||
| Qiong-Yi Zhao | Q56542546 | ||
| Denis C Bauer | Q56787419 | ||
| Zong Hong Zhang | Q57230641 | ||
| Ingrid S Tarr | Q59692085 | ||
| Ian P Blair | Q62071933 | ||
| P2093 | author name string | Garth A Nicholson | |
| Katharine Y Zhang | |||
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| The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients | Q48310101 | ||
| The genotype-phenotype landscape of familial amyotrophic lateral sclerosis in Australia. | Q48331920 | ||
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| Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans | Q59543670 | ||
| Genetic influences on F cells and other hematologic variables: a twin heritability study | Q73295247 | ||
| DNA methylation age is associated with mortality in a longitudinal Danish twin study. | Q34502607 | ||
| Identification of epigenetically altered genes in sporadic amyotrophic lateral sclerosis | Q34541013 | ||
| Superoxide dismutase and the death of motoneurons in ALS. | Q34553806 | ||
| Hypermethylation of repeat expanded C9orf72 is a clinical and molecular disease modifier | Q34810486 | ||
| Up-regulation of neural and cell cycle-related microRNAs in brain of amyotrophic lateral sclerosis mice at late disease stage | Q35052630 | ||
| C9orf72 promoter hypermethylation is neuroprotective: Neuroimaging and neuropathologic evidence | Q35537493 | ||
| Global methylation in exposure biology and translational medical science | Q35579907 | ||
| Overexpression of CCS in G93A-SOD1 mice leads to accelerated neurological deficits with severe mitochondrial pathology | Q35749657 | ||
| The impact of metabolism on DNA methylation | Q36088929 | ||
| Prognostic factors in ALS: A critical review | Q36447824 | ||
| Assessing the effects of high methionine intake on DNA methylation | Q36479628 | ||
| Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray | Q36670000 | ||
| CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia | Q36809438 | ||
| Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin | Q36956646 | ||
| Kv4 accessory protein DPPX (DPP6) is a critical regulator of membrane excitability in hippocampal CA1 pyramidal neurons | Q36956963 | ||
| Additional annotation enhances potential for biologically-relevant analysis of the Illumina Infinium HumanMethylation450 BeadChip array | Q37088466 | ||
| Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood | Q37316040 | ||
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| DNA damage in neurodegenerative diseases | Q38563232 | ||
| Conserved DNA methylation combined with differential frontal cortex and cerebellar expression distinguishes C9orf72-associated and sporadic ALS, and implicates SERPINA1 in disease | Q38624666 | ||
| Clustering of RNA-Seq samples: Comparison study on cancer data | Q38640146 | ||
| Epigenetic differences between monozygotic twins discordant for amyotrophic lateral sclerosis (ALS) provide clues to disease pathogenesis | Q38644299 | ||
| Epigenome-wide DNA methylation analysis in siblings and monozygotic twins discordant for sporadic Parkinson's disease revealed different epigenetic patterns in peripheral blood mononuclear cells | Q38814364 | ||
| Characterization of Gene Expression Phenotype in Amyotrophic Lateral Sclerosis Monocytes. | Q38822774 | ||
| Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons | Q39007648 | ||
| Axonal Excitability in Amyotrophic Lateral Sclerosis : Axonal Excitability in ALS. | Q39017694 | ||
| Rad9B responds to nucleolar stress through ATR and JNK signalling, and delays the G1-S transition. | Q39383444 | ||
| Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion | Q39408417 | ||
| Characterization of the kynurenine pathway in NSC-34 cell line: implications for amyotrophic lateral sclerosis | Q39616472 | ||
| A genome-wide analysis of brain DNA methylation identifies new candidate genes for sporadic amyotrophic lateral sclerosis. | Q39928188 | ||
| Quantification of gene-specific methylation of DNMT3B and MTHFR using sequenom EpiTYPER®. | Q40115079 | ||
| Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis | Q40143586 | ||
| The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter | Q40415783 | ||
| P4510 | describes a project that uses | limma | Q112236343 |
| edgeR | Q113334690 | ||
| minfi | Q113334816 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | amyotrophic lateral sclerosis | Q206901 |
| P304 | page(s) | 8254 | |
| P577 | publication date | 2019-06-04 | |
| P1433 | published in | Scientific Reports | Q2261792 |
| P1476 | title | Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression | |
| P478 | volume | 9 |
| Q89471917 | DNA damage accumulates and responses are engaged in human ALS brain and spinal motor neurons and DNA repair is activatable in iPSC-derived motor neurons with SOD1 mutations |
| Q89581381 | TNF receptor-associated factor 6 interacts with ALS-linked misfolded superoxide dismutase 1 and promotes aggregation |
| Q90615812 | Temporal evolution of the microbiome, immune system and epigenome with disease progression in ALS mice |
| Q93192447 | Twin Registries Moving Forward and Meeting the Future: A Review |
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