Russell L. McLaughlin
University of Dublin Trinity College
34 papers found
Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studies
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
Association of a Locus in theCAMTA1Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis
No association between soil constituents and amyotrophic lateral sclerosis relative risk in Ireland
The selective anatomical vulnerability of ALS: 'disease-defining' and 'disease-defying' brain regions.
Genomic signals of migration and continuity in Britain before the Anglo-Saxons
C9orf72 expansion differentially affects males with spinal onset amyotrophic lateral sclerosis
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Upper Palaeolithic genomes reveal deep roots of modern Eurasians
Social deprivation and population density are not associated with small area risk of amyotrophic lateral sclerosis
Heritability of Amyotrophic Lateral Sclerosis: Insights From Disparate Numbers
Detection of novel germline mutations for breast cancer in non-BRCA1/2families
Homozygosity mapping in an Irish ALS case–control cohort describes local demographic phenomena and points towards potential recessive risk loci
A novel MYH7 Leu1453pro mutation resulting in Laing distal myopathy in an Irish family
A second-generation Irish genome-wide association study for amyotrophic lateral sclerosis
Genome flux and stasis in a five millennium transect of European prehistory
Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS.
Patterns of cerebral and cerebellar white matter degeneration in ALS: Figure 1
Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample
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