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2. Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)

5. Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia

6. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

9. Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes

10. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

12. Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

13. Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia

15. NEK1 and STMN2 short tandem repeat lengths are not associated with Australian amyotrophic lateral sclerosis risk

16. Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS

19. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

22. Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

23. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

24. Genetic Analysis of Tryptophan Metabolism Genes in Sporadic Amyotrophic Lateral Sclerosis

25. Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosis

26. Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia

27. Coexisting Lewy body disease and clinical parkinsonism in amyotrophic lateral sclerosis

28. Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

29. Riluzole is associated with decreasing neuritic plaque severity in amyotrophic lateral sclerosis.

30. Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

31. Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics

36. Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis

37. Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice

46. Safety and tolerability of Triumeq in amyotrophic lateral sclerosis: the Lighthouse trial

47. IBD analysis of Australian amyotrophic lateral sclerosis SOD1-mutation carriers identifies five founder events and links sporadic cases to existing ALS families

48. Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression

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