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2. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

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

4. The toxic metal hypothesis for neurological disorders.

5. Potentially toxic elements in the brains of people with multiple sclerosis.

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

7. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

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

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

10. Mercury is present in neurons and oligodendrocytes in regions of the brain affected by Parkinson's disease and co-localises with Lewy bodies.

11. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)

12. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

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

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

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

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

17. Mercury in the human thyroid gland: Potential implications for thyroid cancer, autoimmune thyroiditis, and hypothyroidism

18. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

19. The Prevalence of Inorganic Mercury in Human Kidneys Suggests a Role for Toxic Metals in Essential Hypertension

20. Mercury in the human adrenal medulla could contribute to increased plasma noradrenaline in aging

21. Elemental imaging shows mercury in cells of the human lateral and medial geniculate nuclei

22. Genome-wide Meta-analysis finds the ACSL5-ZDHHC6 locus Is associated with ALS and links weight loss to the disease genetics

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

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

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

26. The distribution of toxic metals in the human retina and optic nerve head: Implications for age-related macular degeneration.

27. Elemental bioimaging shows mercury and other toxic metals in normal breast tissue and in breast cancers.

28. Mercury in Pancreatic Cells of People with and without Pancreatic Cancer.

29. Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardioyopathy and SNP genotyping in motor neurone disease

34. The Ehlers-danlos syndrome in a xhosa male

35. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

40. Elemental analysis of aging human pituitary glands implicates mercury as a contributor to the somatopause

41. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

43. The Ehlers-Danlos Syndrome in a Xhosa Male

47. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

48. Age-related accumulation of toxic metals in the human locus ceruleus

49. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

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