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30 results on '"Landers J.E."'

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2. List of Contributors

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

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

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

6. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

7. Reconsidering the causality of TIA1 mutations in ALS

8. Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

9. Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort

10. CHCHD10 variants in amyotrophic lateral sclerosis: where Is the evidence?

11. Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology

13. C9orf72 and UNC13A Are Shared Risk Loci for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia: A Genome-Wide Meta-Analysis

14. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

15. Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study

16. No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis

17. Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS

18. Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.

19. Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis

20. A large genome scan for rare CNVs in amyotrophic lateral sclerosis.

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

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

28. Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology

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

30. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

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