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Your search keyword '"Rouleau, G.A."' showing total 17 results

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17 results on '"Rouleau, G.A."'

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1. Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage

2. Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information

3. SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease

4. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

5. A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly.

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

7. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

8. The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

9. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

10. A Locus for Autosomal Dominant Hereditary Spastic Ataxia, SAX1, Maps to Chromosome 12p13.

11. Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

12. Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies

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

14. Genome-wide association study identifies 30 loci associated with bipolar disorder

15. Common variants in P2RY11 are associated with narcolepsy

16. Narcolepsy is strongly associated with the T-cell receptor alpha locus

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

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