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25 results on '"Nicolas, Aude"'

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1. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

2. « Les sinistres seuils » : Sexualité et paranoïa dans la littérature templière

3. Les fantômes d’Isaac Babel : aux confins du texte et de la mémoire

4. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

5. CADPS functional mutations in patients with bipolar disorder increase the sensitivity to stress

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

7. Multiancestry analysis of the HLA locus in Alzheimer’s and Parkinson’s diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes.

8. Genome-Wide Association Analysis of the Sense of Smell in U.S. Older Adults: Identification of Novel Risk Loci in African-Americans and European-Americans

9. Rare missense variant (R251G) on APOE counterbalances the Alzheimer's disease risk associated with APOE‐ε4.

10. Protective association of HLA‐DRB1*04 subtypes in neurodegenerative diseases implicates acetylated tau PHF6 sequences.

11. Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease.

12. Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study

13. A Meta‐Analysis of the Transferability of Bone Mineral Density Genetic Loci Associations From European to African Ancestry Populations.

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

15. Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease.

16. Genome-Wide Association Analysis of the Sense of Smell in U.S. Older Adults: Identification of Novel Risk Loci in African-Americans and European-Americans.

17. Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease.

18. Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.

19. Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability.

20. De novo mutations in HCN1 cause early infantile epileptic encephalopathy.

21. Les rapports franco-britanniques à travers la peinture militaire représentant la guerre de Crimée.

22. Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

23. Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study.

24. F35MUTATIONS IN CADPS IDENTIFIED IN PATIENTS WITH BIPOLAR DISORDER AFFECT PROTEIN FUNCTIONS AND RESULT IN A HIGHER SENSITIVITY TO STRESS.

25. NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases.

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