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1. APOE E4 is associated with impaired self-declared cognition but not disease risk or age of onset in Nigerians with Parkinson’s disease

2. Epigenetic signature of human immune aging in the GESTALT study

3. Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies

4. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

5. MIDN locus structural variants and Parkinson's Disease risk

6. New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk

7. Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels

8. Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.

9. Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.

10. Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts.

11. Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.

12. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.

13. Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis

14. Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24.

15. Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus.

16. Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.

17. Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

18. A genome-wide association study identifies protein quantitative trait loci (pQTLs).

19. Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.

20. A Double‐Blind, Randomized, Placebo‐Controlled Trial of Ursodeoxycholic Acid (<scp>UDCA)</scp> in Parkinson's Disease

21. MAPTallele and haplotype frequencies in Nigerian Africans: population distribution and association with Parkinson’s disease risk and age at onset

22. Epigenetic signature of human immune aging: the GESTALT study

23. Polygenic Parkinson’s disease genetic risk score as risk modifier of parkinsonism in Gaucher disease

24. APOE E4 is associated with cognitive decline but not with disease risk or age of onset in Nigerians with Parkinson’s disease

25. Profiling the NOTCH2NLC GGC Repeat Expansion in Parkinson's Disease in the European Population

26. Unique and shared molecular features of human B and T lymphocyte memory differentiation

27. Candidate Gene Polymorphisms for Ischemic Stroke

28. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

29. Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer’s disease

30. LRP10 in α-synucleinopathies

31. Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease

32. Initial assessment of the pathogenic mechanisms of the recently identified Alzheimer risk Loci

33. Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci

34. Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing

35. A polymorphism in the GALNT2 gene and ovarian cancer risk in four population based case-control studies

36. META-ANALYSIS ON IRON TRAITS REVEALS NOVEL GENETIC LOCI FOR IRON AND FERRITIN LEVELS AND A COMMON VARIANT IN TMPRSS6 THAT INFLUENCES HEPCIDIN LEVELS

37. Neurofibrillary tau pathology modulated by genetic variation of alpha-synuclein

38. Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11

39. A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion

40. X-linked recessive dystonia parkinsonism (XDP; Lubag; DYT3)

41. X-linked dystonia ('Lubag') presenting predominantly with parkinsonism: a more benign phenotype?

43. Case-control study of the α-synuclein interacting protein gene and Parkinson's disease.

44. Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.

45. A Paired RNAi and RabGAP Overexpression Screen Identifies Rab11 as a Regulator of β-Amyloid Production

46. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

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