732 results on '"Orr-Urtreger, Avi"'
Search Results
2. Genome-wide case-only analysis of gene-gene interactions with known Parkinson’s disease risk variants reveals link between LRRK2 and SYT10
3. Longitudinal Measurements of Glucocerebrosidase activity in Parkinson’s patients
4. Variants in PSMB9 and FGR differentially affect Parkinson's disease risk in GBA and LRRK2 mutation carriers
5. Validity of the Short Weekly Calendar Planning Activity in patients with Parkinson disease and nonmanifesting LRRK2 and GBA carriers
6. Decreased delta-band event-related power in dementia with Lewy bodies with a mutation in the glucocerebrosidase gene
7. Feasibility and safety of lumbar puncture in the Parkinson's disease research participants: Parkinson's Progression Marker Initiative (PPMI)
8. Aberrant dopamine transporter and functional connectivity patterns in LRRK2 and GBA mutation carriers
9. Estimation of Genetic Risk Function with Covariates in the Presence of Missing Genotypes
10. Biochemical markers for severity and risk in GBA and LRRK2 Parkinson’s disease
11. FUS-P525L Juvenile Amyotrophic Lateral Sclerosis and Intellectual Disability: Evidence for Association and Oligogenic Inheritance
12. Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study
13. MAPT Locus in Parkinson’s Disease Patients of Ashkenazi Origin: A Stratified Analysis
14. Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium
15. Higher Frequency of Certain Cancers in LRRK2 G2019S Mutation Carriers With Parkinson Disease: A Pooled Analysis
16. Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease genetics
17. Parkinson's disease phenotype is influenced by the severity of the mutations in the GBA gene
18. MAPT Locus in Parkinson's Disease Patients of Ashkenazi Origin: A Stratified Analysis.
19. Altered reward-related neural responses in non-manifesting carriers of the Parkinson disease related LRRK2 mutation
20. Single cell dissection of plasma cell heterogeneity in symptomatic and asymptomatic myeloma
21. CONFIDENTIAL novel variants in genes related to vesicle-mediated-transport modify Parkinson's disease risk
22. Central Role of α7 Nicotinic Receptor in Differentiation of the Stratified Squamous Epithelium
23. A “dose” effect of mutations in the GBA gene on Parkinson's disease phenotype
24. Metabolic syndrome does not influence the phenotype of LRRK2 and GBA related Parkinson’s disease
25. Megacystis, Mydriasis, and Ion Channel Defect in Mice Lacking the α 3 Neuronal Nicotinic Acetylcholine Receptor
26. Central role of alpha7 nicotinic receptor in differentiation of the stratified squamous epithelium.
27. The influence of GBA and LRRK2 on mood disorders in Parkinson's Disease
28. Cellular and humoral immune response to the fourth Pfizer-BioNTech COVID-19 vaccine dose in individuals aged 60 years and older
29. Linkage of a Neurophysiological Deficit in Schizophrenia to a Chromosome 15 Locus
30. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
31. Novel variants in genes related to vesicle-mediated-transport modify Parkinson's disease risk
32. Distinguishing Dementia With Lewy Bodies From Alzheimer Disease: What is the Influence of the GBA Genotype in Ashkenazi Jews?
33. LRRK2 mutations in Parkinson disease; a sex effect or lack thereof? A meta-analysis
34. Genetic markers of Restless Legs Syndrome in Parkinson disease
35. Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's disease
36. Variable PARK2 Mutations Cause Early-Onset Parkinson’s Disease in a Small Restricted Population
37. A cognitive fMRI study in non-manifesting LRRK2 and GBA carriers
38. Efficient estimation of nonparametric genetic risk function with censored data
39. Progression in the LRRK2-Asssociated Parkinson Disease Population
40. Neural correlates of executive functions in healthy G2019S LRRK2 mutation carriers
41. SEPT14 Is Associated with a Reduced Risk for Parkinson’s Disease and Expressed in Human Brain
42. High frequency of C9orf72 hexanucleotide repeat expansion in amyotrophic lateral sclerosis patients from two founder populations sharing the same risk haplotype
43. Interest in Genetic Testing in Ashkenazi Jewish Parkinson’s Disease Patients and Their Unaffected Relatives
44. Glucocerebrosidase Activity Is Not Associated with Parkinson's Disease Risk or Severity
45. Fighting the risk of developing Parkinson's disease; clinical counseling for first degree relatives of patients with Parkinson's disease
46. Familial Clustering of Site-Specific Cancer Risks Associated with BRCA1 and BRCA2 Mutations in the Ashkenazi Jewish Population
47. C9orf72-G4C2 Intermediate Repeats and Parkinson’s Disease
48. Intact working memory in non-manifesting LRRK2 carriers – an fMRI study
49. PARK16 locus: Differential effects of the non-coding rs823114 on Parkinson’s disease risk, RNA expression, and DNA methylation
50. Glucocerebrosidase Activity is not Associated with Parkinson's Disease Risk or Severity
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.