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7. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

8. Deep phenotyping of peripheral tissue facilitates mechanistic disease stratification in sporadic Parkinson’s disease

9. Macro- and micro-structural insights into primary dystonia: a UK Biobank study

10. The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function

11. Reproducibility of Molecular Phenotypes after Long-Term Differentiation to Human iPSC-Derived Neurons: A Multi-Site Omics Study

16. Antiviral activity of bone morphogenetic proteins and activins

17. Artificial intelligence for dementia genetics and omics

18. Correction: The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function

24. Non‐motor phenotypic subgroups in adult‐onset idiopathic, isolated, focal cervical dystonia

25. On the detection of imprinted quantitative trait loci in line crosses: effect of linkage disequilibrium

26. Cerebral small vessel disease genomics and its implications across the lifespan

27. A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

28. Linkage disequilibrium on the bovine X chromosome: characterization and use in quantitative trait locus mapping

29. A human single-cell atlas of the Substantia nigra reveals novel cell-specific pathways associated with the genetic risk of Parkinson’s disease and neuropsychiatric disorders

30. Analysis of shared heritability in common disorders of the brain

31. Universal continuous severity traits underlying hundreds of Parkinson’s disease clinical features

32. The Parkinson's Disease Genome‐Wide Association Study Locus Browser

33. Molecular genetic overlap between migraine and major depressive disorder

34. Correction: The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function

35. The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function

36. Universal latent axes capturing Parkinson’s patient deep phenotypic variation reveals patients with a high genetic risk for Alzheimer’s disease are more likely to develop a more aggressive form of Parkinson’s

37. F80GENOME-WIDE ASSOCIATION OF 45 LOCI WITH MOOD INSTABILITY IN 363,705 UK BIOBANK PARTICIPANTS: GENETIC CORRELATION WITH MULTIPLE PSYCHIATRIC PHENOTYPES AND ASSOCIATION WITH NERVOUS SYSTEM FUNCTION

38. The Parkinson's Disease Genome‐Wide Association Study Locus Browser.

39. Antiviral activity of bone morphogenetic proteins and activins

40. Analysis of shared heritability in common disorders of the brain

41. Analysis of shared heritability in common disorders of the brain

43. Whole-exome sequencing of 228 patients with sporadic Parkinson’s disease

44. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

45. Genome-Wide Association Study of Pain in Parkinson's Disease Implicates TRPM8 as a Risk Factor.

46. Use of a Multiethnic Approach to Identify Rheumatoid- Arthritis-Susceptibility Loci, 1p36 and 17q12

47. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

48. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

49. Common variants at five new loci associated with early-onset inflammatory bowel disease.

50. Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.

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