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684 results on '"Kwok, John B."'

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1. Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

3. A potential patient stratification biomarker for Parkinson´s disease based on LRRK2 kinase-mediated centrosomal alterations in peripheral blood-derived cells

4. Identification of blood eQTLs in older adults

5. Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning

6. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

7. Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group

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

12. Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.

13. Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

14. High polygenic risk score for exceptional longevity is associated with a healthy metabolic profile

15. Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

16. Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.

17. Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

20. Genetic variants associated with longitudinal changes in brain structure across the lifespan

21. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

22. Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume.

25. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

30. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

31. Genetic architecture of subcortical brain structures in 38,851 individuals

34. Genetic variants for head size share genes and pathways with cancer

35. A blood-based marker of mitochondrial DNA damage in Parkinson’s disease

36. Poly‐GA immunohistochemistry is a reliable tool for detecting C9orf72 hexanucleotide repeat expansions.

39. Analysis of DNA methylation associates the cystine–glutamate antiporter SLC7A11 with risk of Parkinson’s disease

42. Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing

43. Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

44. Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia

45. Creating the Pick’s disease International Consortium: Association study ofMAPTH2 haplotype with risk of Pick’s disease

46. A potential patient stratification biomarker for Parkinson's disease based on LRRK2 kinase-mediated centrosomal alterations in peripheral blood-derived cells

48. Frontotemporal dementia and its subtypes: a genome-wide association study

50. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

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