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1. Proteomics identifies potential immunological drivers of postinfection brain atrophy and cognitive decline

2. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

3. Multi-ancestry meta-analysis and fine-mapping in Alzheimer’s disease

5. Characterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing

6. Profiling complex repeat expansions in RFC1 in Parkinson’s disease

8. Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease

9. The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism

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

12. A CRISPRi/a platform in human iPSC-derived microglia uncovers regulators of disease states

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

14. Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

15. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

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

17. Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

18. Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

19. Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

20. Author Correction: The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson’s disease data

21. Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson’s disease in Chinese population

22. The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson’s disease data

23. Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts

27. GenoML: Automated Machine Learning for Genomics

28. FGL1 as a modulator of plasma D‐dimer levels: Exome‐wide marker analysis of plasma tPA, PAI‐1, and D‐dimer

29. Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis

32. Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

33. Stroke genetics informs drug discovery and risk prediction across ancestries

34. A saturated map of common genetic variants associated with human height

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

37. Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

38. Learning the progression and clinical subtypes of Alzheimer's disease from longitudinal clinical data

39. Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium

40. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

41. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.

42. A cellular taxonomy of the adult human spinal cord

43. The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources

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

45. Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

46. The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease

47. GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations

48. Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset

49. Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability

50. MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease

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