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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

20. GenoML: Automated Machine Learning for Genomics

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

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

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

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

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

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

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

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

32. 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

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

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

35. A cellular taxonomy of the adult human spinal cord

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

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

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

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

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

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

42. GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.

43. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

44. Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

45. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

46. Multi-modality machine learning predicting Parkinson’s disease

47. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

49. Identification and prediction of Parkinson’s disease subtypes and progression using machine learning in two cohorts

50. Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects

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