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Author Details

Michael W Nagle
Internal Medicine Research Unit
2008
18
13
PMIDPaper TitleJournal TitlePublished Year
36504281The genetic regulation of protein expression in cerebrospinal fluid.EMBO Mol Med2023
36711569The probability of edge existence due to node degree: a baseline for network-based predictions.bioRxiv2023
37503959Hetnet connectivity search provides rapid insights into how biomedical entities are related.Gigascience2022
34480422The genomics of heart failure: design and rationale of the HERMES consortium.ESC Heart Fail2021
33200983Lymphangiogenic therapy prevents cardiac dysfunction by ameliorating inflammation and hypertension.Elife2020
33067605Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.Nat Metab2020
31694701Multiplex proteomics identifies novel CSF and plasma biomarkers of early Alzheimer's disease.Acta Neuropathol Commun2019
28199695GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci.Hum Mol Genet2017
27479909Identification of 15 genetic loci associated with risk of major depression in individuals of European descent.Nat Genet2016
27869117Genome-wide RNAi screen reveals ALK1 mediates LDL uptake and transcytosis in endothelial cells.Nat Commun2016
27508417The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane.PLoS One2016
19300500A genome-wide association study of pulmonary function measures in the Framingham Heart Study.PLoS Genet2009
19461589Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study.Obesity (Silver Spring)2009
18317470NYD-SP18 is associated with obesity in the NHLBI Family Heart Study.Int J Obes (Lond)2008
18587682Replication of association between ELAVL4 and Parkinson disease: the GenePD study.Hum Genet2008
18509094Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.Neurology2008
18498660Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study.BMC Med Genet2008
18986508The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study.BMC Med2008
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