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Author Details
Full Name
Michael W Nagle
Affiliation
Internal Medicine Research Unit
ORCID
Career Start Year
2008
Papers
18
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36504281
The genetic regulation of protein expression in cerebrospinal fluid.
EMBO Mol Med
2023
36711569
The probability of edge existence due to node degree: a baseline for network-based predictions.
bioRxiv
2023
37503959
Hetnet connectivity search provides rapid insights into how biomedical entities are related.
Gigascience
2022
34480422
The genomics of heart failure: design and rationale of the HERMES consortium.
ESC Heart Fail
2021
33200983
Lymphangiogenic therapy prevents cardiac dysfunction by ameliorating inflammation and hypertension.
Elife
2020
33067605
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Nat Metab
2020
31694701
Multiplex proteomics identifies novel CSF and plasma biomarkers of early Alzheimer's disease.
Acta Neuropathol Commun
2019
28199695
GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci.
Hum Mol Genet
2017
27479909
Identification of 15 genetic loci associated with risk of major depression in individuals of European descent.
Nat Genet
2016
27869117
Genome-wide RNAi screen reveals ALK1 mediates LDL uptake and transcytosis in endothelial cells.
Nat Commun
2016
27508417
The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane.
PLoS One
2016
19300500
A genome-wide association study of pulmonary function measures in the Framingham Heart Study.
PLoS Genet
2009
19461589
Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study.
Obesity (Silver Spring)
2009
18317470
NYD-SP18 is associated with obesity in the NHLBI Family Heart Study.
Int J Obes (Lond)
2008
18587682
Replication of association between ELAVL4 and Parkinson disease: the GenePD study.
Hum Genet
2008
18509094
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.
Neurology
2008
18498660
Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study.
BMC Med Genet
2008
18986508
The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study.
BMC Med
2008
1 - 18 of 18
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