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Author Details
Full Name
Mun-Gwan Hong
Affiliation
KTH Royal Institute of Technology
ORCID
Career Start Year
2007
Papers
42
H Index
20
Expertise
CM4AI Collaborator
Emma Lundberg (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37026541
Characterization of the Mitochondrial Genetic Landscape in Abdominal Aortic Aneurysm.
J Am Heart Assoc
2023
38012230
Author Correction: Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism.
Nat Commun
2023
37604891
Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits.
Nat Commun
2023
37286573
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism.
Nat Commun
2023
37231818
Soluble CD14 and Osteoprotegerin Associate with Ankle-Brachial Index as a Measure of Arterial Stiffness in Patients with Mild-to-Moderate Chronic Kidney Disease in a Five-Year Prospective Study.
Cardiorenal Med
2023
37130959
Author Correction: Discovery of drug-omics associations in type 2 diabetes with generative deep-learning models.
Nat Biotechnol
2023
35106505
Four groups of type 2 diabetes contribute to the etiological and clinical heterogeneity in newly diagnosed individuals: An IMI DIRECT study.
Cell Rep Med
2022
34140485
Multianalyte serology in home-sampled blood enables an unbiased assessment of the immune response against SARS-CoV-2.
Nat Commun
2021
33722194
Circulating proteins associated with allergy development in infants-an exploratory analysis.
Clin Proteomics
2021
34706560
Identification of Endothelial Proteins in Plasma Associated With Cardiovascular Risk Factors.
Arterioscler Thromb Vasc Biol
2021
34759311
Elevated circulating follistatin associates with an increased risk of type 2 diabetes.
Nat Commun
2021
32559194
Predicting and elucidating the etiology of fatty liver disease: A machine learning modeling and validation study in the IMI DIRECT cohorts.
PLoS Med
2020
33261667
Whole blood co-expression modules associate with metabolic traits and type 2 diabetes: an IMI-DIRECT study.
Genome Med
2020
32576278
Whole-genome sequence association analysis of blood proteins in a longitudinal wellness cohort.
Genome Med
2020
32629387
Facets of individual-specific health signatures determined from longitudinal plasma proteome profiling.
EBioMedicine
2020
32737166
Profiles of histidine-rich glycoprotein associate with age and risk of all-cause mortality.
Life Sci Alliance
2020
32235817
Molecular Profiling for Predictors of Radiosensitivity in Patients with Breast or Head-and-Neck Cancer.
Cancers (Basel)
2020
30358838
Targeted Analysis of Serum Proteins Encoded at Known Inflammatory Bowel Disease Risk Loci.
Inflamm Bowel Dis
2019
31772123
The human secretome.
Sci Signal
2019
29444691
Affinity proteomic profiling of plasma for proteins associated to area-based mammographic breast density.
Breast Cancer Res
2018
30175270
Novel Multiomics Profiling of Human Carotid Atherosclerotic Plaques and Plasma Reveals Biliverdin Reductase B as a Marker of Intraplaque Hemorrhage.
JACC Basic Transl Sci
2018
27700103
Identification of a Novel Autoimmune Peptide Epitope of Prostein in Prostate Cancer.
J Proteome Res
2017
28674890
High-Density Serum/Plasma Reverse Phase Protein Arrays.
Methods Mol Biol
2017
25689831
Affinity proteomics discovers decreased levels of AMFR in plasma from Osteoporosis patients.
Proteomics Clin Appl
2016
26558424
Immunocapture strategies in translational proteomics.
Expert Rev Proteomics
2016
27742707
PDGFB, a new candidate plasma biomarker for venous thromboembolism: results from the VEREMA affinity proteomics study.
Blood
2016
27570895
Multidimensional Normalization to Minimize Plate Effects of Suspension Bead Array Data.
J Proteome Res
2016
25356426
Plasma profiling reveals three proteins associated to amyotrophic lateral sclerosis.
Ann Clin Transl Neurol
2014
25231264
Affinity proteomic profiling of plasma, cerebrospinal fluid, and brain tissue within multiple sclerosis.
J Proteome Res
2014
23281178
A genome-wide assessment of variability in human serum metabolism.
Hum Mutat
2013
23631827
Profiling post-centrifugation delay of serum and plasma with antibody bead arrays.
J Proteomics
2013
22190428
Genome-wide and gene-based association implicates FRMD6 in Alzheimer disease.
Hum Mutat
2012
21116047
Associations of gene sequence variation and serum levels of C-reactive protein and interleukin-6 with Alzheimer's disease and dementia.
J Alzheimers Dis
2011
21297263
Genetic association of sequence variants near AGER/NOTCH4 and dementia.
J Alzheimers Dis
2011
19653016
Sequence variation in SORL1 and dementia risk in Swedes.
Neurogenetics
2010
20668461
Genome-wide pathway analysis implicates intracellular transmembrane protein transport in Alzheimer disease.
J Hum Genet
2010
20167577
Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk.
Hum Mol Genet
2010
19408013
Strategies and issues in the detection of pathway enrichment in genome-wide association studies.
Hum Genet
2009
19606474
A survey of ABCA1 sequence variation confirms association with dementia.
Hum Mutat
2009
18448515
Evidence that the gene encoding insulin degrading enzyme influences human lifespan.
Hum Mol Genet
2008
18714388
Transcriptome-wide assessment of human brain and lymphocyte senescence.
PLoS One
2008
17356550
Phenotype selection for detecting variable genes: a survey of cardiovascular quantitative traits and TNF locus polymorphism.
Eur J Hum Genet
2007
1 - 42 of 42
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