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Author Details
Full Name
Matthias Wielscher
Affiliation
School of Public Health, Imperial College London
ORCID
Career Start Year
2011
Papers
40
H Index
18
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36628896
Discovery of a previously unreported deletion in the CDKN2A gene in a case of familial melanoma in Austria.
Eur J Cancer
2023
37749248
Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.
Nat Genet
2023
37675143
Non-IgE-reactive allergen peptides deteriorate the skin barrier in house dust mite-sensitized atopic dermatitis patients.
Front Cell Dev Biol
2023
37012456
Genetic effects on the timing of parturition and links to fetal birth weight.
Nat Genet
2023
37444464
Identification of Genetic Risk Factors for Keratinocyte Cancer in Immunosuppressed Solid Organ Transplant Recipients: A Case-Control Study.
Cancers (Basel)
2023
36936266
The interplay between inflammatory cytokines and cardiometabolic disease: bi-directional mendelian randomisation study.
BMJ Med
2023
36757443
Impact of the COVID-19 pandemic on the epidemiology of severe burns : A single center study from a specialized burn center in Vienna.
Wien Klin Wochenschr
2023
34997067
Single-cell transcriptomics defines keratinocyte differentiation in avian scutate scales.
Sci Rep
2022
35504910
DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases.
Nat Commun
2022
36333467
The transcriptional profile of keloidal Schwann cells.
Exp Mol Med
2022
34154662
Genetic correlation and causal relationships between cardio-metabolic traits and lung function impairment.
Genome Med
2021
33794208
Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study.
Lancet Oncol
2021
34887417
Meta-analyses identify DNA methylation associated with kidney function and damage.
Nat Commun
2021
34588469
Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function.
Sci Rep
2021
34758253
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.
N Engl J Med
2021
34785669
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
Nat Commun
2021
33968070
Single-Cell RNA Sequencing Reveals Tissue Compartment-Specific Plasticity of Mycosis Fungoides Tumor Cells.
Front Immunol
2021
31074781
Exploring the role of genetic confounding in the association between maternal and offspring body mass index: evidence from three birth cohorts.
Int J Epidemiol
2020
31926111
Association of adult lung function with accelerated biological aging.
Aging (Albany NY)
2020
32363781
Determinants of accelerated metabolomic and epigenetic aging in a UK cohort.
Aging Cell
2020
32546146
Role of DNA methylation in the association of lung function with body mass index: a two-step epigenetic Mendelian randomisation study.
BMC Pulm Med
2020
30804560
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Nat Genet
2019
31262328
DNA methylation links prenatal smoking exposure to later life health outcomes in offspring.
Clin Epigenetics
2019
31015461
Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight.
Nat Commun
2019
29481666
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.
Hum Mol Genet
2018
30134983
SERPINA1 methylation and lung function in tobacco-smoke exposed European children and adults: a meta-analysis of ALEC population-based cohorts.
Respir Res
2018
30442561
Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults.
EBioMedicine
2018
29617535
Association of Methylation Signals With Incident Coronary Heart Disease in an Epigenome-Wide Assessment of Circulating Tumor Necrosis Factor α.
JAMA Cardiol
2018
28624884
Age at menarche and lung function: a Mendelian randomization study.
Eur J Epidemiol
2017
28166213
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.
Nat Genet
2017
28320365
Systematic review of lung function and COPD with peripheral blood DNA methylation in population based studies.
BMC Pulm Med
2017
28093691
Middle age enhances expression of innate immunity genes in a female mouse model of pulmonary fibrosis.
Biogerontology
2017
26425700
Diagnostic Performance of Plasma DNA Methylation Profiles in Lung Cancer, Pulmonary Fibrosis and COPD.
EBioMedicine
2015
24512058
Increased antioxidant defense mechanism in human adventitia-derived progenitor cells is associated with therapeutic benefit in ischemia.
Antioxid Redox Signal
2014
25531255
Strategies for validation and testing of DNA methylation biomarkers.
Epigenomics
2014
24044680
Age influence on hypersensitivity pneumonitis induced in mice by exposure to Pantoea agglomerans.
Inhal Toxicol
2013
24466374
Cytosine 5-Hydroxymethylation of the LZTS1 Gene Is Reduced in Breast Cancer.
Transl Oncol
2013
22133121
DNA methylation testing and marker validation using PCR: diagnostic applications.
Expert Rev Mol Diagn
2012
22750649
The stem cell signature of CHH/CHG methylation is not present in 271 cancer associated 5'UTR gene regions.
Biochimie
2012
21896199
Methyl-binding domain protein-based DNA isolation from human blood serum combines DNA analyses and serum-autoantibody testing.
BMC Clin Pathol
2011
1 - 40 of 40
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