H. Eka D. Suchiman
Leiden University Medical Center
33 papers found
A framework for the detection of de novo mutations in family-based sequencing data
Systemic Age-Associated DNA Hypermethylation of ELOVL2 Gene: In Vivo and In Vitro Evidences of a Cell Replication Process.
Genetic and environmental influences interact with age and sex in shaping the human methylome
Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs
Disease variants alter transcription factor levels and methylation of their binding sites
DNA Methylation Landscapes of Human Fetal Development
Design, measurement and processing of region-specific DNA methylation assays: the mass spectrometry-based method EpiTYPER
Population-specific genotype imputations using minimac or IMPUTE2
Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations
Early gestation as the critical time-window for changes in the prenatal environment to affect the adult human blood methylome
Genome of the Netherlands population - specific imputations identify an ABCA6 variant associated with cholesterol levels
EpiTYPER®: a protocol for assay design, measurement and data processing of region-specific DNA methylation using mass spectrometry
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands'
Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markers
Identification of seven loci affecting mean telomere length and their association with disease
The Adult Netherlands Twin Register: Twenty-Five Years of Survey and Biological Data Collection
Identification and systematic annotation of tissue-specific differentially methylated regions using the Illumina 450k array:
Human Longevity and Variation in GH/IGF-1/Insulin Signaling, DNA Damage Signaling and Repair and Pro/antioxidant Pathway Genes: Cross Sectional and Longitudinal Studies
Evidence from case–control and longitudinal studies supports associations of genetic variation in APOE, CETP, and IL6 with human longevity
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