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Publications by Bernard Thienpont

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

American Journal of Human Genetics

English

The H3K9 Dimethyltransferases EHMT1/2 Protect Against Pathological Cardiac Hypertrophy

Journal of Clinical Investigation

English

Regulatory Dynamics of Tet1 and Oct4 Resolve Stages of Global DNA Demethylation and Transcriptomic Changes in Reprogramming

Molecular Biology

English

Genomic and Epigenomic Analysis of High-Risk Prostate Cancer Reveals Changes in Hydroxymethylation and TET1

English

Genetic Biomarkers in the VEGF Pathway Predicting Response to Anti-Vegf Therapy in Age-Related Macular Degeneration

BMJ Open Ophthalmology

English

Systems Genetics Analysis Identify Calcium Signalling Defects as Novel Cause of Congenital Heart Disease

English