Mathias Ehrich
Publications by Year
Research Areas
Epigenetics and DNA Methylation, Prenatal Screening and Diagnostics, RNA modifications and cancer, Cancer Genomics and Diagnostics, Fetal and Pediatric Neurological Disorders
Most-Cited Works
- → Oct4-Induced Pluripotency in Adult Neural Stem Cells(2009)941 cited
- → DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study(2011)931 cited
- → Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry(2005)814 cited
- → DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study(2012)519 cited
- → Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting(2011)475 cited
- → Dnmt3b promotes tumorigenesis in vivo by gene-specific de novo methylation and transcriptional silencing(2007)271 cited
- → Wnt inhibitory factor 1 is epigenetically silenced in human osteosarcoma, and targeted disruption accelerates osteosarcomagenesis in mice(2009)268 cited
- → Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts(2015)238 cited
- → Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants(2016)203 cited
- → Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell‐free DNA from maternal plasma(2013)200 cited