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Mathias Ehrich

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American Journal of Obstetrics and Gynecology|March 25, 2014
Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNARichard P Porreco, Thomas J Garite, Kimberly Maurel, et al.
American Journal of Obstetrics and Gynecology|March 15, 2023
Capillary blood collection: exploring a new method to promote noninvasive prenatal screening accessMathias Ehrich, Katelynn G Sagaser, Richard P Porreco, et al.
Cancer Research|November 17, 2006
Cytosine methylation profiles as a molecular marker in non-small cell lung cancerMathias Ehrich, John K Field, Triantafillos Liloglou, et al.
Clinical Chemistry|February 25, 2015
Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasmaChen Zhao, John Tynan, Mathias Ehrich, et al.
Genome Biology|April 18, 2015
Whole genome bisulfite sequencing of cell-free DNA and its cellular contributors uncovers placenta hypomethylated domainsTaylor J Jensen, Sung K Kim, Zhanyang Zhu, et al.
Cancer Research|February 11, 2010
General transcription factor binding at CpG islands in normal cells correlates with resistance to de novo DNA methylation in cancer cellsClaudia Gebhard, Chris Benner, Mathias Ehrich, et al.
Blood|January 20, 2007
The C/EBPdelta tumor suppressor is silenced by hypermethylation in acute myeloid leukemiaShuchi Agrawal, Wolf-Karsten Hofmann, Nicola Tidow, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 26, 2005
Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometryMathias Ehrich, Matthew R Nelson, Patrick Stanssens, et al.
Journal of Clinical Medicine|August 4, 2015
Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing TwinsSebastian Grömminger, Erbil Yagmur, Sanli Erkan, et al.
The Journal of Molecular Diagnostics : JMD|November 25, 2015
Ultrasensitive Detection of Multiplexed Somatic Mutations Using MALDI-TOF Mass SpectrometryMichael J Mosko, Aleksey A Nakorchevsky, Eunice Flores, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
American Journal of Obstetrics and Gynecology|March 25, 2014
Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNARichard P Porreco, Thomas J Garite, Kimberly Maurel, et al.
American Journal of Obstetrics and Gynecology|March 15, 2023
Capillary blood collection: exploring a new method to promote noninvasive prenatal screening accessMathias Ehrich, Katelynn G Sagaser, Richard P Porreco, et al.
Cancer Research|November 17, 2006
Cytosine methylation profiles as a molecular marker in non-small cell lung cancerMathias Ehrich, John K Field, Triantafillos Liloglou, et al.
Clinical Chemistry|February 25, 2015
Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasmaChen Zhao, John Tynan, Mathias Ehrich, et al.
Genome Biology|April 18, 2015
Whole genome bisulfite sequencing of cell-free DNA and its cellular contributors uncovers placenta hypomethylated domainsTaylor J Jensen, Sung K Kim, Zhanyang Zhu, et al.
Cancer Research|February 11, 2010
General transcription factor binding at CpG islands in normal cells correlates with resistance to de novo DNA methylation in cancer cellsClaudia Gebhard, Chris Benner, Mathias Ehrich, et al.
Blood|January 20, 2007
The C/EBPdelta tumor suppressor is silenced by hypermethylation in acute myeloid leukemiaShuchi Agrawal, Wolf-Karsten Hofmann, Nicola Tidow, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 26, 2005
Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometryMathias Ehrich, Matthew R Nelson, Patrick Stanssens, et al.
Journal of Clinical Medicine|August 4, 2015
Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing TwinsSebastian Grömminger, Erbil Yagmur, Sanli Erkan, et al.
The Journal of Molecular Diagnostics : JMD|November 25, 2015
Ultrasensitive Detection of Multiplexed Somatic Mutations Using MALDI-TOF Mass SpectrometryMichael J Mosko, Aleksey A Nakorchevsky, Eunice Flores, et al.
Pageof 5