Publications by authors named "Mathias Ehrich"

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Capillary blood collection: exploring a new method to promote noninvasive prenatal screening access.
Mathias Ehrich, Katelynn G Sagaser, Richard P Porreco, Deborah Bellesheim, Avinash S Patil

Am J Obstet Gynecol· July 2023

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Genome-Wide Sequencing of Cell-Free DNA Identifies Copy-Number Alterations That Can Be Used for Monitoring Response to Immunotherapy in Cancer Patients.
Taylor J Jensen, Aaron M Goodman, Shumei Kato, Christopher K Ellison, Gregory A Daniels, Mathias Ehrich

Mol Cancer Ther· February 2019

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Incidental Detection of Maternal Neoplasia in Noninvasive Prenatal Testing.
Nilesh G Dharajiya, Daniel S Grosu, Daniel H Farkas, Ron M McCullough, Eyad Almasri, Mathias Ehrich

Clin Chem· February 2018

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Genome-wide cfDNA screening: clinical laboratory experience with the first 10,000 cases.
Mathias Ehrich, John Tynan, Amin Mazloom, Eyad Almasri, Ron McCullough

Genet Med· December 2017

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Using Targeted Sequencing of Paralogous Sequences for Noninvasive Detection of Selected Fetal Aneuploidies.
Christopher K Ellison, Youting Sun, Grant Hogg, Jesse Fox, Helen Tao, Mathias Ehrich

Clin Chem· December 2016

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Mathias Ehrich, Daniel Grosu, Dirk van den Boom, John Tynan

Am J Obstet Gynecol· October 2016

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Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants.
Roy B Lefkowitz, John A Tynan, Tong Liu, Yijin Wu, Amin R Mazloom, Mathias Ehrich

Am J Obstet Gynecol· August 2016

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Ultrasensitive Detection of Multiplexed Somatic Mutations Using MALDI-TOF Mass Spectrometry.
Michael J Mosko, Aleksey A Nakorchevsky, Eunice Flores, Heath Metzler, Mathias Ehrich

J Mol Diagn· January 2016

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Copy-Number Variation and False Positive Results of Prenatal Screening.
Dirk van den Boom, Mathias Ehrich, Sung K Kim

N Engl J Med· December 2015

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Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts.
Sung K Kim, Gregory Hannum, Jennifer Geis, John Tynan, Grant Hogg, Mathias Ehrich

Prenat Diagn· August 2015

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Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma.
Chen Zhao, John Tynan, Mathias Ehrich, Gregory Hannum, Ron McCullough

Clin Chem· April 2015

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Whole genome bisulfite sequencing of cell-free DNA and its cellular contributors uncovers placenta hypomethylated domains.
Taylor J Jensen, Sung K Kim, Zhanyang Zhu, Christine Chin, Claudia Gebhard, Mathias Ehrich

Genome Biol· April 2015

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Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA.
Richard P Porreco, Thomas J Garite, Kimberly Maurel, Barbara Marusiak, , Mathias Ehrich

Am J Obstet Gynecol· October 2014

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Noninvasive detection of a balanced fetal translocation from maternal plasma.
Taylor J Jensen, Sung K Kim, Dirk van den Boom, Cosmin Deciu, Mathias Ehrich

Clin Chem· October 2014

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Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins.
Sebastian Grömminger, Erbil Yagmur, Sanli Erkan, Sándor Nagy, Ulrike Schöck, Mathias Ehrich

J Clin Med· June 2014

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Maternal plasma DNA testing for aneuploidy in pregnancies achieved by assisted reproductive technologies.
Geralyn Lambert-Messerlian, Edward M Kloza, John Williams, Jaroslav Loucky, Barbara O'Brien, Mathias Ehrich

Genet Med· May 2014

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High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasma.
Taylor J Jensen, Tricia Zwiefelhofer, Roger C Tim, Željko Džakula, Sung K Kim, Mathias Ehrich

PLoS One· September 2013

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Optimizing blood collection, transport and storage conditions for cell free DNA increases access to prenatal testing.
David Wong, Sharmili Moturi, Vach Angkachatchai, Reinhold Mueller, Grace DeSantis, Mathias Ehrich

Clin Biochem· August 2013

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Cell-type specific DNA methylation patterns define human breast cellular identity.
Petr Novak, Martha R Stampfer, Jose L Munoz-Rodriguez, James C Garbe, Mathias Ehrich

PLoS One· June 2013

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Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma.
Amin R Mazloom, Željko Džakula, Paul Oeth, Huiquan Wang, Taylor Jensen, Mathias Ehrich

Prenat Diagn· June 2013

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Stemness of the organ of Corti relates to the epigenetic status of Sox2 enhancers.
Jörg Waldhaus, Jelka Cimerman, Henning Gohlke, Mathias Ehrich, Marcus Müller

PLoS One· January 2013

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DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations.
Jacob A Canick, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow, Mathias Ehrich

Prenat Diagn· August 2012

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Detection of microdeletion 22q11.2 in a fetus by next-generation sequencing of maternal plasma.
Taylor J Jensen, Zeljko Dzakula, Cosmin Deciu, Dirk van den Boom, Mathias Ehrich

Clin Chem· July 2012

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DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study.
Glenn E Palomaki, Cosmin Deciu, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow, Mathias Ehrich

Genet Med· March 2012

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DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study.
Glenn E Palomaki, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow, Louis M Neveux, Mathias Ehrich

Genet Med· November 2011

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