Следене
Mathias Ehrich
Mathias Ehrich
Vice President R&D, Sequenom, Inc.
Потвърден имейл адрес: sequenom.com
Заглавие
Позовавания
Позовавания
Година
Oct4-induced pluripotency in adult neural stem cells
JB Kim, V Sebastiano, G Wu, MJ Araúzo-Bravo, P Sasse, L Gentile, K Ko, ...
cell 136 (3), 411-419, 2009
12892009
DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study
GE Palomaki, EM Kloza, GM Lambert-Messerlian, JE Haddow, ...
Genetics in medicine 13 (11), 913-920, 2011
12082011
Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry
M Ehrich, MR Nelson, P Stanssens, M Zabeau, T Liloglou, G Xinarianos, ...
Proceedings of the National Academy of Sciences 102 (44), 15785-15790, 2005
9582005
DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study
GE Palomaki, C Deciu, EM Kloza, GM Lambert-Messerlian, JE Haddow, ...
Genetics in medicine 14 (3), 296-305, 2012
7652012
Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting
M Ehrich, C Deciu, T Zwiefelhofer, JA Tynan, L Cagasan, R Tim, V Lu, ...
American journal of obstetrics and gynecology 204 (3), 205. e1-205. e11, 2011
7462011
Wnt inhibitory factor 1 is epigenetically silenced in human osteosarcoma, and targeted disruption accelerates osteosarcomagenesis in mice
M Kansara, M Tsang, L Kodjabachian, NA Sims, MK Trivett, M Ehrich, ...
The Journal of clinical investigation 119 (4), 837-851, 2009
3302009
Dnmt3b promotes tumorigenesis in vivo by gene-specific de novo methylation and transcriptional silencing
HG Linhart, H Lin, Y Yamada, E Moran, EJ Steine, S Gokhale, G Lo, ...
Genes & development 21 (23), 3110-3122, 2007
3162007
Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell‐free DNA from maternal plasma
AR Mazloom, Ž Džakula, P Oeth, H Wang, T Jensen, J Tynan, ...
Prenatal diagnosis 33 (6), 591-597, 2013
2262013
DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations
JA Canick, EM Kloza, GM Lambert‐Messerlian, JE Haddow, M Ehrich, ...
Prenatal diagnosis 32 (8), 730-734, 2012
2242012
Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts
SK Kim, G Hannum, J Geis, J Tynan, G Hogg, C Zhao, TJ Jensen, ...
Prenatal diagnosis 35 (8), 810-815, 2015
2192015
Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non invasive prenatal diagnoses
M Ehrich, AOH Nygren, TJ Jensen
200*2011
Quantification of fetal DNA by use of methylation-based DNA discrimination
AOH Nygren, J Dean, TJ Jensen, S Kruse, W Kwong, D van den Boom, ...
Clinical Chemistry 56 (10), 1627-1635, 2010
1972010
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
RP Porreco, TJ Garite, K Maurel, B Marusiak, OCR Network, M Ehrich, ...
American journal of obstetrics and gynecology 211 (4), 365. e1-365. e12, 2014
1962014
Quantitative DNA methylation predicts survival in adult acute myeloid leukemia
L Bullinger, M Ehrich, K Döhner, RF Schlenk, H Döhner, MR Nelson, ...
Blood, The Journal of the American Society of Hematology 115 (3), 636-642, 2010
1882010
Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants
RB Lefkowitz, JA Tynan, T Liu, Y Wu, AR Mazloom, E Almasri, G Hogg, ...
American journal of obstetrics and gynecology 215 (2), 227. e1-227. e16, 2016
1872016
Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma
C Zhao, J Tynan, M Ehrich, G Hannum, R McCullough, JS Saldivar, ...
Clinical chemistry 61 (4), 608-616, 2015
1802015
Cytosine methylation profiling of cancer cell lines
M Ehrich, J Turner, P Gibbs, L Lipton, M Giovanneti, C Cantor, ...
Proceedings of the National Academy of Sciences 105 (12), 4844-4849, 2008
1772008
Methods and processes for non-invasive assessment of genetic variations
C Deciu, Z Dzakula, M Ehrich, SK Kim
US Patent 9,367,663, 2016
1742016
Hypermethylation of genes for diagnosis and risk stratification of prostate cancer
DK Vanaja, M Ehrich, D Van den Boom, JC Cheville, RJ Karnes, ...
Cancer investigation 27 (5), 549-560, 2009
1692009
Processes and kits for identifying aneuploidy
M Ehrich, G Del Mistro, C Deciu, YQ Chen, RM McCullough, RC Tim
US Patent 9,926,593, 2018
1602018
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