Author

Paul Oeth

Observed names: P A Oeth, P Oeth, P. A. Oeth, P. Oeth, Paul A. Oeth

Observed institutions: Scripps Research Institute, Albert Einstein College of Medicine, Center for Biologics Evaluation and Research, United States Food and Drug Administration, Wayne State University, University of Michigan, Henry Ford Hospital, Michigan Medicine, National Cancer Institute, Sequenom (United States), Génome Québec

OpenAlex ID: A5079391774

Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting

2011 · Mathias Ehrich, Cosmin Deciu, et al. · American Journal of Obstetrics and Gynecology · 472

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Role of ICAM1 in invasion of human breast cancer cells

2005 · Caridad Rosette, Richard B. Roth, et al. · Carcinogenesis · 271

Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts

2015 · Sung K. Kim, Gregory Hannum, et al. · Prenatal Diagnosis · 238

MALDI-TOF Mass Spectrometry : A Versatile Tool for High-Performance DNA Analysis

2004 · Christian Jurinke, Paul Oeth, et al. · Molecular Biotechnology · 231

Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell‐free DNA from maternal plasma

2013 · Amin R. Mazloom, Željko Džakula, et al. · Prenatal Diagnosis · 199

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Transcriptional Regulation of the Tissue Factor Gene in Human Epithelial Cells Is Mediated by Sp1 and EGR-1

1996 · Mei-Zhen Cui, Graham C.N. Parry, et al. · Journal of Biological Chemistry · 158

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Detection of Fetal Subchromosomal Abnormalities by Sequencing Circulating Cell-Free DNA from Maternal Plasma

2015 · Chen Zhao, John Tynan, et al. · Clinical Chemistry · 154

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Regulation of the Tissue Factor Gene in Human Monocytic Cells: Role of AP-1, NF-κB/Rel, and Sp1 Proteins in Uninduced and Lipopolysaccharide-Induced Expression

1997 · Paul Oeth, Graham C.N. Parry, et al. · Arteriosclerosis Thrombosis and Vascular Biology · 146

Factors affecting levels of circulating cell-free fetal DNA in maternal plasma and their implications for noninvasive prenatal testing

2015 · Sarah L. Kinnings, Jennifer A. Geis, et al. · Prenatal Diagnosis · 138

The Peroxisome Poliferator–Activated Receptor-γ2 Pro12Ala Variant

2001 · Julie A. Douglas, Michael R. Erdos, et al. · Diabetes · 131

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Non-Invasive Prenatal Chromosomal Aneuploidy Testing - Clinical Experience: 100,000 Clinical Samples

2014 · Ron M. McCullough, Eyad A. Almasri, et al. · PLoS ONE · 128

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Lipopolysaccharide Induction of Tissue Factor Gene Expression in Monocytic Cells Is Mediated by Binding of c-Rel/p65 Heterodimers to a κB-Like Site

1994 · P A Oeth, G C Parry, et al. · Molecular and Cellular Biology · 121

Qualitative and Quantitative Genotyping Using Single Base Primer Extension Coupled with Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry (MassARRAY®)

2009 · Paul Oeth, Guy del Mistro, et al. · Methods in molecular biology · 114

High-Throughput Massively Parallel Sequencing for Fetal Aneuploidy Detection from Maternal Plasma

2013 · Taylor J. Jensen, Tricia Zwiefelhofer, et al. · PLoS ONE · 96

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Salicylates inhibit lipopolysaccharide-induced transcriptional activation of the tissue factor gene in human monocytic cells

1995 · P Oeth, N Mackman · Blood · 85

Fetal RHD genotype detection from circulating cell‐free fetal DNA in maternal plasma in non‐sensitized RhD negative women

2011 · Allan T. Bombard, Ranjit Akolekar, et al. · Prenatal Diagnosis · 69

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Sensitive detection of human papillomavirus in cervical, head/neck, and schistosomiasis-associated bladder malignancies

2005 · H. Yang, K. Yang, et al. · Proceedings of the National Academy of Sciences · 69

A single nucleotide polymorphism based approach for the identification and characterization of gene expression modulation using MassARRAY

2005 · Christian Jurinke, Mikhail F. Denissenko, et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 68

Cytosine Methylation Profiles as a Molecular Marker in Non–Small Cell Lung Cancer

2006 · Mathias Ehrich, John K. Field, et al. · Cancer Research · 60

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Clinical validation of a genetic model to estimate the risk of developing choroidal neovascular age-related macular degeneration

2011 · Gregory S Hageman, Karen Gehrs, et al. · Human Genomics · 58

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Mining Disease Susceptibility Genes through SNP Analyses and Expression Profiling Using MALDI-TOF Mass Spectrometry

2004 · Kai Tang, Paul Oeth, et al. · Journal of Proteome Research · 54

Quantitative mutant analysis of viral quasispecies by chip-based matrix-assisted laser desorption/ ionization time-of-flight mass spectrometry

2001 · Georgios Amexis, Paul Oeth, et al. · Proceedings of the National Academy of Sciences · 50

Inclusion of Genotype with Fundus Phenotype Improves Accuracy of Predicting Choroidal Neovascularization and Geographic Atrophy

2013 · Lorah T. Perlee, Aruna T. Bansal, et al. · Ophthalmology · 46

Multiplexed analysis of circulating cell-free fetal nucleic acids for noninvasive prenatal diagnostic RHD testing

2010 · John A. Tynan, Vach Angkachatchai, et al. · American Journal of Obstetrics and Gynecology · 43

Transcript profiling of candidate genes in testis of pigs exhibiting large differences in androstenone levels

2010 · Eli Grindflek, Ingunn Berget, et al. · BMC Genetics · 43

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Works count: 45

Citation count: 3,442

H-index: 27

I10-index: 34