Paul Oeth

3.5k total citations · 1 hit paper
39 papers, 2.7k citations indexed

About

Paul Oeth is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Cancer Research. According to data from OpenAlex, Paul Oeth has authored 39 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Pediatrics, Perinatology and Child Health and 8 papers in Cancer Research. Recurrent topics in Paul Oeth's work include Prenatal Screening and Diagnostics (16 papers), Fetal and Pediatric Neurological Disorders (13 papers) and Molecular Biology Techniques and Applications (8 papers). Paul Oeth is often cited by papers focused on Prenatal Screening and Diagnostics (16 papers), Fetal and Pediatric Neurological Disorders (13 papers) and Molecular Biology Techniques and Applications (8 papers). Paul Oeth collaborates with scholars based in United States, United Kingdom and Sweden. Paul Oeth's co-authors include Dirk van den Boom, Nigel Mackman, Graham C. Parry, Cosmin Deciu, Mathias Ehrich, Christian Jurinke, John A. Tynan, Ron McCullough, Allan T. Bombard and Mikhail F. Denissenko and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Blood.

In The Last Decade

Paul Oeth

39 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

2011 371 citations Mathias Ehrich, Cosmin Deciu et al. American Journal of Obstetrics and Gynecology profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Paul Oeth United States	27	1.2k	950	559	493	449	39	2.7k
Amy J. Sehnert United States	31	2.1k 1.8×	1.3k 1.3×	742 1.3×	856 1.7×	429 1.0×	84	4.6k
David H.K. Chui United States	41	1.7k 1.5×	2.0k 2.1×	814 1.5×	518 1.1×	221 0.5×	225	6.7k
Nury Steuerwald United States	26	564 0.5×	1.1k 1.1×	357 0.6×	57 0.1×	253 0.6×	86	2.5k
Enders K. O. Ng Hong Kong	26	496 0.4×	2.8k 2.9×	193 0.3×	684 1.4×	2.4k 5.3×	42	4.3k
Jung Mi Oh South Korea	6	271 0.2×	974 1.0×	369 0.7×	143 0.3×	102 0.2×	8	2.0k
Yoshiro Koda Japan	31	175 0.1×	1.5k 1.6×	547 1.0×	159 0.3×	162 0.4×	149	3.1k
Thad A. Howard United States	29	527 0.4×	877 0.9×	321 0.6×	92 0.2×	90 0.2×	97	2.8k
Min Fang United States	34	287 0.2×	1.8k 1.9×	386 0.7×	139 0.3×	403 0.9×	182	4.7k
Bertil Glader United States	30	365 0.3×	2.2k 2.3×	1.6k 2.9×	358 0.7×	102 0.2×	131	4.6k
Ann‐Christine Syvänen Sweden	29	185 0.2×	1.1k 1.2×	599 1.1×	66 0.1×	194 0.4×	90	2.5k

Countries citing papers authored by Paul Oeth

Since Specialization

Citations

This map shows the geographic impact of Paul Oeth's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Paul Oeth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paul Oeth more than expected).

Fields of papers citing papers by Paul Oeth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul Oeth. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Paul Oeth. The network helps show where Paul Oeth may publish in the future.

Co-authorship network of co-authors of Paul Oeth

This figure shows the co-authorship network connecting the top 25 collaborators of Paul Oeth. A scholar is included among the top collaborators of Paul Oeth based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Paul Oeth. Paul Oeth is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Tynan, John A., Amin R. Mazloom, Chenglong Zhao, et al.. (2015). Application of risk score analysis to low‐coverage whole genome sequencing data for the noninvasive detection of trisomy 21, trisomy 18, and trisomy 13. Prenatal Diagnosis. 36(1). 56–62. 14 indexed citations

McCullough, Ron, Xiaojun Guan, Jennifer A. Geis, et al.. (2014). Non-Invasive Prenatal Chromosomal Aneuploidy Testing - Clinical Experience: 100,000 Clinical Samples. PLoS ONE. 9(10). e109173–e109173. 94 indexed citations

Perlee, Lorah, Aruna T. Bansal, Karen M. Gehrs, et al.. (2013). Inclusion of Genotype with Fundus Phenotype Improves Accuracy of Predicting Choroidal Neovascularization and Geographic Atrophy. Ophthalmology. 120(9). 1880–1892. 35 indexed citations

Jensen, Taylor J., Željko Džakula, Sung K. Kim, et al.. (2013). High-Throughput Massively Parallel Sequencing for Fetal Aneuploidy Detection from Maternal Plasma. PLoS ONE. 8(3). e57381–e57381. 77 indexed citations

Kamali‐Moghaddam, Masood, Ian Burbulis, Martín Steffen, et al.. (2012). Multiplex protein detection with DNA readout via mass spectrometry. New Biotechnology. 30(2). 153–158. 10 indexed citations

Moise, Kenneth J., R. O’Shaughnessy, L. Simpson, et al.. (2012). Circulating cell‐free fetal DNA for the detection of RHD status and sex using reflex fetal identifiers. Prenatal Diagnosis. 33(1). 95–101. 22 indexed citations

Tynan, John A., et al.. (2011). Restriction Enzyme–Mediated Enhanced Detection of Circulating Cell-Free Fetal DNA in Maternal Plasma. Journal of Molecular Diagnostics. 13(4). 382–389. 15 indexed citations

Bombard, Allan T., et al.. (2011). Fetal RHD genotype detection from circulating cell‐free fetal DNA in maternal plasma in non‐sensitized RhD negative women. Prenatal Diagnosis. 31(8). 802–808. 47 indexed citations

Hageman, Gregory S., Karen M. Gehrs, Serguei Lejnine, et al.. (2011). Clinical validation of a genetic model to estimate the risk of developing choroidal neovascular age-related macular degeneration. Human Genomics. 5(5). 420–420. 46 indexed citations

10.

Ehrich, Mathias, Cosmin Deciu, John A. Tynan, et al.. (2011). Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting. American Journal of Obstetrics and Gynecology. 204(3). 205.e1–205.e11. 371 indexed citations breakdown →

11.

Tynan, John A., Vach Angkachatchai, Mathias Ehrich, et al.. (2010). Multiplexed analysis of circulating cell-free fetal nucleic acids for noninvasive prenatal diagnostic RHD testing. American Journal of Obstetrics and Gynecology. 204(3). 251.e1–251.e6. 30 indexed citations

12.

Grindflek, Eli, et al.. (2010). Transcript profiling of candidate genes in testis of pigs exhibiting large differences in androstenone levels. BMC Genetics. 11(1). 4–4. 35 indexed citations

13.

Patel, Divya A., Duane W. Newton, Claire W. Michael, et al.. (2009). Development and evaluation of a PCR and mass spectroscopy (PCR–MS)-based method for quantitative, type-specific detection of human papillomavirus. Journal of Virological Methods. 160(1-2). 78–84. 13 indexed citations

14.

Ehrich, Mathias, John K. Field, Triantafillos Liloglou, et al.. (2006). Cytosine Methylation Profiles as a Molecular Marker in Non–Small Cell Lung Cancer. Cancer Research. 66(22). 10911–10918. 47 indexed citations

15.

Rosette, Caridad, Richard B. Roth, Paul Oeth, et al.. (2005). Role of ICAM1 in invasion of human breast cancer cells. Carcinogenesis. 26(5). 943–950. 231 indexed citations

16.

Jurinke, Christian, et al.. (2005). A single nucleotide polymorphism based approach for the identification and characterization of gene expression modulation using MassARRAY. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 573(1-2). 83–95. 50 indexed citations

17.

Boom, Dirk van den, Martin Beaulieu, Paul Oeth, et al.. (2004). MALDI-TOF MS: a platform technology for genetic discovery. International Journal of Mass Spectrometry. 238(2). 173–188. 14 indexed citations

18.

Jurinke, Christian, Paul Oeth, & Dirk van den Boom. (2004). MALDI-TOF Mass Spectrometry : A Versatile Tool for High-Performance DNA Analysis. Molecular Biotechnology. 26(2). 147–164. 163 indexed citations

19.

Douglas, Julie A., Michael R. Erdos, Richard M. Watanabe, et al.. (2001). The Peroxisome Poliferator–Activated Receptor-γ2 Pro12Ala Variant. Diabetes. 50(4). 886–890. 120 indexed citations

20.

Graves, John E., et al.. (1990). Biochemical Genetics Of Southern California Basses Of The Genus Paralabrax - Specific Identification Of Fresh And Ethanol-Preserved Individual Eggs And Early Larvae. Fishery Bulletin. 88(1). 59. 12 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact