Cosmin Deciu

3.7k total citations · 3 hit papers
24 papers, 2.7k citations indexed

About

Cosmin Deciu is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Infectious Diseases. According to data from OpenAlex, Cosmin Deciu has authored 24 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Pediatrics, Perinatology and Child Health, 11 papers in Genetics and 5 papers in Infectious Diseases. Recurrent topics in Cosmin Deciu's work include Prenatal Screening and Diagnostics (23 papers), Fetal and Pediatric Neurological Disorders (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). Cosmin Deciu is often cited by papers focused on Prenatal Screening and Diagnostics (23 papers), Fetal and Pediatric Neurological Disorders (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). Cosmin Deciu collaborates with scholars based in United States, Australia and Czechia. Cosmin Deciu's co-authors include Mathias Ehrich, Dirk van den Boom, Allan T. Bombard, Glenn E. Palomaki, Jacob A. Canick, Edward M. Kloza, Geralyn Lambert‐Messerlian, James E. Haddow, Wayne W. Grody and Stanley F. Nelson and has published in prestigious journals such as PLoS ONE, American Journal of Obstetrics and Gynecology and Clinical Chemistry.

In The Last Decade

Cosmin Deciu

24 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.

DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study

2011 660 citations Glenn E. Palomaki, Edward M. Kloza et al. Genetics in Medicine profile →
DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study

2012 392 citations Glenn E. Palomaki, Cosmin Deciu et al. Genetics in Medicine profile →
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
Cosmin Deciu United States	16	2.5k	1.0k	800	516	415	24	2.7k
Ken Song United States	10	1.5k 0.6×	708 0.7×	334 0.4×	324 0.6×	228 0.5×	11	1.6k
Attie T. J. I. Go Netherlands	20	1.2k 0.5×	239 0.2×	433 0.5×	215 0.4×	168 0.4×	59	1.4k
Diane Van Opstal Netherlands	28	2.0k 0.8×	246 0.2×	1.2k 1.5×	457 0.9×	75 0.2×	97	2.6k
Sucheta Bhatt United States	14	747 0.3×	246 0.2×	371 0.5×	202 0.4×	141 0.3×	27	978
Osamu Samura Japan	21	943 0.4×	310 0.3×	272 0.3×	327 0.6×	88 0.2×	68	1.3k
Patricia Devers United States	9	710 0.3×	263 0.3×	225 0.3×	140 0.3×	87 0.2×	14	817
Zhen Yan United States	15	506 0.2×	87 0.1×	204 0.3×	164 0.3×	72 0.2×	19	1.0k
Kirstin Finning United Kingdom	17	857 0.3×	570 0.6×	115 0.1×	124 0.2×	66 0.2×	22	1.1k
Tracy Prosen United States	10	385 0.2×	102 0.1×	156 0.2×	98 0.2×	96 0.2×	18	643
Deborah G. Maddocks United Kingdom	12	544 0.2×	214 0.2×	106 0.1×	193 0.4×	88 0.2×	13	742

Countries citing papers authored by Cosmin Deciu

Since Specialization

Citations

This map shows the geographic impact of Cosmin Deciu'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 Cosmin Deciu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cosmin Deciu more than expected).

Fields of papers citing papers by Cosmin Deciu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cosmin Deciu. 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 Cosmin Deciu. The network helps show where Cosmin Deciu may publish in the future.

Co-authorship network of co-authors of Cosmin Deciu

This figure shows the co-authorship network connecting the top 25 collaborators of Cosmin Deciu. A scholar is included among the top collaborators of Cosmin Deciu 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 Cosmin Deciu. Cosmin Deciu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Pertile, Mark D., Darcy Vavrek, Tasha Kalista, et al.. (2021). Performance of a Paired-End Sequencing-Based Noninvasive Prenatal Screening Test in the Detection of Genome-Wide Fetal Chromosomal Anomalies. Clinical Chemistry. 67(9). 1210–1219. 30 indexed citations

Vavrek, Darcy, Kristen Meier, Tasha Kalista, et al.. (2019). OC02.02: Performance of a genome‐wide PCR‐free, paired‐end sequencing‐based non‐invasive prenatal screening test, VeriSeq NIPT Solution v2. Ultrasound in Obstetrics and Gynecology. 54(S1). 3–4. 1 indexed citations

Jensen, Taylor J., Sung K. Kim, Zhanyang Zhu, et al.. (2015). Whole genome bisulfite sequencing of cell-free DNA and its cellular contributors uncovers placenta hypomethylated domains. Genome Biology. 16(1). 78–78. 54 indexed citations

Jensen, Taylor J., et al.. (2015). Selective Enrichment of Genomic Loci for the Noninvasive Detection of Fetal Aneuploidies [285]. Obstetrics and Gynecology. 125(Supplement 1). 92S–92S. 1 indexed citations

Kim, Sung K., Gregory Hannum, Jennifer A. Geis, et al.. (2015). Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts. Prenatal Diagnosis. 35(8). 810–815. 160 indexed citations

Kinnings, Sarah, Jennifer A. Geis, Eyad Almasri, et al.. (2015). Factors affecting levels of circulating cell-free fetal DNA in maternal plasma and their implications for noninvasive prenatal testing. Prenatal Diagnosis. 35(8). 816–822. 101 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

Porreco, Richard P., Thomas J. Garite, Kimberly Maurel, et al.. (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 DNA. American Journal of Obstetrics and Gynecology. 211(4). 365.e1–365.e12. 142 indexed citations

Jensen, Taylor J., Sung K. Kim, Dirk van den Boom, Cosmin Deciu, & Mathias Ehrich. (2014). Noninvasive Detection of a Balanced Fetal Translocation from Maternal Plasma. Clinical Chemistry. 60(10). 1298–1305. 8 indexed citations

10.

Palomaki, Glenn E., Edward M. Kloza, Geralyn Lambert‐Messerlian, et al.. (2014). Circulating cell free DNA testing: are some test failures informative?. Prenatal Diagnosis. 35(3). 289–293. 68 indexed citations

11.

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

12.

Lambert‐Messerlian, Geralyn, Edward M. Kloza, John Williams, et al.. (2013). Maternal plasma DNA testing for aneuploidy in pregnancies achieved by assisted reproductive technologies. Genetics in Medicine. 16(5). 419–422. 9 indexed citations

13.

Mazloom, Amin R., Željko Džakula, Paul Oeth, et al.. (2013). Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell‐free DNA from maternal plasma. Prenatal Diagnosis. 33(6). 591–597. 156 indexed citations

14.

Palomaki, Glenn E., Cosmin Deciu, Edward M. Kloza, et al.. (2012). DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study. Genetics in Medicine. 14(3). 296–305. 392 indexed citations breakdown →

15.

Palomaki, Glenn E., Edward M. Kloza, Geralyn Lambert‐Messerlian, et al.. (2012). DNA Sequencing of Maternal Plasma to Detect Down Syndrome. Obstetrical & Gynecological Survey. 67(2). 86–88. 3 indexed citations

16.

Canick, Jacob A., Edward M. Kloza, Geralyn Lambert‐Messerlian, et al.. (2012). DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations. Prenatal Diagnosis. 32(8). 730–734. 125 indexed citations

17.

Palomaki, Glenn E., Edward M. Kloza, Geralyn Lambert‐Messerlian, et al.. (2011). DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study. Genetics in Medicine. 13(11). 913–920. 660 indexed citations breakdown →

18.

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

19.

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 →

20.

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. Obstetrical & Gynecological Survey. 66(6). 342–344. 9 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.

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