A citation-based method for searching scientific literature

Marios Ioannides, Achilleas Achilleos, Skevi Kyriakou, Elena Kypri, Charalambos Loizides, Kyriakos Tsangaras, Louiza Constantinou, George Koumbaris, Philippos C Patsalis. Mol Genet Genomic Med 2020
Times Cited: 6







List of co-cited articles
24 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Nonhematopoietically derived DNA is shorter than hematopoietically derived DNA in plasma: a transplantation model.
Yama W L Zheng, K C Allen Chan, Hao Sun, Peiyong Jiang, Xiaoxi Su, Eric Z Chen, Fiona M F Lun, Emily C W Hung, Vincent Lee, John Wong,[...]. Clin Chem 2012
85
16

Non-invasive prenatal testing in the context of IVF and PGT-A.
Dana Kimelman, Mary Ellen Pavone. Best Pract Res Clin Obstet Gynaecol 2021
7
16

Precise genomic mapping of 5-hydroxymethylcytosine via covalent tether-directed sequencing.
Povilas Gibas, Milda Narmontė, Zdislav Staševskij, Juozas Gordevičius, Saulius Klimašauskas, Edita Kriukienė. PLoS Biol 2020
10
16

Cost-effective and accurate method of measuring fetal fraction using SNP imputation.
Minjeong Kim, Jai-Hoon Kim, Kangseok Kim, Sunshin Kim. Bioinformatics 2018
5
20

The Human Pseudoautosomal Region (PAR): Origin, Function and Future.
A Helena Mangs, Brian J Morris. Curr Genomics 2007
138
16

Cell-free fetal DNA testing in singleton IVF conceptions.
Timothy J Lee, Daniel L Rolnik, Melody A Menezes, Andrew C McLennan, Fabricio da Silva Costa. Hum Reprod 2018
31
16

The impact of vanishing fetuses on the outcome of ICSI pregnancies.
Ragaa Mansour, Gamal Serour, Mohamed Aboulghar, Omnia Kamal, Hesham Al-Inany. Fertil Steril 2010
21
16

Disease specific characteristics of fetal epigenetic markers for non-invasive prenatal testing of trisomy 21.
Ji Hyae Lim, Da Eun Lee, So Yeon Park, Do Jin Kim, Hyun Kyong Ahn, You Jung Han, Moon Young Kim, Hyun Mee Ryu. BMC Med Genomics 2014
28
16

International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies.
Glenn E Palomaki, Rossa W K Chiu, Mark D Pertile, Erik A Sistermans, Yuval Yaron, Joris Robert Vermeesch, Neeta L Vora, Robert G Best, Louise Wilkins-Haug. Prenat Diagn 2021
11
16

Sequencing of Circulating Cell-free DNA during Pregnancy.
Diana W Bianchi, Rossa W K Chiu. N Engl J Med 2018
134
16


Next-generation genotype imputation service and methods.
Sayantan Das, Lukas Forer, Sebastian Schönherr, Carlo Sidore, Adam E Locke, Alan Kwong, Scott I Vrieze, Emily Y Chew, Shawn Levy, Matt McGue,[...]. Nat Genet 2016
16

Combination of Fetal Fraction Estimators Based on Fragment Lengths and Fragment Counts in Non-Invasive Prenatal Testing.
Juraj Gazdarica, Rastislav Hekel, Jaroslav Budis, Marcel Kucharik, Frantisek Duris, Jan Radvanszky, Jan Turna, Tomas Szemes. Int J Mol Sci 2019
8
16

Maternal mortality following diagnostic 2nd-trimester amniocentesis.
Uriel Elchalal, Inbar Ben Shachar, Dan Peleg, Joseph G Schenker. Fetal Diagn Ther 2004
21
16

Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA.
Fiona M F Lun, Rossa W K Chiu, Kun Sun, Tak Y Leung, Peiyong Jiang, K C Allen Chan, Hao Sun, Y M Dennis Lo. Clin Chem 2013
97
16


Homologies between X and Y chromosomes detected by DNA probes: localisation and evolution.
M Koenig, J P Moisan, R Heilig, J L Mandel. Nucleic Acids Res 1985
72
16

Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Jinglan Zhang, Jianli Li, Jennifer B Saucier, Yanming Feng, Yanjun Jiang, Jefferson Sinson, Anne K McCombs, Eric S Schmitt, Sandra Peacock, Stella Chen,[...]. Nat Med 2019
99
16

Why NIPT should be publicly funded.
Eline Maria Bunnik, Adriana Kater-Kuipers, Robert-Jan H Galjaard, Inez de Beaufort. J Med Ethics 2020
4
25

Human DNA methylomes at base resolution show widespread epigenomic differences.
Ryan Lister, Mattia Pelizzola, Robert H Dowen, R David Hawkins, Gary Hon, Julian Tonti-Filippini, Joseph R Nery, Leonard Lee, Zhen Ye, Que-Minh Ngo,[...]. Nature 2009
16

Total number of reads affects the accuracy of fetal fraction estimates in NIPT.
Ieva Miceikaitė, Charlotte Brasch-Andersen, Christina Fagerberg, Martin Jakob Larsen. Mol Genet Genomic Med 2021
3
33

Nucleosome positioning and gene regulation: advances through genomics.
Cizhong Jiang, B Franklin Pugh. Nat Rev Genet 2009
695
16

Next-generation sequencing of immunoglobulin gene rearrangements for clonality assessment: a technical feasibility study by EuroClonality-NGS.
Blanca Scheijen, Ruud W J Meijers, Jos Rijntjes, Michèle Y van der Klift, Markus Möbs, Julia Steinhilber, Tomas Reigl, Michiel van den Brand, Michaela Kotrová, Julia-Marie Ritter,[...]. Leukemia 2019
49
16

First- and second-trimester Down syndrome screening markers in pregnancies achieved through assisted reproductive technologies (ART): a FASTER trial study.
G Lambert-Messerlian, L Dugoff, J Vidaver, J A Canick, F D Malone, R H Ball, C H Comstock, D A Nyberg, G Saade, K Eddleman,[...]. Prenat Diagn 2006
40
16

Rare-variant association analysis: study designs and statistical tests.
Seunggeung Lee, Gonçalo R Abecasis, Michael Boehnke, Xihong Lin. Am J Hum Genet 2014
543
16

Maternal plasma fetal DNA fractions in pregnancies with low and high risks for fetal chromosomal aneuploidies.
Irena Hudecova, Daljit Sahota, Macy M S Heung, Yongjie Jin, Wing S Lee, Tak Y Leung, Yuk Ming Dennis Lo, Rossa W K Chiu. PLoS One 2014
70
16

Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management.
Baran Bayindir, Luc Dehaspe, Nathalie Brison, Paul Brady, Simon Ardui, Molka Kammoun, Lars Van der Veken, Klaske Lichtenbelt, Kris Van den Bogaert, Jeroen Van Houdt,[...]. Eur J Hum Genet 2015
74
16

Noninvasive prenatal paternity testing by means of SNP-based targeted sequencing.
Jacqueline Chor Wing Tam, Yee Man Chan, Shui Ying Tsang, Chung In Yau, Shuk Ying Yeung, Ka Ki Au, Chun Kin Chow. Prenat Diagn 2020
7
16

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, Amin R Mazloom, Zhanyang Zhu, John Tynan, Tim Lu, Graham McLennan,[...]. PLoS One 2013
71
16

SNP databases.
Christopher Phillips. Methods Mol Biol 2009
8
16

Sequencing depth and coverage: key considerations in genomic analyses.
David Sims, Ian Sudbery, Nicholas E Ilott, Andreas Heger, Chris P Ponting. Nat Rev Genet 2014
675
16

Screening for trisomies by cell-free DNA testing of maternal blood: consequences of a failed result.
R Revello, L Sarno, A Ispas, R Akolekar, K H Nicolaides. Ultrasound Obstet Gynecol 2016
72
16

Tethered Oligonucleotide-Primed Sequencing, TOP-Seq: A High-Resolution Economical Approach for DNA Epigenome Profiling.
Zdislav Staševskij, Povilas Gibas, Juozas Gordevičius, Edita Kriukienė, Saulius Klimašauskas. Mol Cell 2017
16
16

Abnormal plasma DNA profiles in early ovarian cancer using a non-invasive prenatal testing platform: implications for cancer screening.
Paul A Cohen, Nicola Flowers, Stephen Tong, Natalie Hannan, Mark D Pertile, Lisa Hui. BMC Med 2016
54
16

Factors affecting cell-free DNA fetal fraction and the consequences for test accuracy.
Fergus Perry Scott, Melody Menezes, Ricardo Palma-Dias, Debbie Nisbet, Philip Schluter, Fabricio da Silva Costa, Andrew Cameron McLennan. J Matern Fetal Neonatal Med 2018
33
16

Fetal sex chromosome testing by maternal plasma DNA sequencing: clinical laboratory experience and biology.
Diana W Bianchi, Saba Parsa, Sucheta Bhatt, Meredith Halks-Miller, Kathryn Kurtzman, Amy J Sehnert, Amy Swanson. Obstet Gynecol 2015
95
16


Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory.
Annelies Dheedene, Tom Sante, Matthias De Smet, Jean-François Vanbellinghen, Bernard Grisart, Sarah Vergult, Sandra Janssens, Björn Menten. Prenat Diagn 2016
13
16

Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies.
Diana W Bianchi, Darya Chudova, Amy J Sehnert, Sucheta Bhatt, Kathryn Murray, Tracy L Prosen, Judy E Garber, Louise Wilkins-Haug, Neeta L Vora, Stephen Warsof,[...]. JAMA 2015
231
16

Specifying a Gold Standard for the Validation of Fetal Fraction Estimation in Prenatal Screening.
Nicholas J Wald, King Wai Lau, Jonathan P Bestwick, Robert W Old, Wayne J Huttly, Ray Cheng. Clin Chem 2018
6
16

Initial clinical laboratory experience in noninvasive prenatal testing for fetal aneuploidy from maternal plasma DNA samples.
Tracy Futch, John Spinosa, Sucheta Bhatt, Eileen de Feo, Richard P Rava, Amy J Sehnert. Prenat Diagn 2013
126
16

Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing.
Pe'er Dar, Kirsten J Curnow, Susan J Gross, Megan P Hall, Melissa Stosic, Zachary Demko, Bernhard Zimmermann, Matthew Hill, Styrmir Sigurjonsson, Allison Ryan,[...]. Am J Obstet Gynecol 2014
167
16

Diagnostic mid trimester amniocentesis: how safe?
John W Seeds. Am J Obstet Gynecol 2004
80
16


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.