A citation-based method for searching scientific literature

Jing Yang, Min Chen, Xiaoqing Ye, Fei Chen, Yufan Li, Nan Li, Wenyan Wu, Jimei Sun. Eur J Obstet Gynecol Reprod Biol 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Presence of fetal DNA in maternal plasma and serum.
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
66

Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.
Peter Benn, Antoni Borrell, Rossa W K Chiu, Howard Cuckle, Lorraine Dugoff, Brigitte Faas, Susan Gross, Tianhua Huang, Joann Johnson, Ron Maymon,[...]. Prenat Diagn 2015
179
66


Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
715
33

A first look at women's perspectives on noninvasive prenatal testing to detect sex chromosome aneuploidies and microdeletion syndromes.
Patricia K Agatisa, Mary Beth Mercer, Angela C Leek, Marissa B Smith, Elliot Philipson, Ruth M Farrell. Prenat Diagn 2015
27
33


Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma.
Amin R Mazloom, Željko Džakula, Paul Oeth, Huiquan Wang, Taylor Jensen, John Tynan, Ron McCullough, Juan-Sebastian Saldivar, Mathias Ehrich, Dirk van den Boom,[...]. Prenat Diagn 2013
129
33

Detection of trisomy 21 by quantitative mass spectrometric analysis of single-nucleotide polymorphisms.
Nancy B Y Tsui, Rossa W K Chiu, Chunming Ding, Ahmad El-Sheikhah, Tse N Leung, Tze K Lau, Kypros H Nicolaides, Y M Dennis Lo. Clin Chem 2005
29
33

Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet Med 2016
346
33

Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound.
Lisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Allan J Fisher. Prenat Diagn 2012
155
33


Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection.
Y M Dennis Lo, Nancy B Y Tsui, Rossa W K Chiu, Tze K Lau, Tse N Leung, Macy M S Heung, Ageliki Gerovassili, Yongjie Jin, Kypros H Nicolaides, Charles R Cantor,[...]. Nat Med 2007
260
33

Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes.
Desheng Liang, David S Cram, Hu Tan, Siyuan Linpeng, Yingdi Liu, Huaiyu Sun, Yu Zhang, Feng Tian, Hongmin Zhu, Mengnan Xu,[...]. Genet Med 2019
81
33

Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities.
Mary E Norton, Rebecca J Baer, Ronald J Wapner, Miriam Kuppermann, Laura L Jelliffe-Pawlowski, Robert J Currier. Am J Obstet Gynecol 2016
47
33


Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): A survey of European health-care providers.
Alexandra Benachi, Jessica Caffrey, Pavel Calda, Elena Carreras, Jacques C Jani, Mark D Kilby, Hanns-Georg Klein, Giuseppe Rizzo, Yuval Yaron. Eur J Med Genet 2020
14
33


Survey of US obstetrician opinions regarding NIPT use in general practice: implementation and barriers.
Justin Brewer, Lisa Demers, Thomas Musci. J Matern Fetal Neonatal Med 2017
17
33


Cell-free DNA analysis for noninvasive examination of trisomy.
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
422
33



Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma.
Rossa W K Chiu, K C Allen Chan, Yuan Gao, Virginia Y M Lau, Wenli Zheng, Tak Y Leung, Chris H F Foo, Bin Xie, Nancy B Y Tsui, Fiona M F Lun,[...]. Proc Natl Acad Sci U S A 2008
589
33

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
191
33

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.
Lisa G Shaffer, Mindy P Dabell, Allan J Fisher, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Jill A Rosenfeld. Prenat Diagn 2012
144
33


The use of noninvasive prenatal testing in obstetric care: educational resources, practice patterns, and barriers reported by a national sample of clinicians.
Ruth M Farrell, Patricia K Agatisa, Mary Beth Mercer, Ariane G Mitchum, Marissa B Coleridge. Prenat Diagn 2016
31
33

Karyotype versus genomic hybridization for the prenatal diagnosis of chromosomal abnormalities: a metaanalysis.
Wilmar Saldarriaga, Herney Andrés García-Perdomo, Johanna Arango-Pineda, Javier Fonseca. Am J Obstet Gynecol 2015
23
33

Nearly a third of abnormalities found after first-trimester screening are different than expected: 10-year experience from a single center.
Christina M L Alamillo, David Krantz, Mark Evans, Morris Fiddler, Eugene Pergament. Prenat Diagn 2013
46
33

Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed-methods systematic review.
Eleanor Harding, Jennifer Hammond, Lyn S Chitty, Melissa Hill, Celine Lewis. Prenat Diagn 2020
11
33


Clinical outcome of subchromosomal events detected by whole-genome noninvasive prenatal testing.
J Helgeson, J Wardrop, T Boomer, E Almasri, W B Paxton, J S Saldivar, N Dharajiya, T J Monroe, D H Farkas, D S Grosu,[...]. Prenat Diagn 2015
84
33

Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions.
K Martin, S Iyengar, A Kalyan, C Lan, A L Simon, M Stosic, K Kobara, H Ravi, T Truong, A Ryan,[...]. Clin Genet 2018
50
33

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood.
H Christina Fan, Yair J Blumenfeld, Usha Chitkara, Louanne Hudgins, Stephen R Quake. Proc Natl Acad Sci U S A 2008
683
33

Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe.
Diana Wellesley, Helen Dolk, Patricia A Boyd, Ruth Greenlees, Martin Haeusler, Vera Nelen, Ester Garne, Babak Khoshnood, Berenice Doray, Anke Rissmann,[...]. Eur J Hum Genet 2012
87
33

Analysis of cell-free DNA in maternal blood in screening for aneuploidies: updated meta-analysis.
M M Gil, V Accurti, B Santacruz, M N Plana, K H Nicolaides. Ultrasound Obstet Gynecol 2017
289
33

Global perspectives on clinical adoption of NIPT.
Mollie A Minear, Celine Lewis, Subarna Pradhan, Subhashini Chandrasekharan. Prenat Diagn 2015
89
33

Noninvasive prenatal screening or advanced diagnostic testing: caveat emptor.
Mark I Evans, Ronald J Wapner, Richard L Berkowitz. Am J Obstet Gynecol 2016
55
33

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
Karuna R M van der Meij, Erik A Sistermans, Merryn V E Macville, Servi J C Stevens, Caroline J Bax, Mireille N Bekker, Caterina M Bilardo, Elles M J Boon, Marjan Boter, Karin E M Diderich,[...]. Am J Hum Genet 2019
95
33

Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units.
Lyn S Chitty, David Wright, Melissa Hill, Talitha I Verhoef, Rebecca Daley, Celine Lewis, Sarah Mason, Fiona McKay, Lucy Jenkins, Abigail Howarth,[...]. BMJ 2016
95
33

Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis.
M Grande, F A R Jansen, Y J Blumenfeld, A Fisher, A O Odibo, M C Haak, A Borrell. Ultrasound Obstet Gynecol 2015
93
33

Obstetrical provider knowledge and attitudes towards cell-free DNA screening: results of a cross-sectional national survey.
Wilson V Chan, Jo-Ann Johnson, R Douglas Wilson, Amy Metcalfe. BMC Pregnancy Childbirth 2018
7
33

Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental disease.
Mark D Pertile, Meredith Halks-Miller, Nicola Flowers, Catalin Barbacioru, Sarah L Kinnings, Darcy Vavrek, William K Seltzer, Diana W Bianchi. Sci Transl Med 2017
73
33

Non-invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta-analysis of diagnostic test accuracy studies.
Bounhome Soukkhaphone, Carmen Lindsay, Sylvie Langlois, Julian Little, Francois Rousseau, Daniel Reinharz. Mol Genet Genomic Med 2021
2
50

Effects of HPV-16 E5, E6 and E7 proteins on survival, adhesion, migration and invasion of trophoblastic cells.
Selma Boulenouar, Christine Weyn, Melody Van Noppen, Mohamed Moussa Ali, Michel Favre, Philippe O Delvenne, Françoise Bex, Agnès Noël, Yvon Englert, Véronique Fontaine. Carcinogenesis 2010
55
33


The association between cervical inflammation and histologic evidence of HPV in PAP smears and adverse pregnancy outcome in low risk population.
Maya Nimrodi, Vered Kleitman, Tamar Wainstock, Ofer Gemer, Michai Meirovitz, Eli Maymon, Neta Benshalom-Tirosh, Offer Erez. Eur J Obstet Gynecol Reprod Biol 2018
8
33

Editorial: Causes and Consequences of Intrauterine Growth Restriction.
Ivo Bendix, Suzanne L Miller, Elke Winterhager. Front Endocrinol (Lausanne) 2020
8
33

Tumor necrosis factor a-11 and DR15-DQ6 (B*0602) haplotype increase the risk for cervical intraepithelial neoplasia in human papillomavirus 16 seropositive women in Northern Sweden.
M Ghaderi, L Nikitina, C S Peacock, P Hjelmström, G Hallmans, F Wiklund, P Lenner, J M Blackwell, J Dillner, C B Sanjeevi. Cancer Epidemiol Biomarkers Prev 2000
39
33



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.