A citation-based method for searching scientific literature

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, Christine E M de Die-Smulders, Leonie K Duin, Brigitte H W Faas, Ilse Feenstra, Monique C Haak, Mariëtte J V Hoffer, Nicolette S den Hollander, Iris H I M Hollink, Fernanda S Jehee, Maarten F C M Knapen, Angelique J A Kooper, Irene M van Langen, Klaske D Lichtenbelt, Ingeborg H Linskens, Merel C van Maarle, Dick Oepkes, Mijntje J Pieters, G Heleen Schuring-Blom, Esther Sikkel, Birgit Sikkema-Raddatz, Dominique F C M Smeets, Malgorzata I Srebniak, Ron F Suijkerbuijk, Gita M Tan-Sindhunata, A Jeanine E M van der Ven, Shama L van Zelderen-Bhola, Lidewij Henneman, Robert-Jan H Galjaard, Diane Van Opstal, Marjan M Weiss. Am J Hum Genet 2019
Times Cited: 89







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



Times Cited
  Times     Co-cited
Similarity


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
282
25

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
337
19

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
17

Current use of noninvasive prenatal testing in Europe, Australia and the USA: A graphical presentation.
Kasper Gadsbøll, Olav B Petersen, Vincent Gatinois, Heather Strange, Bo Jacobsson, Ronald Wapner, Joris R Vermeesch, Ida Vogel. Acta Obstet Gynecol Scand 2020
42
38

Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study.
Diane Van Opstal, Merel C van Maarle, Klaske Lichtenbelt, Marjan M Weiss, Heleen Schuring-Blom, Shama L Bhola, Mariette J V Hoffer, Karin Huijsdens-van Amsterdam, Merryn V Macville, Angelique J A Kooper,[...]. Genet Med 2018
48
31

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
20

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
413
16

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
703
14

Sequencing of Circulating Cell-free DNA during Pregnancy.
Diana W Bianchi, Rossa W K Chiu. N Engl J Med 2018
128
14



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
223
13

The clinical utility of genome-wide non invasive prenatal screening.
Francesco Fiorentino, Sara Bono, Francesca Pizzuti, Sara Duca, Arianna Polverari, Monica Faieta, Marina Baldi, Laura Diano, Francesca Spinella. Prenat Diagn 2017
42
26

Rare autosomal trisomies: Important and not so rare.
Fergus Scott, Michael Bonifacio, Rhiannon Sandow, Katie Ellis, Maria-Elisabeth Smet, Andrew McLennan. Prenat Diagn 2018
28
39

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall,[...]. Eur J Hum Genet 2015
152
11

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impact.
Dick Oepkes, G C Lieve Page-Christiaens, Caroline J Bax, Mireille N Bekker, Catia M Bilardo, Elles M J Boon, G Heleen Schuring-Blom, Audrey B C Coumans, Brigitte H Faas, Robert-Jan H Galjaard,[...]. Prenat Diagn 2016
91
11

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
76
13

Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus.
Y M Dennis Lo, K C Allen Chan, Hao Sun, Eric Z Chen, Peiyong Jiang, Fiona M F Lun, Yama W Zheng, Tak Y Leung, Tze K Lau, Charles R Cantor,[...]. Sci Transl Med 2010
618
11

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
46
19

Outcome of publicly funded nationwide first-tier noninvasive prenatal screening.
Kris Van Den Bogaert, Lore Lannoo, Nathalie Brison, Vincent Gatinois, Machteld Baetens, Bettina Blaumeiser, François Boemer, Laura Bourlard, Vincent Bours, Anne De Leener,[...]. Genet Med 2021
13
69

WISECONDOR: detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme.
Roy Straver, Erik A Sistermans, Henne Holstege, Allerdien Visser, Cees B M Oudejans, Marcel J T Reinders. Nucleic Acids Res 2014
90
8

Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts.
Sung K Kim, Gregory Hannum, Jennifer Geis, John Tynan, Grant Hogg, Chen Zhao, Taylor J Jensen, Amin R Mazloom, Paul Oeth, Mathias Ehrich,[...]. Prenat Diagn 2015
119
8

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
127
8

Incidental Detection of Maternal Neoplasia in Noninvasive Prenatal Testing.
Nilesh G Dharajiya, Daniel S Grosu, Daniel H Farkas, Ron M McCullough, Eyad Almasri, Youting Sun, Sung K Kim, Taylor J Jensen, Juan-Sebastian Saldivar, Eric J Topol,[...]. Clin Chem 2018
47
17


Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing.
Nathalie Brison, Maria Neofytou, Luc Dehaspe, Baran Bayindir, Kris Van Den Bogaert, Leila Dardour, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels,[...]. Prenat Diagn 2018
34
20

Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA.
Francesca Romana Grati, Jose Ferreira, Peter Benn, Claudia Izzi, Federica Verdi, Elena Vercellotti, Cristina Dalpiaz, Patrizia D'Ajello, Elisa Filippi, Nicola Volpe,[...]. Genet Med 2020
34
20

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
177
7

Implementing non-invasive prenatal testing for aneuploidy in a national healthcare system: global challenges and national solutions.
Rachèl V van Schendel, Carla G van El, Eva Pajkrt, Lidewij Henneman, Martina C Cornel. BMC Health Serv Res 2017
37
18

Global perspectives on clinical adoption of NIPT.
Mollie A Minear, Celine Lewis, Subarna Pradhan, Subhashini Chandrasekharan. Prenat Diagn 2015
88
7


Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis.
Sian Taylor-Phillips, Karoline Freeman, Julia Geppert, Adeola Agbebiyi, Olalekan A Uthman, Jason Madan, Angus Clarke, Siobhan Quenby, Aileen Clarke. BMJ Open 2016
170
7

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
83
8

Fetal fraction in maternal plasma cell-free DNA at 11-13 weeks' gestation: relation to maternal and fetal characteristics.
G Ashoor, A Syngelaki, L C Y Poon, J C Rezende, K H Nicolaides. Ultrasound Obstet Gynecol 2013
217
7

Uptake of fetal aneuploidy screening after the introduction of the non-invasive prenatal test: A national population-based register study.
Karuna R M van der Meij, Maurike de Groot-van Mooren, Ellen W S Carbo, Mijntje J Pieters, Wendy Rodenburg, Erik A Sistermans, Martina C Cornel, Lidewij Henneman. Acta Obstet Gynecol Scand 2021
10
70

Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.
H Zhang, Y Gao, F Jiang, M Fu, Y Yuan, Y Guo, Z Zhu, M Lin, Q Liu, Z Tian,[...]. Ultrasound Obstet Gynecol 2015
201
7


DNA sequencing versus standard prenatal aneuploidy screening.
Diana W Bianchi, R Lamar Parker, Jeffrey Wentworth, Rajeevi Madankumar, Craig Saffer, Anita F Das, Joseph A Craig, Darya I Chudova, Patricia L Devers, Keith W Jones,[...]. N Engl J Med 2014
401
7

Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta-analysis.
M I Srebniak, M Joosten, M F C M Knapen, L R Arends, M Polak, S van Veen, A T J I Go, D Van Opstal. Ultrasound Obstet Gynecol 2018
46
13

Screening for trisomies by cfDNA testing of maternal blood in twin pregnancy: update of The Fetal Medicine Foundation results and meta-analysis.
M M Gil, S Galeva, J Jani, L Konstantinidou, R Akolekar, M N Plana, K H Nicolaides. Ultrasound Obstet Gynecol 2019
50
12

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
678
6

Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis.
Francesca Malvestiti, Cristina Agrati, Beatrice Grimi, Eva Pompilii, Claudia Izzi, Lorenza Martinoni, Elisa Gaetani, Maria Rosaria Liuti, Anna Trotta, Federico Maggi,[...]. Prenat Diagn 2015
80
7

The impact of maternal plasma DNA fetal fraction on next generation sequencing tests for common fetal aneuploidies.
Jacob A Canick, Glenn E Palomaki, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow. Prenat Diagn 2013
213
6

Detection of rare autosomal trisomies through non-invasive prenatal testing: benefits for pregnancy management.
N Chatron, M Till, C Abel, C Bardel, F Ramond, D Sanlaville, C Schluth-Bolard. Ultrasound Obstet Gynecol 2019
11
54

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
71
8

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
580
6

Discordant non-invasive prenatal testing (NIPT) - a systematic review.
Tanja Schlaikjaer Hartwig, Louise Ambye, Steen Sørensen, Finn Stener Jørgensen. Prenat Diagn 2017
100
6

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
91
6

Is there still a role for nuchal translucency measurement in the changing paradigm of first trimester screening?
Francesca Bardi, Pien Bosschieter, Joke Verheij, Attie Go, Monique Haak, Mireille Bekker, Esther Sikkel, Audrey Coumans, Eva Pajkrt, Caterina Bilardo. Prenat Diagn 2020
15
40

Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing.
Frédéric Amant, Magali Verheecke, Iwona Wlodarska, Luc Dehaspe, Paul Brady, Nathalie Brison, Kris Van Den Bogaert, Daan Dierickx, Vincent Vandecaveye, Thomas Tousseyn,[...]. JAMA Oncol 2015
122
6


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.