A citation-based method for searching scientific literature

Betsy L Gammon, Carolina Jaramillo, Kirsten A Riggan, Megan Allyse. J Matern Fetal Neonatal Med 2020
Times Cited: 4







List of co-cited articles
7 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
289
75

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
50


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
50

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
50

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
52
50

Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies.
Nathalie Brison, Kris Van Den Bogaert, Luc Dehaspe, Jessica M E van den Oever, Katrien Janssens, Bettina Blaumeiser, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels,[...]. Genet Med 2017
35
50

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
25

Confined placental mosaicism revisited: Impact on pregnancy characteristics and outcome.
Jérôme Toutain, Damien Goutte-Gattat, Jacques Horovitz, Robert Saura. PLoS One 2018
30
25

Cell-free DNA testing of an extended range of chromosomal anomalies: clinical experience with 6,388 consecutive cases.
Graziano Pescia, Nicolas Guex, Christian Iseli, Liam Brennan, Magne Osteras, Ioannis Xenarios, Laurent Farinelli, Bernard Conrad. Genet Med 2017
51
25


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
39
25

Low uptake of the combined test in The Netherlands--which factors contribute?
Merel Bakker, Erwin Birnie, Eva Pajkrt, Caterina Maddalena Bilardo, Rosalinde Johanna Maria Snijders. Prenat Diagn 2012
53
25

NIPT-based screening for Down syndrome and beyond: what do pregnant women think?
Rachèl V van Schendel, Wybo J Dondorp, Danielle R M Timmermans, Eline J H van Hugte, Anne de Boer, Eva Pajkrt, Augusta M A Lachmeijer, Lidewij Henneman. Prenat Diagn 2015
45
25


Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing.
S L van der Steen, K E M Diderich, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M Joosten, M F C M Knapen, D Van Opstal, M I Srebniak, A Tibben,[...]. Clin Genet 2015
34
25

The Danish Fetal Medicine Database: establishment, organization and quality assessment of the first trimester screening program for trisomy 21 in Denmark 2008-2012.
Charlotte K Ekelund, Olav B Petersen, Finn S Jørgensen, Susanne Kjaergaard, Torben Larsen, Annette W Olesen, Lillian Skibsted, Peter Skovbo, Steffen Sommer, Lene Sperling,[...]. Acta Obstet Gynecol Scand 2015
40
25

Maternal vitamin B12 deficiency and abnormal cell-free DNA results in pregnancy.
Heleen Schuring-Blom, Klaske Lichtenbelt, Karin van Galen, Martin Elferink, Marjan Weiss, Joris Robert Vermeesch, Lieve Page-Christiaens. Prenat Diagn 2016
11
25

The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia.
Daniel A Arber, Attilio Orazi, Robert Hasserjian, Jürgen Thiele, Michael J Borowitz, Michelle M Le Beau, Clara D Bloomfield, Mario Cazzola, James W Vardiman. Blood 2016
25

Sequencing of Circulating Cell-free DNA during Pregnancy.
Diana W Bianchi, Rossa W K Chiu. N Engl J Med 2018
130
25

The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies.
Malgorzata I Srebniak, Maarten F C M Knapen, Marike Polak, Marieke Joosten, Karin E M Diderich, Lutgarde C P Govaerts, Marjan Boter, Joan N R Kromosoeto, Daniella Aloysia C M van Hassel, Gido Huijbregts,[...]. Hum Mutat 2017
23
25

Noninvasive prenatal testing goes global.
Subhashini Chandrasekharan, Mollie A Minear, Anthony Hung, Megan Allyse. Sci Transl Med 2014
74
25


Chromosomal mosaicisms in prenatal diagnosis: correlation with first trimester screening and clinical outcome.
Christel Eckmann-Scholz, Julia Mallek, Constantin S von Kaisenberg, Norbert K Arnold, Walter Jonat, Siebert Reiner, Almuth Caliebe, Simone Heidemann. J Perinat Med 2012
5
25

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
50
25

A case of confined placental mosaicism with double trisomy associated with stillbirth.
L R Goodfellow, G Batra, V Hall, E McHale, A E P Heazell. Placenta 2011
6
25

Plasma DNA aberrations in systemic lupus erythematosus revealed by genomic and methylomic sequencing.
Rebecca W Y Chan, Peiyong Jiang, Xianlu Peng, Lai-Shan Tam, Gary J W Liao, Edmund K M Li, Priscilla C H Wong, Hao Sun, K C Allen Chan, Rossa W K Chiu,[...]. Proc Natl Acad Sci U S A 2014
70
25

Recommended practice for laboratory reporting of non-invasive prenatal testing of trisomies 13, 18 and 21: a consensus opinion.
Zandra C Deans, Stephanie Allen, Lucy Jenkins, Farrah Khawaja, Ros J Hastings, Kathy Mann, Simon J Patton, Erik A Sistermans, Lyn S Chitty. Prenat Diagn 2017
13
25

Genome-wide cfDNA screening: clinical laboratory experience with the first 10,000 cases.
Mathias Ehrich, John Tynan, Amin Mazloom, Eyad Almasri, Ron McCullough, Theresa Boomer, Daniel Grosu, Jason Chibuk. Genet Med 2017
40
25

Explaining variation in Down's syndrome screening uptake: comparing the Netherlands with England and Denmark using documentary analysis and expert stakeholder interviews.
Neeltje M T H Crombag, Ynke E Vellinga, Sandra A Kluijfhout, Louise D Bryant, Pat A Ward, Rita Iedema-Kuiper, Peter C J I Schielen, Jozien M Bensing, Gerard H A Visser, Ann Tabor,[...]. BMC Health Serv Res 2014
49
25

The future of DNA sequencing.
Eric D Green, Edward M Rubin, Maynard V Olson. Nature 2017
31
25

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
174
25


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
44
25

Impact of transition from analog screening mammography to digital screening mammography on screening outcome in The Netherlands: a population-based study.
J Nederend, L E M Duijm, M W J Louwman, J H Groenewoud, A B Donkers-van Rossum, A C Voogd. Ann Oncol 2012
52
25

Genetic screening and democracy: lessons from debating genetic screening criteria in the Netherlands.
Carla Geertruida van El, Toine Pieters, Martina Cornel. J Community Genet 2012
21
25

Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals.
Melissa Hill, Jo-Ann Johnson, Sylvie Langlois, Hyun Lee, Stephanie Winsor, Brigid Dineley, Marisa Horniachek, Faustina Lalatta, Luisa Ronzoni, Angela N Barrett,[...]. Eur J Hum Genet 2016
35
25

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
92
25

Comparing methods for fetal fraction determination and quality control of NIPT samples.
Daphne M van Beek, Roy Straver, Marian M Weiss, Elles M J Boon, Karin Huijsdens-van Amsterdam, Cees B M Oudejans, Marcel J T Reinders, Erik A Sistermans. Prenat Diagn 2017
34
25

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
92
25


Mosaic maternal 10qter deletions are associated with FRA10B expansions and may cause false-positive noninvasive prenatal screening results.
Karin Huijsdens-van Amsterdam, Roy Straver, Merel C van Maarle, Alida C Knegt, Diane Van Opstal, Frank Sleutels, Dominique Smeets, Erik A Sistermans. Genet Med 2018
8
25

Trends in perinatal health in metropolitan France from 1995 to 2016: Results from the French National Perinatal Surveys.
B Blondel, B Coulm, C Bonnet, F Goffinet, C Le Ray. J Gynecol Obstet Hum Reprod 2017
179
25

Genomewide copy number alteration screening of circulating plasma DNA: potential for the detection of incipient tumors.
L Lenaerts, P Vandenberghe, N Brison, H Che, M Neofytou, M Verheecke, L Leemans, C Maggen, B Dewaele, L Dehaspe,[...]. Ann Oncol 2019
20
25

Calculating the fetal fraction for noninvasive prenatal testing based on genome-wide nucleosome profiles.
Roy Straver, Cees B M Oudejans, Erik A Sistermans, Marcel J T Reinders. Prenat Diagn 2016
56
25

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
122
25

Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphism-based noninvasive prenatal test.
Kirsten J Curnow, Louise Wilkins-Haug, Allison Ryan, Eser Kırkızlar, Melissa Stosic, Megan P Hall, Styrmir Sigurjonsson, Zachary Demko, Matthew Rabinowitz, Susan J Gross. Am J Obstet Gynecol 2015
92
25

Cell-Free DNA Analysis in Maternal Blood: Differences in Estimates between Laboratories with Different Methodologies Using a Propensity Score Approach.
Elisa Bevilacqua, Jacques C Jani, Alexandra Letourneau, Silvia F Duiella, Pascale Kleinfinger, Laurence Lohmann, Serena Resta, Teresa Cos Sanchez, Jean-François Fils, Marilyn Mirra,[...]. Fetal Diagn Ther 2019
2
50

Doubly robust estimation of causal effects.
Michele Jonsson Funk, Daniel Westreich, Chris Wiesen, Til Stürmer, M Alan Brookhart, Marie Davidian. Am J Epidemiol 2011
313
25

Screening for trisomies 21 and 18 in a Spanish public hospital: from the combined test to the cell-free DNA test.
M M Gil, M Brik, C Casanova, R Martin-Alonso, M Verdejo, E Ramírez, B Santacruz. J Matern Fetal Neonatal Med 2017
6
25


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.