A citation-based method for searching scientific literature

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
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


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
273
50

Ensuring high standards for the delivery of NIPT world-wide: Development of an international external quality assessment scheme.
Zandra C Deans, Stephanie Allen, Lucy Jenkins, Farrah Khawaja, Weronika Gutowska-Ding, Simon J Patton, Lyn S Chitty, Ros J Hastings. Prenat Diagn 2019
5
80

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
597
40

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
526
40

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
343
30

Free fetal DNA in maternal plasma in anembryonic pregnancies: confirmation that the origin is the trophoblast.
M Alberry, D Maddocks, M Jones, M Abdel Hadi, S Abdel-Fattah, N Avent, P W Soothill. Prenat Diagn 2007
199
30

Global perspectives on clinical adoption of NIPT.
Mollie A Minear, Celine Lewis, Subarna Pradhan, Subhashini Chandrasekharan. Prenat Diagn 2015
75
30

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
214
30

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
122
20

Gestational age and maternal weight effects on fetal cell-free DNA in maternal plasma.
Eric Wang, Annette Batey, Craig Struble, Thomas Musci, Ken Song, Arnold Oliphant. Prenat Diagn 2013
199
20

Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.
Y M Lo, M S Tein, T K Lau, C J Haines, T N Leung, P M Poon, J S Wainscoat, P J Johnson, A M Chang, N M Hjelm. Am J Hum Genet 1998
20

The importance of determining the limit of detection of non-invasive prenatal testing methods.
Francesco Fiorentino, Sara Bono, Francesca Pizzuti, Martina Mariano, Arianna Polverari, Sara Duca, Mariateresa Sessa, Marina Baldi, Laura Diano, Francesca Spinella. Prenat Diagn 2016
26
20

Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.
M M Gil, M S Quezada, R Revello, R Akolekar, K H Nicolaides. Ultrasound Obstet Gynecol 2015
276
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
147
20

Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases.
Jia-Chi Wang, Trilochan Sahoo, Steven Schonberg, Kimberly A Kopita, Leslie Ross, Kyla Patek, Charles M Strom. Genet Med 2015
57
20

Circulating fetal cell-free DNA fractions differ in autosomal aneuploidies and monosomy X.
Richard P Rava, Anupama Srinivasan, Amy J Sehnert, Diana W Bianchi. Clin Chem 2014
90
20

Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.
Yanlin Wang, Yan Chen, Feng Tian, Jianguang Zhang, Zhuo Song, Yi Wu, Xu Han, Wenjing Hu, Duan Ma, David Cram,[...]. Clin Chem 2014
136
20

Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic).
Mireille Claustres, Viktor Kožich, Els Dequeker, Brain Fowler, Jayne Y Hehir-Kwa, Konstantin Miller, Cor Oosterwijk, Borut Peterlin, Conny van Ravenswaaij-Arts, Uwe Zimmermann,[...]. Eur J Hum Genet 2014
57
20

College of American Pathologists' laboratory standards for next-generation sequencing clinical tests.
Nazneen Aziz, Qin Zhao, Lynn Bry, Denise K Driscoll, Birgit Funke, Jane S Gibson, Wayne W Grody, Madhuri R Hegde, Gerald A Hoeltge, Debra G B Leonard,[...]. Arch Pathol Lab Med 2015
184
20

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
20

Guidelines for diagnostic next-generation sequencing.
Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik Sistermans, Marc Sturm, Marjan Weiss,[...]. Eur J Hum Genet 2016
212
20

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
80
20

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
146
20

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
180
20

Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort.
Eugene Pergament, Howard Cuckle, Bernhard Zimmermann, Milena Banjevic, Styrmir Sigurjonsson, Allison Ryan, Megan P Hall, Michael Dodd, Phil Lacroute, Melissa Stosic,[...]. Obstet Gynecol 2014
153
20


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
20

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
37
20

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
41
20

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
42
20

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
6
33

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
55
20

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
60
20

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
24
20


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
64
20

Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease.
C Michael Osborne, Emily Hardisty, Patricia Devers, Kathleen Kaiser-Rogers, Melissa A Hayden, William Goodnight, Neeta L Vora. Prenat Diagn 2013
119
10


The value of the first trimester ultrasound in the era of cell free DNA screening.
Rashmi R Rao, Stephanie G Valderramos, Neil S Silverman, Christina S Han, Lawrence D Platt. Prenat Diagn 2016
9
11

Cytogenetic Nomenclature: Changes in the ISCN 2013 Compared to the 2009 Edition.
A Simons, L G Shaffer, R J Hastings. Cytogenet Genome Res 2013
133
10

Offering prenatal diagnostic tests: European guidelines for clinical practice [corrected].
Heather Skirton, Lesley Goldsmith, Leigh Jackson, Celine Lewis, Lyn Chitty. Eur J Hum Genet 2014
25
10

Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders.
Rolph Pfundt, Marisol Del Rosario, Lisenka E L M Vissers, Michael P Kwint, Irene M Janssen, Nicole de Leeuw, Helger G Yntema, Marcel R Nelen, Dorien Lugtenberg, Erik-Jan Kamsteeg,[...]. Genet Med 2017
70
10


Pathogenic or not? Assessing the clinical relevance of copy number variants.
J Y Hehir-Kwa, R Pfundt, J A Veltman, N de Leeuw. Clin Genet 2013
35
10

SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control.
N de Leeuw, J Y Hehir-Kwa, A Simons, A Geurts van Kessel, D F Smeets, B H W Faas, R Pfundt. Cytogenet Genome Res 2011
30
10

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
10


Section E9 of the American College of Medical Genetics technical standards and guidelines: fluorescence in situ hybridization.
James T Mascarello, Betsy Hirsch, Hutton M Kearney, Rhett P Ketterling, Susan B Olson, Denise I Quigley, Kathleen W Rao, James H Tepperberg, Karen D Tsuchiya, Anne E Wiktor. Genet Med 2011
38
10

Detection of low-level mosaicism by array CGH in routine diagnostic specimens.
Blake C Ballif, Emily A Rorem, Kyle Sundin, Matt Lincicum, Shannon Gaskin, Justine Coppinger, Catherine D Kashork, Lisa G Shaffer, Bassem A Bejjani. Am J Med Genet A 2006
195
10


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.