A citation-based method for searching scientific literature

M Grande, F A R Jansen, Y J Blumenfeld, A Fisher, A O Odibo, M C Haak, A Borrell. Ultrasound Obstet Gynecol 2015
Times Cited: 75







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



Times Cited
  Times     Co-cited
Similarity


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
597
45

Increased nuchal translucency with normal karyotype.
Athena P Souka, Constantin S Von Kaisenberg, Jonathan A Hyett, Jiri D Sonek, Kypros H Nicolaides. Am J Obstet Gynecol 2005
203
28


Relation between increased fetal nuchal translucency thickness and chromosomal defects.
Karl Oliver Kagan, Kyriaki Avgidou, Francisca S Molina, Katarzyna Gajewska, Kypros H Nicolaides. Obstet Gynecol 2006
78
20

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
142
20

Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype.
T Y Leung, I Vogel, T K Lau, W Chong, J A Hyett, O B Petersen, K W Choy. Ultrasound Obstet Gynecol 2011
73
19


Chromosomal microarray in fetuses with increased nuchal translucency.
I C B Lund, R Christensen, O B Petersen, I Vogel, E M Vestergaard. Ultrasound Obstet Gynecol 2015
29
44

Cut-off value of nuchal translucency as indication for chromosomal microarray analysis.
I Maya, S Yacobson, S Kahana, J Yeshaya, T Tenne, I Agmon-Fishman, L Cohen-Vig, M Shohat, L Basel-Vanagaite, R Sharony. Ultrasound Obstet Gynecol 2017
19
68


Is high fetal nuchal translucency associated with submicroscopic chromosomal abnormalities on array CGH?
J Huang, L C Poon, R Akolekar, K W Choy, T Y Leung, K H Nicolaides. Ultrasound Obstet Gynecol 2014
29
41

Increased nuchal translucency thickness and normal karyotype: time for parental reassurance.
C M Bilardo, M A Müller, E Pajkrt, S A Clur, M M van Zalen, E K Bijlsma. Ultrasound Obstet Gynecol 2007
88
16

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
490
14

Risk of selected structural abnormalities in infants after increased nuchal translucency measurement.
Rebecca J Baer, Mary E Norton, Gary M Shaw, Monica C Flessel, Sara Goldman, Robert J Currier, Laura L Jelliffe-Pawlowski. Am J Obstet Gynecol 2014
50
20

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
129
13

Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis.
F A R Jansen, Y J Blumenfeld, A Fisher, J M Cobben, A O Odibo, A Borrell, M C Haak. Ultrasound Obstet Gynecol 2015
56
17

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
128
13

Challenges in the diagnosis of fetal non-chromosomal abnormalities at 11-13 weeks.
Argyro Syngelaki, Teodora Chelemen, Themistoklis Dagklis, Lindsey Allan, Kypros H Nicolaides. Prenat Diagn 2011
224
12

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
12

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
12


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
126
10


ISUOG practice guidelines: performance of first-trimester fetal ultrasound scan.
L J Salomon, Z Alfirevic, C M Bilardo, G E Chalouhi, T Ghi, K O Kagan, T K Lau, A T Papageorghiou, N J Raine-Fenning, J Stirnemann,[...]. Ultrasound Obstet Gynecol 2013
200
10

Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT.
Malgorzata I Srebniak, Merel C de Wit, Karin E M Diderich, Lutgarde C P Govaerts, Marieke Joosten, Maarten F C M Knapen, Marnix J Bos, Gerda A G Looye-Bruinsma, Mieke Koningen, Attie T J I Go,[...]. Mol Cytogenet 2016
16
50

Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.
M Egloff, B Hervé, T Quibel, S Jaillard, G Le Bouar, K Uguen, A-H Saliou, M Valduga, E Perdriolle, C Coutton,[...]. Ultrasound Obstet Gynecol 2018
17
47

Association of copy number variants with specific ultrasonographically detected fetal anomalies.
Jennifer C Donnelly, Lawrence D Platt, Andrei Rebarber, Julia Zachary, William A Grobman, Ronald J Wapner. Obstet Gynecol 2014
76
9

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Laetitia Gouas, Nina Horelli-Kuitunen, Kwong Wai Choy, Sandra García-Herrero, Alberto Gonzalez de la Vega,[...]. Prenat Diagn 2015
146
9

Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non-invasive prenatal testing?
K D Lichtenbelt, B D M Diemel, M P H Koster, G T R Manten, J Siljee, G H Schuring-Blom, G C M L Page-Christiaens. Prenat Diagn 2015
18
38

Defects and syndromes in chromosomally normal fetuses with increased nuchal translucency thickness at 10-14 weeks of gestation.
A P Souka, R J Snijders, A Novakov, W Soares, K H Nicolaides. Ultrasound Obstet Gynecol 1998
218
9


First-trimester or second-trimester screening, or both, for Down's syndrome.
Fergal D Malone, Jacob A Canick, Robert H Ball, David A Nyberg, Christine H Comstock, Radek Bukowski, Richard L Berkowitz, Susan J Gross, Lorraine Dugoff, Sabrina D Craigo,[...]. N Engl J Med 2005
604
9

Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidies.
Diane Van Opstal, Femke de Vries, Lutgarde Govaerts, Marjan Boter, Debora Lont, Stefanie van Veen, Marieke Joosten, Karin Diderich, Robert-Jan Galjaard, Malgorzata I Srebniak. Hum Mutat 2015
39
17



Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.
Olivier Vanakker, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, Saskia Bulk, Jean-Hubert Caberg, Anne De Leener,[...]. Eur J Med Genet 2014
56
12

Increased nuchal translucency with normal karyotype and anomaly scan: what next?
Merel Bakker, Eva Pajkrt, Caterina M Bilardo. Best Pract Res Clin Obstet Gynaecol 2014
20
35

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
174
9

Outcome of pregnancy in chromosomally normal fetuses with increased nuchal translucency in the first trimester.
A P Souka, E Krampl, S Bakalis, V Heath, K H Nicolaides. Ultrasound Obstet Gynecol 2001
182
9


Testing for Noonan syndrome after increased nuchal translucency.
Marwan M Ali, Stephen T Chasen, Mary E Norton. Prenat Diagn 2017
18
38

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Christine M Armour, Shelley Danielle Dougan, Jo-Ann Brock, Radha Chari, Bernie N Chodirker, Isabelle DeBie, Jane A Evans, William T Gibson, Elena Kolomietz, Tanya N Nelson,[...]. J Med Genet 2018
25
28

Why increased nuchal translucency is associated with congenital heart disease: a systematic review on genetic mechanisms.
Nicole B Burger, Mireille N Bekker, Christianne J M de Groot, Vincent M Christoffels, Monique C Haak. Prenat Diagn 2015
15
40

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
8

Prenatal diagnosis using array-CGH: a French experience.
Caroline Rooryck, Jérôme Toutain, Dorothée Cailley, Julie Bouron, Jacques Horovitz, Didier Lacombe, Benoit Arveiler, Robert Saura. Eur J Med Genet 2013
24
25

DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study.
Glenn E Palomaki, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow, Louis M Neveux, Mathias Ehrich, Dirk van den Boom, Allan T Bombard, Cosmin Deciu, Wayne W Grody,[...]. Genet Med 2011
524
8

The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
56
10

First-trimester detection of structural abnormalities and the role of aneuploidy markers.
M Grande, M Arigita, V Borobio, J M Jimenez, S Fernandez, A Borrell. Ultrasound Obstet Gynecol 2012
51
11

The role of ultrasound in women who undergo cell-free DNA screening.
Mary E Norton, Joseph R Biggio, Jeffrey A Kuller, Sean C Blackwell. Am J Obstet Gynecol 2017
47
12

Pregnancy outcome in fetuses with increased nuchal translucency and normal karyotype.
M V Senat, B De Keersmaecker, F Audibert, G Montcharmont, R Frydman, Y Ville. Prenat Diagn 2002
46
13


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.