A citation-based method for searching scientific literature

M C de Wit, M I Srebniak, L C P Govaerts, D Van Opstal, R J H Galjaard, A T J I Go. Ultrasound Obstet Gynecol 2014
Times Cited: 92







List of co-cited articles
496 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
643
61

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
154
31

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
138
23

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
136
21

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
S C Hillman, S Pretlove, A Coomarasamy, D J McMullan, E V Davison, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2011
154
20

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
20

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
513
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
80
20


Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.
Malgorzata I Srebniak, Marjan Boter, Gretel O Oudesluijs, Titia Cohen-Overbeek, Lutgarde Cp Govaerts, Karin Em Diderich, Renske Oegema, Maarten Fcm Knapen, Ingrid Mbh van de Laar, Marieke Joosten,[...]. Mol Cytogenet 2012
52
26


Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
Francesco Fiorentino, Stefania Napoletano, Fiorina Caiazzo, Mariateresa Sessa, Sara Bono, Letizia Spizzichino, Anthony Gordon, Andrea Nuccitelli, Giuseppe Rizzo, Marina Baldi. Eur J Hum Genet 2013
61
21



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
41
31

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
80
16

Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
129
13

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
184
13

Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.
Malgorzata I Srebniak, Karin Em Diderich, Marieke Joosten, Lutgarde Cp Govaerts, Jeroen Knijnenburg, Femke At de Vries, Marjan Boter, Debora Lont, Maarten Fcm Knapen, Merel C de Wit,[...]. Eur J Hum Genet 2016
38
31

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
81
14

Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases.
Francesco Fiorentino, Fiorina Caiazzo, Stefania Napolitano, Letizia Spizzichino, Sara Bono, Mariateresa Sessa, Andrea Nuccitelli, Anil Biricik, Anthony Gordon, Giuseppe Rizzo,[...]. Prenat Diagn 2011
75
13

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
226
10

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow.
Malgorzata Srebniak, Marjan Boter, Grétel Oudesluijs, Marieke Joosten, Lutgarde Govaerts, Diane Van Opstal, Robert-Jan H Galjaard. Eur J Hum Genet 2011
74
13

Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification.
Malgorzata I Srebniak, Karin E M Diderich, Lutgarde C P Govaerts, Marieke Joosten, Sam Riedijk, Robert Jan H Galjaard, Diane Van Opstal. Eur J Hum Genet 2014
27
37

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
31
32

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis.
R Akolekar, J Beta, G Picciarelli, C Ogilvie, F D'Antonio. Ultrasound Obstet Gynecol 2015
320
10

High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power.
Beatrice Oneda, Rosa Baldinger, Regina Reissmann, Irina Reshetnikova, Pavel Krejci, Rahim Masood, Nicole Ochsenbein-Kölble, Deborah Bartholdi, Katharina Steindl, Denise Morotti,[...]. Prenat Diagn 2014
29
34

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
61
16

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
803
10

High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.
M Tyreman, K M Abbott, L R Willatt, R Nash, C Lees, J Whittaker, I Simonic. J Med Genet 2009
90
10

Karyotype versus microarray testing for genetic abnormalities after stillbirth.
Uma M Reddy, Grier P Page, George R Saade, Robert M Silver, Vanessa R Thorsten, Corette B Parker, Halit Pinar, Marian Willinger, Barbara J Stoll, Josefine Heim-Hall,[...]. N Engl J Med 2012
140
9

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
58
15

The introduction of arrays in prenatal diagnosis: a special challenge.
Annalisa Vetro, Katelijne Bouman, Ros Hastings, Dominic J McMullan, Joris R Vermeesch, Konstantin Miller, Birgit Sikkema-Raddatz, David H Ledbetter, Orsetta Zuffardi, Conny M A van Ravenswaaij-Arts. Hum Mutat 2012
51
15

Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.
I Mademont-Soler, C Morales, A Soler, J M Martínez-Crespo, Y Shen, E Margarit, N Clusellas, M Obón, B L Wu, A Sánchez. Ultrasound Obstet Gynecol 2013
41
19

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
27
29

Non-targeted whole genome 250K SNP array analysis as replacement for karyotyping in fetuses with structural ultrasound anomalies: evaluation of a one-year experience.
Brigitte H W Faas, Ilse Feenstra, Alex J Eggink, Angelique J A Kooper, Rolph Pfundt, John M G van Vugt, Nicole de Leeuw. Prenat Diagn 2012
31
25

Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findings.
Else Marie Vestergaard, Rikke Christensen, Olav B Petersen, Ida Vogel. Acta Obstet Gynecol Scand 2013
23
34

A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.
Paul Daniel Brady, Barbara Delle Chiaie, Gabrielle Christenhusz, Kris Dierickx, Kris Van Den Bogaert, Bjorn Menten, Sandra Janssens, Paul Defoort, Ellen Roets, Elke Sleurs,[...]. Genet Med 2014
45
17

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.
Amy Breman, Amber N Pursley, Patricia Hixson, Weimin Bi, Patricia Ward, Carlos A Bacino, Chad Shaw, James R Lupski, Arthur Beaudet, Ankita Patel,[...]. Prenat Diagn 2012
74
10

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
353
8

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
31
25

Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities.
Suzanne Drury, Hywel Williams, Natalie Trump, Christopher Boustred, Nicholas Lench, Richard H Scott, Lyn S Chitty. Prenat Diagn 2015
108
8

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
154
8

The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
62
12

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences.
S L van der Steen, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M I Srebniak, D Van Opstal, M Joosten, M F C M Knapen, A Tibben, K E M Diderich,[...]. J Genet Couns 2016
26
30

Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
130
8


Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
G D'Amours, Z Kibar, G Mathonnet, R Fetni, F Tihy, V Désilets, S Nizard, J L Michaud, E Lemyre. Clin Genet 2012
58
12

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis.
Lluís Armengol, Julián Nevado, Clara Serra-Juhé, Alberto Plaja, Carmen Mediano, Fe Amalia García-Santiago, Manel García-Aragonés, Olaya Villa, Elena Mansilla, Cristina Preciado,[...]. Hum Genet 2012
61
11



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.