A citation-based method for searching scientific literature

Lijuan Sun, Qingqing Wu, Shi-Wen Jiang, Yani Yan, Xin Wang, Juan Zhang, Yan Liu, Ling Yao, Yuqing Ma, Li Wang. Biomed Res Int 2015
Times Cited: 25







List of co-cited articles
239 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
44

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
44

Evaluation of Fetal Central Nervous System Anomalies by Ultrasound and Its Anatomical Co-relation.
Deepali Onkar, Prashant Onkar, Kajal Mitra. J Clin Diagn Res 2014
18
50

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
32

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
32

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
28



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

High-resolution microarray in the assessment of fetal anomalies detected by ultrasound.
Poonam Charan, Nicole Woodrow, Sue P Walker, Devika Ganesamoorthy, George McGillivray, Ricardo Palma-Dias. Aust N Z J Obstet Gynaecol 2014
12
41

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
20

Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regions.
Sophia K Krutzke, Hartmut Engels, Andrea Hofmann, Madita M Schumann, Kirsten Cremer, Alexander M Zink, Alina Hilger, Michael Ludwig, Ulrich Gembruch, Heiko Reutter,[...]. Birth Defects Res A Clin Mol Teratol 2016
11
45

Chromosome abnormality incidence in fetuses with cerebral ventriculomegaly.
C Gezer, A Ekin, M Ozeren, C E Taner, O Ozer, A Koc, M Bilgin, N S Gezer. J Obstet Gynaecol 2014
17
29


Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
Y Yan, Q Wu, L Zhang, X Wang, S Dan, D Deng, L Sun, L Yao, Y Ma, L Wang. Ultrasound Obstet Gynecol 2014
29
16

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
16


Systematic review and meta-analysis of isolated posterior fossa malformations on prenatal ultrasound imaging (part 1): nomenclature, diagnostic accuracy and associated anomalies.
F D'Antonio, A Khalil, C Garel, G Pilu, G Rizzo, T Lerman-Sagie, A Bhide, B Thilaganathan, L Manzoli, A T Papageorghiou. Ultrasound Obstet Gynecol 2016
34
16

Fetal soft markers in obstetric ultrasound.
Michiel C Van den Hof, R Douglas Wilson. J Obstet Gynaecol Can 2005
69
16

Copy Number Variations with Isolated Fetal Ventriculomegaly.
P Hu, Y Wang, R Sun, L Cao, X Chen, C Liu, C Luo, D Ma, W Wang, X Fu,[...]. Curr Mol Med 2017
11
36

Epidemiology, natural history, progression, and postnatal outcome of severe fetal ventriculomegaly.
Therese Hannon, Peter W G Tennant, Judith Rankin, Stephen C Robson. Obstet Gynecol 2012
40
16


Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.
Trilochan Sahoo, Natasa Dzidic, Michelle N Strecker, Sara Commander, Mary K Travis, Charles Doherty, R Weslie Tyson, Arturo E Mendoza, Mary Stephenson, Craig A Dise,[...]. Genet Med 2017
60
16

Prevalence, natural history, and clinical outcome of mild to moderate ventriculomegaly.
Farah Sethna, Peter W G Tennant, Judith Rankin, Stephen C Robson. Obstet Gynecol 2011
41
16

Molecular genetics in fetal neurology.
Jin Huang, Isabella Y M Wah, Ritsuko K Pooh, Kwong Wai Choy. Semin Fetal Neonatal Med 2012
13
30


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
12

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
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
12

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
12

Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases.
Ioannis Papoulidis, Alexandros Sotiriadis, Elisavet Siomou, Elena Papageorgiou, Makarios Eleftheriades, Vasilios Papadopoulos, Eirini Oikonomidou, Sandro Orru, Emmanouil Manolakos, Apostolos Athanasiadis. Prenat Diagn 2015
23
13

Diagnostic imaging of posterior fossa anomalies in the fetus and neonate: part 2, Posterior fossa disorders.
Teresa Chapman, Sowmya Mahalingam, Gisele E Ishak, Jason N Nixon, Joseph Siebert, Manjiri K Dighe. Clin Imaging 2015
22
13

Perinatal and short-term neonatal outcomes of posterior fossa anomalies.
Rim Ghali, Karen Reidy, A Michelle Fink, Ricardo Palma-Dias. Fetal Diagn Ther 2014
5
60

Anatomical subgroup analysis of the MERIDIAN cohort: ventriculomegaly.
P D Griffiths, K Brackley, M Bradburn, D J A Connolly, M L Gawne-Cain, D I Griffiths, M D Kilby, L Mandefield, C Mooney, S C Robson,[...]. Ultrasound Obstet Gynecol 2017
22
13

Severe apparently isolated fetal ventriculomegaly and neurodevelopmental outcome.
Mathilde Letouzey, Alexandra Chadie, Marie Brasseur-Daudruy, François Proust, Eric Verspyck, Pascal Boileau, Stéphane Marret. Prenat Diagn 2017
10
30

Reference ranges for fetal ventricular width: a non-normal approach.
L J Salomon, J P Bernard, Y Ville. Ultrasound Obstet Gynecol 2007
40
12

Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
Xiangyu Zhu, Jie Li, Tong Ru, Yaping Wang, Yan Xu, Ying Yang, Xing Wu, David S Cram, Yali Hu. Prenat Diagn 2016
37
12

The significance of fetal ventriculomegaly: etiology, short- and long-term outcomes.
Pietro Gaglioti, Manuela Oberto, Tullia Todros. Prenat Diagn 2009
82
12


Mild fetal lateral cerebral ventriculomegaly: clinical course and outcome.
B Bromley, F D Frigoletto, B R Benacerraf. Am J Obstet Gynecol 1991
109
12

Chromosomal and structural anomalies in fetuses with open neural tube defects.
A Ekin, C Gezer, C E Taner, M Ozeren, O Ozer, A Koç, N S Gezer. J Obstet Gynaecol 2014
7
42

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
12

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

Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs.
Madita Schumann, Andrea Hofmann, Sophia K Krutzke, Alina C Hilger, Florian Marsch, Dietlinde Stienen, Ulrich Gembruch, Michael Ludwig, Waltraut M Merz, Heiko Reutter. J Neurodev Disord 2016
8
37

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
28
12

Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia.
Zhiyong Zou, Linhuan Huang, Shaobin Lin, Zhiming He, Hui Zhu, Yi Zhang, Qun Fang, Yanmin Luo. Prenat Diagn 2018
10
30

Copy number variations and fetal ventriculomegaly.
Yan Wang, Ping Hu, Zhengfeng Xu. Curr Opin Obstet Gynecol 2018
8
37

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland,[...]. Genet Med 2020
136
12

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Ellen Hanson, Raphael Bernier, Ken Porche, Frank I Jackson, Robin P Goin-Kochel, LeeAnne Green Snyder, Anne V Snow, Arianne Stevens Wallace, Katherine L Campe, Yuan Zhang,[...]. Biol Psychiatry 2015
128
12


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.