A citation-based method for searching scientific literature

Yan Wang, Ping Hu, Zhengfeng Xu. Curr Opin Obstet Gynecol 2018
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity



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
141
55

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
55

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
86
55

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
43
44

A prospective study of fetuses with isolated ventriculomegaly investigated by antenatal sonography and in utero MR imaging.
P D Griffiths, M J Reeves, J E Morris, G Mason, S A Russell, M N J Paley, E H Whitby. AJNR Am J Neuroradiol 2010
82
44

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
18
44

The significance of fetal ventriculomegaly: etiology, short- and long-term outcomes.
Pietro Gaglioti, Manuela Oberto, Tullia Todros. Prenat Diagn 2009
84
44

Mild fetal ventriculomegaly: diagnosis, evaluation, and management.
Nathan S Fox, Ana Monteagudo, Jeffrey A Kuller, Sabrina Craigo, Mary E Norton. Am J Obstet Gynecol 2018
38
44

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
26
44

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
44
44

The utility of infection screening in isolated mild ventriculomegaly: an observational retrospective study on 141 fetuses.
Lucia Pasquini, Giulia Masini, Claudia Gaini, Chiara Franchi, Michele Trotta, Carlo Dani, Mariarosaria Di Tommaso. Prenat Diagn 2014
17
44

Perinatal and long-term outcomes in fetuses diagnosed with isolated unilateral ventriculomegaly: systematic review and meta-analysis.
C Scala, A Familiari, A Pinas, A T Papageorghiou, A Bhide, B Thilaganathan, A Khalil. Ultrasound Obstet Gynecol 2017
26
33


The application of chromosomal microarray analysis to the prenatal diagnosis of isolated mild ventriculomegaly.
Hong-Lei Duan, Xiang-Yu Zhu, Yu-Jie Zhu, Xing Wu, Guang-Feng Zhao, Wan-Jun Wang, Jie Li. Taiwan J Obstet Gynecol 2019
5
60


Mild fetal lateral cerebral ventriculomegaly: clinical course and outcome.
B Bromley, F D Frigoletto, B R Benacerraf. Am J Obstet Gynecol 1991
109
33

Fetal soft markers in obstetric ultrasound.
Michiel C Van den Hof, R Douglas Wilson. J Obstet Gynaecol Can 2005
71
33

Prognosis of isolated mild to moderate fetal cerebral ventriculomegaly: a systematic review.
Priscilla Devaseelan, Chris Cardwell, Barbara Bell, Stephen Ong. J Perinat Med 2010
25
33

Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis.
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
25
33

Neonatal outcome of congenital ventriculomegaly.
Liz McKechnie, Chakra Vasudevan, Malcolm Levene. Semin Fetal Neonatal Med 2012
24
22

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
664
22

1p deletion syndrome: A prenatal diagnosis characterized by an abnormal 1st trimester combined screening test, yet a normal NIPT result.
Chung-Yuan Yang, Chuan-Chi Kao, Shuenn-Dyn Chang, Shih-Yin Huang. Taiwan J Obstet Gynecol 2018
3
66

Prenatal diagnosis of monosomy 1p36: a focus on brain abnormalities and a review of the literature.
Philippe M Campeau, Nicholas Ah Mew, Lola Cartier, Katherine L Mackay, Lisa G Shaffer, Vazken M Der Kaloustian, Mary Ann Thomas. Am J Med Genet A 2008
34
22

Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.
Sarah Guterman, Claire Beneteau, Sylvia Redon, Céline Dupont, Chantal Missirian, Pauline Jaeger, Berenice Herve, Clémence Jacquin, Nathalie Douet-Guilbert, Marianne Till,[...]. Prenat Diagn 2019
6
33

Postnatal clinical and imaging follow-up of infants with prenatal isolated mild ventriculomegaly: a series of 101 cases.
Céline Falip, Nathalie Blanc, Emmanuelle Maes, Isabelle Zaccaria, Jean François Oury, Guy Sebag, Catherine Garel. Pediatr Radiol 2007
78
22


Counseling in isolated mild fetal ventriculomegaly.
K Melchiorre, A Bhide, A D Gika, G Pilu, A T Papageorghiou. Ultrasound Obstet Gynecol 2009
95
22


The Genetic Basis of Hydrocephalus.
Maria Kousi, Nicholas Katsanis. Annu Rev Neurosci 2016
43
22

The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
64
22

Meta-analysis of second-trimester markers for trisomy 21.
M Agathokleous, P Chaveeva, L C Y Poon, P Kosinski, K H Nicolaides. Ultrasound Obstet Gynecol 2013
123
22

Obstetric and neonatal outcomes in severe fetal ventriculomegaly.
Andrew C G Breeze, Peta M A Alexander, Edile M Murdoch, Hannah H Missfelder-Lobos, Gerald A Hackett, Christoph C Lees. Prenat Diagn 2007
57
22

The clinical significance of fetal isolated cerebral borderline ventriculomegaly: report of 31 cases and review of the literature.
G Pilu, P Falco, S Gabrielli, A Perolo, F Sandri, L Bovicelli. Ultrasound Obstet Gynecol 1999
114
22

Not all ventriculomegaly is created equal: diagnostic overview of fetal, neonatal and pediatric ventriculomegaly.
Smruti K Patel, Jorge Zamorano-Fernandez, Usha Nagaraj, Karin S Bierbrauer, Francesco T Mangano. Childs Nerv Syst 2020
4
50

Is fetal magnetic resonance imaging indicated when ultrasound isolated mild ventriculomegaly is present in pregnancies with no risk factors?
Cecilia Parazzini, Andrea Righini, Chiara Doneda, Filippo Arrigoni, Mariangela Rustico, Mariano Lanna, Fabio Triulzi. Prenat Diagn 2012
28
22

Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with ventriculomegaly.
Qingxian Chang, Yanping Yang, Yixian Peng, Siping Liu, Liyan Li, Xujie Deng, Ming Yang, Yu Lan. Eur J Paediatr Neurol 2020
2
100

Reference ranges for fetal ventricular width: a non-normal approach.
L J Salomon, J P Bernard, Y Ville. Ultrasound Obstet Gynecol 2007
42
22

Nine patients with Xp22.31 microduplication, cognitive deficits, seizures, and talipes anomalies.
Edward D Esplin, Ben Li, Anne Slavotinek, Antonio Novelli, Agatino Battaglia, Robin Clark, Cynthia Curry, Louanne Hudgins. Am J Med Genet A 2014
32
11


Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations.
Céline Dupont, Francesca Romana Grati, Kwong Wai Choy, Sylvie Jaillard, Jérôme Toutain, Marie-Laure Maurin, Jose Antonio Martínez-Conejero, Claire Beneteau, Aurélie Coussement, Denise Molina-Gomes,[...]. Prenat Diagn 2015
17
11

The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.
Cynthia J Curry, Jill A Rosenfeld, Erica Grant, Karen W Gripp, Carol Anderson, Arthur S Aylsworth, Taha Ben Saad, Victor V Chizhikov, Giedre Dybose, Christina Fagerberg,[...]. Am J Med Genet A 2013
41
11

Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication.
Hong-Dan Wang, Lin Liu, Dong Wu, Tao Li, Cun-Ying Cui, Lian-Zhong Zhang, Cheng-Zeng Wang. J Gene Med 2017
9
11

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
190
11

Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?
Feng Li, Yiping Shen, Udo Köhler, Freddie H Sharkey, Deepa Menon, Laurence Coulleaux, Valérie Malan, Marlène Rio, Dominic J McMullan, H Cox,[...]. Eur J Med Genet 2010
53
11

The MECP2 duplication syndrome.
Melissa B Ramocki, Y Jane Tavyev, Sarika U Peters. Am J Med Genet A 2010
189
11

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
820
11

Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes.
Damien L Bruno, Britt-Marie Anderlid, Anna Lindstrand, Conny van Ravenswaaij-Arts, Devika Ganesamoorthy, Johanna Lundin, Christa Lese Martin, Jessica Douglas, Catherine Nowak, Margaret P Adam,[...]. J Med Genet 2010
107
11

Collagen type VI myopathies.
Kate M D Bushby, James Collins, Debbie Hicks. Adv Exp Med Biol 2014
57
11

The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Devin M Cox, Merlin G Butler. Int J Mol Sci 2015
101
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.