A citation-based method for searching scientific literature

Javier Suela, Isabel López-Expósito, María Eugenia Querejeta, Rosa Martorell, Esther Cuatrecasas, Lluis Armengol, Eugenia Antolín, Elena Domínguez Garrido, María José Trujillo-Tiebas, Jordi Rosell, Javier García Planells, Juan Cruz Cigudosa. Med Clin (Barc) 2017
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


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
75

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
630
50

Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature.
Paola Evangelidou, Angelos Alexandrou, Maria Moutafi, Marios Ioannides, Pavlos Antoniou, George Koumbaris, Ioannis Kallikas, Voula Velissariou, Carolina Sismani, Philippos C Patsalis. Biomed Res Int 2013
25
50





Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.
Idit Maya, Bella Davidov, Liron Gershovitz, Yael Zalzstein, Ellen Taub, Justine Coppinger, Lisa G Shaffer, Mordechai Shohat. Prenat Diagn 2010
63
25

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
79
25

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
153
25

Prenatal diagnosis of de novo partial trisomy 18p and partial monosomy 18q recurrent in a family with fatal aortic coarctation.
Hua Hu, Jia Hao, Hong Yao, Qing Chang, Rui Li, Xiaohang Zhang, Zhiqing Liang. Gene 2013
5
25

Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family.
Chih-Ping Chen, Shuenn-Dyh Chang, Tzu-Hao Wang, Liang-Kai Wang, Jeng-Daw Tsai, Yu-Peng Liu, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen,[...]. Taiwan J Obstet Gynecol 2013
14
25


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
23
25

Prenatally diagnosed 17q12 microdeletion syndrome with a novel association with congenital diaphragmatic hernia.
Nancy W Hendrix, Michele Clemens, Timothy P Canavan, Urvashi Surti, Aleksandar Rajkovic. Fetal Diagn Ther 2012
23
25

Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization.
Colyn Cargile Cain, Daniel O Saul, Erin Oehler, Karin Blakemore, Gail Stetten. Fetal Diagn Ther 2008
13
25

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.
Trilochan Sahoo, Sau Wai Cheung, Patricia Ward, Sandra Darilek, Ankita Patel, Daniela del Gaudio, Sung Hae L Kang, Seema R Lalani, Jiangzhen Li, Sallie McAdoo,[...]. Genet Med 2006
121
25

Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review.
Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Wen-Lin Chen, Wayseen Wang. Gene 2013
13
25

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Chih-Ping Chen, Ming Chen, Schu-Rern Chern, Peih-Shan Wu, Shun-Ping Chang, Dong-Jay Lee, Yu-Ting Chen, Li-Feng Chen, Jun-Wei Su, Alan Hwa-Ruey Hsieh,[...]. Taiwan J Obstet Gynecol 2012
8
25

Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH.
Weimin Bi, Amy M Breman, Susan F Venable, Patricia A Eng, Trilochan Sahoo, Xin-Yan Lu, Ankita Patel, Arthur L Beaudet, Sau Wai Cheung, Lisa D White. Prenat Diagn 2008
50
25


Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes.
Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Wen Pan, Wayseen Wang. Gene 2013
13
25

Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13.
A Uwineza, G Pierquin, S Gaillez, M Jamar, A C Hellin, J H Caberg, V Bours. Genet Couns 2013
5
25

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.
Chih-Ping Chen, Ming Chen, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Chin-Yuan Hsu, Pei-Chen Wu, Dai-Dyi Town, Dong-Jay Lee, Gwo-Chin Ma,[...]. Taiwan J Obstet Gynecol 2010
19
25

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
Ignatia B Van den Veyver, Ankita Patel, Chad A Shaw, Amber N Pursley, Sung-Hae L Kang, Marcia J Simovich, Patricia A Ward, Sandra Darilek, Anthony Johnson, Sarah E Neill,[...]. Prenat Diagn 2009
138
25

Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis.
Markus Stumm, Eva Klopocki, Adam Gasiorek-Wiens, Ute Knoll, Deni Wirjadi, Nanette Sarioglu, Rolf-Dieter Wegner, Holger Tönnies. Prenat Diagn 2007
12
25

Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chih-Ping Chen, Schu-Rern Chern, Tzu-Hao Wang, Ding-Wei Hsueh, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang, Tsang-Ming Ko. Prenat Diagn 2005
16
25

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
22
25

A de novo duplication of chromosome 9q34.13-qter in a fetus with Tetralogy of Fallot Syndrome.
Jing Liu, Hao Hu, Na Ma, Zhengjun Jia, Yuchun Zhou, Jiancheng Hu, Hua Wang. Mol Cytogenet 2016
6
25

De novo interstitial direct duplication 1(q23.1q31.1) in a fetus with Pierre Robin sequence and camptodactyly.
A Aboura, A Coulomb-L'Herminé, F Audibert, F Capron, R Frydman, G Tachdjian. Am J Med Genet 2002
24
25


Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.
Chih-Ping Chen, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Taiwan J Obstet Gynecol 2013
10
25

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
25

Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review.
Chih-Ping Chen, Tung-Yao Chang, Wan-Yuo Guo, Pei-Chen Wu, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Li-Feng Chen,[...]. Gene 2013
14
25

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
25

The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration.
Alessandro Liberati, Douglas G Altman, Jennifer Tetzlaff, Cynthia Mulrow, Peter C Gøtzsche, John P A Ioannidis, Mike Clarke, P J Devereaux, Jos Kleijnen, David Moher. J Clin Epidemiol 2009
25

Structural variation in the human genome.
Lars Feuk, Andrew R Carson, Stephen W Scherer. Nat Rev Genet 2006
25

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
Chih-Ping Chen, Ming Chen, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Pei-Chen Wu, Wen-Lin Chen, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang. Taiwan J Obstet Gynecol 2011
8
25

De novo 1q32q44 duplication and distal 1q trisomy syndrome.
Małgorzata J M Nowaczyk, Jane Bayani, Viola Freeman, John Watts, Jeremy Squire, Jie Xu. Am J Med Genet A 2003
28
25

Array-CGH characterization and genotype-phenotype analysis in a patient with a ring chromosome 6.
Laura Ciocca, Cecilia Surace, Maria Cristina Digilio, Maria Cristina Roberti, Pietro Sirleto, Antonietta Lombardo, Serena Russo, Valerio Brizi, Simona Grotta, Claudio Cini,[...]. BMC Med Genomics 2013
8
25

[Cytogenetic analysis of a complex chromosomal imbalance 14q+ in a fetus featuring multiple congenital defects].
Li Li, Xiao-yan Zhou, Xiu-qing Ji, Yin-qiu Yang, Li Cao, Jing Zhou, An Liu, Jian Cheng, Ye Liu, Ping Hu,[...]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2012
1
100

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
25

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
57
25


High resolution comparative genomic hybridisation in clinical cytogenetics.
M Kirchhoff, H Rose, C Lundsteen. J Med Genet 2001
93
25


A fetus with de novo 2q33.2q35 deletion including MAP2 with brain anomalies, esophageal atresia, and laryngeal stenosis.
Ellen van Binsbergen, Richard J Ellis, Nadia Abdelmalik, Joanna Jarvis, Kashmir Randhawa, Josephine Wyatt-Ashmead, Natalie Canham, J Guy Thorpe-Beeston, Grazia M S Mancini, Mieke M Van Haelst. Am J Med Genet A 2014
7
25

Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
Yu-Ling Kuo, Chih-Ping Chen, Liang-Kai Wang, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Shu-Yuan Chang. Taiwan J Obstet Gynecol 2014
6
25

Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH).
Chia-Cheng Hung, Chia-Hui Lin, Shin-Yu Lin, Jin-Chung Shin, Chien-Nan Lee, Yi-Ning Su. Gene 2012
9
25

Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization.
M Chen, Y-S Yang, J-C Shih, W-H Lin, D-J Lee, Y-S Lin, C-H Chou, A D Cameron, N A Ginsberg, C-A Chen,[...]. Ultrasound Obstet Gynecol 2014
17
25


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.