A citation-based method for searching scientific literature

Y Yan, Q Wu, L Zhang, X Wang, S Dan, D Deng, L Sun, L Yao, Y Ma, L Wang. Ultrasound Obstet Gynecol 2014
Times Cited: 33







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



Times Cited
  Times     Co-cited
Similarity


Prenatal diagnosis of congenital heart defect by genome-wide high-resolution SNP array.
Can Liao, Ru Li, Fang Fu, Guie Xie, Yongling Zhang, Min Pan, Jian Li, Dongzhi Li. Prenat Diagn 2014
31
64

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
67
51

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
42
48

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
48

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
42

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
41
39

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
30

Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defects.
Maximilian Schmid, Susanne Stary, Wibke Blaicher, Michaela Gollinger, Peter Husslein, Berthold Streubel. Prenat Diagn 2012
26
34

Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients.
Bernard Thienpont, Luc Mertens, Thomy de Ravel, Benedicte Eyskens, Derize Boshoff, Nicole Maas, Jean-Pierre Fryns, Marc Gewillig, Joris R Vermeesch, Koen Devriendt. Eur Heart J 2007
134
24

The contribution of chromosomal abnormalities to congenital heart defects: a population-based study.
Robert J Hartman, Sonja A Rasmussen, Lorenzo D Botto, Tiffany Riehle-Colarusso, Christa L Martin, Janet D Cragan, Mikyong Shin, Adolfo Correa. Pediatr Cardiol 2011
104
24


Extracardiac lesions and chromosomal abnormalities associated with major fetal heart defects: comparison of intrauterine, postnatal and postmortem diagnoses.
M S Song, A Hu, U Dyamenahalli, D Chitayat, E J T Winsor, G Ryan, J Smallhorn, J Barrett, S-J Yoo, L K Hornberger. Ultrasound Obstet Gynecol 2009
56
24

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
156
21

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
30


Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects.
Jeroen Breckpot, Bernard Thienpont, Hilde Peeters, Thomy de Ravel, Amihood Singer, Maissa Rayyan, Karel Allegaert, Christine Vanhole, Benedicte Eyskens, Joris Robert Vermeesch,[...]. J Pediatr 2010
61
18

Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies.
Lorenzo D Botto, Angela E Lin, Tiffany Riehle-Colarusso, Sadia Malik, Adolfo Correa. Birth Defects Res A Clin Mol Teratol 2007
278
18

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
18

Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis.
Rivka Sukenik-Halevy, Shay Sukenik, Arie Koifman, Yoav Alpert, Reli Hershkovitz, Alex Levi, Tal Biron-Shental. Prenat Diagn 2016
12
50

Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies.
Elizabeth Goldmuntz, Prasuna Paluru, Joseph Glessner, Hakon Hakonarson, Jaclyn A Biegel, Peter S White, Xiaowu Gai, Tamim H Shaikh. Congenit Heart Dis 2011
54
15

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Rachel Soemedi, Ian J Wilson, Jamie Bentham, Rebecca Darlay, Ana Töpf, Diana Zelenika, Catherine Cosgrove, Kerry Setchfield, Chris Thornborough, Javier Granados-Riveron,[...]. Am J Hum Genet 2012
183
15

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
15

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
15

Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis.
Denise van der Linde, Elisabeth E M Konings, Maarten A Slager, Maarten Witsenburg, Willem A Helbing, Johanna J M Takkenberg, Jolien W Roos-Hesselink. J Am Coll Cardiol 2011
15

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
533
15


The importance of copy number variation in congenital heart disease.
Gregory Costain, Candice K Silversides, Anne S Bassett. NPJ Genom Med 2016
29
17

Cryptic chromosomal abnormalities identified in children with congenital heart disease.
Ashleigh A Richards, Lane Jaeckle Santos, Haley A Nichols, Bill P Crider, Frederick F Elder, Natalie S Hauser, Andrew R Zinn, Vidu Garg. Pediatr Res 2008
66
12



High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.
F Erdogan, L A Larsen, L Zhang, Z Tümer, N Tommerup, W Chen, J R Jacobsen, M Schubert, J Jurkatis, A Tzschach,[...]. J Med Genet 2008
91
12

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
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

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
139
12

Genetics of congenital heart disease: the glass half empty.
Akl C Fahed, Bruce D Gelb, J G Seidman, Christine E Seidman. Circ Res 2013
310
12

Isolated ventricular septal defects in the era of advanced fetal echocardiography: risk of chromosomal anomalies and spontaneous closure rate from diagnosis to age of 1 year.
O Gómez, J M Martínez, A Olivella, M Bennasar, F Crispi, N Masoller, J Bartrons, B Puerto, E Gratacós. Ultrasound Obstet Gynecol 2014
33
12

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Steven C Greenway, Alexandre C Pereira, Jennifer C Lin, Steven R DePalma, Samuel J Israel, Sonia M Mesquita, Emel Ergul, Jessie H Conta, Joshua M Korn, Steven A McCarroll,[...]. Nat Genet 2009
297
12

Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
Mary Ella Pierpont, Craig T Basson, D Woodrow Benson, Bruce D Gelb, Therese M Giglia, Elizabeth Goldmuntz, Glenn McGee, Craig A Sable, Deepak Srivastava, Catherine L Webb. Circulation 2007
532
12

Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defects.
J Breckpot, B Thienpont, Y Arens, L C Tranchevent, J R Vermeesch, Y Moreau, M Gewillig, K Devriendt. Cytogenet Genome Res 2011
42
12

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
158
12

Rare copy number variants contribute to congenital left-sided heart disease.
Marc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, Yassamin Feroz-Zada, Robbie Davies, Shi Wei Yang, Anath Christopher Lionel, Guylaine D'Amours, Emmanuelle Lemyre, Rebecca Cullum,[...]. PLoS Genet 2012
89
12

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
16

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
76
12

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
16

Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population.
Yu An, Wenyuan Duan, Guoying Huang, Xiaoli Chen, Li Li, Chenxia Nie, Jia Hou, Yonghao Gui, Yiming Wu, Feng Zhang,[...]. BMC Med Genomics 2016
17
23

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
12

Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease.
Areti Syrmou, Maria Tzetis, Helen Fryssira, Konstantina Kosma, Vasilis Oikonomakis, Krinio Giannikou, Periklis Makrythanasis, Sophia Kitsiou-Tzeli, Emmanuel Kanavakis. Pediatr Res 2013
19
15

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
23

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
9

[Prenatal diagnosis of heart defects and associated chromosomal aberrations].
R Chaoui, H Körner, C Bommer, B Göldner, A Bierlich, R Bollmann. Ultraschall Med 1999
22
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.