A citation-based method for searching scientific literature

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
Times Cited: 56







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



Times Cited
  Times     Co-cited
Similarity


The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
26

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
21

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
21

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
28

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
32

Prenatal ultrasound screening of congenital heart disease in an unselected national population: a 21-year experience.
Jan Marek, Viktor Tomek, Jan Skovránek, Viera Povysilová, Milan Samánek. Heart 2011
123
16

Prenatal detection of congenital heart disease.
Mark K Friedberg, Norman H Silverman, Anita J Moon-Grady, Elizabeth Tong, Jennifer Nourse, Beatrice Sorenson, Jaimie Lee, Lisa K Hornberger. J Pediatr 2009
175
14

Prenatal diagnosis of congenital heart disease in the Naples area during the years 1994-1999 -- the experience of a joint fetal-pediatric cardiology unit.
Dario Paladini, MariaGiovanna Russo, Adele Teodoro, Giuseppe Pacileo, Giovanni Capozzi, Pasquale Martinelli, Carmine Nappi, Raffaele Calabrò. Prenat Diagn 2002
48
16


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
14

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
14

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
33
24

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
14

[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
31

Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study.
C Ferencz, C A Neill, J A Boughman, J D Rubin, J I Brenner, L W Perry. J Pediatr 1989
198
12

Prenatal detection of heart defects in a non-selected population of 30,149 fetuses--detection rates and outcome.
E Tegnander, W Williams, O J Johansen, H-G K Blaas, S H Eik-Nes. Ultrasound Obstet Gynecol 2006
168
12

Prospective diagnosis of 1,006 consecutive cases of congenital heart disease in the fetus.
L D Allan, G K Sharland, A Milburn, S M Lockhart, A M Groves, R H Anderson, A C Cook, N L Fagg. J Am Coll Cardiol 1994
317
12

Trends in prenatal diagnosis, pregnancy termination, and perinatal mortality of newborns with congenital heart disease in France, 1983-2000: a population-based evaluation.
Babak Khoshnood, Catherine De Vigan, Véronique Vodovar, Janine Goujard, Anne Lhomme, Damien Bonnet, François Goffinet. Pediatrics 2005
204
10

Improved surgical outcome after fetal diagnosis of hypoplastic left heart syndrome.
W Tworetzky, D B McElhinney, V M Reddy, M M Brook, F L Hanley, N H Silverman. Circulation 2001
399
10

Extracardiac abnormalities in infants with congenital heart disease.
R D Greenwood, A Rosenthal, L Parisi, D C Fyler, A S Nadas. Pediatrics 1975
145
10

Detection of transposition of the great arteries in fetuses reduces neonatal morbidity and mortality.
D Bonnet, A Coltri, G Butera, L Fermont, J Le Bidois, J Kachaner, D Sidi. Circulation 1999
447
10

Investigating 22q11.2 deletion and other chromosomal aberrations in fetuses with heart defects detected by prenatal echocardiography.
Fernanda Teixeira da Silva Bellucco, Sintia Iole Nogueira Belangero, Leila Montenegro Silveira Farah, Maria Virgínia Lima Machado, Adriano Pastor Cruz, Lílian Maria Lopes, Marco Antonio Borges Lopes, Marcelo Zugaib, Mirlene Cecília Cernach, Maria Isabel Melaragno. Pediatr Cardiol 2010
15
40

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
10

Diagnosis and treatment of fetal cardiac disease: a scientific statement from the American Heart Association.
Mary T Donofrio, Anita J Moon-Grady, Lisa K Hornberger, Joshua A Copel, Mark S Sklansky, Alfred Abuhamad, Bettina F Cuneo, James C Huhta, Richard A Jonas, Anita Krishnan,[...]. Circulation 2014
444
10

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
14

The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy.
Jeffrey P Jacobs, Robert H Anderson, Paul M Weinberg, Henry L Walters, Christo I Tchervenkov, Danny Del Duca, Rodney C G Franklin, Vera D Aiello, Marie J Béland, Steven D Colan,[...]. Cardiol Young 2007
144
8

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
Lorenzo D Botto, Kristin May, Paul M Fernhoff, Adolfo Correa, Karlene Coleman, Sonja A Rasmussen, Robert K Merritt, Leslie A O'Leary, Lee-Yang Wong, E Marsha Elixson,[...]. Pediatrics 2003
414
8

Population-based study of congenital heart defects in Down syndrome.
S B Freeman, L F Taft, K J Dooley, K Allran, S L Sherman, T J Hassold, M J Khoury, D M Saker. Am J Med Genet 1998
216
8



Tetralogy of Fallot in the fetus in the current era.
L C Y Poon, I C Huggon, V Zidere, L D Allan. Ultrasound Obstet Gynecol 2007
27
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
8

Congenital heart disease in 56,109 births. Incidence and natural history.
S C Mitchell, S B Korones, H W Berendes. Circulation 1971
794
8

Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
Kathy J Jenkins, Adolfo Correa, Jeffrey A Feinstein, Lorenzo Botto, Amy E Britt, Stephen R Daniels, Marsha Elixson, Carole A Warnes, Catherine L Webb. Circulation 2007
466
8

Recurrence of congenital heart defects in families.
Nina Øyen, Gry Poulsen, Heather A Boyd, Jan Wohlfahrt, Peter K A Jensen, Mads Melbye. Circulation 2009
191
8

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
8

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
8

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
8

Prevalence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan, Richard R Liberthson. Am Heart J 2004
493
8

Congenital heart disease: current knowledge about causes and inheritance.
Gillian M Blue, Edwin P Kirk, Gary F Sholler, Richard P Harvey, David S Winlaw. Med J Aust 2012
130
8

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
8

Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia.
Marcus P Kennedy, Heymut Omran, Margaret W Leigh, Sharon Dell, Lucy Morgan, Paul L Molina, Blair V Robinson, Susan L Minnix, Heike Olbrich, Thomas Severin,[...]. Circulation 2007
248
7

Prenatal diagnosis of congenital heart disease and fetal karyotyping.
D Paladini, R Calabrò, S Palmieri, T D'Andrea. Obstet Gynecol 1993
45
8

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
7

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
7

Frequency of 22q11 deletions in patients with conotruncal defects.
E Goldmuntz, B J Clark, L E Mitchell, A F Jawad, B F Cuneo, L Reed, D McDonald-McGinn, P Chien, J Feuer, E H Zackai,[...]. J Am Coll Cardiol 1998
359
7

Foetal echocardiographic assessment of tetralogy of Fallot and post-natal outcome.
Florentia Kaguelidou, Laurent Fermont, Younes Boudjemline, Jérôme Le Bidois, Alain Batisse, Damien Bonnet. Eur Heart J 2008
24
16




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.