A citation-based method for searching scientific literature

Abigail S Carey, Li Liang, Jonathan Edwards, Tracy Brandt, Hui Mei, Andrew J Sharp, Daphne T Hsu, Jane W Newburger, Richard G Ohye, Wendy K Chung, Mark W Russell, Jill A Rosenfeld, Lisa G Shaffer, Michael K Parides, Lisa Edelmann, Bruce D Gelb. Circ Cardiovasc Genet 2013
Times Cited: 53







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



Times Cited
  Times     Co-cited
Similarity


De novo mutations in histone-modifying genes in congenital heart disease.
Samir Zaidi, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D Overton, Angela Romano-Adesman, Robert D Bjornson, Roger E Breitbart, Kerry K Brown,[...]. Nature 2013
523
49

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
88
33

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
30

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
182
30

The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.
Dorothy Warburton, Michael Ronemus, Jennie Kline, Vaidehi Jobanputra, Ismee Williams, Kwame Anyane-Yeboa, Wendy Chung, Lan Yu, Nancy Wong, Danielle Awad,[...]. Hum Genet 2014
78
26

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

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.
Jason Homsy, Samir Zaidi, Yufeng Shen, James S Ware, Kaitlin E Samocha, Konrad J Karczewski, Steven R DePalma, David McKean, Hiroko Wakimoto, Josh Gorham,[...]. Science 2015
342
24

Genetics of congenital heart disease: the glass half empty.
Akl C Fahed, Bruce D Gelb, J G Seidman, Christine E Seidman. Circ Res 2013
304
22

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
22

Early developmental outcome in children with hypoplastic left heart syndrome and related anomalies: the single ventricle reconstruction trial.
Jane W Newburger, Lynn A Sleeper, David C Bellinger, Caren S Goldberg, Sarah Tabbutt, Minmin Lu, Kathleen A Mussatto, Ismee A Williams, Kathryn E Gustafson, Seema Mital,[...]. Circulation 2012
190
22

Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.
Candice K Silversides, Anath C Lionel, Gregory Costain, Daniele Merico, Ohsuke Migita, Ben Liu, Tracy Yuen, Jessica Rickaby, Bhooma Thiruvahindrapuram, Christian R Marshall,[...]. PLoS Genet 2012
106
20

Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Joseph T Glessner, Alexander G Bick, Kaoru Ito, Jason Homsy, Laura Rodriguez-Murillo, Menachem Fromer, Erica Mazaika, Badri Vardarajan, Michael Italia, Jeremy Leipzig,[...]. Circ Res 2014
129
20

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
18

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
530
18

Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.
Daniel Seung Kim, Jerry H Kim, Amber A Burt, David R Crosslin, Nancy Burnham, Cecilia E Kim, Donna M McDonald-McGinn, Elaine H Zackai, Susan C Nicolson, Thomas L Spray,[...]. J Thorac Cardiovasc Surg 2016
29
34

Hypoplastic left heart syndrome is heritable.
Robert B Hinton, Lisa J Martin, Meredith E Tabangin, Mjaye L Mazwi, Linda H Cripe, D Woodrow Benson. J Am Coll Cardiol 2007
124
16

Congenital heart disease caused by mutations in the transcription factor NKX2-5.
J J Schott, D W Benson, C T Basson, W Pease, G M Silberbach, J P Moak, B J Maron, C E Seidman, J G Seidman. Science 1998
891
16

Mutations in NOTCH1 cause aortic valve disease.
Vidu Garg, Alecia N Muth, Joshua F Ransom, Marie K Schluterman, Robert Barnes, Isabelle N King, Paul D Grossfeld, Deepak Srivastava. Nature 2005
903
16

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
16

Brain volume and metabolism in fetuses with congenital heart disease: evaluation with quantitative magnetic resonance imaging and spectroscopy.
Catherine Limperopoulos, Wayne Tworetzky, Doff B McElhinney, Jane W Newburger, David W Brown, Richard L Robertson, Nicolas Guizard, Ellen McGrath, Judith Geva, David Annese,[...]. Circulation 2010
342
16

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Vidu Garg, Irfan S Kathiriya, Robert Barnes, Marie K Schluterman, Isabelle N King, Cheryl A Butler, Caryn R Rothrock, Reenu S Eapen, Kayoko Hirayama-Yamada, Kunitaka Joo,[...]. Nature 2003
798
15

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
102
15

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

Genetics and genetic testing in congenital heart disease.
Jason R Cowan, Stephanie M Ware. Clin Perinatol 2015
48
16

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Alejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, Jeroen Breckpot, Saeed H Al Turki, Bernard Thienpont, Jeremy McRae, Tomas W Fitzgerald, Tarjinder Singh, Ganesh Jawahar Swaminathan,[...]. Nat Genet 2016
160
15

Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning.
Khalid A Fakhro, Murim Choi, Stephanie M Ware, John W Belmont, Jeffrey A Towbin, Richard P Lifton, Mustafa K Khokha, Martina Brueckner. Proc Natl Acad Sci U S A 2011
158
13

Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.
Kim L McBride, Ricardo Pignatelli, Mark Lewin, Trang Ho, Susan Fernbach, Andres Menesses, Wilbur Lam, Suzanne M Leal, Norman Kaplan, Paul Schliekelman,[...]. Am J Med Genet A 2005
123
13

Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy.
Edwin P Kirk, Margaret Sunde, Mauro W Costa, Scott A Rankin, Orit Wolstein, M Leticia Castro, Tanya L Butler, Changbaig Hyun, Guanglan Guo, Robyn Otway,[...]. Am J Hum Genet 2007
221
13

Rare variants in NR2F2 cause congenital heart defects in humans.
Saeed Al Turki, Ashok K Manickaraj, Catherine L Mercer, Sebastian S Gerety, Marc-Phillip Hitz, Sarah Lindsay, Lisa C A D'Alessandro, G Jawahar Swaminathan, Jamie Bentham, Anne-Karin Arndt,[...]. Am J Hum Genet 2014
93
13

Recurrence of congenital heart defects in families.
Nina Øyen, Gry Poulsen, Heather A Boyd, Jan Wohlfahrt, Peter K A Jensen, Mads Melbye. Circulation 2009
185
13

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
16

Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve.
Robert B Hinton, Lisa J Martin, Smitha Rame-Gowda, Meredith E Tabangin, Linda H Cripe, D Woodrow Benson. J Am Coll Cardiol 2009
83
13

Abnormal brain development in newborns with congenital heart disease.
Steven P Miller, Patrick S McQuillen, Shannon Hamrick, Duan Xu, David V Glidden, Natalie Charlton, Tom Karl, Anthony Azakie, Donna M Ferriero, A James Barkovich,[...]. N Engl J Med 2007
464
13

Brain maturation is delayed in infants with complex congenital heart defects.
Daniel J Licht, David M Shera, Robert R Clancy, Gil Wernovsky, Lisa M Montenegro, Susan C Nicolson, Robert A Zimmerman, Thomas L Spray, J William Gaynor, Arastoo Vossough. J Thorac Cardiovasc Surg 2009
347
13

Patient characteristics are important determinants of neurodevelopmental outcome at one year of age after neonatal and infant cardiac surgery.
J William Gaynor, Gil Wernovsky, Gail P Jarvik, Judy Bernbaum, Marsha Gerdes, Elaine Zackai, Alex S Nord, Robert R Clancy, Susan C Nicolson, Thomas L Spray. J Thorac Cardiovasc Surg 2007
164
13

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
Rachel Soemedi, Ana Topf, Ian J Wilson, Rebecca Darlay, Thahira Rahman, Elise Glen, Darroch Hall, Ni Huang, Jamie Bentham, Shoumo Bhattacharya,[...]. Hum Mol Genet 2012
72
13

Genetic testing practices in infants with congenital heart disease.
Jessica A Connor, Robert B Hinton, Erin M Miller, Kristen L Sund, Jennifer G Ruschman, Stephanie M Ware. Congenit Heart Dis 2014
30
23

Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
Juan Geng, Jonathan Picker, Zhaojing Zheng, Xiaoqing Zhang, Jian Wang, Fuki Hisama, David W Brown, Mary P Mullen, David Harris, Joan Stoler,[...]. BMC Genomics 2014
47
14

Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection Fraction.
Jeanne L Theis, Michael T Zimmermann, Jared M Evans, Bruce W Eckloff, Eric D Wieben, Muhammad Y Qureshi, Patrick W O'Leary, Timothy M Olson. Circ Cardiovasc Genet 2015
39
17

Reduced fetal cerebral oxygen consumption is associated with smaller brain size in fetuses with congenital heart disease.
Liqun Sun, Christopher K Macgowan, John G Sled, Shi-Joon Yoo, Cedric Manlhiot, Prashob Porayette, Lars Grosse-Wortmann, Edgar Jaeggi, Brian W McCrindle, John Kingdom,[...]. Circulation 2015
230
13

Neurodevelopmental outcomes in children with congenital heart disease: evaluation and management: a scientific statement from the American Heart Association.
Bradley S Marino, Paul H Lipkin, Jane W Newburger, Georgina Peacock, Marsha Gerdes, J William Gaynor, Kathleen A Mussatto, Karen Uzark, Caren S Goldberg, Walter H Johnson,[...]. Circulation 2012
658
13

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah Morton, Steven R DePalma, Xue Zeng, Hongjian Qi, Weni Chang, Michael C Sierant,[...]. Nat Genet 2017
271
13

Haploinsufficiency of TAB2 causes congenital heart defects in humans.
Bernard Thienpont, Litu Zhang, Alex V Postma, Jeroen Breckpot, Léon-Charles Tranchevent, Peter Van Loo, Kjeld Møllgård, Niels Tommerup, Iben Bache, Zeynep Tümer,[...]. Am J Hum Genet 2010
60
11

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
60
11

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
271
11

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
458
11

Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects.
James R Priest, Santhosh Girirajan, Tiffany H Vu, Aaron Olson, Evan E Eichler, Michael A Portman. Am J Med Genet A 2012
30
20

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Heather C Mefford, Andrew J Sharp, Carl Baker, Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K Maloney, John A Crolla, Diana Baralle,[...]. N Engl J Med 2008
515
11

Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease.
Jesse Christiansen, John D Dyck, Basil G Elyas, Margaret Lilley, J Stephen Bamforth, Mark Hicks, Kathleen A Sprysak, Robert Tomaszewski, Shelagh M Haase, Leanne M Vicen-Wyhony,[...]. Circ Res 2004
104
11

Adolescents with d-transposition of the great arteries corrected with the arterial switch procedure: neuropsychological assessment and structural brain imaging.
David C Bellinger, David Wypij, Michael J Rivkin, David R DeMaso, Richard L Robertson, Carolyn Dunbar-Masterson, Leonard A Rappaport, Gil Wernovsky, Richard A Jonas, Jane W Newburger. Circulation 2011
255
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.