A citation-based method for searching scientific literature

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, B S Emanuel, D A Driscoll. J Am Coll Cardiol 1998
Times Cited: 356







List of co-cited articles
1615 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
32

22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases.
Shabnam Peyvandi, Philip J Lupo, Jennifer Garbarini, Stacy Woyciechowski, Sharon Edman, Beverly S Emanuel, Laura E Mitchell, Elizabeth Goldmuntz. Pediatr Cardiol 2013
54
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
296
17

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
527
16

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
15

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur,[...]. J Med Genet 1997
819
14

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
180
14

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
517
13

Deletion of chromosome 22q11.2 and outcome in patients with pulmonary atresia and ventricular septal defect.
William T Mahle, Joseph Crisalli, Karlene Coleman, Robert M Campbell, Vincent K H Tam, Robert N Vincent, Kirk R Kanter. Ann Thorac Surg 2003
64
18

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
408
12


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
12

Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching.
D B McElhinney, B J Clark, P M Weinberg, M L Kenton, D McDonald-McGinn, D A Driscoll, E H Zackai, E Goldmuntz. J Am Coll Cardiol 2001
150
11

Impact of DEL22q11, trisomy 21, and other genetic syndromes on surgical outcome of conotruncal heart defects.
Guido Michielon, Bruno Marino, Gianluca Oricchio, Maria Cristina Digilio, Fiore Iorio, Sergio Filippelli, Silvia Placidi, Roberto M Di Donato. J Thorac Cardiovasc Surg 2009
40
27


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
133
11

Recurrence of congenital heart defects in families.
Nina Øyen, Gry Poulsen, Heather A Boyd, Jan Wohlfahrt, Peter K A Jensen, Mads Melbye. Circulation 2009
182
11

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
E A Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, G Ogunrinu, H F Sutherland, P J Scambler,[...]. Nature 2001
677
11

Role of TBX1 in human del22q11.2 syndrome.
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
523
11

Genetic syndromes and outcome after surgical correction of tetralogy of Fallot.
Guido Michielon, Bruno Marino, Roberto Formigari, Gaetano Gargiulo, Fernando Picchio, Maria C Digilio, Silvia Anaclerio, Gianluca Oricchio, Stephen P Sanders, Roberto M Di Donato. Ann Thorac Surg 2006
72
13

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Heather J Cordell, Ana Töpf, Chrysovalanto Mamasoula, Alex V Postma, Jamie Bentham, Diana Zelenika, Simon Heath, Gillian Blue, Catherine Cosgrove, Javier Granados Riveron,[...]. Hum Mol Genet 2013
58
17

Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.
Lidia Ziolkowska, Wanda Kawalec, Anna Turska-Kmiec, Malgorzata Krajewska-Walasek, Grazyna Brzezinska-Rajszys, Jadwiga Daszkowska, Bogdan Maruszewski, Piotr Burczynski. Eur J Pediatr 2008
45
20

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
90
10

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
897
9



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
9

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!
D M McDonald-McGinn, M K Tonnesen, A Laufer-Cahana, B Finucane, D A Driscoll, B S Emanuel, E H Zackai. Genet Med 2001
199
9


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
9

Conotruncal heart defects: impact of genetic syndromes on immediate operative mortality.
Silvia Anaclerio, Vincenzo Di Ciommo, Guido Michielon, Maria Cristina Digilio, Roberto Formigari, Ferdinando Maria Picchio, Gaetano Gargiulo, Roberto Di Donato, Maria Antonietta De Ioris, Bruno Marino. Ital Heart J 2004
48
18

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Heather J Cordell, Jamie Bentham, Ana Topf, Diana Zelenika, Simon Heath, Chrysovalanto Mamasoula, Catherine Cosgrove, Gillian Blue, Javier Granados-Riveron, Kerry Setchfield,[...]. Nat Genet 2013
74
12

Anatomic patterns of conotruncal defects associated with deletion 22q11.
B Marino, M C Digilio, A Toscano, S Anaclerio, A Giannotti, C Feltri, M A de Ioris, A Angioni, B Dallapiccola. Genet Med 2001
79
10

Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.
Ralf Rauch, Michael Hofbeck, Christiane Zweier, Andreas Koch, Stefan Zink, Udo Trautmann, Juliane Hoyer, Renate Kaulitz, Helmut Singer, Anita Rauch. J Med Genet 2010
86
9

Deletion 22q11.2 syndrome--implications for the intensive care physician.
Vishal Jatana, Jonathan Gillis, Boyd H Webster, Lesley C Adès. Pediatr Crit Care Med 2007
17
47

Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomalies.
Doff B McElhinney, Deborah A Driscoll, Elissa R Levin, Abbas F Jawad, Beverly S Emanuel, Elizabeth Goldmuntz. Pediatrics 2003
48
16

Microduplication 22q11.2: a new chromosomal syndrome.
Marie-France Portnoï. Eur J Med Genet 2009
145
8

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
D M McDonald-McGinn, R Kirschner, E Goldmuntz, K Sullivan, P Eicher, M Gerdes, E Moss, C Solot, P Wang, I Jacobs,[...]. Genet Couns 1999
311
8

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
S Merscher, B Funke, J A Epstein, J Heyer, A Puech, M M Lu, R J Xavier, M B Demay, R G Russell, S Factor,[...]. Cell 2001
650
8

Impact of 22q11.2 deletion on the postoperative course of children after cardiac surgery.
Rachel McDonald, Andrew Dodgen, Sunali Goyal, Jeffrey M Gossett, Takeshi Shinkawa, Santosh C Uppu, Carlos Blanco, Xiomara Garcia, Adnan T Bhutta, Michiaki Imamura,[...]. Pediatr Cardiol 2013
33
24

Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study.
J Burn, P Brennan, J Little, S Holloway, R Coffey, J Somerville, N R Dennis, L Allan, R Arnold, J E Deanfield,[...]. Lancet 1998
222
8

Long-term outcome in patients undergoing surgical repair of tetralogy of Fallot.
J G Murphy, B J Gersh, D D Mair, V Fuster, M D McGoon, D M Ilstrup, D C McGoon, J W Kirklin, G K Danielson. N Engl J Med 1993
663
8

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
101
8

22q11.2 Deletion syndrome is associated with increased perioperative events and more complicated postoperative course in infants undergoing infant operative correction of truncus arteriosus communis or interrupted aortic arch.
Michael L O'Byrne, Wei Yang, Laura Mercer-Rosa, Aimee S Parnell, Matthew E Oster, Yosef Levenbrown, Ronn E Tanel, Elizabeth Goldmuntz. J Thorac Cardiovasc Surg 2014
38
21

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
260
8

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
888
7

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
9

22q11 deletions in isolated and syndromic patients with tetralogy of Fallot.
F Amati, A Mari, M C Digilio, R Mingarelli, B Marino, A Giannotti, G Novelli, B Dallapiccola. Hum Genet 1995
109
7

Determinants of outcome after surgical treatment of pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries.
Adriano Carotti, Sonia B Albanese, Sergio Filippelli, Lucilla Ravà, Paolo Guccione, Giacomo Pongiglione, Roberto M Di Donato. J Thorac Cardiovasc Surg 2010
86
8

Clinical features of 78 adults with 22q11 Deletion Syndrome.
Anne S Bassett, Eva W C Chow, Janice Husted, Rosanna Weksberg, Oana Caluseriu, Gary D Webb, Michael A Gatzoulis. Am J Med Genet A 2005
285
7


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.