A citation-based method for searching scientific literature

E Goldmuntz, E Geiger, D W Benson. Circulation 2001
Times Cited: 228







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



Times Cited
  Times     Co-cited
Similarity


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
48

NKX2.5 mutations in patients with congenital heart disease.
Doff B McElhinney, Elizabeth Geiger, Joshua Blinder, D Woodrow Benson, Elizabeth Goldmuntz. J Am Coll Cardiol 2003
239
45

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways.
D W Benson, G M Silberbach, A Kavanaugh-McHugh, C Cottrill, Y Zhang, S Riggs, O Smalls, M C Johnson, M S Watson, J G Seidman,[...]. J Clin Invest 1999
418
39

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
797
27

Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5.
I Lyons, L M Parsons, L Hartley, R Li, J E Andrews, L Robb, R P Harvey. Genes Dev 1995
858
24

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
24

Familial Tetralogy of Fallot caused by mutation in the jagged1 gene.
Z A Eldadah, A Hamosh, N J Biery, R A Montgomery, M Duke, R Elkins, H C Dietz. Hum Mol Genet 2001
171
22

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
21

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect.
Kayoko Hirayama-Yamada, Mitsuhiro Kamisago, Kaoru Akimoto, Hiroyuki Aotsuka, Yoshihide Nakamura, Hideshi Tomita, Michiko Furutani, Shin-ichiro Imamura, Atsuyoshi Takao, Makoto Nakazawa,[...]. Am J Med Genet A 2005
150
20

Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.
David A Elliott, Edwin P Kirk, Thomas Yeoh, Suchitra Chandar, Fiona McKenzie, Peter Taylor, Paul Grossfeld, Diane Fatkin, Owen Jones, Peter Hayes,[...]. J Am Coll Cardiol 2003
167
20

Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease.
H Kasahara, B Lee, J J Schott, D W Benson, J G Seidman, C E Seidman, S Izumo. J Clin Invest 2000
125
20

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
23



GATA4 sequence variants in patients with congenital heart disease.
A Tomita-Mitchell, C L Maslen, C D Morris, V Garg, E Goldmuntz. J Med Genet 2007
139
19

NKX2.5 mutations in patients with non-syndromic congenital heart disease.
Luciana Gioli-Pereira, Alexandre Costa Pereira, Sônia M Mesquita, José Xavier-Neto, Antônio Augusto Lopes, José Eduardo Krieger. Int J Cardiol 2010
44
40

An Nkx2-5/Bmp2/Smad1 negative feedback loop controls heart progenitor specification and proliferation.
Owen W J Prall, Mary K Menon, Mark J Solloway, Yusuke Watanabe, Stéphane Zaffran, Fanny Bajolle, Christine Biben, Jim J McBride, Bronwyn R Robertson, Hervé Chaulet,[...]. Cell 2007
359
18

Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block.
Mohammad Pashmforoush, Jonathan T Lu, Hanying Chen, Tara St Amand, Richard Kondo, Sylvain Pradervand, Sylvia M Evans, Bob Clark, James R Feramisco, Wayne Giles,[...]. Cell 2004
298
16

Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors.
A Sarkozy, E Conti, C Neri, R D'Agostino, M C Digilio, G Esposito, A Toscano, B Marino, A Pizzuti, B Dallapiccola. J Med Genet 2005
112
15

A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot.
Georges Nemer, Fatimah Fadlalah, Julnar Usta, Mona Nemer, Ghassan Dbaibo, Mounir Obeid, Fadi Bitar. Hum Mutat 2006
119
15

New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle.
Alessandro De Luca, A Sarkozy, R Ferese, F Consoli, F Lepri, M L Dentici, P Vergara, A De Zorzi, P Versacci, M C Digilio,[...]. Clin Genet 2011
50
30

The effect of p.Arg25Cys alteration in NKX2-5 on conotruncal heart anomalies: mutation or polymorphism?
M I Akçaboy, F B Cengiz, B Inceoğlu, T Uçar, S Atalay, E Tutar, M Tekin. Pediatr Cardiol 2008
25
56

A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?
Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, Thierry Sluysmans, Koen Devriendt, Han G Brunner, Miikka Vikkula. Eur J Hum Genet 2006
52
26

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
14

Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 gene.
Ilse Gutierrez-Roelens, Thierry Sluysmans, Marc Gewillig, Koen Devriendt, Miikka Vikkula. Hum Mutat 2002
51
27

Investigation of somatic NKX2-5 mutations in congenital heart disease.
J M Draus, M A Hauck, M Goetsch, E H Austin, A Tomita-Mitchell, M E Mitchell. J Med Genet 2009
49
28

Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot.
Antonio Pizzuti, Anna Sarkozy, Anthea L Newton, Emanuela Conti, Elisabetta Flex, Maria Cristina Digilio, Francesca Amati, Debora Gianni, Caterina Tandoi, Bruno Marino,[...]. Hum Mutat 2003
83
16


Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation.
Y Hiroi, S Kudoh, K Monzen, Y Ikeda, Y Yazaki, R Nagai, I Komuro. Nat Genet 2001
413
13

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
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
220
13


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
12

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
11

Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5.
C Biben, R Weber, S Kesteven, E Stanley, L McDonald, D A Elliott, L Barnett, F Köentgen, L Robb, M Feneley,[...]. Circ Res 2000
249
11


Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis.
Monica Dentice, Viviana Cordeddu, Annamaria Rosica, Alfonso Massimiliano Ferrara, Libero Santarpia, Domenico Salvatore, Luca Chiovato, Anna Perri, Lidia Moschini, Cristina Fazzini,[...]. J Clin Endocrinol Metab 2006
100
11

Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations.
Stella Marie Reamon-Buettner, Hartmut Hecker, Katharina Spanel-Borowski, Steffen Craatz, Eberhard Kuenzel, Juergen Borlak. Am J Pathol 2004
69
15

Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants.
Helen R Griffin, Ana Töpf, Elise Glen, Christiane Zweier, A Graham Stuart, Jonathan Parsons, Ian Peart, John Deanfield, John O'Sullivan, Anita Rauch,[...]. Heart 2010
45
24

GATA4 mutations in 486 Chinese patients with congenital heart disease.
Weimin Zhang, Xiaofeng Li, Adong Shen, Weiwei Jiao, Xiaolei Guan, Zhongzhi Li. Eur J Med Genet 2008
73
13

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.
C T Basson, D R Bachinsky, R C Lin, T Levi, J A Elkins, J Soults, D Grayzel, E Kroumpouzou, T A Traill, J Leblanc-Straceski,[...]. Nat Genet 1997
769
10

Perinatal loss of Nkx2-5 results in rapid conduction and contraction defects.
Laura E Briggs, Morihiko Takeda, Adolfo E Cuadra, Hiroko Wakimoto, Melissa H Marks, Alexandra J Walker, Tsugio Seki, Suk P Oh, Jonathan T Lu, Colin Sumners,[...]. Circ Res 2008
70
14

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
10

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

The cardiac transcription factors Nkx2-5 and GATA-4 are mutual cofactors.
D Durocher, F Charron, R Warren, R J Schwartz, M Nemer. EMBO J 1997
496
10


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
10

Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects.
Maximilian G Posch, Andreas Perrot, Katharina Schmitt, Sebastian Mittelhaus, Eva-Maria Esenwein, Brigitte Stiller, Christian Geier, Rainer Dietz, Reinhard Gessner, Cemil Ozcelik,[...]. Am J Med Genet A 2008
70
12

Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease.
Yuichi Ikeda, Yukio Hiroi, Toru Hosoda, Toshinori Utsunomiya, Shuzo Matsuo, Tsuyoshi Ito, Jun-ichi Inoue, Tetsuya Sumiyoshi, Hiroyuki Takano, Ryozo Nagai,[...]. Circ J 2002
68
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.