A citation-based method for searching scientific literature

Hong Gu, Frank C Smith, Steven M Taffet, Mario Delmar. Circ Res 2003
Times Cited: 91







List of co-cited articles
1216 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Cardiac malformation in neonatal mice lacking connexin43.
A G Reaume, P A de Sousa, S Kulkarni, B L Langille, D Zhu, T C Davies, S C Juneja, G M Kidder, J Rossant. Science 1995
30

Abnormal cardiac conduction and morphogenesis in connexin40 and connexin43 double-deficient mice.
S Kirchhoff, J S Kim, A Hagendorff, E Thönnissen, O Krüger, W H Lamers, K Willecke. Circ Res 2000
103
27

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
27

Loss of connexin45 causes a cushion defect in early cardiogenesis.
M Kumai, K Nishii, K Nakamura, N Takeda, M Suzuki, Y Shibata. Development 2000
173
23

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
23


Reduced cardiac conduction velocity and predisposition to arrhythmias in connexin40-deficient mice.
S Kirchhoff, E Nelles, A Hagendorff, O Krüger, O Traub, K Willecke. Curr Biol 1998
299
20

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
26

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
18

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation.
Michael H Gollob, Douglas L Jones, Andrew D Krahn, Lynne Danis, Xiang-Qun Gong, Qing Shao, Xiaoqin Liu, John P Veinot, Anthony S L Tang, Alexandre F R Stewart,[...]. N Engl J Med 2006
353
17

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

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi,[...]. Nat Genet 2008
390
15

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
14

Conduction slowing and sudden arrhythmic death in mice with cardiac-restricted inactivation of connexin43.
D E Gutstein, G E Morley, H Tamaddon, D Vaidya, M D Schneider, J Chen, K R Chien, H Stuhlmann, G I Fishman. Circ Res 2001
520
13

Gap junctions and the connexin protein family.
Goran Söhl, Klaus Willecke. Cardiovasc Res 2004
660
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
182
13

Cardiac conduction abnormalities in mice lacking the gap junction protein connexin40.
S Verheule, C A van Batenburg, F E Coenjaerts, S Kirchhoff, K Willecke, H J Jongsma. J Cardiovasc Electrophysiol 1999
127
12

Defective vascular development in connexin 45-deficient mice.
O Krüger, A Plum, J S Kim, E Winterhager, S Maxeiner, G Hallas, S Kirchhoff, O Traub, W H Lamers, K Willecke. Development 2000
263
12

Chamber-related differences in connexin expression in the human heart.
C Vozzi, E Dupont, S R Coppen, H I Yeh, N J Severs. J Mol Cell Cardiol 1999
170
12

Heart defects in connexin43-deficient mice.
J Ya, E B Erdtsieck-Ernste, P A de Boer, M J van Kempen, H Jongsma, D Gros, A F Moorman, W H Lamers. Circ Res 1998
108
12

Gap junction-mediated cell-cell communication modulates mouse neural crest migration.
G Y Huang, E S Cooper, K Waldo, M L Kirby, N B Gilula, C W Lo. J Cell Biol 1998
194
12

Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.
William A Paznekas, Simeon A Boyadjiev, Robert E Shapiro, Otto Daniels, Bernd Wollnik, Catherine E Keegan, Jeffrey W Innis, Mary Beth Dinulos, Cathy Christian, Mark C Hannibal,[...]. Am J Hum Genet 2003
440
12

Mutations of the Connexin43 gap-junction gene in patients with heart malformations and defects of laterality.
S H Britz-Cunningham, M M Shah, C W Zuppan, W H Fletcher. N Engl J Med 1995
305
12

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
12

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
12

Heart and neural tube defects in transgenic mice overexpressing the Cx43 gap junction gene.
J L Ewart, M F Cohen, R A Meyer, G Y Huang, A Wessels, R G Gourdie, A J Chin, S M Park, B O Lazatin, S Villabon,[...]. Development 1997
155
10

An essential role for connexin43 gap junctions in mouse coronary artery development.
W E I Li, K Waldo, K L Linask, T Chen, A Wessels, M S Parmacek, M L Kirby, C W Lo. Development 2002
99
10

Mice lacking connexin45 conditionally in cardiac myocytes display embryonic lethality similar to that of germline knockout mice without endocardial cushion defect.
Kiyomasa Nishii, Madoka Kumai, Katsuko Egashira, Takeshi Miwa, Kanako Hashizume, Yumi Miyano, Yosaburo Shibata. Cell Commun Adhes 2003
43
23

Heart and head defects in mice lacking pairs of connexins.
Alexander M Simon, Andrea R McWhorter, Julie A Dones, Charity L Jackson, HwuDauRw Chen. Dev Biol 2004
31
32

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
10

A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot.
Valentina Guida, Rosangela Ferese, Marcella Rocchetti, Monica Bonetti, Anna Sarkozy, Serena Cecchetti, Vania Gelmetti, Francesca Lepri, Massimiliano Copetti, Giuseppe Lamorte,[...]. Eur J Hum Genet 2013
24
41

Downregulation of connexin 45 gene products during mouse heart development.
S Alcoléa, M Théveniau-Ruissy, T Jarry-Guichard, I Marics, E Tzouanacou, J P Chauvin, J P Briand, A F Moorman, W H Lamers, D B Gros. Circ Res 1999
111
9



Expression pattern of connexin gene products at the early developmental stages of the mouse cardiovascular system.
B Delorme, E Dahl, T Jarry-Guichard, J P Briand, K Willecke, D Gros, M Théveniau-Ruissy. Circ Res 1997
177
9

Alteration in connexin 43 gap junction gene dosage impairs conotruncal heart development.
G Y Huang, A Wessels, B R Smith, K K Linask, J L Ewart, C W Lo. Dev Biol 1998
128
9


A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.
W Antoinette Groenewegen, Mehran Firouzi, Connie R Bezzina, Saskia Vliex, Irene M van Langen, Lodewijk Sandkuijl, Jeroen P P Smits, Miriam Hulsbeek, Martin B Rook, Habo J Jongsma,[...]. Circ Res 2003
187
9

Lack of vascular connexin 40 is associated with hypertension and irregular arteriolar vasomotion.
Cor de Wit, Frederik Roos, Steffen-Sebastian Bolz, Ulrich Pohl. Physiol Genomics 2003
157
9

Plasma membrane channels formed by connexins: their regulation and functions.
Juan C Saez, Viviana M Berthoud, Maria C Branes, Agustin D Martinez, Eric C Beyer. Physiol Rev 2003
855
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

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
9

Unique and shared functions of different connexins in mice.
A Plum, G Hallas, T Magin, F Dombrowski, A Hagendorff, B Schumacher, C Wolpert, J Kim, W H Lamers, M Evert,[...]. Curr Biol 2000
217
8



Comparison of connexin expression patterns in the developing mouse heart and human foetal heart.
Steven R Coppen, Riyaz A Kaba, Deborah Halliday, Emmanuel Dupont, Jeremy N Skepper, Suzy Elneil, Nicholas J Severs. Mol Cell Biochem 2003
65
12


Impaired conduction of vasodilation along arterioles in connexin40-deficient mice.
C de Wit, F Roos, S S Bolz, S Kirchhoff, O Krüger, K Willecke, U Pohl. Circ Res 2000
271
8

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease.
B G Bruneau, G Nemer, J P Schmitt, F Charron, L Robitaille, S Caron, D A Conner, M Gessler, M Nemer, C E Seidman,[...]. Cell 2001
720
8

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
524
8


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.