A citation-based method for searching scientific literature

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
Times Cited: 888







List of co-cited articles
1285 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
35

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
25

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
23

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
22

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

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
20

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
20

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
331
18

Genetics and Genomics of Congenital Heart Disease.
Samir Zaidi, Martina Brueckner. Circ Res 2017
140
17

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
16

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
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
154
15

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.
Q Y Li, R A Newbury-Ecob, J A Terrett, D I Wilson, A R Curtis, C H Yi, T Gebuhr, P J Bullen, S C Robson, T Strachan,[...]. Nat Genet 1997
648
13

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
13

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
13

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
719
13

NKX2.5 mutations in patients with tetralogy of fallot.
E Goldmuntz, E Geiger, D W Benson. Circulation 2001
228
12

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
12

Building the mammalian heart from two sources of myocardial cells.
Margaret Buckingham, Sigolène Meilhac, Stéphane Zaffran. Nat Rev Genet 2005
763
12

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.
Mary Ella Pierpont, Martina Brueckner, Wendy K Chung, Vidu Garg, Ronald V Lacro, Amy L McGuire, Seema Mital, James R Priest, William T Pu, Amy Roberts,[...]. Circulation 2018
101
12

Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system.
Patrick Y Jay, Brett S Harris, Colin T Maguire, Antje Buerger, Hiroko Wakimoto, Makoto Tanaka, Sabina Kupershmidt, Dan M Roden, Thomas M Schultheiss, Terrence X O'Brien,[...]. J Clin Invest 2004
176
11

Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart.
Chen-Leng Cai, Xingqun Liang, Yunqing Shi, Po-Hsien Chu, Samuel L Pfaff, Ju Chen, Sylvia Evans. Dev Cell 2003
11

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
11


Complex Interdependence Regulates Heterotypic Transcription Factor Distribution and Coordinates Cardiogenesis.
Luis Luna-Zurita, Christian U Stirnimann, Sebastian Glatt, Bogac L Kaynak, Sean Thomas, Florence Baudin, Md Abul Hassan Samee, Daniel He, Eric M Small, Maria Mileikovsky,[...]. Cell 2016
112
11

Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis.
Yen-Sin Ang, Renee N Rivas, Alexandre J S Ribeiro, Rohith Srivas, Janell Rivera, Nicole R Stone, Karishma Pratt, Tamer M A Mohamed, Ji-Dong Fu, C Ian Spencer,[...]. Cell 2016
101
11

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
10

Genetics of Congenital Heart Defects: The NKX2-5 Gene, a Key Player.
Ill-Min Chung, Govindasamy Rajakumar. Genes (Basel) 2016
40
22

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
9

A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system development.
Ivan P G Moskowitz, Jae B Kim, Meredith L Moore, Cordula M Wolf, Michael A Peterson, Jay Shendure, Marcelo A Nobrega, Yoshifumi Yokota, Charles Berul, Seigo Izumo,[...]. Cell 2007
183
9

Genetic analysis of essential cardiac transcription factors in 256 patients with non-syndromic congenital heart defects.
Kazuki Kodo, Tsutomu Nishizawa, Michiko Furutani, Shoichi Arai, Kazuaki Ishihara, Mayumi Oda, Shinji Makino, Keiichi Fukuda, Takao Takahashi, Rumiko Matsuoka,[...]. Circ J 2012
42
21

Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.
Sabrina Gade Ellesøe, Morten Munk Johansen, Jesper Vandborg Bjerre, Vibeke Elisabeth Hjortdal, Søren Brunak, Lars Allan Larsen. Congenit Heart Dis 2016
42
21

The changing epidemiology of congenital heart disease.
Teun van der Bom, A Carla Zomer, Aeilko H Zwinderman, Folkert J Meijboom, Berto J Bouma, Barbara J M Mulder. Nat Rev Cardiol 2011
318
9

Co-occupancy by multiple cardiac transcription factors identifies transcriptional enhancers active in heart.
Aibin He, Sek Won Kong, Qing Ma, William T Pu. Proc Natl Acad Sci U S A 2011
247
9

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
9

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
8

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
128
8

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
8

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
8

Tbx5-hedgehog molecular networks are essential in the second heart field for atrial septation.
Linglin Xie, Andrew D Hoffmann, Ozanna Burnicka-Turek, Joshua M Friedland-Little, Ke Zhang, Ivan P Moskowitz. Dev Cell 2012
85
9


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
8

Congenital heart disease-causing Gata4 mutation displays functional deficits in vivo.
Chaitali Misra, Nita Sachan, Caryn Rothrock McNally, Sara N Koenig, Haley A Nichols, Anuradha Guggilam, Pamela A Lucchesi, William T Pu, Deepak Srivastava, Vidu Garg. PLoS Genet 2012
55
14

HCN4 dynamically marks the first heart field and conduction system precursors.
Xingqun Liang, Gang Wang, Lizhu Lin, Jennifer Lowe, Qingquang Zhang, Lei Bu, Yihan Chen, Ju Chen, Yunfu Sun, Sylvia M Evans. Circ Res 2013
124
8

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
8


Spectrum of heart disease associated with murine and human GATA4 mutation.
Satish K Rajagopal, Qing Ma, Dita Obler, Jie Shen, Ani Manichaikul, Aoy Tomita-Mitchell, Kari Boardman, Christine Briggs, Vidu Garg, Deepak Srivastava,[...]. J Mol Cell Cardiol 2007
166
8

Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families.
Wilhelmina S Kerstjens-Frederikse, Ingrid M B H van de Laar, Yvonne J Vos, Judith M A Verhagen, Rolf M F Berger, Klaske D Lichtenbelt, Jolien S Klein Wassink-Ruiter, Paul A van der Zwaag, Gideon J du Marchie Sarvaas, Klasien A Bergman,[...]. Genet Med 2016
58
13

Genetics and genetic testing in congenital heart disease.
Jason R Cowan, Stephanie M Ware. Clin Perinatol 2015
46
17


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.