A citation-based method for searching scientific literature

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, Rumiko Matsuoka, Jonathan C Cohen, Deepak Srivastava. Nature 2003
Times Cited: 797







List of co-cited articles
941 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
24

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
20

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
19

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
19

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
18


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
17

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
16

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
15

Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development.
Meenakshi Maitra, Marie K Schluterman, Haley A Nichols, James A Richardson, Cecilia W Lo, Deepak Srivastava, Vidu Garg. Dev Biol 2009
122
14

Genetics and Genomics of Congenital Heart Disease.
Samir Zaidi, Martina Brueckner. Circ Res 2017
140
13

Dynamic GATA4 enhancers shape the chromatin landscape central to heart development and disease.
Aibin He, Fei Gu, Yong Hu, Qing Ma, Lillian Yi Ye, Jennifer A Akiyama, Axel Visel, Len A Pennacchio, William T Pu. Nat Commun 2014
93
13

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
13

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

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

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

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
12

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
12

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

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
11

Direct reprogramming of fibroblasts into functional cardiomyocytes by defined factors.
Masaki Ieda, Ji-Dong Fu, Paul Delgado-Olguin, Vasanth Vedantham, Yohei Hayashi, Benoit G Bruneau, Deepak Srivastava. Cell 2010
11

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
11

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

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling.
Kazuki Kodo, Tsutomu Nishizawa, Michiko Furutani, Shoichi Arai, Eiji Yamamura, Kunitaka Joo, Takao Takahashi, Rumiko Matsuoka, Hiroyuki Yamagishi. Proc Natl Acad Sci U S A 2009
130
10

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
16

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
9


Cardiomyocyte GATA4 functions as a stress-responsive regulator of angiogenesis in the murine heart.
Joerg Heineke, Mannix Auger-Messier, Jian Xu, Toru Oka, Michelle A Sargent, Allen York, Raisa Klevitsky, Sachin Vaikunth, Stephen A Duncan, Bruce J Aronow,[...]. J Clin Invest 2007
162
9


Cardiac-specific deletion of Gata4 reveals its requirement for hypertrophy, compensation, and myocyte viability.
Toru Oka, Marjorie Maillet, Alistair J Watt, Robert J Schwartz, Bruce J Aronow, Stephen A Duncan, Jeffery D Molkentin. Circ Res 2006
296
9

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
9

Morphogenesis of the right ventricle requires myocardial expression of Gata4.
Elisabeth M Zeisberg, Qing Ma, Amy L Juraszek, Kelvin Moses, Robert J Schwartz, Seigo Izumo, William T Pu. J Clin Invest 2005
176
8

TBX5 drives Scn5a expression to regulate cardiac conduction system function.
David E Arnolds, Fang Liu, John P Fahrenbach, Gene H Kim, Kurt J Schillinger, Scott Smemo, Elizabeth M McNally, Marcelo A Nobrega, Vickas V Patel, Ivan P Moskowitz. J Clin Invest 2012
88
9

GATA4 is a dosage-sensitive regulator of cardiac morphogenesis.
William T Pu, Takahiro Ishiwata, Amy L Juraszek, Qing Ma, Seigo Izumo. Dev Biol 2004
157
8


GATA4 is essential for formation of the proepicardium and regulates cardiogenesis.
Alistair J Watt, Michele A Battle, Jixuan Li, Stephen A Duncan. Proc Natl Acad Sci U S A 2004
242
8

GATA4 transcription factor is required for ventral morphogenesis and heart tube formation.
C T Kuo, E E Morrisey, R Anandappa, K Sigrist, M M Lu, M S Parmacek, C Soudais, J M Leiden. Genes Dev 1997
782
8

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
8

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
8

Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.
Scott Smemo, Luciene C Campos, Ivan P Moskowitz, José E Krieger, Alexandre C Pereira, Marcelo A Nobrega. Hum Mol Genet 2012
114
8

An endocardial pathway involving Tbx5, Gata4, and Nos3 required for atrial septum formation.
Mathieu Nadeau, Romain O Georges, Brigitte Laforest, Abir Yamak, Chantal Lefebvre, Janie Beauregard, Pierre Paradis, Benoit G Bruneau, Gregor Andelfinger, Mona Nemer. Proc Natl Acad Sci U S A 2010
48
16

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Donna J Page, Matthieu J Miossec, Simon G Williams, Richard M Monaghan, Elisavet Fotiou, Heather J Cordell, Louise Sutcliffe, Ana Topf, Mathieu Bourgey, Guillaume Bourque,[...]. Circ Res 2019
45
17

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
7

The T-Box transcription factor Tbx5 is required for the patterning and maturation of the murine cardiac conduction system.
Ivan P G Moskowitz, Anne Pizard, Vickas V Patel, Benoit G Bruneau, Jae B Kim, Sabina Kupershmidt, Dan Roden, Charles I Berul, Christine E Seidman, Jonathan G Seidman. Development 2004
143
7

Disruption of myocardial Gata4 and Tbx5 results in defects in cardiomyocyte proliferation and atrioventricular septation.
Chaitali Misra, Sheng-Wei Chang, Madhumita Basu, Nianyuan Huang, Vidu Garg. Hum Mol Genet 2014
30
23

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
7

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.
Margaret J Wat, Oleg A Shchelochkov, Ashley M Holder, Amy M Breman, Aditi Dagli, Carlos Bacino, Fernando Scaglia, Roberto T Zori, Sau Wai Cheung, Daryl A Scott,[...]. Am J Med Genet A 2009
102
7


Of mice and men: molecular genetics of congenital heart disease.
Troels Askhøj Andersen, Karin de Linde Lind Troelsen, Lars Allan Larsen. Cell Mol Life Sci 2014
110
7

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
9


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.