Brigitte Laforest, Gregor Andelfinger, Mona Nemer. J Clin Invest 2011
Times Cited: 119
Times Cited: 119
Times Cited
Times Co-cited
Similarity
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
Vidu Garg, Alecia N Muth, Joshua F Ransom, Marie K Schluterman, Robert Barnes, Isabelle N King, Paul D Grossfeld, Deepak Srivastava. Nature 2005
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Rare non-synonymous variations in the transcriptional activation domains of GATA5 in bicuspid aortic valve disease.
Ratnasari Padang, Richard D Bagnall, David R Richmond, Paul G Bannon, Christopher Semsarian. J Mol Cell Cardiol 2012
Ratnasari Padang, Richard D Bagnall, David R Richmond, Paul G Bannon, Christopher Semsarian. J Mol Cell Cardiol 2012
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Abnormal aortic valve development in mice lacking endothelial nitric oxide synthase.
T C Lee, Y D Zhao, D W Courtman, D J Stewart. Circulation 2000
T C Lee, Y D Zhao, D W Courtman, D J Stewart. Circulation 2000
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31
Bicuspid aortic valve is heritable.
Linda Cripe, Gregor Andelfinger, Lisa J Martin, Kerry Shooner, D Woodrow Benson. J Am Coll Cardiol 2004
Linda Cripe, Gregor Andelfinger, Lisa J Martin, Kerry Shooner, D Woodrow Benson. J Am Coll Cardiol 2004
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Bicuspid aortic valves with different spatial orientations of the leaflets are distinct etiological entities.
Borja Fernández, Ana C Durán, Teresa Fernández-Gallego, M Carmen Fernández, Miguel Such, Josep M Arqué, Valentín Sans-Coma. J Am Coll Cardiol 2009
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Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve.
Elizabeth M Bonachea, Sheng-Wei Chang, Gloria Zender, Stephanie LaHaye, Sara Fitzgerald-Butt, Kim L McBride, Vidu Garg. Pediatr Res 2014
Elizabeth M Bonachea, Sheng-Wei Chang, Gloria Zender, Stephanie LaHaye, Sara Fitzgerald-Butt, Kim L McBride, Vidu Garg. Pediatr Res 2014
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Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease.
Kevin Bosse, Chetan P Hans, Ning Zhao, Sara N Koenig, Nianyuan Huang, Anuradha Guggilam, Stephanie LaHaye, Ge Tao, Pamela A Lucchesi, Joy Lincoln,[...]. J Mol Cell Cardiol 2013
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Cardiac neural crest orchestrates remodeling and functional maturation of mouse semilunar valves.
Rajan Jain, Kurt A Engleka, Stacey L Rentschler, Lauren J Manderfield, Li Li, Lijun Yuan, Jonathan A Epstein. J Clin Invest 2011
Rajan Jain, Kurt A Engleka, Stacey L Rentschler, Lauren J Manderfield, Li Li, Lijun Yuan, Jonathan A Epstein. J Clin Invest 2011
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Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysms.
Stephen H McKellar, David J Tester, Marineh Yagubyan, Ramanath Majumdar, Michael J Ackerman, Thoralf M Sundt. J Thorac Cardiovasc Surg 2007
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Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5.
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GATA5 interacts with GATA4 and GATA6 in outflow tract development.
Brigitte Laforest, Mona Nemer. Dev Biol 2011
Brigitte Laforest, Mona Nemer. Dev Biol 2011
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Notch promotes epithelial-mesenchymal transition during cardiac development and oncogenic transformation.
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Extracellular matrix remodeling and organization in developing and diseased aortic valves.
Robert B Hinton, Joy Lincoln, Gail H Deutsch, Hanna Osinska, Peter B Manning, D Woodrow Benson, Katherine E Yutzey. Circ Res 2006
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Sequential Ligand-Dependent Notch Signaling Activation Regulates Valve Primordium Formation and Morphogenesis.
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Novel missense mutations (p.T596M and p.P1797H) in NOTCH1 in patients with bicuspid aortic valve.
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Deficient signaling via Alk2 (Acvr1) leads to bicuspid aortic valve development.
Penny S Thomas, Somyoth Sridurongrit, Pilar Ruiz-Lozano, Vesa Kaartinen. PLoS One 2012
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GATA6 Regulates Aortic Valve Remodeling, and Its Haploinsufficiency Leads to Right-Left Type Bicuspid Aortic Valve.
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Sequencing of NOTCH1, GATA5, TGFBR1 and TGFBR2 genes in familial cases of bicuspid aortic valve.
Ilenia Foffa, Lamia Ait Alì, Paola Panesi, Massimiliano Mariani, Pierluigi Festa, Nicoletta Botto, Cecilia Vecoli, Maria Grazia Andreassi. BMC Med Genet 2013
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A roadmap to investigate the genetic basis of bicuspid aortic valve and its complications: insights from the International BAVCon (Bicuspid Aortic Valve Consortium).
Siddharth K Prakash, Yohan Bossé, Jochen D Muehlschlegel, Hector I Michelena, Giuseppe Limongelli, Alessandro Della Corte, Francesca R Pluchinotta, Maria Giovanna Russo, Artur Evangelista, D Woodrow Benson,[...]. J Am Coll Cardiol 2014
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Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.
Dong-Chuan Guo, Hariyadarshi Pannu, Van Tran-Fadulu, Christina L Papke, Robert K Yu, Nili Avidan, Scott Bourgeois, Anthony L Estrera, Hazim J Safi, Elizabeth Sparks,[...]. Nat Genet 2007
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A prospective study to assess the frequency of familial clustering of congenital bicuspid aortic valve.
K Huntington, A G Hunter, K L Chan. J Am Coll Cardiol 1997
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A classification system for the bicuspid aortic valve from 304 surgical specimens.
Hans-H Sievers, Claudia Schmidtke. J Thorac Cardiovasc Surg 2007
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GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve.
Lin-Mei Shi, Ju-Wei Tao, Xing-Biao Qiu, Juan Wang, Fang Yuan, Lei Xu, Hua Liu, Ruo-Gu Li, Ying-Jia Xu, Qian Wang,[...]. Int J Mol Med 2014
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Notch1 represses osteogenic pathways in aortic valve cells.
Vishal Nigam, Deepak Srivastava. J Mol Cell Cardiol 2009
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Endothelial nitric oxide synthase in bicuspid aortic valve disease.
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Frequency by decades of unicuspid, bicuspid, and tricuspid aortic valves in adults having isolated aortic valve replacement for aortic stenosis, with or without associated aortic regurgitation.
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Lineage and morphogenetic analysis of the cardiac valves.
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The incidence of congenital heart disease.
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Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve.
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NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling.
Kim L McBride, Maurisa F Riley, Gloria A Zender, Sara M Fitzgerald-Butt, Jeffrey A Towbin, John W Belmont, Susan E Cole. Hum Mol Genet 2008
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Nfatc1 coordinates valve endocardial cell lineage development required for heart valve formation.
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Development of heart valve leaflets and supporting apparatus in chicken and mouse embryos.
Joy Lincoln, Christina M Alfieri, Katherine E Yutzey. Dev Dyn 2004
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Aortic dilatation in patients with bicuspid aortic valve.
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Fate of the mammalian cardiac neural crest.
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Diet-induced aortic valve disease in mice haploinsufficient for the Notch pathway effector RBPJK/CSL.
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Incidence of aortic complications in patients with bicuspid aortic valves.
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Heart valve development: regulatory networks in development and disease.
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Heart valve structure and function in development and disease.
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Neural crest cells are required for correct positioning of the developing outflow cushions and pattern the arterial valve leaflets.
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Human disease modeling reveals integrated transcriptional and epigenetic mechanisms of NOTCH1 haploinsufficiency.
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ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.
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Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.
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Genetic insights into bicuspid aortic valve formation.
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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.