A citation-based method for searching scientific literature

Vidu Garg, Alecia N Muth, Joshua F Ransom, Marie K Schluterman, Robert Barnes, Isabelle N King, Paul D Grossfeld, Deepak Srivastava. Nature 2005
Times Cited: 953







List of co-cited articles
3420 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
332
16

Bicuspid aortic valve is heritable.
Linda Cripe, Gregor Andelfinger, Lisa J Martin, Kerry Shooner, D Woodrow Benson. J Am Coll Cardiol 2004
375
16

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
100
15

Notch1 represses osteogenic pathways in aortic valve cells.
Vishal Nigam, Deepak Srivastava. J Mol Cell Cardiol 2009
138
14

Loss of Gata5 in mice leads to bicuspid aortic valve.
Brigitte Laforest, Gregor Andelfinger, Mona Nemer. J Clin Invest 2011
119
14

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
190
14

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
131
13

Human disease modeling reveals integrated transcriptional and epigenetic mechanisms of NOTCH1 haploinsufficiency.
Christina V Theodoris, Molong Li, Mark P White, Lei Liu, Daniel He, Katherine S Pollard, Benoit G Bruneau, Deepak Srivastava. Cell 2015
122
13

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
13

Genetic associations with valvular calcification and aortic stenosis.
George Thanassoulis, Catherine Y Campbell, David S Owens, J Gustav Smith, Albert V Smith, Gina M Peloso, Kathleen F Kerr, Sonali Pechlivanis, Matthew J Budoff, Tamara B Harris,[...]. N Engl J Med 2013
548
13

GATA6 Regulates Aortic Valve Remodeling, and Its Haploinsufficiency Leads to Right-Left Type Bicuspid Aortic Valve.
Lara Gharibeh, Hiba Komati, Yohan Bossé, Munir Boodhwani, Mahyar Heydarpour, Megan Fortier, Romina Hassanzadeh, Janet Ngu, Patrick Mathieu, Simon Body,[...]. Circulation 2018
38
31

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
195
12

Bicuspid aortic valve disease.
Samuel C Siu, Candice K Silversides. J Am Coll Cardiol 2010
538
12

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
66
16

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
168
11

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
829
11

Aortic dilatation in patients with bicuspid aortic valve.
Subodh Verma, Samuel C Siu. N Engl J Med 2014
281
11

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
119
11

Novel missense mutations (p.T596M and p.P1797H) in NOTCH1 in patients with bicuspid aortic valve.
Salah A Mohamed, Zouhair Aherrahrou, Henrike Liptau, Armin W Erasmi, Carolin Hagemann, Sandra Wrobel, Katja Borzym, Heribert Schunkert, Hans H Sievers, Jeanette Erdmann. Biochem Biophys Res Commun 2006
156
11

Incidence of aortic complications in patients with bicuspid aortic valves.
Hector I Michelena, Amber D Khanna, Douglas Mahoney, Edit Margaryan, Yan Topilsky, Rakesh M Suri, Ben Eidem, William D Edwards, Thoralf M Sundt, Maurice Enriquez-Sarano. JAMA 2011
474
11

ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.
Russell A Gould, Hamza Aziz, Courtney E Woods, Manuel Alejandro Seman-Senderos, Elizabeth Sparks, Christoph Preuss, Florian Wünnemann, Djahida Bedja, Cassandra R Moats, Sarah A McClymont,[...]. Nat Genet 2019
58
18

Calcific aortic valve disease: not simply a degenerative process: A review and agenda for research from the National Heart and Lung and Blood Institute Aortic Stenosis Working Group. Executive summary: Calcific aortic valve disease-2011 update.
Nalini M Rajamannan, Frank J Evans, Elena Aikawa, K Jane Grande-Allen, Linda L Demer, Donald D Heistad, Craig A Simmons, Kristyn S Masters, Patrick Mathieu, Kevin D O'Brien,[...]. Circulation 2011
504
11

Valve Interstitial Cells: The Key to Understanding the Pathophysiology of Heart Valve Calcification.
Arkady Rutkovskiy, Anna Malashicheva, Gareth Sullivan, Maria Bogdanova, Anna Kostareva, Kåre-Olav Stensløkken, Arnt Fiane, Jarle Vaage. J Am Heart Assoc 2017
117
11

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
914
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
554
10

Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor.
Elisabeth Gillis, Ajay A Kumar, Ilse Luyckx, Christoph Preuss, Elyssa Cannaerts, Gerarda van de Beek, Björn Wieschendorf, Maaike Alaerts, Nikhita Bolar, Geert Vandeweyer,[...]. Front Physiol 2017
55
18


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
238
10

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
394
10

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
60
15

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

Bicuspid aortic valve: identifying knowledge gaps and rising to the challenge from the International Bicuspid Aortic Valve Consortium (BAVCon).
Hector I Michelena, Siddharth K Prakash, Alessandro Della Corte, Malenka M Bissell, Nandan Anavekar, Patrick Mathieu, Yohan Bossé, Giuseppe Limongelli, Eduardo Bossone, D Woodrow Benson,[...]. Circulation 2014
233
9

Altered DNA Methylation of Long Noncoding RNA H19 in Calcific Aortic Valve Disease Promotes Mineralization by Silencing NOTCH1.
Fayez Hadji, Marie-Chloé Boulanger, Simon-Pierre Guay, Nathalie Gaudreault, Soumiya Amellah, Guada Mkannez, Rihab Bouchareb, Joël Tremblay Marchand, Mohamed Jalloul Nsaibia, Sandra Guauque-Olarte,[...]. Circulation 2016
138
9

Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome.
Jeanne L Theis, Sybil C L Hrstka, Jared M Evans, Megan M O'Byrne, Mariza de Andrade, Patrick W O'Leary, Timothy J Nelson, Timothy M Olson. Hum Genet 2015
42
21

Valvular interstitial cells suppress calcification of valvular endothelial cells.
Jesper Hjortnaes, Kayle Shapero, Claudia Goettsch, Joshua D Hutcheson, Joshua Keegan, Jolanda Kluin, John E Mayer, Joyce Bischoff, Elena Aikawa. Atherosclerosis 2015
90
10

Spatiotemporal Multi-Omics Mapping Generates a Molecular Atlas of the Aortic Valve and Reveals Networks Driving Disease.
Florian Schlotter, Arda Halu, Shinji Goto, Mark C Blaser, Simon C Body, Lang H Lee, Hideyuki Higashi, Daniel M DeLaughter, Joshua D Hutcheson, Payal Vyas,[...]. Circulation 2018
99
9

Clinical factors associated with calcific aortic valve disease. Cardiovascular Health Study.
B F Stewart, D Siscovick, B K Lind, J M Gardin, J S Gottdiener, V E Smith, D W Kitzman, C M Otto. J Am Coll Cardiol 1997
9

The complex genetics of hypoplastic left heart syndrome.
Xiaoqin Liu, Hisato Yagi, Shazina Saeed, Abha S Bais, George C Gabriel, Zhaohan Chen, Kevin A Peterson, You Li, Molly C Schwartz, William T Reynolds,[...]. Nat Genet 2017
102
8

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
54
14


Natural history of asymptomatic patients with normally functioning or minimally dysfunctional bicuspid aortic valve in the community.
Hector I Michelena, Valerie A Desjardins, Jean-François Avierinos, Antonio Russo, Vuyisile T Nkomo, Thoralf M Sundt, Patricia A Pellikka, A Jamil Tajik, Maurice Enriquez-Sarano. Circulation 2008
341
8


A randomized trial of intensive lipid-lowering therapy in calcific aortic stenosis.
S Joanna Cowell, David E Newby, Robin J Prescott, Peter Bloomfield, John Reid, David B Northridge, Nicholas A Boon. N Engl J Med 2005
718
8

Familial clustering of bicuspid aortic valve and its relationship with aortic dilation in first-degree relatives.
Laura Galian-Gay, Amelia Carro Hevia, Gisela Teixido-Turà, José Rodríguez Palomares, Laura Gutiérrez-Moreno, Giuliana Maldonado, María Teresa Gonzàlez-Alujas, Augusto Sao-Aviles, Pastora Gallego, Francisco Calvo-Iglesias,[...]. Heart 2019
33
24

Genetics and Genomics of Congenital Heart Disease.
Samir Zaidi, Martina Brueckner. Circ Res 2017
183
8

Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis.
Sébastien Thériault, Christian Dina, David Messika-Zeitoun, Solena Le Scouarnec, Romain Capoulade, Nathalie Gaudreault, Sidwell Rigade, Zhonglin Li, Floriane Simonet, Maxime Lamontagne,[...]. Circ Genom Precis Med 2019
20
40

Aortic stenosis in the elderly: disease prevalence and number of candidates for transcatheter aortic valve replacement: a meta-analysis and modeling study.
Ruben L J Osnabrugge, Darren Mylotte, Stuart J Head, Nicolas M Van Mieghem, Vuyisile T Nkomo, Corinne M LeReun, Ad J J C Bogers, Nicolo Piazza, A Pieter Kappetein. J Am Coll Cardiol 2013
573
8

Calcific aortic stenosis.
Brian R Lindman, Marie-Annick Clavel, Patrick Mathieu, Bernard Iung, Patrizio Lancellotti, Catherine M Otto, Philippe Pibarot. Nat Rev Dis Primers 2016
330
8


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
255
7


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.