A citation-based method for searching scientific literature

Shannon N Nees, Wendy K Chung. Cold Spring Harb Perspect Biol 2020
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
132
50

In Vivo and In Vitro Genetic Models of Congenital Heart Disease.
Uddalak Majumdar, Jun Yasuhara, Vidu Garg. Cold Spring Harb Perspect Biol 2021
7
42

Single-cell analysis of cardiogenesis reveals basis for organ-level developmental defects.
T Yvanka de Soysa, Sanjeev S Ranade, Satoshi Okawa, Srikanth Ravichandran, Yu Huang, Hazel T Salunga, Amelia Schricker, Antonio Del Sol, Casey A Gifford, Deepak Srivastava. Nature 2019
67
37

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
37

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
290
37


Genetics of Congenital Heart Defects: The NKX2-5 Gene, a Key Player.
Ill-Min Chung, Govindasamy Rajakumar. Genes (Basel) 2016
40
25

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
61
25

Advanced maturation of human cardiac tissue grown from pluripotent stem cells.
Kacey Ronaldson-Bouchard, Stephen P Ma, Keith Yeager, Timothy Chen, LouJin Song, Dario Sirabella, Kumi Morikawa, Diogo Teles, Masayuki Yazawa, Gordana Vunjak-Novakovic. Nature 2018
444
25

Single-Cell Transcriptome Analysis Maps the Developmental Track of the Human Heart.
Yueli Cui, Yuxuan Zheng, Xixi Liu, Liying Yan, Xiaoying Fan, Jun Yong, Yuqiong Hu, Ji Dong, Qingqing Li, Xinglong Wu,[...]. Cell Rep 2019
137
25

Human cardiac organoids for the modelling of myocardial infarction and drug cardiotoxicity.
Dylan J Richards, Yang Li, Charles M Kerr, Jenny Yao, Gyda C Beeson, Robert C Coyle, Xun Chen, Jia Jia, Brooke Damon, Robert Wilson,[...]. Nat Biomed Eng 2020
65
25

Human Pluripotent Stem Cell-Derived Atrial and Ventricular Cardiomyocytes Develop from Distinct Mesoderm Populations.
Jee Hoon Lee, Stephanie I Protze, Zachary Laksman, Peter H Backx, Gordon M Keller. Cell Stem Cell 2017
159
25

Human-iPSC-Derived Cardiac Stromal Cells Enhance Maturation in 3D Cardiac Microtissues and Reveal Non-cardiomyocyte Contributions to Heart Disease.
Elisa Giacomelli, Viviana Meraviglia, Giulia Campostrini, Amy Cochrane, Xu Cao, Ruben W J van Helden, Ana Krotenberg Garcia, Maria Mircea, Sarantos Kostidis, Richard P Davis,[...]. Cell Stem Cell 2020
109
25

Notch and interacting signalling pathways in cardiac development, disease, and regeneration.
Donal MacGrogan, Juliane Münch, José Luis de la Pompa. Nat Rev Cardiol 2018
68
25

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
172
25

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
532
25

Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.
Kim L McBride, Ricardo Pignatelli, Mark Lewin, Trang Ho, Susan Fernbach, Andres Menesses, Wilbur Lam, Suzanne M Leal, Norman Kaplan, Paul Schliekelman,[...]. Am J Med Genet A 2005
125
25

Oligogenic inheritance of a human heart disease involving a genetic modifier.
Casey A Gifford, Sanjeev S Ranade, Ryan Samarakoon, Hazel T Salunga, T Yvanka de Soysa, Yu Huang, Ping Zhou, Aryé Elfenbein, Stacia K Wyman, Yen Kim Bui,[...]. Science 2019
61
25

Hypoplastic Left Heart Syndrome: A New Paradigm for an Old Disease?
Paul Grossfeld, Shuyi Nie, Lizhu Lin, Lu Wang, Robert H Anderson. J Cardiovasc Dev Dis 2019
14
25

The T-box transcription factor Eomesodermin acts upstream of Mesp1 to specify cardiac mesoderm during mouse gastrulation.
Ita Costello, Inga-Marie Pimeisl, Sarah Dräger, Elizabeth K Bikoff, Elizabeth J Robertson, Sebastian J Arnold. Nat Cell Biol 2011
148
25

Heart fields and cardiac morphogenesis.
Robert G Kelly, Margaret E Buckingham, Antoon F Moorman. Cold Spring Harb Perspect Med 2014
115
25

The deployment of cell lineages that form the mammalian heart.
Sigolène M Meilhac, Margaret E Buckingham. Nat Rev Cardiol 2018
74
25

Inhibition of Wnt activity induces heart formation from posterior mesoderm.
M J Marvin, G Di Rocco, A Gardiner, S M Bush, A B Lassar. Genes Dev 2001
413
25

Environmental Risk Factors for Congenital Heart Disease.
Jacinta Isabelle Kalisch-Smith, Nikita Ved, Duncan Burnaby Sparrow. Cold Spring Harb Perspect Biol 2020
20
25

Defining the earliest step of cardiovascular lineage segregation by single-cell RNA-seq.
Fabienne Lescroart, Xiaonan Wang, Xionghui Lin, Benjamin Swedlund, Souhir Gargouri, Adriana Sànchez-Dànes, Victoria Moignard, Christine Dubois, Catherine Paulissen, Sarah Kinston,[...]. Science 2018
111
25

Genetics and Genomics of Congenital Heart Disease.
Samir Zaidi, Martina Brueckner. Circ Res 2017
159
25


Utility of genetic evaluation in infants with congenital heart defects admitted to the cardiac intensive care unit.
Rebecca C Ahrens-Nicklas, Shama Khan, Jennifer Garbarini, Stacy Woyciechowski, Lisa D'Alessandro, Elaine H Zackai, Matthew A Deardorff, Elizabeth Goldmuntz. Am J Med Genet A 2016
16
25

Genetic Testing Protocol Reduces Costs and Increases Rate of Genetic Diagnosis in Infants with Congenital Heart Disease.
Gabrielle C Geddes, Donald Basel, Peter Frommelt, Aaron Kinney, Michael Earing. Pediatr Cardiol 2017
16
25

Chromosome microarray analysis in the investigation of children with congenital heart disease.
Xiao-Li Wu, Ru Li, Fang Fu, Min Pan, Jin Han, Xin Yang, Yong-Ling Zhang, Fa-Tao Li, Can Liao. BMC Pediatr 2017
16
25

Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies.
Lorenzo D Botto, Angela E Lin, Tiffany Riehle-Colarusso, Sadia Malik, Adolfo Correa. Birth Defects Res A Clin Mol Teratol 2007
278
25

Current Practice and Utility of Chromosome Microarray Analysis in Infants Undergoing Cardiac Surgery.
Jason R Buckley, Minoo N Kavarana, Shahryar M Chowdhury, Mark A Scheurer. Congenit Heart Dis 2015
10
25

Genetics and genetic testing in congenital heart disease.
Jason R Cowan, Stephanie M Ware. Clin Perinatol 2015
54
25

Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
Juan Geng, Jonathan Picker, Zhaojing Zheng, Xiaoqing Zhang, Jian Wang, Fuki Hisama, David W Brown, Mary P Mullen, David Harris, Joan Stoler,[...]. BMC Genomics 2014
51
25

Generation of conditional alleles for Foxc1 and Foxc2 in mice.
Amy Sasman, Carey Nassano-Miller, Kyoo Seok Shim, Hyun Young Koo, Ting Liu, Kathryn M Schultz, Meredith Millay, Atsushi Nanano, Myengmo Kang, Takashi Suzuki,[...]. Genesis 2012
27
12

Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase.
P S Danielian, D Muccino, D H Rowitch, S K Michael, A P McMahon. Curr Biol 1998
999
12


Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growth.
Seungwoon Seo, Hardeep P Singh, Pedro M Lacal, Amy Sasman, Anees Fatima, Ting Liu, Kathryn M Schultz, Douglas W Losordo, Ordan J Lehmann, Tsutomu Kume. Proc Natl Acad Sci U S A 2012
65
12

Cardiac Neural Crest.
Hiroyuki Yamagishi. Cold Spring Harb Perspect Biol 2021
8
12

Foxc2 is required for proper cardiac neural crest cell migration, outflow tract septation, and ventricle expansion.
Kimberly E Inman, Carlo Donato Caiaffa, Kristin R Melton, Lisa L Sandell, Annita Achilleos, Tsutomu Kume, Paul A Trainor. Dev Dyn 2018
10
12


Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles.
G E Winnier, T Kume, K Deng, R Rogers, J Bundy, C Raines, M A Walter, B L Hogan, S J Conway. Dev Biol 1999
138
12

Histology atlas of the developing mouse heart with emphasis on E11.5 to E18.5.
Saija M Savolainen, Julie F Foley, Susan A Elmore. Toxicol Pathol 2009
81
12

The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development.
Seungwoon Seo, Hideo Fujita, Atsushi Nakano, Myengmo Kang, Antonio Duarte, Tsutomu Kume. Dev Biol 2006
199
12

Functionally significant, rare transcription factor variants in tetralogy of Fallot.
Ana Töpf, Helen R Griffin, Elise Glen, Rachel Soemedi, Danielle L Brown, Darroch Hall, Thahira J Rahman, Jyrki J Eloranta, Christoph Jüngst, A Graham Stuart,[...]. PLoS One 2014
40
12

Foxc2 in pharyngeal arch mesenchyme is important for aortic arch artery remodelling and ventricular septum formation.
Mohammad Khaja Mafij Uddin, Wataru Kimura, Tomoyuki Ishikura, Haruhiko Koseki, Nobuaki Yoshida, Mohammad Johirul Islam, Mohammed Badrul Amin, Kasumi Nakamura, Yi-Xin Wu, Eiji Sato,[...]. Biomed Res 2015
7
14

Essential roles of the winged helix transcription factor MFH-1 in aortic arch patterning and skeletogenesis.
K Iida, H Koseki, H Kakinuma, N Kato, Y Mizutani-Koseki, H Ohuchi, H Yoshioka, S Noji, K Kawamura, Y Kataoka,[...]. Development 1997
188
12

A global double-fluorescent Cre reporter mouse.
Mandar Deepak Muzumdar, Bosiljka Tasic, Kazunari Miyamichi, Ling Li, Liqun Luo. Genesis 2007
12

Foxc1 and Foxc2 in the Neural Crest Are Required for Ocular Anterior Segment Development.
Seungwoon Seo, Lisheng Chen, Wenzhong Liu, Demin Zhao, Kathryn M Schultz, Amy Sasman, Ting Liu, Hao F Zhang, Philip J Gage, Tsutomu Kume. Invest Ophthalmol Vis Sci 2017
22
12



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.