A citation-based method for searching scientific literature

Hayato Tada, Noboru Fujino, Akihiro Nomura, Chiaki Nakanishi, Kenshi Hayashi, Masayuki Takamura, Masa-Aki Kawashiri. J Hum Genet 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Variable cardiovascular phenotypes associated with SMAD2 pathogenic variants.
Jorge L Granadillo, Wendy K Chung, Leah Hecht, Nicole Corsten-Janssen, Daniel Wegner, Sebastiaan W A Nij Bijvank, Tomi L Toler, Daniel E Pineda-Alvarez, Ganka Douglas, Joshua J Murphy,[...]. Hum Mutat 2018
12
33

National Trends in Hospitalizations of Adults With Tetralogy of Fallot.
Ada C Stefanescu Schmidt, Doreen DeFaria Yeh, Sara Tabtabai, Kevin F Kennedy, Robert W Yeh, Ami B Bhatt. Am J Cardiol 2016
17
33

Gene ontology: tool for the unification of biology. The Gene Ontology Consortium.
M Ashburner, C A Ball, J A Blake, D Botstein, H Butler, J M Cherry, A P Davis, K Dolinski, S S Dwight, J T Eppig,[...]. Nat Genet 2000
33

Acrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction.
K Nicole Weaver, Kristin E Noack Watt, Robert B Hufnagel, Joaquin Navajas Acedo, Luke L Linscott, Kristen L Sund, Patricia L Bender, Rainer König, Charles M Lourenco, Ute Hehr,[...]. Am J Hum Genet 2015
37
33

The NuRD complex and macrocephaly associated neurodevelopmental disorders.
Tyler Mark Pierson, Maria G Otero, Katheryn Grand, Andrew Choi, John M Graham, Juan I Young, Joel P Mackay. Am J Med Genet C Semin Med Genet 2019
12
33

Genetics of congenital heart disease: the glass half empty.
Akl C Fahed, Bruce D Gelb, J G Seidman, Christine E Seidman. Circ Res 2013
310
33

Familial pulmonary arterial hypertension by KDR heterozygous loss of function.
Mélanie Eyries, David Montani, Barbara Girerd, Nicolas Favrolt, Marianne Riou, Laurence Faivre, Grégoire Manaud, Frédéric Perros, Stefan Gräf, Nicholas W Morrell,[...]. Eur Respir J 2020
18
33

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
33

KEGG: kyoto encyclopedia of genes and genomes.
M Kanehisa, S Goto. Nucleic Acids Res 2000
33

Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes.
Mark W Russell, Wendy K Chung, Jonathan R Kaltman, Thomas A Miller. J Am Heart Assoc 2018
38
33

Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot.
Miriam S Reuter, Rebekah Jobling, Rajiv R Chaturvedi, Roozbeh Manshaei, Gregory Costain, Tracy Heung, Meredith Curtis, S Mohsen Hosseini, Eriskay Liston, Chelsea Lowther,[...]. Genet Med 2019
31
33

The reactome pathway knowledgebase.
Bijay Jassal, Lisa Matthews, Guilherme Viteri, Chuqiao Gong, Pascual Lorente, Antonio Fabregat, Konstantinos Sidiropoulos, Justin Cook, Marc Gillespie, Robin Haw,[...]. Nucleic Acids Res 2020
666
33

Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort.
Josephina A N Meester, Maja Sukalo, Kim C Schröder, Denny Schanze, Gareth Baynam, Guntram Borck, Nuria C Bramswig, Duygu Duman, Brigitte Gilbert-Dussardier, Muriel Holder-Espinasse,[...]. Hum Mutat 2018
18
33


De novo variants in exomes of congenital heart disease patients identify risk genes and pathways.
Cigdem Sevim Bayrak, Peng Zhang, Martin Tristani-Firouzi, Bruce D Gelb, Yuval Itan. Genome Med 2020
14
33

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
49
33

STRING v11: protein-protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets.
Damian Szklarczyk, Annika L Gable, David Lyon, Alexander Junge, Stefan Wyder, Jaime Huerta-Cepas, Milan Simonovic, Nadezhda T Doncheva, John H Morris, Peer Bork,[...]. Nucleic Acids Res 2019
33

Tetralogy of Fallot. The first 300 years.
C A Neill, E B Clark. Tex Heart Inst J 1994
13
33

Genetic Origins of Tetralogy of Fallot.
Ari Morgenthau, William H Frishman. Cardiol Rev 2018
28
33

Low expression VEGF haplotype increases the risk for tetralogy of Fallot: a family based association study.
D Lambrechts, K Devriendt, D A Driscoll, E Goldmuntz, M Gewillig, R Vlietinck, D Collen, P Carmeliet. J Med Genet 2005
49
33

GATA6 haploinsufficiency causes pancreatic agenesis in humans.
Hana Lango Allen, Sarah E Flanagan, Charles Shaw-Smith, Elisa De Franco, Ildem Akerman, Richard Caswell, Jorge Ferrer, Andrew T Hattersley, Sian Ellard. Nat Genet 2011
165
33

Tetralogy of fallot and alterations in vascular endothelial growth factor-A signaling and notch signaling in mouse embryos solely expressing the VEGF120 isoform.
Nynke M S van den Akker, Daniël G M Molin, Patricia P W M Peters, Saskia Maas, Lambertus J Wisse, Ronald van Brempt, Conny J van Munsteren, Margot M Bartelings, Robert E Poelmann, Peter Carmeliet,[...]. Circ Res 2007
43
33

Echocardiographic Screening for Pulmonary Hypertension in Congenital Heart Disease: JACC Review Topic of the Week.
Konstantinos Dimopoulos, Robin Condliffe, Robert M R Tulloh, Paul Clift, Rafael Alonso-Gonzalez, Radwa Bedair, Natali A Y Chung, Gerry Coghlan, Samantha Fitzsimmons, Alessandra Frigiola,[...]. J Am Coll Cardiol 2018
20
33

Lifetime prevalence of congenital heart disease in the general population from 2000 to 2010.
Ariane J Marelli, Raluca Ionescu-Ittu, Andrew S Mackie, Liming Guo, Nandini Dendukuri, Mohammed Kaouache. Circulation 2014
529
33

Fog1 is required for cardiac looping in zebrafish.
R Zaak Walton, Ashley E E Bruce, Harold E Olivey, Khalid Najib, Vanitha Johnson, Judy U Earley, Robert K Ho, Eric C Svensson. Dev Biol 2006
23
33

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.
Bhagyalaxmi Mohapatra, Brett Casey, Hua Li, Trang Ho-Dawson, Liana Smith, Susan D Fernbach, Laura Molinari, Stephen R Niesh, John Lynn Jefferies, William J Craigen,[...]. Hum Mol Genet 2009
95
33

Haploinsufficiency of TAB2 causes congenital heart defects in humans.
Bernard Thienpont, Litu Zhang, Alex V Postma, Jeroen Breckpot, Léon-Charles Tranchevent, Peter Van Loo, Kjeld Møllgård, Niels Tommerup, Iben Bache, Zeynep Tümer,[...]. Am J Hum Genet 2010
65
33

Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies.
Yingjuan Liu, Sen Chen, Liesl Zühlke, Graeme C Black, Mun-Kit Choy, Ningxiu Li, Bernard D Keavney. Int J Epidemiol 2019
159
33

The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Karin Weiss, Hayley P Lazar, Alina Kurolap, Ariel F Martinez, Tamar Paperna, Lior Cohen, Marie F Smeland, Sandra Whalen, Solveig Heide, Boris Keren,[...]. Genet Med 2020
21
33

Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humans.
J D Karkera, J S Lee, E Roessler, S Banerjee-Basu, M V Ouspenskaia, J Mez, E Goldmuntz, P Bowers, J Towbin, J W Belmont,[...]. Am J Hum Genet 2007
76
33

The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects.
Yaojuan Jia, Jacoba J Louw, Jeroen Breckpot, Bert Callewaert, Catherine Barrea, Yves Sznajer, Marc Gewillig, Erika Souche, Luc Dehaspe, Joris Robert Vermeesch,[...]. Am J Med Genet A 2015
32
33

A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Mark A DePristo, Eric Banks, Ryan Poplin, Kiran V Garimella, Jared R Maguire, Christopher Hartl, Anthony A Philippakis, Guillermo del Angel, Manuel A Rivas, Matt Hanna,[...]. Nat Genet 2011
33

Survival Prospects and Circumstances of Death in Contemporary Adult Congenital Heart Disease Patients Under Follow-Up at a Large Tertiary Centre.
Gerhard-Paul Diller, Aleksander Kempny, Rafael Alonso-Gonzalez, Lorna Swan, Anselm Uebing, Wei Li, Sonya Babu-Narayan, Stephen J Wort, Konstantinos Dimopoulos, Michael A Gatzoulis. Circulation 2015
252
33

Mutational analysis of the human MESP1 gene in patients with congenital heart disease reveals a highly variable sequence in exon 1.
Harald Lahm, Marcus-André Deutsch, Martina Dreßen, Stefanie Doppler, Astrid Werner, Jürgen Hörer, Julie Cleuziou, Christian Schreiber, Johannes Böhm, Karl-Ludwig Laugwitz,[...]. Eur J Med Genet 2013
11
33


MESP1 Mutations in Patients with Congenital Heart Defects.
Petra Werner, Brande Latney, Matthew A Deardorff, Elizabeth Goldmuntz. Hum Mutat 2016
22
33

Tetralogy of Fallot and Hypoplastic Left Heart Syndrome - Complex Clinical Phenotypes Meet Complex Genetic Networks.
Harald Lahm, Patric Schön, Stefanie Doppler, Martina Dreßen, Julie Cleuziou, Marcus-André Deutsch, Peter Ewert, Rüdiger Lange, Markus Krane. Curr Genomics 2015
14
33

Tetralogy of Fallot.
Frederique Bailliard, Robert H Anderson. Orphanet J Rare Dis 2009
122
33

Cardiovascular Precision Medicine in the Genomics Era.
Alexandra M Dainis, Euan A Ashley. JACC Basic Transl Sci 2018
23
33

The European Genome-phenome Archive of human data consented for biomedical research.
Ilkka Lappalainen, Jeff Almeida-King, Vasudev Kumanduri, Alexander Senf, John Dylan Spalding, Saif Ur-Rehman, Gary Saunders, Jag Kandasamy, Mario Caccamo, Rasko Leinonen,[...]. Nat Genet 2015
182
33

The importance of copy number variation in congenital heart disease.
Gregory Costain, Candice K Silversides, Anne S Bassett. NPJ Genom Med 2016
29
33

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
33

Age- and Lesion-Related Comorbidity Burden Among US Adults With Congenital Heart Disease: A Population-Based Study.
Anushree Agarwal, Robert Thombley, Craig S Broberg, Ian S Harris, Elyse Foster, Vaikom S Mahadevan, Anitha John, Eric Vittinghoff, Greg M Marcus, R Adams Dudley. J Am Heart Assoc 2019
15
33

The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease.
Miriam S Reuter, Rajiv R Chaturvedi, Eriskay Liston, Roozbeh Manshaei, Ritu B Aul, Sarah Bowdin, Iris Cohn, Meredith Curtis, Priya Dhir, Robin Z Hayeems,[...]. Genet Med 2020
12
33

Cytoscape: a software environment for integrated models of biomolecular interaction networks.
Paul Shannon, Andrew Markiel, Owen Ozier, Nitin S Baliga, Jonathan T Wang, Daniel Ramage, Nada Amin, Benno Schwikowski, Trey Ideker. Genome Res 2003
33

Genetic syndromes and outcome after surgical correction of tetralogy of Fallot.
Guido Michielon, Bruno Marino, Roberto Formigari, Gaetano Gargiulo, Fernando Picchio, Maria C Digilio, Silvia Anaclerio, Gianluca Oricchio, Stephen P Sanders, Roberto M Di Donato. Ann Thorac Surg 2006
71
33

Hot topics in tetralogy of Fallot.
Juan Villafañe, Jeffrey A Feinstein, Kathy J Jenkins, Robert N Vincent, Edward P Walsh, Anne M Dubin, Tal Geva, Jeffrey A Towbin, Meryl S Cohen, Charles Fraser,[...]. J Am Coll Cardiol 2013
92
33

Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences.
Roozbeh Manshaei, Daniele Merico, Miriam S Reuter, Worrawat Engchuan, Bahareh A Mojarad, Rajiv Chaturvedi, Tracy Heung, Giovanna Pellecchia, Mehdi Zarrei, Thomas Nalpathamkalam,[...]. Front Genet 2020
6
33

Cellular decisions in cardiac outflow tract and coronary development: an act by VEGF and NOTCH.
Nynke M S van den Akker, Vincenza Caolo, Daniël G M Molin. Differentiation 2012
24
33

IQGAP1 and its binding proteins control diverse biological functions.
Colin D White, Huseyin H Erdemir, David B Sacks. Cell Signal 2012
155
33


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.