A citation-based method for searching scientific literature

Kazuki Kodo, Keiko Uchida, Hiroyuki Yamagishi. Front Cardiovasc Med 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity



Role of TBX1 in human del22q11.2 syndrome.
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
526
100

Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome.
Silvia E Racedo, Erica Hasten, Mingyan Lin, Gnanapackiam Sheela Devakanmalai, Tingwei Guo, Ertugrul M Ozbudak, Chen-Leng Cai, Deyou Zheng, Bernice E Morrow. PLoS Genet 2017
15
100

Tbx1 regulates proliferation and differentiation of multipotent heart progenitors.
Li Chen, Filomena Gabriella Fulcoli, Susan Tang, Antonio Baldini. Circ Res 2009
94
100

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
E A Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, G Ogunrinu, H F Sutherland, P J Scambler,[...]. Nature 2001
687
100

T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field.
Christopher De Bono, Charlotte Thellier, Nicolas Bertrand, Rachel Sturny, Estelle Jullian, Claudio Cortes, Sonia Stefanovic, Stéphane Zaffran, Magali Théveniau-Ruissy, Robert G Kelly. Hum Mol Genet 2018
27
100

Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer.
Hiroyuki Yamagishi, Jun Maeda, Tonghuan Hu, John McAnally, Simon J Conway, Tsutomu Kume, Erik N Meyers, Chihiro Yamagishi, Deepak Srivastava. Genes Dev 2003
190
100

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
S Merscher, B Funke, J A Epstein, J Heyer, A Puech, M M Lu, R J Xavier, M B Demay, R G Russell, S Factor,[...]. Cell 2001
662
100

TBX1 regulates epithelial polarity and dynamic basal filopodia in the second heart field.
Alexandre Francou, Edouard Saint-Michel, Karim Mesbah, Robert G Kelly. Development 2014
40
100

Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field.
Sonja Nowotschin, Jun Liao, Philip J Gage, Jonathan A Epstein, Marina Campione, Bernice E Morrow. Development 2006
104
100

Identification of downstream genetic pathways of Tbx1 in the second heart field.
Jun Liao, Vimla S Aggarwal, Sonja Nowotschin, Alexei Bondarev, Shari Lipner, Bernice E Morrow. Dev Biol 2008
95
100

Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.
Huansheng Xu, Masae Morishima, John N Wylie, Robert J Schwartz, Benoit G Bruneau, Elizabeth A Lindsay, Antonio Baldini. Development 2004
272
100


Wnt2 is a direct downstream target of GATA6 during early cardiogenesis.
Alexander Alexandrovich, Matthew Arno, Roger K Patient, Ajay M Shah, John A Pizzey, Alison C Brewer. Mech Dev 2006
31
50

Perspectives on ENCODE.
Michael P Snyder, Thomas R Gingeras, Jill E Moore, Zhiping Weng, Mark B Gerstein, Bing Ren, Ross C Hardison, John A Stamatoyannopoulos, Brenton R Graveley, Elise A Feingold,[...]. Nature 2020
41
50


Mechanisms of T-box gene function in the developing heart.
Franziska Greulich, Carsten Rudat, Andreas Kispert. Cardiovasc Res 2011
150
50

A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
Xiaoqing Zhang, Yuejuan Xu, Deyuan Liu, Juan Geng, Sun Chen, Zhengwen Jiang, Qihua Fu, Kun Sun. BMC Genomics 2015
32
50

Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer.
Luna Simona Pane, Filomena Gabriella Fulcoli, Andrea Cirino, Alessandra Altomonte, Rosa Ferrentino, Marchesa Bilio, Antonio Baldini. Dis Model Mech 2018
5
50

Tbx1 is regulated by forkhead proteins in the secondary heart field.
Jun Maeda, Hiroyuki Yamagishi, John McAnally, Chihiro Yamagishi, Deepak Srivastava. Dev Dyn 2006
56
50

JASPAR 2020: update of the open-access database of transcription factor binding profiles.
Oriol Fornes, Jaime A Castro-Mondragon, Aziz Khan, Robin van der Lee, Xi Zhang, Phillip A Richmond, Bhavi P Modi, Solenne Correard, Marius Gheorghe, Damir Baranašić,[...]. Nucleic Acids Res 2020
424
50

Pax2 may play a role in kidney development by regulating the expression of TBX1.
Hongkun Jiang, Lei Li, Hailing Yang, Yinglong Bai, Hong Jiang, Yunpeng Li. Mol Biol Rep 2014
9
50


Systematic localization of common disease-associated variation in regulatory DNA.
Matthew T Maurano, Richard Humbert, Eric Rynes, Robert E Thurman, Eric Haugen, Hao Wang, Alex P Reynolds, Richard Sandstrom, Hongzhu Qu, Jennifer Brody,[...]. Science 2012
50

Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome.
Erica Hasten, Donna M McDonald-McGinn, Terrence B Crowley, Elaine Zackai, Beverly S Emanuel, Bernice E Morrow, Silvia E Racedo. Hum Mol Genet 2018
10
50

GATA transcription factors in the developing and adult heart.
Sampsa Pikkarainen, Heikki Tokola, Risto Kerkelä, Heikki Ruskoaho. Cardiovasc Res 2004
263
50

TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome.
Shan Gao, Myriam Moreno, Steven Eliason, Huojun Cao, Xiao Li, Wenjie Yu, Felicitas B Bidlack, Henry C Margolis, Antonio Baldini, Brad A Amendt. Hum Mol Genet 2015
35
50

Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis.
Helen M Phillips, Catherine A Stothard, Wasay M Shaikh Qureshi, Anastasia I Kousa, J Alberto Briones-Leon, Ramada R Khasawneh, Chloe O'Loughlin, Rachel Sanders, Silvia Mazzotta, Rebecca Dodds,[...]. Development 2019
10
50

Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors.
Tonghuan Hu, Hiroyuki Yamagishi, Jun Maeda, John McAnally, Chihiro Yamagishi, Deepak Srivastava. Development 2004
168
50

Cardiac cell type-specific gene regulatory programs and disease risk association.
James D Hocker, Olivier B Poirion, Fugui Zhu, Justin Buchanan, Kai Zhang, Joshua Chiou, Tsui-Min Wang, Qingquan Zhang, Xiaomeng Hou, Yang E Li,[...]. Sci Adv 2021
5
50

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
35
50

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.
Marta Unolt, Paolo Versacci, Silvia Anaclerio, Caterina Lambiase, Giulio Calcagni, Matteo Trezzi, Adriano Carotti, Terrence Blaine Crowley, Elaine H Zackai, Elizabeth Goldmuntz,[...]. Am J Med Genet A 2018
19
50

Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Yingjie Zhao, Alexander Diacou, H Richard Johnston, Fadi I Musfee, Donna M McDonald-McGinn, Daniel McGinn, T Blaine Crowley, Gabriela M Repetto, Ann Swillen, Jeroen Breckpot,[...]. Am J Hum Genet 2020
16
50

Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions.
Christiane Zweier, Heinrich Sticht, Inci Aydin-Yaylagül, Christine E Campbell, Anita Rauch. Am J Hum Genet 2007
142
50

The transcription factor GATA-4 regulates cytochrome P4502C19 gene expression.
Jessica Mwinyi, Yvonne Hofmann, Rasmus Steen Pedersen, Jana Nekvindová, Isa Cavaco, Souren Mkrtchian, Magnus Ingelman-Sundberg. Life Sci 2010
22
50

Cardiac T-box factor Tbx20 directly interacts with Nkx2-5, GATA4, and GATA5 in regulation of gene expression in the developing heart.
Fiona A Stennard, Mauro W Costa, David A Elliott, Scott Rankin, Saskia J P Haast, Donna Lai, Lachlan P A McDonald, Karen Niederreither, Pascal Dolle, Benoit G Bruneau,[...]. Dev Biol 2003
200
50

Variants in the Regulatory Region of WNT5A Reduced Risk of Cardiac Conotruncal Malformations in the Chinese Population.
Peiqiang Li, Haijie Li, Yufang Zheng, Bin Qiao, Wenyuan Duan, Lijuan Huang, Weiqi Liu, Hongyan Wang. Sci Rep 2015
6
50

A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.
Yun Pan, Zha-Gen Wang, Xing-Yuan Liu, Hong Zhao, Ning Zhou, Gui-Fen Zheng, Xing-Biao Qiu, Ruo-Gu Li, Fang Yuan, Hong-Yu Shi,[...]. Pediatr Cardiol 2015
24
50

Human cardiac cis-regulatory elements, their cognate transcription factors, and regulatory DNA sequence variants.
Dongwon Lee, Ashish Kapoor, Alexias Safi, Lingyun Song, Marc K Halushka, Gregory E Crawford, Aravinda Chakravarti. Genome Res 2018
11
50

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
136
50

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.
Richard Paylor, Beate Glaser, Annalisa Mupo, Paris Ataliotis, Corinne Spencer, Angela Sobotka, Chelsey Sparks, Chul-Hee Choi, John Oghalai, Sarah Curran,[...]. Proc Natl Acad Sci U S A 2006
197
50

Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.
Ralf Rauch, Michael Hofbeck, Christiane Zweier, Andreas Koch, Stefan Zink, Udo Trautmann, Juliane Hoyer, Renate Kaulitz, Helmut Singer, Anita Rauch. J Med Genet 2010
87
50



Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene.
C Chieffo, N Garvey, W Gong, B Roe, G Zhang, L Silver, B S Emanuel, M L Budarf. Genomics 1997
120
50

Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome.
Deborah L Guris, Gregg Duester, Virginia E Papaioannou, Akira Imamoto. Dev Cell 2006
135
50

In vivo response to high-resolution variation of Tbx1 mRNA dosage.
Zhen Zhang, Antonio Baldini. Hum Mol Genet 2008
83
50

The UCSC Genome Browser database: 2021 update.
Jairo Navarro Gonzalez, Ann S Zweig, Matthew L Speir, Daniel Schmelter, Kate R Rosenbloom, Brian J Raney, Conner C Powell, Luis R Nassar, Nathan D Maulding, Christopher M Lee,[...]. Nucleic Acids Res 2021
57
50

GATA-6 regulates semaphorin 3C and is required in cardiac neural crest for cardiovascular morphogenesis.
John J Lepore, Patricia A Mericko, Lan Cheng, Min Min Lu, Edward E Morrisey, Michael S Parmacek. J Clin Invest 2006
96
50

The roles of GATA-4, -5 and -6 in vertebrate heart development.
Tessa Peterkin, Abigail Gibson, Matthew Loose, Roger Patient. Semin Cell Dev Biol 2005
128
50


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.