A citation-based method for searching scientific literature

Hiroyuki Yamagishi, Jun Maeda, Tonghuan Hu, John McAnally, Simon J Conway, Tsutomu Kume, Erik N Meyers, Chihiro Yamagishi, Deepak Srivastava. Genes Dev 2003
Times Cited: 191







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



Times Cited
  Times     Co-cited
Similarity



Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development.
V Garg, C Yamagishi, T Hu, I S Kathiriya, H Yamagishi, D Srivastava. Dev Biol 2001
207
41

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
692
37

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
665
34

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
170
33

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
274
27

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
533
22

Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart.
Chen-Leng Cai, Xingqun Liang, Yunqing Shi, Po-Hsien Chu, Samuel L Pfaff, Ju Chen, Sylvia Evans. Dev Cell 2003
21

Building the mammalian heart from two sources of myocardial cells.
Margaret Buckingham, Sigolène Meilhac, Stéphane Zaffran. Nat Rev Genet 2005
791
21

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways.
Francesca Vitelli, Masae Morishima, Ilaria Taddei, Elizabeth A Lindsay, Antonio Baldini. Hum Mol Genet 2002
244
21

Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.
D L Chapman, N Garvey, S Hancock, M Alexiou, S I Agulnik, J J Gibson-Brown, J Cebra-Thomas, R J Bollag, L M Silver, V E Papaioannou. Dev Dyn 1996
489
21



A genetic link between Tbx1 and fibroblast growth factor signaling.
Francesca Vitelli, Ilaria Taddei, Masae Morishima, Erik N Meyers, Elizabeth A Lindsay, Antonio Baldini. Development 2002
211
20

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
32


Tbx1 regulates proliferation and differentiation of multipotent heart progenitors.
Li Chen, Filomena Gabriella Fulcoli, Susan Tang, Antonio Baldini. Circ Res 2009
95
18

In vivo response to high-resolution variation of Tbx1 mRNA dosage.
Zhen Zhang, Antonio Baldini. Hum Mol Genet 2008
83
20


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
137
15

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
15

Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm.
Amélie Calmont, Sarah Ivins, Kelly Lammerts Van Bueren, Irinna Papangeli, Vanessa Kyriakopoulou, William D Andrews, James F Martin, Anne M Moon, Elizabeth A Illingworth, M Albert Basson,[...]. Development 2009
88
17

Conotruncal myocardium arises from a secondary heart field.
K L Waldo, D H Kumiski, K T Wallis, H A Stadt, M R Hutson, D H Platt, M L Kirby. Development 2001
452
14

The outflow tract of the heart is recruited from a novel heart-forming field.
C H Mjaatvedt, T Nakaoka, R Moreno-Rodriguez, R A Norris, M J Kern, C A Eisenberg, D Turner, R R Markwald. Dev Biol 2001
386
14


Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage.
Jun Liao, Lazaros Kochilas, Sonja Nowotschin, Jelena S Arnold, Vimla S Aggarwal, Jonathan A Epstein, M Christian Brown, Joe Adams, Bernice E Morrow. Hum Mol Genet 2004
167
14

Tbx1 regulates the BMP-Smad1 pathway in a transcription independent manner.
F Gabriella Fulcoli, Tuong Huynh, Peter J Scambler, Antonio Baldini. PLoS One 2009
71
19


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
13

An Nkx2-5/Bmp2/Smad1 negative feedback loop controls heart progenitor specification and proliferation.
Owen W J Prall, Mary K Menon, Mark J Solloway, Yusuke Watanabe, Stéphane Zaffran, Fanny Bajolle, Christine Biben, Jim J McBride, Bronwyn R Robertson, Hervé Chaulet,[...]. Cell 2007
371
13

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
199
13


Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations.
Jelena S Arnold, Uwe Werling, Evan M Braunstein, Jun Liao, Sonja Nowotschin, Winfried Edelmann, Jean M Hebert, Bernice E Morrow. Development 2006
106
12

Mef2c is a direct transcriptional target of ISL1 and GATA factors in the anterior heart field during mouse embryonic development.
Evdokia Dodou, Michael P Verzi, Joshua P Anderson, Shan-Mei Xu, Brian L Black. Development 2004
264
12

Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling.
Eon Joo Park, Lisa A Ogden, Amy Talbot, Sylvia Evans, Chen-Leng Cai, Brian L Black, Deborah U Frank, Anne M Moon. Development 2006
184
12

The del22q11.2 candidate gene Tbx1 controls regional outflow tract identity and coronary artery patterning.
Magali Théveniau-Ruissy, Mathieu Dandonneau, Karim Mesbah, Olivier Ghez, Marie-Geneviève Mattei, Lucile Miquerol, Robert G Kelly. Circ Res 2008
97
12

A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field.
Tuong Huynh, Li Chen, Phillip Terrell, Antonio Baldini. Genesis 2007
75
16

Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development.
Zhen Zhang, Fabiana Cerrato, Huansheng Xu, Francesca Vitelli, Masae Morishima, Joshua Vincentz, Yasuhide Furuta, Lijiang Ma, James F Martin, Antonio Baldini,[...]. Development 2005
98
12

Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1.
Sarah Ivins, Kelly Lammerts van Beuren, Catherine Roberts, Chela James, Elizabeth Lindsay, Antonio Baldini, Paris Ataliotis, Peter J Scambler. Dev Biol 2005
66
18


Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome.
Hiroyuki Yamagishi, Deepak Srivastava. Trends Mol Med 2003
95
11

Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse.
Radwan Abu-Issa, Graham Smyth, Ida Smoak, Ken-ichi Yamamura, Erik N Meyers. Development 2002
330
11

An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.
Deborah U Frank, Lori K Fotheringham, Judson A Brewer, Louis J Muglia, Martin Tristani-Firouzi, Mario R Capecchi, Anne M Moon. Development 2002
265
11

Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development.
Jun K Takeuchi, Maria Mileikovskaia, Kazuko Koshiba-Takeuchi, Analeah B Heidt, Alessandro D Mori, Eric P Arruda, Marina Gertsenstein, Romain Georges, Lorinda Davidson, Rong Mo,[...]. Development 2005
164
11

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
144
11

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease.
B G Bruneau, G Nemer, J P Schmitt, F Charron, L Robitaille, S Caron, D A Conner, M Gessler, M Nemer, C E Seidman,[...]. Cell 2001
730
11

Cre-mediated excision of Fgf8 in the Tbx1 expression domain reveals a critical role for Fgf8 in cardiovascular development in the mouse.
Christopher B Brown, Jennifer M Wenning, Min Min Lu, Douglas J Epstein, Erik N Meyers, Jonathan A Epstein. Dev Biol 2004
107
11

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
139
11


Foxh1 is essential for development of the anterior heart field.
Ingo von Both, Cristoforo Silvestri, Tuba Erdemir, Heiko Lickert, Johnathon R Walls, R Mark Henkelman, Janet Rossant, Richard P Harvey, Liliana Attisano, Jeffrey L Wrana. Dev Cell 2004
130
10


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.