A citation-based method for searching scientific literature

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, Peter J Scambler. Development 2009
Times Cited: 87







List of co-cited articles
1073 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
681
52


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
654
45

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
42

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
269
34

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
32

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
209
31


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
133
28

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
524
27

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice.
Victoria Randall, Karen McCue, Catherine Roberts, Vanessa Kyriakopoulou, Sarah Beddow, Angela N Barrett, Francesca Vitelli, Katrina Prescott, Charles Shaw-Smith, Koen Devriendt,[...]. J Clin Invest 2009
95
26

In vivo response to high-resolution variation of Tbx1 mRNA dosage.
Zhen Zhang, Antonio Baldini. Hum Mol Genet 2008
83
26

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
206
25

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
94
24

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
30

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
21

Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome.
Kelly Lammerts van Bueren, Irinna Papangeli, Francesca Rochais, Kerra Pearce, Catherine Roberts, Amelie Calmont, Dorota Szumska, Robert G Kelly, Shoumo Bhattacharya, Peter J Scambler. Dev Biol 2010
47
40


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
267
20

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
194
19

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
181
19

Ablation of specific expression domains reveals discrete functions of ectoderm- and endoderm-derived FGF8 during cardiovascular and pharyngeal development.
Timothy L Macatee, Benjamin P Hammond, Benjamin R Arenkiel, Lily Francis, Deborah U Frank, Anne M Moon. Development 2003
188
19


Congenital heart disease in mice deficient for the DiGeorge syndrome region.
E A Lindsay, A Botta, V Jurecic, S Carattini-Rivera, Y C Cheah, H M Rosenblatt, A Bradley, A Baldini. Nature 1999
299
18


Tbx1 regulates proliferation and differentiation of multipotent heart progenitors.
Li Chen, Filomena Gabriella Fulcoli, Susan Tang, Antonio Baldini. Circ Res 2009
93
16

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
105
16

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
188
16

Fate of the mammalian cardiac neural crest.
X Jiang, D H Rowitch, P Soriano, A P McMahon, H M Sucov. Development 2000
820
16

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
96
16

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
141
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
164
14

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
329
14


Neural crest cells contribute to normal aorticopulmonary septation.
M L Kirby, T F Gale, D E Stewart. Science 1983
853
14

Targeted disruption of semaphorin 3C leads to persistent truncus arteriosus and aortic arch interruption.
L Feiner, A L Webber, C B Brown, M M Lu, L Jia, P Feinstein, P Mombaerts, J A Epstein, J A Raper. Development 2001
219
13

A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field.
Tuong Huynh, Li Chen, Phillip Terrell, Antonio Baldini. Genesis 2007
72
16


An essential role for Notch in neural crest during cardiovascular development and smooth muscle differentiation.
Frances A High, Maozhen Zhang, Aaron Proweller, Lili Tu, Michael S Parmacek, Warren S Pear, Jonathan A Epstein. J Clin Invest 2007
186
13

Murine Jagged1/Notch signaling in the second heart field orchestrates Fgf8 expression and tissue-tissue interactions during outflow tract development.
Frances A High, Rajan Jain, Jason Z Stoller, Nicole B Antonucci, Min Min Lu, Kathleen M Loomes, Klaus H Kaestner, Warren S Pear, Jonathan A Epstein. J Clin Invest 2009
124
13

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
486
13

Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome.
Lucile Ryckebüsch, Nicolas Bertrand, Karim Mesbah, Fanny Bajolle, Karen Niederreither, Robert G Kelly, Stéphane Zaffran. Circ Res 2010
53
22

The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1.
Irinna Papangeli, Peter Scambler. Wiley Interdiscip Rev Dev Biol 2013
41
29


The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
342
12


VEGF: a modifier of the del22q11 (DiGeorge) syndrome?
Ingeborg Stalmans, Diether Lambrechts, Frederik De Smet, Sandra Jansen, Jian Wang, Sunit Maity, Paige Kneer, Maren von der Ohe, Ann Swillen, Christa Maes,[...]. Nat Med 2003
214
12



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
15


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.