A citation-based method for searching scientific literature

Jelena S Arnold, Uwe Werling, Evan M Braunstein, Jun Liao, Sonja Nowotschin, Winfried Edelmann, Jean M Hebert, Bernice E Morrow. Development 2006
Times Cited: 106







List of co-cited articles
1080 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
687
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
662
47


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
38

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
99
36

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
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
272
30

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
210
27

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
27

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
26

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
488
22

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
20

The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis.
Robert G Kelly, Loydie A Jerome-Majewska, Virginia E Papaioannou. Hum Mol Genet 2004
172
19

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
266
19


The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans.
Tatjana Piotrowski, Dae-gwon Ahn, Thomas F Schilling, Sreelaja Nair, Ilya Ruvinsky, Robert Geisler, Gerd-Jörg Rauch, Pascal Haffter, Leonard I Zon, Yi Zhou,[...]. Development 2003
161
18

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
18

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
328
17

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur,[...]. J Med Genet 1997
821
15

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
15

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
15

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
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

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
14

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
21

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
14

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
14


Building the mammalian heart from two sources of myocardial cells.
Margaret Buckingham, Sigolène Meilhac, Stéphane Zaffran. Nat Rev Genet 2005
773
13


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
13


Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients.
Jelena S Arnold, Evan M Braunstein, Takahiro Ohyama, Andrew K Groves, Joe C Adams, M Christian Brown, Bernice E Morrow. Hum Mol Genet 2006
63
19

Fate of the mammalian cardiac neural crest.
X Jiang, D H Rowitch, P Soriano, A P McMahon, H M Sucov. Development 2000
819
12


TBX1 is required for inner ear morphogenesis.
Francesca Vitelli, Antonella Viola, Masae Morishima, Tiziano Pramparo, Antonio Baldini, Elizabeth Lindsay. Hum Mol Genet 2003
95
11

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
11

In vivo response to high-resolution variation of Tbx1 mRNA dosage.
Zhen Zhang, Antonio Baldini. Hum Mol Genet 2008
83
13

Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects.
W Gong, S Gottlieb, J Collins, A Blescia, H Dietz, E Goldmuntz, D M McDonald-McGinn, E H Zackai, B S Emanuel, D A Driscoll,[...]. J Med Genet 2001
100
11

Tbx1 regulates proliferation and differentiation of multipotent heart progenitors.
Li Chen, Filomena Gabriella Fulcoli, Susan Tang, Antonio Baldini. Circ Res 2009
94
11

Suppression of neural fate and control of inner ear morphogenesis by Tbx1.
Steven Raft, Sonja Nowotschin, Jun Liao, Bernice E Morrow. Development 2004
122
10

The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
343
10

Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants.
Francesca Vitelli, Zhen Zhang, Tuong Huynh, Angela Sobotka, Annalisa Mupo, Antonio Baldini. Dev Biol 2006
40
25


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
380
10


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
10

Gain of function of Tbx1 affects pharyngeal and heart development in the mouse.
Francesca Vitelli, Tuong Huynh, Antonio Baldini. Genesis 2009
31
32

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
411
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.