A citation-based method for searching scientific literature

Ingeborg Stalmans, Diether Lambrechts, Frederik De Smet, Sandra Jansen, Jian Wang, Sunit Maity, Paige Kneer, Maren von der Ohe, Ann Swillen, Christa Maes, Marc Gewillig, Daniel G M Molin, Peter Hellings, Thurid Boetel, Maartin Haardt, Veerle Compernolle, Mieke Dewerchin, Stephane Plaisance, Robert Vlietinck, Beverly Emanuel, Adriana C Gittenberger-de Groot, Peter Scambler, Bernice Morrow, Deborah A Driscol, Lieve Moons, Camila V Esguerra, Geert Carmeliet, Annett Behn-Krappa, Koen Devriendt, Désiré Collen, Simon J Conway, Peter Carmeliet. Nat Med 2003
Times Cited: 214







List of co-cited articles
1020 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
30


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
23

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
19

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
17

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
16


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
301
13

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
13

Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele.
P Carmeliet, V Ferreira, G Breier, S Pollefeyt, L Kieckens, M Gertsenstein, M Fahrig, A Vandenhoeck, K Harpal, C Eberhardt,[...]. Nature 1996
13


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
12

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
12

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


A requirement for neuropilin-1 in embryonic vessel formation.
T Kawasaki, T Kitsukawa, Y Bekku, Y Matsuda, M Sanbo, T Yagi, H Fujisawa. Development 1999
556
12

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
11

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
25

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
217
11

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
12


Neural crest cells contribute to normal aorticopulmonary septation.
M L Kirby, T F Gale, D E Stewart. Science 1983
856
10

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
10


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
10


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
10

The biology of VEGF and its receptors.
Napoleone Ferrara, Hans-Peter Gerber, Jennifer LeCouter. Nat Med 2003
10

Heterozygous embryonic lethality induced by targeted inactivation of the VEGF gene.
N Ferrara, K Carver-Moore, H Chen, M Dowd, L Lu, K S O'Shea, L Powell-Braxton, K J Hillan, M W Moore. Nature 1996
10

Neuropilin-1 conveys semaphorin and VEGF signaling during neural and cardiovascular development.
Chenghua Gu, E Rene Rodriguez, Dorothy V Reimert, Tianzhi Shu, Bernd Fritzsch, Linda J Richards, Alex L Kolodkin, David D Ginty. Dev Cell 2003
512
10

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
9

The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
343
9

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
9


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
97
9

In vivo response to high-resolution variation of Tbx1 mRNA dosage.
Zhen Zhang, Antonio Baldini. Hum Mol Genet 2008
83
10

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
9

Arteriolar and venular patterning in retinas of mice selectively expressing VEGF isoforms.
Ingeborg Stalmans, Yin-Shan Ng, Richard Rohan, Marcus Fruttiger, Ann Bouché, Ali Yuce, Hajime Fujisawa, Bart Hermans, Moshe Shani, Sandra Jansen,[...]. J Clin Invest 2002
370
9

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
8

Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes.
Anne M Moon, Deborah L Guris, Ji-heui Seo, Leiming Li, Jennetta Hammond, Amy Talbot, Akira Imamoto. Dev Cell 2006
100
8

Frequency of 22q11 deletions in patients with conotruncal defects.
E Goldmuntz, B J Clark, L E Mitchell, A F Jawad, B F Cuneo, L Reed, D McDonald-McGinn, P Chien, J Feuer, E H Zackai,[...]. J Am Coll Cardiol 1998
359
8

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
8



The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
8

Spatially restricted patterning cues provided by heparin-binding VEGF-A control blood vessel branching morphogenesis.
Christiana Ruhrberg, Holger Gerhardt, Matthew Golding, Rose Watson, Sofia Ioannidou, Hajime Fujisawa, Christer Betsholtz, David T Shima. Genes Dev 2002
610
8


Impaired myocardial angiogenesis and ischemic cardiomyopathy in mice lacking the vascular endothelial growth factor isoforms VEGF164 and VEGF188.
P Carmeliet, Y S Ng, D Nuyens, G Theilmeier, K Brusselmans, I Cornelissen, E Ehler, V V Kakkar, I Stalmans, V Mattot,[...]. Nat Med 1999
505
8

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
14

Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.
B Morrow, R Goldberg, C Carlson, R Das Gupta, H Sirotkin, J Collins, I Dunham, H O'Donnell, P Scambler, R Shprintzen. Am J Hum Genet 1995
215
7


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.