A citation-based method for searching scientific literature

Julien Vermot, Karen Niederreither, Jean-Marie Garnier, Pierre Chambon, Pascal Dollé. Proc Natl Acad Sci U S A 2003
Times Cited: 108







List of co-cited articles
1433 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Embryonic retinoic acid synthesis is essential for early mouse post-implantation development.
K Niederreither, V Subbarayan, P Dollé, P Chambon. Nat Genet 1999
780
38

The regional pattern of retinoic acid synthesis by RALDH2 is essential for the development of posterior pharyngeal arches and the enteric nervous system.
Karen Niederreither, Julien Vermot, Isabelle Le Roux, Brigitte Schuhbaur, Pierre Chambon, Pascal Dollé. Development 2003
157
33



Embryonic retinoic acid synthesis is essential for heart morphogenesis in the mouse.
K Niederreither, J Vermot, N Messaddeq, B Schuhbaur, P Chambon, P Dollé. Development 2001
265
27

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
26


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
24

Retinoic acid down-regulates Tbx1 expression in vivo and in vitro.
Catherine Roberts, Sarah M Ivins, Chela T James, Peter J Scambler. Dev Dyn 2005
77
29


Retinoic acid synthesis and hindbrain patterning in the mouse embryo.
K Niederreither, J Vermot, B Schuhbaur, P Chambon, P Dollé. Development 2000
271
20

Retinoic acid signalling in the development of branchial arches.
Manuel Mark, Norbert B Ghyselinck, Pierre Chambon. Curr Opin Genet Dev 2004
65
30

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
37

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
19



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
19

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
18

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
18

Retinoic acid embryopathy.
E J Lammer, D T Chen, R M Hoar, N D Agnish, P J Benke, J T Braun, C J Curry, P M Fernhoff, A W Grix, I T Lott. N Engl J Med 1985
18

Function of the retinoic acid receptors (RARs) during development (I). Craniofacial and skeletal abnormalities in RAR double mutants.
D Lohnes, M Mark, C Mendelsohn, P Dollé, A Dierich, P Gorry, A Gansmuller, P Chambon. Development 1994
602
17


Retinoic acid-induced developmental defects are mediated by RARbeta/RXR heterodimers in the pharyngeal endoderm.
Nicolas Matt, Norbert B Ghyselinck, Olivia Wendling, Pierre Chambon, Manuel Mark. Development 2003
79
20

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
15


RDH10 is essential for synthesis of embryonic retinoic acid and is required for limb, craniofacial, and organ development.
Lisa L Sandell, Brian W Sanderson, Gennadiy Moiseyev, Teri Johnson, Arcady Mushegian, Kendra Young, Jean-Philippe Rey, Jian-xing Ma, Karen Staehling-Hampton, Paul A Trainor. Genes Dev 2007
207
15

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
14



Retinoic acid in development: towards an integrated view.
Karen Niederreither, Pascal Dollé. Nat Rev Genet 2008
455
13

RXR alpha mutant mice establish a genetic basis for vitamin A signaling in heart morphogenesis.
H M Sucov, E Dyson, C L Gumeringer, J Price, K R Chien, R M Evans. Genes Dev 1994
518
12

Genetic analysis of RXR alpha developmental function: convergence of RXR and RAR signaling pathways in heart and eye morphogenesis.
P Kastner, J M Grondona, M Mark, A Gansmuller, M LeMeur, D Decimo, J L Vonesch, P Dollé, P Chambon. Cell 1994
578
12

The zebrafish neckless mutation reveals a requirement for raldh2 in mesodermal signals that pattern the hindbrain.
G Begemann, T F Schilling, G J Rauch, R Geisler, P W Ingham. Development 2001
279
12


A newborn lethal defect due to inactivation of retinaldehyde dehydrogenase type 3 is prevented by maternal retinoic acid treatment.
Valérie Dupé, Nicolas Matt, Jean-Marie Garnier, Pierre Chambon, Manuel Mark, Norbert B Ghyselinck. Proc Natl Acad Sci U S A 2003
215
12

Retinoic acid deficiency alters second heart field formation.
Lucile Ryckebusch, Zengxin Wang, Nicolas Bertrand, Song-Chang Lin, Xuan Chi, Robert Schwartz, Stéphane Zaffran, Karen Niederreither. Proc Natl Acad Sci U S A 2008
129
12

Genetic evidence that oxidative derivatives of retinoic acid are not involved in retinoid signaling during mouse development.
Karen Niederreither, Suzan Abu-Abed, Brigitte Schuhbaur, Martin Petkovich, Pierre Chambon, Pascal Dollé. Nat Genet 2002
172
11

Normal fate and altered function of the cardiac neural crest cell lineage in retinoic acid receptor mutant embryos.
Xiaobing Jiang, Bibha Choudhary, Esther Merki, Kenneth R Chien, Robert E Maxson, Henry M Sucov. Mech Dev 2002
78
14

Effects of excess vitamin A on development of cranial neural crest-derived structures: a neonatal and embryologic study.
G B Mulder, N Manley, J Grant, K Schmidt, W Zeng, C Eckhoff, L Maggio-Price. Teratology 2000
61
18

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
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
329
11

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
11

Local retinoid signaling coordinates forebrain and facial morphogenesis by maintaining FGF8 and SHH.
R A Schneider, D Hu, J L Rubenstein, M Maden, J A Helms. Development 2001
202
11

Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6.
Christelle Golzio, Jelena Martinovic-Bouriel, Sophie Thomas, Soumaya Mougou-Zrelli, Bettina Grattagliano-Bessieres, Maryse Bonniere, Sophie Delahaye, Arnold Munnich, Ferechte Encha-Razavi, Stanislas Lyonnet,[...]. Am J Hum Genet 2007
136
11

Retinoic acid signalling during development.
Muriel Rhinn, Pascal Dollé. Development 2012
499
11

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
397
11


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
159
10

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
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.