A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


A Smad transcriptional corepressor.
D Wotton, R S Lo, S Lee, J Massagué. Cell 1999
451
55

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke,[...]. Nat Genet 2000
303
55


TGIF inhibits retinoid signaling.
Laurent Bartholin, Shannon E Powers, Tiffany A Melhuish, Samuel Lasse, Michael Weinstein, David Wotton. Mol Cell Biol 2006
90
49

Multiple modes of repression by the Smad transcriptional corepressor TGIF.
D Wotton, R S Lo, L A Swaby, J Massagué. J Biol Chem 1999
156
34

Expression and functional analysis of Tgif during mouse midline development.
Jiu-Zhen Jin, Shi Gu, Patrick McKinney, Jixiang Ding. Dev Dyn 2006
29
75

TGIF2 interacts with histone deacetylase 1 and represses transcription.
T A Melhuish, C M Gallo, D Wotton. J Biol Chem 2001
100
33


Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
30

Genetics of ventral forebrain development and holoprosencephaly.
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
201
26

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
856
26

Intragenic deletion of Tgif causes defectsin brain development.
Chenzhong Kuang, Yan Xiao, Ling Yang, Qian Chen, Zhenzhen Wang, Simon J Conway, Yan Chen. Hum Mol Genet 2006
34
50

Loss of Tgif function causes holoprosencephaly by disrupting the SHH signaling pathway.
Kenichiro Taniguchi, Anoush E Anderson, Ann E Sutherland, David Wotton. PLoS Genet 2012
60
26

The Smad transcriptional corepressor TGIF recruits mSin3.
D Wotton, P S Knoepfler, C D Laherty, R N Eisenman, J Massagué. Cell Growth Differ 2001
103
23



Functional analysis of mutations in TGIF associated with holoprosencephaly.
Kenia B El-Jaick, Shannon E Powers, Laurent Bartholin, Kenneth R Myers, Jin Hahn, Ieda M Orioli, Maia Ouspenskaia, Felicitas Lacbawan, Erich Roessler, David Wotton,[...]. Mol Genet Metab 2007
56
25

Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation.
Shannon E Powers, Kenichiro Taniguchi, Weiwei Yen, Tiffany A Melhuish, Jun Shen, Christopher A Walsh, Ann E Sutherland, David Wotton. Development 2010
48
29

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
369
20

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
L Nanni, J E Ming, M Bocian, K Steinhaus, D W Bianchi, C Die-Smulders, A Giannotti, K Imaizumi, K L Jones, M D Campo,[...]. Hum Mol Genet 1999
263
20

Drosophila TGIF proteins are transcriptional activators.
Cathy A Hyman, Laurent Bartholin, Stuart J Newfeld, David Wotton. Mol Cell Biol 2003
31
38

A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
June M de la Cruz, Richard N Bamford, Rebecca D Burdine, Erich Roessler, A James Barkovich, Dian Donnai, Alexander F Schier, Maximilian Muenke. Hum Genet 2002
81
19


Zic2 regulates the kinetics of neurulation.
T Nagai, J Aruga, O Minowa, T Sugimoto, Y Ohno, T Noda, K Mikoshiba. Proc Natl Acad Sci U S A 2000
180
19

The Tgif2 gene contains a retained intron within the coding sequence.
Tiffany A Melhuish, David Wotton. BMC Mol Biol 2006
26
46

Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
139
19

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
Jeffrey E Ming, Michelle E Kaupas, Erich Roessler, Han G Brunner, Mahin Golabi, Mustafa Tekin, Robert F Stratton, Eva Sujansky, Sherri J Bale, Maximilian Muenke. Hum Genet 2002
161
17

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
D E Wallis, E Roessler, U Hehr, L Nanni, T Wiltshire, A Richieri-Costa, G Gillessen-Kaesbach, E H Zackai, J Rommens, M Muenke. Nat Genet 1999
285
17

Maternal Tgif is required for vascularization of the embryonic placenta.
Laurent Bartholin, Tiffany A Melhuish, Shannon E Powers, Sophie Goddard-Léon, Isabelle Treilleux, Ann E Sutherland, David Wotton. Dev Biol 2008
39
28

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
E Belloni, M Muenke, E Roessler, G Traverso, J Siegel-Bartelt, A Frumkin, H F Mitchell, H Donis-Keller, C Helms, A V Hing,[...]. Nat Genet 1996
492
15

Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos.
K K Sulik, D B Dehart, J M Rogers, N Chernoff. Teratology 1995
110
15



Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
132
15


Amplification and overexpression of TGIF2, a novel homeobox gene of the TALE superclass, in ovarian cancer cell lines.
I Imoto, A Pimkhaokham, T Watanabe, F Saito-Ohara, E Soeda, J Inazawa. Biochem Biophys Res Commun 2000
84
15

Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations.
Céline Aguilella, Christèle Dubourg, Jocelyne Attia-Sobol, Jacqueline Vigneron, Martine Blayau, Laurent Pasquier, Leila Lazaro, Sylvie Odent, Véronique David. Hum Genet 2003
39
25

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
Erich Roessler, Yang-Zhu Du, Jose L Mullor, Esther Casas, William P Allen, Gabriele Gillessen-Kaesbach, Elizabeth R Roeder, Jeffrey E Ming, Ariel Ruiz i Altaba, Maximilian Muenke. Proc Natl Acad Sci U S A 2003
238
15

Smad transcription factors.
Joan Massagué, Joan Seoane, David Wotton. Genes Dev 2005
15

Mutations in holoprosencephaly.
D Wallis, M Muenke. Hum Mutat 2000
138
15

Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers.
Elaine E Storm, Sonia Garel, Ugo Borello, Jean M Hebert, Salvador Martinez, Susan K McConnell, Gail R Martin, John L R Rubenstein. Development 2006
266
15


Mouse models of holoprosencephaly.
Monica Hayhurst, Susan K McConnell. Curr Opin Neurol 2003
49
18


Cdo functions at multiple points in the Sonic Hedgehog pathway, and Cdo-deficient mice accurately model human holoprosencephaly.
Wei Zhang, Jong-Sun Kang, Francesca Cole, Min-Jeong Yi, Robert S Krauss. Dev Cell 2006
195
14

Hedgehog-mediated patterning of the mammalian embryo requires transporter-like function of dispatched.
Yong Ma, Alfrun Erkner, Ruoyu Gong, Shenqin Yao, Jussi Taipale, Konrad Basler, Philip A Beachy. Cell 2002
222
14

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
232
14

Chordin and noggin promote organizing centers of forebrain development in the mouse.
Ryan M Anderson, Alison R Lawrence, Rolf W Stottmann, Daniel Bachiller, John Klingensmith. Development 2002
141
12

Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype.
C Bendavid, B R Haddad, A Griffin, M Huizing, C Dubourg, I Gicquel, L R Cavalli, L Pasquier, A L Shanske, R Long,[...]. J Med Genet 2006
36
22

Three-amino acid extension loop homeodomain proteins Meis2 and TGIF differentially regulate transcription.
Y Yang, C K Hwang, U M D'Souza, S H Lee, E Junn, M M Mouradian. J Biol Chem 2000
67
12


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.