A citation-based method for searching scientific literature

Yotam Menuchin-Lasowski, Pazit Oren-Giladi, Qing Xie, Raaya Ezra-Elia, Ron Ofri, Shany Peled-Hajaj, Chen Farhy, Yujiro Higashi, Tom Van de Putte, Hisato Kondoh, Danny Huylebroeck, Ales Cvekl, Ruth Ashery-Padan. Development 2016
Times Cited: 9







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



Times Cited
  Times     Co-cited
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Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome.
Tom Van de Putte, Mitsuji Maruhashi, Annick Francis, Luc Nelles, Hisato Kondoh, Danny Huylebroeck, Yujiro Higashi. Am J Hum Genet 2003
212
66

SIP1, a novel zinc finger/homeodomain repressor, interacts with Smad proteins and binds to 5'-CACCT sequences in candidate target genes.
K Verschueren, J E Remacle, C Collart, H Kraft, B S Baker, P Tylzanowski, L Nelles, G Wuytens, M T Su, R Bodmer,[...]. J Biol Chem 1999
378
55

Ocular coloboma and high myopia with Hirschsprung disease associated with a novel ZFHX1B missense mutation and trisomy 21.
C Y Gregory-Evans, H Vieira, R Dalton, G G W Adams, A Salt, K Gregory-Evans. Am J Med Genet A 2004
43
44

Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.
Chiea Chuen Khor, Masahiro Miyake, Li Jia Chen, Yi Shi, Veluchamy A Barathi, Fan Qiao, Isao Nakata, Kenji Yamashiro, Xin Zhou, Pancy O S Tam,[...]. Hum Mol Genet 2013
37
44

Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease.
N Wakamatsu, Y Yamada, K Yamada, T Ono, N Nomura, H Taniguchi, H Kitoh, N Mutoh, T Yamanaka, K Mushiake,[...]. Nat Genet 2001
236
44

Dual-mode modulation of Smad signaling by Smad-interacting protein Sip1 is required for myelination in the central nervous system.
Qinjie Weng, Ying Chen, Haibo Wang, Xiaomei Xu, Bo Yang, Qiaojun He, Weinian Shou, Yan Chen, Yujiro Higashi, Veronique van den Berghe,[...]. Neuron 2012
114
44

ZFHX1B mutations in patients with Mowat-Wilson syndrome.
Florence Dastot-Le Moal, Meredith Wilson, David Mowat, Nathalie Collot, Florence Niel, Michel Goossens. Hum Mutat 2007
102
44

Directed migration of cortical interneurons depends on the cell-autonomous action of Sip1.
Veronique van den Berghe, Elke Stappers, Bram Vandesande, Jordane Dimidschstein, Roel Kroes, Annick Francis, Andrea Conidi, Flore Lesage, Ruben Dries, Silvia Cazzola,[...]. Neuron 2013
79
44

Sip1 regulates sequential fate decisions by feedback signaling from postmitotic neurons to progenitors.
Eve Seuntjens, Anjana Nityanandam, Amaya Miquelajauregui, Joke Debruyn, Agata Stryjewska, Sandra Goebbels, Klaus-Armin Nave, Danny Huylebroeck, Victor Tarabykin. Nat Neurosci 2009
153
44

Generation of the floxed allele of the SIP1 (Smad-interacting protein 1) gene for Cre-mediated conditional knockout in the mouse.
Yujiro Higashi, Mitsuji Maruhashi, Luc Nelles, Tom Van de Putte, Kristin Verschueren, Tomoya Miyoshi, Aki Yoshimoto, Hisato Kondoh, Danny Huylebroeck. Genesis 2002
81
44

Interaction between Smad-interacting protein-1 and the corepressor C-terminal binding protein is dispensable for transcriptional repression of E-cadherin.
Leo A van Grunsven, Christine Michiels, Tom Van de Putte, Luc Nelles, Gunther Wuytens, Kristin Verschueren, Danny Huylebroeck. J Biol Chem 2003
87
44

Loss of Sip1 leads to migration defects and retention of ectodermal markers during lens development.
Abby L Manthey, Salil A Lachke, Paul G FitzGerald, Robert W Mason, David A Scheiblin, John H McDonald, Melinda K Duncan. Mech Dev 2014
33
33

Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease.
V Cacheux, F Dastot-Le Moal, H Kääriäinen, N Bondurand, R Rintala, B Boissier, M Wilson, D Mowat, M Goossens. Hum Mol Genet 2001
172
33

ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat-Wilson syndrome.
Jamal Ghoumid, Loïc Drevillon, Seyedeh Maryam Alavi-Naini, Nadège Bondurand, Marlène Rio, Audrey Briand-Suleau, Mayssa Nasser, Linda Goodwin, Patrick Raymond, Constantin Yanicostas,[...]. Hum Mol Genet 2013
33
33

Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2.
Michelle Ariss, Kristina Natan, Neil Friedman, Elias I Traboulsi. Ophthalmic Genet 2012
14
33

Ptf1a determines horizontal and amacrine cell fates during mouse retinal development.
Yoshio Fujitani, Shuko Fujitani, Huijun Luo, Feng Qiu, Jared Burlison, Qiaoming Long, Yoshiya Kawaguchi, Helena Edlund, Raymond J MacDonald, Takahisa Furukawa,[...]. Development 2006
165
33

Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat-Wilson syndrome.
Tom Van de Putte, Annick Francis, Luc Nelles, Leo A van Grunsven, Danny Huylebroeck. Hum Mol Genet 2007
60
33

Foxn4 controls the genesis of amacrine and horizontal cells by retinal progenitors.
Shengguo Li, Zeqian Mo, Xuejie Yang, Sandy M Price, Michael M Shen, Mengqing Xiang. Neuron 2004
177
33

Clinical and mutational spectrum of Mowat-Wilson syndrome.
Christiane Zweier, Christian T Thiel, Andreas Dufke, Yanick J Crow, Peter Meinecke, Mohnish Suri, Sirpa Ala-Mello, Frits Beemer, Sergio Bernasconi, Paolo Bianchi,[...]. Eur J Med Genet 2005
91
33

Dlx1&2-dependent expression of Zfhx1b (Sip1, Zeb2) regulates the fate switch between cortical and striatal interneurons.
Gabriel L McKinsey, Susan Lindtner, Brett Trzcinski, Axel Visel, Len A Pennacchio, Danny Huylebroeck, Yujiro Higashi, John L R Rubenstein. Neuron 2013
102
33

Zeb2: A multifunctional regulator of nervous system development.
Shane V Hegarty, Aideen M Sullivan, Gerard W O'Keeffe. Prog Neurobiol 2015
49
33

A natural antisense transcript regulates Zeb2/Sip1 gene expression during Snail1-induced epithelial-mesenchymal transition.
Manuel Beltran, Isabel Puig, Cristina Peña, José Miguel García, Ana Belén Alvarez, Raúl Peña, Félix Bonilla, Antonio García de Herreros. Genes Dev 2008
445
33


Four amino acids within a tandem QxVx repeat in a predicted extended α-helix of the Smad-binding domain of Sip1 are necessary for binding to activated Smad proteins.
Andrea Conidi, Veronique van den Berghe, Kris Leslie, Agata Stryjewska, Hua Xue, Ye-Guang Chen, Eve Seuntjens, Danny Huylebroeck. PLoS One 2013
15
33

SIP1 mediates cell-fate decisions between neuroectoderm and mesendoderm in human pluripotent stem cells.
Zhenzhi Chng, Adrian Teo, Roger A Pedersen, Ludovic Vallier. Cell Stem Cell 2010
98
33

Zeb2 Regulates Cell Fate at the Exit from Epiblast State in Mouse Embryonic Stem Cells.
Agata Stryjewska, Ruben Dries, Tim Pieters, Griet Verstappen, Andrea Conidi, Kathleen Coddens, Annick Francis, Lieve Umans, Wilfred F J van IJcken, Geert Berx,[...]. Stem Cells 2017
29
33

XSip1 neuralizing activity involves the co-repressor CtBP and occurs through BMP dependent and independent mechanisms.
Leo A van Grunsven, Vincent Taelman, Christine Michiels, Griet Verstappen, Jacob Souopgui, Massimo Nichane, Emmanuelle Moens, Karin Opdecamp, Jessica Vanhomwegen, Sadia Kricha,[...]. Dev Biol 2007
44
33

Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex.
Griet Verstappen, Leo A van Grunsven, Christine Michiels, Tom Van de Putte, Jacob Souopgui, Jozef Van Damme, Eric Bellefroid, Joël Vandekerckhove, Danny Huylebroeck. Hum Mol Genet 2008
63
33

Zeb2 recruits HDAC-NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination.
Lai Man Natalie Wu, Jincheng Wang, Andrea Conidi, Chuntao Zhao, Haibo Wang, Zachary Ford, Liguo Zhang, Christiane Zweier, Brian G Ayee, Patrice Maurel,[...]. Nat Neurosci 2016
74
33

New mode of DNA binding of multi-zinc finger transcription factors: deltaEF1 family members bind with two hands to two target sites.
J E Remacle, H Kraft, W Lerchner, G Wuytens, C Collart, K Verschueren, J C Smith, D Huylebroeck. EMBO J 1999
217
33

Terminal NK cell maturation is controlled by concerted actions of T-bet and Zeb2 and is essential for melanoma rejection.
Mary J van Helden, Steven Goossens, Cécile Daussy, Anne-Laure Mathieu, Fabrice Faure, Antoine Marçais, Niels Vandamme, Natalie Farla, Katia Mayol, Sébastien Viel,[...]. J Exp Med 2015
80
33

Focus on molecules: Smad Interacting Protein 1 (Sip1, ZEB2, ZFHX1B).
Abby L Grabitz, Melinda K Duncan. Exp Eye Res 2012
9
22


Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical features.
K Yamada, Y Yamada, N Nomura, K Miura, R Wakako, C Hayakawa, A Matsumoto, T Kumagai, I Yoshimura, S Miyazaki,[...]. Am J Hum Genet 2001
84
22

Genetic interaction between Sox10 and Zfhx1b during enteric nervous system development.
Laure Stanchina, Tom Van de Putte, Michel Goossens, Danny Huylebroeck, Nadege Bondurand. Dev Biol 2010
33
22

Regulation of trunk neural crest delamination by δEF1 and Sip1 in the chicken embryo.
Takahiro Yasumi, Masashi Inoue, Mitsuji Maruhashi, Yusuke Kamachi, Yujiro Higashi, Hisato Kondoh, Masanori Uchikawa. Dev Growth Differ 2016
8
25

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome.
L Garavelli, A Donadio, C Zanacca, G Banchini, E Della Giustina, G Bertani, G Albertini, C Del Rossi, C Zweier, A Rauch,[...]. Am J Med Genet A 2003
52
22

Onecut1 is essential for horizontal cell genesis and retinal integrity.
Fuguo Wu, Renzhong Li, Yumiko Umino, Tadeusz J Kaczynski, Darshan Sapkota, Shengguo Li, Mengqing Xiang, Steven J Fliesler, David M Sherry, Maureen Gannon,[...]. J Neurosci 2013
42
22

The role of the transcriptional regulator Ptf1a in converting intestinal to pancreatic progenitors.
Yoshiya Kawaguchi, Bonnie Cooper, Maureen Gannon, Michael Ray, Raymond J MacDonald, Christopher V E Wright. Nat Genet 2002
707
22

From progenitors to differentiated cells in the vertebrate retina.
Michalis Agathocleous, William A Harris. Annu Rev Cell Dev Biol 2009
167
22

Tfap2a and 2b act downstream of Ptf1a to promote amacrine cell differentiation during retinogenesis.
Kangxin Jin, Haisong Jiang, Dongchang Xiao, Min Zou, Jun Zhu, Mengqing Xiang. Mol Brain 2015
28
22

Prdm13 regulates subtype specification of retinal amacrine interneurons and modulates visual sensitivity.
Satoshi Watanabe, Rikako Sanuki, Yuko Sugita, Wataru Imai, Ryoji Yamazaki, Takashi Kozuka, Mizuki Ohsuga, Takahisa Furukawa. J Neurosci 2015
29
22

Ocular phenotype of Mowat-Wilson syndrome in the first reported Cypriot patients: an under-recognized association.
George A Tanteles, Violetta Christophidou-Anastasiadou. Clin Dysmorphol 2014
5
40


Smad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formation.
Amaya Miquelajauregui, Tom Van de Putte, Alexander Polyakov, Anjana Nityanandam, Sridhar Boppana, Eve Seuntjens, Anton Karabinos, Yujiro Higashi, Danny Huylebroeck, Victor Tarabykin. Proc Natl Acad Sci U S A 2007
70
22

Regulation of ocular lens development by Smad-interacting protein 1 involving Foxe3 activation.
Aki Yoshimoto, Yuka Saigou, Yujiro Higashi, Hisato Kondoh. Development 2005
61
22

Recurrence of Mowat-Wilson syndrome in siblings with the same proven mutation.
Julie McGaughran, Stephen Sinnott, Florence Dastot-Le Moal, Meredith Wilson, David Mowat, Bridget Sutton, Michel Goossens. Am J Med Genet A 2005
32
22

Mowat-Wilson syndrome.
Livia Garavelli, Paola Cerruti Mainardi. Orphanet J Rare Dis 2007
90
22

Ptf1a is essential for the differentiation of GABAergic and glycinergic amacrine cells and horizontal cells in the mouse retina.
Hassan Nakhai, Saadettin Sel, Jack Favor, Lidia Mendoza-Torres, Friedrich Paulsen, Gernot I W Duncker, Roland M Schmid. Development 2007
137
22



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.