A citation-based method for searching scientific literature

I Sakamoto, S Kishida, A Fukui, M Kishida, H Yamamoto, S Hino, T Michiue, S Takada, M Asashima, A Kikuchi. J Biol Chem 2000
Times Cited: 75







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



Times Cited
  Times     Co-cited
Similarity


CHD8 suppresses p53-mediated apoptosis through histone H1 recruitment during early embryogenesis.
Masaaki Nishiyama, Kiyotaka Oshikawa, Yu-ichi Tsukada, Tadashi Nakagawa, Shun-ichiro Iemura, Tohru Natsume, Yuhong Fan, Akira Kikuchi, Arthur I Skoultchi, Keiichi I Nakayama. Nat Cell Biol 2009
118
36

Early embryonic death in mice lacking the beta-catenin-binding protein Duplin.
Masaaki Nishiyama, Keiko Nakayama, Ryosuke Tsunematsu, Tadasuke Tsukiyama, Akira Kikuchi, Keiichi I Nakayama. Mol Cell Biol 2004
49
46

Disruptive CHD8 mutations define a subtype of autism early in development.
Raphael Bernier, Christelle Golzio, Bo Xiong, Holly A Stessman, Bradley P Coe, Osnat Penn, Kali Witherspoon, Jennifer Gerdts, Carl Baker, Anneke T Vulto-van Silfhout,[...]. Cell 2014
382
28

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
25

Inhibition of Wnt signaling by ICAT, a novel beta-catenin-interacting protein.
K Tago, T Nakamura, M Nishita, J Hyodo, S Nagai, Y Murata, S Adachi, S Ohwada, Y Morishita, H Shibuya,[...]. Genes Dev 2000
268
22

The chromatin remodeling factor CHD8 interacts with elongating RNA polymerase II and controls expression of the cyclin E2 gene.
M Rodríguez-Paredes, M Ceballos-Chávez, M Esteller, M García-Domínguez, J C Reyes. Nucleic Acids Res 2009
57
29

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Brian J O'Roak, Laura Vives, Wenqing Fu, Jarrett D Egertson, Ian B Stanaway, Ian G Phelps, Gemma Carvill, Akash Kumar, Choli Lee, Katy Ankenman,[...]. Science 2012
773
22

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
22

Histone H1 recruitment by CHD8 is essential for suppression of the Wnt-β-catenin signaling pathway.
Masaaki Nishiyama, Arthur I Skoultchi, Keiichi I Nakayama. Mol Cell Biol 2012
82
21

XTcf-3 transcription factor mediates beta-catenin-induced axis formation in Xenopus embryos.
M Molenaar, M van de Wetering, M Oosterwegel, J Peterson-Maduro, S Godsave, V Korinek, J Roose, O Destrée, H Clevers. Cell 1996
20

CHD8 is an ATP-dependent chromatin remodeling factor that regulates beta-catenin target genes.
Brandi A Thompson, Véronique Tremblay, Grace Lin, Daniel A Bochar. Mol Cell Biol 2008
124
20

CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.
Aarathi Sugathan, Marta Biagioli, Christelle Golzio, Serkan Erdin, Ian Blumenthal, Poornima Manavalan, Ashok Ragavendran, Harrison Brand, Diane Lucente, Judith Miles,[...]. Proc Natl Acad Sci U S A 2014
163
20

Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling.
Omer Durak, Fan Gao, Yea Jin Kaeser-Woo, Richard Rueda, Anthony J Martorell, Alexi Nott, Carol Y Liu, L Ashley Watson, Li-Huei Tsai. Nat Neurosci 2016
108
20


Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.
Michael E Talkowski, Jill A Rosenfeld, Ian Blumenthal, Vamsee Pillalamarri, Colby Chiang, Adrian Heilbut, Carl Ernst, Carrie Hanscom, Elizabeth Rossin, Amelia M Lindgren,[...]. Cell 2012
375
18

CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
Yuta Katayama, Masaaki Nishiyama, Hirotaka Shoji, Yasuyuki Ohkawa, Atsuki Kawamura, Tetsuya Sato, Mikita Suyama, Toru Takumi, Tsuyoshi Miyakawa, Keiichi I Nakayama. Nature 2016
141
18

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Lisenka E L M Vissers, Conny M A van Ravenswaaij, Ronald Admiraal, Jane A Hurst, Bert B A de Vries, Irene M Janssen, Walter A van der Vliet, Erik H L P G Huys, Pieter J de Jong, Ben C J Hamel,[...]. Nat Genet 2004
756
17

Functional interaction of beta-catenin with the transcription factor LEF-1.
J Behrens, J P von Kries, M Kühl, L Bruhn, D Wedlich, R Grosschedl, W Birchmeier. Nature 1996
16

Constitutive transcriptional activation by a beta-catenin-Tcf complex in APC-/- colon carcinoma.
V Korinek, N Barker, P J Morin, D van Wichen, R de Weger, K W Kinzler, B Vogelstein, H Clevers. Science 1997
16


Mechanisms of Wnt signaling in development.
A Wodarz, R Nusse. Annu Rev Cell Dev Biol 1998
16

The Chd family of chromatin remodelers.
Concetta G A Marfella, Anthony N Imbalzano. Mutat Res 2007
231
16

Chd8 Mutation Leads to Autistic-like Behaviors and Impaired Striatal Circuits.
Randall J Platt, Yang Zhou, Ian M Slaymaker, Ashwin S Shetty, Niels R Weisbach, Jin-Ah Kim, Jitendra Sharma, Mitul Desai, Sabina Sood, Hannah R Kempton,[...]. Cell Rep 2017
86
16

Identification of c-MYC as a target of the APC pathway.
T C He, A B Sparks, C Rago, H Hermeking, L Zawel, L T da Costa, P J Morin, B Vogelstein, K W Kinzler. Science 1998
14


CTCF-dependent chromatin insulator is linked to epigenetic remodeling.
Ko Ishihara, Mitsuo Oshimura, Mitsuyoshi Nakao. Mol Cell 2006
191
14

CHD8 associates with human Staf and contributes to efficient U6 RNA polymerase III transcription.
Chih-Chi Yuan, Xinyang Zhao, Laurence Florens, Selene K Swanson, Michael P Washburn, Nouria Hernandez. Mol Cell Biol 2007
47
23

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
14




Nuclear localization of Duplin, a beta-catenin-binding protein, is essential for its inhibitory activity on the Wnt signaling pathway.
Masashi Kobayashi, Shosei Kishida, Akimasa Fukui, Tatsuo Michiue, Yoichi Miyamoto, Tetsuji Okamoto, Yoshihiro Yoneda, Makoto Asashima, Akira Kikuchi. J Biol Chem 2002
16
62

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
13

The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment.
Justin Cotney, Rebecca A Muhle, Stephan J Sanders, Li Liu, A Jeremy Willsey, Wei Niu, Wenzhong Liu, Lambertus Klei, Jing Lei, Jun Yin,[...]. Nat Commun 2015
162
13

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
13

The cyclin D1 gene is a target of the beta-catenin/LEF-1 pathway.
M Shtutman, J Zhurinsky, I Simcha, C Albanese, M D'Amico, R Pestell, A Ben-Ze'ev. Proc Natl Acad Sci U S A 1999
12

Functional interaction of an axin homolog, conductin, with beta-catenin, APC, and GSK3beta.
J Behrens, B A Jerchow, M Würtele, J Grimm, C Asbrand, R Wirtz, M Kühl, D Wedlich, W Birchmeier. Science 1998
12

Inhibition of the Wnt signaling pathway by Idax, a novel Dvl-binding protein.
S Hino, S Kishida, T Michiue, A Fukui, I Sakamoto, S Takada, M Asashima, A Kikuchi. Mol Cell Biol 2001
103
12

Pontin52 and reptin52 function as antagonistic regulators of beta-catenin signalling activity.
A Bauer, S Chauvet, O Huber, F Usseglio, U Rothbächer, D Aragnol, R Kemler, J Pradel. EMBO J 2000
224
12

Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC.
P J Morin, A B Sparks, V Korinek, N Barker, H Clevers, B Vogelstein, K W Kinzler. Science 1997
12

Wnt signaling and cancer.
P Polakis. Genes Dev 2000
12

Regulation of androgen-responsive transcription by the chromatin remodeling factor CHD8.
Tushar Menon, Joel A Yates, Daniel A Bochar. Mol Endocrinol 2010
29
31

The chromatin remodeller CHD8 is required for E2F-dependent transcription activation of S-phase genes.
Alicia Subtil-Rodríguez, Elena Vázquez-Chávez, María Ceballos-Chávez, Manuel Rodríguez-Paredes, José I Martín-Subero, Manel Esteller, José C Reyes. Nucleic Acids Res 2014
43
20

Germline Chd8 haploinsufficiency alters brain development in mouse.
Andrea L Gompers, Linda Su-Feher, Jacob Ellegood, Nycole A Copping, M Asrafuzzaman Riyadh, Tyler W Stradleigh, Michael C Pride, Melanie D Schaffler, A Ayanna Wade, Rinaldo Catta-Preta,[...]. Nat Neurosci 2017
99
12

An F-box protein, FWD1, mediates ubiquitin-dependent proteolysis of beta-catenin.
M Kitagawa, S Hatakeyama, M Shirane, M Matsumoto, N Ishida, K Hattori, I Nakamichi, A Kikuchi, K Nakayama, K Nakayama. EMBO J 1999
450
10





Inhibition of Wnt signaling pathway by a novel axin-binding protein.
T Kadoya, S Kishida, A Fukui, T Hinoi, T Michiue, M Asashima, A Kikuchi. J Biol Chem 2000
48
16


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.