A citation-based method for searching scientific literature

M Rodríguez-Paredes, M Ceballos-Chávez, M Esteller, M García-Domínguez, J C Reyes. Nucleic Acids Res 2009
Times Cited: 57







List of co-cited articles
673 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
59

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
50

The Chd family of chromatin remodelers.
Concetta G A Marfella, Anthony N Imbalzano. Mutat Res 2007
231
36

CTCF-dependent chromatin insulator is linked to epigenetic remodeling.
Ko Ishihara, Mitsuo Oshimura, Mitsuyoshi Nakao. Mol Cell 2006
191
33

A novel beta-catenin-binding protein inhibits beta-catenin-dependent Tcf activation and axis formation.
I Sakamoto, S Kishida, A Fukui, M Kishida, H Yamamoto, S Hino, T Michiue, S Takada, M Asashima, A Kikuchi. J Biol Chem 2000
75
29

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
29

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
34

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
30

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
26

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
26

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
26

Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns.
Michael P Schnetz, Cynthia F Bartels, Kuntal Shastri, Dheepa Balasubramanian, Gabriel E Zentner, Ravishankar Balaji, Xiaodong Zhang, Lingyun Song, Zhenghe Wang, Thomas Laframboise,[...]. Genome Res 2009
164
24

CHD7 cooperates with PBAF to control multipotent neural crest formation.
Ruchi Bajpai, Denise A Chen, Alvaro Rada-Iglesias, Junmei Zhang, Yiqin Xiong, Jill Helms, Ching-Pin Chang, Yingming Zhao, Tomek Swigut, Joanna Wysocka. Nature 2010
364
24

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
24

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
24

Regulation of HOXA2 gene expression by the ATP-dependent chromatin remodeling enzyme CHD8.
Joel A Yates, Tushar Menon, Brandi A Thompson, Daniel A Bochar. FEBS Lett 2010
29
44

Regulation of androgen-responsive transcription by the chromatin remodeling factor CHD8.
Tushar Menon, Joel A Yates, Daniel A Bochar. Mol Endocrinol 2010
29
44

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

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
30

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
22

The Drosophila trithorax group protein Kismet facilitates an early step in transcriptional elongation by RNA Polymerase II.
Shrividhya Srinivasan, Jennifer A Armstrong, Renate Deuring, Ina K Dahlsveen, Helen McNeill, John W Tamkun. Development 2005
96
19

Drosophila Kismet regulates histone H3 lysine 27 methylation and early elongation by RNA polymerase II.
Shrividhya Srinivasan, Kristel M Dorighi, John W Tamkun. PLoS Genet 2008
92
19

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
19

CHD proteins: a diverse family with strong ties.
J Adam Hall, Philippe T Georgel. Biochem Cell Biol 2007
140
19

Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children.
Farah Zahir, Helen V Firth, Agnes Baross, Allen D Delaney, Patrice Eydoux, William T Gibson, Sylvie Langlois, Howard Martin, Lionel Willatt, Marco A Marra,[...]. J Med Genet 2007
54
20

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
19

Double chromodomains cooperate to recognize the methylated histone H3 tail.
John F Flanagan, Li-Zhi Mi, Maksymilian Chruszcz, Marcin Cymborowski, Katrina L Clines, Youngchang Kim, Wladek Minor, Fraydoon Rastinejad, Sepideh Khorasanizadeh. Nature 2005
380
17

CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome.
Tserendulam Batsukh, Lasse Pieper, Anna M Koszucka, Nina von Velsen, Sigrid Hoyer-Fender, Miriam Elbracht, Jorieke E H Bergman, Lies H Hoefsloot, Silke Pauli. Hum Mol Genet 2010
51
19

The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes.
B Wilkinson, N Grepo, B L Thompson, J Kim, K Wang, O V Evgrafov, W Lu, J A Knowles, D B Campbell. Transl Psychiatry 2015
53
18

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
17

Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues.
Elizabeth A Hurd, Patrice L Capers, Marsha N Blauwkamp, Meredith E Adams, Yehoash Raphael, Heather K Poucher, Donna M Martin. Mamm Genome 2007
106
15

Chd1 regulates open chromatin and pluripotency of embryonic stem cells.
Alexandre Gaspar-Maia, Adi Alajem, Fanny Polesso, Rupa Sridharan, Mike J Mason, Amy Heidersbach, João Ramalho-Santos, Michael T McManus, Kathrin Plath, Eran Meshorer,[...]. Nature 2009
349
14

Characterization of the CHD family of proteins.
T Woodage, M A Basrai, A D Baxevanis, P Hieter, F S Collins. Proc Natl Acad Sci U S A 1997
275
14

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
14

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

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
14

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
14

Multiple mutations in mouse Chd7 provide models for CHARGE syndrome.
Erika A Bosman, Andrew C Penn, John C Ambrose, Ross Kettleborough, Derek L Stemple, Karen P Steel. Hum Mol Genet 2005
144
12

CHD5 is a tumor suppressor at human 1p36.
Anindya Bagchi, Cristian Papazoglu, Ying Wu, Daniel Capurso, Michael Brodt, Dailia Francis, Markus Bredel, Hannes Vogel, Alea A Mills. Cell 2007
244
12

CHD6 is a DNA-dependent ATPase and localizes at nuclear sites of mRNA synthesis.
Thomas Lutz, Reinhard Stöger, Amelia Nieto. FEBS Lett 2006
29
24

The Drosophila kismet gene is related to chromatin-remodeling factors and is required for both segmentation and segment identity.
G Daubresse, R Deuring, L Moore, O Papoulas, I Zakrajsek, W R Waldrip, M P Scott, J A Kennison, J W Tamkun. Development 1999
113
12


Altered Neocortical Gene Expression, Brain Overgrowth and Functional Over-Connectivity in Chd8 Haploinsufficient Mice.
Philipp Suetterlin, Shaun Hurley, Conor Mohan, Kimberley L H Riegman, Marco Pagani, Angela Caruso, Jacob Ellegood, Alberto Galbusera, Ivan Crespo-Enriquez, Caterina Michetti,[...]. Cereb Cortex 2018
49
14

Estrogen regulation of cyclin E2 requires cyclin D1 but not c-Myc.
C Elizabeth Caldon, C Marcelo Sergio, Judith Schütte, Marijke N Boersma, Robert L Sutherland, Jason S Carroll, Elizabeth A Musgrove. Mol Cell Biol 2009
47
12

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.
M C J Jongmans, R J Admiraal, K P van der Donk, L E L M Vissers, A F Baas, L Kapusta, J M van Hagen, D Donnai, T J de Ravel, J A Veltman,[...]. J Med Genet 2006
251
10

Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome.
W S Layman, D P McEwen, L A Beyer, S R Lalani, S D Fernbach, E Oh, A Swaroop, C C Hegg, Y Raphael, J R Martens,[...]. Hum Mol Genet 2009
73
10

PRIC320, a transcription coactivator, isolated from peroxisome proliferator-binding protein complex.
Sailesh Surapureddi, Navin Viswakarma, Songtao Yu, Dongsheng Guo, M Sambasiva Rao, Janardan K Reddy. Biochem Biophys Res Commun 2006
29
20

The dMi-2 chromodomains are DNA binding modules important for ATP-dependent nucleosome mobilization.
Karim Bouazoune, Angelika Mitterweger, Gernot Längst, Axel Imhof, Asifa Akhtar, Peter B Becker, Alexander Brehm. EMBO J 2002
111
10

A histone lysine methyltransferase activated by non-canonical Wnt signalling suppresses PPAR-gamma transactivation.
Ichiro Takada, Masatomo Mihara, Miyuki Suzawa, Fumiaki Ohtake, Shinji Kobayashi, Mamoru Igarashi, Min-Young Youn, Ken-ichi Takeyama, Takashi Nakamura, Yoshihiro Mezaki,[...]. Nat Cell Biol 2007
318
10

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.
S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein, M Mistry, P Pavlidis, R Solomon, E Ghiban,[...]. Mol Psychiatry 2014
226
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.