A citation-based method for searching scientific literature

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
Times Cited: 118







List of co-cited articles
1095 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
40

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
37

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
36

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
41

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
31

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
31

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
28

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
28

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
45

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
53

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
26

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
32

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
24

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
23

The Chd family of chromatin remodelers.
Concetta G A Marfella, Anthony N Imbalzano. Mutat Res 2007
231
23

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
26

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

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
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
20

CTCF-dependent chromatin insulator is linked to epigenetic remodeling.
Ko Ishihara, Mitsuo Oshimura, Mitsuyoshi Nakao. Mol Cell 2006
191
18

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
41

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
18

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
34

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
31

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
15

A de novo convergence of autism genetics and molecular neuroscience.
Niklas Krumm, Brian J O'Roak, Jay Shendure, Evan E Eichler. Trends Neurosci 2014
272
15

Sexually dimorphic behavior, neuronal activity, and gene expression in Chd8-mutant mice.
Hwajin Jung, Haram Park, Yeonsoo Choi, Hyojin Kang, Eunee Lee, Hanseul Kweon, Junyeop Daniel Roh, Jacob Ellegood, Woochul Choi, Jaeseung Kang,[...]. Nat Neurosci 2018
55
27

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
29

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
14

CHD proteins: a diverse family with strong ties.
J Adam Hall, Philippe T Georgel. Biochem Cell Biol 2007
140
14

De novo gene disruptions in children on the autistic spectrum.
Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoon-Ha Lee, Giuseppe Narzisi, Anthony Leotta,[...]. Neuron 2012
899
14

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
26

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
12

Chromatin remodelling during development.
Lena Ho, Gerald R Crabtree. Nature 2010
690
12

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
41

Regulation of androgen-responsive transcription by the chromatin remodeling factor CHD8.
Tushar Menon, Joel A Yates, Daniel A Bochar. Mol Endocrinol 2010
29
41

Dual Requirement of CHD8 for Chromatin Landscape Establishment and Histone Methyltransferase Recruitment to Promote CNS Myelination and Repair.
Chuntao Zhao, Chen Dong, Magali Frah, Yaqi Deng, Corentine Marie, Feng Zhang, Lingli Xu, Zhixing Ma, Xinran Dong, Yifeng Lin,[...]. Dev Cell 2018
45
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
11

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.
Da Wei Huang, Brad T Sherman, Richard A Lempicki. Nat Protoc 2009
11

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
760
10

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
A Jeremy Willsey, Stephan J Sanders, Mingfeng Li, Shan Dong, Andrew T Tebbenkamp, Rebecca A Muhle, Steven K Reilly, Leon Lin, Sofia Fertuzinhos, Jeremy A Miller,[...]. Cell 2013
475
10

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, Jacinta M McMahon, Brian J O'Roak, Joseph Cook, Adiba Khan, Michael O Dorschner, Molly Weaver, Sophie Calvert,[...]. Nat Genet 2013
398
10

Oligodendrocyte precursor survival and differentiation requires chromatin remodeling by Chd7 and Chd8.
Corentine Marie, Adrien Clavairoly, Magali Frah, Hatem Hmidan, Jun Yan, Chuntao Zhao, Juliette Van Steenwinckel, Romain Daveau, Bernard Zalc, Bassem Hassan,[...]. Proc Natl Acad Sci U S A 2018
42
23

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
9

Mutation of the SNF2 family member Chd2 affects mouse development and survival.
Concetta G A Marfella, Yasuyuki Ohkawa, Andrew H Coles, David S Garlick, Stephen N Jones, Anthony N Imbalzano. J Cell Physiol 2006
63
14

The biology of chromatin remodeling complexes.
Cedric R Clapier, Bradley R Cairns. Annu Rev Biochem 2009
9

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
802
9

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
16

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
9

From neural development to cognition: unexpected roles for chromatin.
Jehnna L Ronan, Wei Wu, Gerald R Crabtree. Nat Rev Genet 2013
281
9


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.