A citation-based method for searching scientific literature

Elliot S Stolerman, Brooke Smith, Alka Chaubey, Julie R Jones. Eur J Med Genet 2016
Times Cited: 16







List of co-cited articles
177 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
87

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
75

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
68

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
50

A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.
Nancy Merner, Baudouin Forgeot d'Arc, Scott C Bell, Gilles Maussion, Huashan Peng, Julie Gauthier, Liam Crapper, Fadi F Hamdan, Jacques L Michaud, Laurent Mottron,[...]. Am J Med Genet A 2016
27
50

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
43

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
43

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
43

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

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 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
31

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
31

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
31

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
31

Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly.
Paolo Prontera, Valentina Ottaviani, Daniela Toccaceli, Daniela Rogaia, Carmen Ardisia, Rita Romani, Gabriela Stangoni, Angiolo Pierini, Emilio Donti. Am J Med Genet A 2014
24
31

White-matter relaxation time and myelin water fraction differences in young adults with autism.
S C L Deoni, J R Zinkstok, E Daly, C Ecker, S C R Williams, D G M Murphy. Psychol Med 2015
38
25


Chd7 cooperates with Sox10 and regulates the onset of CNS myelination and remyelination.
Danyang He, Corentine Marie, Chuntao Zhao, Bongwoo Kim, Jincheng Wang, Yaqi Deng, Adrien Clavairoly, Magali Frah, Haibo Wang, Xuelian He,[...]. Nat Neurosci 2016
79
25

Brg1-dependent chromatin remodelling is not essentially required during oligodendroglial differentiation.
Melanie Bischof, Matthias Weider, Melanie Küspert, Klaus-Armin Nave, Michael Wegner. J Neurosci 2015
40
25

Olig2 targets chromatin remodelers to enhancers to initiate oligodendrocyte differentiation.
Yang Yu, Ying Chen, Bongwoo Kim, Haibo Wang, Chuntao Zhao, Xuelian He, Lei Liu, Wei Liu, Lai Man N Wu, Meng Mao,[...]. Cell 2013
199
25

lncRNA Functional Networks in Oligodendrocytes Reveal Stage-Specific Myelination Control by an lncOL1/Suz12 Complex in the CNS.
Danyang He, Jincheng Wang, Yulan Lu, Yaqi Deng, Chuntao Zhao, Lingli Xu, Yinhuai Chen, Yueh-Chiang Hu, Wenhao Zhou, Q Richard Lu. Neuron 2017
55
25

Brg1 directly regulates Olig2 transcription and is required for oligodendrocyte progenitor cell specification.
Steven Matsumoto, Fatima Banine, Kerstin Feistel, Scott Foster, Rubing Xing, Jaime Struve, Larry S Sherman. Dev Biol 2016
20
25

Recurrent de novo mutations implicate novel genes underlying simplex autism risk.
B J O'Roak, H A Stessman, E A Boyle, K T Witherspoon, B Martin, C Lee, L Vives, C Baker, J B Hiatt, D A Nickerson,[...]. Nat Commun 2014
182
25

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
25

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
Holly A F Stessman, Bo Xiong, Bradley P Coe, Tianyun Wang, Kendra Hoekzema, Michaela Fenckova, Malin Kvarnung, Jennifer Gerdts, Sandy Trinh, Nele Cosemans,[...]. Nat Genet 2017
219
25

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
25

Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology.
Rebecca A Barnard, Matthew B Pomaville, Brian J O'Roak. Front Neurosci 2015
40
25

CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment.
Ping Wang, Mingyan Lin, Erika Pedrosa, Anastasia Hrabovsky, Zheng Zhang, Wenjun Guo, Herbert M Lachman, Deyou Zheng. Mol Autism 2015
78
25

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
25

Autism.
Meng-Chuan Lai, Michael V Lombardo, Simon Baron-Cohen. Lancet 2014
892
18

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

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
18

Sirt2 is a novel in vivo downstream target of Nkx2.2 and enhances oligodendroglial cell differentiation.
Shaoping Ji, J Ronald Doucette, Adil J Nazarali. J Mol Cell Biol 2011
51
18

The molecular hallmarks of epigenetic control.
C David Allis, Thomas Jenuwein. Nat Rev Genet 2016
878
18


Olig1 Acetylation and Nuclear Export Mediate Oligodendrocyte Development.
Jinxiang Dai, Kathryn K Bercury, Weilin Jin, Wendy B Macklin. J Neurosci 2015
37
18


Histone deacetylases: unique players in shaping the epigenetic histone code.
Sam Thiagalingam, Kuang-Hung Cheng, Hyunjoo J Lee, Nora Mineva, Arunthathi Thiagalingam, Jose F Ponte. Ann N Y Acad Sci 2003
505
18


A histone deacetylase 3-dependent pathway delimits peripheral myelin growth and functional regeneration.
Xuelian He, Liguo Zhang, Luis F Queme, Xuezhao Liu, Andrew Lu, Ronald R Waclaw, Xinran Dong, Wenhao Zhou, Grahame Kidd, Sung-Ok Yoon,[...]. Nat Med 2018
40
18

Chromatin remodelling in mammalian differentiation: lessons from ATP-dependent remodellers.
Ivana L de la Serna, Yasuyuki Ohkawa, Anthony N Imbalzano. Nat Rev Genet 2006
279
18

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
18


A proton spectroscopy study of white matter in children with autism.
Antonio Y Hardan, Lawrence K Fung, Thomas Frazier, Sean W Berquist, Nancy J Minshew, Matcheri S Keshavan, Jeffrey A Stanley. Prog Neuropsychopharmacol Biol Psychiatry 2016
14
21


Nicotinamide phosphoribosyltransferase protects against ischemic stroke through SIRT1-dependent adenosine monophosphate-activated kinase pathway.
Pei Wang, Tian-Ying Xu, Yun-Feng Guan, Wei-Wei Tian, Benoit Viollet, Yao-Cheng Rui, Qi-Wei Zhai, Ding-Feng Su, Chao-Yu Miao. Ann Neurol 2011
230
18

HDAC1 and HDAC2 regulate oligodendrocyte differentiation by disrupting the beta-catenin-TCF interaction.
Feng Ye, Ying Chen, ThaoNguyen Hoang, Rusty L Montgomery, Xian-hui Zhao, Hong Bu, Tom Hu, Makoto M Taketo, Johan H van Es, Hans Clevers,[...]. Nat Neurosci 2009
401
18

Intrinsic and extrinsic control of oligodendrocyte development.
J Bradley Zuchero, Ben A Barres. Curr Opin Neurobiol 2013
96
18

Expansion of oligodendrocyte progenitor cells following SIRT1 inactivation in the adult brain.
Victoria A Rafalski, Peggy P Ho, Jamie O Brett, Duygu Ucar, Jason C Dugas, Elizabeth A Pollina, Lionel M L Chow, Adiljan Ibrahim, Suzanne J Baker, Ben A Barres,[...]. Nat Cell Biol 2013
99
18

Nuclear receptor co-repressors are required for the histone-deacetylase activity of HDAC3 in vivo.
Seo-Hee You, Hee-Woong Lim, Zheng Sun, Molly Broache, Kyoung-Jae Won, Mitchell A Lazar. Nat Struct Mol Biol 2013
108
18


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.