A citation-based method for searching scientific literature

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, Gerald R Crabtree, Guoping Feng, Feng Zhang. Cell Rep 2017
Times Cited: 86



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
Times Cited: 108




List of shared articles



Times cited

What we can learn from a genetic rodent model about autism.
Dorit Möhrle, Marta Fernández, Olga Peñagarikano, Andreas Frick, Brian Allman, Susanne Schmid. Neurosci Biobehav Rev 2020
11

A spontaneous missense mutation in the chromodomain helicase DNA-binding protein 8 (CHD8) gene: a novel association with congenital myasthenic syndrome.
C Y Lee, M Petkova, S Morales-Gonzalez, N Gimber, J Schmoranzer, A Meisel, W Böhmerle, W Stenzel, M Schuelke, J M Schwarz. Neuropathol Appl Neurobiol 2020
1

Neural circuit dysfunction in mouse models of neurodevelopmental disorders.
Isabel Del Pino, Beatriz Rico, Oscar Marín. Curr Opin Neurobiol 2018
37

Overexpression of microRNA-221 promotes the differentiation of stem cells from human exfoliated deciduous teeth to neurons through activation of Wnt/β-catenin pathway via inhibition of CHD8.
Bing Wen, Chenjiang He, Qin Zhang, Fanglin Zhang, Na Li, Yan Pan, Mengting Deng, Yue Wang, Jianping Li, Jiaxuan Qiu. Cell Cycle 2020
0

Excitatory neuronal CHD8 in the regulation of neocortical development and sensory-motor behaviors.
Hanseul Kweon, Won Beom Jung, Geun Ho Im, Jia Ryoo, Joon-Hyuk Lee, Hogyeong Do, Yeonsoo Choi, You-Hyang Song, Hwajin Jung, Haram Park,[...]. Cell Rep 2021
0


Epigenetic cues modulating the generation of cell-type diversity in the cerebral cortex.
Nicole Amberg, Susanne Laukoter, Simon Hippenmeyer. J Neurochem 2019
8


Chd8 haploinsufficiency impairs early brain development and protein homeostasis later in life.
Jessica A Jiménez, Travis S Ptacek, Alex H Tuttle, Ralf S Schmid, Sheryl S Moy, Jeremy M Simon, Mark J Zylka. Mol Autism 2020
4

Distinct, dosage-sensitive requirements for the autism-associated factor CHD8 during cortical development.
Shaun Hurley, Conor Mohan, Philipp Suetterlin, Robert Ellingford, Kimberley L H Riegman, Jacob Ellegood, Angela Caruso, Caterina Michetti, Olivier Brock, Romy Evans,[...]. Mol Autism 2021
0

Experimental Models to Study Autism Spectrum Disorders: hiPSCs, Rodents and Zebrafish.
Alba Pensado-López, Sara Veiga-Rúa, Ángel Carracedo, Catarina Allegue, Laura Sánchez. Genes (Basel) 2020
1


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

Characterizing vulnerable brain areas and circuits in mouse models of autism: Towards understanding pathogenesis and new therapeutic approaches.
Kelvin Hui, Yuta Katayama, Keiichi I Nakayama, Jun Nomura, Takeshi Sakurai. Neurosci Biobehav Rev 2020
6

Chd2 Is Necessary for Neural Circuit Development and Long-Term Memory.
Young J Kim, Sattar Khoshkhoo, Jan C Frankowski, Bingyao Zhu, Saad Abbasi, Sunyoung Lee, Ye Emily Wu, Robert F Hunt. Neuron 2018
22

Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of CHD8 Haploinsufficiency.
A Ayanna Wade, Kenneth Lim, Rinaldo Catta-Preta, Alex S Nord. Front Mol Neurosci 2019
12

The autism-associated protein CHD8 is required for cerebellar development and motor function.
Atsuki Kawamura, Yuta Katayama, Wataru Kakegawa, Daisuke Ino, Masaaki Nishiyama, Michisuke Yuzaki, Keiichi I Nakayama. Cell Rep 2021
0

Sequencing perturbed cortex development.
Barbara Treutlein, J Gray Camp. Science 2020
1

Regulatory genes and pathways disrupted in autism spectrum disorders.
Fatma Ayhan, Genevieve Konopka. Prog Neuropsychopharmacol Biol Psychiatry 2019
8

Lineage specific transcription factors and epigenetic regulators mediate TGFβ-dependent enhancer activation.
Raquel Fueyo, Simona Iacobucci, Stella Pappa, Conchi Estarás, Sergio Lois, Marta Vicioso-Mantis, Claudia Navarro, Sara Cruz-Molina, José Carlos Reyes, Álvaro Rada-Iglesias,[...]. Nucleic Acids Res 2018
10

Autism spectrum disorder: neuropathology and animal models.
Merina Varghese, Neha Keshav, Sarah Jacot-Descombes, Tahia Warda, Bridget Wicinski, Dara L Dickstein, Hala Harony-Nicolas, Silvia De Rubeis, Elodie Drapeau, Joseph D Buxbaum,[...]. Acta Neuropathol 2017
127

Oxytocin ameliorates impaired social behavior in a Chd8 haploinsufficiency mouse model of autism.
Stanislav M Cherepanov, Maria Gerasimenko, Teruko Yuhi, Kazumi Furuhara, Chiharu Tsuji, Shigeru Yokoyama, Keiichi I Nakayama, Masaaki Nishiyama, Haruhiro Higashida. BMC Neurosci 2021
0

The human chd8 gene is transcribed from two distant upstream promoters.
Gary R Kunkel, Hannah G Lisciandro, Hannah L Winter. Biochem Biophys Res Commun 2020
0

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

Neural stem cells in neuropsychiatric disorders.
Roberto Sacco, Emanuele Cacci, Gaia Novarino. Curr Opin Neurobiol 2018
22

Chromatin modification and epigenetic control in functional nerve regeneration.
Kalen P Berry, Q Richard Lu. Semin Cell Dev Biol 2020
1

Chd8 Rescued TBI-Induced Neurological Deficits by Suppressing Apoptosis and Autophagy Via Wnt Signaling Pathway.
Jie Chen, Haochen Wang, Chengliang Luo, Cheng Gao, Yalai Zhang, Guang Chen, Wei Chen, Xiping Chen, Luyang Tao. Cell Mol Neurobiol 2020
3

Morphological study of embryonic Chd8+/- mouse brains using light-sheet microscopy.
Harold F Gómez, Leonie Hodel, Odyssé Michos, Dagmar Iber. BMC Res Notes 2021
0

Chromatin Remodeler CHD8 in Autism and Brain Development.
Anke Hoffmann, Dietmar Spengler. J Clin Med 2021
2

Linking Autism Risk Genes to Disruption of Cortical Development.
Marta Garcia-Forn, Andrea Boitnott, Zeynep Akpinar, Silvia De Rubeis. Cells 2020
4

Autism Spectrum Disorder: Signaling Pathways and Prospective Therapeutic Targets.
Juliana Baranova, Guilherme Dragunas, Mayara C S Botellho, Ana Luisa P Ayub, Rebeca Bueno-Alves, Rebeca R Alencar, Debora D Papaiz, Mari C Sogayar, Henning Ulrich, Ricardo G Correa. Cell Mol Neurobiol 2021
7

Autism-associated CHD8 deficiency impairs axon development and migration of cortical neurons.
Qiong Xu, Yuan-Yuan Liu, Xiaoming Wang, Guo-He Tan, Hui-Ping Li, Samuel W Hulbert, Chun-Yang Li, Chun-Chun Hu, Zhi-Qi Xiong, Xiu Xu,[...]. Mol Autism 2018
29

Overlapping Molecular Pathways Leading to Autism Spectrum Disorders, Fragile X Syndrome, and Targeted Treatments.
Maria Jimena Salcedo-Arellano, Ana Maria Cabal-Herrera, Ruchi Harendra Punatar, Courtney Jessica Clark, Christopher Allen Romney, Randi J Hagerman. Neurotherapeutics 2021
2



The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective.
Britt Mossink, Moritz Negwer, Dirk Schubert, Nael Nadif Kasri. Cell Mol Life Sci 2021
3


Oligodendrocyte dysfunction due to Chd8 mutation gives rise to behavioral deficits in mice.
Atsuki Kawamura, Yuta Katayama, Masaaki Nishiyama, Hirotaka Shoji, Kota Tokuoka, Yoshifumi Ueta, Mariko Miyata, Tadashi Isa, Tsuyoshi Miyakawa, Akiko Hayashi-Takagi,[...]. Hum Mol Genet 2020
9

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

Exploring the role of RALYL in Alzheimer's disease reserve by network-based approaches.
Yixuan Zhang, Jiali Wang, Xiaoquan Liu, Haochen Liu. Alzheimers Res Ther 2020
0

Pathogenic POGZ mutation causes impaired cortical development and reversible autism-like phenotypes.
Kensuke Matsumura, Kaoru Seiriki, Shota Okada, Masashi Nagase, Shinya Ayabe, Ikuko Yamada, Tamio Furuse, Hirotoshi Shibuya, Yuka Yasuda, Hidenaga Yamamori,[...]. Nat Commun 2020
10

In vivo Perturb-Seq reveals neuronal and glial abnormalities associated with autism risk genes.
Xin Jin, Sean K Simmons, Amy Guo, Ashwin S Shetty, Michelle Ko, Lan Nguyen, Vahbiz Jokhi, Elise Robinson, Paul Oyler, Nathan Curry,[...]. Science 2020
15

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