A citation-based method for searching scientific literature

Thomas Smol, Caroline Thuillier, Elise Boudry-Labis, Anne Dieux-Coeslier, Bénédicte Duban-Bedu, Roseline Caumes, Sonia Bouquillon, Sylvie Manouvrier-Hanu, Catherine Roche-Lestienne, Jamal Ghoumid. Neurogenetics 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Novel 14q11.2 microduplication including the CHD8 and SUPT16H genes associated with developmental delay.
Marta Smyk, Anna Poluha, Ilona Jaszczuk, Magdalena Bartnik, Joanna Bernaciak, Beata Nowakowska. Am J Med Genet A 2016
9
66

Identifying facial phenotypes of genetic disorders using deep learning.
Yaron Gurovich, Yair Hanani, Omri Bar, Guy Nadav, Nicole Fleischer, Dekel Gelbman, Lina Basel-Salmon, Peter M Krawitz, Susanne B Kamphausen, Martin Zenker,[...]. Nat Med 2019
129
33

Heterogeneous nuclear ribonucleoprotein C1/C2, MeCP1, and SWI/SNF form a chromatin remodeling complex at the beta-globin locus control region.
Milind C Mahajan, Geeta J Narlikar, Gokul Boyapaty, Robert E Kingston, Sherman M Weissman. Proc Natl Acad Sci U S A 2005
42
33

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
33

Elevated zero maze: a paradigm to evaluate antianxiety effects of drugs.
S K Kulkarni, K Singh, M Bishnoi. Methods Find Exp Clin Pharmacol 2007
61
33

Deficiency of Shank2 causes mania-like behavior that responds to mood stabilizers.
Andrea L Pappas, Alexandra L Bey, Xiaoming Wang, Mark Rossi, Yong Ho Kim, Haidun Yan, Fiona Porkka, Lara J Duffney, Samantha M Phillips, Xinyu Cao,[...]. JCI Insight 2017
23
33

Overview of mouse models of autism spectrum disorders.
Alexandra L Bey, Yong-hui Jiang. Curr Protoc Pharmacol 2014
32
33

Animal models of restricted repetitive behavior in autism.
Mark H Lewis, Yoko Tanimura, Linda W Lee, James W Bodfish. Behav Brain Res 2007
145
33

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
100


De novo variants in the Helicase-C domain of CHD8 are associated with severe phenotypes including autism, language disability and overgrowth.
Yu An, Linna Zhang, Wenwen Liu, Yunyun Jiang, Xue Chen, Xiaoping Lan, Gan Li, Qiang Hang, Jian Wang, James F Gusella,[...]. Hum Genet 2020
8
33

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
33

Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors.
Patrick E Rothwell, Marc V Fuccillo, Stephan Maxeiner, Scott J Hayton, Ozgun Gokce, Byung Kook Lim, Stephen C Fowler, Robert C Malenka, Thomas C Südhof. Cell 2014
240
33

Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.
Jinchen Li, Lin Wang, Hui Guo, Leisheng Shi, Kun Zhang, Meina Tang, Shanshan Hu, Shanshan Dong, Yanling Liu, Tianyun Wang,[...]. Mol Psychiatry 2017
39
33

Glutamatergic and GABAergic modulations of ultrasonic vocalizations during maternal separation distress in mouse pups.
Aki Takahashi, Jasmine J Yap, Dawnya Zitzman Bohager, Sara Faccidomo, Terry Clayton, James M Cook, Klaus A Miczek. Psychopharmacology (Berl) 2009
33
33

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
33

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
33

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
33

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
33

The clinical presentation caused by truncating CHD8 variants.
Sofia Douzgou, Hui Wen Liang, Kay Metcalfe, Suresh Somarathi, Marc Tischkowitz, Wafik Mohamed, Usha Kini, Shane McKee, Laura Yates, Marta Bertoli,[...]. Clin Genet 2019
15
33

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
33

A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf-Hirschhorn syndrome.
Gaetano Terrone, Gerarda Cappuccio, Rita Genesio, Annalisa Esposito, Valeria Fiorentino, Marina Riccitelli, Lucio Nitsch, Nicola Brunetti-Pierri, Ennio Del Giudice. Am J Med Genet A 2014
13
33

Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing.
Jinyu Wu, Ping Yu, Xin Jin, Xiu Xu, Jinchen Li, Zhongshan Li, Mingbang Wang, Tao Wang, Xueli Wu, Yi Jiang,[...]. J Genet Genomics 2018
7
33

Translational animal models of autism and neurodevelopmental disorders.
Jacqueline N Crawley. Dialogues Clin Neurosci 2012
106
33

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
33

A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8.
Heba Yasin, William T Gibson, Sylvie Langlois, Robert M Stowe, Erica S Tsang, Leora Lee, Jenny Poon, Grant Tran, Christine Tyson, Chi Kin Wong,[...]. J Hum Genet 2019
15
33


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
33

Prevalence of Motor Difficulties in Autism Spectrum Disorder: Analysis of a Population-Based Cohort.
Melissa K Licari, Gail A Alvares, Kandice Varcin, Kiah L Evans, Dominique Cleary, Siobhan L Reid, Emma J Glasson, Keely Bebbington, Jess E Reynolds, John Wray,[...]. Autism Res 2020
22
33

Behavioural phenotyping assays for mouse models of autism.
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
839
33

De novo genic mutations among a Chinese autism spectrum disorder cohort.
Tianyun Wang, Hui Guo, Bo Xiong, Holly A F Stessman, Huidan Wu, Bradley P Coe, Tychele N Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema,[...]. Nat Commun 2016
147
33

Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3.
Xiaoming Wang, Portia A McCoy, Ramona M Rodriguiz, Yanzhen Pan, H Shawn Je, Adam C Roberts, Caroline J Kim, Janet Berrios, Jennifer S Colvin, Danielle Bousquet-Moore,[...]. Hum Mol Genet 2011
325
33

Autism spectrum disorder early in development associated with CHD8 mutations among two Chinese children.
Jiangping Wang, Jinling Liu, Yi Gao, Kaixuan Wang, Kewen Jiang. BMC Pediatr 2018
5
33

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
33


Genetic Diagnostic Evaluation of Trio-Based Whole Exome Sequencing Among Children With Diagnosed or Suspected Autism Spectrum Disorder.
Xiujuan Du, Xueren Gao, Xin Liu, Lixiao Shen, Kai Wang, Yanjie Fan, Yu Sun, Xiaomei Luo, Huili Liu, Lili Wang,[...]. Front Genet 2018
10
33

Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice.
S S Moy, J J Nadler, A Perez, R P Barbaro, J M Johns, T R Magnuson, J Piven, J N Crawley. Genes Brain Behav 2004
807
33

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
33


Altered mGluR5-Homer scaffolds and corticostriatal connectivity in a Shank3 complete knockout model of autism.
Xiaoming Wang, Alexandra L Bey, Brittany M Katz, Alexandra Badea, Namsoo Kim, Lisa K David, Lara J Duffney, Sunil Kumar, Stephen D Mague, Samuel W Hulbert,[...]. Nat Commun 2016
131
33

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
33

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
33

Designing mouse behavioral tasks relevant to autistic-like behaviors.
Jacqueline N Crawley. Ment Retard Dev Disabil Res Rev 2004
313
33

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.
Y H Jiang, D Armstrong, U Albrecht, C M Atkins, J L Noebels, G Eichele, J D Sweatt, A L Beaudet. Neuron 1998
584
33

CHD8 intragenic deletion associated with autism spectrum disorder.
Elliot S Stolerman, Brooke Smith, Alka Chaubey, Julie R Jones. Eur J Med Genet 2016
16
33

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
33

Impact of MYH6 variants in hypoplastic left heart syndrome.
Aoy Tomita-Mitchell, Karl D Stamm, Donna K Mahnke, Min-Su Kim, Pip M Hidestrand, Huan Ling Liang, Mary A Goetsch, Mats Hidestrand, Pippa Simpson, Andrew N Pelech,[...]. Physiol Genomics 2016
34
33

Turner's syndrome in fetal life.
E Surerus, I C Huggon, L D Allan. Ultrasound Obstet Gynecol 2003
46
33

Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects.
Javier T Granados-Riveron, Tushar K Ghosh, Mark Pope, Frances Bu'Lock, Christopher Thornborough, Jacqueline Eason, Edwin P Kirk, Diane Fatkin, Michael P Feneley, Richard P Harvey,[...]. Hum Mol Genet 2010
81
33

Effect of copy number variants on outcomes for infants with single ventricle heart defects.
Abigail S Carey, Li Liang, Jonathan Edwards, Tracy Brandt, Hui Mei, Andrew J Sharp, Daphne T Hsu, Jane W Newburger, Richard G Ohye, Wendy K Chung,[...]. Circ Cardiovasc Genet 2013
53
33


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.