A citation-based method for searching scientific literature

Hongyuan Wei, Yunjiao Zhu, Tianli Wang, Xueqing Zhang, Kexin Zhang, Zhihua Zhang. J Neural Transm (Vienna) 2021
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


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
40

Heritability of autism spectrum disorders: a meta-analysis of twin studies.
Beata Tick, Patrick Bolton, Francesca Happé, Michael Rutter, Frühling Rijsdijk. J Child Psychol Psychiatry 2016
334
40

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
40

Childhood Functional Gastrointestinal Disorders: Neonate/Toddler.
Marc A Benninga, Christophe Faure, Paul E Hyman, Ian St James Roberts, Neil L Schechter, Samuel Nurko. Gastroenterology 2016
208
40


Neural Subtype Specification from Human Pluripotent Stem Cells.
Yunlong Tao, Su-Chun Zhang. Cell Stem Cell 2016
144
20

Transcriptome-wide transmission disequilibrium analysis identifies novel risk genes for autism spectrum disorder.
Kunling Huang, Yuchang Wu, Junha Shin, Ye Zheng, Alireza Fotuhi Siahpirani, Yupei Lin, Zheng Ni, Jiawen Chen, Jing You, Sunduz Keles,[...]. PLoS Genet 2021
6
20


Comparing the MicroRNA spectrum between serum and plasma.
Kai Wang, Yue Yuan, Ji-Hoon Cho, Sara McClarty, David Baxter, David J Galas. PLoS One 2012
461
20

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
841
20


A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden.
S Steffenburg, C Gillberg, L Hellgren, L Andersson, I C Gillberg, G Jakobsson, M Bohman. J Child Psychol Psychiatry 1989
543
20

Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
Christel Depienne, Daniel Moreno-De-Luca, Delphine Heron, Delphine Bouteiller, Aurélie Gennetier, Richard Delorme, Pauline Chaste, Jean-Pierre Siffroi, Sandra Chantot-Bastaraud, Baya Benyahia,[...]. Biol Psychiatry 2009
90
20

Most mammalian mRNAs are conserved targets of microRNAs.
Robin C Friedman, Kyle Kai-How Farh, Christopher B Burge, David P Bartel. Genome Res 2009
20

EEG endophenotypes in autism spectrum disorder.
Jamie K Capal, Christopher Carosella, Elora Corbin, Paul S Horn, Rebecca Caine, Patricia Manning-Courtney. Epilepsy Behav 2018
11
20



Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders.
Elaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, Christine Stevens, Aniko Sabo, Daniel G MacArthur, Benjamin M Neale, Andrew Kirby, Douglas M Ruderfer, Menachem Fromer,[...]. Neuron 2013
171
20

Neuroimaging endophenotypes in autism spectrum disorder.
Rajneesh Mahajan, Stewart H Mostofsky. CNS Spectr 2015
21
20

Language delay aggregates in toddler siblings of children with autism spectrum disorder.
N Marrus, L P Hall, S J Paterson, J T Elison, J J Wolff, M R Swanson, J Parish-Morris, A T Eggebrecht, J R Pruett, H C Hazlett,[...]. J Neurodev Disord 2018
20
20


The multilayered complexity of ceRNA crosstalk and competition.
Yvonne Tay, John Rinn, Pier Paolo Pandolfi. Nature 2014
20

Aberrant expression of long noncoding RNAs in autistic brain.
Mark N Ziats, Owen M Rennert. J Mol Neurosci 2013
141
20

CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in cerebral organoids derived from iPS cells.
Ping Wang, Ryan Mokhtari, Erika Pedrosa, Michael Kirschenbaum, Can Bayrak, Deyou Zheng, Herbert M Lachman. Mol Autism 2017
144
20


Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
20


Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene.
Ashok Patowary, So Yeon Won, Shin Ji Oh, Ryan R Nesbitt, Marilyn Archer, Debbie Nickerson, Wendy H Raskind, Raphael Bernier, Ji Eun Lee, Zoran Brkanac. Transl Psychiatry 2019
6
20


Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
706
20

Exome sequencing makes medical genomics a reality.
Leslie G Biesecker. Nat Genet 2010
108
20

Gene regulation by long non-coding RNAs and its biological functions.
Luisa Statello, Chun-Jie Guo, Ling-Ling Chen, Maite Huarte. Nat Rev Mol Cell Biol 2021
686
20

NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism.
Hui Guo, Qiumeng Zhang, Rujia Dai, Bin Yu, Kendra Hoekzema, Jieqiong Tan, Senwei Tan, Xiangbin Jia, Wendy K Chung, Rebecca Hernan,[...]. Am J Hum Genet 2020
5
20

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
6
20

Genomic Patterns of De Novo Mutation in Simplex Autism.
Tychele N Turner, Bradley P Coe, Diane E Dickel, Kendra Hoekzema, Bradley J Nelson, Michael C Zody, Zev N Kronenberg, Fereydoun Hormozdiari, Archana Raja, Len A Pennacchio,[...]. Cell 2017
163
20

Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder.
Namshin Kim, Kyoung Hyoun Kim, Won-Jun Lim, Jiwoong Kim, Soon Ae Kim, Hee Jeong Yoo. Genes (Basel) 2020
5
20

Serum microRNA profiles in children with autism.
Mahesh Mundalil Vasu, Ayyappan Anitha, Ismail Thanseem, Katsuaki Suzuki, Kohei Yamada, Taro Takahashi, Tomoyasu Wakuda, Keiko Iwata, Masatsugu Tsujii, Toshirou Sugiyama,[...]. Mol Autism 2014
130
20

Transcriptional Gene Silencing of the Autism-Associated Long Noncoding RNA MSNP1AS in Human Neural Progenitor Cells.
Jessica J DeWitt, Patrick M Hecht, Nicole Grepo, Brent Wilkinson, Oleg V Evgrafov, Kevin V Morris, James A Knowles, Daniel B Campbell. Dev Neurosci 2016
13
20

Clinical Genetic Aspects of ASD Spectrum Disorders.
G Bradley Schaefer. Int J Mol Sci 2016
42
20

Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
Daniel Benjamin Callaghan, Sanja Rogic, Powell Patrick Cheng Tan, Kristina Calli, Ying Qiao, Robert Baldwin, Matthew Jacobson, Manuel Belmadani, Nathan Holmes, Chang Yu,[...]. Clin Genet 2019
10
20

A genome-wide scan for common alleles affecting risk for autism.
Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams, Nuala Sykes, Alistair T Pagnamenta,[...]. Hum Mol Genet 2010
412
20

The genetics of autism.
Rebecca Muhle, Stephanie V Trentacoste, Isabelle Rapin. Pediatrics 2004
661
20

Mechanisms of Long Non-Coding RNAs in the Assembly and Plasticity of Neural Circuitry.
Andi Wang, Junbao Wang, Ying Liu, Yan Zhou. Front Neural Circuits 2017
25
20

Beyond the Exome: The Non-coding Genome and Enhancers in Neurodevelopmental Disorders and Malformations of Cortical Development.
Elena Perenthaler, Soheil Yousefi, Eva Niggl, Tahsin Stefan Barakat. Front Cell Neurosci 2019
27
20


Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.
Maricela Alarcón, Rita M Cantor, Jianjun Liu, T Conrad Gilliam, Daniel H Geschwind. Am J Hum Genet 2002
203
20

History, Discovery, and Classification of lncRNAs.
Julien Jarroux, Antonin Morillon, Marina Pinskaya. Adv Exp Med Biol 2017
407
20

Genome-wide differential expression of synaptic long noncoding RNAs in autism spectrum disorder.
Y Wang, X Zhao, W Ju, M Flory, J Zhong, S Jiang, P Wang, X Dong, X Tao, Q Chen,[...]. Transl Psychiatry 2015
54
20

Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.
Tychele N Turner, Fereydoun Hormozdiari, Michael H Duyzend, Sarah A McClymont, Paul W Hook, Ivan Iossifov, Archana Raja, Carl Baker, Kendra Hoekzema, Holly A Stessman,[...]. Am J Hum Genet 2016
168
20



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.