A citation-based method for searching scientific literature

Anke Hoffmann, Dietmar Spengler. J Clin Med 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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
100

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
115
100

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
100

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
100

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
100

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
100

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
100

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
100

The CHD8 overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patients.
Philip J Ostrowski, Anna Zachariou, Chey Loveday, Ana Beleza-Meireles, Marta Bertoli, John Dean, Andrew G L Douglas, Ian Ellis, Alison Foster, John M Graham,[...]. Am J Med Genet C Semin Med Genet 2019
10
50

Excitation/Inhibition Imbalance in Animal Models of Autism Spectrum Disorders.
Eunee Lee, Jiseok Lee, Eunjoon Kim. Biol Psychiatry 2017
169
50

Chromatin remodelers: We are the drivers!!
Monica Tyagi, Nasir Imam, Kirtika Verma, Ashok K Patel. Nucleus 2016
44
50

Complex Oscillatory Waves Emerging from Cortical Organoids Model Early Human Brain Network Development.
Cleber A Trujillo, Richard Gao, Priscilla D Negraes, Jing Gu, Justin Buchanan, Sebastian Preissl, Allen Wang, Wei Wu, Gabriel G Haddad, Isaac A Chaim,[...]. Cell Stem Cell 2019
148
50

Whole-Neuron Synaptic Mapping Reveals Spatially Precise Excitatory/Inhibitory Balance Limiting Dendritic and Somatic Spiking.
Daniel Maxim Iascone, Yujie Li, Uygar Sümbül, Michael Doron, Hanbo Chen, Valentine Andreu, Finola Goudy, Heike Blockus, Larry F Abbott, Idan Segev,[...]. Neuron 2020
14
50


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
50

Auditory encoding abnormalities in children with autism spectrum disorder suggest delayed development of auditory cortex.
J Christopher Edgar, Charles L Fisk Iv, Jeffrey I Berman, Darina Chudnovskaya, Song Liu, Juhi Pandey, John D Herrington, Russell G Port, Robert T Schultz, Timothy P L Roberts. Mol Autism 2015
43
50

The Evf-2 noncoding RNA is transcribed from the Dlx-5/6 ultraconserved region and functions as a Dlx-2 transcriptional coactivator.
Jianchi Feng, Chunming Bi, Brian S Clark, Rina Mady, Palak Shah, Jhumku D Kohtz. Genes Dev 2006
504
50

Fragility and volatility of structural hubs in the human connectome.
Leonardo L Gollo, James A Roberts, Vanessa L Cropley, Maria A Di Biase, Christos Pantelis, Andrew Zalesky, Michael Breakspear. Nat Neurosci 2018
43
50

Structure and mechanism of helicases and nucleic acid translocases.
Martin R Singleton, Mark S Dillingham, Dale B Wigley. Annu Rev Biochem 2007
804
50

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
50

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
50

Maturation of auditory neural processes in autism spectrum disorder - A longitudinal MEG study.
Russell G Port, J Christopher Edgar, Matthew Ku, Luke Bloy, Rebecca Murray, Lisa Blaskey, Susan E Levy, Timothy P L Roberts. Neuroimage Clin 2016
40
50

Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures.
Roy Ben-Shalom, Caroline M Keeshen, Kiara N Berrios, Joon Y An, Stephan J Sanders, Kevin J Bender. Biol Psychiatry 2017
90
50

Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.
Huidan Wu, Honghui Li, Ting Bai, Lin Han, Jianjun Ou, Guanglei Xun, Yu Zhang, Yazhe Wang, Guiqin Duan, Ningxia Zhao,[...]. Clin Genet 2020
9
50


An in vivo model of functional and vascularized human brain organoids.
Abed AlFatah Mansour, J Tiago Gonçalves, Cooper W Bloyd, Hao Li, Sarah Fernandes, Daphne Quang, Stephen Johnston, Sarah L Parylak, Xin Jin, Fred H Gage. Nat Biotechnol 2018
319
50


Mechanisms underlying spontaneous patterned activity in developing neural circuits.
Aaron G Blankenship, Marla B Feller. Nat Rev Neurosci 2010
421
50

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
50

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
50

FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders.
Jessica Mariani, Gianfilippo Coppola, Ping Zhang, Alexej Abyzov, Lauren Provini, Livia Tomasini, Mariangela Amenduni, Anna Szekely, Dean Palejev, Michael Wilson,[...]. Cell 2015
508
50

Clinical Phenotypes of Carriers of Mutations in CHD8 or Its Conserved Target Genes.
Jennifer S Beighley, Caitlin M Hudac, Anne B Arnett, Jessica L Peterson, Jennifer Gerdts, Arianne S Wallace, Heather C Mefford, Kendra Hoekzema, Tychele N Turner, Brian J O'Roak,[...]. Biol Psychiatry 2020
12
50

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
50

Glia keep synapse distribution under wraps.
Laura E Clarke, Ben A Barres. Cell 2013
10
50

Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism.
Neelroop N Parikshak, Rui Luo, Alice Zhang, Hyejung Won, Jennifer K Lowe, Vijayendran Chandran, Steve Horvath, Daniel H Geschwind. Cell 2013
547
50

Metabolite alterations in autistic children: a 1H MR spectroscopy study.
B Kubas, W Kułak, W Sobaniec, E Tarasow, U Lebkowska, J Walecki. Adv Med Sci 2012
44
50

An early cell shape transition drives evolutionary expansion of the human forebrain.
Silvia Benito-Kwiecinski, Stefano L Giandomenico, Magdalena Sutcliffe, Erlend S Riis, Paula Freire-Pritchett, Iva Kelava, Stephanie Wunderlich, Ulrich Martin, Gregory A Wray, Kate McDole,[...]. Cell 2021
10
50

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
310
50

Revisiting the excitation/inhibition imbalance hypothesis of ASD through a clinical lens.
Russell G Port, Lindsay M Oberman, Timothy Pl Roberts. Br J Radiol 2019
8
50

A fully automated high-throughput workflow for 3D-based chemical screening in human midbrain organoids.
Henrik Renner, Martha Grabos, Katharina J Becker, Theresa E Kagermeier, Jie Wu, Mandy Otto, Stefan Peischard, Dagmar Zeuschner, Yaroslav TsyTsyura, Paul Disse,[...]. Elife 2020
21
50

Gene hunting in autism spectrum disorder: on the path to precision medicine.
Daniel H Geschwind, Matthew W State. Lancet Neurol 2015
240
50

Large-scale cellular-resolution gene profiling in human neocortex reveals species-specific molecular signatures.
Hongkui Zeng, Elaine H Shen, John G Hohmann, Seung Wook Oh, Amy Bernard, Joshua J Royall, Katie J Glattfelder, Susan M Sunkin, John A Morris, Angela L Guillozet-Bongaarts,[...]. Cell 2012
174
50

An SNP in an ultraconserved regulatory element affects Dlx5/Dlx6 regulation in the forebrain.
Luc Poitras, Man Yu, Cindy Lesage-Pelletier, Ryan B Macdonald, Jean-Philippe Gagné, Gary Hatch, Isabelle Kelly, Steven P Hamilton, John L R Rubenstein, Guy G Poirier,[...]. Development 2010
43
50

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
50

Individual brain organoids reproducibly form cell diversity of the human cerebral cortex.
Silvia Velasco, Amanda J Kedaigle, Sean K Simmons, Allison Nash, Marina Rocha, Giorgia Quadrato, Bruna Paulsen, Lan Nguyen, Xian Adiconis, Aviv Regev,[...]. Nature 2019
225
50

Excitation-inhibition dysbalance as predictor of autistic phenotypes.
Bárbara Oliveira, Marina Mitjans, Michael A Nitsche, Min-Fang Kuo, Hannelore Ehrenreich. J Psychiatr Res 2018
10
50

Human induced pluripotent stem cells for modelling neurodevelopmental disorders.
Karthikeyan Ardhanareeswaran, Jessica Mariani, Gianfilippo Coppola, Alexej Abyzov, Flora M Vaccarino. Nat Rev Neurol 2017
75
50

Glutamate and GABA in autism spectrum disorder-a translational magnetic resonance spectroscopy study in man and rodent models.
Jamie Horder, Marija M Petrinovic, Maria A Mendez, Andreas Bruns, Toru Takumi, Will Spooren, Gareth J Barker, Basil Künnecke, Declan G Murphy. Transl Psychiatry 2018
77
50

Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
Irina Voineagu, Xinchen Wang, Patrick Johnston, Jennifer K Lowe, Yuan Tian, Steve Horvath, Jonathan Mill, Rita M Cantor, Benjamin J Blencowe, Daniel H Geschwind. Nature 2011
50

Early nutrition influences developmental myelination and cognition in infants and young children.
Sean Deoni, Douglas Dean, Sarah Joelson, Jonathan O'Regan, Nora Schneider. Neuroimage 2018
35
50


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.