A citation-based method for searching scientific literature

Sahar Avazzadeh, Katya McDonagh, Jamie Reilly, Yanqin Wang, Stephanie D Boomkamp, Veronica McInerney, Janusz Krawczyk, Jacqueline Fitzgerald, Niamh Feerick, Matthew O'Sullivan, Amirhossein Jalali, Eva B Forman, Sally A Lynch, Sean Ennis, Nele Cosemans, Hilde Peeters, Peter Dockery, Timothy O'Brien, Leo R Quinlan, Louise Gallagher, Sanbing Shen. Mol Autism 2019
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality.
Matti Lam, Mohsen Moslem, Julien Bryois, Robin J Pronk, Elias Uhlin, Ivar Dehnisch Ellström, Loora Laan, Jessica Olive, Rebecca Morse, Harriet Rönnholm,[...]. Exp Cell Res 2019
19
63

Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1.
ChangHui Pak, Tamas Danko, Yingsha Zhang, Jason Aoto, Garret Anderson, Stephan Maxeiner, Fei Yi, Marius Wernig, Thomas C Südhof. Cell Stem Cell 2015
115
63

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
45

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
45

Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons.
Eric Deneault, Sean H White, Deivid C Rodrigues, P Joel Ross, Muhammad Faheem, Kirill Zaslavsky, Zhuozhi Wang, Roumiana Alexandrova, Giovanna Pellecchia, Wei Wei,[...]. Stem Cell Reports 2018
35
45

SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neurons.
Kirill Zaslavsky, Wen-Bo Zhang, Fraser P McCready, Deivid C Rodrigues, Eric Deneault, Caitlin Loo, Melody Zhao, P Joel Ross, Joelle El Hajjar, Asli Romm,[...]. Nat Neurosci 2019
48
45

Uncovering the Functional Link Between SHANK3 Deletions and Deficiency in Neurodevelopment Using iPSC-Derived Human Neurons.
Guanqun Huang, Shuting Chen, Xiaoxia Chen, Jiajun Zheng, Zhuoran Xu, Abolfazl Doostparast Torshizi, Siyi Gong, Qingpei Chen, Xiaokuang Ma, Jiandong Yu,[...]. Front Neuroanat 2019
18
45

Stem cell-derived neurons from autistic individuals with SHANK3 mutation show morphogenetic abnormalities during early development.
A Kathuria, P Nowosiad, R Jagasia, S Aigner, R D Taylor, L C Andreae, N J F Gatford, W Lucchesi, D P Srivastava, J Price. Mol Psychiatry 2018
45
45

Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations.
Laura Gouder, Aline Vitrac, Hany Goubran-Botros, Anne Danckaert, Jean-Yves Tinevez, Gwenaëlle André-Leroux, Ekaterina Atanasova, Nathalie Lemière, Anne Biton, Claire S Leblond,[...]. Sci Rep 2019
27
45

Pathological priming causes developmental gene network heterochronicity in autistic subject-derived neurons.
Simon T Schafer, Apua C M Paquola, Shani Stern, David Gosselin, Manching Ku, Monique Pena, Thomas J M Kuret, Marvin Liyanage, Abed AlFatah Mansour, Baptiste N Jaeger,[...]. Nat Neurosci 2019
91
36

Synaptic Dysfunction in Human Neurons With Autism-Associated Deletions in PTCHD1-AS.
P Joel Ross, Wen-Bo Zhang, Rebecca S F Mok, Kirill Zaslavsky, Eric Deneault, Lia D'Abate, Deivid C Rodrigues, Ryan K C Yuen, Muhammad Faheem, Marat Mufteev,[...]. Biol Psychiatry 2020
23
36

Neuroligin-4 Regulates Excitatory Synaptic Transmission in Human Neurons.
Samuele G Marro, Soham Chanda, Nan Yang, Justyna A Janas, Giulio Valperga, Justin Trotter, Bo Zhou, Sean Merrill, Issa Yousif, Hannah Shelby,[...]. Neuron 2019
25
36

Autism-associated SHANK3 haploinsufficiency causes Ih channelopathy in human neurons.
Fei Yi, Tamas Danko, Salome Calado Botelho, Christopher Patzke, ChangHui Pak, Marius Wernig, Thomas C Südhof. Science 2016
150
36

Human Pluripotent Stem Cell-derived Cortical Neurons for High Throughput Medication Screening in Autism: A Proof of Concept Study in SHANK3 Haploinsufficiency Syndrome.
Hélène Darville, Aurélie Poulet, Frédérique Rodet-Amsellem, Laure Chatrousse, Julie Pernelle, Claire Boissart, Delphine Héron, Caroline Nava, Anselme Perrier, Margot Jarrige,[...]. EBioMedicine 2016
48
36

Neuronal impact of patient-specific aberrant NRXN1α splicing.
Erin Flaherty, Shijia Zhu, Natalie Barretto, Esther Cheng, P J Michael Deans, Michael B Fernando, Nadine Schrode, Nancy Francoeur, Alesia Antoine, Khaled Alganem,[...]. Nat Genet 2019
24
36

Assembly of functionally integrated human forebrain spheroids.
Fikri Birey, Jimena Andersen, Christopher D Makinson, Saiful Islam, Wu Wei, Nina Huber, H Christina Fan, Kimberly R Cordes Metzler, Georgia Panagiotakos, Nicholas Thom,[...]. Nature 2017
411
36

Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models.
Liyun Zeng, Peilin Zhang, Lingling Shi, Vicky Yamamoto, Wange Lu, Kai Wang. PLoS One 2013
38
36

Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons.
Brooke A DeRosa, Jimmy El Hokayem, Elena Artimovich, Catherine Garcia-Serje, Andre W Phillips, Derek Van Booven, Jonathan E Nestor, Lily Wang, Michael L Cuccaro, Jeffery M Vance,[...]. Sci Rep 2018
37
36

Single-cell genomics identifies cell type-specific molecular changes in autism.
Dmitry Velmeshev, Lucas Schirmer, Diane Jung, Maximilian Haeussler, Yonatan Perez, Simone Mayer, Aparna Bhaduri, Nitasha Goyal, David H Rowitch, Arnold R Kriegstein. Science 2019
136
36

CNTN5-/+or EHMT2-/+human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networks.
Eric Deneault, Muhammad Faheem, Sean H White, Deivid C Rodrigues, Song Sun, Wei Wei, Alina Piekna, Tadeo Thompson, Jennifer L Howe, Leon Chalil,[...]. Elife 2019
25
36

SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients.
Aleksandr Shcheglovitov, Olesya Shcheglovitova, Masayuki Yazawa, Thomas Portmann, Rui Shu, Vittorio Sebastiano, Anna Krawisz, Wendy Froehlich, Jonathan A Bernstein, Joachim F Hallmayer,[...]. Nature 2013
288
36

Altered neuronal network and rescue in a human MECP2 duplication model.
S Nageshappa, C Carromeu, C A Trujillo, P Mesci, I Espuny-Camacho, E Pasciuto, P Vanderhaeghen, C M Verfaillie, S Raitano, A Kumar,[...]. Mol Psychiatry 2016
65
36

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
36

Atypical behaviour and connectivity in SHANK3-mutant macaques.
Yang Zhou, Jitendra Sharma, Qiong Ke, Rogier Landman, Jingli Yuan, Hong Chen, David S Hayden, John W Fisher, Minqing Jiang, William Menegas,[...]. Nature 2019
53
27

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.
Michael J Gandal, Jillian R Haney, Neelroop N Parikshak, Virpi Leppa, Gokul Ramaswami, Chris Hartl, Andrew J Schork, Vivek Appadurai, Alfonso Buil, Thomas M Werge,[...]. Science 2018
398
27

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
27

Disrupted neuronal maturation in Angelman syndrome-derived induced pluripotent stem cells.
James J Fink, Tiwanna M Robinson, Noelle D Germain, Carissa L Sirois, Kaitlyn A Bolduc, Amanda J Ward, Frank Rigo, Stormy J Chamberlain, Eric S Levine. Nat Commun 2017
44
27

Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling.
Stuart M Chambers, Christopher A Fasano, Eirini P Papapetrou, Mark Tomishima, Michel Sadelain, Lorenz Studer. Nat Biotechnol 2009
27

Fused cerebral organoids model interactions between brain regions.
Joshua A Bagley, Daniel Reumann, Shan Bian, Julie Lévi-Strauss, Juergen A Knoblich. Nat Methods 2017
232
27

Environmental risk factors for autism: an evidence-based review of systematic reviews and meta-analyses.
Amirhossein Modabbernia, Eva Velthorst, Abraham Reichenberg. Mol Autism 2017
216
27

Induction of pluripotent stem cells from adult human fibroblasts by defined factors.
Kazutoshi Takahashi, Koji Tanabe, Mari Ohnuki, Megumi Narita, Tomoko Ichisaka, Kiichiro Tomoda, Shinya Yamanaka. Cell 2007
27

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
27

Transcriptome of iPSC-derived neuronal cells reveals a module of co-expressed genes consistently associated with autism spectrum disorder.
K Griesi-Oliveira, M S Fogo, B G G Pinto, A Y Alves, A M Suzuki, A G Morales, S Ezquina, O J Sosa, G J Sutton, D Y Sunaga-Franze,[...]. Mol Psychiatry 2021
16
27

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
27

Generation of pure GABAergic neurons by transcription factor programming.
Nan Yang, Soham Chanda, Samuele Marro, Yi-Han Ng, Justyna A Janas, Daniel Haag, Cheen Euong Ang, Yunshuo Tang, Quetzal Flores, Moritz Mall,[...]. Nat Methods 2017
121
27

Modeling the Interplay Between Neurons and Astrocytes in Autism Using Human Induced Pluripotent Stem Cells.
Fabiele Baldino Russo, Beatriz Camille Freitas, Graciela Conceição Pignatari, Isabella Rodrigues Fernandes, Jonathan Sebat, Alysson Renato Muotri, Patricia Cristina Baleeiro Beltrão-Braga. Biol Psychiatry 2018
59
27

Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome.
Sergiu P Paşca, Thomas Portmann, Irina Voineagu, Masayuki Yazawa, Aleksandr Shcheglovitov, Anca M Paşca, Branden Cord, Theo D Palmer, Sachiko Chikahisa, Seiji Nishino,[...]. Nat Med 2011
378
27

Altered proliferation and networks in neural cells derived from idiopathic autistic individuals.
Maria C Marchetto, Haim Belinson, Yuan Tian, Beatriz C Freitas, Chen Fu, Krishna Vadodaria, Patricia Beltrao-Braga, Cleber A Trujillo, Ana P D Mendes, Krishnan Padmanabhan,[...]. Mol Psychiatry 2017
170
27

Cellular Phenotypes in Human iPSC-Derived Neurons from a Genetic Model of Autism Spectrum Disorder.
Aditi Deshpande, Smita Yadav, Dang Q Dao, Zhi-Yong Wu, Kenton C Hokanson, Michelle K Cahill, Arun P Wiita, Yuh-Nung Jan, Erik M Ullian, Lauren A Weiss. Cell Rep 2017
48
27

Idiopathic Autism: Cellular and Molecular Phenotypes in Pluripotent Stem Cell-Derived Neurons.
Xiaozhuo Liu, Emilie Campanac, Hoi-Hung Cheung, Mark N Ziats, Lucile Canterel-Thouennon, Margarita Raygada, Vanessa Baxendale, Alan Lap-Yin Pang, Lu Yang, Susan Swedo,[...]. Mol Neurobiol 2017
32
27

Rapid single-step induction of functional neurons from human pluripotent stem cells.
Yingsha Zhang, Changhui Pak, Yan Han, Henrik Ahlenius, Zhenjie Zhang, Soham Chanda, Samuele Marro, Christopher Patzke, Claudio Acuna, Jason Covy,[...]. Neuron 2013
571
27

A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells.
Maria C N Marchetto, Cassiano Carromeu, Allan Acab, Diana Yu, Gene W Yeo, Yangling Mu, Gong Chen, Fred H Gage, Alysson R Muotri. Cell 2010
856
27

Induced pluripotent stem cell technology: a decade of progress.
Yanhong Shi, Haruhisa Inoue, Joseph C Wu, Shinya Yamanaka. Nat Rev Drug Discov 2017
487
27

Autism spectrum disorder: insights into convergent mechanisms from transcriptomics.
Mathieu Quesnel-Vallières, Robert J Weatheritt, Sabine P Cordes, Benjamin J Blencowe. Nat Rev Genet 2019
49
27

Heterozygous deletion of α-neurexin I or α-neurexin II results in behaviors relevant to autism and schizophrenia.
James Dachtler, Jose L Ivorra, Tessa E Rowland, Colin Lever, R John Rodgers, Steven J Clapcote. Behav Neurosci 2015
39
27

LRRTMs and neuroligins bind neurexins with a differential code to cooperate in glutamate synapse development.
Tabrez J Siddiqui, Raika Pancaroglu, Yunhee Kang, Amanda Rooyakkers, Ann Marie Craig. J Neurosci 2010
190
27


Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature.
Frédérique Béna, Damien L Bruno, Mats Eriksson, Conny van Ravenswaaij-Arts, Zornitza Stark, Trijnie Dijkhuizen, Erica Gerkes, Stefania Gimelli, Devika Ganesamoorthy, Ann Charlotte Thuresson,[...]. Am J Med Genet B Neuropsychiatr Genet 2013
68
27

Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons.
K Griesi-Oliveira, A Acab, A R Gupta, D Y Sunaga, T Chailangkarn, X Nicol, Y Nunez, M F Walker, J D Murdoch, S J Sanders,[...]. Mol Psychiatry 2015
125
27

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
27


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.