A citation-based method for searching scientific literature

Eduarda Morgana da Silva Montenegro, Claudia Samogy Costa, Gabriele Campos, Marília Scliar, Tatiana Ferreira de Almeida, Elaine Cristina Zachi, Isabela Maya Wahys Silva, Ada J S Chan, Mehdi Zarrei, Naila C V Lourenço, Guilherme Lopes Yamamoto, Stephen Scherer, Maria Rita Passos-Bueno. Autism Res 2020
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Rare RELN variants affect Reelin-DAB1 signal transduction in autism spectrum disorder.
Sandra M Sánchez-Sánchez, Juliana Magdalon, Karina Griesi-Oliveira, Guilherme L Yamamoto, Carolina Santacruz-Perez, Mariana Fogo, Maria Rita Passos-Bueno, Andrea L Sertié. Hum Mutat 2018
13
40

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
40

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
40

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
601
40

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
40

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

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
40


Cullin-3 targets cyclin E for ubiquitination and controls S phase in mammalian cells.
J D Singer, M Gurian-West, B Clurman, J M Roberts. Genes Dev 1999
315
40

Constitutive turnover of cyclin E by Cul3 maintains quiescence.
Justina D McEvoy, Uta Kossatz, Nisar Malek, Jeffrey D Singer. Mol Cell Biol 2007
45
40


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
20


The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.
Cynthia J Curry, Jill A Rosenfeld, Erica Grant, Karen W Gripp, Carol Anderson, Arthur S Aylsworth, Taha Ben Saad, Victor V Chizhikov, Giedre Dybose, Christina Fagerberg,[...]. Am J Med Genet A 2013
37
20

The familial risk of autism.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
482
20

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
20

Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with post-mortem adult brains.
Gabriel E Hoffman, Brigham J Hartley, Erin Flaherty, Ian Ladran, Peter Gochman, Douglas M Ruderfer, Eli A Stahl, Judith Rapoport, Pamela Sklar, Kristen J Brennand. Nat Commun 2017
64
20

Immune transcriptome alterations in the temporal cortex of subjects with autism.
Krassimira Garbett, Philip J Ebert, Amanda Mitchell, Carla Lintas, Barbara Manzi, Károly Mirnics, Antonio M Persico. Neurobiol Dis 2008
247
20

Head circumference and brain size in autism spectrum disorder: A systematic review and meta-analysis.
Roberto Sacco, Stefano Gabriele, Antonio M Persico. Psychiatry Res 2015
90
20

Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome.
Yuan Tian, Irina Voineagu, Sergiu P Paşca, Hyejung Won, Vijayendran Chandran, Steve Horvath, Ricardo E Dolmetsch, Daniel H Geschwind. Genome Med 2014
56
20


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
20

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
20

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.
Jack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, Stephan J Sanders, Kamil Slowikowski, Monkol Lek, Konrad J Karczewski, David J Cutler, Bernie Devlin, Kathryn Roeder,[...]. Nat Genet 2017
152
20

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
20

Searching for convergent pathways in autism spectrum disorders: insights from human brain transcriptome studies.
Akira Gokoolparsadh, Gavin J Sutton, Alexiy Charamko, Nicole F Oldham Green, Christopher J Pardy, Irina Voineagu. Cell Mol Life Sci 2016
13
20

Blood transcriptomic comparison of individuals with and without autism spectrum disorder: A combined-samples mega-analysis.
Daniel S Tylee, Jonathan L Hess, Thomas P Quinn, Rahul Barve, Hailiang Huang, Yanli Zhang-James, Jeffrey Chang, Boryana S Stamova, Frank R Sharp, Irva Hertz-Picciotto,[...]. Am J Med Genet B Neuropsychiatr Genet 2017
25
20

Spatio-temporal transcriptome of the human brain.
Hyo Jung Kang, Yuka Imamura Kawasawa, Feng Cheng, Ying Zhu, Xuming Xu, Mingfeng Li, André M M Sousa, Mihovil Pletikos, Kyle A Meyer, Goran Sedmak,[...]. Nature 2011
20

Normalization of RNA-seq data using factor analysis of control genes or samples.
Davide Risso, John Ngai, Terence P Speed, Sandrine Dudoit. Nat Biotechnol 2014
667
20

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
20

TopHat: discovering splice junctions with RNA-Seq.
Cole Trapnell, Lior Pachter, Steven L Salzberg. Bioinformatics 2009
20

Novel roles of amyloid-beta precursor protein metabolites in fragile X syndrome and autism.
C J Westmark, D K Sokol, B Maloney, D K Lahiri. Mol Psychiatry 2016
24
20

Is my network module preserved and reproducible?
Peter Langfelder, Rui Luo, Michael C Oldham, Steve Horvath. PLoS Comput Biol 2011
443
20

Autism Spectrum Symptomatology in Children with Williams Syndrome Who Have Phrase Speech or Fluent Language.
Bonita P Klein-Tasman, Faye van der Fluit, Carolyn B Mervis. J Autism Dev Disord 2018
16
20

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
20

Ion Mobility-Enhanced Data-Independent Acquisitions Enable a Deep Proteomic Landscape of Oligodendrocytes.
Juliana S Cassoli, Caroline Brandão-Teles, Aline G Santana, Gustavo H M F Souza, Daniel Martins-de-Souza. Proteomics 2017
4
25

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).
Brett S Abrahams, Dan E Arking, Daniel B Campbell, Heather C Mefford, Eric M Morrow, Lauren A Weiss, Idan Menashe, Tim Wadkins, Sharmila Banerjee-Basu, Alan Packer. Mol Autism 2013
250
20

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
20

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
A Jeremy Willsey, Stephan J Sanders, Mingfeng Li, Shan Dong, Andrew T Tebbenkamp, Rebecca A Muhle, Steven K Reilly, Leon Lin, Sofia Fertuzinhos, Jeremy A Miller,[...]. Cell 2013
475
20

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
20

A quantitative framework to evaluate modeling of cortical development by neural stem cells.
Jason L Stein, Luis de la Torre-Ubieta, Yuan Tian, Neelroop N Parikshak, Israel A Hernández, Maria C Marchetto, Dylan K Baker, Daning Lu, Cassidy R Hinman, Jennifer K Lowe,[...]. Neuron 2014
113
20


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
20

Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014.
Jon Baio, Lisa Wiggins, Deborah L Christensen, Matthew J Maenner, Julie Daniels, Zachary Warren, Margaret Kurzius-Spencer, Walter Zahorodny, Cordelia Robinson Rosenberg, Tiffany White,[...]. MMWR Surveill Summ 2018
20

IDGenetics: a comprehensive database for genes and mutations of intellectual disability related disorders.
Chong Chen, Denghui Chen, Huangqi Xue, Xinting Liu, Tao Zhang, Shaohua Tang, Wei Li, Xueqin Xu. Neurosci Lett 2018
5
20

Genetics and epigenetics of autism spectrum disorder-current evidence in the field.
Barbara Wiśniowiecka-Kowalnik, Beata Anna Nowakowska. J Appl Genet 2019
46
20

iPSC-derived forebrain neurons from FXS individuals show defects in initial neurite outgrowth.
Matthew E Doers, Michael T Musser, Robert Nichol, Erich R Berndt, Mei Baker, Timothy M Gomez, Su-Chun Zhang, Leonard Abbeduto, Anita Bhattacharyya. Stem Cells Dev 2014
103
20

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.
Michael J Gandal, Pan Zhang, Evi Hadjimichael, Rebecca L Walker, Chao Chen, Shuang Liu, Hyejung Won, Harm van Bakel, Merina Varghese, Yongjun Wang,[...]. Science 2018
298
20

HTSeq--a Python framework to work with high-throughput sequencing data.
Simon Anders, Paul Theodor Pyl, Wolfgang Huber. Bioinformatics 2015
20

WGCNA: an R package for weighted correlation network analysis.
Peter Langfelder, Steve Horvath. BMC Bioinformatics 2008
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.