A citation-based method for searching scientific literature

Marta Garcia-Forn, Andrea Boitnott, Zeynep Akpinar, Silvia De Rubeis. Cells 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


A Translational Repression Complex in Developing Mammalian Neural Stem Cells that Regulates Neuronal Specification.
Siraj K Zahr, Guang Yang, Hilal Kazan, Michael J Borrett, Scott A Yuzwa, Anastassia Voronova, David R Kaplan, Freda D Miller. Neuron 2018
56
50

Translational derepression of Elavl4 isoforms at their alternative 5' UTRs determines neuronal development.
Tatiana Popovitchenko, Yongkyu Park, Nicholas F Page, Xiaobing Luo, Zeljka Krsnik, Yuan Liu, Iva Salamon, Jessica D Stephenson, Matthew L Kraushar, Nicole L Volk,[...]. Nat Commun 2020
9
50

Thalamic WNT3 Secretion Spatiotemporally Regulates the Neocortical Ribosome Signature and mRNA Translation to Specify Neocortical Cell Subtypes.
Matthew L Kraushar, Barbara Viljetic, H R Sagara Wijeratne, Kevin Thompson, Xinfu Jiao, Jack W Pike, Vera Medvedeva, Matthias Groszer, Megerditch Kiledjian, Ronald P Hart,[...]. J Neurosci 2015
27
50

The RNA binding protein HuR determines the differential translation of autism-associated FoxP subfamily members in the developing neocortex.
T Popovitchenko, K Thompson, B Viljetic, X Jiao, D L Kontonyiannis, M Kiledjian, R P Hart, M R Rasin. Sci Rep 2016
22
50

Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development.
Ashley L Lennox, Mariah L Hoye, Ruiji Jiang, Bethany L Johnson-Kerner, Lindsey A Suit, Srivats Venkataramanan, Charles J Sheehan, Fernando C Alsina, Brieana Fregeau, Kimberly A Aldinger,[...]. Neuron 2020
28
50

Prenatal deletion of the RNA-binding protein HuD disrupts postnatal cortical circuit maturation and behavior.
Erik M DeBoer, Ricardo Azevedo, Taylor A Vega, Jesse Brodkin, Wado Akamatsu, Hideyuki Okano, George C Wagner, Mladen-Roko Rasin. J Neurosci 2014
36
50

Temporally defined neocortical translation and polysome assembly are determined by the RNA-binding protein Hu antigen R.
Matthew L Kraushar, Kevin Thompson, H R Sagara Wijeratne, Barbara Viljetic, Kristina Sakers, Justin W Marson, Dimitris L Kontoyiannis, Steven Buyske, Ronald P Hart, Mladen-Roko Rasin. Proc Natl Acad Sci U S A 2014
52
50

Translational Diagnostics: An In-House Pipeline to Validate Genetic Variants in Children with Undiagnosed and Rare Diseases.
Jordi Pijuan, María Rodríguez-Sanz, Daniel Natera-de Benito, Carlos Ortez, Arola Altimir, Mireia Osuna-López, Montserrat Roura, Maddi Ugalde, Liedewei Van de Vondel, Judith Reina-Castillón,[...]. J Mol Diagn 2021
2
50

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
25

Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia.
S Mah, M R Nelson, L E Delisi, R H Reneland, N Markward, M R James, D R Nyholt, N Hayward, H Handoko, B Mowry,[...]. Mol Psychiatry 2006
99
25

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
533
25

STRING v11: protein-protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets.
Damian Szklarczyk, Annika L Gable, David Lyon, Alexander Junge, Stefan Wyder, Jaime Huerta-Cepas, Milan Simonovic, Nadezhda T Doncheva, John H Morris, Peer Bork,[...]. Nucleic Acids Res 2019
25

NGL-2 Deletion Leads to Autistic-like Behaviors Responsive to NMDAR Modulation.
Seung Min Um, Seungmin Ha, Hyejin Lee, Jihye Kim, Kyungdeok Kim, Wangyong Shin, Yi Sul Cho, Junyeop Daniel Roh, Jaeseung Kang, Taesun Yoo,[...]. Cell Rep 2018
19
25

Punch biopsy of the skin.
Thomas J Zuber. Am Fam Physician 2002
40
25

Neuropilins lock secreted semaphorins onto plexins in a ternary signaling complex.
Bert J C Janssen, Tomas Malinauskas, Greg A Weir, M Zameel Cader, Christian Siebold, E Yvonne Jones. Nat Struct Mol Biol 2012
107
25

Semaphorin 5A inhibits synaptogenesis in early postnatal- and adult-born hippocampal dentate granule cells.
Yuntao Duan, Shih-Hsiu Wang, Juan Song, Yevgeniya Mironova, Guo-li Ming, Alex L Kolodkin, Roman J Giger. Elife 2014
56
25

Anxiety and comorbid measures associated with PLXNA2.
Naomi R Wray, Michael R James, Steven P Mah, Matthew Nelson, Gavin Andrews, Patrick F Sullivan, Grant W Montgomery, Andrew J Birley, Andreas Braun, Nicholas G Martin. Arch Gen Psychiatry 2007
41
25

The leucine-rich repeat structure.
J Bella, K L Hindle, P A McEwan, S C Lovell. Cell Mol Life Sci 2008
279
25

CSVS, a crowdsourcing database of the Spanish population genetic variability.
María Peña-Chilet, Gema Roldán, Javier Perez-Florido, Francisco M Ortuño, Rosario Carmona, Virginia Aquino, Daniel Lopez-Lopez, Carlos Loucera, Jose L Fernandez-Rueda, Asunción Gallego,[...]. Nucleic Acids Res 2021
7
25

Autism as a strongly genetic disorder: evidence from a British twin study.
A Bailey, A Le Couteur, I Gottesman, P Bolton, E Simonoff, E Yuzda, M Rutter. Psychol Med 1995
25

Leucine-Rich Repeat (LRR) Domains Containing Intervening Motifs in Plants.
Norio Matsushima, Hiroki Miyashita. Biomolecules 2012
43
25

Getting neural circuits into shape with semaphorins.
R Jeroen Pasterkamp. Nat Rev Neurosci 2012
157
25

Development and validation of a CGH microarray for clinical cytogenetic diagnosis.
Sau W Cheung, Chad A Shaw, Wei Yu, Jiangzham Li, Zhishuo Ou, Ankita Patel, Svetlana A Yatsenko, Mitchell L Cooper, Patti Furman, Pawel Stankiewicz,[...]. Genet Med 2005
200
25

PlexinA2 Forward Signaling through Rap1 GTPases Regulates Dentate Gyrus Development and Schizophrenia-like Behaviors.
Xiao-Feng Zhao, Rafi Kohen, Rachel Parent, Yuntao Duan, Grace L Fisher, Matthew J Korn, Lingchao Ji, Guoqiang Wan, Jing Jin, Andreas W Püschel,[...]. Cell Rep 2018
12
25

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
25

A 7q31.33q32.1 microdeletion including LRRC4 and GRM8 is associated with severe intellectual disability and characteristics of autism.
Noriko Sangu, Keiko Shimojima, Yuya Takahashi, Tsukasa Ohashi, Jun Tohyama, Toshiyuki Yamamoto. Hum Genome Var 2017
9
25

CUPSAT: prediction of protein stability upon point mutations.
Vijaya Parthiban, M Michael Gromiha, Dietmar Schomburg. Nucleic Acids Res 2006
331
25

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses.
Sarah R Gilman, Ivan Iossifov, Dan Levy, Michael Ronemus, Michael Wigler, Dennis Vitkup. Neuron 2011
426
25

Linkage and candidate gene studies of autism spectrum disorders in European populations.
Richard Holt, Gabrielle Barnby, Elena Maestrini, Elena Bacchelli, Denise Brocklebank, Inês Sousa, Erik J Mulder, Katri Kantojärvi, Irma Järvelä, Sabine M Klauck,[...]. Eur J Hum Genet 2010
50
25

The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.
Peter D Stenson, Matthew Mort, Edward V Ball, Katy Evans, Matthew Hayden, Sally Heywood, Michelle Hussain, Andrew D Phillips, David N Cooper. Hum Genet 2017
592
25

Pharmacologic Treatment of Severe Irritability and Problem Behaviors in Autism: A Systematic Review and Meta-analysis.
Lawrence K Fung, Rajneesh Mahajan, Alixandra Nozzolillo, Pilar Bernal, Aaron Krasner, Booil Jo, Daniel Coury, Agnes Whitaker, Jeremy Veenstra-Vanderweele, Antonio Y Hardan. Pediatrics 2016
83
25

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
25


Plexin-A2 and its ligand, Sema6A, control nucleus-centrosome coupling in migrating granule cells.
Julie Renaud, Géraldine Kerjan, Itsuko Sumita, Yvrick Zagar, Virginie Georget, Doyeun Kim, Coralie Fouquet, Kazunori Suda, Makoto Sanbo, Fumikazu Suto,[...]. Nat Neurosci 2008
104
25

A standard curve based method for relative real time PCR data processing.
Alexey Larionov, Andreas Krause, William Miller. BMC Bioinformatics 2005
561
25

Identification of two inherited copy number variants in a male with autism supports two-hit and compound heterozygosity models of autism.
Susan Shur-Fen Gau, Hsiao-Mei Liao, Chao-Chun Hong, Wei-Hsien Chien, Chia-Hsiang Chen. Am J Med Genet B Neuropsychiatr Genet 2012
24
25

Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
Yong-hui Jiang, Ryan K C Yuen, Xin Jin, Mingbang Wang, Nong Chen, Xueli Wu, Jia Ju, Junpu Mei, Yujian Shi, Mingze He,[...]. Am J Hum Genet 2013
276
25

Multicenter, randomized, double-blind, active comparator and placebo-controlled trial of a corticotropin-releasing factor receptor-1 antagonist in generalized anxiety disorder.
Vladimir Coric, Howard H Feldman, Dan A Oren, Anantha Shekhar, Joseph Pultz, Randy C Dockens, Xiaoling Wu, Kimberly A Gentile, Shu-Pang Huang, Eileen Emison,[...]. Depress Anxiety 2010
111
25

Global prevalence of autism and other pervasive developmental disorders.
Mayada Elsabbagh, Gauri Divan, Yun-Joo Koh, Young Shin Kim, Shuaib Kauchali, Carlos Marcín, Cecilia Montiel-Nava, Vikram Patel, Cristiane S Paula, Chongying Wang,[...]. Autism Res 2012
925
25

Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder.
Jinchen Li, Lin Wang, Ping Yu, Leisheng Shi, Kun Zhang, Zhong Sheng Sun, Kun Xia. Am J Med Genet B Neuropsychiatr Genet 2017
13
25

Structural Basis for Plexin Activation and Regulation.
Youxin Kong, Bert J C Janssen, Tomas Malinauskas, Vamshidhar R Vangoor, Charlotte H Coles, Rainer Kaufmann, Tao Ni, Robert J C Gilbert, Sergi Padilla-Parra, R Jeroen Pasterkamp,[...]. Neuron 2016
53
25

Expression patterns of plexins and neuropilins are consistent with cooperative and separate functions during neural development.
Olivier Mauti, Rejina Sadhu, Joelle Gemayel, Matthias Gesemann, Esther T Stoeckli. BMC Dev Biol 2006
34
25

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
25

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases.
Michelle M Clark, Zornitza Stark, Lauge Farnaes, Tiong Y Tan, Susan M White, David Dimmock, Stephen F Kingsmore. NPJ Genom Med 2018
150
25

MutationTaster2: mutation prediction for the deep-sequencing age.
Jana Marie Schwarz, David N Cooper, Markus Schuelke, Dominik Seelow. Nat Methods 2014
25

Genetics of autism spectrum disorders.
Daniel H Geschwind. Trends Cogn Sci 2011
313
25

Autism spectrum disorder.
Catherine Lord, Traolach S Brugha, Tony Charman, James Cusack, Guillaume Dumas, Thomas Frazier, Emily J H Jones, Rebecca M Jones, Andrew Pickles, Matthew W State,[...]. Nat Rev Dis Primers 2020
100
25

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
25

DANN: a deep learning approach for annotating the pathogenicity of genetic variants.
Daniel Quang, Yifei Chen, Xiaohui Xie. Bioinformatics 2015
369
25

CADD: predicting the deleteriousness of variants throughout the human genome.
Philipp Rentzsch, Daniela Witten, Gregory M Cooper, Jay Shendure, Martin Kircher. Nucleic Acids Res 2019
773
25


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.