A citation-based method for searching scientific literature

Tzyy-Nan Huang, Hsiu-Chun Chuang, Wen-Hsi Chou, Chiung-Ya Chen, Hsiao-Fang Wang, Shen-Ju Chou, Yi-Ping Hsueh. Nat Neurosci 2014
Times Cited: 108







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



Times Cited
  Times     Co-cited
Similarity


Tbr1 regulates differentiation of the preplate and layer 6.
R F Hevner, L Shi, N Justice, Y Hsueh, M Sheng, S Smiga, A Bulfone, A M Goffinet, A T Campagnoni, J L Rubenstein. Neuron 2001
641
29

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
29

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Brian J O'Roak, Laura Vives, Wenqing Fu, Jarrett D Egertson, Ian B Stanaway, Ian G Phelps, Gemma Carvill, Akash Kumar, Choli Lee, Katy Ankenman,[...]. Science 2012
810
26

De novo TBR1 mutations in sporadic autism disrupt protein functions.
Pelagia Deriziotis, Brian J O'Roak, Sarah A Graham, Sara B Estruch, Danai Dimitropoulou, Raphael A Bernier, Jennifer Gerdts, Jay Shendure, Evan E Eichler, Simon E Fisher. Nat Commun 2014
78
32

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
22

Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function.
Hyejung Won, Hye-Ryeon Lee, Heon Yung Gee, Won Mah, Jae-Ick Kim, Jiseok Lee, Seungmin Ha, Changuk Chung, Eun Suk Jung, Yi Sul Cho,[...]. Nature 2012
437
21


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
20

Trans-synaptic zinc mobilization improves social interaction in two mouse models of autism through NMDAR activation.
Eun-Jae Lee, Hyejin Lee, Tzyy-Nan Huang, Changuk Chung, Wangyong Shin, Kyungdeok Kim, Jae-Young Koh, Yi-Ping Hsueh, Eunjoon Kim. Nat Commun 2015
63
30

Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex.
Francesco Bedogni, Rebecca D Hodge, Gina E Elsen, Branden R Nelson, Ray A M Daza, Richard P Beyer, Theo K Bammler, John L R Rubenstein, Robert F Hevner. Proc Natl Acad Sci U S A 2010
220
18

T-Brain-1--A Potential Master Regulator in Autism Spectrum Disorders.
Hsiu-Chun Chuang, Tzyy-Nan Huang, Yi-Ping Hsueh. Autism Res 2015
36
47

Neocortical excitation/inhibition balance in information processing and social dysfunction.
Ofer Yizhar, Lief E Fenno, Matthias Prigge, Franziska Schneider, Thomas J Davidson, Daniel J O'Shea, Vikaas S Sohal, Inbal Goshen, Joel Finkelstein, Jeanne T Paz,[...]. Nature 2011
15

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
15

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
677
15

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
931
14

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
14

Tbr1 and Fezf2 regulate alternate corticofugal neuronal identities during neocortical development.
William L McKenna, Jennifer Betancourt, Kathryn A Larkin, Benjamin Abrams, Chao Guo, John L R Rubenstein, Bin Chen. J Neurosci 2011
167
14

T-brain-1: a homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex.
A Bulfone, S M Smiga, K Shimamura, A Peterson, L Puelles, J L Rubenstein. Neuron 1995
348
14

Behavioural phenotyping assays for mouse models of autism.
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
895
13

NMDA receptor dysfunction in autism spectrum disorders.
Eun-Jae Lee, Su Yeon Choi, Eunjoon Kim. Curr Opin Pharmacol 2015
105
13

TBR1 regulates autism risk genes in the developing neocortex.
James H Notwell, Whitney E Heavner, Siavash Fazel Darbandi, Sol Katzman, William L McKenna, Christian F Ortiz-Londono, David Tastad, Matthew J Eckler, John L R Rubenstein, Susan K McConnell,[...]. Genome Res 2016
37
35

Haploinsufficiency of autism causative gene Tbr1 impairs olfactory discrimination and neuronal activation of the olfactory system in mice.
Tzyy-Nan Huang, Tzu-Li Yen, Lily R Qiu, Hsiu-Chun Chuang, Jason P Lerch, Yi-Ping Hsueh. Mol Autism 2019
20
65

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.
João Peça, Cátia Feliciano, Jonathan T Ting, Wenting Wang, Michael F Wells, Talaignair N Venkatraman, Christopher D Lascola, Zhanyan Fu, Guoping Feng. Nature 2011
856
12

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
613
12


Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2.
Michael J Schmeisser, Elodie Ey, Stephanie Wegener, Juergen Bockmann, A Vanessa Stempel, Angelika Kuebler, Anna-Lena Janssen, Patrick T Udvardi, Ehab Shiban, Christina Spilker,[...]. Nature 2012
397
11

Identification of Tbr-1/CASK complex target genes in neurons.
Ting-Fang Wang, Chia-Nung Ding, Guey-Shin Wang, Shih-Chi Luo, Yi-Ling Lin, Youlin Ruan, Robert Hevner, John L R Rubenstein, Yi-Ping Hsueh. J Neurochem 2004
63
17

Modeling autism by SHANK gene mutations in mice.
Yong-Hui Jiang, Michael D Ehlers. Neuron 2013
292
11

Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior.
Jacqueline Blundell, Cory A Blaiss, Mark R Etherton, Felipe Espinosa, Katsuhiko Tabuchi, Christopher Walz, Marc F Bolliger, Thomas C Südhof, Craig M Powell. J Neurosci 2010
305
11

Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators.
Lara J Duffney, Ping Zhong, Jing Wei, Emmanuel Matas, Jia Cheng, Luye Qin, Kaijie Ma, David M Dietz, Yuji Kajiwara, Joseph D Buxbaum,[...]. Cell Rep 2015
160
11

An olfactory sensory map develops in the absence of normal projection neurons or GABAergic interneurons.
A Bulfone, F Wang, R Hevner, S Anderson, T Cutforth, S Chen, J Meneses, R Pedersen, R Axel, J L Rubenstein. Neuron 1998
256
11

Transcriptional modification by a CASK-interacting nucleosome assembly protein.
Guey-Shin Wang, Chen-Jei Hong, Tsen-Yann Yen, Hsin-Yi Huang, Yvonne Ou, Tzyy-Nan Huang, Wei-Gang Jung, Ting-Yu Kuo, Morgan Sheng, Ting-Fang Wang,[...]. Neuron 2004
109
10

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication.
Ozlem Bozdagi, Takeshi Sakurai, Danae Papapetrou, Xiaobin Wang, Dara L Dickstein, Nagahide Takahashi, Yuji Kajiwara, Mu Yang, Adam M Katz, Maria Luisa Scattoni,[...]. Mol Autism 2010
368
10

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice.
Katsuhiko Tabuchi, Jacqueline Blundell, Mark R Etherton, Robert E Hammer, Xinran Liu, Craig M Powell, Thomas C Südhof. Science 2007
648
10

Loss of predominant Shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission.
Mehreen Kouser, Haley E Speed, Colleen M Dewey, Jeremy M Reimers, Allie J Widman, Natasha Gupta, Shunan Liu, Thomas C Jaramillo, Muhammad Bangash, Bo Xiao,[...]. J Neurosci 2013
166
10

TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract.
Wenqi Han, Kenneth Y Kwan, Sungbo Shim, Mandy M S Lam, Yurae Shin, Xuming Xu, Ying Zhu, Mingfeng Li, Nenad Sestan. Proc Natl Acad Sci U S A 2011
125
10

Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 Microdeletions.
R N Traylor, W B Dobyns, J A Rosenfeld, P Wheeler, J E Spence, A M Bandholz, E V Bawle, E P Carmany, C M Powell, B Hudson,[...]. Mol Syndromol 2012
24
41

Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity.
Siavash Fazel Darbandi, Sarah E Robinson Schwartz, Qihao Qi, Rinaldo Catta-Preta, Emily Ling-Lin Pai, Jeffrey D Mandell, Amanda Everitt, Anna Rubin, Rebecca A Krasnoff, Sol Katzman,[...]. Neuron 2018
38
26


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
9

Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3.
Xiaoming Wang, Portia A McCoy, Ramona M Rodriguiz, Yanzhen Pan, H Shawn Je, Adam C Roberts, Caroline J Kim, Janet Berrios, Jennifer S Colvin, Danielle Bousquet-Moore,[...]. Hum Mol Genet 2011
350
9


Social deficits in IRSp53 mutant mice improved by NMDAR and mGluR5 suppression.
Woosuk Chung, Su Yeon Choi, Eunee Lee, Haram Park, Jaeseung Kang, Hanwool Park, Yeonsoo Choi, Dongsoo Lee, Sae-Geun Park, Ryunhee Kim,[...]. Nat Neurosci 2015
112
9

Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses.
James P Clement, Massimiliano Aceti, Thomas K Creson, Emin D Ozkan, Yulin Shi, Nicholas J Reish, Antoine G Almonte, Brooke H Miller, Brian J Wiltgen, Courtney A Miller,[...]. Cell 2012
198
9

TBR1 is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion.
Orazio Palumbo, Marco Fichera, Pietro Palumbo, Renata Rizzo, Elisabetta Mazzolla, Donatella Maria Cocuzza, Massimo Carella, Teresa Mattina. Am J Med Genet A 2014
38
23

Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex.
Chris Englund, Andy Fink, Charmaine Lau, Diane Pham, Ray A M Daza, Alessandro Bulfone, Tom Kowalczyk, Robert F Hevner. J Neurosci 2005
917
9


Adult restoration of Shank3 expression rescues selective autistic-like phenotypes.
Yuan Mei, Patricia Monteiro, Yang Zhou, Jin-Ah Kim, Xian Gao, Zhanyan Fu, Guoping Feng. Nature 2016
204
9

Advancing the understanding of autism disease mechanisms through genetics.
Luis de la Torre-Ubieta, Hyejung Won, Jason L Stein, Daniel H Geschwind. Nat Med 2016
401
9

SHANK proteins: roles at the synapse and in autism spectrum disorder.
Patricia Monteiro, Guoping Feng. Nat Rev Neurosci 2017
270
9


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.