A citation-based method for searching scientific literature

Samuele G Marro, Soham Chanda, Nan Yang, Justyna A Janas, Giulio Valperga, Justin Trotter, Bo Zhou, Sean Merrill, Issa Yousif, Hannah Shelby, Hannes Vogel, M Yashar S Kalani, Thomas C Südhof, Marius Wernig. Neuron 2019
Times Cited: 28







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



Times Cited
  Times     Co-cited
Similarity


Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, I Carina Gillberg, Henrik Soderstrom, Bruno Giros, Marion Leboyer, Christopher Gillberg,[...]. Nat Genet 2003
46

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
589
42

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
628
35

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
120
35


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
40
32

Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors.
Patrick E Rothwell, Marc V Fuccillo, Stephan Maxeiner, Scott J Hayton, Ozgun Gokce, Byung Kook Lim, Stephen C Fowler, Robert C Malenka, Thomas C Südhof. Cell 2014
245
28

The cellular and molecular landscape of neuroligins.
Michael A Bemben, Seth L Shipman, Roger A Nicoll, Katherine W Roche. Trends Neurosci 2015
87
28

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Ryan K C Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang,[...]. Nat Neurosci 2017
341
28

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
154
28

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
50
28

CRISPR Interference-Based Platform for Multimodal Genetic Screens in Human iPSC-Derived Neurons.
Ruilin Tian, Mariam A Gachechiladze, Connor H Ludwig, Matthew T Laurie, Jason Y Hong, Diane Nathaniel, Anika V Prabhu, Michael S Fernandopulle, Rajan Patel, Mehrnoosh Abshari,[...]. Neuron 2019
83
25

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family.
Frédéric Laumonnier, Frédérique Bonnet-Brilhault, Marie Gomot, Romuald Blanc, Albert David, Marie-Pierre Moizard, Martine Raynaud, Nathalie Ronce, Eric Lemonnier, Patrick Calvas,[...]. Am J Hum Genet 2004
510
25

Neuroligin-4 is localized to glycinergic postsynapses and regulates inhibition in the retina.
Mrinalini Hoon, Tolga Soykan, Björn Falkenburger, Matthieu Hammer, Annarita Patrizi, Karl-Friedrich Schmidt, Marco Sassoè-Pognetto, Siegrid Löwel, Tobias Moser, Holger Taschenberger,[...]. Proc Natl Acad Sci U S A 2011
141
25

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients.
J Yan, G Oliveira, A Coutinho, C Yang, J Feng, C Katz, J Sram, A Bockholt, I R Jones, N Craddock,[...]. Mol Psychiatry 2005
217
25

Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2.
Alexander A Chubykin, Deniz Atasoy, Mark R Etherton, Nils Brose, Ege T Kavalali, Jay R Gibson, Thomas C Südhof. Neuron 2007
389
25

Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function.
Mark Etherton, Csaba Földy, Manu Sharma, Katsuhiko Tabuchi, Xinran Liu, Mehrdad Shamloo, Robert C Malenka, Thomas C Südhof. Proc Natl Acad Sci U S A 2011
207
25


Binding of neuroligins to PSD-95.
M Irie, Y Hata, M Takeuchi, K Ichtchenko, A Toyoda, K Hirao, Y Takai, T W Rosahl, T C Südhof. Science 1997
547
21

Functional maturation of hPSC-derived forebrain interneurons requires an extended timeline and mimics human neural development.
Cory R Nicholas, Jiadong Chen, Yunshuo Tang, Derek G Southwell, Nadine Chalmers, Daniel Vogt, Christine M Arnold, Ying-Jiun J Chen, Edouard G Stanley, Andrew G Elefanty,[...]. Cell Stem Cell 2013
336
21

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
131
21

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
175
21

Structural analysis of the synaptic protein neuroligin and its beta-neurexin complex: determinants for folding and cell adhesion.
Igor P Fabrichny, Philippe Leone, Gerlind Sulzenbacher, Davide Comoletti, Meghan T Miller, Palmer Taylor, Yves Bourne, Pascale Marchot. Neuron 2007
117
21

Structures of neuroligin-1 and the neuroligin-1/neurexin-1 beta complex reveal specific protein-protein and protein-Ca2+ interactions.
Demet Araç, Antony A Boucard, Engin Ozkan, Pavel Strop, Evan Newell, Thomas C Südhof, Axel T Brunger. Neuron 2007
143
21

Homodimerization and isoform-specific heterodimerization of neuroligins.
Alexandros Poulopoulos, Tolga Soykan, Liam P Tuffy, Matthieu Hammer, Frédérique Varoqueaux, Nils Brose. Biochem J 2012
44
21

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
98
21

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
21

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
21

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
46
21

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
30
21

Neuroligin 2 is exclusively localized to inhibitory synapses.
Frédérique Varoqueaux, Stéphane Jamain, Nils Brose. Eur J Cell Biol 2004
350
21

Functional significance of rare neuroligin 1 variants found in autism.
Moe Nakanishi, Jun Nomura, Xiao Ji, Kota Tamada, Takashi Arai, Eiki Takahashi, Maja Bućan, Toru Takumi. PLoS Genet 2017
42
21

Autism-associated neuroligin-3 mutations commonly disrupt tonic endocannabinoid signaling.
Csaba Földy, Robert C Malenka, Thomas C Südhof. Neuron 2013
172
21

Identification and functional characterization of rare mutations of the neuroligin-2 gene (NLGN2) associated with schizophrenia.
Chicheng Sun, Min-Chih Cheng, Rosie Qin, Ding-Lieh Liao, Tzu-Ting Chen, Farn-Jong Koong, Gong Chen, Chia-Hsiang Chen. Hum Mol Genet 2011
87
21

Neuroligins determine synapse maturation and function.
Frédérique Varoqueaux, Gayane Aramuni, Randi L Rawson, Ralf Mohrmann, Markus Missler, Kurt Gottmann, Weiqi Zhang, Thomas C Südhof, Nils Brose. Neuron 2006
535
21


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
432
17

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.
Stephane Jamain, Konstantin Radyushkin, Kurt Hammerschmidt, Sylvie Granon, Susann Boretius, Frederique Varoqueaux, Nelina Ramanantsoa, Jorge Gallego, Anja Ronnenberg, Dorina Winter,[...]. Proc Natl Acad Sci U S A 2008
363
17

A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export.
Chen Zhang, Jeff M Milunsky, Stephanie Newton, Jaewon Ko, Geping Zhao, Tom A Maher, Helen Tager-Flusberg, Marc F Bolliger, Alice S Carter, Antony A Boucard,[...]. J Neurosci 2009
125
17



Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.
Xiaojuan Xu, Zhimin Xiong, Lusi Zhang, Yalan Liu, Lina Lu, Yu Peng, Hui Guo, Jingping Zhao, Kun Xia, Zhengmao Hu. Mol Biol Rep 2014
23
21

Perturbed Hippocampal Synaptic Inhibition and γ-Oscillations in a Neuroligin-4 Knockout Mouse Model of Autism.
Matthieu Hammer, Dilja Krueger-Burg, Liam Patrick Tuffy, Benjamin Hillman Cooper, Holger Taschenberger, Sarit Pati Goswami, Hannelore Ehrenreich, Peter Jonas, Frederique Varoqueaux, Jeong-Seop Rhee,[...]. Cell Rep 2015
38
17

Using whole-exome sequencing to identify inherited causes of autism.
Timothy W Yu, Maria H Chahrour, Michael E Coulter, Sarn Jiralerspong, Kazuko Okamura-Ikeda, Bulent Ataman, Klaus Schmitz-Abe, David A Harmin, Mazhar Adli, Athar N Malik,[...]. Neuron 2013
266
17

Unusually rapid evolution of Neuroligin-4 in mice.
Marc F Bolliger, Jimin Pei, Stephan Maxeiner, Antony A Boucard, Nick V Grishin, Thomas C Südhof. Proc Natl Acad Sci U S A 2008
61
17

Autism-associated neuroligin-4 mutation selectively impairs glycinergic synaptic transmission in mouse brainstem synapses.
Bo Zhang, Ozgun Gokce, W Dylan Hale, Nils Brose, Thomas C Südhof. J Exp Med 2018
13
38

Posttranslational modifications of neuroligins regulate neuronal and glial signaling.
Jaehoon Jeong, Jeremiah D Paskus, Katherine W Roche. Curr Opin Neurobiol 2017
17
29

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
122
17

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
524
17

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
28
17


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.