A citation-based method for searching scientific literature

Zhonghua Hu, Xiao Xiao, Zhuohua Zhang, Ming Li. Mol Psychiatry 2019
Times Cited: 24







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



Times Cited
  Times     Co-cited
Similarity


Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
398
33



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
25

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
506
25

Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review.
Paola Castronovo, Marco Baccarin, Arianna Ricciardello, Chiara Picinelli, Pasquale Tomaiuolo, Francesca Cucinotta, Myriam Frittoli, Carla Lintas, Roberto Sacco, Antonio M Persico. Clin Genet 2020
13
46

Analysis of copy number variations at 15 schizophrenia-associated loci.
Elliott Rees, James T R Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D Chambert, Alexander L Richards, Gerwyn Mahoney-Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll,[...]. Br J Psychiatry 2014
218
20

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
20

Conditional Deletion of All Neurexins Defines Diversity of Essential Synaptic Organizer Functions for Neurexins.
Lulu Y Chen, Man Jiang, Bo Zhang, Ozgun Gokce, Thomas C Südhof. Neuron 2017
79
20

Presynaptic neurexin-3 alternative splicing trans-synaptically controls postsynaptic AMPA receptor trafficking.
Jason Aoto, David C Martinelli, Robert C Malenka, Katsuhiko Tabuchi, Thomas C Südhof. Cell 2013
171
20


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
16

Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders.
Hannah Mary Grayton, Markus Missler, David Andrew Collier, Cathy Fernandes. PLoS One 2013
92
16

The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran,[...]. Biol Psychiatry 2014
194
16

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
16

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Alden Y Huang, Dongmei Yu, Lea K Davis, Jae Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen,[...]. Neuron 2017
71
16

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis.
Markus Missler, Weiqi Zhang, Astrid Rohlmann, Gunnar Kattenstroth, Robert E Hammer, Kurt Gottmann, Thomas C Südhof. Nature 2003
446
16

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
16


Distinct circuit-dependent functions of presynaptic neurexin-3 at GABAergic and glutamatergic synapses.
Jason Aoto, Csaba Földy, Silviana Maria Ciurea Ilcus, Katsuhiko Tabuchi, Thomas C Südhof. Nat Neurosci 2015
53
16


Neurexins and neuropsychiatric disorders.
Enas Kasem, Taiga Kurihara, Katsuhiko Tabuchi. Neurosci Res 2018
38
16

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
G Kirov, A J Pocklington, P Holmans, D Ivanov, M Ikeda, D Ruderfer, J Moran, K Chambert, D Toncheva, L Georgieva,[...]. Mol Psychiatry 2012
515
12

Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling.
Yingwei Mao, Xuecai Ge, Christopher L Frank, Jon M Madison, Angela N Koehler, Mary Kathryn Doud, Carlos Tassa, Erin M Berry, Takahiro Soda, Karun K Singh,[...]. Cell 2009
573
12


Disrupted-in-Schizophrenia 1 (DISC1) regulates spines of the glutamate synapse via Rac1.
Akiko Hayashi-Takagi, Manabu Takaki, Nick Graziane, Saurav Seshadri, Hannah Murdoch, Allan J Dunlop, Yuichi Makino, Anupamaa J Seshadri, Koko Ishizuka, Deepak P Srivastava,[...]. Nat Neurosci 2010
298
12




Selective Loss of Smaller Spines in Schizophrenia.
Matthew L MacDonald, Jamil Alhassan, Jason T Newman, Michelle Richard, Hong Gu, Ryan M Kelly, Alan R Sampson, Kenneth N Fish, Peter Penzes, Zachary P Wills,[...]. Am J Psychiatry 2017
51
12

Synaptic loss in schizophrenia: a meta-analysis and systematic review of synaptic protein and mRNA measures.
Emanuele Felice Osimo, Katherine Beck, Tiago Reis Marques, Oliver D Howes. Mol Psychiatry 2019
54
12

Beyond GWASs: illuminating the dark road from association to function.
Stacey L Edwards, Jonathan Beesley, Juliet D French, Alison M Dunning. Am J Hum Genet 2013
412
12

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies.
Patrick F Sullivan, Kenneth S Kendler, Michael C Neale. Arch Gen Psychiatry 2003
12

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
12

Dendritic structural plasticity and neuropsychiatric disease.
Marc P Forrest, Euan Parnell, Peter Penzes. Nat Rev Neurosci 2018
138
12

Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis.
Andrew E Jaffe, Richard E Straub, Joo Heon Shin, Ran Tao, Yuan Gao, Leonardo Collado-Torres, Tony Kam-Thong, Hualin S Xi, Jie Quan, Qiang Chen,[...]. Nat Neurosci 2018
121
12

Dendritic spine pathology in neuropsychiatric disorders.
Peter Penzes, Michael E Cahill, Kelly A Jones, Jon-Eric VanLeeuwen, Kevin M Woolfrey. Nat Neurosci 2011
864
12

Gene expression elucidates functional impact of polygenic risk for schizophrenia.
Menachem Fromer, Panos Roussos, Solveig K Sieberts, Jessica S Johnson, David H Kavanagh, Thanneer M Perumal, Douglas M Ruderfer, Edwin C Oh, Aaron Topol, Hardik R Shah,[...]. Nat Neurosci 2016
447
12

Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets.
Zhihong Zhu, Futao Zhang, Han Hu, Andrew Bakshi, Matthew R Robinson, Joseph E Powell, Grant W Montgomery, Michael E Goddard, Naomi R Wray, Peter M Visscher,[...]. Nat Genet 2016
630
12

Schizophrenia risk from complex variation of complement component 4.
Aswin Sekar, Allison R Bialas, Heather de Rivera, Avery Davis, Timothy R Hammond, Nolan Kamitaki, Katherine Tooley, Jessy Presumey, Matthew Baum, Vanessa Van Doren,[...]. Nature 2016
12

A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus.
Ming Li, Andrew E Jaffe, Richard E Straub, Ran Tao, Joo Heon Shin, Yanhong Wang, Qiang Chen, Chao Li, Yankai Jia, Kazutaka Ohi,[...]. Nat Med 2016
86
12

Open Chromatin Profiling in hiPSC-Derived Neurons Prioritizes Functional Noncoding Psychiatric Risk Variants and Highlights Neurodevelopmental Loci.
Marc P Forrest, Hanwen Zhang, Winton Moy, Heather McGowan, Catherine Leites, Leonardo E Dionisio, Zihui Xu, Jianxin Shi, Alan R Sanders, William J Greenleaf,[...]. Cell Stem Cell 2017
62
12

Significant association of the neurexin-1 gene (NRXN1) with nicotine dependence in European- and African-American smokers.
Justin Nussbaum, Qing Xu, Thomas J Payne, Jennie Z Ma, Weihua Huang, Joel Gelernter, Ming D Li. Hum Mol Genet 2008
65
12

CNVs in neuropsychiatric disorders.
George Kirov. Hum Mol Genet 2015
77
12

Copy number variation in bipolar disorder.
E K Green, E Rees, J T R Walters, K-G Smith, L Forty, D Grozeva, J L Moran, P Sklar, S Ripke, K D Chambert,[...]. Mol Psychiatry 2016
92
12

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
371
12

Disruption of neurexin 1 associated with autism spectrum disorder.
Hyung-Goo Kim, Shotaro Kishikawa, Anne W Higgins, Ihn-Sik Seong, Diana J Donovan, Yiping Shen, Eric Lally, Lauren A Weiss, Juliane Najm, Kerstin Kutsche,[...]. Am J Hum Genet 2008
398
12

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.
Kimberley M Kendall, Matthew Bracher-Smith, Harry Fitzpatrick, Amy Lynham, Elliott Rees, Valentina Escott-Price, Michael J Owen, Michael C O'Donovan, James T R Walters, George Kirov. Br J Psychiatry 2019
31
12

Disruption of the neurexin 1 gene is associated with schizophrenia.
Dan Rujescu, Andres Ingason, Sven Cichon, Olli P H Pietiläinen, Michael R Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon,[...]. Hum Mol Genet 2009
334
12

Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.
Mark R Etherton, Cory A Blaiss, Craig M Powell, Thomas C Südhof. Proc Natl Acad Sci U S A 2009
279
12


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.