A citation-based method for searching scientific literature

Thomas J Turner, Clara Zourray, Stephanie Schorge, Gabriele Lignani. J Neurochem 2021
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


CRISPR/dCas9-based Scn1a gene activation in inhibitory neurons ameliorates epileptic and behavioral phenotypes of Dravet syndrome model mice.
Tetsushi Yamagata, Matthieu Raveau, Kenta Kobayashi, Hiroyuki Miyamoto, Tetsuya Tatsukawa, Ikuo Ogiwara, Shigeyoshi Itohara, Takao K Hensch, Kazuhiro Yamakawa. Neurobiol Dis 2020
19
50

dCas9-Based Scn1a Gene Activation Restores Inhibitory Interneuron Excitability and Attenuates Seizures in Dravet Syndrome Mice.
Gaia Colasante, Gabriele Lignani, Simone Brusco, Claudia Di Berardino, Jenna Carpenter, Serena Giannelli, Nicholas Valassina, Simone Bido, Raffaele Ricci, Valerio Castoldi,[...]. Mol Ther 2020
53
50

RNAi-Based Gene Therapy Rescues Developmental and Epileptic Encephalopathy in a Genetic Mouse Model.
Osasumwen V Aimiuwu, Allison M Fowler, Megha Sah, Jia Jie Teoh, Ayla Kanber, Nettie K Pyne, Sabrina Petri, Chana Rosenthal-Weiss, Mu Yang, Scott Q Harper,[...]. Mol Ther 2020
5
60

Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage.
Alexis C Komor, Yongjoo B Kim, Michael S Packer, John A Zuris, David R Liu. Nature 2016
37

In vivo CRISPRa decreases seizures and rescues cognitive deficits in a rodent model of epilepsy.
Gaia Colasante, Yichen Qiu, Luca Massimino, Claudia Di Berardino, Jonathan H Cornford, Albert Snowball, Mikail Weston, Steffan P Jones, Serena Giannelli, Andreas Lieb,[...]. Brain 2020
24
37

Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome.
Guy M Lenk, Paymaan Jafar-Nejad, Sophie F Hill, Lucas D Huffman, Corrine E Smolen, Jacy L Wagnon, Hayley Petit, Wenxi Yu, Julie Ziobro, Kritika Bhatia,[...]. Ann Neurol 2020
31
37

Epilepsy and developmental disorders: Next generation sequencing in the clinic.
Joseph D Symonds, Amy McTague. Eur J Paediatr Neurol 2020
25
37

In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration.
Keiichiro Suzuki, Yuji Tsunekawa, Reyna Hernandez-Benitez, Jun Wu, Jie Zhu, Euiseok J Kim, Fumiyuki Hatanaka, Mako Yamamoto, Toshikazu Araoka, Zhe Li,[...]. Nature 2016
527
37


Search-and-replace genome editing without double-strand breaks or donor DNA.
Andrew V Anzalone, Peyton B Randolph, Jessie R Davis, Alexander A Sousa, Luke W Koblan, Jonathan M Levy, Peter J Chen, Christopher Wilson, Gregory A Newby, Aditya Raguram,[...]. Nature 2019
830
37

Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage.
Nicole M Gaudelli, Alexis C Komor, Holly A Rees, Michael S Packer, Ahmed H Badran, David I Bryson, David R Liu. Nature 2017
37

Highly efficient Cas9-mediated transcriptional programming.
Alejandro Chavez, Jonathan Scheiman, Suhani Vora, Benjamin W Pruitt, Marcelle Tuttle, Eswar P R Iyer, Shuailiang Lin, Samira Kiani, Christopher D Guzman, Daniel J Wiegand,[...]. Nat Methods 2015
688
37

Advances in genome editing through control of DNA repair pathways.
Charles D Yeh, Christopher D Richardson, Jacob E Corn. Nat Cell Biol 2019
93
37


Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy.
Amy McTague, Umesh Nair, Sony Malhotra, Esther Meyer, Natalie Trump, Elena V Gazina, Apostolos Papandreou, Adeline Ngoh, Sally Ackermann, Gautam Ambegaonkar,[...]. Neurology 2018
42
25


Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression.
Lei S Qi, Matthew H Larson, Luke A Gilbert, Jennifer A Doudna, Jonathan S Weissman, Adam P Arkin, Wendell A Lim. Cell 2013
25

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
195
25

The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegeneration.
Jing-Qiong Kang, Wangzhen Shen, Chengwen Zhou, Dong Xu, Robert L Macdonald. Nat Neurosci 2015
56
25

Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum.
Amy McTague, Richard Appleton, Shivaram Avula, J Helen Cross, Mary D King, Thomas S Jacques, Sanjay Bhate, Anthony Cronin, Andrew Curran, Archana Desurkar,[...]. Brain 2013
82
25

PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity.
Floriana Fruscione, Pierluigi Valente, Bruno Sterlini, Alessandra Romei, Simona Baldassari, Manuela Fadda, Cosimo Prestigio, Giorgia Giansante, Jacopo Sartorelli, Pia Rossi,[...]. Brain 2018
51
25

Gene Therapy Tools for Brain Diseases.
Selene Ingusci, Gianluca Verlengia, Marie Soukupova, Silvia Zucchini, Michele Simonato. Front Pharmacol 2019
48
25

UBE3A and Its Link With Autism.
Naman Vatsa, Nihar Ranjan Jana. Front Mol Neurosci 2018
21
25

Angelman syndrome - insights into a rare neurogenetic disorder.
Karin Buiting, Charles Williams, Bernhard Horsthemke. Nat Rev Neurol 2016
140
25

The Neurotropic Properties of AAV-PHP.B Are Limited to C57BL/6J Mice.
Juliette Hordeaux, Qiang Wang, Nathan Katz, Elizabeth L Buza, Peter Bell, James M Wilson. Mol Ther 2018
169
25

Cre-dependent selection yields AAV variants for widespread gene transfer to the adult brain.
Benjamin E Deverman, Piers L Pravdo, Bryan P Simpson, Sripriya Ravindra Kumar, Ken Y Chan, Abhik Banerjee, Wei-Li Wu, Bin Yang, Nina Huber, Sergiu P Pasca,[...]. Nat Biotechnol 2016
412
25

Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model.
Sara Silva-Santos, Geeske M van Woerden, Caroline F Bruinsma, Edwin Mientjes, Mehrnoush Aghadavoud Jolfaei, Ben Distel, Steven A Kushner, Ype Elgersma. J Clin Invest 2015
111
25

Adenovirus-Mediated Somatic Genome Editing of Pten by CRISPR/Cas9 in Mouse Liver in Spite of Cas9-Specific Immune Responses.
Dan Wang, Haiwei Mou, Shaoyong Li, Yingxiang Li, Soren Hough, Karen Tran, Jia Li, Hao Yin, Daniel G Anderson, Erik J Sontheimer,[...]. Hum Gene Ther 2015
186
25

Adeno-associated virus-mediated rescue of the cognitive defects in a mouse model for Angelman syndrome.
Jennifer L Daily, Kevin Nash, Umesh Jinwal, Todd Golde, Justin Rogers, Melinda M Peters, Rebecca D Burdine, Chad Dickey, Jessica L Banko, Edwin J Weeber. PLoS One 2011
61
25

Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy.
Jennifer A Kearney, Anna K Wiste, Ulrich Stephani, Michelle M Trudeau, Anne Siegel, Rajesh RamachandranNair, Roy D Elterman, Hiltrud Muhle, Juliane Reinsdorf, W Donald Shields,[...]. Pediatr Neurol 2006
41
25

Towards a therapy for Angelman syndrome by targeting a long non-coding RNA.
Linyan Meng, Amanda J Ward, Seung Chun, C Frank Bennett, Arthur L Beaudet, Frank Rigo. Nature 2015
273
25

Epileptogenic Q555X SYN1 mutant triggers imbalances in release dynamics and short-term plasticity.
Gabriele Lignani, Andrea Raimondi, Enrico Ferrea, Anna Rocchi, Francesco Paonessa, Fabrizia Cesca, Marta Orlando, Tatiana Tkatch, Flavia Valtorta, Patrick Cossette,[...]. Hum Mol Genet 2013
47
25


Presynaptic dysfunction in neurodevelopmental disorders: Insights from the synaptic vesicle life cycle.
Katherine Bonnycastle, Elizabeth C Davenport, Michael A Cousin. J Neurochem 2021
10
25

Re-expression of SynGAP protein in adulthood improves translatable measures of brain function and behavior.
Thomas K Creson, Camilo Rojas, Ernie Hwaun, Thomas Vaissiere, Murat Kilinc, Andres Jimenez-Gomez, Jimmy Lloyd Holder, Jianrong Tang, Laura L Colgin, Courtney A Miller,[...]. Elife 2019
22
25

Efficient CRISPR-Cas9-mediated generation of knockin human pluripotent stem cells lacking undesired mutations at the targeted locus.
Florian T Merkle, Werner M Neuhausser, David Santos, Eivind Valen, James A Gagnon, Kristi Maas, Jackson Sandoe, Alexander F Schier, Kevin Eggan. Cell Rep 2015
85
25

Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome.
Nina Xie, He Gong, Joshua A Suhl, Pankaj Chopra, Tao Wang, Stephen T Warren. PLoS One 2016
60
25

Off-target Effects in CRISPR/Cas9-mediated Genome Engineering.
Xiao-Hui Zhang, Louis Y Tee, Xiao-Gang Wang, Qun-Shan Huang, Shi-Hua Yang. Mol Ther Nucleic Acids 2015
420
25

Biological concepts in human sodium channel epilepsies and their relevance in clinical practice.
Andreas Brunklaus, Juanjiangmeng Du, Felix Steckler, Ismael I Ghanty, Katrine M Johannesen, Christina Dühring Fenger, Stephanie Schorge, David Baez-Nieto, Hao-Ran Wang, Andrew Allen,[...]. Epilepsia 2020
20
25

Modulating gene regulation to treat genetic disorders.
Navneet Matharu, Nadav Ahituv. Nat Rev Drug Discov 2020
8
25

Genome editing with CRISPR-Cas nucleases, base editors, transposases and prime editors.
Andrew V Anzalone, Luke W Koblan, David R Liu. Nat Biotechnol 2020
285
25

A TALE nuclease architecture for efficient genome editing.
Jeffrey C Miller, Siyuan Tan, Guijuan Qiao, Kyle A Barlow, Jianbin Wang, Danny F Xia, Xiangdong Meng, David E Paschon, Elo Leung, Sarah J Hinkley,[...]. Nat Biotechnol 2011
25

Breaking the code of DNA binding specificity of TAL-type III effectors.
Jens Boch, Heidi Scholze, Sebastian Schornack, Angelika Landgraf, Simone Hahn, Sabine Kay, Thomas Lahaye, Anja Nickstadt, Ulla Bonas. Science 2009
25

Efficient construction of sequence-specific TAL effectors for modulating mammalian transcription.
Feng Zhang, Le Cong, Simona Lodato, Sriram Kosuri, George M Church, Paola Arlotta. Nat Biotechnol 2011
523
25

Epigenome editing by a CRISPR-Cas9-based acetyltransferase activates genes from promoters and enhancers.
Isaac B Hilton, Anthony M D'Ippolito, Christopher M Vockley, Pratiksha I Thakore, Gregory E Crawford, Timothy E Reddy, Charles A Gersbach. Nat Biotechnol 2015
906
25

Genome Editing for CNS Disorders.
Fábio Duarte, Nicole Déglon. Front Neurosci 2020
4
50

Genome-scale transcriptional activation by an engineered CRISPR-Cas9 complex.
Silvana Konermann, Mark D Brigham, Alexandro E Trevino, Julia Joung, Omar O Abudayyeh, Clea Barcena, Patrick D Hsu, Naomi Habib, Jonathan S Gootenberg, Hiroshi Nishimasu,[...]. Nature 2015
25


The Epidemiology of Epilepsy.
Ettore Beghi. Neuroepidemiology 2020
84
25

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.
Julia Oyrer, Snezana Maljevic, Ingrid E Scheffer, Samuel F Berkovic, Steven Petrou, Christopher A Reid. Pharmacol Rev 2018
79
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.