A citation-based method for searching scientific literature

Leighton B N Hinkley, Corby L Dale, Tracy L Luks, Anne M Findlay, Polina Bukshpun, Nick Pojman, Tony Thieu, Wendy K Chung, Jeffrey Berman, Timothy P L Roberts, Pratik Mukherjee, Elliott H Sherr, Srikantan S Nagarajan. J Neurosci 2019
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


FieldTrip: Open source software for advanced analysis of MEG, EEG, and invasive electrophysiological data.
Robert Oostenveld, Pascal Fries, Eric Maris, Jan-Mathijs Schoffelen. Comput Intell Neurosci 2011
50

Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain.
N Tzourio-Mazoyer, B Landeau, D Papathanassiou, F Crivello, O Etard, N Delcroix, B Mazoyer, M Joliot. Neuroimage 2002
50

Progressive ataxia related to PRRT2 gene mutation.
Giovanni Castelnovo, Dimitri Renard, Marie De Verdal, JeanJean Luc, Eric Thouvenot, Florence Riant. J Neurol Sci 2016
4
25

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.
Wan-Jin Chen, Yu Lin, Zhi-Qi Xiong, Wei Wei, Wang Ni, Guo-He Tan, Shun-Ling Guo, Jin He, Ya-Fang Chen, Qi-Jie Zhang,[...]. Nat Genet 2011
292
25

[Adolescent with a schizophreniform disorder and recurrent 16p11.2 duplication].
L Castelein, J Steyaert, H Peeters, G van Buggenhout. Tijdschr Psychiatr 2019
1
100

Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene.
Xiao-Rong Liu, Dan Huang, Jie Wang, Yi-Fan Wang, Hui Sun, Bin Tang, Wen Li, Jin-Xing Lai, Na He, Mei Wu,[...]. Neurol Genet 2016
22
25

Novel and de novo point and large microdeletion mutation in PRRT2-related epilepsy.
Li Yang, Cuiping You, Shiyan Qiu, Xiaofan Yang, Yufen Li, Feng Liu, Dongqing Zhang, Yue Niu, Liyun Xu, Na Xu,[...]. Brain Behav 2020
5
25

Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.
Hsien-Yang Lee, Yong Huang, Nadine Bruneau, Patrice Roll, Elisha D O Roberson, Mark Hermann, Emily Quinn, James Maas, Robert Edwards, Tetsuo Ashizawa,[...]. Cell Rep 2012
168
25

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine.
Robin Cloarec, Nadine Bruneau, Gabrielle Rudolf, Annick Massacrier, Manal Salmi, Marc Bataillard, Clotilde Boulay, Roberto Caraballo, Natalio Fejerman, Pierre Genton,[...]. Neurology 2012
67
25

Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutation.
Margherita Fabbri, Carla Marini, Francesca Bisulli, Lidia Di Vito, Antonio Elia, Renzo Guerrini, Davide Mei, Paolo Tinuper. Epileptic Disord 2013
10
25

Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis.
Atsushi Ishii, Sawa Yasumoto, Yukiko Ihara, Takahito Inoue, Takako Fujita, Noriko Nakamura, Masaharu Ohfu, Yushiro Yamashita, Hideo Takatsuka, Toshiaki Taga,[...]. Brain Dev 2013
19
25

16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions.
Mu Yang, Elena J Mahrt, Freeman Lewis, Gillian Foley, Thomas Portmann, Ricardo E Dolmetsch, Christine V Portfors, Jacqueline N Crawley. Autism Res 2015
46
25

PRRT2 mutations: exploring the phenotypical boundaries.
Tania Djémié, Sarah Weckhuysen, Philip Holmgren, Katia Hardies, Tine Van Dyck, Rik Hendrickx, An-Sofie Schoonjans, Wim Van Paesschen, Anna C Jansen, Linda De Meirleir,[...]. J Neurol Neurosurg Psychiatry 2014
22
25

Acute-Onset Ataxia and Transient Cerebellar Diffusion Restriction Associated with a PRRT2 Mutation.
Nicolas Legris, Olivier Chassin, Ghaidaa Nasser, Florence Riant, Elisabeth Tournier-Lasserve, Christian Denier. J Stroke Cerebrovasc Dis 2019
5
25

Atypical neural variability in carriers of 16p11.2 copy number variants.
Reem Al-Jawahiri, Myles Jones, Elizabeth Milne. Autism Res 2019
3
33

PRRT2 Mutant Leads to Dysfunction of Glutamate Signaling.
Ming Li, Fenghe Niu, Xilin Zhu, Xiaopan Wu, Ning Shen, Xiaozhong Peng, Ying Liu. Int J Mol Sci 2015
45
25

Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences.
Angelo Labate, Patrizia Tarantino, Maurizio Viri, Laura Mumoli, Monica Gagliardi, Antonino Romeo, Federico Zara, Grazia Annesi, Antonio Gambardella. Epilepsia 2012
54
25

PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.
Sarah E Heron, Bronwyn E Grinton, Sara Kivity, Zaid Afawi, Sameer M Zuberi, James N Hughes, Clair Pridmore, Bree L Hodgson, Xenia Iona, Lynette G Sadleir,[...]. Am J Hum Genet 2012
171
25

A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2): HINTS FOR AN INTRACELLULAR FUNCTION AT THE SYNAPSE.
Pia Rossi, Bruno Sterlini, Enrico Castroflorio, Antonella Marte, Franco Onofri, Flavia Valtorta, Luca Maragliano, Anna Corradi, Fabio Benfenati. J Biol Chem 2016
38
25

[PRRT2 mutation and infantile convulsions].
M Mathot, D Lederer, S Gerard, E Gueulette, M Deprez. Arch Pediatr 2017
2
50

PRRT2 Is a Key Component of the Ca(2+)-Dependent Neurotransmitter Release Machinery.
Pierluigi Valente, Enrico Castroflorio, Pia Rossi, Manuela Fadda, Bruno Sterlini, Romina Ines Cervigni, Cosimo Prestigio, Silvia Giovedì, Franco Onofri, Elisa Mura,[...]. Cell Rep 2016
71
25

The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
125
25

Benign infantile seizures followed by autistic regression in a boy with 16p11.2 deletion.
Roberta Milone, Angelo Valetto, Veronica Bertini, Federico Sicca. Epileptic Disord 2017
2
50

Benign infantile convulsions (IC) and subsequent paroxysmal kinesigenic dyskinesia (PKD) in a patient with 16p11.2 microdeletion syndrome.
Axel Weber, Angelika Köhler, Andreas Hahn, Bernd Neubauer, Ulrich Müller. Neurogenetics 2013
21
25

PRRT2 deficiency induces paroxysmal kinesigenic dyskinesia by regulating synaptic transmission in cerebellum.
Guo-He Tan, Yuan-Yuan Liu, Lu Wang, Kui Li, Ze-Qiang Zhang, Hong-Fu Li, Zhong-Fei Yang, Yang Li, Dan Li, Ming-Yue Wu,[...]. Cell Res 2018
34
25

Expanding phenotype of PRRT2 gene mutations: A new case with epilepsy and benign myoclonus of early infancy.
Ilenia Maini, Alessandro Iodice, Carlotta Spagnoli, Grazia Gabriella Salerno, Gianna Bertani, Daniele Frattini, Carlo Fusco. Eur J Paediatr Neurol 2016
13
25

Paroxysmal kinesigenic dyskinesia caused by 16p11.2 microdeletion.
Pichet Termsarasab, Amy C Yang, Jennifer Reiner, Hui Mei, Stuart A Scott, Steven J Frucht. Tremor Other Hyperkinet Mov (N Y) 2014
7
25

Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2-related disorders.
Shao-Yun Zhao, Li-Xi Li, Yu-Lan Chen, Yi-Jun Chen, Gong-Lu Liu, Hai-Lin Dong, Dian-Fu Chen, Hong-Fu Li, Zhi-Ying Wu. CNS Neurosci Ther 2020
4
25

Focal seizures and epileptic spasms in a child with Down syndrome from a family with a PRRT2 mutation.
Ayuko Igarashi, Akihisa Okumura, Keiko Shimojima, Shinpei Abe, Mitsuru Ikeno, Toshiaki Shimizu, Toshiyuki Yamamoto. Brain Dev 2016
7
25

Early childhood myoclonic epilepsy: An independent genetic generalized epilepsy with myoclonic seizures as the main seizure type.
Zhixian Yang, Jiao Xue, Hui Li, Ping Qian, Xiaoyan Liu, Yuwu Jiang, Yuehua Zhang. Clin Neurophysiol 2017
3
33

16p11.2 deletion in patients with paroxysmal kinesigenic dyskinesia but without intellectual disability.
Wen Li, Yifan Wang, Bin Li, Bin Tang, Hui Sun, Jinxing Lai, Na He, Bingmei Li, Heng Meng, Weiping Liao,[...]. Brain Behav 2018
2
50

Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
M T Siu, D T Butcher, A L Turinsky, C Cytrynbaum, D J Stavropoulos, S Walker, O Caluseriu, M Carter, Y Lou, R Nicolson,[...]. Clin Epigenetics 2019
23
25

Child Neurology: PRRT2-associated movement disorders and differential diagnoses.
Darius Ebrahimi-Fakhari, Keun-Sun Kang, Urania Kotzaeridou, Juergen Kohlhase, Christine Klein, Birgit E Assmann. Neurology 2014
10
25

Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study.
Russell C Dale, Padraic Grattan-Smith, Michelle Nicholson, Greg B Peters. Dev Med Child Neurol 2012
56
25

Severe phenotypic spectrum of biallelic mutations in PRRT2 gene.
Marion Delcourt, Florence Riant, Josette Mancini, Mathieu Milh, Vincent Navarro, Emmanuel Roze, Véronique Humbertclaude, Christian Korff, Vincent Des Portes, Pierre Szepetowski,[...]. J Neurol Neurosurg Psychiatry 2015
41
25


Phenotypes, genotypes, and the management of paroxysmal movement disorders.
Laura Silveira-Moriyama, Stjepana Kovac, Manju A Kurian, Henry Houlden, Andrew J Lees, Matthew C Walker, Emmanuel Roze, Alex R Paciorkowski, Jonathan W Mink, Thomas T Warner. Dev Med Child Neurol 2018
19
25

Identification of a Premature Termination Mutation in the Proline-Rich Transmembrane Protein 2 Gene in a Chinese Family with Febrile Seizures.
Wen Zheng, Jie Zhang, Xiong Deng, Jingjing Xiao, Lamei Yuan, Yan Yang, Liping Guan, Zhi Song, Zhijian Yang, Hao Deng. Mol Neurobiol 2016
16
25

PRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesia.
Akihisa Okumura, Keiko Shimojima, Hirokazu Kurahashi, Shingo Numoto, Shino Shimada, Atsushi Ishii, Iori Ohmori, Satoru Takahashi, Tomonari Awaya, Tetsuo Kubota,[...]. Seizure 2019
7
25

Excitation/Inhibition Imbalance in Animal Models of Autism Spectrum Disorders.
Eunee Lee, Jiseok Lee, Eunjoon Kim. Biol Psychiatry 2017
169
25

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
386
25

Altered Excitatory-Inhibitory Balance in the NMDA-Hypofunction Model of Schizophrenia.
Colin Kehrer, Nino Maziashvili, Tamar Dugladze, Tengis Gloveli. Front Mol Neurosci 2008
164
25

Mechanisms underlying the EEG biomarker in Dup15q syndrome.
Joel Frohlich, Lawrence T Reiter, Vidya Saravanapandian, Charlotte DiStefano, Scott Huberty, Carly Hyde, Stormy Chamberlain, Carrie E Bearden, Peyman Golshani, Andrei Irimia,[...]. Mol Autism 2019
14
25


A Review of the Functional and Anatomical Default Mode Network in Schizophrenia.
Mao-Lin Hu, Xiao-Fen Zong, J John Mann, Jun-Jie Zheng, Yan-Hui Liao, Zong-Chang Li, Ying He, Xiao-Gang Chen, Jin-Song Tang. Neurosci Bull 2017
91
25

Prodromal assessment with the structured interview for prodromal syndromes and the scale of prodromal symptoms: predictive validity, interrater reliability, and training to reliability.
Tandy J Miller, Thomas H McGlashan, Joanna L Rosen, Kristen Cadenhead, Tyrone Cannon, Joseph Ventura, William McFarlane, Diana O Perkins, Godfrey D Pearlson, Scott W Woods. Schizophr Bull 2003
25


Default mode network connectivity and reciprocal social behavior in 22q11.2 deletion syndrome.
Matthew J Schreiner, Katherine H Karlsgodt, Lucina Q Uddin, Carolyn Chow, Eliza Congdon, Maria Jalbrzikowski, Carrie E Bearden. Soc Cogn Affect Neurosci 2014
47
25

Measuring the cortical correlation structure of spontaneous oscillatory activity with EEG and MEG.
Marcus Siems, Anna-Antonia Pape, Joerg F Hipp, Markus Siegel. Neuroimage 2016
40
25

Auditory Evoked M100 Response Latency is Delayed in Children with 16p11.2 Deletion but not 16p11.2 Duplication.
Julian Jenkins, Vivian Chow, Lisa Blaskey, Emily Kuschner, Saba Qasmieh, Leah Gaetz, J Christopher Edgar, Pratik Mukherjee, Randall Buckner, Srikantan S Nagarajan,[...]. Cereb Cortex 2016
18
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.