A citation-based method for searching scientific literature

Norimichi Higurashi, Taku Uchida, Christoph Lossin, Yoshio Misumi, Yohei Okada, Wado Akamatsu, Yoichi Imaizumi, Bo Zhang, Kazuki Nabeshima, Masayuki X Mori, Shutaro Katsurabayashi, Yukiyoshi Shirasaka, Hideyuki Okano, Shinichi Hirose. Mol Brain 2013
Times Cited: 73







List of co-cited articles
1124 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Modeling Dravet syndrome using induced pluripotent stem cells (iPSCs) and directly converted neurons.
Jiao Jiao, Yuanyuan Yang, Yiwu Shi, Jiayu Chen, Rui Gao, Yong Fan, Hui Yao, Weiping Liao, Xiao-Fang Sun, Shaorong Gao. Hum Mol Genet 2013
79
67

Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism.
Yu Liu, Luis F Lopez-Santiago, Yukun Yuan, Julie M Jones, Helen Zhang, Heather A O'Malley, Gustavo A Patino, Janelle E O'Brien, Raffaella Rusconi, Ajay Gupta,[...]. Ann Neurol 2013
148
64

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy.
Frank H Yu, Massimo Mantegazza, Ruth E Westenbroek, Carol A Robbins, Franck Kalume, Kimberly A Burton, William J Spain, G Stanley McKnight, Todd Scheuer, William A Catterall. Nat Neurosci 2006
643
45

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
Ikuo Ogiwara, Hiroyuki Miyamoto, Noriyuki Morita, Nafiseh Atapour, Emi Mazaki, Ikuyo Inoue, Tamaki Takeuchi, Shigeyoshi Itohara, Yuchio Yanagawa, Kunihiko Obata,[...]. J Neurosci 2007
499
39

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
38

A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells.
Maria C N Marchetto, Cassiano Carromeu, Allan Acab, Diana Yu, Gene W Yeo, Yangling Mu, Gong Chen, Fred H Gage, Alysson R Muotri. Cell 2010
865
31

A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients.
Yishan Sun, Sergiu P Paşca, Thomas Portmann, Carleton Goold, Kathleen A Worringer, Wendy Guan, Karen C Chan, Hui Gai, Daniel Vogt, Ying-Jiun J Chen,[...]. Elife 2016
65
33

Cerebral organoids model human brain development and microcephaly.
Madeline A Lancaster, Magdalena Renner, Carol-Anne Martin, Daniel Wenzel, Louise S Bicknell, Matthew E Hurles, Tessa Homfray, Josef M Penninger, Andrew P Jackson, Juergen A Knoblich. Nature 2013
28

CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation.
J Liu, C Gao, W Chen, W Ma, X Li, Y Shi, H Zhang, L Zhang, Y Long, H Xu,[...]. Transl Psychiatry 2016
55
34

Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome.
Sergiu P Paşca, Thomas Portmann, Irina Voineagu, Masayuki Yazawa, Aleksandr Shcheglovitov, Anca M Paşca, Branden Cord, Theo D Palmer, Sachiko Chikahisa, Seiji Nishino,[...]. Nat Med 2011
381
24

Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome.
Christine S Cheah, Frank H Yu, Ruth E Westenbroek, Franck K Kalume, John C Oakley, Gregory B Potter, John L Rubenstein, William A Catterall. Proc Natl Acad Sci U S A 2012
168
24

Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells.
Achia Urbach, Ori Bar-Nur, George Q Daley, Nissim Benvenisty. Cell Stem Cell 2010
276
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
20

Directed differentiation and functional maturation of cortical interneurons from human embryonic stem cells.
Asif M Maroof, Sotirios Keros, Jennifer A Tyson, Shui-Wang Ying, Yosif M Ganat, Florian T Merkle, Becky Liu, Adam Goulburn, Edouard G Stanley, Andrew G Elefanty,[...]. Cell Stem Cell 2013
359
20

SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients.
Aleksandr Shcheglovitov, Olesya Shcheglovitova, Masayuki Yazawa, Thomas Portmann, Rui Shu, Vittorio Sebastiano, Anna Krawisz, Wendy Froehlich, Jonathan A Bernstein, Joachim F Hallmayer,[...]. Nature 2013
291
20

Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice.
Akshitkumar M Mistry, Christopher H Thompson, Alison R Miller, Carlos G Vanoye, Alfred L George, Jennifer A Kearney. Neurobiol Dis 2014
90
20

Impaired excitability of somatostatin- and parvalbumin-expressing cortical interneurons in a mouse model of Dravet syndrome.
Chao Tai, Yasuyuki Abe, Ruth E Westenbroek, Todd Scheuer, William A Catterall. Proc Natl Acad Sci U S A 2014
112
20

Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation.
Aaron Y L Cheung, Lindsay M Horvath, Daria Grafodatskaya, Peter Pasceri, Rosanna Weksberg, Akitsu Hotta, Laura Carrel, James Ellis. Hum Mol Genet 2011
188
19

Induced pluripotent stem cells from a spinal muscular atrophy patient.
Allison D Ebert, Junying Yu, Ferrill F Rose, Virginia B Mattis, Christian L Lorson, James A Thomson, Clive N Svendsen. Nature 2009
979
19

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
238
19

Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons.
John T Dimos, Kit T Rodolfa, Kathy K Niakan, Laurin M Weisenthal, Hiroshi Mitsumoto, Wendy Chung, Gist F Croft, Genevieve Saphier, Rudy Leibel, Robin Goland,[...]. Science 2008
17

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
17

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
17

Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes.
Stormy J Chamberlain, Pin-Fang Chen, Khong Y Ng, Fany Bourgois-Rocha, Fouad Lemtiri-Chlieh, Eric S Levine, Marc Lalande. Proc Natl Acad Sci U S A 2010
215
17

Nav1.1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome.
Ikuo Ogiwara, Takuji Iwasato, Hiroyuki Miyamoto, Ryohei Iwata, Tetsushi Yamagata, Emi Mazaki, Yuchio Yanagawa, Nobuaki Tamamaki, Takao K Hensch, Shigeyoshi Itohara,[...]. Hum Mol Genet 2013
99
17

Impaired action potential initiation in GABAergic interneurons causes hyperexcitable networks in an epileptic mouse model carrying a human Na(V)1.1 mutation.
Ulrike B S Hedrich, Camille Liautard, Daniel Kirschenbaum, Martin Pofahl, Jennifer Lavigne, Yuanyuan Liu, Stephan Theiss, Johannes Slotta, Andrew Escayg, Marcel Dihné,[...]. J Neurosci 2014
72
18

CDKL5 ensures excitatory synapse stability by reinforcing NGL-1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons.
Sara Ricciardi, Federica Ungaro, Melanie Hambrock, Nils Rademacher, Gilda Stefanelli, Dario Brambilla, Alessandro Sessa, Cinzia Magagnotti, Angela Bachi, Elisa Giarda,[...]. Nat Cell Biol 2012
161
16

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, Jacinta M McMahon, Brian J O'Roak, Joseph Cook, Adiba Khan, Michael O Dorschner, Molly Weaver, Sophie Calvert,[...]. Nat Genet 2013
405
16

Autistic-like behaviour in Scn1a+/- mice and rescue by enhanced GABA-mediated neurotransmission.
Sung Han, Chao Tai, Ruth E Westenbroek, Frank H Yu, Christine S Cheah, Gregory B Potter, John L Rubenstein, Todd Scheuer, Horacio O de la Iglesia, William A Catterall. Nature 2012
372
16

Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibility.
Stacey B Dutton, Christopher D Makinson, Ligia A Papale, Anupama Shankar, Bindu Balakrishnan, Kazu Nakazawa, Andrew Escayg. Neurobiol Dis 2013
76
16

Mitochondrial dysfunction associated with increased oxidative stress and α-synuclein accumulation in PARK2 iPSC-derived neurons and postmortem brain tissue.
Yoichi Imaizumi, Yohei Okada, Wado Akamatsu, Masato Koike, Naoko Kuzumaki, Hideki Hayakawa, Tomoko Nihira, Tetsuro Kobayashi, Manabu Ohyama, Shigeto Sato,[...]. Mol Brain 2012
252
15

Disease-specific induced pluripotent stem cells.
In-Hyun Park, Natasha Arora, Hongguang Huo, Nimet Maherali, Tim Ahfeldt, Akiko Shimamura, M William Lensch, Chad Cowan, Konrad Hochedlinger, George Q Daley. Cell 2008
15

Modelling schizophrenia using human induced pluripotent stem cells.
Kristen J Brennand, Anthony Simone, Jessica Jou, Chelsea Gelboin-Burkhart, Ngoc Tran, Sarah Sangar, Yan Li, Yangling Mu, Gong Chen, Diana Yu,[...]. Nature 2011
872
15

Signaling defects in iPSC-derived fragile X premutation neurons.
Jing Liu, Katarzyna A Koscielska, Zhengyu Cao, Susan Hulsizer, Natalie Grace, Gaela Mitchell, Catherine Nacey, Jackline Githinji, Jeannine McGee, Dolores Garcia-Arocena,[...]. Hum Mol Genet 2012
95
15

Induced pluripotent stem cell lines derived from human somatic cells.
Junying Yu, Maxim A Vodyanik, Kim Smuga-Otto, Jessica Antosiewicz-Bourget, Jennifer L Frane, Shulan Tian, Jeff Nie, Gudrun A Jonsdottir, Victor Ruotti, Ron Stewart,[...]. Science 2007
15

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
A Escayg, B T MacDonald, M H Meisler, S Baulac, G Huberfeld, I An-Gourfinkel, A Brice, E LeGuern, B Moulard, D Chaigne,[...]. Nat Genet 2000
693
15

De novo mutations in epileptic encephalopathies.
Andrew S Allen, Samuel F Berkovic, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E Eichler, Michael P Epstein, Tracy Glauser, David B Goldstein, Yujun Han,[...]. Nature 2013
925
15

Brain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure.
Xuyu Qian, Ha Nam Nguyen, Mingxi M Song, Christopher Hadiono, Sarah C Ogden, Christy Hammack, Bing Yao, Gregory R Hamersky, Fadi Jacob, Chun Zhong,[...]. Cell 2016
916
15

Probing sporadic and familial Alzheimer's disease using induced pluripotent stem cells.
Mason A Israel, Shauna H Yuan, Cedric Bardy, Sol M Reyna, Yangling Mu, Cheryl Herrera, Michael P Hefferan, Sebastiaan Van Gorp, Kristopher L Nazor, Francesca S Boscolo,[...]. Nature 2012
728
13

Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.
Steven D Sheridan, Kraig M Theriault, Surya A Reis, Fen Zhou, Jon M Madison, Laurence Daheron, Jeanne F Loring, Stephen J Haggarty. PLoS One 2011
210
13

Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome.
Kun-Yong Kim, Eriona Hysolli, In-Hyun Park. Proc Natl Acad Sci U S A 2011
148
13

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.
Giulia Barcia, Matthew R Fleming, Aline Deligniere, Valeswara-Rao Gazula, Maile R Brown, Maeva Langouet, Haijun Chen, Jack Kronengold, Avinash Abhyankar, Roberta Cilio,[...]. Nat Genet 2012
265
13

De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.
Krishna R Veeramah, Janelle E O'Brien, Miriam H Meisler, Xiaoyang Cheng, Sulayman D Dib-Hajj, Stephen G Waxman, Dinesh Talwar, Santhosh Girirajan, Evan E Eichler, Linda L Restifo,[...]. Am J Hum Genet 2012
254
13

Embryonic stem cell lines derived from human blastocysts.
J A Thomson, J Itskovitz-Eldor, S S Shapiro, M A Waknitz, J J Swiergiel, V S Marshall, J M Jones. Science 1998
13

Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAergic) interneuron abnormalities.
Melinda S Martin, Karoni Dutt, Ligia A Papale, Céline M Dubé, Stacey B Dutton, Georgius de Haan, Anupama Shankar, Sergio Tufik, Miriam H Meisler, Tallie Z Baram,[...]. J Biol Chem 2010
147
13

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
L Claes, J Del-Favero, B Ceulemans, L Lagae, C Van Broeckhoven, P De Jonghe. Am J Hum Genet 2001
785
13

Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus.
Michael J Devine, Mina Ryten, Petr Vodicka, Alison J Thomson, Tom Burdon, Henry Houlden, Fatima Cavaleri, Masumi Nagano, Nicola J Drummond, Jan-Willem Taanman,[...]. Nat Commun 2011
295
12

Induced pluripotent stem cell models from X-linked adrenoleukodystrophy patients.
Jiho Jang, Hoon-Chul Kang, Han-Soo Kim, Ji Young Kim, Yong Jun Huh, Dae-Sung Kim, Jeong-Eun Yoo, Jeong-Ah Lee, Boyoung Lim, Jiwon Lee,[...]. Ann Neurol 2011
71
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.