A citation-based method for searching scientific literature

Bruno Sterlini, Floriana Fruscione, Simona Baldassari, Fabio Benfenati, Federico Zara, Anna Corradi. Int J Mol Sci 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E Scheffer, Samuel Berkovic, Giuseppe Capovilla, Mary B Connolly, Jacqueline French, Laura Guilhoto, Edouard Hirsch, Satish Jain, Gary W Mathern, Solomon L Moshé,[...]. Epilepsia 2017
75

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
50

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
50


Fused cerebral organoids model interactions between brain regions.
Joshua A Bagley, Daniel Reumann, Shan Bian, Julie Lévi-Strauss, Juergen A Knoblich. Nat Methods 2017
259
50

Layer-By-Layer: The Case for 3D Bioprinting Neurons to Create Patient-Specific Epilepsy Models.
Natasha Antill-O'Brien, Justin Bourke, Cathal D O'Connell. Materials (Basel) 2019
13
50

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
460
50

Complex Oscillatory Waves Emerging from Cortical Organoids Model Early Human Brain Network Development.
Cleber A Trujillo, Richard Gao, Priscilla D Negraes, Jing Gu, Justin Buchanan, Sebastian Preissl, Allen Wang, Wei Wu, Gabriel G Haddad, Isaac A Chaim,[...]. Cell Stem Cell 2019
179
50

Self-organization of axial polarity, inside-out layer pattern, and species-specific progenitor dynamics in human ES cell-derived neocortex.
Taisuke Kadoshima, Hideya Sakaguchi, Tokushige Nakano, Mika Soen, Satoshi Ando, Mototsugu Eiraku, Yoshiki Sasai. Proc Natl Acad Sci U S A 2013
435
50

The use of brain organoids to investigate neural development and disease.
Elizabeth Di Lullo, Arnold R Kriegstein. Nat Rev Neurosci 2017
255
50

Cell diversity and network dynamics in photosensitive human brain organoids.
Giorgia Quadrato, Tuan Nguyen, Evan Z Macosko, John L Sherwood, Sung Min Yang, Daniel R Berger, Natalie Maria, Jorg Scholvin, Melissa Goldman, Justin P Kinney,[...]. Nature 2017
479
50


Investigation of Rett syndrome using pluripotent stem cells.
Rana Dajani, Sung-Eun Koo, Gareth J Sullivan, In-Hyun Park. J Cell Biochem 2013
18
25

Synapse alterations precede neuronal damage and storage pathology in a human cerebral organoid model of CLN3-juvenile neuronal ceroid lipofuscinosis.
Gemma Gomez-Giro, Jonathan Arias-Fuenzalida, Javier Jarazo, Dagmar Zeuschner, Muhammad Ali, Nina Possemis, Silvia Bolognin, Rashi Halder, Christian Jäger, Willemijn F E Kuper,[...]. Acta Neuropathol Commun 2019
14
25

Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation.
Yunyao Xie, Nathan N Ng, Olga S Safrina, Carmen M Ramos, Kevin C Ess, Philip H Schwartz, Martin A Smith, Diane K O'Dowd. Neurobiol Dis 2020
8
25


Efficient specification of interneurons from human pluripotent stem cells by dorsoventral and rostrocaudal modulation.
Tae-Gon Kim, Ruiqin Yao, Travis Monnell, Jun-Hyeong Cho, Anju Vasudevan, Alice Koh, Kumar T Peeyush, Minho Moon, Debkanya Datta, Vadim Y Bolshakov,[...]. Stem Cells 2014
64
25

The L1 adhesion molecule normalizes neuritogenesis in Rett syndrome-derived neural precursor cells.
Myungsik Yoo, Cassiano Carromeu, Ohyoon Kwon, Alysson Muotri, Melitta Schachner. Biochem Biophys Res Commun 2017
9
25

Generation of D1-1 TALEN isogenic control cell line from Dravet syndrome patient iPSCs using TALEN-mediated editing of the SCN1A gene.
Yasuyoshi Tanaka, Takefumi Sone, Norimichi Higurashi, Tetsushi Sakuma, Sadafumi Suzuki, Mitsuru Ishikawa, Takashi Yamamoto, Jun Mitsui, Hitomi Tsuji, Hideyuki Okano,[...]. Stem Cell Res 2018
8
25

Unverricht-Lundborg disease.
Arielle Crespel, Edoardo Ferlazzo, Silvana Franceschetti, Pierre Genton, Riadh Gouider, Reetta Kälviäinen, Miikka Korja, Maria K Lehtinen, Esa Mervaala, Michele Simonato,[...]. Epileptic Disord 2016
22
25

Transcriptomes of Dravet syndrome iPSC derived GABAergic cells reveal dysregulated pathways for chromatin remodeling and neurodevelopment.
Jens Schuster, Loora Laan, Joakim Klar, Zhe Jin, Mikael Huss, Sergiy Korol, Feria Hikmet Noraddin, Maria Sobol, Bryndis Birnir, Niklas Dahl. Neurobiol Dis 2019
14
25

A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome.
Ikuo Ogiwara, Tojo Nakayama, Tetsushi Yamagata, Hideyuki Ohtani, Emi Mazaki, Shigeru Tsuchiya, Yushi Inoue, Kazuhiro Yamakawa. Epilepsia 2012
55
25

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
189
25

Human induced pluripotent stem cells free of vector and transgene sequences.
Junying Yu, Kejin Hu, Kim Smuga-Otto, Shulan Tian, Ron Stewart, Igor I Slukvin, James A Thomson. Science 2009
25

Abnormal γ-aminobutyric acid neurotransmission in a Kcnq2 model of early onset epilepsy.
Taku Uchida, Christoph Lossin, Yukiko Ihara, Masanobu Deshimaru, Yuchio Yanagawa, Susumu Koyama, Shinichi Hirose. Epilepsia 2017
9
25

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.
Jana Stanurova, Anika Neureiter, Michaela Hiber, Hannah de Oliveira Kessler, Kristin Stolp, Roman Goetzke, Diana Klein, Agnes Bankfalvi, Hannes Klump, Laura Steenpass. Sci Rep 2016
41
25

Animal models of epilepsy: use and limitations.
Ludmyla Kandratavicius, Priscila Alves Balista, Cleiton Lopes-Aguiar, Rafael Naime Ruggiero, Eduardo Henrique Umeoka, Norberto Garcia-Cairasco, Lezio Soares Bueno-Junior, Joao Pereira Leite. Neuropsychiatr Dis Treat 2014
208
25

PCDH19 mutation in Japanese females with epilepsy.
Norimichi Higurashi, Xiuyu Shi, Sawa Yasumoto, Hirokazu Oguni, Masako Sakauchi, Kazuya Itomi, Akie Miyamoto, Hideaki Shiraishi, Takeo Kato, Yoshio Makita,[...]. Epilepsy Res 2012
37
25


Sodium channels, inherited epilepsy, and antiepileptic drugs.
William A Catterall. Annu Rev Pharmacol Toxicol 2014
99
25

Disrupted neuronal maturation in Angelman syndrome-derived induced pluripotent stem cells.
James J Fink, Tiwanna M Robinson, Noelle D Germain, Carissa L Sirois, Kaitlyn A Bolduc, Amanda J Ward, Frank Rigo, Stormy J Chamberlain, Eric S Levine. Nat Commun 2017
49
25

Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome.
Hiroshi Maeda, Tomohiro Chiyonobu, Michiko Yoshida, Satoshi Yamashita, Masashi Zuiki, Satoshi Kidowaki, Kenichi Isoda, Kazuhiro Yamakawa, Masafumi Morimoto, Tatsutoshi Nakahata,[...]. J Hum Genet 2016
13
25

Human Pluripotent Stem Cell-Derived TSC2-Haploinsufficient Smooth Muscle Cells Recapitulate Features of Lymphangioleiomyomatosis.
Lisa M Julian, Sean P Delaney, Ying Wang, Alexander A Goldberg, Carole Doré, Julien Yockell-Lelièvre, Roger Y Tam, Krinio Giannikou, Fiona McMurray, Molly S Shoichet,[...]. Cancer Res 2017
20
25

Efficient and Precise CRISPR/Cas9-Mediated MECP2 Modifications in Human-Induced Pluripotent Stem Cells.
Thi Thanh Huong Le, Ngoc Tung Tran, Thi Mai Lan Dao, Dinh Dung Nguyen, Huy Duong Do, Thi Lien Ha, Ralf Kühn, Thanh Liem Nguyen, Klaus Rajewsky, Van Trung Chu. Front Genet 2019
8
25

Imbalance of excitatory/inhibitory synaptic protein expression in iPSC-derived neurons from FOXG1(+/-) patients and in foxg1(+/-) mice.
Tommaso Patriarchi, Sonia Amabile, Elisa Frullanti, Elisa Landucci, Caterina Lo Rizzo, Francesca Ariani, Mario Costa, Francesco Olimpico, Johannes W Hell, Flora M Vaccarino,[...]. Eur J Hum Genet 2016
33
25

Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation.
Jiong Tao, Hilde Van Esch, M Hagedorn-Greiwe, Kirsten Hoffmann, Bettina Moser, Martine Raynaud, Jürgen Sperner, Jean-Pierre Fryns, Eberhard Schwinger, Jozef Gécz,[...]. Am J Hum Genet 2004
205
25


Male patients affected by mosaic PCDH19 mutations: five new cases.
I M de Lange, P Rump, R F Neuteboom, P B Augustijn, K Hodges, A I Kistemaker, O F Brouwer, G M S Mancini, H A Newman, Y J Vos,[...]. Neurogenetics 2017
23
25

Valproic acid-induced hepatotoxicity in Alpers syndrome is associated with mitochondrial permeability transition pore opening-dependent apoptotic sensitivity in an induced pluripotent stem cell model.
Shengbiao Li, Jingyi Guo, Zhongfu Ying, Shen Chen, Liang Yang, Keshi Chen, Qi Long, Dajiang Qin, Duanqing Pei, Xingguo Liu. Hepatology 2015
49
25

Induced Pluripotent Stem Cells Derived from a CLN5 Patient Manifest Phenotypic Characteristics of Neuronal Ceroid Lipofuscinoses.
Kristiina Uusi-Rauva, Tea Blom, Carina von Schantz-Fant, Tomas Blom, Anu Jalanko, Aija Kyttälä. Int J Mol Sci 2017
22
25

The tuberous sclerosis complex.
Peter B Crino, Katherine L Nathanson, Elizabeth Petri Henske. N Engl J Med 2006
25

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
25

Generation of three human induced pluripotent stem cell (iPSC) lines from three patients with Dravet syndrome carrying distinct SCN1A gene mutations.
Jens Schuster, Ambrin Fatima, Maria Sobol, Feria Hikmet Norradin, Loora Laan, Niklas Dahl. Stem Cell Res 2019
3
33

STXBP1 encephalopathy: Connecting neurodevelopmental disorders with α-synucleinopathies?
Vanessa Lanoue, Ye Jin Chai, Julie Z Brouillet, Sarah Weckhuysen, Elizabeth E Palmer, Brett M Collins, Frederic A Meunier. Neurology 2019
13
25

Zinc finger nucleases: custom-designed molecular scissors for genome engineering of plant and mammalian cells.
Sundar Durai, Mala Mani, Karthikeyan Kandavelou, Joy Wu, Matthew H Porteus, Srinivasan Chandrasegaran. Nucleic Acids Res 2005
255
25

In Vitro Modeling of the Bipolar Disorder and Schizophrenia Using Patient-Derived Induced Pluripotent Stem Cells with Copy Number Variations of PCDH15 and RELN.
Takaya Ishii, Mitsuru Ishikawa, Koki Fujimori, Takuji Maeda, Itaru Kushima, Yuko Arioka, Daisuke Mori, Yuhki Nakatake, Bun Yamagata, Shintaro Nio,[...]. eNeuro 2019
17
25

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
872
25

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Hsiao-Tuan Chao, Hongmei Chen, Rodney C Samaco, Mingshan Xue, Maria Chahrour, Jong Yoo, Jeffrey L Neul, Shiaoching Gong, Hui-Chen Lu, Nathaniel Heintz,[...]. Nature 2010
754
25

Integration of CpG-free DNA induces de novo methylation of CpG islands in pluripotent stem cells.
Yuta Takahashi, Jun Wu, Keiichiro Suzuki, Paloma Martinez-Redondo, Mo Li, Hsin-Kai Liao, Min-Zu Wu, Reyna Hernández-Benítez, Tomoaki Hishida, Maxim Nikolaievich Shokhirev,[...]. Science 2017
28
25

PCDH19-related epilepsy in two mosaic male patients.
Alessandra Terracciano, Marina Trivisano, Raffaella Cusmai, Luca De Palma, Lucia Fusco, Claudia Compagnucci, Enrico Bertini, Federico Vigevano, Nicola Specchio. Epilepsia 2016
41
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.