A citation-based method for searching scientific literature

Parviz Daniel Hejazi Pastor, Xiaofei Du, Sarah Fazal, Andre N Davies, Christopher M Gomez. Cerebellum 2018
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Second cistron in CACNA1A gene encodes a transcription factor mediating cerebellar development and SCA6.
Xiaofei Du, Jun Wang, Haipeng Zhu, Lorenzo Rinaldo, Kay-Marie Lamar, Ann C Palmenberg, Christian Hansel, Christopher M Gomez. Cell 2013
94
63

An miRNA-mediated therapy for SCA6 blocks IRES-driven translation of the CACNA1A second cistron.
Yu Miyazaki, Xiaofei Du, Shin-Ichi Muramatsu, Christopher M Gomez. Sci Transl Med 2016
35
45

Mammalian Polycistronic mRNAs and Disease.
Timofey A Karginov, Daniel Parviz Hejazi Pastor, Bert L Semler, Christopher M Gomez. Trends Genet 2017
16
27

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
27

α1ACT Is Essential for Survival and Early Cerebellar Programming in a Critical Neonatal Window.
Xiaofei Du, Cenfu Wei, Daniel Parviz Hejazi Pastor, Eshaan R Rao, Yan Li, Giorgio Grasselli, Jack Godfrey, Ann C Palmenberg, Jorge Andrade, Christian Hansel,[...]. Neuron 2019
8
37

RNA regulons in Hox 5' UTRs confer ribosome specificity to gene regulation.
Shifeng Xue, Siqi Tian, Kotaro Fujii, Wipapat Kladwang, Rhiju Das, Maria Barna. Nature 2015
172
18


Local RNA flexibility perturbation of the IRES element induced by a novel ligand inhibits viral RNA translation.
Gloria Lozano, Alejandro Trapote, Jorge Ramajo, Xavier Elduque, Anna Grandas, Jordi Robles, Enrique Pedroso, Encarnación Martínez-Salas. RNA Biol 2015
17
18


Bicistronic CACNA1A Gene Expression in Neurons Derived from Spinocerebellar Ataxia Type 6 Patient-Induced Pluripotent Stem Cells.
Carlo Bavassano, Andreas Eigentler, Ruslan Stanika, Gerald J Obermair, Sylvia Boesch, Georg Dechant, Roxana Nat. Stem Cells Dev 2017
13
18

RNAi silencing of P/Q-type calcium channels in Purkinje neurons of adult mouse leads to episodic ataxia type 2.
Julie Salvi, Federica Bertaso, Anne-Laure Mausset-Bonnefont, Alexandra Metz, Céline Lemmers, Fabrice Ango, Laurent Fagni, Philippe Lory, Alexandre Mezghrani. Neurobiol Dis 2014
13
18

RORalpha-mediated Purkinje cell development determines disease severity in adult SCA1 mice.
Heliane G Serra, Lisa Duvick, Tao Zu, Kerri Carlson, Sam Stevens, Nathan Jorgensen, Alana Lysholm, Eric Burright, Huda Y Zoghbi, H Brent Clark,[...]. Cell 2006
149
18

Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels.
Kei Watase, Curtis F Barrett, Taisuke Miyazaki, Taro Ishiguro, Kinya Ishikawa, Yuanxin Hu, Toshinori Unno, Yaling Sun, Sayumi Kasai, Masahiko Watanabe,[...]. Proc Natl Acad Sci U S A 2008
104
18

CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.
Lena Damaj, Alexis Lupien-Meilleur, Anne Lortie, Émilie Riou, Luis H Ospina, Louise Gagnon, Catherine Vanasse, Elsa Rossignol. Eur J Hum Genet 2015
86
18

Polyglutamine spinocerebellar ataxias - from genes to potential treatments.
Henry L Paulson, Vikram G Shakkottai, H Brent Clark, Harry T Orr. Nat Rev Neurosci 2017
128
18

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Igor Splawski, Katherine W Timothy, Leah M Sharpe, Niels Decher, Pradeep Kumar, Raffaella Bloise, Carlo Napolitano, Peter J Schwartz, Robert M Joseph, Karen Condouris,[...]. Cell 2004
976
18

Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6.
K Ishikawa, H Fujigasaki, H Saegusa, K Ohwada, T Fujita, H Iwamoto, Y Komatsuzaki, S Toru, H Toriyama, M Watanabe,[...]. Hum Mol Genet 1999
140
18

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1.
Y Kawaguchi, T Okamoto, M Taniwaki, M Aizawa, M Inoue, S Katayama, H Kawakami, S Nakamura, M Nishimura, I Akiguchi. Nat Genet 1994
18

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
H T Orr, M Y Chung, S Banfi, T J Kwiatkowski, A Servadio, A L Beaudet, A E McCall, L A Duvick, L P Ranum, H Y Zoghbi. Nat Genet 1993
18

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
S M Pulst, A Nechiporuk, T Nechiporuk, S Gispert, X N Chen, I Lopes-Cendes, S Pearlman, S Starkman, G Orozco-Diaz, A Lunkes,[...]. Nat Genet 1996
867
18

Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trial.
Silvia Romano, Giulia Coarelli, Christian Marcotulli, Luca Leonardi, Francesca Piccolo, Maria Spadaro, Marina Frontali, Michela Ferraldeschi, Maria Chiara Vulpiani, Federica Ponzelli,[...]. Lancet Neurol 2015
94
18

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
18

A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia.
Marie Coutelier, Iulia Blesneac, Arnaud Monteil, Marie-Lorraine Monin, Kunie Ando, Emeline Mundwiller, Alfredo Brusco, Isabelle Le Ber, Mathieu Anheim, Anna Castrioto,[...]. Am J Hum Genet 2015
58
18

Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42.
Shunta Hashiguchi, Hiroshi Doi, Misako Kunii, Yukihiro Nakamura, Misa Shimuta, Etsuko Suzuki, Shigeru Koyano, Masaki Okubo, Hitaru Kishida, Masaaki Shiina,[...]. Neurobiol Dis 2019
9
22

A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia.
Hiroyuki Morino, Yukiko Matsuda, Keiko Muguruma, Ryosuke Miyamoto, Ryosuke Ohsawa, Toshiyuki Ohtake, Reiko Otobe, Masahiko Watanabe, Hirofumi Maruyama, Kouichi Hashimoto,[...]. Mol Brain 2015
49
18

Splice isoform-specific suppression of the Cav2.1 variant underlying spinocerebellar ataxia type 6.
Wei-Ling Tsou, Bing-Wen Soong, Henry L Paulson, Edgardo Rodríguez-Lebrón. Neurobiol Dis 2011
24
18

Properties of human Cav2.1 channel with a spinocerebellar ataxia type 6 mutation expressed in Purkinje cells.
Hironao Saegusa, Minoru Wakamori, Yoshihiro Matsuda, Junyang Wang, Yasuo Mori, Shuqin Zong, Tsutomu Tanabe. Mol Cell Neurosci 2007
49
18

Migration of Interneuron Precursors in the Nascent Cerebellar Cortex.
Annika K Wefers, Christian Haberlandt, Lachezar Surchev, Christian Steinhäuser, Ronald Jabs, Karl Schilling. Cerebellum 2018
6
16




Epigenetic Drivers in Pediatric Medulloblastoma.
Martine F Roussel, Jennifer L Stripay. Cerebellum 2018
28
9




Climbing Fiber Development Is Impaired in Postnatal Car8 wdl Mice.
Lauren N Miterko, Roy V Sillitoe. Cerebellum 2018
4
25


C2'-endo nucleotides as molecular timers suggested by the folding of an RNA domain.
Stefanie A Mortimer, Kevin M Weeks. Proc Natl Acad Sci U S A 2009
32
9

LOOP IIId of the HCV IRES is essential for the structural rearrangement of the 40S-HCV IRES complex.
Jenniffer Angulo, Nathalie Ulryck, Jules Deforges, Nathalie Chamond, Marcelo Lopez-Lastra, Benoît Masquida, Bruno Sargueil. Nucleic Acids Res 2016
22
9

Alternative Mechanisms to Initiate Translation in Eukaryotic mRNAs.
Encarnación Martínez-Salas, David Piñeiro, Noemí Fernández. Comp Funct Genomics 2012
36
9


An accurately preorganized IRES RNA structure enables eIF4G capture for initiation of viral translation.
Shunsuke Imai, Parimal Kumar, Christopher U T Hellen, Victoria M D'Souza, Gerhard Wagner. Nat Struct Mol Biol 2016
23
9


Picornavirus IRES elements: RNA structure and host protein interactions.
Encarnación Martínez-Salas, Rosario Francisco-Velilla, Javier Fernandez-Chamorro, Gloria Lozano, Rosa Diaz-Toledano. Virus Res 2015
70
9


Signals Involved in Regulation of Hepatitis C Virus RNA Genome Translation and Replication.
Michael Niepmann, Lyudmila A Shalamova, Gesche K Gerresheim, Oliver Rossbach. Front Microbiol 2018
22
9

A novel protein encoded by the circular form of the SHPRH gene suppresses glioma tumorigenesis.
Maolei Zhang, Nunu Huang, Xuesong Yang, Jingyan Luo, Sheng Yan, Feizhe Xiao, Wenping Chen, Xinya Gao, Kun Zhao, Huangkai Zhou,[...]. Oncogene 2018
257
9


Gemin5 promotes IRES interaction and translation control through its C-terminal region.
David Piñeiro, Noemi Fernández, Jorge Ramajo, Encarnación Martínez-Salas. Nucleic Acids Res 2013
45
9

Foot-and-mouth disease virus infection induces proteolytic cleavage of PTB, eIF3a,b, and PABP RNA-binding proteins.
Miguel Rodríguez Pulido, Paula Serrano, Margarita Sáiz, Encarnación Martínez-Salas. Virology 2007
53
9


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.