A citation-based method for searching scientific literature

Kerri M Carlson, Laura Melcher, Shaojuan Lai, Huda Y Zoghbi, H Brent Clark, Harry T Orr. J Neurogenet 2009
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


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
35

The AXH domain of Ataxin-1 mediates neurodegeneration through its interaction with Gfi-1/Senseless proteins.
Hiroshi Tsuda, Hamed Jafar-Nejad, Akash J Patel, Yaling Sun, Hung-Kai Chen, Matthew F Rose, Koen J T Venken, Juan Botas, Harry T Orr, Hugo J Bellen,[...]. Cell 2005
147
35

Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice.
I A Klement, P J Skinner, M D Kaytor, H Yi, S M Hersch, H B Clark, H Y Zoghbi, H T Orr. Cell 1998
800
35


ATAXIN-1 interacts with the repressor Capicua in its native complex to cause SCA1 neuropathology.
Yung C Lam, Aaron B Bowman, Paymaan Jafar-Nejad, Janghoo Lim, Ronald Richman, John D Fryer, Eric D Hyun, Lisa A Duvick, Harry T Orr, Juan Botas,[...]. Cell 2006
213
28

Serine 776 of ataxin-1 is critical for polyglutamine-induced disease in SCA1 transgenic mice.
Effat S Emamian, Michael D Kaytor, Lisa A Duvick, Tao Zu, Susan K Tousey, Huda Y Zoghbi, H Brent Clark, Harry T Orr. Neuron 2003
224
28

Anatomy of zebrafish cerebellum and screen for mutations affecting its development.
Young-Ki Bae, Shuichi Kani, Takashi Shimizu, Koji Tanabe, Hideaki Nojima, Yukiko Kimura, Shin-ichi Higashijima, Masahiko Hibi. Dev Biol 2009
171
21

Zebrafish lacking Alzheimer presenilin enhancer 2 (Pen-2) demonstrate excessive p53-dependent apoptosis and neuronal loss.
William A Campbell, Hongwei Yang, Henrik Zetterberg, Stéphanie Baulac, Jacqueline A Sears, Tianming Liu, Stephen T C Wong, Tao P Zhong, Weiming Xia. J Neurochem 2006
87
21

Effective targeted gene 'knockdown' in zebrafish.
A Nasevicius, S C Ekker. Nat Genet 2000
21

Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
985
21

A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration.
Kei Watase, Edwin J Weeber, Bisong Xu, Barbara Antalffy, Lisa Yuva-Paylor, Kouichi Hashimoto, Masanobu Kano, Richard Atkinson, Yaling Sun, Dawna L Armstrong,[...]. Neuron 2002
219
21

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
152
21

Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1.
Janghoo Lim, Juan Crespo-Barreto, Paymaan Jafar-Nejad, Aaron B Bowman, Ronald Richman, David E Hill, Harry T Orr, Huda Y Zoghbi. Nature 2008
226
21

SCA1 transgenic mice: a model for neurodegeneration caused by an expanded CAG trinucleotide repeat.
E N Burright, H B Clark, A Servadio, T Matilla, R M Feddersen, W S Yunis, L A Duvick, H Y Zoghbi, H T Orr. Cell 1995
464
21

Mice lacking ataxin-1 display learning deficits and decreased hippocampal paired-pulse facilitation.
A Matilla, E D Roberson, S Banfi, J Morales, D L Armstrong, E N Burright, H T Orr, J D Sweatt, H Y Zoghbi, M M Matzuk. J Neurosci 1998
143
21

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes.
Michael F Waters, Natali A Minassian, Giovanni Stevanin, Karla P Figueroa, John P A Bannister, Dagmar Nolte, Allan F Mock, Virgilio Gerald H Evidente, Dominic B Fee, Ulrich Müller,[...]. Nat Genet 2006
205
21

Phosphorylation of ATXN1 at Ser776 in the cerebellum.
Nathan D Jorgensen, J Michael Andresen, Sara Lagalwar, Ben Armstrong, Sam Stevens, Courtney E Byam, Lisa A Duvick, Shaojuan Lai, Paymaan Jafar-Nejad, Huda Y Zoghbi,[...]. J Neurochem 2009
40
21

Identification of genes that modify ataxin-1-induced neurodegeneration.
P Fernandez-Funez, M L Nino-Rosales, B de Gouyon, W C She, J M Luchak, P Martinez, E Turiegano, J Benito, M Capovilla, P J Skinner,[...]. Nature 2000
483
21

Zebrafish models of human motor neuron diseases: advantages and limitations.
Patrick J Babin, Cyril Goizet, Demetrio Raldúa. Prog Neurobiol 2014
102
21

Calpain Inhibition Is Protective in Machado-Joseph Disease Zebrafish Due to Induction of Autophagy.
Maxinne Watchon, Kristy C Yuan, Nick Mackovski, Adam J Svahn, Nicholas J Cole, Claire Goldsbury, Silke Rinkwitz, Thomas S Becker, Garth A Nicholson, Angela S Laird. J Neurosci 2017
38
21

I-SceI meganuclease mediates highly efficient transgenesis in fish.
Violette Thermes, Clemens Grabher, Filomena Ristoratore, Franck Bourrat, André Choulika, Jochen Wittbrodt, Jean-Stéphane Joly. Mech Dev 2002
392
14

Complex splicing and neural expression of duplicated tau genes in zebrafish embryos.
Mengqi Chen, Ralph N Martins, Michael Lardelli. J Alzheimers Dis 2009
32
14

A large-scale insertional mutagenesis screen in zebrafish.
A Amsterdam, S Burgess, G Golling, W Chen, Z Sun, K Townsend, S Farrington, M Haldi, N Hopkins. Genes Dev 1999
363
14


Decreased BDNF levels are a major contributor to the embryonic phenotype of huntingtin knockdown zebrafish.
Heike Diekmann, Oleg Anichtchik, Angeleen Fleming, Marie Futter, Paul Goldsmith, Alan Roach, David C Rubinsztein. J Neurosci 2009
61
14

Overexpression of mutant superoxide dismutase 1 causes a motor axonopathy in the zebrafish.
Robin Lemmens, Annelies Van Hoecke, Nicole Hersmus, Veerle Geelen, Isabel D'Hollander, Vincent Thijs, Ludo Van Den Bosch, Peter Carmeliet, Wim Robberecht. Hum Mol Genet 2007
101
14



Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
D R Rosen, T Siddique, D Patterson, D A Figlewicz, P Sapp, A Hentati, D Donaldson, J Goto, J P O'Regan, H X Deng. Nature 1993
14


Zebrafish DJ-1 is evolutionarily conserved and expressed in dopaminergic neurons.
Qing Bai, Steven J Mullett, Jessica A Garver, David A Hinkle, Edward A Burton. Brain Res 2006
50
14


Characterization of the Huntington's disease (HD) gene homologue in the zebrafish Danio rerio.
C A Karlovich, R M John, L Ramirez, D Y Stainier, R M Myers. Gene 1998
57
14

Identification of a second presenilin gene in zebrafish with similarity to the human Alzheimer's disease gene presenilin2.
Casper Groth, Svanhild Nornes, Rosa McCarty, Richard Tamme, Michael Lardelli. Dev Genes Evol 2002
41
14

In vivo drug discovery in the zebrafish.
Leonard I Zon, Randall T Peterson. Nat Rev Drug Discov 2005
905
14

CHIP suppresses polyglutamine aggregation and toxicity in vitro and in vivo.
Victor M Miller, Rick F Nelson, Cynthia M Gouvion, Aislinn Williams, Edgardo Rodriguez-Lebron, Scott Q Harper, Beverly L Davidson, Michael R Rebagliati, Henry L Paulson. J Neurosci 2005
177
14

Loss of PINK1 function affects development and results in neurodegeneration in zebrafish.
Oleg Anichtchik, Heike Diekmann, Angeleen Fleming, Alan Roach, Paul Goldsmith, David C Rubinsztein. J Neurosci 2008
108
14


p53-dependent neuronal cell death in a DJ-1-deficient zebrafish model of Parkinson's disease.
Sandrine Bretaud, Claire Allen, Phillip W Ingham, Oliver Bandmann. J Neurochem 2007
151
14

Identification of anti-prion compounds as efficient inhibitors of polyglutamine protein aggregation in a zebrafish model.
Niclas W Schiffer, Sarah A Broadley, Thomas Hirschberger, Paul Tavan, Hans A Kretzschmar, Armin Giese, Christian Haass, F Ulrich Hartl, Bettina Schmid. J Biol Chem 2007
78
14

Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio).
Laura Flinn, Heather Mortiboys, Katrin Volkmann, Reinhard W Köster, Phillip W Ingham, Oliver Bandmann. Brain 2009
118
14

A transposon-mediated gene trap approach identifies developmentally regulated genes in zebrafish.
Koichi Kawakami, Hisashi Takeda, Noriko Kawakami, Makoto Kobayashi, Naoto Matsuda, Masayoshi Mishina. Dev Cell 2004
600
14

Huntingtin-deficient zebrafish exhibit defects in iron utilization and development.
Amanda L Lumsden, Tanya L Henshall, Sonia Dayan, Michael T Lardelli, Robert I Richards. Hum Mol Genet 2007
109
14


Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase.
H X Deng, A Hentati, J A Tainer, Z Iqbal, A Cayabyab, W Y Hung, E D Getzoff, P Hu, B Herzfeldt, R P Roos. Science 1993
14

A highly conserved regulatory element controls hematopoietic expression of GATA-2 in zebrafish.
Zhongan Yang, Hong Jiang, Fang Zhao, Deepa B Shankar, Kathleen M Sakamoto, Michael Q Zhang, Shuo Lin. BMC Dev Biol 2007
6
33

Patterning the brain of the zebrafish embryo.
C B Kimmel. Annu Rev Neurosci 1993
133
14

A zebrafish model of tauopathy allows in vivo imaging of neuronal cell death and drug evaluation.
Dominik Paquet, Ratan Bhat, Astrid Sydow, Eva-Maria Mandelkow, Stefan Berg, Sven Hellberg, Johanna Fälting, Martin Distel, Reinhard W Köster, Bettina Schmid,[...]. J Clin Invest 2009
174
14

Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice.
Heliane G Serra, Courtney E Byam, Jeffrey D Lande, Susan K Tousey, Huda Y Zoghbi, Harry T Orr. Hum Mol Genet 2004
132
14

Spinocerebellar ataxia type 1.
H Y Zoghbi. Clin Neurosci 1995
22
14


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.