A citation-based method for searching scientific literature

A R La Spada, E M Wilson, D B Lubahn, A E Harding, K H Fischbeck. Nature 1991
Times Cited: 1700







List of co-cited articles
1298 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy.
Masahisa Katsuno, Hiroaki Adachi, Akito Kume, Mei Li, Yuji Nakagomi, Hisayoshi Niwa, Chen Sang, Yasushi Kobayashi, Manabu Doyu, Gen Sobue. Neuron 2002
315
22


Peripheral androgen receptor gene suppression rescues disease in mouse models of spinal and bulbar muscular atrophy.
Andrew P Lieberman, Zhigang Yu, Sue Murray, Raechel Peralta, Audrey Low, Shuling Guo, Xing Xian Yu, Constanza J Cortes, C Frank Bennett, Brett P Monia,[...]. Cell Rep 2014
107
19

Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy.
Constanza J Cortes, Shuo-Chien Ling, Ling T Guo, Gene Hung, Taiji Tsunemi, Linda Ly, Seiya Tokunaga, Edith Lopez, Bryce L Sopher, C Frank Bennett,[...]. Neuron 2014
102
16

Natural history of spinal and bulbar muscular atrophy (SBMA): a study of 223 Japanese patients.
Naoki Atsuta, Hirohisa Watanabe, Mizuki Ito, Haruhiko Banno, Keisuke Suzuki, Masahisa Katsuno, Fumiaki Tanaka, Akiko Tamakoshi, Gen Sobue. Brain 2006
148
16

Clinical features of spinal and bulbar muscular atrophy.
Lindsay E Rhodes, Brandi K Freeman, Sungyoung Auh, Angela D Kokkinis, Alison La Pean, Cheunju Chen, Tanya J Lehky, Joseph A Shrader, Ellen W Levy, Michael Harris-Love,[...]. Brain 2009
99
15

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
15

Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
919
15

Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy.
Masahisa Katsuno, Hiroaki Adachi, Manabu Doyu, Makoto Minamiyama, Chen Sang, Yasushi Kobayashi, Akira Inukai, Gen Sobue. Nat Med 2003
203
14

Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial.
Masahisa Katsuno, Haruhiko Banno, Keisuke Suzuki, Yu Takeuchi, Motoshi Kawashima, Ichiro Yabe, Hidenao Sasaki, Masashi Aoki, Mitsuya Morita, Imaharu Nakano,[...]. Lancet Neurol 2010
115
14

Overexpression of IGF-1 in muscle attenuates disease in a mouse model of spinal and bulbar muscular atrophy.
Isabella Palazzolo, Conor Stack, Lingling Kong, Antonio Musaro, Hiroaki Adachi, Masahisa Katsuno, Gen Sobue, J Paul Taylor, Charlotte J Sumner, Kenneth H Fischbeck,[...]. Neuron 2009
152
14

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
686
13

Correlation of clinical and molecular features in spinal bulbar muscular atrophy.
Pietro Fratta, Niranjanan Nirmalananthan, Luc Masset, Iwona Skorupinska, Toby Collins, Andrea Cortese, Sally Pemble, Andrea Malaspina, Elizabeth M C Fisher, Linda Greensmith,[...]. Neurology 2014
45
26

Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet.
Anna Rocchi, Carmelo Milioto, Sara Parodi, Andrea Armirotti, Doriana Borgia, Matteo Pellegrini, Anna Urciuolo, Sibilla Molon, Valeria Morbidoni, Manuela Marabita,[...]. Acta Neuropathol 2016
44
27

Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients.
Hiroaki Adachi, Masahisa Katsuno, Makoto Minamiyama, Masahiro Waza, Chen Sang, Yuji Nakagomi, Yasushi Kobayashi, Fumiaki Tanaka, Manabu Doyu, Akira Inukai,[...]. Brain 2005
133
12

Nuclear inclusions of the androgen receptor protein in spinal and bulbar muscular atrophy.
M Li, S Miwa, Y Kobayashi, D E Merry, M Yamamoto, F Tanaka, M Doyu, Y Hashizume, K H Fischbeck, G Sobue. Ann Neurol 1998
215
12

X-linked recessive bulbospinal neuronopathy. A clinicopathological study.
G Sobue, Y Hashizume, E Mukai, M Hirayama, T Mitsuma, A Takahashi. Brain 1989
251
12

Polyglutamine-expanded androgen receptor interferes with TFEB to elicit autophagy defects in SBMA.
Constanza J Cortes, Helen C Miranda, Harald Frankowski, Yakup Batlevi, Jessica E Young, Amy Le, Nishi Ivanov, Bryce L Sopher, Cassiano Carromeu, Alysson R Muotri,[...]. Nat Neurosci 2014
96
12

Cytoplasmic retention of polyglutamine-expanded androgen receptor ameliorates disease via autophagy in a mouse model of spinal and bulbar muscular atrophy.
Heather L Montie, Maria S Cho, Latia Holder, Yuhong Liu, Andrey S Tsvetkov, Steven Finkbeiner, Diane E Merry. Hum Mol Genet 2009
102
12

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
12

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
V Campuzano, L Montermini, M D Moltò, L Pianese, M Cossée, F Cavalcanti, E Monros, F Rodius, F Duclos, A Monticelli,[...]. Science 1996
12

Efficacy and safety of dutasteride in patients with spinal and bulbar muscular atrophy: a randomised placebo-controlled trial.
Lindsay E Fernández-Rhodes, Angela D Kokkinis, Michelle J White, Charlotte A Watts, Sungyoung Auh, Neal O Jeffries, Joseph A Shrader, Tanya J Lehky, Li Li, Jennifer E Ryder,[...]. Lancet Neurol 2011
97
11

Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females.
Gianni Sorarù, Carla D'Ascenzo, Alberto Polo, Arianna Palmieri, Linda Baggio, Lodovica Vergani, Cinzia Gellera, Giuseppe Moretto, Elena Pegoraro, Corrado Angelini. J Neurol Sci 2008
84
13

Androgen-dependent pathology demonstrates myopathic contribution to the Kennedy disease phenotype in a mouse knock-in model.
Zhigang Yu, Nahid Dadgar, Megan Albertelli, Kirsten Gruis, Cynthia Jordan, Diane M Robins, Andrew P Lieberman. J Clin Invest 2006
119
11

Phase 2 trial of leuprorelin in patients with spinal and bulbar muscular atrophy.
Haruhiko Banno, Masahisa Katsuno, Keisuke Suzuki, Yu Takeuchi, Motoshi Kawashima, Noriaki Suga, Motoko Takamori, Mizuki Ito, Tomohiko Nakamura, Koji Matsuo,[...]. Ann Neurol 2009
102
10

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
10

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
10

Polyglutamine Repeats in Neurodegenerative Diseases.
Andrew P Lieberman, Vikram G Shakkottai, Roger L Albin. Annu Rev Pathol 2019
55
18

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
R Koide, T Ikeuchi, O Onodera, H Tanaka, S Igarashi, K Endo, H Takahashi, R Kondo, A Ishikawa, T Hayashi. Nat Genet 1994
713
10

Long-term treatment with leuprorelin for spinal and bulbar muscular atrophy: natural history-controlled study.
Atsushi Hashizume, Masahisa Katsuno, Keisuke Suzuki, Akihiro Hirakawa, Yasuhiro Hijikata, Shinichiro Yamada, Tomonori Inagaki, Haruhiko Banno, Gen Sobue. J Neurol Neurosurg Psychiatry 2017
21
42

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion.
G David, N Abbas, G Stevanin, A Dürr, G Yvert, G Cancel, C Weber, G Imbert, F Saudou, E Antoniou,[...]. Nat Genet 1997
453
9

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p.
S Nagafuchi, H Yanagisawa, K Sato, T Shirayama, E Ohsaki, M Bundo, T Takeda, K Tadokoro, I Kondo, N Murayama. Nat Genet 1994
470
9

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.
K Sanpei, H Takano, S Igarashi, T Sato, M Oyake, H Sasaki, A Wakisaka, K Tashiro, Y Ishida, T Ikeuchi,[...]. Nat Genet 1996
463
9

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
978
9

Mitochondrial abnormalities in spinal and bulbar muscular atrophy.
Srikanth Ranganathan, George G Harmison, Kristin Meyertholen, Maria Pennuto, Barrington G Burnett, Kenneth H Fischbeck. Hum Mol Genet 2009
107
9

Castration restores function and neurofilament alterations of aged symptomatic males in a transgenic mouse model of spinal and bulbar muscular atrophy.
Erica S Chevalier-Larsen, Christopher J O'Brien, Huiyi Wang, Shannon C Jenkins, Latia Holder, Andrew P Lieberman, Diane E Merry. J Neurosci 2004
152
9

CAG repeat size correlates to electrophysiological motor and sensory phenotypes in SBMA.
Keisuke Suzuki, Masahisa Katsuno, Haruhiko Banno, Yu Takeuchi, Naoki Atsuta, Mizuki Ito, Hirohisa Watanabe, Fumitada Yamashita, Norio Hori, Tomohiko Nakamura,[...]. Brain 2008
66
13

Non-ATG-initiated translation directed by microsatellite expansions.
Tao Zu, Brian Gibbens, Noelle S Doty, Mário Gomes-Pereira, Aline Huguet, Matthew D Stone, Jamie Margolis, Mark Peterson, Todd W Markowski, Melissa A C Ingram,[...]. Proc Natl Acad Sci U S A 2011
496
9

Motoneuronal cell death is not correlated with aggregate formation of androgen receptors containing an elongated polyglutamine tract.
S Simeoni, M A Mancini, D L Stenoien, M Marcelli, N L Weigel, M Zanisi, L Martini, A Poletti. Hum Mol Genet 2000
95
9

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
A J Verkerk, M Pieretti, J S Sutcliffe, Y H Fu, D P Kuhl, A Pizzuti, O Reiner, S Richards, M F Victoria, F P Zhang. Cell 1991
9

Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.
S E Holmes, E E O'Hearn, M G McInnis, D A Gorelick-Feldman, J J Kleiderlein, C Callahan, N G Kwak, R G Ingersoll-Ashworth, M Sherr, A J Sumner,[...]. Nat Genet 1999
270
9

Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy.
S Igarashi, Y Tanno, O Onodera, M Yamazaki, S Sato, A Ishikawa, N Miyatani, M Nagashima, Y Ishikawa, K Sahashi. Neurology 1992
118
8

Nonalcoholic fatty liver disease in spinal and bulbar muscular atrophy.
Robert D Guber, Varun Takyar, Angela Kokkinis, Derrick A Fox, Hawwa Alao, Ilona Kats, Dara Bakar, Alan T Remaley, Stephen M Hewitt, David E Kleiner,[...]. Neurology 2017
15
53


DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Conceição Bettencourt, Davina Hensman-Moss, Michael Flower, Sarah Wiethoff, Alexis Brice, Cyril Goizet, Giovanni Stevanin, Georgios Koutsis, Georgia Karadima, Marios Panas,[...]. Ann Neurol 2016
102
8

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein.
K Nakamura, S Y Jeong, T Uchihara, M Anno, K Nagashima, T Nagashima, S Ikeda, S Tsuji, I Kanazawa. Hum Mol Genet 2001
382
8

A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophy.
Eric D Wieben, Ross A Aleff, Nirubol Tosakulwong, Malinda L Butz, W Edward Highsmith, Albert O Edwards, Keith H Baratz. PLoS One 2012
120
8

Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients.
Doriana Borgia, Adriana Malena, Marco Spinazzi, Maria Andrea Desbats, Leonardo Salviati, Aaron P Russell, Giovanni Miotto, Laura Tosatto, Elena Pegoraro, Gianni Sorarù,[...]. Hum Mol Genet 2017
22
36

GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome.
Amy J LaCroix, Deborah Stabley, Rebecca Sahraoui, Margaret P Adam, Michele Mehaffey, Kelly Kernan, Candace T Myers, Carrie Fagerstrom, George Anadiotis, Yassmine M Akkari,[...]. Am J Hum Genet 2019
24
33


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.