A citation-based method for searching scientific literature

Wai Yan Yau, Emer O'Connor, Roisin Sullivan, Layan Akijian, Nicholas W Wood. FEBS J 2018
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


The central role of DNA damage and repair in CAG repeat diseases.
Thomas H Massey, Lesley Jones. Dis Model Mech 2018
37
50

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
50

Genetics, Mechanisms, and Therapeutic Progress in Polyglutamine Spinocerebellar Ataxias.
Ronald A M Buijsen, Lodewijk J A Toonen, Sarah L Gardiner, Willeke M C van Roon-Mom. Neurotherapeutics 2019
37
50

Inositol 1,4,5-trisphosphate receptors and neurodegenerative disorders.
Polina A Egorova, Ilya B Bezprozvanny. FEBS J 2018
22
33

Xpa deficiency reduces CAG trinucleotide repeat instability in neuronal tissues in a mouse model of SCA1.
Leroy Hubert, Yunfu Lin, Vincent Dion, John H Wilson. Hum Mol Genet 2011
56
33


Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3.
Rui Gao, Yongping Liu, Anabela Silva-Fernandes, Xiang Fang, Adriana Paulucci-Holthauzen, Arpita Chatterjee, Hang L Zhang, Tohru Matsuura, Sanjeev Choudhary, Tetsuo Ashizawa,[...]. PLoS Genet 2015
45
33



Spinocerebellar ataxias: prospects and challenges for therapy development.
Tetsuo Ashizawa, Gülin Öz, Henry L Paulson. Nat Rev Neurol 2018
70
33

Inhibition of polyglutamine protein aggregation and cell death by novel peptides identified by phage display screening.
Y Nagai, T Tucker, H Ren, D J Kenan, B S Henderson, J D Keene, W J Strittmatter, J R Burke. J Biol Chem 2000
140
33

Prevention of polyglutamine oligomerization and neurodegeneration by the peptide inhibitor QBP1 in Drosophila.
Yoshitaka Nagai, Nobuhiro Fujikake, Katsuhito Ohno, Hiroyuki Higashiyama, Helena A Popiel, Julia Rahadian, Masamitsu Yamaguchi, Warren J Strittmatter, James R Burke, Tatsushi Toda. Hum Mol Genet 2003
104
33

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
107
33


DNA triplet repeat expansion and mismatch repair.
Ravi R Iyer, Anna Pluciennik, Marek Napierala, Robert D Wells. Annu Rev Biochem 2015
72
33

DNA repair in the trinucleotide repeat disorders.
Lesley Jones, Henry Houlden, Sarah J Tabrizi. Lancet Neurol 2017
45
33

Update on genetic predisposition to colorectal cancer and polyposis.
Laura Valle, Richarda M de Voer, Yael Goldberg, Wenche Sjursen, Asta Försti, Clara Ruiz-Ponte, Trinidad Caldés, Pilar Garré, Maren F Olsen, Margareta Nordling,[...]. Mol Aspects Med 2019
34
33


Endonucleolytic function of MutLalpha in human mismatch repair.
Farid A Kadyrov, Leonid Dzantiev, Nicoleta Constantin, Paul Modrich. Cell 2006
407
33

Disease-associated repeat instability and mismatch repair.
Monika H M Schmidt, Christopher E Pearson. DNA Repair (Amst) 2016
115
33

Alzheimer disease: progress or profit?
Claire Mount, Christian Downton. Nat Med 2006
176
16

Shedding light on aberrant interactions - a review of modern tools for studying protein aggregates.
Franziska Kundel, Laura Tosatto, Daniel R Whiten, David C Wirthensohn, Mathew H Horrocks, David Klenerman. FEBS J 2018
7
16




Preventing neurodegeneration by adrenergic astroglial excitation.
Robert Zorec, Vladimir Parpura, Alexei Verkhratsky. FEBS J 2018
14
16

Interaction of misfolded proteins and mitochondria in neurodegenerative disorders.
Andrey Y Abramov, Alexey V Berezhnov, Evgeniya I Fedotova, Valery P Zinchenko, Ludmila P Dolgacheva. Biochem Soc Trans 2017
35
16

The role of glucocerebrosidase in Parkinson disease pathogenesis.
Matthew E Gegg, Anthony H V Schapira. FEBS J 2018
65
16


Bridging the gap: from protein misfolding to protein misfolding diseases.
Leila M Luheshi, Christopher M Dobson. FEBS Lett 2009
66
16


The role of Nrf2 signaling in counteracting neurodegenerative diseases.
Albena T Dinkova-Kostova, Rumen V Kostov, Aleksey G Kazantsev. FEBS J 2018
99
16

Expanded polyglutamine-binding peptoid as a novel therapeutic agent for treatment of Huntington's disease.
Xuesong Chen, Jun Wu, Yuan Luo, Xia Liang, Charlene Supnet, Mee Whi Kim, Gregor P Lotz, Guocheng Yang, Paul J Muchowski, Thomas Kodadek,[...]. Chem Biol 2011
31
16

Tremor in the Degenerative Cerebellum: Towards the Understanding of Brain Circuitry for Tremor.
Ruo-Yah Lai, Darya Tomishon, Karla P Figueroa, Stefan M Pulst, Susan Perlman, George Wilmot, Christopher M Gomez, Jeremy D Schmahmann, Henry Paulson, Vikram G Shakkottai,[...]. Cerebellum 2019
8
16

Structure of two tRNA genes from Dictyostelium discoideum.
T Dingermann, W Bertling, T Brechner, K Nerke, D M Peffley, M L Sogin. Nucleic Acids Res 1986
12
16

On the distribution of intranuclear and cytoplasmic aggregates in the brainstem of patients with spinocerebellar ataxia type 2 and 3.
Kay Seidel, Sonny Siswanto, Michaela Fredrich, Mohamed Bouzrou, Wilfred F A den Dunnen, Inci Özerden, Horst-Werner Korf, Bela Melegh, Jeroen J de Vries, Ewout R Brunt,[...]. Brain Pathol 2017
21
16

Abnormalities in the climbing fiber-Purkinje cell circuitry contribute to neuronal dysfunction in ATXN1[82Q] mice.
Justin A Barnes, Blake A Ebner, Lisa A Duvick, Wangcai Gao, Gang Chen, Harry T Orr, Timothy J Ebner. J Neurosci 2011
54
16

Structural Complexity of the Cerebellum and Cerebral Cortex is Reduced in Spinocerebellar Ataxia Type 2.
Chiara Marzi, Stefano Ciulli, Marco Giannelli, Andrea Ginestroni, Carlo Tessa, Mario Mascalchi, Stefano Diciotti. J Neuroimaging 2018
8
16


The complex structure of ATXN2 genetic variation.
Stefan M Pulst. Neurol Genet 2018
4
25

Nerve ultrasound as a diagnostic tool for sensory neuronopathy in spinocerebellar ataxia syndrome.
Ruth Leadbetter, Mark Weatherall, Luciana Pelosi. Clin Neurophysiol 2019
7
16

Microbiome Influences Prenatal and Adult Microglia in a Sex-Specific Manner.
Morgane Sonia Thion, Donovan Low, Aymeric Silvin, Jinmiao Chen, Pauline Grisel, Jonas Schulte-Schrepping, Ronnie Blecher, Thomas Ulas, Paola Squarzoni, Guillaume Hoeffel,[...]. Cell 2018
255
16

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
T Schmitz-Hübsch, M Coudert, P Bauer, P Giunti, C Globas, L Baliko, A Filla, C Mariotti, M Rakowicz, P Charles,[...]. Neurology 2008
167
16

Progression of corticospinal tract dysfunction in pre-ataxic spinocerebellar ataxia type 2: A two-years follow-up TMS study.
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Reidenis Torres-Vega, Ricardo Ortega-Sánchez, Jacqueline Medrano-Montero, Rigoberto González-Piña, Yaimeé Vázquez-Mojena, Georg Auburger, Ulf Ziemann. Clin Neurophysiol 2018
9
16


Behavioral changes in rats following bufotenine injection.
G Winocur, S P Bagchi, J D Young. Percept Mot Skills 1969
7
16

Roles of Post-translational Modifications in Spinocerebellar Ataxias.
Linlin Wan, Keqin Xu, Zhao Chen, Beisha Tang, Hong Jiang. Front Cell Neurosci 2018
7
16





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.