A citation-based method for searching scientific literature

Miaozhen Huang, Dineke S Verbeek. Neurosci Lett 2019
Times Cited: 21







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



Times Cited
  Times     Co-cited
Similarity


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
28

Spinocerebellar ataxias.
Bing-Wen Soong, Patrick J Morrison. Handb Clin Neurol 2018
28
19

Spinocerebellar ataxia: an update.
Roisin Sullivan, Wai Yan Yau, Emer O'Connor, Henry Houlden. J Neurol 2019
48
19

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n.
Nozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, Shuichi Asakawa, Taro Ishiguro, Taiji Tsunemi, Makoto Takahashi, Tohru Matsuura, Kevin M Flanigan, Sawa Iwasaki,[...]. Am J Hum Genet 2009
171
14

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
14

Scale for the assessment and rating of ataxia: development of a new clinical scale.
T Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, J Berciano, S Boesch, C Depondt, P Giunti, C Globas, J Infante, J-S Kang,[...]. Neurology 2006
907
14

Ataxia telangiectasia: a review.
Cynthia Rothblum-Oviatt, Jennifer Wright, Maureen A Lefton-Greif, Sharon A McGrath-Morrow, Thomas O Crawford, Howard M Lederman. Orphanet J Rare Dis 2016
185
14


XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia.
Nicolas C Hoch, Hana Hanzlikova, Stuart L Rulten, Martine Tétreault, Emilia Komulainen, Limei Ju, Peter Hornyak, Zhihong Zeng, William Gittens, Stephanie A Rey,[...]. Nature 2017
123
14

Aberrant topoisomerase-1 DNA lesions are pathogenic in neurodegenerative genome instability syndromes.
Sachin Katyal, Youngsoo Lee, Karin C Nitiss, Susanna M Downing, Yang Li, Mikio Shimada, Jingfeng Zhao, Helen R Russell, John H J Petrini, John L Nitiss,[...]. Nat Neurosci 2014
85
14

Neuropathologic findings in essential tremor.
E D Louis, J P G Vonsattel, L S Honig, G W Ross, K E Lyons, R Pahwa. Neurology 2006
104
14


Purkinje Cell Signaling Deficits in Animal Models of Ataxia.
Eriola Hoxha, Ilaria Balbo, Maria Concetta Miniaci, Filippo Tempia. Front Synaptic Neurosci 2018
34
14

Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
Dong-Hui Chen, Zoran Brkanac, Christophe L M J Verlinde, Xiao-Jian Tan, Laura Bylenok, David Nochlin, Mark Matsushita, Hillary Lipe, John Wolff, Magali Fernandez,[...]. Am J Hum Genet 2003
175
14

Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia.
Maxime Cadieux-Dion, Maude Turcotte-Gauthier, Anne Noreau, Caroline Martin, Caroline Meloche, Micheline Gravel, Christian Allen Drouin, Guy A Rouleau, Dang Khoa Nguyen, Patrick Cossette. JAMA Neurol 2014
61
14

The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
Luis Ruano, Claudia Melo, M Carolina Silva, Paula Coutinho. Neuroepidemiology 2014
243
14

A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34.
Kokoro Ozaki, Hiroshi Doi, Jun Mitsui, Nozomu Sato, Yoichiro Iikuni, Takamasa Majima, Kiyomi Yamane, Takashi Irioka, Hiroyuki Ishiura, Koichiro Doi,[...]. JAMA Neurol 2015
39
14

A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia.
Ana I Seixas, Joana R Loureiro, Cristina Costa, Andrés Ordóñez-Ugalde, Hugo Marcelino, Cláudia L Oliveira, José L Loureiro, Ashutosh Dhingra, Eva Brandão, Vitor T Cruz,[...]. Am J Hum Genet 2017
47
9

Purkinje cell ataxin-1 modulates climbing fiber synaptic input in developing and adult mouse cerebellum.
Blake A Ebner, Melissa A Ingram, Justin A Barnes, Lisa A Duvick, Jill L Frisch, H Brent Clark, Huda Y Zoghbi, Timothy J Ebner, Harry T Orr. J Neurosci 2013
31
9

Profile of extrapyramidal manifestations in 85 patients with spinocerebellar ataxia type 1, 2 and 3.
Ketan Jhunjhunwala, M Netravathi, Meera Purushottam, Sanjeev Jain, Pramod Kumar Pal. J Clin Neurosci 2014
17
11

Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrument.
H Jacobi, M Rakowicz, R Rola, R Fancellu, C Mariotti, P Charles, A Dürr, M Küper, D Timmann, C Linnemann,[...]. Cerebellum 2013
58
9

Depression comorbidity in spinocerebellar ataxia.
Tanja Schmitz-Hübsch, Mathieu Coudert, Sophie Tezenas du Montcel, Paola Giunti, Robyn Labrum, Alexandra Dürr, Pascale Ribai, Perrine Charles, Christoph Linnemann, Ludger Schöls,[...]. Mov Disord 2011
44
9

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.
H Jacobi, P Bauer, P Giunti, R Labrum, M G Sweeney, P Charles, A Dürr, C Marelli, C Globas, C Linnemann,[...]. Neurology 2011
120
9

The preclinical stage of spinocerebellar ataxias.
Roderick P P W M Maas, Judith van Gaalen, Thomas Klockgether, Bart P C van de Warrenburg. Neurology 2015
53
9

Tyrosyl-DNA phosphodiesterases: rescuing the genome from the risks of relaxation.
Ajinkya S Kawale, Lawrence F Povirk. Nucleic Acids Res 2018
43
9

Mitochondrial dysfunction in ataxia-telangiectasia.
Yasmine A Valentin-Vega, Kirsteen H Maclean, Jacqueline Tait-Mulder, Sandra Milasta, Meredith Steeves, Frank C Dorsey, John L Cleveland, Douglas R Green, Michael B Kastan. Blood 2012
234
9

The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder.
G S Stewart, R S Maser, T Stankovic, D A Bressan, M I Kaplan, N G Jaspers, A Raams, P J Byrd, J H Petrini, A M Taylor. Cell 1999
761
9

Ataxia telangiectasia mutated activation by transcription- and topoisomerase I-induced DNA double-strand breaks.
Olivier Sordet, Christophe E Redon, Josée Guirouilh-Barbat, Susan Smith, Stéphanie Solier, Céline Douarre, Chiara Conti, Asako J Nakamura, Benu B Das, Estelle Nicolas,[...]. EMBO Rep 2009
152
9

Nijmegen breakage syndrome (NBS).
Krystyna H Chrzanowska, Hanna Gregorek, Bożenna Dembowska-Bagińska, Maria A Kalina, Martin Digweed. Orphanet J Rare Dis 2012
123
9

Optimal function of the DNA repair enzyme TDP1 requires its phosphorylation by ATM and/or DNA-PK.
Benu Brata Das, Smitha Antony, Shalu Gupta, Thomas S Dexheimer, Christophe E Redon, Susan Garfield, Yosef Shiloh, Yves Pommier. EMBO J 2009
96
9

Localization of a portion of extranuclear ATM to peroxisomes.
D Watters, P Kedar, K Spring, J Bjorkman, P Chen, M Gatei, G Birrell, B Garrone, P Srinivasa, D I Crane,[...]. J Biol Chem 1999
150
9

Phosphorylation of polynucleotide kinase/ phosphatase by DNA-dependent protein kinase and ataxia-telangiectasia mutated regulates its association with sites of DNA damage.
Angela E Zolner, Ismail Abdou, Ruiqiong Ye, Rajam S Mani, Mesfin Fanta, Yaping Yu, Pauline Douglas, Nasser Tahbaz, Shujuan Fang, Tracey Dobbs,[...]. Nucleic Acids Res 2011
48
9

TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural function.
Fernando Gómez-Herreros, Janneke H M Schuurs-Hoeijmakers, Mark McCormack, Marie T Greally, Stuart Rulten, Rocío Romero-Granados, Timothy J Counihan, Elijah Chaila, Judith Conroy, Sean Ennis,[...]. Nat Genet 2014
94
9

Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder.
Regina Waltes, Reinhard Kalb, Magtouf Gatei, Amanda W Kijas, Markus Stumm, Alexandra Sobeck, Britta Wieland, Raymonda Varon, Yaniv Lerenthal, Martin F Lavin,[...]. Am J Hum Genet 2009
155
9

Intrinsic mitochondrial dysfunction in ATM-deficient lymphoblastoid cells.
Mark Ambrose, Jimena V Goldstine, Richard A Gatti. Hum Mol Genet 2007
120
9

ATM-mediated phosphorylation of polynucleotide kinase/phosphatase is required for effective DNA double-strand break repair.
Hava Segal-Raz, Gilad Mass, Keren Baranes-Bachar, Yaniv Lerenthal, Shih-Ya Wang, Young Min Chung, Shelly Ziv-Lehrman, Cecilia E Ström, Thomas Helleday, Mickey C-T Hu,[...]. EMBO Rep 2011
45
9

Neurodegeneration in ataxia telangiectasia: what is new? What is evident?
Franziska Hoche, Kay Seidel, Marius Theis, Stefan Vlaho, Ralf Schubert, Stefan Zielen, Matthias Kieslich. Neuropediatrics 2012
46
9

NAD+ Replenishment Improves Lifespan and Healthspan in Ataxia Telangiectasia Models via Mitophagy and DNA Repair.
Evandro Fei Fang, Henok Kassahun, Deborah L Croteau, Morten Scheibye-Knudsen, Krisztina Marosi, Huiming Lu, Raghavendra A Shamanna, Sumana Kalyanasundaram, Ravi Chand Bollineni, Mark A Wilson,[...]. Cell Metab 2016
206
9


SMRT compounds abrogate cellular phenotypes of ataxia telangiectasia in neural derivatives of patient-specific hiPSCs.
Peiyee Lee, Nathan T Martin, Kotoka Nakamura, Soheila Azghadi, Mandana Amiri, Uri Ben-David, Susan Perlman, Richard A Gatti, Hailiang Hu, William E Lowry. Nat Commun 2013
27
9


ATM activation by oxidative stress.
Zhi Guo, Sergei Kozlov, Martin F Lavin, Maria D Person, Tanya T Paull. Science 2010
694
9

Genotype-phenotype relationships in ataxia-telangiectasia and variants.
S Gilad, L Chessa, R Khosravi, P Russell, Y Galanty, M Piane, R A Gatti, T J Jorgensen, Y Shiloh, A Bar-Shira. Am J Hum Genet 1998
187
9

ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage.
Shuhei Matsuoka, Bryan A Ballif, Agata Smogorzewska, E Robert McDonald, Kristen E Hurov, Ji Luo, Corey E Bakalarski, Zhenming Zhao, Nicole Solimini, Yaniv Lerenthal,[...]. Science 2007
9

Fiji: an open-source platform for biological-image analysis.
Johannes Schindelin, Ignacio Arganda-Carreras, Erwin Frise, Verena Kaynig, Mark Longair, Tobias Pietzsch, Stephan Preibisch, Curtis Rueden, Stephan Saalfeld, Benjamin Schmid,[...]. Nat Methods 2012
9

Torpedo formation and Purkinje cell loss: modeling their relationship in cerebellar disease.
Elan D Louis, Sheng-Han Kuo, Jean-Paul G Vonsattel, Phyllis L Faust. Cerebellum 2014
28
9

Development of Purkinje cell degeneration in a knockin mouse model reveals lysosomal involvement in the pathogenesis of SCA6.
Toshinori Unno, Minoru Wakamori, Masato Koike, Yasuo Uchiyama, Kinya Ishikawa, Hisahiko Kubota, Takashi Yoshida, Hiroko Sasakawa, Christoph Peters, Hidehiro Mizusawa,[...]. Proc Natl Acad Sci U S A 2012
32
9

Clec16a is Critical for Autolysosome Function and Purkinje Cell Survival.
Veronika Redmann, Christopher A Lamb, Seungmin Hwang, Robert C Orchard, Sungsu Kim, Minoo Razi, Ashley Milam, Sunmin Park, Christine C Yokoyama, Amal Kambal,[...]. Sci Rep 2016
21
9

Motor neuron vulnerability and resistance in amyotrophic lateral sclerosis.
Jik Nijssen, Laura H Comley, Eva Hedlund. Acta Neuropathol 2017
101
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.