A citation-based method for searching scientific literature

David Genis, Sara Ortega-Cubero, Hector San Nicolás, Jordi Corral, Josep Gardenyes, Laura de Jorge, Eva López, Berta Campos, Elena Lorenzo, Raúl Tonda, Sergi Beltran, Montserrat Negre, María Obón, Brigitte Beltran, Laura Fàbregas, Berta Alemany, Fabián Márquez, Lluís Ramió-Torrentà, Jordi Gich, Víctor Volpini, Pau Pastor. Neurology 2018
Times Cited: 48







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



Times Cited
  Times     Co-cited
Similarity


Identification of CHIP as a novel causative gene for autosomal recessive cerebellar ataxia.
Yuting Shi, Junling Wang, Jia-Da Li, Haigang Ren, Wenjuan Guan, Miao He, Weiqian Yan, Ying Zhou, Zhengmao Hu, Jianguo Zhang,[...]. PLoS One 2013
62
45

Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian families.
Giovanna De Michele, Maria Lieto, Daniele Galatolo, Elena Salvatore, Sirio Cocozza, Melissa Barghigiani, Alessandra Tessa, Jacopo Baldacci, Sabina Pappatà, Alessandro Filla,[...]. Parkinsonism Relat Disord 2019
30
70

Ataxia and hypogonadism caused by the loss of ubiquitin ligase activity of the U box protein CHIP.
Chang-He Shi, Jonathan C Schisler, Carrie E Rubel, Song Tan, Bo Song, Holly McDonough, Lei Xu, Andrea L Portbury, Cheng-Yuan Mao, Cadence True,[...]. Hum Mol Genet 2014
92
37

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
286
33

Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts.
Matthis Synofzik, Rebecca Schüle, Martin Schulze, Janina Gburek-Augustat, Roland Schweizer, Anja Schirmacher, Ingeborg Krägeloh-Mann, Michael Gonzalez, Peter Young, Stephan Züchner,[...]. Orphanet J Rare Dis 2014
43
34

The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families.
M Lieto, V Riso, D Galatolo, G De Michele, S Rossi, M Barghigiani, S Cocozza, G Pontillo, R Trovato, F Saccà,[...]. Eur J Neurol 2020
30
50

STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations.
Stefanie Nicole Hayer, Tine Deconinck, Benjamin Bender, Katrien Smets, Stephan Züchner, Selina Reich, Ludger Schöls, Rebecca Schüle, Peter De Jonghe, Jonathan Baets,[...]. Orphanet J Rare Dis 2017
35
40

STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity.
Ketil Heimdal, Monica Sanchez-Guixé, Ingvild Aukrust, Jens Bollerslev, Ove Bruland, Greg Eigner Jablonski, Anne Kjersti Erichsen, Einar Gude, Jeanette A Koht, Sigrid Erdal,[...]. Orphanet J Rare Dis 2014
41
34

Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutations.
Chantal Depondt, Simona Donatello, Nicolas Simonis, Myriam Rai, Roxane van Heurck, Marc Abramowicz, Marc D'Hooghe, Massimo Pandolfo. Neurology 2014
32
40

Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1.
Conceição Bettencourt, Justo García de Yébenes, José Luis López-Sendón, Orr Shomroni, Xingqian Zhang, Shu-Bing Qian, Ingrid M C Bakker, Sasja Heetveld, Raquel Ros, Beatriz Quintáns,[...]. Cerebellum 2015
25
48

Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 family.
R Palvadeau, Z E Kaya-Güleç, G Şimşir, A Vural, Ö Öztop-Çakmak, G Genç, M S Aygün, O Falay, A Nazlı Başak, S Ertan. Neurogenetics 2020
14
85



Inaugural cognitive decline, late disease onset and novel STUB1 variants in SCAR16.
José Gazulla, Silvia Izquierdo-Alvarez, Esther Sierra-Martínez, María Eugenia Marta-Moreno, Sara Alvarez. Neurol Sci 2018
11
90

In vitro characterization of six STUB1 variants in spinocerebellar ataxia 16 reveals altered structural properties for the encoded CHIP proteins.
Yasaman Pakdaman, Monica Sanchez-Guixé, Rune Kleppe, Sigrid Erdal, Helene J Bustad, Lise Bjørkhaug, Kristoffer Haugarvoll, Charalampos Tzoulis, Ketil Heimdal, Per M Knappskog,[...]. Biosci Rep 2017
18
50


Ataxia plus myoclonus in a 23-year-old patient due to STUB1 mutations.
Marta Cordoba, Sergio Rodriguez-Quiroga, Emilia Mabel Gatto, Agustín Alurralde, Marcelo Andrés Kauffman. Neurology 2014
24
37

Spinocerebellar ataxia.
Thomas Klockgether, Caterina Mariotti, Henry L Paulson. Nat Rev Dis Primers 2019
164
18

Clinical and pathologic phenotype of a large family with heterozygous STUB1 mutation.
Merel O Mol, Jeroen G J van Rooij, Esther Brusse, Annemieke J M H Verkerk, Shamiram Melhem, Wilfred F A den Dunnen, Patrizia Rizzu, Chiara Cupidi, John C van Swieten, Laura Donker Kaat. Neurol Genet 2020
9
100

Heterozygous STUB1 missense variants cause ataxia, cognitive decline, and STUB1 mislocalization.
Dong-Hui Chen, Caitlin Latimer, Mayumi Yagi, Mesaki Kenneth Ndugga-Kabuye, Elyana Heigham, Suman Jayadev, James S Meabon, Christopher M Gomez, C Dirk Keene, David G Cook,[...]. Neurol Genet 2020
10
90

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Thomas Roux, Mathieu Barbier, Mélanie Papin, Claire-Sophie Davoine, Sabrina Sayah, Giulia Coarelli, Perrine Charles, Cecilia Marelli, Livia Parodi, Christine Tranchant,[...]. Genet Med 2020
10
90

STUB1 polyadenylation signal variant AACAAA does not affect polyadenylation but decreases STUB1 translation causing SCAR16.
Burcu Turkgenc, Burcin Sanlidag, Amber Eker, Aslı Giray, Ozgur Kutuk, Cengiz Yakicier, Aslıhan Tolun, Sehime G Temel. Hum Mutat 2018
8
100

Changes in protein function underlie the disease spectrum in patients with CHIP mutations.
Sabrina C Madrigal, Zipporah McNeil, Rebekah Sanchez-Hodge, Chang-He Shi, Cam Patterson, Kenneth Matthew Scaglione, Jonathan C Schisler. J Biol Chem 2019
12
66

STUB1 regulates TFEB-induced autophagy-lysosome pathway.
Youbao Sha, Lang Rao, Carmine Settembre, Andrea Ballabio, N Tony Eissa. EMBO J 2017
83
14

Disrupted structure and aberrant function of CHIP mediates the loss of motor and cognitive function in preclinical models of SCAR16.
Chang-He Shi, Carrie Rubel, Sarah E Soss, Rebekah Sanchez-Hodge, Shuo Zhang, Sabrina C Madrigal, Saranya Ravi, Holly McDonough, Richard C Page, Walter J Chazin,[...]. PLoS Genet 2018
23
30

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings With Autosomal Recessive Spinocerebellar Ataxia Type 16.
Toshitaka Kawarai, Ryosuke Miyamoto, Yoshimitsu Shimatani, Antonio Orlacchio, Ryuji Kaji. JAMA Neurol 2016
12
58

Spinocerebellar ataxia: an update.
Roisin Sullivan, Wai Yan Yau, Emer O'Connor, Henry Houlden. J Neurol 2019
69
14

Spinocerebellar ataxia type 48: last but not least.
Giovanna De Michele, Daniele Galatolo, Melissa Barghigiani, Diletta Dello Iacovo, Rosanna Trovato, Alessandra Tessa, Elena Salvatore, Alessandro Filla, Giuseppe De Michele, Filippo M Santorelli. Neurol Sci 2020
16
43

Chaperoned ubiquitylation--crystal structures of the CHIP U box E3 ubiquitin ligase and a CHIP-Ubc13-Uev1a complex.
Minghao Zhang, Mark Windheim, S Mark Roe, Mark Peggie, Philip Cohen, Chrisostomos Prodromou, Laurence H Pearl. Mol Cell 2005
317
12

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
990
12

Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.
Esther A R Nibbeling, Anna Duarri, Corien C Verschuuren-Bemelmans, Michiel R Fokkens, Juha M Karjalainen, Cleo J L M Smeets, Jelkje J de Boer-Bergsma, Gerben van der Vries, Dennis Dooijes, Giovana B Bampi,[...]. Brain 2017
60
12

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
12

Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan.
Hsu-Huai Chiu, Cheng-Tsung Hsaio, Yu-Shuen Tsai, Yi-Chu Liao, Yi-Chung Lee, Bing-Wen Soong. Cerebellum 2020
7
85

Expanding the clinical spectrum of STIP1 homology and U-box containing protein 1-associated ataxia.
Jean-Marie Ravel, Mehdi Benkirane, Nadège Calmels, Cecilia Marelli, Fabienne Ory-Magne, Claire Ewenczyk, Yosra Halleb, François Tison, Claire Lecocq, Guillaume Pische,[...]. J Neurol 2021
9
66

Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.
Hélio A G Teive, Renato P Munhoz, Walter O Arruda, Iscia Lopes-Cendes, Salmo Raskin, Lineu C Werneck, Tetsuo Ashizawa. Clinics (Sao Paulo) 2012
48
10

Dimerization of the human E3 ligase CHIP via a coiled-coil domain is essential for its activity.
Rainer Nikolay, Thomas Wiederkehr, Wolfgang Rist, Günter Kramer, Matthias P Mayer, Bernd Bukau. J Biol Chem 2004
88
10

CHIP protects from the neurotoxicity of expanded and wild-type ataxin-1 and promotes their ubiquitination and degradation.
Ismael Al-Ramahi, Yung C Lam, Hung-Kai Chen, Beatrice de Gouyon, Minghang Zhang, Alma M Pérez, Joana Branco, Maria de Haro, Cam Patterson, Huda Y Zoghbi,[...]. J Biol Chem 2006
143
10

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
10


In vivo evidence of CHIP up-regulation attenuating tau aggregation.
Naruhiko Sahara, Miyuki Murayama, Tatsuya Mizoroki, Makoto Urushitani, Yuzuru Imai, Ryosuke Takahashi, Shigeo Murata, Keiji Tanaka, Akihiko Takashima. J Neurochem 2005
158
10

Ataxia, dementia, and hypogonadotropism caused by disordered ubiquitination.
David H Margolin, Maria Kousi, Yee-Ming Chan, Elaine T Lim, Jeremy D Schmahmann, Marios Hadjivassiliou, Janet E Hall, Ibrahim Adam, Andrew Dwyer, Lacey Plummer,[...]. N Engl J Med 2013
133
10

A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies.
Marie Coutelier, Giulia Coarelli, Marie-Lorraine Monin, Juliette Konop, Claire-Sophie Davoine, Christelle Tesson, Rémi Valter, Mathieu Anheim, Anthony Behin, Giovanni Castelnovo,[...]. Brain 2017
60
10

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
10

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.
Heike Jacobi, Sophie Tezenas du Montcel, Peter Bauer, Paola Giunti, Arron Cook, Robyn Labrum, Michael H Parkinson, Alexandra Durr, Alexis Brice, Perrine Charles,[...]. Lancet Neurol 2015
127
10

The "crab sign": an imaging feature of spinocerebellar ataxia type 48.
Sirio Cocozza, Giuseppe Pontillo, Giovanna De Michele, Teresa Perillo, Elvira Guerriero, Lorenzo Ugga, Elena Salvatore, Daniele Galatolo, Vittorio Riso, Francesco Saccà,[...]. Neuroradiology 2020
8
62

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
61
8

Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor development.
Stefano Lise, Yvonne Clarkson, Emma Perkins, Alexandra Kwasniewska, Elham Sadighi Akha, Ricardo Parolin Schnekenberg, Daumante Suminaite, Jilly Hope, Ian Baker, Lorna Gregory,[...]. PLoS Genet 2012
66
8

SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V.
E Sánchez-Ferrero, E Coto, C Beetz, J Gámez, A I Corao, M Díaz, J Esteban, E del Castillo, G Moris, J Infante,[...]. Clin Genet 2013
70
8

Autosomal Recessive Cerebellar Ataxias: Paving the Way toward Targeted Molecular Therapies.
Matthis Synofzik, Hélène Puccio, Fanny Mochel, Ludger Schöls. Neuron 2019
29
13

CHIP controls necroptosis through ubiquitylation- and lysosome-dependent degradation of RIPK3.
Jinho Seo, Eun-Woo Lee, Hyerim Sung, Daehyeon Seong, Yves Dondelinger, Jihye Shin, Manhyung Jeong, Hae-Kyung Lee, Jung-Hoon Kim, Su Yeon Han,[...]. Nat Cell Biol 2016
85
8


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.