A citation-based method for searching scientific literature

Justyna Jezierska, Giovanni Stevanin, Hiroyuki Watanabe, Michiel R Fokkens, Fabien Zagnoli, Jérôme Kok, Jean-Yves Goas, Pierre Bertrand, Christophe Robin, Alexis Brice, Georgy Bakalkin, Alexandra Durr, Dineke S Verbeek. J Neurol 2013
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23.
Georgy Bakalkin, Hiroyuki Watanabe, Justyna Jezierska, Cloë Depoorter, Corien Verschuuren-Bemelmans, Igor Bazov, Konstantin A Artemenko, Tatjana Yakovleva, Dennis Dooijes, Bart P C Van de Warrenburg,[...]. Am J Hum Genet 2010
72
75

Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.
D S Verbeek, B P van de Warrenburg, P Wesseling, P L Pearson, H P Kremer, R J Sinke. Brain 2004
48
43

The frequency of spinocerebellar ataxia type 23 in a UK population.
Katherine Fawcett, Mohadeseh Mehrabian, Yo-Tsen Liu, Sherifa Hamed, Elahe Elahi, Tamas Revesz, Georgios Koutsis, Joshua Herscheson, Lucia Schottlaender, Mark Wardle,[...]. J Neurol 2013
11
54

Non-opioid nociceptive activity of human dynorphin mutants that cause neurodegenerative disorder spinocerebellar ataxia type 23.
Hiroyuki Watanabe, Hirokazu Mizoguchi, Dineke S Verbeek, Alexander Kuzmin, Fred Nyberg, Oleg Krishtal, Shinobu Sakurada, Georgy Bakalkin. Peptides 2012
11
45

Elevated mutant dynorphin A causes Purkinje cell loss and motor dysfunction in spinocerebellar ataxia type 23.
Cleo J L M Smeets, Justyna Jezierska, Hiroyuki Watanabe, Anna Duarri, Michiel R Fokkens, Michel Meijer, Qin Zhou, Tania Yakovleva, Erik Boddeke, Wilfred den Dunnen,[...]. Brain 2015
25
31

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
203
25

Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia.
Brent L Fogel, Ji Yong Lee, Jessica Lane, Amanda Wahnich, Sandy Chan, Alden Huang, Greg E Osborn, Eric Klein, Catherine Mamah, Susan Perlman,[...]. Mov Disord 2012
25
25

Translocation of dynorphin neuropeptides across the plasma membrane. A putative mechanism of signal transmission.
Zoya Marinova, Vladana Vukojevic, Slavina Surcheva, Tatiana Yakovleva, Gvido Cebers, Natalia Pasikova, Ivan Usynin, Loïc Hugonin, Weijie Fang, Mathias Hallberg,[...]. J Biol Chem 2005
44
18

Perturbations of model membranes induced by pathogenic dynorphin A mutants causing neurodegeneration in human brain.
Fatemeh Madani, Malik Mumtaz Taqi, Sebastian K T S Wärmländer, Dineke S Verbeek, Georgy Bakalkin, Astrid Gräslund. Biochem Biophys Res Commun 2011
10
30

Membrane leakage induced by dynorphins.
Loïc Hugonin, Vladana Vukojević, Georgy Bakalkin, Astrid Gräslund. FEBS Lett 2006
27
18

Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation.
A Herman-Bert, G Stevanin, J C Netter, O Rascol, D Brassat, P Calvas, A Camuzat, Q Yuan, M Schalling, A Dürr,[...]. Am J Hum Genet 2000
98
18

Big dynorphin as a putative endogenous ligand for the kappa-opioid receptor.
Florence Merg, Dominique Filliol, Ivan Usynin, Igor Bazov, Niklas Bark, Yasmin L Hurd, Tatjana Yakovleva, Brigitte L Kieffer, Georgy Bakalkin. J Neurochem 2006
47
18

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
263
18

Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization.
Yuh-Cherng Guo, Juei-Jueng Lin, Yi-Chu Liao, Pei-Chien Tsai, Yi-Chung Lee, Bing-Wen Soong. Neurology 2014
26
18

A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia.
Ho Tsoi, Allen C S Yu, Zhefan S Chen, Nelson K N Ng, Anne Y Y Chan, Liz Y P Yuen, Jill M Abrigo, Suk Ying Tsang, Stephen K W Tsui, Tony M F Tong,[...]. J Med Genet 2014
42
18

Spinocerebellar ataxia type 23: a genetic update.
Dineke S Verbeek. Cerebellum 2009
12
25


The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene.
Kazumasa Saigoh, Jun Mitsui, Makito Hirano, Mitsuaki Shioyama, Makoto Samukawa, Yaeko Ichikawa, Jun Goto, Shoji Tsuji, Susumu Kusunoki. Parkinsonism Relat Disord 2015
6
50

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
57
18

The dynorphin/κ-opioid receptor system and its role in psychiatric disorders.
H A Tejeda, T S Shippenberg, R Henriksson. Cell Mol Life Sci 2012
99
12

Amino acid sequence pattern in the regulatory peptides.
G Y Bakalkin, A B Rakhmaninova, V K Akparov, A A Volodin, V V Ovchinnikov, R A Sarkisyan. Int J Pept Protein Res 1991
12
16

Nonopiate effects of dynorphin and des-Tyr-dynorphin.
J M Walker, H C Moises, D H Coy, G Baldrighi, H Akil. Science 1982
233
12



Cytotoxic effects of dynorphins through nonopioid intracellular mechanisms.
K Tan-No, G Cebers, T Yakovleva, B Hoon Goh, I Gileva, K Reznikov, M Aguilar-Santelises, K F Hauser, L Terenius, G Bakalkin. Exp Cell Res 2001
45
12

Membrane interaction of disease-related dynorphin A variants.
Johannes Björnerås, Astrid Gräslund, Lena Mäler. Biochemistry 2013
9
22

Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds.
Peter Bauer, Giovanni Stevanin, Christian Beetz, Matthis Synofzik, Tanja Schmitz-Hübsch, Ullrich Wüllner, Eric Berthier, Elisabeth Ollagnon-Roman, Olaf Riess, Sylvie Forlani,[...]. J Neurol Neurosurg Psychiatry 2010
35
12

KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients.
Karla P Figueroa, Natali A Minassian, Giovanni Stevanin, Michael Waters, Vartan Garibyan, Sylvie Forlani, Adam Strzelczyk, Katrin Bürk, Alexis Brice, Alexandra Dürr,[...]. Hum Mutat 2010
64
12

Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.
Anna Duarri, Justyna Jezierska, Michiel Fokkens, Michel Meijer, Helenius J Schelhaas, Wilfred F A den Dunnen, Freerk van Dijk, Corien Verschuuren-Bemelmans, Gerard Hageman, Pieter van de Vlies,[...]. Ann Neurol 2012
86
12

Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias.
Claudia Cagnoli, Giovanni Stevanin, Alessandro Brussino, Marco Barberis, Cecilia Mancini, Russell L Margolis, Susan E Holmes, Marcello Nobili, Sylvie Forlani, Sergio Padovan,[...]. Hum Mutat 2010
59
12


Big dynorphin, a prodynorphin-derived peptide produces NMDA receptor-mediated effects on memory, anxiolytic-like and locomotor behavior in mice.
Alexander Kuzmin, Nather Madjid, Lars Terenius, Sven Ove Ogren, Georgy Bakalkin. Neuropsychopharmacology 2006
53
12

High-affinity interaction of (des-Tyrosyl)dynorphin A(2-17) with NMDA receptors.
Q Tang, R Gandhoke, A Burritt, V J Hruby, F Porreca, J Lai. J Pharmacol Exp Ther 1999
54
12

Neuropathic pain: the paradox of dynorphin.
J Lai, M H Ossipov, T W Vanderah, T P Malan, F Porreca. Mol Interv 2001
55
12



Pathobiology of dynorphins in trauma and disease.
Kurt F Hauser, Jane V Aldrich, Kevin J Anderson, Georgy Bakalkin, MacDonald J Christie, Edward D Hall, Pamela E Knapp, Stephen W Scheff, Indrapal N Singh, Bryce Vissel,[...]. Front Biosci 2005
64
12


Pronociceptive role of dynorphins in uninjured animals: N-ethylmaleimide-induced nociceptive behavior mediated through inhibition of dynorphin degradation.
Koichi Tan-No, Hiroaki Takahashi, Osamu Nakagawasai, Fukie Niijima, Takumi Sato, Susumu Satoh, Shinobu Sakurada, Zoya Marinova, Tatjana Yakovleva, Georgy Bakalkin,[...]. Pain 2005
37
12


Calcium influx into phospholipid vesicles caused by dynorphin neuropeptides.
Loïc Hugonin, Vladana Vukojević, Georgy Bakalkin, Astrid Gräslund. Biochim Biophys Acta 2008
9
22

Intrathecally administered big dynorphin, a prodynorphin-derived peptide, produces nociceptive behavior through an N-methyl-D-aspartate receptor mechanism.
Koichi Tan-No, Akihisa Esashi, Osamu Nakagawasai, Fukie Niijima, Takeshi Tadano, Chikai Sakurada, Tsukasa Sakurada, Georgy Bakalkin, Lars Terenius, Kensuke Kisara. Brain Res 2002
49
12

Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred.
K Bürk, C Zühlke, I R König, A Ziegler, E Schwinger, C Globas, J Dichgans, Y Hellenbroich. Neurology 2004
44
12

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
456
12

Mutations in KCND3 cause spinocerebellar ataxia type 22.
Yi-Chung Lee, Alexandra Durr, Karen Majczenko, Yen-Hua Huang, Yu-Chao Liu, Cheng-Chang Lien, Pei-Chien Tsai, Yaeko Ichikawa, Jun Goto, Marie-Lorraine Monin,[...]. Ann Neurol 2012
98
12


Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.
Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, Massimo Plumari, Giorgio Battaglia, Annalisa Pastore, Adele Finardi, Claudia Cagnoli, Filippo Tempia, Marina Frontali,[...]. Nat Genet 2010
210
12

A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult.
Katherine E Hekman, Guo-Yun Yu, Christopher D Brown, Haipeng Zhu, Xiaofei Du, Kristina Gervin, Dag Erik Undlien, April Peterson, Giovanni Stevanin, H Brent Clark,[...]. Hum Mol Genet 2012
38
12

Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16.
A Iwaki, Y Kawano, S Miura, H Shibata, D Matsuse, W Li, H Furuya, Y Ohyagi, T Taniwaki, J Kira,[...]. J Med Genet 2008
91
12

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.
Lijia Huang, Jodi Warman Chardon, Melissa T Carter, Kathie L Friend, Tracy E Dudding, Jeremy Schwartzentruber, Ruobing Zou, Peter W Schofield, Stuart Douglas, Dennis E Bulman,[...]. Orphanet J Rare Dis 2012
87
12


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.