A citation-based method for searching scientific literature

Yuhei Hasuike, Hana Tanaka, Terence Gall-Duncan, Mustafa Mehkary, Kazuhiko Nakatani, Christopher E Pearson, Shoji Tsuji, Hideki Mochizuki, Masayuki Nakamori. Neurobiol Dis 2022
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease.
C A Maurage, B Udd, M M Ruchoux, P Vermersch, H Kalimo, R Krahe, A Delacourte, N Sergeant. Neurology 2005
64
100

Aberrant axon branching via Fos-B dysregulation in FUS-ALS motor neurons.
Tetsuya Akiyama, Naoki Suzuki, Mitsuru Ishikawa, Koki Fujimori, Takefumi Sone, Jiro Kawada, Ryo Funayama, Fumiyoshi Fujishima, Shio Mitsuzawa, Kensuke Ikeda,[...]. EBioMedicine 2019
25
100

Mutant human embryonic stem cells reveal neurite and synapse formation defects in type 1 myotonic dystrophy.
Antoine Marteyn, Yves Maury, Morgane M Gauthier, Camille Lecuyer, Remi Vernet, Jérôme A Denis, Geneviève Pietu, Marc Peschanski, Cécile Martinat. Cell Stem Cell 2011
76
100

Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions.
Haishan Jiang, Hiroshi Shimizu, Atsushi Shiga, Masami Tanaka, Osamu Onodera, Akiyoshi Kakita, Hitoshi Takahashi. Neuropathology 2017
5
100

Aberrantly spliced alpha-dystrobrevin alters alpha-syntrophin binding in myotonic dystrophy type 1.
M Nakamori, T Kimura, T Kubota, T Matsumura, H Sumi, H Fujimura, M P Takahashi, S Sakoda. Neurology 2008
25
100

Peripheral neuropathy in myotonic dystrophy type 1.
Mieke C E Hermans, Catharina G Faber, Els K Vanhoutte, Mayienne Bakkers, Marc H De Baets, Christine E M de Die-Smulders, Ingemar S J Merkies. J Peripher Nerv Syst 2011
23
100

Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of Ca(V)1.1 calcium channel.
Zhen Zhi Tang, Viktor Yarotskyy, Lan Wei, Krzysztof Sobczak, Masayuki Nakamori, Katy Eichinger, Richard T Moxley, Robert T Dirksen, Charles A Thornton. Hum Mol Genet 2012
109
100

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy.
Fernande Freyermuth, Frédérique Rau, Yosuke Kokunai, Thomas Linke, Chantal Sellier, Masayuki Nakamori, Yoshihiro Kino, Ludovic Arandel, Arnaud Jollet, Christelle Thibault,[...]. Nat Commun 2016
97
100

Differences in splicing defects between the grey and white matter in myotonic dystrophy type 1 patients.
Masamitsu Nishi, Takashi Kimura, Masataka Igeta, Mitsuru Furuta, Koichi Suenaga, Tsuyoshi Matsumura, Harutoshi Fujimura, Kenji Jinnai, Hiroo Yoshikawa. PLoS One 2020
6
100

Gene ontology analysis for RNA-seq: accounting for selection bias.
Matthew D Young, Matthew J Wakefield, Gordon K Smyth, Alicia Oshlack. Genome Biol 2010
100

Trimmomatic: a flexible trimmer for Illumina sequence data.
Anthony M Bolger, Marc Lohse, Bjoern Usadel. Bioinformatics 2014
100

Somatic instability of CTG repeat in myotonic dystrophy.
T Ashizawa, J R Dubel, Y Harati. Neurology 1993
152
100


Disrupted prenatal RNA processing and myogenesis in congenital myotonic dystrophy.
James D Thomas, Łukasz J Sznajder, Olgert Bardhi, Faaiq N Aslam, Zacharias P Anastasiadis, Marina M Scotti, Ichizo Nishino, Masayuki Nakamori, Eric T Wang, Maurice S Swanson. Genes Dev 2017
57
100

Neurocognitive Features of Motor Premanifest Individuals With Myotonic Dystrophy Type 1.
Ellen van der Plas, Timothy R Koscik, Vincent Magnotta, Sarah A Cumming, Darren Monckton, Laurie Gutmann, Peggy Nopoulos. Neurol Genet 2021
3
100

Differential effects of PKA-controlled CaMKK2 variants on neuronal differentiation.
Wenguang Cao, Muhammad Sohail, Guodong Liu, Geremy A Koumbadinga, Vincent G Lobo, Jiuyong Xie. RNA Biol 2011
24
100


Peripheral neuropathy in patients with myotonic dystrophy type 1.
Stojan Peric, Vidosava Rakocevic Stojanovic, Ana Nikolic, Aleksandra Kacar, Ivana Basta, Sanja Pavlovic, Dragana Lavrnic. Neurol Res 2013
16
100

Targeting Expanded Repeats by Small Molecules in Repeat Expansion Disorders.
Masayuki Nakamori, Hideki Mochizuki. Mov Disord 2021
5
100

Amyotrophic Lateral Sclerosis with Pallidonigroluysian Degeneration: A Clinicopathological Study.
Junko Ito, Hiroshi Shimizu, Kentaro Ohta, Jiro Idezuka, Hajime Tanaka, Hiroshi Kondo, Takashi Nakajima, Hitoshi Takahashi, Kohei Akazawa, Osamu Onodera,[...]. Ann Neurol 2020
5
100

Synaptic protein dysregulation in myotonic dystrophy type 1: Disease neuropathogenesis beyond missplicing.
Oscar Hernández-Hernández, Géraldine Sicot, Diana M Dinca, Aline Huguet, Annie Nicole, Luc Buée, Arnold Munnich, Nicolas Sergeant, Geneviève Gourdon, Mário Gomes-Pereira. Rare Dis 2013
13
100


Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy.
Frédérique Rau, Jeanne Lainé, Laetitita Ramanoudjame, Arnaud Ferry, Ludovic Arandel, Olivier Delalande, Arnaud Jollet, Florent Dingli, Kuang-Yung Lee, Cécile Peccate,[...]. Nat Commun 2015
54
100

Molecular genetics of congenital myotonic dystrophy.
Stella Lanni, Christopher E Pearson. Neurobiol Dis 2019
20
100

Laser capture microdissection.
M R Emmert-Buck, R F Bonner, P D Smith, R F Chuaqui, Z Zhuang, S R Goldstein, R A Weiss, L A Liotta. Science 1996
100

Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy.
Charlotte Fugier, Arnaud F Klein, Caroline Hammer, Stéphane Vassilopoulos, Ylva Ivarsson, Anne Toussaint, Valérie Tosch, Alban Vignaud, Arnaud Ferry, Nadia Messaddeq,[...]. Nat Med 2011
213
100

Ribonuclear foci at the neuromuscular junction in myotonic dystrophy type 1.
T M Wheeler, M C Krym, C A Thornton. Neuromuscul Disord 2007
38
100

Unique transcriptome patterns of the white and grey matter corroborate structural and functional heterogeneity in the human frontal lobe.
James D Mills, Tomas Kavanagh, Woojin S Kim, Bei Jun Chen, Yoshihiro Kawahara, Glenda M Halliday, Michael Janitz. PLoS One 2013
34
100


Muscleblind-like 1 knockout mice reveal novel splicing defects in the myotonic dystrophy brain.
Koichi Suenaga, Kuang-Yung Lee, Masayuki Nakamori, Yoshiki Tatsumi, Masanori P Takahashi, Harutoshi Fujimura, Kenji Jinnai, Hiroo Yoshikawa, Hongqing Du, Manuel Ares,[...]. PLoS One 2012
58
100

Splicing biomarkers of disease severity in myotonic dystrophy.
Masayuki Nakamori, Krzysztof Sobczak, Araya Puwanant, Steve Welle, Katy Eichinger, Shree Pandya, Jeannne Dekdebrun, Chad R Heatwole, Michael P McDermott, Tian Chen,[...]. Ann Neurol 2013
139
100

Myotonic dystrophy transgenic mice exhibit pathologic abnormalities in diaphragm neuromuscular junctions and phrenic nerves.
Petrica-Adrian Panaite, Emilien Gantelet, Rudolf Kraftsik, Geneviève Gourdon, Thierry Kuntzer, Ibtissam Barakat-Walter. J Neuropathol Exp Neurol 2008
24
100

Scaled-down genetic analysis of myotonic dystrophy type 1 and type 2.
Masayuki Nakamori, Krzysztof Sobczak, Richard T Moxley, Charles A Thornton. Neuromuscul Disord 2009
12
100

Current Progress in CNS Imaging of Myotonic Dystrophy.
Martina Minnerop, Carla Gliem, Cornelia Kornblum. Front Neurol 2018
32
100

Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing.
Nicolas Charlet-B, Rajesh S Savkur, Gopal Singh, Anne V Philips, Elizabeth A Grice, Thomas A Cooper. Mol Cell 2002
429
100

Distinct Functions for Mammalian CLASP1 and -2 During Neurite and Axon Elongation.
Carmen Laura Sayas, Sreya Basu, Michael van der Reijden, Eugenio Bustos-Morán, Marcia Liz, Monica Sousa, Wilfred F J van IJcken, Jesus Avila, Niels Galjart. Front Cell Neurosci 2019
9
100

The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease.
Martina Minnerop, Bernd Weber, Jan-Christoph Schoene-Bake, Sandra Roeske, Sandra Mirbach, Christian Anspach, Christiane Schneider-Gold, Regina C Betz, Christoph Helmstaedter, Marc Tittgemeyer,[...]. Brain 2011
164
100

STAR: ultrafast universal RNA-seq aligner.
Alexander Dobin, Carrie A Davis, Felix Schlesinger, Jorg Drenkow, Chris Zaleski, Sonali Jha, Philippe Batut, Mark Chaisson, Thomas R Gingeras. Bioinformatics 2013
100

Axonal motor and sensory neuropathy in myotonic dystrophy.
M Mondelli, A Rossi, A Malandrini, P Della Porta, G C Guzaai. Acta Neurol Scand 1993
37
100


Small increase in triplet repeat length of cerebellum from patients with myotonic dystrophy.
S Ishii, T Nishio, N Sunohara, T Yoshihara, K Takemura, K Hikiji, S Tsujino, N Sakuragawa. Hum Genet 1996
42
100

Muscle histopathology in myotonic dystrophy in relation to age and muscular weakness.
H Tohgi, A Kawamorita, K Utsugisawa, M Yamagata, M Sano. Muscle Nerve 1994
26
100

Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain.
Peggy F Shelbourne, Christine Keller-McGandy, Wenya Linda Bi, Song-Ro Yoon, Louis Dubeau, Nicola J Veitch, Jean Paul Vonsattel, Nancy S Wexler, Norman Arnheim, Sarah J Augood. Hum Mol Genet 2007
128
100

Core Clinical Phenotypes in Myotonic Dystrophies.
Stephan Wenninger, Federica Montagnese, Benedikt Schoser. Front Neurol 2018
59
100

Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy.
Ami Mankodi, Masanori P Takahashi, Hong Jiang, Carol L Beck, William J Bowers, Richard T Moxley, Stephen C Cannon, Charles A Thornton. Mol Cell 2002
465
100


Myotonic dystrophy: approach to therapy.
Charles A Thornton, Eric Wang, Ellie M Carrell. Curr Opin Genet Dev 2017
54
100

Human brain pathology in myotonic dystrophy type 1: A systematic review.
Ralf Weijs, Kees Okkersen, Baziel van Engelen, Benno Küsters, Martin Lammens, Eleonora Aronica, Joost Raaphorst, Anne-Marie van Cappellen van Walsum. Neuropathology 2021
11
100

Transcriptional signatures of synaptic vesicle genes define myotonic dystrophy type I neurodegeneration.
Antonio Jimenez-Marin, Ibai Diez, Garazi Labayru, Andone Sistiaga, Maria C Caballero, Pol Andres-Benito, Jorge Sepulcre, Isidro Ferrer, Adolfo Lopez de Munain, Jesus M Cortes. Neuropathol Appl Neurobiol 2021
7
100

Dysregulation of human brain microtubule-associated tau mRNA maturation in myotonic dystrophy type 1.
N Sergeant, B Sablonnière, S Schraen-Maschke, A Ghestem, C A Maurage, A Wattez, P Vermersch, A Delacourte. Hum Mol Genet 2001
215
100


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.