A citation-based method for searching scientific literature

Honghao Li, Qi Chen, Fuchen Liu, Xuemei Zhang, Wei Li, Shuping Liu, Yuying Zhao, Yaoqin Gong, Chuanzhu Yan. PLoS One 2013
Times Cited: 24







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



Times Cited
  Times     Co-cited
Similarity


The proteomic profile of hereditary inclusion body myopathy.
Ilan Sela, Irit Milman Krentsis, Zipora Shlomai, Menachem Sadeh, Ron Dabby, Zohar Argov, Hannah Ben-Bassat, Stella Mitrani-Rosenbaum. PLoS One 2011
39
45

A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.
May Christine V Malicdan, Satoru Noguchi, Ikuya Nonaka, Yukiko K Hayashi, Ichizo Nishino. Hum Mol Genet 2007
89
45

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.
I Eisenberg, N Avidan, T Potikha, H Hochner, M Chen, T Olender, M Barash, M Shemesh, M Sadeh, G Grabov-Nardini,[...]. Nat Genet 2001
373
41


Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model.
May Christine V Malicdan, Satoru Noguchi, Yukiko K Hayashi, Ikuya Nonaka, Ichizo Nishino. Nat Med 2009
116
33


Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine.
Belinda Galeano, Riko Klootwijk, Irini Manoli, MaoSen Sun, Carla Ciccone, Daniel Darvish, Matthew F Starost, Patricia M Zerfas, Victoria J Hoffmann, Shelley Hoogstraten-Miller,[...]. J Clin Invest 2007
145
29


UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: novel pathways in skeletal muscle?
Shira Amsili, Hagit Zer, Stephan Hinderlich, Sabine Krause, Michal Becker-Cohen, Daniel G MacArthur, Kathryn N North, Stella Mitrani-Rosenbaum. PLoS One 2008
41
29

Sialylation is essential for early development in mice.
Martina Schwarzkopf, Klaus-Peter Knobeloch, Elvira Rohde, Stephan Hinderlich, Nicola Wiechens, Lothar Lucka, Ivan Horak, Werner Reutter, Rüdiger Horstkorte. Proc Natl Acad Sci U S A 2002
252
29

Cell stress molecules in the skeletal muscle of GNE myopathy.
Charlotte Fischer, Konstanze Kleinschnitz, Arne Wrede, Ingrid Muth, Niels Kruse, Ichizo Nishino, Jens Schmidt. BMC Neurol 2013
13
53

Variable phenotypes of knockin mice carrying the M712T Gne mutation.
Ilan Sela, Lena Yakovlev, Michal Becker Cohen, Moran Elbaz, Nurit Yanay, Uri Ben Shlomo, Hagit Yotvat, Yakov Fellig, Zohar Argov, Stella Mitrani-Rosenbaum. Neuromolecular Med 2013
20
35

GNE Myopathy and Cell Apoptosis: A Comparative Mutation Analysis.
Reema Singh, Ranjana Arya. Mol Neurobiol 2016
17
41

Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model mice.
Takahiro Yonekawa, May Christine V Malicdan, Anna Cho, Yukiko K Hayashi, Ikuya Nonaka, Toshiki Mine, Takeshi Yamamoto, Ichizo Nishino, Satoru Noguchi. Brain 2014
32
29

Aceneuramic Acid Extended Release Administration Maintains Upper Limb Muscle Strength in a 48-week Study of Subjects with GNE Myopathy: Results from a Phase 2, Randomized, Controlled Study.
Zohar Argov, Yoseph Caraco, Heather Lau, Alan Pestronk, Perry B Shieh, Alison Skrinar, Tony Koutsoukos, Ruhi Ahmed, Julia Martinisi, Emil Kakkis. J Neuromuscul Dis 2016
23
30

NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations.
E Ricci, A Broccolini, T Gidaro, R Morosetti, C Gliubizzi, R Frusciante, G M Di Lella, P A Tonali, M Mirabella. Neurology 2006
53
25

Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles.
Satoru Noguchi, Yoko Keira, Kumiko Murayama, Megumu Ogawa, Masako Fujita, Genri Kawahara, Yasushi Oya, Masaoki Imazawa, Yu-Ichi Goto, Yukiko K Hayashi,[...]. J Biol Chem 2004
119
25

Serum neural cell adhesion molecule is hyposialylated in hereditary inclusion body myopathy.
Yadira Valles-Ayoub, Saghi Esfandiarifard, Pedram Sinai, Rosangela Carbajo, Zeshan Khokher, Daniel No, Marvin Pietruszka, Babak Darvish, Emil Kakkis, Daniel Darvish. Genet Test Mol Biomarkers 2012
12
50

Hereditary inclusion-body myopathies.
Aldobrando Broccolini, Massimiliano Mirabella. Biochim Biophys Acta 2015
23
26

Mutation update for GNE gene variants associated with GNE myopathy.
Frank V Celeste, Thierry Vilboux, Carla Ciccone, John Karl de Dios, May Christine V Malicdan, Petcharat Leoyklang, John C McKew, William A Gahl, Nuria Carrillo-Carrasco, Marjan Huizing. Hum Mutat 2014
63
25

Characterization of hereditary inclusion body myopathy myoblasts: possible primary impairment of apoptotic events.
S Amsili, Z Shlomai, R Levitzki, S Krause, H Lochmuller, H Ben-Bassat, S Mitrani-Rosenbaum. Cell Death Differ 2007
45
25

Increased amyloid β-peptide uptake in skeletal muscle is induced by hyposialylation and may account for apoptosis in GNE myopathy.
Mònica Bosch-Morató, Cinta Iriondo, Biuse Guivernau, Victòria Valls-Comamala, Noemí Vidal, Montse Olivé, Henry Querfurth, Francisco J Muñoz. Oncotarget 2016
12
50

Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy.
Anna Cho, May Christine, V Malicdan, Miho Miyakawa, Ikuya Nonaka, Ichizo Nishino, Satoru Noguchi. Hum Mol Genet 2017
26
25

Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutations.
Madoka Mori-Yoshimura, Kazunari Monma, Naoki Suzuki, Masashi Aoki, Toshihide Kumamoto, Keiko Tanaka, Hiroyuki Tomimitsu, Satoshi Nakano, Masahiro Sonoo, Jun Shimizu,[...]. J Neurol Sci 2012
32
20


Hypoglycosylation of alpha-dystroglycan in patients with hereditary IBM due to GNE mutations.
Marjan Huizing, Goran Rakocevic, Susan E Sparks, Ioanna Mamali, Alexey Shatunov, Lev Goldfarb, Donna Krasnewich, William A Gahl, Marinos C Dalakas. Mol Genet Metab 2004
83
20

No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation.
Ilan Salama, Stephan Hinderlich, Zipora Shlomai, Iris Eisenberg, Sabine Krause, Kevin Yarema, Zohar Argov, Hanns Lochmuller, Werner Reutter, Ron Dabby,[...]. Biochem Biophys Res Commun 2005
65
20

Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle.
Aldobrando Broccolini, Teresa Gidaro, Raimondo De Cristofaro, Roberta Morosetti, Carla Gliubizzi, Enzo Ricci, Pietro A Tonali, Massimiliano Mirabella. J Neurochem 2008
40
20

Glycoprotein hyposialylation gives rise to a nephrotic-like syndrome that is prevented by sialic acid administration in GNE V572L point-mutant mice.
Mitutoshi Ito, Kazushi Sugihara, Tomoya Asaka, Tadashi Toyama, Toru Yoshihara, Kengo Furuichi, Takashi Wada, Masahide Asano. PLoS One 2012
29
20

Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy.
I Nishino, S Noguchi, K Murayama, A Driss, K Sugie, Y Oya, T Nagata, K Chida, T Takahashi, Y Takusa,[...]. Neurology 2002
160
20

Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy).
Anna Cho, Yukiko K Hayashi, Kazunari Monma, Yasushi Oya, Satoru Noguchi, Ikuya Nonaka, Ichizo Nishino. J Neurol Neurosurg Psychiatry 2014
37
20

Peracetylated N-acetylmannosamine, a synthetic sugar molecule, efficiently rescues muscle phenotype and biochemical defects in mouse model of sialic acid-deficient myopathy.
May Christine V Malicdan, Satoru Noguchi, Tomoharu Tokutomi, Yu-ichi Goto, Ikuya Nonaka, Yukiko K Hayashi, Ichizo Nishino. J Biol Chem 2012
30
20

Gne depletion during zebrafish development impairs skeletal muscle structure and function.
Alon Daya, Gad David Vatine, Michal Becker-Cohen, Tzukit Tal-Goldberg, Adam Friedmann, Yoav Gothilf, Shao Jun Du, Stella Mitrani-Rosenbaum. Hum Mol Genet 2014
11
45

Mitochondrial processes are impaired in hereditary inclusion body myopathy.
Iris Eisenberg, Noa Novershtern, Zohar Itzhaki, Michal Becker-Cohen, Menachem Sadeh, Peter H G M Willems, Nir Friedman, Werner J H Koopman, Stella Mitrani-Rosenbaum. Hum Mol Genet 2008
33
20

GNE myopathy: new name and new mutation nomenclature.
Marjan Huizing, Nuria Carrillo-Carrasco, May Christine V Malicdan, Satoru Noguchi, William A Gahl, Stella Mitrani-Rosenbaum, Zohar Argov, Ichizo Nishino. Neuromuscul Disord 2014
47
20

GNE myopathy in India.
Atchayaram Nalini, Narayanappa Gayathri, Ischizo Nishino, Yukiko K Hayashi. Neurol India 2013
25
20

Oral monosaccharide therapies to reverse renal and muscle hyposialylation in a mouse model of GNE myopathy.
Terren K Niethamer, Tal Yardeni, Petcharat Leoyklang, Carla Ciccone, Adrian Astiz-Martinez, Katherine Jacobs, Heidi M Dorward, Patricia M Zerfas, William A Gahl, Marjan Huizing. Mol Genet Metab 2012
30
20

GNE myopathy: current update and future therapy.
Ichizo Nishino, Nuria Carrillo-Carrasco, Zohar Argov. J Neurol Neurosurg Psychiatry 2015
91
20

The Interaction of UDP-N-Acetylglucosamine 2-Epimerase/N-Acetylmannosamine Kinase (GNE) and Alpha-Actinin 2 Is Altered in GNE Myopathy M743T Mutant.
Avi Harazi, Michal Becker-Cohen, Hagit Zer, Ofra Moshel, Stephan Hinderlich, Stella Mitrani-Rosenbaum. Mol Neurobiol 2017
26
20


Endoplasmic reticulum stress and unfolded protein response in inclusion body myositis muscle.
Gaetano Vattemi, W King Engel, Janis McFerrin, Valerie Askanas. Am J Pathol 2004
145
16

Muscle imaging findings in GNE myopathy.
Giorgio Tasca, Enzo Ricci, Mauro Monforte, Francesco Laschena, Pierfrancesco Ottaviani, Carmelo Rodolico, Emanuele Barca, Gabriella Silvestri, Elisabetta Iannaccone, Massimiliano Mirabella,[...]. J Neurol 2012
40
16

Reduced sialylation status in UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (GNE)-deficient mice.
Daniel Gagiannis, André Orthmann, Ilona Danssmann, Martina Schwarzkopf, Wenke Weidemann, Rüdiger Horstkorte. Glycoconj J 2007
33
16

Limb-girdle phenotype is frequent in patients with myopathy associated with GNE mutations.
Young-Eun Park, Hyang-Suk Kim, Eun-Suk Choi, Jin-Hong Shin, Sun-Young Kim, Eun-Hui Son, Chang-Hoon Lee, Dae-Seong Kim. J Neurol Sci 2012
25
16

Influence of UDP-GlcNAc 2-epimerase/ManNAc kinase mutant proteins on hereditary inclusion body myopathy.
Juliane Penner, Lars R Mantey, Sharona Elgavish, Darius Ghaderi, Sebahattin Cirak, Markus Berger, Sabine Krause, Lothar Lucka, Thomas Voit, Stella Mitrani-Rosenbaum,[...]. Biochemistry 2006
47
16


Loss of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) induces apoptotic processes in pancreatic carcinoma cells.
Wolfgang Kemmner, Pia Kessel, Hugo Sanchez-Ruderisch, Heinz Möller, Stephan Hinderlich, Peter M Schlag, Katharina Detjen. FASEB J 2012
16
25

Hereditary inclusion body myopathy: a decade of progress.
Marjan Huizing, Donna M Krasnewich. Biochim Biophys Acta 2009
65
16


Non-specific accumulation of glycosphingolipids in GNE myopathy.
Katherine A Patzel, Tal Yardeni, Erell Le Poëc-Celic, Petcharat Leoyklang, Heidi Dorward, Dominic S Alonzi, Nikolay V Kukushkin, Bixue Xu, Yongmin Zhang, Matthieu Sollogoub,[...]. J Inherit Metab Dis 2014
7
57


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.