A citation-based method for searching scientific literature

H-J Kim, S H Hong, C-S Ki, B-J Kim, J-S Shim, S-H Cho, J-H Park, J-W Kim. Neurology 2005
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Connexin mutations in X-linked Charcot-Marie-Tooth disease.
J Bergoffen, S S Scherer, S Wang, M O Scott, L J Bone, D L Paul, K Chen, M W Lensch, P F Chance, K H Fischbeck. Science 1993
897
50

X-linked motor-sensory neuropathy type-II with deafness and mental retardation: a new disorder.
F S Cowchock, S W Duckett, L J Streletz, L J Graziani, L G Jackson. Am J Med Genet 1985
74
44

Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy.
V V Ionasescu, J Trofatter, J L Haines, A M Summers, R Ionasescu, C Searby. Am J Hum Genet 1991
60
38

Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (cmtx5).
Hee-Jin Kim, Kwang-Min Sohn, Michael E Shy, Karen M Krajewski, Miok Hwang, June-Hee Park, Sue-Yon Jang, Hong-Hee Won, Byung-Ok Choi, Sung Hwa Hong,[...]. Am J Hum Genet 2007
84
38


X-linked recessive Charcot-Marie-Tooth neuropathy: clinical and genetic study.
V V Ionasescu, J Trofatter, J L Haines, A M Summers, R Ionasescu, C Searby. Muscle Nerve 1992
30
33

Proof of genetic heterogeneity in X-linked Charcot-Marie-Tooth disease.
I G Huttner, M L Kennerson, S W Reddel, D Radovanovic, G A Nicholson. Neurology 2006
16
37

Familial opticoacoustic nerve degeneration and polyneuropathy.
R N Rosenberg, A Chutorian. Neurology 1967
84
27

Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study.
E Nelis, C Van Broeckhoven, P De Jonghe, A Löfgren, A Vandenberghe, P Latour, E Le Guern, A Brice, M L Mostacciuolo, F Schiavon,[...]. Eur J Hum Genet 1996
358
22


N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom.
L Kalaydjieva, D Gresham, R Gooding, L Heather, F Baas, R de Jonge, K Blechschmidt, D Angelicheva, D Chandler, P Worsley,[...]. Am J Hum Genet 2000
294
22

Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease.
Henry L Paulson, James Y Garbern, Timothy F Hoban, Karen M Krajewski, Richard A Lewis, Kenneth H Fischbeck, Robert I Grossman, Robert Lenkinski, John A Kamholz, Michael E Shy. Ann Neurol 2002
124
22

A second locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 19q13.3.
A Leal, B Morera, Del Valle G, D Heuss, C Kayser, M Berghoff, R Villegas, E Hernández, M Méndez, H C Hennies,[...]. Am J Hum Genet 2001
52
22

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.
Rachel V Baxter, Kamel Ben Othmane, Julie M Rochelle, Jason E Stajich, Christine Hulette, Susan Dew-Knight, Faycal Hentati, Mongi Ben Hamida, S Bel, Judy E Stenger,[...]. Nat Genet 2002
272
22

Periaxin mutations cause recessive Dejerine-Sottas neuropathy.
C F Boerkoel, H Takashima, P Stankiewicz, C A Garcia, S M Leber, L Rhee-Morris, J R Lupski. Am J Hum Genet 2001
149
22

Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1.
K Grohmann, M Schuelke, A Diers, K Hoffmann, B Lucke, C Adams, E Bertini, H Leonhardt-Horti, F Muntoni, R Ouvrier,[...]. Nat Genet 2001
244
22

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
Stephan Züchner, Maher Noureddine, Marina Kennerson, Kristien Verhoeven, Kristl Claeys, Peter De Jonghe, John Merory, Sofia A Oliveira, Marcy C Speer, Judith E Stenger,[...]. Nat Genet 2005
259
22


Molecular genetics of X-linked Charcot-Marie-Tooth disease.
Kleopas A Kleopa, Steven S Scherer. Neuromolecular Med 2006
80
22

Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J.
Clement Y Chow, Yanling Zhang, James J Dowling, Natsuko Jin, Maja Adamska, Kensuke Shiga, Kinga Szigeti, Michael E Shy, Jun Li, Xuebao Zhang,[...]. Nature 2007
363
22

X-linked dominant hereditary motor and sensory neuropathy.
A F Hahn, W F Brown, W J Koopman, T E Feasby. Brain 1990
133
16

The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity.
O Dubourg, S Tardieu, N Birouk, R Gouider, J M Léger, T Maisonobe, A Brice, P Bouche, E LeGuern. Neuromuscul Disord 2001
38
16

Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease.
O Dubourg, S Tardieu, N Birouk, R Gouider, J M Léger, T Maisonobe, A Brice, P Bouche, E LeGuern. Brain 2001
97
16


The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease.
Ana Cuesta, Laia Pedrola, Teresa Sevilla, Javier García-Planells, María José Chumillas, Fernando Mayordomo, Eric LeGuern, Ignacio Marín, Juan J Vílchez, Francesc Palau. Nat Genet 2002
258
16

Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect.
R Claramunt, L Pedrola, T Sevilla, A López de Munain, J Berciano, A Cuesta, B Sánchez-Navarro, J M Millán, G M Saifi, J R Lupski,[...]. J Med Genet 2005
111
16

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene.
I V Mersiyanova, A V Perepelov, A V Polyakov, V F Sitnikov, E L Dadali, R B Oparin, A N Petrin, O V Evgrafov. Am J Hum Genet 2000
318
16

X-linked neuropathy: gene localization with DNA probes.
K H Fischbeck, N ar-Rushdi, M Pericak-Vance, M Rozear, A D Roses, J P Fryns. Ann Neurol 1986
105
16

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2.
Stephan Züchner, Peter De Jonghe, Albena Jordanova, Kristl G Claeys, Velina Guergueltcheva, Sylvia Cherninkova, Steven R Hamilton, Greg Van Stavern, Karen M Krajewski, Jeffery Stajich,[...]. Ann Neurol 2006
258
16

Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy.
Jan Senderek, Carsten Bergmann, Claudia Stendel, Jutta Kirfel, Nathalie Verpoorten, Peter De Jonghe, Vincent Timmerman, Roman Chrast, Mark H G Verheijen, Greg Lemke,[...]. Am J Hum Genet 2003
141
16

Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathy.
E Nelis, S Erdem, P Y K Van Den Bergh, M-C Belpaire-Dethiou, C Ceuterick, V Van Gerwen, A Cuesta, L Pedrola, F Palau, A A W M Gabreëls-Festen,[...]. Neurology 2002
116
16

Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan Gypsies.
P K Thomas, L Kalaydjieva, B Youl, T Rogers, D Angelicheva, R H King, V Guergueltcheva, J Colomer, C Lupu, A Corches,[...]. Ann Neurol 2001
34
16


Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.
A Quattrone, A Gambardella, F Bono, U Aguglia, A Bolino, A C Bruni, M P Montesi, R L Oliveri, M Sabatelli, O Tamburrini,[...]. Neurology 1996
90
16

Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy.
Albena Jordanova, Joy Irobi, Florian P Thomas, Patrick Van Dijck, Kris Meerschaert, Maarten Dewil, Ines Dierick, An Jacobs, Els De Vriendt, Velina Guergueltcheva,[...]. Nat Genet 2006
278
16

Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene.
K Hayasaka, M Himoro, W Sato, G Takada, K Uyemura, N Shimizu, T D Bird, P M Conneally, P F Chance. Nat Genet 1993
330
16

Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.
Oleg V Evgrafov, Irena Mersiyanova, Joy Irobi, Ludo Van Den Bosch, Ines Dierick, Conrad L Leung, Olga Schagina, Nathalie Verpoorten, Katrien Van Impe, Valeriy Fedotov,[...]. Nat Genet 2004
444
16

Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.
Louis Viollet, Annie Barois, Jean G Rebeiz, Ziad Rifai, Philippe Burlet, Mohammed Zarhrate, Elodie Vial, Michel Dessainte, Brigitte Estournet, Bernard Kleinknecht,[...]. Ann Neurol 2002
40
16

Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15.
Jan Senderek, Carsten Bergmann, Susanne Weber, Uwe-Peter Ketelsen, Hubert Schorle, Sabine Rudnik-Schöneborn, Reinhard Büttner, Eckhard Buchheim, Klaus Zerres. Hum Mol Genet 2003
190
16

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.
Annachiara De Sandre-Giovannoli, Malika Chaouch, Serguei Kozlov, Jean-Michel Vallat, Meriem Tazir, Nadia Kassouri, Pierre Szepetowski, Tarik Hammadouche, Antoon Vandenberghe, Colin L Stewart,[...]. Am J Hum Genet 2002
400
16

A novel form of distal hereditary motor neuronopathy maps to chromosome 9p21.1-p12.
K Christodoulou, E Zamba, M Tsingis, A Mubaidin, K Horani, S Abu-Sheik, M El-Khateeb, K Kyriacou, T Kyriakides, A K Al-Qudah,[...]. Ann Neurol 2000
32
16

Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies.
L E Warner, P Mancias, I J Butler, C M McDonald, L Keppen, K G Koob, J R Lupski. Nat Genet 1998
370
16

Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy.
Joy Irobi, Katrien Van Impe, Pavel Seeman, Albena Jordanova, Ines Dierick, Nathalie Verpoorten, Andrej Michalik, Els De Vriendt, An Jacobs, Veerle Van Gerwen,[...]. Nat Genet 2004
319
16

The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem.
Robert A Taylor, Erin M Simon, Harold G Marks, Steven S Scherer. Neurology 2003
121
16

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome.
Christian Windpassinger, Michaela Auer-Grumbach, Joy Irobi, Heema Patel, Erwin Petek, Gerd Hörl, Roland Malli, Johanna A Reed, Ines Dierick, Nathalie Verpoorten,[...]. Nat Genet 2004
279
16

Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3.
Corinna Berghoff, Martin Berghoff, Alejandro Leal, Bernal Morera, Ramiro Barrantes, André Reis, Bernhard Neundörfer, Bernd Rautenstrauss, Gerardo Del Valle, Dieter Heuss. Neuromuscul Disord 2004
16
18

Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11.
A De Sandre-Giovannoli, V Delague, T Hamadouche, M Chaouch, M Krahn, I Boccaccio, T Maisonobe, E Chouery, R Jabbour, S Atweh,[...]. J Med Genet 2005
32
16

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.
Anthony Antonellis, Rachel E Ellsworth, Nyamkhishig Sambuughin, Imke Puls, Annette Abel, Shih-Queen Lee-Lin, Albena Jordanova, Ivo Kremensky, Kyproula Christodoulou, Lefkos T Middleton,[...]. Am J Hum Genet 2003
411
16

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta.
C Zhao, J Takita, Y Tanaka, M Setou, T Nakagawa, S Takeda, H W Yang, S Terada, T Nakata, Y Takei,[...]. Cell 2001
549
16

Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2.
A Bolino, M Muglia, F L Conforti, E LeGuern, M A Salih, D M Georgiou, K Christodoulou, I Hausmanowa-Petrusewicz, P Mandich, A Schenone,[...]. Nat Genet 2000
360
16


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.