A citation-based method for searching scientific literature

E Nelis, N Haites, C Van Broeckhoven. Hum Mutat 1999
Times Cited: 174







List of co-cited articles
788 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
888
23

The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype.
P De Jonghe, V Timmerman, C Ceuterick, E Nelis, E De Vriendt, A Löfgren, A Vercruyssen, C Verellen, L Van Maldergem, J J Martin,[...]. Brain 1999
177
20


Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination.
L E Warner, M J Hilz, S H Appel, J M Killian, E H Kolodry, G Karpati, S Carpenter, G V Watters, C Wheeler, D Witt,[...]. Neuron 1996
309
18

DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
J R Lupski, R M de Oca-Luna, S Slaugenhaupt, L Pentao, V Guzzetta, B J Trask, O Saucedo-Cardenas, D F Barker, J M Killian, C A Garcia,[...]. Cell 1991
18

DNA deletion associated with hereditary neuropathy with liability to pressure palsies.
P F Chance, M K Alderson, K A Leppig, M W Lensch, N Matsunami, B Smith, P D Swanson, S J Odelberg, C M Disteche, T D Bird. Cell 1993
678
17

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
367
15



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
354
15

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
357
13


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
308
12

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
327
12

Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies.
S Bort, E Nelis, V Timmerman, T Sevilla, A Cruz-Martínez, F Martínez, J M Millán, J Arpa, J J Vílchez, F Prieto,[...]. Hum Genet 1997
119
12

Connexin32-null mice develop demyelinating peripheral neuropathy.
S S Scherer, Y T Xu, E Nelles, K Fischbeck, K Willecke, L J Bone. Glia 1998
221
12


Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene.
F Chapon, P Latour, P Diraison, S Schaeffer, A Vandenberghe. J Neurol Neurosurg Psychiatry 1999
103
11

Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero gene.
M G Marrosu, S Vaccargiu, G Marrosu, A Vannelli, C Cianchetti, F Muntoni. Neurology 1998
132
11


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
286
10


Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies.
K Silander, P Meretoja, V Juvonen, J Ignatius, H Pihko, A Saarinen, T Wallden, E Herrgård, P Aula, M L Savontaus. Hum Mutat 1998
66
15

Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A.
L J Valentijn, F Baas, R A Wolterman, J E Hoogendijk, N H van den Bosch, I Zorn, A W Gabreëls-Festen, M de Visser, P A Bolhuis. Nat Genet 1992
417
10

Role of myelin P0 protein as a homophilic adhesion molecule.
M T Filbin, F S Walsh, B D Trapp, J A Pizzey, G I Tennekoon. Nature 1990
311
10

Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype correlation.
Cornelius F Boerkoel, Hiroshi Takashima, Carlos A Garcia, Richard K Olney, John Johnson, Katherine Berry, Paul Russo, Shelley Kennedy, Ahmad S Teebi, Mena Scavina,[...]. Ann Neurol 2002
183
10

Phenotypic clustering in MPZ mutations.
Michael E Shy, Agnes Jáni, Karen Krajewski, Marina Grandis, Richard A Lewis, Jun Li, Rosemary R Shy, Janne Balsamo, Jack Lilien, James Y Garbern,[...]. Brain 2004
195
10

Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease.
A A Gabreëls-Festen, J E Hoogendijk, P H Meijerink, F J Gabreëls, P A Bolhuis, S van Beersum, T Kulkens, E Nelis, F G Jennekens, M de Visser,[...]. Neurology 1996
120
9

Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1).
E A Janssen, S Kemp, G W Hensels, O G Sie, C E de Die-Smulders, J E Hoogendijk, M de Visser, P A Bolhuis. Hum Genet 1997
50
18

Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32.
P Anzini, D H Neuberg, M Schachner, E Nelles, K Willecke, J Zielasek, K V Toyka, U Suter, R Martini. J Neurosci 1997
247
9


Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice.
K Adlkofer, R Martini, A Aguzzi, J Zielasek, K V Toyka, U Suter. Nat Genet 1995
299
9

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse.
U Suter, J J Moskow, A A Welcher, G J Snipes, B Kosaras, R L Sidman, A M Buchberg, E M Shooter. Proc Natl Acad Sci U S A 1992
269
9


Krox-20 controls myelination in the peripheral nervous system.
P Topilko, S Schneider-Maunoury, G Levi, A Baron-Van Evercooren, A B Chennoufi, T Seitanidou, C Babinet, P Charnay. Nature 1994
609
9

Mutations in the cytoplasmic domain of P0 reveal a role for PKC-mediated phosphorylation in adhesion and myelination.
W Xu, M Shy, J Kamholz, L Elferink, G Xu, J Lilien, J Balsamo. J Cell Biol 2001
61
14

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.
N Birouk, E LeGuern, T Maisonobe, H Rouger, R Gouider, S Tardieu, M Gugenheim, M C Routon, J M Léger, Y Agid,[...]. Neurology 1998
136
8

Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease.
S Oh, Y Ri, M V Bennett, E B Trexler, V K Verselis, T A Bargiello. Neuron 1997
203
8



Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene.
B B Roa, C A Garcia, U Suter, D A Kulpa, C A Wise, J Mueller, A A Welcher, G J Snipes, E M Shooter, P I Patel,[...]. N Engl J Med 1993
327
8

Trembler mouse carries a point mutation in a myelin gene.
U Suter, A A Welcher, T Ozcelik, G J Snipes, B Kosaras, U Francke, S Billings-Gagliardi, R L Sidman, E M Shooter. Nature 1992
383
8



Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 gene.
V V Ionasescu, C C Searby, R Ionasescu, S Chatkupt, N Patel, R Koenigsberger. Muscle Nerve 1997
55
14

Structural and functional diversity of connexin genes in the mouse and human genome.
Klaus Willecke, Jürgen Eiberger, Joachim Degen, Dominik Eckardt, Alessandro Romualdi, Martin Güldenagel, Urban Deutsch, Goran Söhl. Biol Chem 2002
893
8

Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field.
E Nelis, V Timmerman, P De Jonghe, C Van Broeckhoven, B Rautenstrauss. Neurogenetics 1999
29
24

Charcot-Marie-Tooth neuropathy type 2 and P0 point mutations: two novel amino acid substitutions (Asp61Gly; Tyr119Cys) and a possible "hotspot" on Thr124Met.
J Senderek, B Hermanns, U Lehmann, C Bergmann, G Marx, C Kabus, V Timmerman, G Stoltenburg-Didinger, J M Schröder. Brain Pathol 2000
55
12

Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene.
V Delague, C Bareil, S Tuffery, P Bouvagnet, E Chouery, S Koussa, T Maisonobe, J Loiselet, A Mégarbané, M Claustres. Am J Hum Genet 2000
62
11

Protein composition of myelin of the peripheral nervous system.
S Greenfield, S Brostoff, E H Eylar, P Morell. J Neurochem 1973
397
7


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.