A citation-based method for searching scientific literature

J Amiel, V Raclin, J M Jouannic, N Morichon, H Hoffman-Radvanyi, M Dommergues, J Feingold, A Munnich, J P Bonnefont. J Med Genet 2001
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
J D Brook, M E McCurrach, H G Harley, A J Buckler, D Church, H Aburatani, K Hunter, V P Stanton, J P Thirion, T Hudson. Cell 1992
80


Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy patients.
L Martorell, D G Monckton, J Gamez, K J Johnson, I Gich, A Lopez de Munain, M Baiget. Hum Mol Genet 1998
108
40

Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins.
Walther J A A van den Broek, Marcel R Nelen, Derick G Wansink, Marga M Coerwinkel, Hein te Riele, Patricia J T A Groenen, Bé Wieringa. Hum Mol Genet 2002
210
40

Congenital myotonic dystrophy: report of paternal transmission.
Y Tanaka, Y Suzuki, N Shimozawa, E Nanba, N Kondo. Brain Dev 2000
7
40

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.
T Ashizawa, M Anvret, M Baiget, J M Barceló, H Brunner, A M Cobo, B Dallapiccola, R G Fenwick, U Grandell, H Harley. Am J Hum Genet 1994
113
40


Defective satellite cells in congenital myotonic dystrophy.
D Furling, L Coiffier, V Mouly, J P Barbet, J L St Guily, K Taneja, G Gourdon, C Junien, G S Butler-Browne. Hum Mol Genet 2001
84
20

Myotonic dystrophy with no trinucleotide repeat expansion.
C A Thornton, R C Griggs, R T Moxley. Ann Neurol 1994
145
20

Proximal myotonic myopathy: a syndrome with a favourable prognosis?
Giovanni Meola, V Sansone, K Marinou, M Cotelli, R T Moxley, C A Thornton, L De Ambroggi. J Neurol Sci 2002
26
20

Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2).
J W Day, R Roelofs, B Leroy, I Pech, K Benzow, L P Ranum. Neuromuscul Disord 1999
82
20

Myotonic dystrophy protein kinase is involved in the modulation of the Ca2+ homeostasis in skeletal muscle cells.
A A Benders, P J Groenen, F T Oerlemans, J H Veerkamp, B Wieringa. J Clin Invest 1997
53
20

A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene.
S Nagamitsu, T Matsuura, M Khajavi, R Armstrong, C Gooch, Y Harati, T Ashizawa. Neurology 2000
32
20

Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.
A Mankodi, C R Urbinati, Q P Yuan, R T Moxley, V Sansone, M Krym, D Henderson, M Schalling, M S Swanson, C A Thornton. Hum Mol Genet 2001
309
20

Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts.
K Ricker, M C Koch, F Lehmann-Horn, D Pongratz, M Otto, R Heine, R T Moxley. Neurology 1994
178
20



Visualization of double-stranded RNAs from the myotonic dystrophy protein kinase gene and interactions with CUG-binding protein.
S Michalowski, J W Miller, C R Urbinati, M Paliouras, M S Swanson, J Griffith. Nucleic Acids Res 1999
101
20

Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells.
Majid Fardaei, Mark T Rogers, Helena M Thorpe, Kenneth Larkin, Marion G Hamshere, Peter S Harper, J David Brook. Hum Mol Genet 2002
319
20

CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus.
G N Filippova, C P Thienes, B H Penn, D H Cho, Y J Hu, J M Moore, T R Klesert, V V Lobanenkov, S J Tapscott. Nat Genet 2001
233
20

Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene.
C A Thornton, J P Wymer, Z Simmons, C McClain, R T Moxley. Nat Genet 1997
165
20

Specific tau variants in the brains of patients with myotonic dystrophy.
P Vermersch, N Sergeant, M M Ruchoux, H Hofmann-Radvanyi, A Wattez, H Petit, P Dwailly, A Delacourte. Neurology 1996
122
20

Human MSH2 binds to trinucleotide repeat DNA structures associated with neurodegenerative diseases.
C E Pearson, A Ewel, S Acharya, R A Fishel, R R Sinden. Hum Mol Genet 1997
118
20

Age and causes of death in adult-onset myotonic dystrophy.
C E de Die-Smulders, C J Höweler, C Thijs, J F Mirandolle, H B Anten, H J Smeets, K E Chandler, J P Geraedts. Brain 1998
144
20

Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts.
P S Sarkar, B Appukuttan, J Han, Y Ito, C Ai, W Tsai, Y Chai, J T Stout, S Reddy. Nat Genet 2000
127
20

Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy.
T R Klesert, D H Cho, J I Clark, J Maylie, J Adelman, L Snider, E C Yuen, P Soriano, S J Tapscott. Nat Genet 2000
163
20

Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.
G Jansen, P Willems, M Coerwinkel, W Nillesen, H Smeets, L Vits, C Höweler, H Brunner, B Wieringa. Am J Hum Genet 1994
146
20


RNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1.
N A Timchenko, Z J Cai, A L Welm, S Reddy, T Ashizawa, L T Timchenko. J Biol Chem 2001
224
20

Linkage of proximal myotonic myopathy to chromosome 3q.
K Ricker, T Grimm, M C Koch, C Schneider, W Kress, C D Reimers, W Schulte-Mattler, B Mueller-Myhsok, K V Toyka, C R Mueller. Neurology 1999
60
20

Molecular basis for impaired muscle differentiation in myotonic dystrophy.
N A Timchenko, P Iakova, Z J Cai, J R Smith, L T Timchenko. Mol Cell Biol 2001
138
20

Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP.
T R Klesert, A D Otten, T D Bird, S J Tapscott. Nat Genet 1997
183
20

Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat.
A Mankodi, E Logigian, L Callahan, C McClain, R White, D Henderson, M Krym, C A Thornton. Science 2000
487
20

Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues.
K L Taneja, M McCurrach, M Schalling, D Housman, R H Singer. J Cell Biol 1995
449
20



Genetic mapping of a second myotonic dystrophy locus.
L P Ranum, P F Rasmussen, K A Benzow, M D Koob, J W Day. Nat Genet 1998
180
20


Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.
H Seznec, O Agbulut, N Sergeant, C Savouret, A Ghestem, N Tabti, J C Willer, L Ourth, C Duros, E Brisson,[...]. Hum Mol Genet 2001
174
20


A new mutation in a family with cold-aggravated myotonia disrupts Na(+) channel inactivation.
F F Wu, M P Takahashi, E Pegoraro, C Angelini, P Colleselli, S C Cannon, E P Hoffman. Neurology 2001
30
20

Progressive atrioventricular conduction block in a mouse myotonic dystrophy model.
C I Berul, C T Maguire, J Gehrmann, S Reddy. J Interv Card Electrophysiol 2000
38
20

Modafinil for excessive daytime sleepiness in myotonic dystrophy.
M S Damian, A Gerlach , F Schmidt, E Lehmann , H Reichmann. Neurology 2001
67
20

Myotonic dystrophy protein kinase phosphorylates the myosin phosphatase targeting subunit and inhibits myosin phosphatase activity.
A Murányi, R Zhang, F Liu, K Hirano, M Ito, H F Epstein, D J Hartshorne. FEBS Lett 2001
72
20


Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy.
J W Miller, C R Urbinati, P Teng-Umnuay, M G Stenberg, B J Byrne, C A Thornton, M S Swanson. EMBO J 2000
623
20

The skeletal muscle chloride channel in dominant and recessive human myotonia.
M C Koch, K Steinmeyer, C Lorenz, K Ricker, F Wolf, M Otto, B Zoll, F Lehmann-Horn, K H Grzeschik, T J Jentsch. Science 1992
591
20


Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy.
S Reddy, D B Smith, M M Rich, J M Leferovich, P Reilly, B M Davis, K Tran, H Rayburn, R Bronson, D Cros,[...]. Nat Genet 1996
246
20

Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.
G Jansen, P J Groenen, D Bächner, P H Jap, M Coerwinkel, F Oerlemans, W van den Broek, B Gohlsch, D Pette, J J Plomp,[...]. Nat Genet 1996
235
20


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.