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List of co-cited articles
1171 articles co-cited >1



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Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity.
Fernando Morales, Jillian M Couto, Catherine F Higham, Grant Hogg, Patricia Cuenca, Claudia Braida, Richard H Wilson, Berit Adam, Gerardo del Valle, Roberto Brian,[...]. Hum Mol Genet 2012
98
50

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
45

Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent.
L J Wong, T Ashizawa, D G Monckton, C T Caskey, C S Richards. Am J Hum Genet 1995
169
40

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.
M Mahadevan, C Tsilfidis, L Sabourin, G Shutler, C Amemiya, G Jansen, C Neville, M Narang, J Barceló, K O'Hoy. Science 1992
39

Highly unstable sequence interruptions of the CTG repeat in the myotonic dystrophy gene.
Zuzana Musova, Radim Mazanec, Anna Krepelova, Edvard Ehler, Jiri Vales, Radka Jaklova, Tomas Prochazka, Petr Koukal, Tatana Marikova, Josef Kraus,[...]. Am J Med Genet A 2009
93
33

Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.
H G Harley, S A Rundle, J C MacMillan, J Myring, J D Brook, S Crow, W Reardon, I Fenton, D J Shaw, P S Harper. Am J Hum Genet 1993
307
31

An unstable triplet repeat in a gene related to myotonic muscular dystrophy.
Y H Fu, A Pizzuti, R G Fenwick, J King, S Rajnarayan, P W Dunne, J Dubel, G A Nasser, T Ashizawa, P de Jong. Science 1992
31

Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients.
Claudia Braida, Rhoda K A Stefanatos, Berit Adam, Navdeep Mahajan, Hubert J M Smeets, Florence Niel, Cyril Goizet, Benoit Arveiler, Michel Koenig, Clotilde Lagier-Tourenne,[...]. Hum Mol Genet 2010
97
31


Analysis of unstable triplet repeats using small-pool polymerase chain reaction.
Mário Gomes-Pereira, Sanjay I Bidichandani, Darren G Monckton. Methods Mol Biol 2004
57
49

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
26

Myotonic dystrophy: size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism.
C Lavedan, H Hofmann-Radvanyi, P Shelbourne, J P Rabes, C Duros, D Savoy, I Dehaupas, S Luce, K Johnson, C Junien. Am J Hum Genet 1993
213
24

Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy.
M Anvret, G Ahlberg, U Grandell, B Hedberg, K Johnson, L Edström. Hum Mol Genet 1993
161
23

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
109
23

A general method for the detection of large CAG repeat expansions by fluorescent PCR.
J P Warner, L H Barron, D Goudie, K Kelly, D Dow, D R Fitzpatrick, D J Brock. J Med Genet 1996
188
21


Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability.
H Seznec, A S Lia-Baldini, C Duros, C Fouquet, C Lacroix, H Hofmann-Radvanyi, C Junien, G Gourdon. Hum Mol Genet 2000
119
20

Somatic instability of CTG repeat in myotonic dystrophy.
T Ashizawa, J R Dubel, Y Harati. Neurology 1993
149
19

Repeat instability as the basis for human diseases and as a potential target for therapy.
Arturo López Castel, John D Cleary, Christopher E Pearson. Nat Rev Mol Cell Biol 2010
293
19

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
C L Liquori, K Ricker, M L Moseley, J F Jacobsen, W Kress, S L Naylor, J W Day, L P Ranum. Science 2001
819
19

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
18

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy.
J Buxton, P Shelbourne, J Davies, C Jones, T Van Tongeren, C Aslanidis, P de Jong, G Jansen, M Anvret, B Riley. Nature 1992
570
18

Repeat instability: mechanisms of dynamic mutations.
Christopher E Pearson, Kerrie Nichol Edamura, John D Cleary. Nat Rev Genet 2005
608
18

High levels of somatic DNA diversity at the myotonic dystrophy type 1 locus are driven by ultra-frequent expansion and contraction mutations.
Catherine F Higham, Fernando Morales, Christina A Cobbold, Daniel T Haydon, Darren G Monckton. Hum Mol Genet 2012
31
58

The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy.
A Hunter, C Tsilfidis, G Mettler, P Jacob, M Mahadevan, L Surh, R Korneluk. J Med Genet 1992
199
17

Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues.
Arturo López Castel, Masayuki Nakamori, Stephanie Tomé, David Chitayat, Geneviève Gourdon, Charles A Thornton, Christopher E Pearson. Hum Mol Genet 2011
93
18

A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients.
Fernando Morales, Melissa Vásquez, Carolina Santamaría, Patricia Cuenca, Eyleen Corrales, Darren G Monckton. DNA Repair (Amst) 2016
48
35

Dramatic, expansion-biased, age-dependent, tissue-specific somatic mosaicism in a transgenic mouse model of triplet repeat instability.
M T Fortune, C Vassilopoulos, M I Coolbaugh, M J Siciliano, D G Monckton. Hum Mol Genet 2000
104
16

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
114
16


Pms2 is a genetic enhancer of trinucleotide CAG.CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion.
Mário Gomes-Pereira, M Teresa Fortune, Laura Ingram, John P McAbney, Darren G Monckton. Hum Mol Genet 2004
129
16

Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum.
Vanessa C Wheeler, Lori-Anne Lebel, Vladimir Vrbanac, Allison Teed, Hein te Riele, Marcy E MacDonald. Hum Mol Genet 2003
158
15

Hypermutable myotonic dystrophy CTG repeats in transgenic mice.
D G Monckton, M I Coolbaugh, K T Ashizawa, M J Siciliano, C T Caskey. Nat Genet 1997
102
15

Germline mutational dynamics in myotonic dystrophy type 1 males: allele length and age effects.
L Martorell, J Gámez, M L Cayuela, F K Gould, J P McAbney, T Ashizawa, D G Monckton, M Baiget. Neurology 2004
35
42

Cloning of the essential myotonic dystrophy region and mapping of the putative defect.
C Aslanidis, G Jansen, C Amemiya, G Shutler, M Mahadevan, C Tsilfidis, C Chen, J Alleman, N G Wormskamp, M Vooijs. Nature 1992
450
15

Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).
H G Brunner, H T Brüggenwirth, W Nillesen, G Jansen, B C Hamel, R L Hoppe, C E de Die, C J Höweler, B A van Oost, B Wieringa. Am J Hum Genet 1993
87
17


Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classification.
M De Antonio, C Dogan, D Hamroun, M Mati, S Zerrouki, B Eymard, S Katsahian, G Bassez. Rev Neurol (Paris) 2016
92
16

Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice.
Laurent Foiry, Li Dong, Cédric Savouret, Laurence Hubert, Hein te Riele, Claudine Junien, Geneviève Gourdon. Hum Genet 2006
100
14

CTG repeat instability and size variation timing in DNA repair-deficient mice.
Cédric Savouret, Edith Brisson, Jeroen Essers, Roland Kanaar, Albert Pastink, Hein te Riele, Claudine Junien, Geneviève Gourdon. EMBO J 2003
146
14


Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset.
Meera Swami, Audrey E Hendricks, Tammy Gillis, Tiffany Massood, Jayalakshmi Mysore, Richard H Myers, Vanessa C Wheeler. Hum Mol Genet 2009
159
14

Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat.
T Ashizawa, J R Dubel, P W Dunne, C J Dunne, Y H Fu, A Pizzuti, C T Caskey, E Boerwinkle, M B Perryman, H F Epstein. Neurology 1992
125
14

Complex patterns of male germline instability and somatic mosaicism in myotonic dystrophy type 1.
L Martorell, D G Monckton, J Gamez, M Baiget. Eur J Hum Genet 2000
34
41


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
632
13

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy.
H G Harley, J D Brook, S A Rundle, S Crow, W Reardon, A J Buckler, P S Harper, D E Housman, D J Shaw. Nature 1992
650
13

Anticipation in myotonic dystrophy: fact or fiction?
C J Höweler, H F Busch, J P Geraedts, M F Niermeijer, A Staal. Brain 1989
211
13




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.