A citation-based method for searching scientific literature

L Martorell, D G Monckton, J Gamez, K J Johnson, I Gich, A Lopez de Munain, M Baiget. Hum Mol Genet 1998
Times Cited: 112







List of co-cited articles
1077 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



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
171
54


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
46

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

Somatic instability of CTG repeat in myotonic dystrophy.
T Ashizawa, J R Dubel, Y Harati. Neurology 1993
150
32

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
30

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
30


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
309
28

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
27

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
211
27

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
214
24

Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?
M Zatz, M R Passos-Bueno, A Cerqueira, S K Marie, M Vainzof, R C Pavanello. Hum Mol Genet 1995
61
37

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
574
22


Somatic instability of the myotonic dystrophy (CTG)n repeat during human fetal development.
L Martorell, K Johnson, C A Boucher, M Baiget. Hum Mol Genet 1997
58
34

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
656
20


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
125
20

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
103
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
836
19

Anticipation in myotonic dystrophy: new light on an old problem.
P S Harper, H G Harley, W Reardon, D J Shaw. Am J Hum Genet 1992
238
18


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
99
18

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
105
18

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
103
17

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
502
17


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
149
17

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
103
17

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
201
16

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
47

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
241
16


Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy.
C Tsilfidis, A E MacKenzie, G Mettler, J Barceló, R G Korneluk. Nat Genet 1992
324
15

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
456
15




Trinucleotide repeats affect DNA replication in vivo.
G M Samadashwily, G Raca, S M Mirkin. Nat Genet 1997
263
15

Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells.
John D Cleary, Kerrie Nichol, Yuh-Hwa Wang, Christopher E Pearson. Nat Genet 2002
150
15

"Mitotic drive" of expanded CTG repeats in myotonic dystrophy type 1 (DM1).
M Khajavi, A M Tari, N B Patel, K Tsuji, D R Siwak, M L Meistrich, N H Terry, T Ashizawa. Hum Mol Genet 2001
37
37

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
644
14

Frequency and stability of the myotonic dystrophy type 1 premutation.
L Martorell, D G Monckton, A Sanchez, A Lopez De Munain, M Baiget. Neurology 2001
53
26

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
116
14


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
16

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
186
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.