A citation-based method for searching scientific literature

M Anvret, G Ahlberg, U Grandell, B Hedberg, K Johnson, L Edström. Hum Mol Genet 1993
Times Cited: 161







List of co-cited articles
945 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
66


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
53


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
48

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
47

Somatic instability of CTG repeat in myotonic dystrophy.
T Ashizawa, J R Dubel, Y Harati. Neurology 1993
150
43

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
38

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
36

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
112
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
309
31

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
30

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
26

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
42


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
23

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
21

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

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
20

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
20

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
21



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


Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.
H Telenius, B Kremer, Y P Goldberg, J Theilmann, S E Andrew, J Zeisler, S Adam, C Greenberg, E J Ives, L A Clarke. Nat Genet 1994
304
18

Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.
L Mangiarini, K Sathasivam, A Mahal, R Mott, M Seller, G P Bates. Nat Genet 1997
248
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

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
29

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
17

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
460
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
15

Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genes.
M G Hamshere, E E Newman, M Alwazzan, B S Athwal, J D Brook. Proc Natl Acad Sci U S A 1997
109
15

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
15

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
15

Anticipation in myotonic dystrophy: fact or fiction?
C J Höweler, H F Busch, J P Geraedts, M F Niermeijer, A Staal. Brain 1989
213
15

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
128
14

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
14


Small increase in triplet repeat length of cerebellum from patients with myotonic dystrophy.
S Ishii, T Nishio, N Sunohara, T Yoshihara, K Takemura, K Hikiji, S Tsujino, N Sakuragawa. Hum Genet 1996
41
31

Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice.
G Gourdon, F Radvanyi, A S Lia, C Duros, M Blanche, M Abitbol, C Junien, H Hofmann-Radvanyi. Nat Genet 1997
93
13


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
13

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
38

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
13

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
13

Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1.
S S Chong, A E McCall, J Cota, S H Subramony, H T Orr, M R Hughes, H Y Zoghbi. Nat Genet 1995
154
12


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.