A citation-based method for searching scientific literature

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, Jean-Louis Mandel, Catharina G Faber, Christine E M de Die-Smulders, Frank Spaans, Darren G Monckton. Hum Mol Genet 2010
Times Cited: 111







List of co-cited articles
1162 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
106
64

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
51

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
42

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
114
37


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
34

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
197
30

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
176
27

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
317
27

De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1.
Sarah A Cumming, Mark J Hamilton, Yvonne Robb, Helen Gregory, Catherine McWilliam, Anneli Cooper, Berit Adam, Josephine McGhie, Graham Hamilton, Pawel Herzyk,[...]. Eur J Hum Genet 2018
53
47

Non-ATG-initiated translation directed by microsatellite expansions.
Tao Zu, Brian Gibbens, Noelle S Doty, Mário Gomes-Pereira, Aline Huguet, Matthew D Stone, Jamie Margolis, Mark Peterson, Todd W Markowski, Melissa A C Ingram,[...]. Proc Natl Acad Sci U S A 2011
592
23

Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions.
Massimo Santoro, Marcella Masciullo, Roberta Pietrobono, Giulia Conte, Anna Modoni, Maria Laura E Bianchi, Valentina Rizzo, Maria Grazia Pomponi, Giorgio Tasca, Giovanni Neri,[...]. J Neurol 2013
33
69

Identification and characterization of 5' CCG interruptions in complex DMPK expanded alleles.
Annalisa Botta, Giulia Rossi, Marzia Marcaurelio, Luana Fontana, Maria Rosaria D'Apice, Francesco Brancati, Roberto Massa, Darren G Monckton, Federica Sangiuolo, Giuseppe Novelli. Eur J Hum Genet 2017
28
82


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
849
22

Effect of unexpected sequence interruptions to conventional PCR and repeat primed PCR in myotonic dystrophy type 1 testing.
Jan Radvansky, Andrej Ficek, Gabriel Minarik, Roland Palffy, Ludevit Kadasi. Diagn Mol Pathol 2011
30
73

Repeat instability: mechanisms of dynamic mutations.
Christopher E Pearson, Kerrie Nichol Edamura, John D Cleary. Nat Rev Genet 2005
625
21


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
218
20

Unusual association of a unique CAG interruption in 5' of DM1 CTG repeats with intergenerational contractions and low somatic mosaicism.
Stéphanie Tomé, Elodie Dandelot, Céline Dogan, Alexis Bertrand, David Geneviève, Yann Péréon, Marie Simon, Jean-Paul Bonnefont, Guillaume Bassez, Geneviève Gourdon. Hum Mutat 2018
26
76

Genetic determinants of disease severity in the myotonic dystrophy type 1 OPTIMISTIC cohort.
Sarah A Cumming, Cecilia Jimenez-Moreno, Kees Okkersen, Stephan Wenninger, Ferroudja Daidj, Fiona Hogarth, Roberta Littleford, Gráinne Gorman, Guillaume Bassez, Benedikt Schoser,[...]. Neurology 2019
50
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
116
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
121
17

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
56
30

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
310
16


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
666
16

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
99
16

Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1).
Massimo Santoro, Luana Fontana, Marcella Masciullo, Maria Laura Ester Bianchi, Salvatore Rossi, Emanuele Leoncini, Giuseppe Novelli, Annalisa Botta, Gabriella Silvestri. Biochim Biophys Acta 2015
26
61

Repeat Interruptions Modify Age at Onset in Myotonic Dystrophy Type 1 by Stabilizing DMPK Expansions in Somatic Cells.
Jovan Pešović, Stojan Perić, Miloš Brkušanin, Goran Brajušković, Vidosava Rakočević-Stojanović, Dušanka Savić-Pavićević. Front Genet 2018
26
61

Somatic instability of CTG repeat in myotonic dystrophy.
T Ashizawa, J R Dubel, Y Harati. Neurology 1993
153
15

Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2.
Erik-Jan Kamsteeg, Wolfram Kress, Claudio Catalli, Jens M Hertz, Martina Witsch-Baumgartner, Michael F Buckley, Baziel G M van Engelen, Marianne Schwartz, Hans Scheffer. Eur J Hum Genet 2012
75
20

Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions.
Jovan Pešović, S Perić, M Brkušanin, G Brajušković, V Rakočević-Stojanović, Dušanka Savić-Pavićević. Neurogenetics 2017
18
83

CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.
Lise Barbé, Stella Lanni, Arturo López-Castel, Silvie Franck, Claudia Spits, Kathelijn Keymolen, Sara Seneca, Stephanie Tomé, Ioana Miron, Julie Letourneau,[...]. Am J Hum Genet 2017
48
31


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
163
14

Length of uninterrupted CGG repeats determines instability in the FMR1 gene.
E E Eichler, J J Holden, B W Popovich, A L Reiss, K Snow, S N Thibodeau, C S Richards, P A Ward, D L Nelson. Nat Genet 1994
393
14

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
246
13

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
118
13

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
149
13

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
13

A muscleblind knockout model for myotonic dystrophy.
Rahul N Kanadia, Karen A Johnstone, Ami Mankodi, Codrin Lungu, Charles A Thornton, Douglas Esson, Adrian M Timmers, William W Hauswirth, Maurice S Swanson. Science 2003
542
13

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
576
13

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.
M Y Chung, L P Ranum, L A Duvick, A Servadio, H Y Zoghbi, H T Orr. Nat Genet 1993
430
13


Triplet-primed PCR is more sensitive than southern blotting-long PCR for the diagnosis of myotonic dystrophy type1.
Maria Addis, Marianna Serrenti, Cristiana Meloni, Milena Cau, Maria Antonietta Melis. Genet Test Mol Biomarkers 2012
19
68

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
323
12

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
512
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.