A citation-based method for searching scientific literature

Fernando Morales, Melissa Vásquez, Eyleen Corrales, Rebeca Vindas-Smith, Carolina Santamaría-Ulloa, Baili Zhang, Mario Sirito, Marcos R Estecio, Ralf Krahe, Darren G Monckton. Hum Mol Genet 2020
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


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
55

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
55

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
33
44

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
44


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
36
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
33

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
33

A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotype.
Alfonsina Ballester-Lopez, Emma Koehorst, Miriam Almendrote, Alicia Martínez-Piñeiro, Giuseppe Lucente, Ian Linares-Pardo, Judit Núñez-Manchón, Nicolau Guanyabens, Antoni Cano, Alejandro Lucia,[...]. Hum Mutat 2020
9
33

Cognitive impairment in myotonic dystrophy type 1 is associated with white matter damage.
Francesca Caso, Federica Agosta, Stojan Peric, Vidosava Rakočević-Stojanović, Massimiliano Copetti, Vladimir S Kostic, Massimo Filippi. PLoS One 2014
53
33

Neuropathology does not Correlate with Regional Differences in the Extent of Expansion of CTG Repeats in the Brain with Myotonic Dystrophy Type 1.
Kyoko Itoh, Maki Mitani, Kunihiko Kawamoto, Naonobu Futamura, Itaru Funakawa, Kenji Jinnai, Shinji Fushiki. Acta Histochem Cytochem 2010
39
33


Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1.
Stefano Zanigni, Stefania Evangelisti, Maria Pia Giannoccaro, Federico Oppi, Roberto Poda, Antonio Giorgio, Claudia Testa, David Neil Manners, Patrizia Avoni, Laura Ludovica Gramegna,[...]. Neuroimage Clin 2016
36
33


The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease.
Martina Minnerop, Bernd Weber, Jan-Christoph Schoene-Bake, Sandra Roeske, Sandra Mirbach, Christian Anspach, Christiane Schneider-Gold, Regina C Betz, Christoph Helmstaedter, Marc Tittgemeyer,[...]. Brain 2011
154
33

MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1.
Michael Flower, Vilija Lomeikaite, Marc Ciosi, Sarah Cumming, Fernando Morales, Kitty Lo, Davina Hensman Moss, Lesley Jones, Peter Holmans, Darren G Monckton,[...]. Brain 2019
43
33

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
33

Length-dependent CTG·CAG triplet-repeat expansion in myotonic dystrophy patient-derived induced pluripotent stem cells.
Jintang Du, Erica Campau, Elisabetta Soragni, Christine Jespersen, Joel M Gottesfeld. Hum Mol Genet 2013
56
33

Parental age effects, but no evidence for an intrauterine effect in the transmission of myotonic dystrophy type 1.
Fernando Morales, Melissa Vásquez, Patricia Cuenca, Domingo Campos, Carolina Santamaría, Gerardo Del Valle, Roberto Brian, Mauricio Sittenfeld, Darren G Monckton. Eur J Hum Genet 2015
17
33

DNA methylation at the DMPK gene locus is associated with cognitive functions in myotonic dystrophy type 1.
Édith Breton, Cécilia Légaré, Gayle Overend, Simon-Pierre Guay, Darren Monckton, Jean Mathieu, Cynthia Gagnon, Louis Richer, Benjamin Gallais, Luigi Bouchard. Epigenomics 2020
4
75

Transcriptionally Repressive Chromatin Remodelling and CpG Methylation in the Presence of Expanded CTG-Repeats at the DM1 Locus.
Judith Rixt Brouwer, Aline Huguet, Annie Nicole, Arnold Munnich, Geneviève Gourdon. J Nucleic Acids 2013
28
33

Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus.
Aline Huguet, Fadia Medja, Annie Nicole, Alban Vignaud, Céline Guiraud-Dogan, Arnaud Ferry, Valérie Decostre, Jean-Yves Hogrel, Friedrich Metzger, Andreas Hoeflich,[...]. PLoS Genet 2012
62
33

Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing.
Nicolas Charlet-B, Rajesh S Savkur, Gopal Singh, Anne V Philips, Elizabeth A Grice, Thomas A Cooper. Mol Cell 2002
420
22

Anticipation in myotonic dystrophy. I. Statistical verification based on clinical and haplotype findings.
T Ashizawa, C J Dunne, J R Dubel, M B Perryman, H F Epstein, E Boerwinkle, J F Hejtmancik. Neurology 1992
49
22

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
36
22



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
22

Prevalence of muscular dystrophies: a systematic literature review.
Alice Theadom, Miriam Rodrigues, Richard Roxburgh, Shiavnthi Balalla, Chris Higgins, Rohit Bhattacharjee, Kelly Jones, Rita Krishnamurthi, Valery Feigin. Neuroepidemiology 2014
100
22

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
22

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
30
22

Myotonic dystrophies type 1 and 2: a summary on current aspects.
Ulrike Schara, Benedikt G H Schoser. Semin Pediatr Neurol 2006
69
22

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
20
22

DMPK gene DNA methylation levels are associated with muscular and respiratory profiles in DM1.
Cécilia Légaré, Gayle Overend, Simon-Pierre Guay, Darren G Monckton, Jean Mathieu, Cynthia Gagnon, Luigi Bouchard. Neurol Genet 2019
10
22

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
18
22

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
16
22

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
22


An autopsy case of myotonic dystrophy with mental disorders and various neuropathologic features.
K Mizukami, M Sasaki, A Baba, T Suzuki, H Shiraishi. Psychiatry Clin Neurosci 1999
26
22

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
51
22

Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2.
Y G Weber, R Roebling, J Kassubek, S Hoffmann, A Rosenbohm, M Wolf, P Steinbach, K Jurkat-Rott, H Walter, S N Reske,[...]. Neurology 2010
85
22

Central nervous system magnetic resonance imaging findings in myotonic dystrophy.
R H Glantz, R B Wright, M S Huckman, D C Garron, I M Siegel. Arch Neurol 1988
82
22

How genetics affects the brain to produce higher-level dysfunctions in myotonic dystrophy type 1.
Laura Serra, Antonio Petrucci, Barbara Spanò, Mario Torso, Giusy Olivito, Ludovico Lispi, Sandro Costanzi-Porrini, Giovanni Giulietti, Giacomo Koch, Manlio Giacanelli,[...]. Funct Neurol 2015
26
22

Abnormal functional brain connectivity and personality traits in myotonic dystrophy type 1.
Laura Serra, Gabriella Silvestri, Antonio Petrucci, Barbara Basile, Marcella Masciullo, Elena Makovac, Mario Torso, Barbara Spanò, Chiara Mastropasqua, Neil A Harrison,[...]. JAMA Neurol 2014
48
22

Characterization of the pattern of cognitive impairment in myotonic dystrophy type 1.
Anna Modoni, Gabriella Silvestri, Maria Grazia Pomponi, Fortunato Mangiola, Pietro A Tonali, Camillo Marra. Arch Neurol 2004
102
22

"I Know that You Know that I Know": Neural Substrates Associated with Social Cognition Deficits in DM1 Patients.
Laura Serra, Mara Cercignani, Michela Bruschini, Lisa Cipolotti, Matteo Mancini, Gabriella Silvestri, Antonio Petrucci, Elisabetta Bucci, Giovanni Antonini, Loretta Licchelli,[...]. PLoS One 2016
34
22

Cerebral involvement in myotonic dystrophies.
Giovanni Meola, Valeria Sansone. Muscle Nerve 2007
167
22

Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2).
G Meola, V Sansone, D Perani, S Scarone, S Cappa, C Dragoni, E Cattaneo, M Cotelli, C Gobbo, F Fazio,[...]. Neuromuscul Disord 2003
156
22

Abnormal Cortical Thickness Is Associated With Deficits in Social Cognition in Patients With Myotonic Dystrophy Type 1.
Laura Serra, Guendalina Bianchi, Michela Bruschini, Giovanni Giulietti, Carlotta Di Domenico, Sabrina Bonarota, Antonio Petrucci, Gabriella Silvestri, Alessia Perna, Giovanni Meola,[...]. Front Neurol 2020
9
22

Dilated Virchow-Robin spaces in myotonic dystrophy: frequency, extent and significance.
A Di Costanzo, F Di Salle, L Santoro, V Bonavita, G Tedeschi. Eur Neurol 2001
34
22


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.