A citation-based method for searching scientific literature

Gregory M Williams, Vasileios Paschalis, Janice Ortega, Frederick W Muskett, James T Hodgkinson, Guo-Min Li, John W R Schwabe, Robert S Lahue. Proc Natl Acad Sci U S A 2020
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Sperm capacitation is associated with phosphorylation of the testis-specific radial spoke protein Rsph6a†.
Bidur Paudel, María Gracia Gervasi, James Porambo, Diego A Caraballo, Darya A Tourzani, Jesse Mager, Mark D Platt, Ana María Salicioni, Pablo E Visconti. Biol Reprod 2019
9
11

Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene.
Y H Wang, S Amirhaeri, S Kang, R D Wells, J D Griffith. Science 1994
204
11

Phenylbutazone induces expression of MBNL1 and suppresses formation of MBNL1-CUG RNA foci in a mouse model of myotonic dystrophy.
Guiying Chen, Akio Masuda, Hiroyuki Konishi, Bisei Ohkawara, Mikako Ito, Masanobu Kinoshita, Hiroshi Kiyama, Tohru Matsuura, Kinji Ohno. Sci Rep 2016
23
11

Dynamic DNA Methylation During Aging: A "Prophet" of Age-Related Outcomes.
Fu-Hui Xiao, Hao-Tian Wang, Qing-Peng Kong. Front Genet 2019
37
11

Molecular genetics of congenital myotonic dystrophy.
Stella Lanni, Christopher E Pearson. Neurobiol Dis 2019
20
11

Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy.
Charlotte Fugier, Arnaud F Klein, Caroline Hammer, Stéphane Vassilopoulos, Ylva Ivarsson, Anne Toussaint, Valérie Tosch, Alban Vignaud, Arnaud Ferry, Nadia Messaddeq,[...]. Nat Med 2011
213
11

Therapeutic application of histone deacetylase inhibitors for central nervous system disorders.
Aleksey G Kazantsev, Leslie M Thompson. Nat Rev Drug Discov 2008
556
11

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
113
11

Longitudinal increases in somatic mosaicism of the expanded CTG repeat in myotonic dystrophy type 1 are associated with variation in age-at-onset.
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
17
11


Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells.
Shira Yanovsky-Dagan, Michal Avitzour, Gheona Altarescu, Paul Renbaum, Talia Eldar-Geva, Oshrat Schonberger, Stella Mitrani-Rosenbaum, Ephrat Levy-Lahad, Ramon Y Birnbaum, Lior Gepstein,[...]. Stem Cell Reports 2015
30
11

DNA methylation-calling tools for Oxford Nanopore sequencing: a survey and human epigenome-wide evaluation.
Yang Liu, Wojciech Rosikiewicz, Ziwei Pan, Nathaniel Jillette, Ping Wang, Aziz Taghbalout, Jonathan Foox, Christopher Mason, Martin Carroll, Albert Cheng,[...]. Genome Biol 2021
7
14

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
13
11

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
102
11

Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1.
Christine Voellenkle, Alessandra Perfetti, Matteo Carrara, Paola Fuschi, Laura Valentina Renna, Marialucia Longo, Simona Baghai Sain, Rosanna Cardani, Rea Valaperta, Gabriella Silvestri,[...]. Int J Mol Sci 2019
20
11

Myotonic dystrophy type 1 (DM1) clinical subtypes and CTCF site methylation status flanking the CTG expansion are mutant allele length-dependent.
Fernando Morales, Eyleen Corrales, Baili Zhang, Melissa Vásquez, Carolina Santamaría-Ulloa, Hazel Quesada, Mario Sirito, Marcos R Estecio, Darren G Monckton, Ralf Krahe. Hum Mol Genet 2021
5
20

(CTG)n expansions in various tissues from a myotonic dystrophy patient.
M Kinoshita, R Takahashi, T Hasegawa, T Komori, R Nagasawa, K Hirose, H Tanabe. Muscle Nerve 1996
28
11

Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.
H Seznec, O Agbulut, N Sergeant, C Savouret, A Ghestem, N Tabti, J C Willer, L Ourth, C Duros, E Brisson,[...]. Hum Mol Genet 2001
179
11


Allele length of the DMPK CTG repeat is a predictor of progressive myotonic dystrophy type 1 phenotypes.
Gayle Overend, Cécilia Légaré, Jean Mathieu, Luigi Bouchard, Cynthia Gagnon, Darren G Monckton. Hum Mol Genet 2019
24
11

Neuromuscular Diseases.
Brett M Morrison. Semin Neurol 2016
22
11

5-Hydroxymethylcytosine is an essential intermediate of active DNA demethylation processes in primary human monocytes.
Maja Klug, Sandra Schmidhofer, Claudia Gebhard, Reinhard Andreesen, Michael Rehli. Genome Biol 2013
67
11


High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional Study.
Alessia Perna, Daria Maccora, Salvatore Rossi, Tommaso Filippo Nicoletti, Maria Assunta Zocco, Vittorio Riso, Anna Modoni, Antonio Petrucci, Venanzio Valenza, Antonio Grieco,[...]. Front Neurol 2020
6
16

Histone deacetylase inhibitors as therapeutics for polyglutamine disorders.
Rachel Butler, Gillian P Bates. Nat Rev Neurosci 2006
161
11

Germline DNA demethylation dynamics and imprint erasure through 5-hydroxymethylcytosine.
Jamie A Hackett, Roopsha Sengupta, Jan J Zylicz, Kazuhiro Murakami, Caroline Lee, Thomas A Down, M Azim Surani. Science 2013
476
11


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
239
11

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
536
11

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
26
11

Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1.
Jacob N Miller, Ellen van der Plas, Mark Hamilton, Timothy R Koscik, Laurie Gutmann, Sarah A Cumming, Darren G Monckton, Peggy C Nopoulos. Neurol Genet 2020
10
11

Genome-wide analysis of 5-hydroxymethylcytosine distribution reveals its dual function in transcriptional regulation in mouse embryonic stem cells.
Hao Wu, Ana C D'Alessio, Shinsuke Ito, Zhibin Wang, Kairong Cui, Keji Zhao, Yi Eve Sun, Yi Zhang. Genes Dev 2011
407
11

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
22
11

Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program.
Nicholas E Johnson, Russell J Butterfield, Katie Mayne, Tara Newcomb, Carina Imburgia, Diane Dunn, Brett Duval, Marcia L Feldkamp, Robert B Weiss. Neurology 2021
13
11

Age and anesthetic effects on murine electrocardiography.
Alysia A Chaves, Spencer J Dech, Tomohiro Nakayama, Robert L Hamlin, John Anthony Bauer, Cynthia A Carnes. Life Sci 2003
26
11


Sex influences DNA methylation and gene expression in human skeletal muscle myoblasts and myotubes.
Cajsa Davegårdh, Elin Hall Wedin, Christa Broholm, Tora Ida Henriksen, Maria Pedersen, Bente Klarlund Pedersen, Camilla Scheele, Charlotte Ling. Stem Cell Res Ther 2019
30
11


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.