A citation-based method for searching scientific literature

Sergei M Mirkin. Nature 2007
Times Cited: 583







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



Times Cited
  Times     Co-cited
Similarity


Repeat instability: mechanisms of dynamic mutations.
Christopher E Pearson, Kerrie Nichol Edamura, John D Cleary. Nat Rev Genet 2005
607
20


Disease-associated repeat instability and mismatch repair.
Monika H M Schmidt, Christopher E Pearson. DNA Repair (Amst) 2016
119
16

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
293
15

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
14


Repeat instability during DNA repair: Insights from model systems.
Karen Usdin, Nealia C M House, Catherine H Freudenreich. Crit Rev Biochem Mol Biol 2015
101
14

Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
968
13

Trinucleotide repeats that expand in human disease form hairpin structures in vitro.
A M Gacy, G Goellner, N Juranić, S Macura, C T McMurray. Cell 1995
465
13


Abundant contribution of short tandem repeats to gene expression variation in humans.
Melissa Gymrek, Thomas Willems, Audrey Guilmatre, Haoyang Zeng, Barak Markus, Stoyan Georgiev, Mark J Daly, Alkes L Price, Jonathan K Pritchard, Andrew J Sharp,[...]. Nat Genet 2016
143
10


Repeat expansion disease: progress and puzzles in disease pathogenesis.
Albert R La Spada, J Paul Taylor. Nat Rev Genet 2010
285
10


Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
9

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
9

Rationally designed small molecules that target both the DNA and RNA causing myotonic dystrophy type 1.
Lien Nguyen, Long M Luu, Shaohong Peng, Julio F Serrano, H Y Edwin Chan, Steven C Zimmerman. J Am Chem Soc 2015
62
14

Replication-dependent instability at (CTG) x (CAG) repeat hairpins in human cells.
Guoqi Liu, Xiaomi Chen, John J Bissler, Richard R Sinden, Michael Leffak. Nat Chem Biol 2010
106
9


Slipped-strand DNAs formed by long (CAG)*(CTG) repeats: slipped-out repeats and slip-out junctions.
Christopher E Pearson, Mandy Tam, Yuh-Hwa Wang, S Erin Montgomery, Arvin C Dar, John D Cleary, Kerrie Nichol. Nucleic Acids Res 2002
113
8

Small-molecule ligand induces nucleotide flipping in (CAG)n trinucleotide repeats.
Kazuhiko Nakatani, Shinya Hagihara, Yuki Goto, Akio Kobori, Masaki Hagihara, Gosuke Hayashi, Motoki Kyo, Makoto Nomura, Masaki Mishima, Chojiro Kojima. Nat Chem Biol 2005
99
8



On the wrong DNA track: Molecular mechanisms of repeat-mediated genome instability.
Alexandra N Khristich, Sergei M Mirkin. J Biol Chem 2020
41
19

On the wrong DNA track: Molecular mechanisms of repeat-mediated genome instability.
Alexandra N Khristich, Sergei M Mirkin. J Biol Chem 2020
44
18


DNA triplet repeat expansion and mismatch repair.
Ravi R Iyer, Anna Pluciennik, Marek Napierala, Robert D Wells. Annu Rev Biochem 2015
72
9

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.
A R La Spada, E M Wilson, D B Lubahn, A E Harding, K H Fischbeck. Nature 1991
7


A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
7

A simple ligand that selectively targets CUG trinucleotide repeats and inhibits MBNL protein binding.
Jonathan F Arambula, Sreenivasa Rao Ramisetty, Anne M Baranger, Steven C Zimmerman. Proc Natl Acad Sci U S A 2009
146
7


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
536
7

Slipped (CTG)*(CAG) repeats can be correctly repaired, escape repair or undergo error-prone repair.
Gagan B Panigrahi, Rachel Lau, S Erin Montgomery, Michelle R Leonard, Christopher E Pearson. Nat Struct Mol Biol 2005
114
7

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
A J Verkerk, M Pieretti, J S Sutcliffe, Y H Fu, D P Kuhl, A Pizzuti, O Reiner, S Richards, M F Victoria, F P Zhang. Cell 1991
7

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
V Campuzano, L Montermini, M D Moltò, L Pianese, M Cossée, F Cavalcanti, E Monros, F Rodius, F Duclos, A Monticelli,[...]. Science 1996
7

Advances in mechanisms of genetic instability related to hereditary neurological diseases.
Robert D Wells, Ruhee Dere, Micheal L Hebert, Marek Napierala, Leslie S Son. Nucleic Acids Res 2005
158
7

OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells.
Irina V Kovtun, Yuan Liu, Magnar Bjoras, Arne Klungland, Samuel H Wilson, Cynthia T McMurray. Nature 2007
322
7

Detection of slipped-DNAs at the trinucleotide repeats of the myotonic dystrophy type I disease locus in patient tissues.
Michelle M Axford, Yuh-Hwa Wang, Masayuki Nakamori, Maria Zannis-Hadjopoulos, Charles A Thornton, Christopher E Pearson. PLoS Genet 2013
42
16

Variable tandem repeats accelerate evolution of coding and regulatory sequences.
Rita Gemayel, Marcelo D Vinces, Matthieu Legendre, Kevin J Verstrepen. Annu Rev Genet 2010
323
6

Genome-wide profiling of heritable and de novo STR variations.
Thomas Willems, Dina Zielinski, Jie Yuan, Assaf Gordon, Melissa Gymrek, Yaniv Erlich. Nat Methods 2017
73
8


lobSTR: A short tandem repeat profiler for personal genomes.
Melissa Gymrek, David Golan, Saharon Rosset, Yaniv Erlich. Genome Res 2012
168
6

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Conceição Bettencourt, Davina Hensman-Moss, Michael Flower, Sarah Wiethoff, Alexis Brice, Cyril Goizet, Giovanni Stevanin, Georgios Koutsis, Georgia Karadima, Marios Panas,[...]. Ann Neurol 2016
112
6

RNA-DNA hybrids promote the expansion of Friedreich's ataxia (GAA)n repeats via break-induced replication.
Alexander J Neil, Miranda U Liang, Alexandra N Khristich, Kartik A Shah, Sergei M Mirkin. Nucleic Acids Res 2018
33
18

R-loops associated with triplet repeat expansions promote gene silencing in Friedreich ataxia and fragile X syndrome.
Matthias Groh, Michele M P Lufino, Richard Wade-Martins, Natalia Gromak. PLoS Genet 2014
195
6

Crosstalk between MSH2-MSH3 and polβ promotes trinucleotide repeat expansion during base excision repair.
Yanhao Lai, Helen Budworth, Jill M Beaver, Nelson L S Chan, Zunzhen Zhang, Cynthia T McMurray, Yuan Liu. Nat Commun 2016
31
19

Comparative genomics and molecular dynamics of DNA repeats in eukaryotes.
Guy-Franck Richard, Alix Kerrest, Bernard Dujon. Microbiol Mol Biol Rev 2008
276
6

RNA phase transitions in repeat expansion disorders.
Ankur Jain, Ronald D Vale. Nature 2017
313
6



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.