A citation-based method for searching scientific literature

Rachel Adihe Lokanga, Ali Entezam, Daman Kumari, Dmitry Yudkin, Mei Qin, Carolyn Beebe Smith, Karen Usdin. Hum Mutat 2013
Times Cited: 55







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



Times Cited
  Times     Co-cited
Similarity



Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model.
Ali Entezam, Rea Biacsi, Bonnie Orrison, Tapas Saha, Gloria E Hoffman, Ed Grabczyk, Robert L Nussbaum, Karen Usdin. Gene 2007
139
40

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
30

Role of mismatch repair enzymes in GAA·TTC triplet-repeat expansion in Friedreich ataxia induced pluripotent stem cells.
Jintang Du, Erica Campau, Elisabetta Soragni, Sherman Ku, James W Puckett, Peter B Dervan, Joel M Gottesfeld. J Biol Chem 2012
77
30

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
207
30


Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes.
Ella Dragileva, Audrey Hendricks, Allison Teed, Tammy Gillis, Edith T Lopez, Errol C Friedberg, Raju Kucherlapati, Winfried Edelmann, Kathryn L Lunetta, Marcy E MacDonald,[...]. Neurobiol Dis 2009
138
29

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.
F Tassone, R J Hagerman, A K Taylor, L W Gane, T E Godfrey, P J Hagerman. Am J Hum Genet 2000
604
27

Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice.
Laurent Foiry, Li Dong, Cédric Savouret, Laurence Hubert, Hein te Riele, Claudine Junien, Geneviève Gourdon. Hum Genet 2006
102
27

MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice.
Stéphanie Tomé, Kevin Manley, Jodie P Simard, Greg W Clark, Meghan M Slean, Meera Swami, Peggy F Shelbourne, Elisabeth R M Tillier, Darren G Monckton, Anne Messer,[...]. PLoS Genet 2013
83
27

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
Y H Fu, D P Kuhl, A Pizzuti, M Pieretti, J S Sutcliffe, S Richards, A J Verkerk, J J Holden, R G Fenwick, S T Warren. Cell 1991
27


Heterozygosity for a hypomorphic Polβ mutation reduces the expansion frequency in a mouse model of the Fragile X-related disorders.
Rachel Adihe Lokanga, Alireza Ghodsi Senejani, Joann Balazs Sweasy, Karen Usdin. PLoS Genet 2015
29
48

Potassium bromate, a potent DNA oxidizing agent, exacerbates germline repeat expansion in a fragile X premutation mouse model.
Ali Entezam, Adihe Rachel Lokanga, Wei Le, Gloria Hoffman, Karen Usdin. Hum Mutat 2010
45
28

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


CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles.
Dalyir I Pretto, Guadalupe Mendoza-Morales, Joyce Lo, Ru Cao, Andrew Hadd, Gary J Latham, Blythe Durbin-Johnson, Randi Hagerman, Flora Tassone. J Med Genet 2014
56
23

Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.
Ricardo Mouro Pinto, Ella Dragileva, Andrew Kirby, Alejandro Lloret, Edith Lopez, Jason St Claire, Gagan B Panigrahi, Caixia Hou, Kim Holloway, Tammy Gillis,[...]. PLoS Genet 2013
115
23


A MutSβ-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice?
Xiao-Nan Zhao, Rachel Lokanga, Kimaada Allette, Inbal Gazy, Di Wu, Karen Usdin. PLoS Genet 2016
29
44



AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome.
Carolyn M Yrigollen, Blythe Durbin-Johnson, Louise Gane, David L Nelson, Randi Hagerman, Paul J Hagerman, Flora Tassone. Genet Med 2012
108
21

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
327
21

Mosaicism in fragile X affected males.
S L Nolin, A Glicksman, G E Houck, W T Brown, C S Dobkin. Am J Med Genet 1994
126
21

Transcription-associated R-loop formation across the human FMR1 CGG-repeat region.
Erick W Loomis, Lionel A Sanz, Frédéric Chédin, Paul J Hagerman. PLoS Genet 2014
126
21

Mutsβ generates both expansions and contractions in a mouse model of the Fragile X-associated disorders.
Xiao-Nan Zhao, Daman Kumari, Shikha Gupta, Di Wu, Maya Evanitsky, Wei Yang, Karen Usdin. Hum Mol Genet 2015
39
30

At physiological pH, d(CCG)15 forms a hairpin containing protonated cytosines and a distorted helix.
A Yu, M D Barron, R M Romero, M Christy, B Gold, J Dai, D M Gray, I S Haworth, M Mitas. Biochemistry 1997
64
20

Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum.
Vanessa C Wheeler, Lori-Anne Lebel, Vladimir Vrbanac, Allison Teed, Hein te Riele, Marcy E MacDonald. Hum Mol Genet 2003
158
20

CTG repeat instability and size variation timing in DNA repair-deficient mice.
Cédric Savouret, Edith Brisson, Jeroen Essers, Roland Kanaar, Albert Pastink, Hein te Riele, Claudine Junien, Geneviève Gourdon. EMBO J 2003
149
20

Neil1 is a genetic modifier of somatic and germline CAG trinucleotide repeat instability in R6/1 mice.
Linda Møllersen, Alexander D Rowe, Jennifer L Illuzzi, Gunn A Hildrestrand, Katharina J Gerhold, Linda Tveterås, Anja Bjølgerud, David M Wilson, Magnar Bjørås, Arne Klungland. Hum Mol Genet 2012
52
21

DNA mismatch repair complex MutSβ promotes GAA·TTC repeat expansion in human cells.
Anasheh Halabi, Scott Ditch, Jeffrey Wang, Ed Grabczyk. J Biol Chem 2012
49
22


(CAG)(n)-hairpin DNA binds to Msh2-Msh3 and changes properties of mismatch recognition.
Barbara A L Owen, Zungyoon Yang, Maoyi Lai, Maciej Gajec, John D Badger, Jeffrey J Hayes, Winfried Edelmann, Raju Kucherlapati, Teresa M Wilson, Cynthia T McMurray. Nat Struct Mol Biol 2005
163
20

Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers.
Sarah L Nolin, Anne Glicksman, Nicole Ersalesi, Carl Dobkin, W Ted Brown, Ru Cao, Eliot Blatt, Sachin Sah, Gary J Latham, Andrew G Hadd. Genet Med 2015
79
20

Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population.
Sébastien Jacquemont, Randi J Hagerman, Maureen A Leehey, Deborah A Hall, Richard A Levine, James A Brunberg, Lin Zhang, Tristan Jardini, Louise W Gane, Susan W Harris,[...]. JAMA 2004
440
18

Pms2 suppresses large expansions of the (GAA·TTC)n sequence in neuronal tissues.
Rebecka L Bourn, Irene De Biase, Ricardo Mouro Pinto, Chiranjeevi Sandi, Sahar Al-Mahdawi, Mark A Pook, Sanjay I Bidichandani. PLoS One 2012
32
31


DNA instability in postmitotic neurons.
Roman Gonitel, Hilary Moffitt, Kirupa Sathasivam, Ben Woodman, Peter J Detloff, Richard L M Faull, Gillian P Bates. Proc Natl Acad Sci U S A 2008
134
18

A novel approach to investigate tissue-specific trinucleotide repeat instability.
Jong-Min Lee, Jie Zhang, Andrew I Su, John R Walker, Tim Wiltshire, Kihwa Kang, Ella Dragileva, Tammy Gillis, Edith T Lopez, Marie-Josee Boily,[...]. BMC Syst Biol 2010
73
18

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
297
18

The mismatch repair system protects against intergenerational GAA repeat instability in a Friedreich ataxia mouse model.
Vahid Ezzatizadeh, Ricardo Mouro Pinto, Chiranjeevi Sandi, Madhavi Sandi, Sahar Al-Mahdawi, Hein Te Riele, Mark A Pook. Neurobiol Dis 2012
44
22




The DNA replication program is altered at the FMR1 locus in fragile X embryonic stem cells.
Jeannine Gerhardt, Mark J Tomishima, Nikica Zaninovic, Dilek Colak, Zi Yan, Qiansheng Zhan, Zev Rosenwaks, Samie R Jaffrey, Carl L Schildkraut. Mol Cell 2014
69
18

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
470
18

AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission.
Carolyn M Yrigollen, Loreto Martorell, Blythe Durbin-Johnson, Montserrat Naudo, Jordi Genoves, Alessandra Murgia, Roberta Polli, Lili Zhou, Deborah Barbouth, Abigail Rupchock,[...]. J Neurodev Disord 2014
61
18

Absence of expression of the FMR-1 gene in fragile X syndrome.
M Pieretti, F P Zhang, Y H Fu, S T Warren, B A Oostra, C T Caskey, D L Nelson. Cell 1991
16



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.