A citation-based method for searching scientific literature

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
Times Cited: 1689







List of co-cited articles
1235 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
41

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
21

FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism.
Jennifer C Darnell, Sarah J Van Driesche, Chaolin Zhang, Ka Ying Sharon Hung, Aldo Mele, Claire E Fraser, Elizabeth F Stone, Cynthia Chen, John J Fak, Sung Wook Chi,[...]. Cell 2011
14

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.
I Oberlé, F Rousseau, D Heitz, C Kretz, D Devys, A Hanauer, J Boué, M F Bertheas, J L Mandel. Science 1991
14

Altered synaptic plasticity in a mouse model of fragile X mental retardation.
Kimberly M Huber, Sean M Gallagher, Stephen T Warren, Mark F Bear. Proc Natl Acad Sci U S A 2002
933
12

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.
R J Hagerman, M Leehey, W Heinrichs, F Tassone, R Wilson, J Hills, J Grigsby, B Gage, P J Hagerman. Neurology 2001
643
12

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
12

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
11

DNA methylation represses FMR-1 transcription in fragile X syndrome.
J S Sutcliffe, D L Nelson, F Zhang, M Pieretti, C T Caskey, D Saxe, S T Warren. Hum Mol Genet 1992
471
11

Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.
Sarah L Nolin, W Ted Brown, Anne Glicksman, George E Houck, Alice D Gargano, Amy Sullivan, Valérie Biancalana, Karen Bröndum-Nielsen, Helle Hjalgrim, Elke Holinski-Feder,[...]. Am J Hum Genet 2003
240
11

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
69
15

Fragile X genotype characterized by an unstable region of DNA.
S Yu, M Pritchard, E Kremer, M Lynch, J Nancarrow, E Baker, K Holman, J C Mulley, S T Warren, D Schlessinger. Science 1991
691
11




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
10

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
98
10

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
289
10

The FMR1 premutation and reproduction.
Michael D Wittenberger, Randi J Hagerman, Stephanie L Sherman, Allyn McConkie-Rosell, Corrine K Welt, Robert W Rebar, Emily C Corrigan, Joe Leigh Simpson, Lawrence M Nelson. Fertil Steril 2007
249
10


FMR1 protein: conserved RNP family domains and selective RNA binding.
C T Ashley, K D Wilkinson, D Reines, S T Warren. Science 1993
572
9

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.
E J Kremer, M Pritchard, M Lynch, S Yu, K Holman, E Baker, S T Warren, D Schlessinger, G R Sutherland, R I Richards. Science 1991
800
9

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
379
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
9

FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States.
Flora Tassone, Ka Pou Iong, Tzu-Han Tong, Joyce Lo, Louise W Gane, Elizabeth Berry-Kravis, Danh Nguyen, Lisa Y Mu, Jennifer Laffin, Don B Bailey,[...]. Genome Med 2012
163
9

Reversion of FMR1 Methylation and Silencing by Editing the Triplet Repeats in Fragile X iPSC-Derived Neurons.
Chul-Yong Park, Tomer Halevy, Dongjin R Lee, Jin Jea Sung, Jae Souk Lee, Ofra Yanuka, Nissim Benvenisty, Dong-Wook Kim. Cell Rep 2015
102
9

Molecular mechanisms of fragile X syndrome: a twenty-year perspective.
Michael R Santoro, Steven M Bray, Stephen T Warren. Annu Rev Pathol 2012
333
9


Examination of reproductive aging milestones among women who carry the FMR1 premutation.
E G Allen, A K Sullivan, M Marcus, C Small, C Dominguez, M P Epstein, K Charen, W He, K C Taylor, S L Sherman. Hum Reprod 2007
139
9

Association of FMR1 repeat size with ovarian dysfunction.
A K Sullivan, M Marcus, M P Epstein, E G Allen, A E Anido, J J Paquin, M Yadav-Shah, S L Sherman. Hum Reprod 2005
296
9

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
462
9

The mGluR theory of fragile X mental retardation.
Mark F Bear, Kimberly M Huber, Stephen T Warren. Trends Neurosci 2004
8

Promoter-bound trinucleotide repeat mRNA drives epigenetic silencing in fragile X syndrome.
Dilek Colak, Nikica Zaninovic, Michael S Cohen, Zev Rosenwaks, Wang-Yong Yang, Jeannine Gerhardt, Matthew D Disney, Samie R Jaffrey. Science 2014
179
8

Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
961
8

Repeat instability: mechanisms of dynamic mutations.
Christopher E Pearson, Kerrie Nichol Edamura, John D Cleary. Nat Rev Genet 2005
606
8


Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome.
Bradford Coffee, Fuping Zhang, Stephanie Ceman, Stephen T Warren, Daniel Reines. Am J Hum Genet 2002
121
8

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
807
8

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
524
8

CGG repeat-associated translation mediates neurodegeneration in fragile X tremor ataxia syndrome.
Peter K Todd, Seok Yoon Oh, Amy Krans, Fang He, Chantal Sellier, Michelle Frazer, Abigail J Renoux, Kai-chun Chen, K Matthew Scaglione, Venkatesha Basrur,[...]. Neuron 2013
279
8

Epidemiology of fragile X syndrome: a systematic review and meta-analysis.
Jessica Hunter, Oliver Rivero-Arias, Angel Angelov, Edward Kim, Iain Fotheringham, Jose Leal. Am J Med Genet A 2014
143
8


Expansion of an FMR1 grey-zone allele to a full mutation in two generations.
Isabel Fernandez-Carvajal, Blanca Lopez Posadas, Ruiqin Pan, Christopher Raske, Paul J Hagerman, Flora Tassone. J Mol Diagn 2009
85
9

Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome.
Nina Xie, He Gong, Joshua A Suhl, Pankaj Chopra, Tao Wang, Stephen T Warren. PLoS One 2016
57
14

Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics.
Claudia Bagni, Flora Tassone, Giovanni Neri, Randi Hagerman. J Clin Invest 2012
180
8

An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysis.
Liangjing Chen, Andrew Hadd, Sachin Sah, Stela Filipovic-Sadic, Julie Krosting, Edward Sekinger, Ruiqin Pan, Paul J Hagerman, Timothy T Stenzel, Flora Tassone,[...]. J Mol Diagn 2010
117
8


A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.
J P Martin, J Bell. J Neurol Psychiatry 1943
322
8




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.