A citation-based method for searching scientific literature

Kathryn B Garber, Jeannie Visootsak, Stephen T Warren. Eur J Hum Genet 2008
Times Cited: 245







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



Times Cited
  Times     Co-cited
Similarity


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
30

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
23

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
978
21

The mGluR theory of fragile X mental retardation.
Mark F Bear, Kimberly M Huber, Stephen T Warren. Trends Neurosci 2004
18

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits.
T A Comery, J B Harris, P J Willems, B A Oostra, S A Irwin, I J Weiler, W T Greenough. Proc Natl Acad Sci U S A 1997
782
17

Molecular mechanisms of fragile X syndrome: a twenty-year perspective.
Michael R Santoro, Steven M Bray, Stephen T Warren. Annu Rev Pathol 2012
361
16

FMRP targets distinct mRNA sequence elements to regulate protein expression.
Manuel Ascano, Neelanjan Mukherjee, Pradeep Bandaru, Jason B Miller, Jeffrey D Nusbaum, David L Corcoran, Christine Langlois, Mathias Munschauer, Scott Dewell, Markus Hafner,[...]. Nature 2012
458
16

Correction of fragile X syndrome in mice.
Gül Dölen, Emily Osterweil, B S Shankaranarayana Rao, Gordon B Smith, Benjamin D Auerbach, Sumantra Chattarji, Mark F Bear. Neuron 2007
702
13

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome.
V Brown, P Jin, S Ceman, J C Darnell, W T O'Donnell, S A Tenenbaum, X Jin, Y Feng, K D Wilkinson, J D Keene,[...]. Cell 2001
864
13

Co-occurring conditions associated with FMR1 gene variations: findings from a national parent survey.
Donald B Bailey, Melissa Raspa, Murrey Olmsted, David B Holiday. Am J Med Genet A 2008
306
13

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
12

Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization.
Lisa Cordeiro, Elizabeth Ballinger, Randi Hagerman, David Hessl. J Neurodev Disord 2011
195
12



A randomized double-blind, placebo-controlled trial of minocycline in children and adolescents with fragile x syndrome.
Mary Jacena S Leigh, Danh V Nguyen, Yi Mu, Tri I Winarni, Andrea Schneider, Tasleem Chechi, Jonathan Polussa, Paul Doucet, Flora Tassone, Susan M Rivera,[...]. J Dev Behav Pediatr 2013
159
11

Advances in the treatment of fragile X syndrome.
Randi J Hagerman, Elizabeth Berry-Kravis, Walter E Kaufmann, Michele Y Ono, Nicole Tartaglia, Ave Lachiewicz, Rebecca Kronk, Carol Delahunty, David Hessl, Jeannie Visootsak,[...]. Pediatrics 2009
371
11

FMR1 protein: conserved RNP family domains and selective RNA binding.
C T Ashley, K D Wilkinson, D Reines, S T Warren. Science 1993
588
11

Fragile X syndrome: a review of associated medical problems.
Sharon A Kidd, Ave Lachiewicz, Deborah Barbouth, Robin K Blitz, Carol Delahunty, Dianne McBrien, Jeannie Visootsak, Elizabeth Berry-Kravis. Pediatrics 2014
118
11

Fragile X syndrome.
Randi J Hagerman, Elizabeth Berry-Kravis, Heather Cody Hazlett, Donald B Bailey, Herve Moine, R Frank Kooy, Flora Tassone, Ilse Gantois, Nahum Sonenberg, Jean Louis Mandel,[...]. Nat Rev Dis Primers 2017
260
11

Chronic pharmacological mGlu5 inhibition corrects fragile X in adult mice.
Aubin Michalon, Michael Sidorov, Theresa M Ballard, Laurence Ozmen, Will Spooren, Joseph G Wettstein, Georg Jaeschke, Mark F Bear, Lothar Lindemann. Neuron 2012
355
10

What can we learn about autism from studying fragile X syndrome?
Dejan B Budimirovic, Walter E Kaufmann. Dev Neurosci 2011
114
10




Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP.
Q J Yan, M Rammal, M Tranfaglia, R P Bauchwitz. Neuropharmacology 2005
395
9

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
9

Minocycline promotes dendritic spine maturation and improves behavioural performance in the fragile X mouse model.
T V Bilousova, L Dansie, M Ngo, J Aye, J R Charles, D W Ethell, I M Ethell. J Med Genet 2009
321
9


Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function.
J C Darnell, K B Jensen, P Jin, V Brown, S T Warren, R B Darnell. Cell 2001
742
9

Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.
Bradford Coffee, Krayton Keith, Igor Albizua, Tamika Malone, Julie Mowrey, Stephanie L Sherman, Stephen T Warren. Am J Hum Genet 2009
260
9

Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome.
Elizabeth M Berry-Kravis, Lothar Lindemann, Aia E Jønch, George Apostol, Mark F Bear, Randall L Carpenter, Jacqueline N Crawley, Aurore Curie, Vincent Des Portes, Farah Hossain,[...]. Nat Rev Drug Discov 2018
168
9

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
8


FMRP regulates neurotransmitter release and synaptic information transmission by modulating action potential duration via BK channels.
Pan-Yue Deng, Ziv Rotman, Jay A Blundon, Yongcheol Cho, Jianmin Cui, Valeria Cavalli, Stanislav S Zakharenko, Vitaly A Klyachko. Neuron 2013
223
8

Altered Neuronal and Circuit Excitability in Fragile X Syndrome.
Anis Contractor, Vitaly A Klyachko, Carlos Portera-Cailliau. Neuron 2015
212
8

FMR1 and the fragile X syndrome: human genome epidemiology review.
D C Crawford, J M Acuña, S L Sherman. Genet Med 2001
429
8

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.
S A Irwin, B Patel, M Idupulapati, J B Harris, R A Crisostomo, B P Larsen, F Kooy, P J Willems, P Cras, P B Kozlowski,[...]. Am J Med Genet 2001
523
8

The generation of a conditional Fmr1 knock out mouse model to study Fmrp function in vivo.
E J Mientjes, I Nieuwenhuizen, L Kirkpatrick, T Zu, M Hoogeveen-Westerveld, L Severijnen, M Rifé, R Willemsen, D L Nelson, B A Oostra. Neurobiol Dis 2006
144
8

Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function.
Y Q Zhang, A M Bailey, H J Matthies, R B Renden, M A Smith, S D Speese, G M Rubin, K Broadie. Cell 2001
509
8

Dynamic translational and proteasomal regulation of fragile X mental retardation protein controls mGluR-dependent long-term depression.
Lingfei Hou, Marcia D Antion, Daoying Hu, Corinne M Spencer, Richard Paylor, Eric Klann. Neuron 2006
352
7

Genetic reduction of group 1 metabotropic glutamate receptors alters select behaviors in a mouse model for fragile X syndrome.
Alexia M Thomas, Nghiem Bui, Deanna Graham, Jennifer R Perkins, Lisa A Yuva-Paylor, Richard Paylor. Behav Brain Res 2011
56
12

Increased expression of the PI3K enhancer PIKE mediates deficits in synaptic plasticity and behavior in fragile X syndrome.
Christina Gross, Chia-Wei Chang, Seth M Kelly, Aditi Bhattacharya, Sean M J McBride, Scott W Danielson, Michael Q Jiang, Chi Bun Chan, Keqiang Ye, Jay R Gibson,[...]. Cell Rep 2015
74
9

Analysis of neocortex in three males with the fragile X syndrome.
V J Hinton, W T Brown, K Wisniewski, R D Rudelli. Am J Med Genet 1991
399
7

Prevalence of fragile X syndrome.
G Turner, T Webb, S Wake, H Robinson. Am J Med Genet 1996
526
7

Expression of the GABAergic system in animal models for fragile X syndrome and fragile X associated tremor/ataxia syndrome (FXTAS).
Charlotte D'Hulst, Inge Heulens, Judith R Brouwer, Rob Willemsen, Natalie De Geest, Simon P Reeve, Peter P De Deyn, Bassem A Hassan, R Frank Kooy. Brain Res 2009
123
7

A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability.
Francesca Zalfa, Boris Eleuteri, Kirsten S Dickson, Valentina Mercaldo, Silvia De Rubeis, Alessandra di Penta, Elisabetta Tabolacci, Pietro Chiurazzi, Giovanni Neri, Seth G N Grant,[...]. Nat Neurosci 2007
277
7

Autism spectrum disorder in fragile X syndrome: communication, social interaction, and specific behaviors.
Walter E Kaufmann, Ranon Cortell, Alice S M Kau, Irena Bukelis, Elaine Tierney, Robert M Gray, Christiane Cox, George T Capone, Pia Stanard. Am J Med Genet A 2004
284
7

Evidence that fragile X mental retardation protein is a negative regulator of translation.
B Laggerbauer, D Ostareck, E M Keidel, A Ostareck-Lederer, U Fischer. Hum Mol Genet 2001
446
7

A chromatin-dependent role of the fragile X mental retardation protein FMRP in the DNA damage response.
Roman Alpatov, Bluma J Lesch, Mika Nakamoto-Kinoshita, Andres Blanco, Shuzhen Chen, Alexandra Stützer, Karim J Armache, Matthew D Simon, Chao Xu, Muzaffar Ali,[...]. Cell 2014
99
7

Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back.
Christina Gross, Anne Hoffmann, Gary J Bassell, Elizabeth M Berry-Kravis. Neurotherapeutics 2015
65
10


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.