A citation-based method for searching scientific literature

Dejan B Budimirovic, Annette Schlageter, Stela Filipovic-Sadic, Dragana D Protic, Eran Bram, E Mark Mahone, Kimberly Nicholson, Kristen Culp, Kamyab Javanmardi, Jon Kemppainen, Andrew Hadd, Kevin Sharp, Tatyana Adayev, Giuseppe LaFauci, Carl Dobkin, Lili Zhou, William Ted Brown, Elizabeth Berry-Kravis, Walter E Kaufmann, Gary J Latham. Brain Sci 2020
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity


Updated report on tools to measure outcomes of clinical trials in fragile X syndrome.
Dejan B Budimirovic, Elizabeth Berry-Kravis, Craig A Erickson, Scott S Hall, David Hessl, Allan L Reiss, Margaret K King, Leonard Abbeduto, Walter E Kaufmann. J Neurodev Disord 2017
62
40


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
135
35

Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment.
Walter E Kaufmann, Sharon A Kidd, Howard F Andrews, Dejan B Budimirovic, Amy Esler, Barbara Haas-Givler, Tracy Stackhouse, Catharine Riley, Georgina Peacock, Stephanie L Sherman,[...]. Pediatrics 2017
77
30

What can we learn about autism from studying fragile X syndrome?
Dejan B Budimirovic, Walter E Kaufmann. Dev Neurosci 2011
106
30

The mGluR theory of fragile X mental retardation.
Mark F Bear, Kimberly M Huber, Stephen T Warren. Trends Neurosci 2004
30

Arbaclofen in fragile X syndrome: results of phase 3 trials.
Elizabeth Berry-Kravis, Randi Hagerman, Jeannie Visootsak, Dejan Budimirovic, Walter E Kaufmann, Maryann Cherubini, Peter Zarevics, Karen Walton-Bowen, Paul Wang, Mark F Bear,[...]. J Neurodev Disord 2017
78
25

Mavoglurant in fragile X syndrome: Results of two randomized, double-blind, placebo-controlled trials.
Elizabeth Berry-Kravis, Vincent Des Portes, Randi Hagerman, Sébastien Jacquemont, Perrine Charles, Jeannie Visootsak, Marc Brinkman, Karin Rerat, Barbara Koumaras, Liansheng Zhu,[...]. Sci Transl Med 2016
145
25

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
351
25

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
25

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
25

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
192
25

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
177
25

Effects of STX209 (arbaclofen) on neurobehavioral function in children and adults with fragile X syndrome: a randomized, controlled, phase 2 trial.
Elizabeth M Berry-Kravis, David Hessl, Barbara Rathmell, Peter Zarevics, Maryann Cherubini, Karen Walton-Bowen, Yi Mu, Danh V Nguyen, Joseph Gonzalez-Heydrich, Paul P Wang,[...]. Sci Transl Med 2012
217
20

Improving IQ measurement in intellectual disabilities using true deviation from population norms.
Stephanie M Sansone, Andrea Schneider, Erika Bickel, Elizabeth Berry-Kravis, Christina Prescott, David Hessl. J Neurodev Disord 2014
55
20

A Randomized, Double-Blind, Placebo-Controlled Trial of Low-Dose Sertraline in Young Children With Fragile X Syndrome.
Laura Greiss Hess, Sarah E Fitzpatrick, Danh V Nguyen, Yanjun Chen, Kimberly N Gaul, Andrea Schneider, Kerrie Lemons Chitwood, Marwa Abd Al Azaim Eldeeb, Jonathan Polussa, David Hessl,[...]. J Dev Behav Pediatr 2016
37
20

Closing the Gender Gap in Fragile X Syndrome: Review on Females with FXS and Preliminary Research Findings.
Kristi L Bartholomay, Cindy H Lee, Jennifer L Bruno, Amy A Lightbody, Allan L Reiss. Brain Sci 2019
26
20

Reduced Expression of Cerebral Metabotropic Glutamate Receptor Subtype 5 in Men with Fragile X Syndrome.
James R Brašić, Ayon Nandi, David S Russell, Danna Jennings, Olivier Barret, Anil Mathur, Keith Slifer, Thomas Sedlak, Samuel D Martin, Zabecca Brinson,[...]. Brain Sci 2020
4
100

Association between IQ and FMR1 protein (FMRP) across the spectrum of CGG repeat expansions.
Kyoungmi Kim, David Hessl, Jamie L Randol, Glenda M Espinal, Andrea Schneider, Dragana Protic, Elber Yuksel Aydin, Randi J Hagerman, Paul J Hagerman. PLoS One 2019
15
26

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
125
20

FMR1 and the fragile X syndrome: human genome epidemiology review.
D C Crawford, J M Acuña, S L Sherman. Genet Med 2001
403
20

Best Practices in Fragile X Syndrome Treatment Development.
Craig A Erickson, Walter E Kaufmann, Dejan B Budimirovic, Ave Lachiewicz, Barbara Haas-Givler, Robert M Miller, Jayne Dixon Weber, Leonard Abbeduto, David Hessl, Randi J Hagerman,[...]. Brain Sci 2018
18
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
422
15

Clinical Development of Targeted Fragile X Syndrome Treatments: An Industry Perspective.
Anna W Lee, Pamela Ventola, Dejan Budimirovic, Elizabeth Berry-Kravis, Jeannie Visootsak. Brain Sci 2018
21
15

A solution to limitations of cognitive testing in children with intellectual disabilities: the case of fragile X syndrome.
David Hessl, Danh V Nguyen, Cherie Green, Alyssa Chavez, Flora Tassone, Randi J Hagerman, Damla Senturk, Andrea Schneider, Amy Lightbody, Allan L Reiss,[...]. J Neurodev Disord 2009
108
15

Genotype, molecular phenotype, and cognitive phenotype: correlations in fragile X syndrome.
W E Kaufmann, M T Abrams, W Chen, A L Reiss. Am J Med Genet 1999
96
15

Translation-relevant EEG phenotypes in a mouse model of Fragile X Syndrome.
Jonathan W Lovelace, Iryna M Ethell, Devin K Binder, Khaleel A Razak. Neurobiol Dis 2018
49
15

Auditory EEG Biomarkers in Fragile X Syndrome: Clinical Relevance.
Lauren E Ethridge, Lisa A De Stefano, Lauren M Schmitt, Nicholas E Woodruff, Kara L Brown, Morgan Tran, Jun Wang, Ernest V Pedapati, Craig A Erickson, John A Sweeney. Front Integr Neurosci 2019
16
18

Psychometric study of the Aberrant Behavior Checklist in Fragile X Syndrome and implications for targeted treatment.
Stephanie M Sansone, Keith F Widaman, Scott S Hall, Allan L Reiss, Amy Lightbody, Walter E Kaufmann, Elizabeth Berry-Kravis, Ave Lachiewicz, Elaine C Brown, David Hessl. J Autism Dev Disord 2012
93
15

A pilot open label, single dose trial of fenobam in adults with fragile X syndrome.
E Berry-Kravis, D Hessl, S Coffey, C Hervey, A Schneider, J Yuhas, J Hutchison, M Snape, M Tranfaglia, D V Nguyen,[...]. J Med Genet 2009
264
15

Developmental studies in fragile X syndrome.
Khaleel A Razak, Kelli C Dominick, Craig A Erickson. J Neurodev Disord 2020
17
17

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
15

Molecular Biomarkers in Fragile X Syndrome.
Marwa Zafarullah, Flora Tassone. Brain Sci 2019
8
37

Kinetic analysis of the metabotropic glutamate subtype 5 tracer [(18)F]FPEB in bolus and bolus-plus-constant-infusion studies in humans.
Jenna M Sullivan, Keunpoong Lim, David Labaree, Shu-Fei Lin, Timothy J McCarthy, John P Seibyl, Gilles Tamagnan, Yiyun Huang, Richard E Carson, Yu-Shin Ding,[...]. J Cereb Blood Flow Metab 2013
44
15

18F-FPEB, a PET radiopharmaceutical for quantifying metabotropic glutamate 5 receptors: a first-in-human study of radiochemical safety, biokinetics, and radiation dosimetry.
Dean F Wong, Rikki Waterhouse, Hiroto Kuwabara, Jongho Kim, James R Brašić, Wichana Chamroonrat, Michael Stabins, Daniel P Holt, Robert F Dannals, Terence G Hamill,[...]. J Nucl Med 2013
69
15

Autism spectrum disorder in Fragile X syndrome: differential contribution of adaptive socialization and social withdrawal.
Dejan B Budimirovic, Irena Bukelis, Christiane Cox, Robert M Gray, Elaine Tierney, Walter E Kaufmann. Am J Med Genet A 2006
64
15

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.
H L Hinds, C T Ashley, J S Sutcliffe, D L Nelson, S T Warren, D E Housman, M Schalling. Nat Genet 1993
297
15

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
15

Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics.
Claudia Bagni, Flora Tassone, Giovanni Neri, Randi Hagerman. J Clin Invest 2012
188
15

Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations.
Beatrice Primerano, Flora Tassone, Randi J Hagerman, Paul Hagerman, Francesco Amaldi, Claudia Bagni. RNA 2002
138
15

Size and methylation mosaicism in males with Fragile X syndrome.
Poonnada Jiraanont, Madhur Kumar, Hiu-Tung Tang, Glenda Espinal, Paul J Hagerman, Randi J Hagerman, Nuanchan Chutabhakdikul, Flora Tassone. Expert Rev Mol Diagn 2017
20
15

FORWARD: A Registry and Longitudinal Clinical Database to Study Fragile X Syndrome.
Stephanie L Sherman, Sharon A Kidd, Catharine Riley, Elizabeth Berry-Kravis, Howard F Andrews, Robert M Miller, Sharyn Lincoln, Mark Swanson, Walter E Kaufmann, W Ted Brown. Pediatrics 2017
20
15

Fragile X syndrome: a review of clinical and molecular diagnoses.
Claudia Ciaccio, Laura Fontana, Donatella Milani, Silvia Tabano, Monica Miozzo, Susanna Esposito. Ital J Pediatr 2017
52
15

The molecular biology of FMRP: new insights into fragile X syndrome.
Joel D Richter, Xinyu Zhao. Nat Rev Neurosci 2021
14
21


Phenotypic variation and FMRP levels in fragile X.
Danuta Z Loesch, Richard M Huggins, Randi J Hagerman. Ment Retard Dev Disabil Res Rev 2004
191
15

Clinic-based retrospective analysis of psychopharmacology for behavior in fragile x syndrome.
Elizabeth Berry-Kravis, Allison Sumis, Crystal Hervey, Shaguna Mathur. Int J Pediatr 2012
25
15

Clinical and molecular implications of mosaicism in FMR1 full mutations.
Dalyir Pretto, Carolyn M Yrigollen, Hiu-Tung Tang, John Williamson, Glenda Espinal, Chris K Iwahashi, Blythe Durbin-Johnson, Randi J Hagerman, Paul J Hagerman, Flora Tassone. Front Genet 2014
60
15

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
288
15

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
174
15


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.