Hagerman, Randi J.
University of California Davis Medical Center · University of California, Davis
56 papers on CoChatORCID 0000-0001-5029-8448
Most cited papers
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Fragile X syndrome
Hagerman, R. J., Berry-Kravis, E., Hazlett, H. C., Bailey, D. B., Moine, H., Kooy, R. F., Tassone, F., Gantois, I., Sonenberg, N., Mandel, J. L., et al. (2017) · Nature Reviews Disease Primers
Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases
Cited by 838
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Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056
Jacquemont, S., Curie, A., des Portes, V., Torrioli, M. G., Berry-Kravis, E., Hagerman, R. J., Ramos, F. J., Cornish, K., He, Y., Paulding, C., et al. (2011) · Science Translational Medicine
Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases
Cited by 609
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Advances in the Treatment of Fragile X Syndrome
Hagerman, R. J., Berry-Kravis, E., Kaufmann, W. E., Ono, M. Y., Tartaglia, N., Lachiewicz, A., Kronk, R., Delahunty, C., Hessl, D., Visootsak, J., et al. (2009) · Pediatrics
Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases
Cited by 596
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The Gut Microbiota and Autism Spectrum Disorders
Li, Q., Han, Y., Dy, A. B. C., & Hagerman, R. J. (2017) · Frontiers in Cellular Neuroscience
Gut microbiota and healthAutism Spectrum Disorder Research
Cited by 462
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A pilot open label, single dose trial of fenobam in adults with fragile X syndrome
Berry-Kravis, E., Hessl, D., Coffey, S., Hervey, C., Schneider, A., Yuhas, J., Hutchison, J., Snape, M., Tranfaglia, M., Nguyen, D. V., et al. (2009) · Journal of Medical Genetics
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 411
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Autism Profiles of Males With Fragile X Syndrome
Harris, S. W., Hessl, D., Goodlin-Jones, B., Ferranti, J., Bacalman, S., Barbato, I., Tassone, F., Hagerman, P. J., Herman, K., & Hagerman, R. J. (2008) · American Journal on Mental Retardation
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 396
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Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome
Berry-Kravis, E. M., Lindemann, L., Jønch, A. E., Apostol, G., Bear, M. F., Carpenter, R. L., Crawley, J. N., Curie, A., Des Portes, V., Hossain, F., et al. (2018) · Nature Reviews Drug Discovery
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 336
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Effects of STX209 (Arbaclofen) on Neurobehavioral Function in Children and Adults with Fragile X Syndrome: A Randomized, Controlled, Phase 2 Trial
Berry-Kravis, E. M., Hessl, D., Rathmell, B., Zarevics, P., Cherubini, M., Walton-Bowen, K., Mu, Y., Nguyen, D. V., Gonzalez-Heydrich, J., Wang, P. P., et al. (2012) · Science Translational Medicine
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 328
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Autism Spectrum Disorders and Attention-Deficit/Hyperactivity Disorder in Boys with the Fragile X Premutation
FARZIN, F., PERRY, H., HESSL, D., LOESCH, D., COHEN, J., BACALMAN, S., GANE, L., TASSONE, F., HAGERMAN, P., & HAGERMAN, R. (2006) · Journal of Developmental & Behavioral Pediatrics
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 325
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Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics
Bagni, C., Tassone, F., Neri, G., & Hagerman, R. (2012) · Journal of Clinical Investigation
Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases
Cited by 321
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Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization
Cordeiro, L., Ballinger, E., Hagerman, R., & Hessl, D. (2011) · Journal of Neurodevelopmental Disorders
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 316
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Fragile X Syndrome
Hagerman, R. J. (2002) · Johns Hopkins University Press eBooks
Genetics and Neurodevelopmental DisordersDown syndrome and intellectual disability research
Cited by 299
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A Randomized Double-Blind, Placebo-Controlled Trial of Minocycline in Children and Adolescents with Fragile X Syndrome
Leigh, M. J. S., Nguyen, D. V., Mu, Y., Winarni, T. I., Schneider, A., Chechi, T., Polussa, J., Doucet, P., Tassone, F., Rivera, S. M., et al. (2013) · Journal of Developmental & Behavioral Pediatrics
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 298
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Mavoglurant in fragile X syndrome: Results of two randomized, double-blind, placebo-controlled trials
Berry-Kravis, E., Des Portes, V., Hagerman, R., Jacquemont, S., Charles, P., Visootsak, J., Brinkman, M., Rerat, K., Koumaras, B., Zhu, L., et al. (2016) · Science Translational Medicine
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 270
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Fragile X and autism: intertwined at the molecular level leading to targeted treatments
Hagerman, R., Hoem, G., & Hagerman, P. (2010) · Molecular Autism
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 247
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An analysis of autism in fifty males with the fragile X syndrome
Hagerman, R. J., Jackson, A. W., Levitas, A., Rimland, B., Braden, M., Opitz, J. M., & Reynolds, J. F. (1986) · American Journal of Medical Genetics
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 238
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An Update on Psychopharmacological Treatment of Autism Spectrum Disorder
Aishworiya, R., Valica, T., Hagerman, R., & Restrepo, B. (2022) · Neurotherapeutics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 233
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Fragile X-Associated Neuropsychiatric Disorders (FXAND)
Hagerman, R. J., Protic, D., Rajaratnam, A., Salcedo-Arellano, M. J., Aydin, E. Y., & Schneider, A. (2018) · Frontiers in Psychiatry
Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases
Cited by 204
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Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with fragile X syndrome
Hoeffer, C. A., Sanchez, E., Hagerman, R. J., Mu, Y., Nguyen, D. V., Wong, H., Whelan, A. M., Zukin, R. S., Klann, E., & Tassone, F. (2012) · Genes, Brain and Behavior
Genetics and Neurodevelopmental DisordersRNA and protein synthesis mechanisms
Cited by 198
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Fragile X spectrum disorders
Lozano, R., Rosero, C. A., & Hagerman, R. J. (2014) · Intractable & Rare Diseases Research
Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases
Cited by 186
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Arbaclofen in fragile X syndrome: results of phase 3 trials
Berry-Kravis, E., Hagerman, R., Visootsak, J., Budimirovic, D., Kaufmann, W. E., Cherubini, M., Zarevics, P., Walton-Bowen, K., Wang, P., Bear, M. F., et al. (2017) · Journal of Neurodevelopmental Disorders
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 183
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A solution to limitations of cognitive testing in children with intellectual disabilities: the case of fragile X syndrome
Hessl, D., Nguyen, D. V., Green, C., Chavez, A., Tassone, F., Hagerman, R. J., Senturk, D., Schneider, A., Lightbody, A., Reiss, A. L., et al. (2009) · Journal of Neurodevelopmental Disorders
Genetics and Neurodevelopmental DisordersDown syndrome and intellectual disability research
Cited by 182
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AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome
Yrigollen, C. M., Durbin-Johnson, B., Gane, L., Nelson, D. L., Hagerman, R., Hagerman, P. J., & Tassone, F. (2012) · Genetics in Medicine
Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases
Cited by 179
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Fragile X: Leading the Way for Targeted Treatments in Autism
Wang, L. W., Berry-Kravis, E., & Hagerman, R. J. (2010) · Neurotherapeutics
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 176
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