Understanding fragile X syndrome
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Relative strengths in Fragile X syndrome include receptive language skills, visual memory, acquisition of factual information, imitation skills and gestalt processing.
“Relative strengths include receptive language skills, visual memory, acquisition of factual information, imitation skills and gestalt processing (Berry-Kravis et al., 2002).”
From Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders (2014) · cites this paper as Berry-Kravis et al., 2002
Individuals with Fragile X syndrome exhibit deficits in visuospatial tasks, quantitative skills, short-term and working memory, expressive language skills, sequential processing and executive function.
“FXS individuals exhibit deficits in visuospatial tasks, quantitative skills, short-term and working memory, expressive language skills, sequential processing and executive function (Berry-Kravis et al., 2002; Cornish et al., 1999; Freund and Reiss, 1991; Hall et al., 2012; Kwon et al., 2001; Maes et al., 1994).”
From Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders (2014) · cites this paper as Berry-Kravis et al., 2002
Of individuals with Fragile X syndrome and autistic behaviors, 15-40% of males and a few females meet the diagnostic criteria for ASD.
“Of the individuals with FXS and autistic behaviors, 15–40% of males and a few females meet the diagnostic criteria for ASD (Berry-Kravis et al., 2002).”
From Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders (2014) · cites this paper as Berry-Kravis et al., 2002
The behavioral and cognitive deficits of Fmr1 KO mice are actually quite subtle and parallel Fragile X syndrome patients.
“By most accounts Fmr1 KO mice appear to have relatively normal behavior, but research has shown that the behavioral and cognitive deficits of the KO are actually quite subtle and parallel FXS patients (Berry-Kravis et al., 2002; D’Hooge et al., 1997; Paradee et al., 1999; Peier et al., 2000).”
From Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders (2014) · cites this paper as Berry-Kravis et al., 2002
Cites
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X
Hagerman, R. J., Leehey, M. A., Heinrichs, W. L., Tassone, F., Wilson, R., Hills, J. D., Grigsby, J., Gage, B. F., & Hagerman, P. J. (2001) · Neurology · doi:10.1212/wnl.57.1.127 · Cited by 966 · see citing works
Fragile X Syndrome: Diagnosis, Treatment, And Research
Silverman, & Cronister, A. (1991) · Johns Hopkins University Press eBooks · Cited by 481 · see citing works
Epilepsy and EEG Findings in Males with Fragile X Syndrome
Musumeci, S. A., Hagerman, R. J., Ferri, R., Bosco, P., Bernardina, B. D., Tassinari, C. A., Sarro, G. D., & Elia, M. (1999) · Epilepsia · doi:10.1111/j.1528-1157.1999.tb00824.x · Cited by 250 · see citing works
Hessl, D., Dyer-Friedman, J., Glaser, B., Wisbeck, J., Barajas, R. G., Taylor, A., & Reiss, A. L. (2001) · Pediatrics · doi:10.1542/peds.108.5.e88 · Cited by 201 · see citing works
Cognitive profiles associated with the fra(X) syndrome in males and females
Freund, L. S., & Reiss, A. L. (1991) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320380409 · Cited by 189 · see citing works
Attention, Development, and Psychopathology
Merrill, E. C., & Atwell, J. A. (1998) · American Journal on Mental Retardation · doi:10.1352/0895-8017(1998)103 · Cited by 170 · see citing works
A controlled trial of stimulant medication in children with the fragile X syndrome
Hagerman, R. J., Murphy, M. A., & Wittenberger, M. D. (1988) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320300138 · Cited by 158 · see citing works
Profile of cognitive functioning in women with the fragile X mutation.
Bennetto, L., Taylor, A. K., Pennington, B. F., Porter, D., & Hagerman, R. J. (2001) · Neuropsychology · doi:10.1037/0894-4105.15.2.290 · Cited by 135 · see citing works
The Trajectory of Cognitive Development in Males with Fragile X Syndrome
Dykens, E. M., Hodapp, R. M., Ort, S., Finucane, B. M., SHAPIRO, L. R., & Leckman, J. F. (1989) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/00004583-198905000-00020 · Cited by 106 · see citing works
Autistic Behaviors Among Girls with Fragile X Syndrome
Mazzocco, M. M. M., Kates, W. R., Baumgardner, T. L., Freund, L. S., & Reiss, A. L. (1997) · Journal of Autism and Developmental Disorders · doi:10.1023/a:1025857422026 · Cited by 101 · see citing works
Hodapp, R. M., Leckman, J. F., Dykens, E. M., Sparrow, S. S., Zelinsky, D. G., & Ort, S. I. (1992) · PubMed · Cited by 98 · see citing works
Gravholt, C. H., & Næraa, R. W. (1997) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19971112)72:4 · Cited by 92 · see citing works
Biology of the fragile X mental retardation protein, an RNA-binding protein
Khandjian, É. W. (1999) · Biochemistry and Cell Biology · doi:10.1139/bcb-77-4-331 · Cited by 79 · see citing works
Lachiewicz, A. M., Dawson, D. V., & Spiridigliozzi, G. A. (2000) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(20000605)92:4 · Cited by 75 · see citing works
Transmitting males and carrier females in fragile X–revisited
Loesch, D. Z., Hay, D. A., & Mulley, J. C. (1994) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320510418 · Cited by 73 · see citing works
Noninvasive Test for Fragile X Syndrome, Using Hair Root Analysis
Willemsen, R., Anar, B., de Diego‐Otero, Y., Vries, B. B. A. D., Hilhorst‐Hofstee, Y., Smits, A. P. T., van Looveren, E., Willems, P. J., GALJAARD, H., & Oostra, B. A. (1999) · The American Journal of Human Genetics · doi:10.1086/302462 · Cited by 72 · see citing works
Neri, G., & Chiurazzi, P. (1999) · Advances in Genetics · doi:10.1002/1096-8628(200023)97:3 · Cited by 66 · see citing works
Standards for Selected Anthropometric Measurements in Males With the Fragile X Syndrome
Butler, M. G., Brunschwig, A., Miller, L. K., & Hagerman, R. J. (1992) · PEDIATRICS · doi:10.1542/peds.89.6.1059 · Cited by 65 · see citing works
Biology of the fragile X mental retardation protein, an RNA-binding protein
Khandjian, É. W. (1999) · Biochemistry and Cell Biology · doi:10.1139/o99-035 · Cited by 62 · see citing works
A converging‐methods approach to fragile X syndrome
Churchill, J. D., Grossman, A. W., Irwin, S. A., Galvez, R., Klintsova, A. Y., Weiler, I. J., & Greenough, W. T. (2002) · Developmental Psychobiology · doi:10.1002/dev.10036 · Cited by 46 · see citing works
Self-citationFragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction
Syrrou, M., Georgiou, I. A., Patsalis, P. C., Bouba, I., Adonakis, G., & Pagoulatos, G. N. (1999) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19990528)84:3 · Cited by 33 · see citing works
Ocular anomalies in fragile X syndrome.
Maino, D. M., Schlange, D. G., Maino, J. H., & Caden, B. W. (1990) · PubMed · Cited by 11 · see citing works
Miller (1999) · doi:10.1002/(sici)1096-8628(19990402)83:4
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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 · doi:10.1038/nrdp.2017.65 · Cited by 838 · see citing works
Self-citationOpen-label add-on treatment trial of minocycline in fragile X syndrome.
Paribello, C., Tao, L., Folino, A., Berry-Kravis, E., Tranfaglia, M., Ethell, I. M., & Ethell, D. W. (2010) · BMC Neurology · doi:10.1186/1471-2377-10-91 · Cited by 223 · see citing works
Self-citationOpen-Label Treatment Trial of Lithium to Target the Underlying Defect in Fragile X Syndrome
Berry-Kravis, E., Sumis, A., Hervey, C., Nelson, M., Porges, S. W., Weng, N., Weiler, I. J., & Greenough, W. T. (2008) · Journal of Developmental & Behavioral Pediatrics · doi:10.1097/dbp.0b013e31817dc447 · Cited by 215 · see citing works
Self-citationExperience effects on brain development: possible contributions to psychopathology
Grossman, A. W., Churchill, J. D., McKinney, B. C., Kodish, I. M., Otte, S. L., & Greenough, W. T. (2002) · Journal of Child Psychology and Psychiatry · doi:10.1111/1469-7610.t01-1-00102 · Cited by 186 · see citing works
Self-citationBehavioral phenotypes of genetic mouse models of autism
Kazdoba, T. M., Leach, P. T., & Crawley, J. N. (2015) · Genes Brain & Behavior · doi:10.1111/gbb.12256 · Cited by 179 · see citing works
Flores-Dorantes, M. T., Díaz‐López, Y. E., & Gutiérrez‐Aguilar, R. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00863 · Cited by 159 · see citing works
Seizures in Fragile X Syndrome: Characteristics and Comorbid Diagnoses
Berry-Kravis, E., Raspa, M., Loggin-Hester, L., Bishop, E., Holiday, D., & Bailey, D. B. (2010) · American Journal on Intellectual and Developmental Disabilities · doi:10.1352/1944-7558-115.6.461 · Cited by 155 · see citing works
Self-citationPsychopharmacology in fragile X syndrome—Present and future
Berry‐Kravis, E., & Potanos, K. (2004) · Mental Retardation and Developmental Disabilities Research Reviews · doi:10.1002/mrdd.20007 · Cited by 151 · see citing works
Self-citationTherapeutic Strategies in Fragile X Syndrome: Dysregulated mGluR Signaling and Beyond
Groß, C., Berry‐Kravis, E., & Bassell, G. J. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.137 · Cited by 103 · see citing works
Self-citationOxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders
Francis, S. M., Sagar, A., Levin-Decanini, T., Liu, W., Carter, C. S., & Jacob, S. (2014) · Brain Research · doi:10.1016/j.brainres.2014.01.021 · Cited by 101 · see citing works
Early‐phase ERK activation as a biomarker for metabolic status in fragile X syndrome
Weng, N., Weiler, I. J., Sumis, A. M., Berry‐Kravis, E., & Greenough, W. T. (2008) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30765 · Cited by 72 · see citing works
Self-citationModulation of the GABAergic pathway for the treatment of fragile X syndrome
Hagerman, R. J., Lozano, R., & Hare, E. B. (2014) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s42919 · Cited by 66 · see citing works
Fragile X syndrome and fragile X-associated tremor ataxia syndrome
Hall, D. A., & Berry‐Kravis, E. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63233-3.00025-7 · Cited by 63 · see citing works
Self-citationPublic Health Literature Review of Fragile X Syndrome
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Cholesterol levels in Fragile X syndrome
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Self-citationClinic-Based Retrospective Analysis of Psychopharmacology for Behavior in Fragile X Syndrome
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Self-citationCharacterization of Potential Outcome Measures for Future Clinical Trials in Fragile X Syndrome
Berry‐Kravis, E., Sumis, A. M., Kim, O.-K., Lara, R., & Wuu, J. (2008) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-008-0564-8 · Cited by 25 · see citing works
Self-citationCaregiver Preferences for the Treatment of Males with Fragile X Syndrome
Cross, J. D., Yang, J., Johnson, F. R., Quiroz, J. A., Dunn, J., Raspa, M., & Bailey, D. B. (2015) · Journal of Developmental & Behavioral Pediatrics · doi:10.1097/dbp.0000000000000234 · Cited by 19 · see citing works
Raspa, M., Franco, V. D. F., Bishop, E. E., Wheeler, A., Wylie, A. C., & Bailey, D. B. (2018) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2018.04.024 · Cited by 17 · see citing works
Targeted treatments in fragile X syndrome
Hare, E. B., Hagerman, R. J., & Lozano, R. (2014) · Expert Opinion on Orphan Drugs · doi:10.1517/21678707.2014.903795 · Cited by 14 · see citing works
Risperidone Treatment for Irritability in Fragile X Syndrome
Dominick, K. C., Wink, L. K., Pedapati, E. V., Shaffer, R. C., Sweeney, J. A., & Erickson, C. A. (2018) · Journal of Child and Adolescent Psychopharmacology · doi:10.1089/cap.2017.0057 · Cited by 12 · see citing works
Molecular mechanisms for targeted treatments in fragile X syndrome
Miranda, I., & Hagerman, R. J. (2023) · Rare Disease and Orphan Drugs Journal · doi:10.20517/rdodj.2023.21 · Cited by 3 · see citing works
Hoffmann, A., & Berry‐Kravis, E. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800109-7.00020-0 · Cited by 3 · see citing works
Self-citationMotor stereotypies in fragile X syndrome
Kaytser, V., Berry‐Kravis, E., Ouyang, B., Doll, E. R., & Hall, D. (2015) · Journal of Pediatric Neurology · doi:10.3233/jpn-140635 · Cited by 2 · see citing works
Self-citationHare, E. B., Lozano, R., Partington, L. C., & Hagerman, R. J. (2016) · Springer eBooks · doi:10.1007/978-3-319-18096-0_64 · Cited by 2 · see citing works
Investigating Therapeutic Strategies for Fragile X Syndrome in Mice
Michalon, A., & Lindemann, L. (2012) · BioValley monographs · doi:10.1159/000339190 · Cited by 1 · see citing works
Grossman, A. W., Greenough, W. T., & Berry‐Kravis, E. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00794-4 · Cited by 1 · see citing works
Self-citationDysregulated ERK signal pathway and immune profiles in Fragile X Syndrome
Weng, N. (2012) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign)
Oxytocin and Vasopressin in Autism and Genetic Syndromes
Levin‐Decanini, T., Francis, S. M., Sagar, A., Liu, W., Carter, C. S., & Jacob, S. (2015) · Contemporary clinical neuroscience · doi:10.1007/978-1-4939-2190-4_14
- Authors
- Berry-Kravis, E., Grossman, A. W., Crnic, L. S., & Greenough, W. T.
- Affiliations
- University of Illinois Urbana-Champaign (US)
- University of Colorado Anschutz (US)
- ORCID
- Grossman, Aaron W.
- Venue
- Current Paediatrics
- Publisher
- Elsevier BV
- Published
- 2002-08
- Volume
- 12
- Issue
- 4
- Pages
- 316-324
- ISSN
- 0957-5839 (ISSN-L)
- OpenAlex
- W2079802852
- Cited by
- 29
- References
- 23
- Citations by year
- 2023: 1 · 2020: 1 · 2018: 3 · 2017: 2 · 2016: 2 · 2015: 4 · 2014: 4 · 2012: 3
- FWCI
- 0.35
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Current Paediatrics (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Down syndrome and intellectual disability research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Keywords
- fragile X syndrome, FMRP, intellectual disability, hyperactivity, anxiety, mitral valve prolapse, gastroesophageal reflux, otitis media, genetic counseling, behavior management
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