Randi J. Hagerman - Concepedia

Author

Randi J. Hagerman

University of California, Davis

Also Known As

Hagerman, Randi J., R J Hagerman, R. J. Hagerman, Randi Hagerman, Randi J. Hagerman

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

University of California, Davis University of California Davis Medical Center University of Colorado Health University of Colorado Denver Children's Hospital Colorado

About

Randi J. Hagerman is an author at University of California, Davis specializing in medicine, developmental delay, and fragile x premutation.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	1.2K
2	Education	2	2	204
3	Arts	1	1	33
4	Health Sciences	1	1	190
5	Social Sciences	1	1	44

Randi J. Hagerman

Publications

Citations

H-Index

Page 1

	Year	Citations
Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics Claudia Bagni, Flora Tassone, Giovanni Neri, Journal of Clinical Investigation Fragile X SyndromeFmr1 GeneMendelian DisorderGenetic DisorderMedicine	2012	321
Heterozygous fragile X female: Historical, physical, cognitive, and cytogenetic features Amy Cronister, Rebecca Schreiner, Michael D. Wittenberger, American Journal of Medical Genetics CytogeneticsGeneticsReproductive BiologyOsteoporosisNormal Iq	1991	190
AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome Carolyn M. Yrigollen, Blythe Durbin‐Johnson, Louise W. Gane, Genetics in Medicine Fragile X SyndromeDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2012	174
Fragile X checklist Randi J. Hagerman, Khaled M. A. Amiri, Amy Cronister American Journal of Medical Genetics	1991	160
Girls With Fragile X Syndrome: Physical and Neurocognitive Status and Outcome Randi J. Hagerman, Carey Jackson, Khaled M. A. Amiri, PEDIATRICS DisabilityEducationFragile X GenePsychologyNeurodiversity	1992	159
Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration Y. Chen, F. Tassone, Robert F. Berman, Human Molecular Genetics	2009	150
Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndrome Eleonora Napoli, Catherine Ross‐Inta, Sarah Wong, Human Molecular Genetics	2011	106
Molecular/clinical correlations in females with fragile X William E. Sobesky, Annette K. Taylor, Bruce F. Pennington, American Journal of Medical Genetics	1996	105
Tissue heterogeneity of theFMR1 mutation in a high-functioning male with fragile X syndrome Annette K. Taylor, Flora Tassone, Pamela N. Dyer, American Journal of Medical Genetics	1999	77
Parkinsonism in FMR1 premutation carriers may be indistinguishable from Parkinson disease Deborah A. Hall, Katherine L. Howard, Randi J. Hagerman, Parkinsonism & Related Disorders Parkinson DiseaseDegenerative DiseaseFmr1 Premutation CarriersClinical NeuroscienceNeurology	2008	68

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