Randi Hagerman

Tsakopoulos-Vismara Chair in Pediatrics

Departments

Pediatrics - Medicine

Offices and Labs

UC Davis Health System, Sacramento, CA 95817
(916)734-6348

CBS Grad Group Affiliations

Neuroscience

Specialties / Focus

Neuroscience
  • Development and Plasticity
  • Cognitive Neuroscience
  • Medical Neuroscience

Labs

Publications

5/21/2010 9:26:34 AM
  • Simon JA, Keenan JM, Pennington BF, Taylor AK, Hagerman RJ. (2001) Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence. Cognitive Neuropsychology 18(1),1-18
  • Mangeot SD, Miller LJ, McIntosh DN, McGrath-Clark J, Simon J, Hagerman RJ, Goldson E. (2001) Sensory modulation dysfunction in children with attention-deficit-hyperactivity disorder. Developmental Medicine & Child Neurology 43:399-406
  • Tassone F, Hagerman RJ, Taylor AK, Hagerman PJ. (2001) A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA. J Med Genet. 38:0-3
  • Hagerman RJ, Leehey M, Heinrichs W, Tassone F, Wilson R, Hills J, Grigsby J, Gage B, Hagerman PJ. (2001) Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology 57:127-130
  • Simon JA, Keenan JM, Pennington BF, Taylor A, Hagerman RJ. (2001) Discourse processing in women with fragile X syndrome: Coherence. Cognitive Neuropsychology 18:1-18.
  • Bennetto L, Pennington BF, Porter D, Taylor AK, Hagerman RJ. (2001) Profile of cognitive functioning in women with the fragile X mutation. Neuropsychology 15:290-299.
  • Gould EL, Loesch DZ, Martin MJ, Hagerman RJ, Armstrong SM, Huggins RM. (2000) Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study. Am J Med Genet 95:307-315.
  • Tassone F, Hagerman RJ, Chamberlain WD, Hagerman PJ. (2000b) Transcription of the FMR1 gene in individuals with fragile X syndrome. Am J Med Genet (Semin. Med. Genet.) 97:195-203.
  • Tassone F, Hagerman RJ, Loesch D, Lachiewicz A, Taylor A, Hagerman PJ. (2000a) Fragile X males with unmethylated full mutation trinucleotide repeat expansion have elevated levels of FMR1 messenger RNA. Am J Med Genet 94:232-236.
  • Tassone F, Hagerman RJ, Taylor AK, Mills JB, Harris SW, Gane LW, Hagerman PJ. (2000) Clinical Involvement and Protein Expression in Individuals with the FMR1 Premutation. Am J Med Genet 91:144-152.
  • Tassone F, Hagerman RJ, Taylor AK, Gane LW, Godfrey T, Hagerman PJ. (2000b) Elevated levels of FMR1 messenger RNA in carrier males: A new mechanism of involvement in fragile X syndrome. Am J Human Genet 66:6-15.