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Nolin, Sarah L; Sah, Sachin; Glicksman, Anne et al. (2013) Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles. Am J Med Genet A 161A:771-8
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Visootsak, Jeannie; Charen, Krista; Rohr, Julia et al. (2012) Diagnosis of fragile X syndrome: a qualitative study of African American families. J Genet Couns 21:845-53
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Hunter, Jessica Ezzell; Sherman, Stephanie; Grigsby, Jim et al. (2012) Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts. Neuropsychology 26:156-64
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Hunter, Jessica Ezzell; Leslie, Mary; Novak, Gloria et al. (2012) Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms. Am J Med Genet B Neuropsychiatr Genet 159B:549-59
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Juncos, Jorge L; Lazarus, Joash T; Rohr, Julia et al. (2012) Olfactory dysfunction in fragile X tremor ataxia syndrome. Mov Disord 27:1556-9
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Hunter, Jessica Ezzell; Epstein, Michael P; Tinker, Stuart W et al. (2012) The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance. Behav Genet 42:415-22
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Chang, Martin C; DeCaro, John J; Zheng, Mei et al. (2011) Ovarian histopathological and ubiquitin-immunophenotypic features in fragile X-associated primary ovarian insufficiency: a study of five cases and selected controls. Histopathology 59:1018-23
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Allen, Emily Graves; Hunter, Jessica E; Rusin, Michele et al. (2011) Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome. Neuropsychology 25:404-411
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