Gail A. Spiridigliozzi

Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.

Allyn McConkie‐Rosell, Ave M. Lachiewicz, Gail A. Spiridigliozzi et al. · PubMed · 1993 · 169 citations

IRF2BPL Is Associated with Neurological Phenotypes

Paul C. Marcogliese, Vandana Shashi, Rebecca C. Spillmann et al. · The American Journal of Human Genetics · 2018 · 108 citations · Full text

Neurology, Neuroscience, Molecular Neurobiology +4

Assessment of Cognitive Scales to Examine Memory, Executive Function and Language in Individuals with Down Syndrome: Implications of a 6-month Observational Study

Xavier Liogier D’ardhuy, Jamie O. Edgin, Charles Bouis et al. · Frontiers in Behavioral Neuroscience · 2015 · 90 citations · Full text

Neuropsychology, Neurolinguistics, Psycholinguistics +18

Parental attitudes regarding carrier testing in children at risk for fragile X syndrome

Allyn McConkie‐Rosell, Gail A. Spiridigliozzi, Kathleen A. Rounds et al. · American Journal of Medical Genetics · 1999 · 89 citations

Donepezil for treatment of cognitive dysfunction in children with Down syndrome aged 10–17

Priya S. Kishnani, James H. Heller, Gail A. Spiridigliozzi et al. · American Journal of Medical Genetics Part A · 2010 · 84 citations