Hagerman, Randi J.

Sertraline May Improve Language Developmental Trajectory in Young Children with Fragile X Syndrome: A Retrospective Chart Review

Indah Winarni, T., Chonchaiya, W., Adams, E., Au, J., Mu, Y., Rivera, S. M., Nguyen, D. V., & Hagerman, R. J. (2012) · Autism Research and Treatment

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 52

Social cognition skills among females with fragile X

Mazzocco, M. M. M., Pennington, B. F., & Hagerman, R. J. (1994) · Journal of Autism and Developmental Disorders

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 46

A randomized controlled trial of sertraline in young children with autism spectrum disorder

Potter, L. A., Scholze, D. A., Biag, H. M. B., Schneider, A., Chen, Y., Nguyen, D. V., Rajaratnam, A., Rivera, S. M., Dwyer, P. S., Tassone, F., et al. (2019) · Frontiers in Psychiatry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 43

Fragile X-associated tremor/ataxia syndrome: Pathophysiology and management

Hagerman, R., & Hagerman, P. (2021) · Current Opinion in Neurology

Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases

Cited by 40

Cognitive and behavioral improvement in adults with fragile X syndrome treated with metformin‐two cases

Protic, D., Aydin, E. Y., Tassone, F., Tan, M. M., Hagerman, R. J., & Schneider, A. (2019) · Molecular Genetics & Genomic Medicine

Genetics and Neurodevelopmental DisordersDown syndrome and intellectual disability research

Cited by 34

Group I metabotropic glutamate receptor mediated dynamic immune dysfunction in children with fragile X syndrome

Careaga, M., Noyon, T., Basuta, K., Van de Water, J., Tassone, F., Hagerman, R. J., & Ashwood, P. (2014) · Journal of Neuroinflammation

Genetics and Neurodevelopmental DisordersImmunodeficiency and Autoimmune Disorders

Cited by 20

Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in fragile X premutation carriers: case series

Tassanakijpanich, N., McKenzie, F. J., McLennan, Y. A., Makhoul, E., Tassone, F., Jasoliya, M. J., Romney, C., Petrasic, I. C., Napalinga, K., Buchanan, C. B., et al. (2022) · Journal of Medical Genetics

Genetics and Neurodevelopmental DisordersConnective tissue disorders research

Cited by 9

In utero alcohol and unsuitable home environmental exposure combined with FMR1 full mutation allele cause severe fragile X syndrome phenotypes

Winarni, T. I., Aishworiya, R., Culpepper, H., Zafarullah, M., Mendoza, G., Wilaisakditipakorn, T. J., Likhitweerawong, N., Law, J., Hagerman, R., & Tassone, F. (2025) · International Journal of Molecular Sciences

Genetics and Neurodevelopmental DisordersPrenatal Substance Exposure Effects

Cited by 3