Hagerman, Paul J.

Fragile X syndrome

Hagerman, R. J., Berry-Kravis, E., Hazlett, H. C., Bailey, D. B., Moine, H., Kooy, R. F., Tassone, F., Gantois, I., Sonenberg, N., Mandel, J. L., et al. (2017) · Nature Reviews Disease Primers

Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases

Cited by 838

Autism Profiles of Males With Fragile X Syndrome

Harris, S. W., Hessl, D., Goodlin-Jones, B., Ferranti, J., Bacalman, S., Barbato, I., Tassone, F., Hagerman, P. J., Herman, K., & Hagerman, R. J. (2008) · American Journal on Mental Retardation

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 396

Autism Spectrum Disorders and Attention-Deficit/Hyperactivity Disorder in Boys with the Fragile X Premutation

FARZIN, F., PERRY, H., HESSL, D., LOESCH, D., COHEN, J., BACALMAN, S., GANE, L., TASSONE, F., HAGERMAN, P., & HAGERMAN, R. (2006) · Journal of Developmental & Behavioral Pediatrics

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 325

Fragile X and autism: intertwined at the molecular level leading to targeted treatments

Hagerman, R., Hoem, G., & Hagerman, P. (2010) · Molecular Autism

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 247

Screening for Expanded Alleles of the FMR1 Gene in Blood Spots from Newborn Males in a Spanish Population

Fernandez-Carvajal, I., Walichiewicz, P., Xiaosen, X., Pan, R., Hagerman, P. J., & Tassone, F. (2009) · The Journal of Molecular Diagnostics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 204

AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome

Yrigollen, C. M., Durbin-Johnson, B., Gane, L., Nelson, D. L., Hagerman, R., Hagerman, P. J., & Tassone, F. (2012) · Genetics in Medicine

Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases

Cited by 179

Expansion of an FMR1 Grey-Zone Allele to a Full Mutation in Two Generations

Fernandez-Carvajal, I., Lopez Posadas, B., Pan, R., Raske, C., Hagerman, P. J., & Tassone, F. (2009) · The Journal of Molecular Diagnostics

Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases

Cited by 164

Advances in understanding the molecular basis of FXTAS

Garcia-Arocena, D., & Hagerman, P. J. (2010) · Human Molecular Genetics

Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases

Cited by 136

Tremor and ataxia in fragile X premutation carriers: Blinded videotape study

Berry‐Kravis, E., Lewin, F., Wuu, J., Leehey, M., Hagerman, R., Hagerman, P., & Goetz, C. G. (2003) · Annals of Neurology

Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases

Cited by 109

Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome

Greco, C. M., Navarro, C. S., Hunsaker, M. R., Maezawa, I., Shuler, J. F., Tassone, F., Delany, M., Au, J. W., Berman, R. F., Jin, L.-W., et al. (2011) · Molecular Autism

Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases

Cited by 90

FMR1 premutation and full mutation molecular mechanisms related to autism

Hagerman, R., Au, J., & Hagerman, P. (2011) · Journal of Neurodevelopmental Disorders

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 85

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

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