• 19705 Citations
  • 79 h-Index
1969 …2019
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  • 9 Similar Profiles
Fragile X Syndrome Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Tremor Medicine & Life Sciences
Alleles Medicine & Life Sciences
Genes Medicine & Life Sciences
RNA Medicine & Life Sciences
Messenger RNA Medicine & Life Sciences
Fragile X Mental Retardation Protein Medicine & Life Sciences

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Projects 1980 2019

Epigenetic regulation of the FMR1 gene

Hagerman, P. J., Tassone, F. & Chedin, F. L.

National Institutes of Health


Project: Research project

Gene Silencing
Double-Stranded DNA Breaks
Induced Pluripotent Stem Cells
Intellectual Disability
Gait Ataxia
Small Interfering RNA
Glutamic Acid
Therapeutic Human Experimentation
Neurodegenerative Diseases
Research Personnel

Research Output 1969 2018

  • 19705 Citations
  • 79 h-Index
  • 246 Article
  • 7 Chapter
  • 3 Review article

Autism phenotype in fragile X premutation males is not associated with FMR1 expression: A preliminary evaluation

Sumekar, T. A., Winarni, T. I., Mu, Y., Chonchaiya, W., Tassone, F., Iwahashi, C., Cheung, K., Faradz, S. M. H., Hagerman, P. J., Nguyen, D. V. & Hagerman, R. J., May 1 2018, In : Hiroshima Journal of Medical Sciences. 67, p. 166-173 8 p.

Research output: Contribution to journalArticle

Autistic Disorder
Messenger RNA

Fragile X syndrome and connective tissue dysregulation

Ramírez-Cheyne, J. A., Duque, G. A., Ayala-Zapata, S., Saldarriaga-Gil, W., Hagerman, P. J., Hagerman, R. J. & Payán-Gómez, C., Jan 1 2018, (Accepted/In press) In : Clinical Genetics.

Research output: Contribution to journalArticle

Fragile X Syndrome
Connective Tissue
Extracellular Matrix
Fragile X Mental Retardation Protein
Urogenital System

Microglial cell activation and senescence are characteristic of the pathology FXTAS

Martínez Cerdeño, V., Hong, T., Amina, S., Lechpammer, M., Ariza, J., Tassone, F., Noctor, S. C., Hagerman, P. J. & Hagerman, R. J., Dec 1 2018, In : Movement Disorders. 33, 12, p. 1887-1894 8 p.

Research output: Contribution to journalArticle

Cell Aging
Fragile X Tremor Ataxia Syndrome
Intranuclear Inclusion Bodies
7 Citations (Scopus)

Calcium dysregulation and Cdk5-ATM pathway involved in a mouse model of fragile X-associated tremor/ataxia syndrome

Robin, G., López, J. R., Espinal, G. M., Hulsizer, S., Hagerman, P. J. & Pessah, I. N., Jul 15 2017, In : Human Molecular Genetics. 26, 14, p. 2649-2666 18 p.

Research output: Contribution to journalArticle

DNA Damage
Intranuclear Inclusion Bodies

Clinical and molecular correlates in fragile X premutation females

Jiraanont, P., Sweha, S. R., AlOlaby, R. R., Silva, M., Tang, H. T., Durbin-Johnson, B., Schneider, A., Espinal, G. M., Hagerman, P. J., Rivera, S. M., Hessl, D. R., Hagerman, R. J., Chutabhakdikul, N. & Tassone, F., Jun 1 2017, In : eNeurologicalSci. 7, p. 49-56 8 p.

Research output: Contribution to journalArticle

Executive Function
Messenger RNA