• 19372 Citations
  • 78 h-Index
1969 …2019
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  • 8 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

9/21/155/31/19

Project: Research projectResearch Project

Epigenomics
Methylation
Gene Silencing
Double-Stranded DNA Breaks
Genes

Human iPSC neuronal models for early and late phases of FXTAS neurodegeneration

Hagerman, P. J.

National Institutes of Health

9/30/098/31/11

Project: Research projectNIH Challenge Grants and Partnerships Program

Induced Pluripotent Stem Cells
Intellectual Disability
Alleles
Fibroblasts
Gait Ataxia
RNA
Small Interfering RNA
Oligonucleotides
Astrocytes
Glutamic Acid

Neuro Therapeutics Research Institute

Hagerman, P. J.

National Institutes of Health

9/15/076/30/12

Project: Research projectLinked Specialized Center Cooperative Agreement

Neuro Therapeutics Research Institute (1 of 6)

Hagerman, P. J.

National Institutes of Health

9/15/076/30/12

Project: Research projectLinked Specialized Center Cooperative Agreement

Therapeutic Human Experimentation
Ataxia
Research
Neurodegenerative Diseases
Research Personnel

Research Output 1969 2017

  • 19372 Citations
  • 78 h-Index
  • 243 Article
  • 7 Chapter
  • 3 Review article
6 Citations

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
Calcium
Brain
Dantrolene
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

Phenotype
Anxiety
Executive Function
Depression
Messenger RNA
1 Citations

Concomitant occurrence of FXTAS and clinically defined sporadic inclusion body myositis: Report of two cases

Lechpammer, M., Martinez-Cerdeno, V., Hunsaker, M. R., Hah, M., Gonzales, H., Tisch, S., Joffe, R., Pamphlett, R., Tassone, F., Hagerman, P. J., Bolitho, S. J. & Hagerman, R. J., Aug 1 2017, In : Croatian Medical Journal. 58, 4, p. 310-315 6 p.

Research output: Contribution to journalArticle

Inclusion Body Myositis
Fragile X Syndrome
Fatal Outcome
Tremor
Ataxia
14 Citations

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. & Hagerman, P. J., Sep 29 2017, In : Nature reviews. Disease primers. 3, 1 p.

Research output: Contribution to journalReview article

Fragile X Mental Retardation Protein
Fragile X Syndrome
Trinucleotide Repeats
Language Development
Neuronal Plasticity
3 Citations

Iron accumulation and dysregulation in the putamen in fragile X-associated tremor/ataxia syndrome

Ariza, J., Rogers, H., Hartvigsen, A., Snell, M., Dill, M., Judd, D., Hagerman, P. J. & Martinez-Cerdeno, V., 2017, (Accepted/In press) In : Movement Disorders.

Research output: Contribution to journalArticle

Putamen
Iron
Ceruloplasmin
Iron-Binding Proteins
Transferrin