• 16443 Citations
  • 70 h-Index
1977 …2019
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  • 10 Similar Profiles
Fragile X Syndrome Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Alleles Medicine & Life Sciences
Genes Medicine & Life Sciences
Tremor Medicine & Life Sciences
Mutation Medicine & Life Sciences
Messenger RNA Medicine & Life Sciences
Fragile X Mental Retardation Protein Medicine & Life Sciences

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Projects 1977 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


Schwartzkroin, P. A., Tassone, F., Garden, G., La Spada, A., Spieker, S. J., Farrell, D., Kucewicz, J., Burbacher, T., Chance, P. F., Maravilla, K., Guralnick, M., Kucewicz, J., Morris, D., Beach, K., Laird, C., Greenough, W., Tapscott, S. J., Dawson, G., Owen, G., Moritz, W., Ruppenthal, G. & Scott, R.

National Institutes of Health


Project: Research project

handicapped child
quality of life

Research Output 1987 2019

FMRpolyG alters mitochondrial transcripts level and respiratory chain complex assembly in Fragile X associated tremor/ataxia syndrome [FXTAS]

Gohel, D., Sripada, L., Prajapati, P., Singh, K., Roy, M., Kotadia, D., Tassone, F., Charlet-Berguerand, N. & Singh, R., Jan 1 2019, In : Biochimica et Biophysica Acta - Molecular Basis of Disease.

Research output: Contribution to journalArticle

Electron Transport
Animal Models
Intranuclear Inclusion Bodies
Mitochondrial DNA

Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)

Zafarullah, M. & Tassone, F., Jan 1 2019, In : Methods in molecular biology (Clifton, N.J.). 1942, p. 173-189 17 p.

Research output: Contribution to journalArticle

Gait Ataxia
Intranuclear Inclusion Bodies
Parkinsonian Disorders

Increased severity of fragile X spectrum disorders in the agricultural community of Ricaurte, Colombia

Saldarriaga, W., Salcedo-Arellano, M. J., Rodriguez-Guerrero, T., Ríos, M., Fandiño-Losada, A., Ramirez-Cheyne, J., Lein, P. J., Tassone, F. & Hagerman, R. J., Feb 1 2019, In : International Journal of Developmental Neuroscience. 72, p. 1-5 5 p.

Research output: Contribution to journalArticle

Primary Ovarian Insufficiency
Rural Population
2 Citations (Scopus)

Age- and CGG repeat-related slowing of manual movement in fragile X carriers: A prodrome of fragile X-associated tremor ataxia syndrome?

Shickman, R., Famula, J., Tassone, F., Leehey, M., Ferrer, E., Rivera, S. M. & Hessl, D. R., Apr 1 2018, In : Movement Disorders. 33, 4, p. 628-636 9 p.

Research output: Contribution to journalArticle

Prodromal Symptoms
Executive Function
Neurologic Examination
3 Citations (Scopus)

A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome

Jensen, M., Kooy, R. F., Simon, T. J., Reyniers, E., Girirajan, S. & Tassone, F., Apr 1 2018, In : European Journal of Medical Genetics. 61, 4, p. 209-212 4 p.

Research output: Contribution to journalArticle

DiGeorge Syndrome
Intellectual Disability
Chromosomes, Human, Pair 22