• 16013 Citations
  • 69 h-Index
1977 …2019
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  • 7 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

9/21/155/31/19

Project: Research projectResearch Project

Epigenomics
Methylation
Gene Silencing
Double-Stranded DNA Breaks
Genes

RESEARCH IN MENTAL RETARDATION AND CHILD DEVELOPMENT

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

9/1/776/30/14

Project: Research projectCenter Core Grants

neurosciences
handicapped child
quality of life
knowledge

Research Output 1987 2018

2 Citations

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

Cytosine
Ataxia
Prodromal Symptoms
Executive Function
Neurologic Examination
2 Citations

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
Phenotype
Genome
Chromosomes, Human, Pair 22
Pregnanolone
Metabolomics
gamma-Aminobutyric Acid
Neurodegenerative Diseases
Mitochondria

Assessment of molecular measures in non-FXTAS male premutation carriers

Al Olaby, R. R., Tang, H. T., Durbin-Johnson, B., Schneider, A., Hessl, D. R., Rivera, S. M. & Tassone, F., Aug 22 2018, In : Frontiers in Genetics. 9, AUG, 302.

Research output: Contribution to journalArticle

Protein Isoforms
Tremor
Alternative Splicing
Gait Ataxia
Movement Disorders

Congnitive deficits and associated ERP N400 abnormalities in FXTAS with parkinsonism

Wang, X. H., Yang, J. C., Soohoo, R., Cotter, D., Yuan, M., Xia, J., Yaqub, S., Doty, J., Niu, Y. Q., Tassone, F., Hagerman, R. J., Zhang, L. & Olichney, J. M., Sep 18 2018, In : Frontiers in Genetics. 9, SEP, 327.

Research output: Contribution to journalArticle

Parkinsonian Disorders
Evoked Potentials
Verbal Learning
Brain
Neurologic Examination