Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Chiurazzi, Pietro
Neri, Giovanni
and
Oostra, Ben A.
2003.
Understanding the biological underpinnings of fragile X syndrome.
Current Opinion in Pediatrics,
Vol. 15,
Issue. 6,
p.
559.
Jin, Peng
Zarnescu, Daniela C.
Zhang, Fuping
Pearson, Christopher E.
Lucchesi, John C.
Moses, Kevin
and
Warren, Stephen T.
2003.
RNA-Mediated Neurodegeneration Caused by the Fragile X Premutation rCGG Repeats in Drosophila.
Neuron,
Vol. 39,
Issue. 5,
p.
739.
Berry‐Kravis, Elizabeth
Lewin, Foster
Wuu, Joanne
Leehey, Maureen
Hagerman, Randi
Hagerman, Paul
and
Goetz, Christopher G.
2003.
Tremor and ataxia in fragile X premutation carriers: Blinded videotape study.
Annals of Neurology,
Vol. 53,
Issue. 5,
p.
616.
Hagerman, Paul J.
and
Hagerman, Randi J.
2004.
The Fragile-X Premutation: A Maturing Perspective.
The American Journal of Human Genetics,
Vol. 74,
Issue. 5,
p.
805.
GOODLIN-JONES, BETH L.
TASSONE, FLORA
GANE, LOUISE W.
and
HAGERMAN, RANDI J.
2004.
Autistic Spectrum Disorder and the Fragile X Premutation.
Journal of Developmental & Behavioral Pediatrics,
Vol. 25,
Issue. 6,
p.
392.
Macpherson, James N.
2004.
Encyclopedia of Medical Genomics and Proteomics.
p.
513.
Zeesman, Susan
Zwaigenbaum, Lonnie
Whelan, Donald T.
Hagerman, Randi J.
Tassone, Flora
and
Taylor, Sherryl A.M.
2004.
Paternal transmission of fragile X syndrome.
American Journal of Medical Genetics Part A,
Vol. 129A,
Issue. 2,
p.
184.
Hagerman, Paul J.
and
Hagerman, Randi J.
2004.
Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS).
Mental Retardation and Developmental Disabilities Research Reviews,
Vol. 10,
Issue. 1,
p.
25.
Pietrobono, Roberta
Tabolacci, Elisabetta
Zalfa, Francesca
Zito, Ilaria
Terracciano, Alessandra
Moscato, Umberto
Bagni, Claudia
Oostra, Ben
Chiurazzi, Pietro
and
Neri, Giovanni
2005.
Molecular dissection of the events leading to inactivation of the FMR1 gene.
Human Molecular Genetics,
Vol. 14,
Issue. 2,
p.
267.
Gatchel, Jennifer R.
and
Zoghbi, Huda Y.
2005.
Diseases of Unstable Repeat Expansion: Mechanisms and Common Principles.
Nature Reviews Genetics,
Vol. 6,
Issue. 10,
p.
743.
Osborne, Robert J.
and
Thornton, Charles A.
2006.
RNA-dominant diseases.
Human Molecular Genetics,
Vol. 15,
Issue. suppl_2,
p.
R162.
Han, Xiao‐Dong
Powell, Berkley R.
Phalin, Judith L.
and
Chehab, Farid F.
2006.
Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high‐functioning fragile X male.
American Journal of Medical Genetics Part A,
Vol. 140A,
Issue. 13,
p.
1463.
Tassone, Flora
and
Hagerman, Paul J.
2006.
Human Nucleotide Expansion Disorders.
Vol. 19,
Issue. ,
p.
57.
Toniolo, Daniela
2006.
X-linked premature ovarian failure: a complex disease.
Current Opinion in Genetics & Development,
Vol. 16,
Issue. 3,
p.
293.
HAGERMAN, RANDI J.
2006.
Lessons from Fragile X Regarding Neurobiology, Autism, and Neurodegeneration.
Journal of Developmental & Behavioral Pediatrics,
Vol. 27,
Issue. 1,
p.
63.
OOSTRA, BEN A.
and
NELSON, DAVID L.
2006.
Genetic Instabilities and Neurological Diseases.
p.
175.
Ennis, S.
Murray, A.
Youings, S.
Brightwell, G.
Herrick, D.
Ring, S.
Pembrey, M.
Morton, N. E.
and
Jacobs, P. A.
2006.
An Investigation of FRAXA Intermediate Allele Phenotype in A Longitudinal Sample.
Annals of Human Genetics,
Vol. 70,
Issue. 2,
p.
170.
Bourgeois, James A.
Farzin, Faraz
Brunberg, James A.
Tassone, Flora
Hagerman, Paul
Zhang, Lin
Hessl, David
and
Hagerman, Randi
2006.
Dementia With Mood Symptoms in a Fragile X Premutation Carrier With the Fragile X-Associated Tremor/Ataxia Syndrome: Clinical Intervention With Donepezil and Venlafaxine.
The Journal of Neuropsychiatry and Clinical Neurosciences,
Vol. 18,
Issue. 2,
p.
171.
Mahishi, Lata
and
Usdin, Karen
2006.
NF-Y, AP2, Nrf1 and Sp1 regulate the fragile X-related gene 2 (FXR2).
Biochemical Journal,
Vol. 400,
Issue. 2,
p.
327.
Brouwer, J.R.
Mientjes, E.J.
Bakker, C.E.
Nieuwenhuizen, I.M.
Severijnen, L.A.
Van der Linde, H.C.
Nelson, D.L.
Oostra, B.A.
and
Willemsen, R.
2007.
Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation.
Experimental Cell Research,
Vol. 313,
Issue. 2,
p.
244.