Wilmar Saldarriaga Gil

Dr. Wilmar Saldarriaga Gil

orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 December 2014
Verified
Journal Article
Open access
WGWilmar Saldarriaga Gil
Wilmar Saldarriaga Gil
FTFlora Tassone
Flora Tassone
LGLaura Yuriko González-Teshima
Laura Yuriko González-Teshima
JFJose Vicente Forero-Forero
Jose Vicente Forero-Forero
SASebastián Ayala-Zapata
Sebastián Ayala-Zapata
RHRandi Hagerman
Randi Hagerman
Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full mutation (greater than 200 CGG repeats), in the fragile X mental retardation 1 gene locus Xq27.3; which leads to an hypermethylated region in the gene promoter therefore silencing it and lowering the expression levels of the fragile X mental retardation 1, a protein involved in synaptic plasticity and maturation. Individuals with FXS present with intellectual disability, autism, hyperactivity, long face, large or prominent ears and macroorchidism at puberty and thereafter. Most of the young children with FXS will present with language delay, sensory hyper arousal and anxiety. Girls are less affected than boys, only 25% have intellectual disability. Given the genomic features of the syndrome, there are patients with a number of triplet repeats between 55 and 200, known as premutation carriers. Most carriers have a normal IQ but some have developmental problems. The diagnosis of FXS has evolved from karyotype with special culture medium, to molecular techniques that are more sensitive and specific including PCR and Southern Blot. During the last decade, the advances in the knowledge of FXS, has led to the development of investigations on pharmaceutical management or targeted treatments for FXS. Minocycline and sertraline have shown efficacy in children.

1 March 2015 in American Journal of Obstetrics and Gynecology
Verified
Journal Article
Closed access
WGWilmar Saldarriaga Gil
Wilmar Saldarriaga Gil
HGHerney Andres García-Perdomo
Herney Andres García-Perdomo
JAJohanna Arango-Pineda
Johanna Arango-Pineda
JFJavier Fonseca
Javier Fonseca

16 September 2008 in American Journal of Medical Genetics Part A
Verified
Journal Article
Closed access
PDF file
ECEduardo E. Castilla
Eduardo E. Castilla
PMPierpaolo Mastroiacovo
Pierpaolo Mastroiacovo
JLJorge S. López‐Camelo
Jorge S. López‐Camelo
WGWilmar Saldarriaga Gil
Wilmar Saldarriaga Gil
CICarolina Isaza
Carolina Isaza
IOIêda M. Orioli
Iêda M. Orioli

29 January 2018 in Journal of Human Genetics
Verified
Journal Article
Closed access
PDF file
WGWilmar Saldarriaga Gil
Wilmar Saldarriaga Gil
JFJose Forero
Jose Forero
LGLaura Yuriko González-Teshima
Laura Yuriko González-Teshima
AFAndrés Fandiño-Losada
Andrés Fandiño-Losada
CICarolina Isaza
Carolina Isaza
FTFlora Tassone
Flora Tassone

10 November 2018 in Clinical Genetics
Verified
Journal Article
Closed access
PDF file
JRJulián Andrés Ramírez‐Cheyne
Julián Andrés Ramírez‐Cheyne
GDGustavo Andrés Duque
Gustavo Andrés Duque
SASebastián Ayala‐Zapata
Sebastián Ayala‐Zapata
WGWilmar Saldarriaga Gil
Wilmar Saldarriaga Gil
PHPaul Hagerman
Paul Hagerman
CPCésar Payán‐Gómez
César Payán‐Gómez

6 February 2009 in Birth Defects Research Part A: Clinical and Molecular Teratology
Verified
Journal Article
Closed access
PDF file
IOIêda M. Orioli
Iêda M. Orioli
PMPierpaolo Mastroiacovo
Pierpaolo Mastroiacovo
JLJorge S. López‐Camelo
Jorge S. López‐Camelo
WGWilmar Saldarriaga Gil
Wilmar Saldarriaga Gil
CICarolina Isaza
Carolina Isaza
ECEduardo E. Castilla
Eduardo E. Castilla