Position - Company  
Research Associate - The University of South Dakota

Bioinformatics (Sequence analysis: UCSC, Galaxy, NCBI, EBI...)
BioExtract Server Tools development and workflows creation
Setup of bioinformatics workshops and trainings over the BRIN colleges (South Dakota Biomedical Research Infrastructure Network)

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Mar 2010 - Jun 2011
Superviseur Gestion de la Realtion Client - Tunisiana Aug 2003 - Feb 2010
Research student - Institut National de Neurologie Dec 2001 - Jun 2009
postdoc - University of California, San Francisco Jun 2011 - Present
Postdoc - UCSF Medical Center

Genomic analysis
High-Throughput Sequencing
Exome Sequencing
SNP detection
Twins Biology

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Jul 2011 - Present
Degree - University  
PhD, Moelcular Biology & Human Genetics - National Institute of Neurology (TUNISIA) 2002 - 2009
Master, Biomedical Sciences - Universite Josepf Fourier grenoble 2000 - 2001
Bachelor's degree, Biological Sciences - Facutle des Sciences de Monastir 1996 - 2000
Publication Info
Ataxia with vitamin E deficiency and abetalipoproteinemia. Hentati F, El-Euch G, Bouhlal Y, Amouri R Handb Clin Neurol. 103:295-305. doi: 10.1016/B978-0-444-51892-7.00018-8. 2012. View on PubMed.
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overview. Bouhlal Y, Amouri R, El Euch-Fayeche G, Hentati F Parkinsonism Relat Disord. 17(6):418-22. doi: 10.1016/j.parkreldis.2011.03.005. March 30, 2011. View on PubMed.
Computational analysis of a novel SACS gene mutation with BioExtract server. Bouhlal Y, Jennewein DM, Anderson B, Reynoldson J, Maamouri W, Hentati F, Amouri R, Lushbough C J Mol Neurosci. 44(1):53-8. doi: 10.1007/s12031-011-9512-8. March 17, 2011. View on PubMed.
Socio-economic status, racial composition and the affordability of fresh fruits and vegetables in neighborhoods of a large rural region in Texas. Dunn RA, Sharkey JR, Lotade-Manje J, Bouhlal Y, Nayga RM Jr Nutr J. 10:6. doi: 10.1186/1475-2891-10-6. January 18, 2011. View on PubMed.
Spinal muscular atrophy due to double gene conversion event. Maamouri W, Hammer MB, Bouhlel Y, Souilem S, Khmiri N, Nehdi H, Hentati F, Amouri R Int J Neurosci. 121(2):107-11. doi: 10.3109/00207454.2010.529209. November 3, 2010. View on PubMed.
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays. H'mida-Ben Brahim D, M'zahem A, Assoum M, Bouhlal Y, Fattori F, Anheim M, Ali-Pacha L and 16 others J Neurol. 258(1):56-67. doi: 10.1007/s00415-010-5682-5. August 27, 2010. View on PubMed.
Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosis. Amouri R, Nehdi H, Bouhlal Y, Kefi M, Larnaout A, Hentati F J Mol Neurosci. 39(3):337-41. doi: 10.1007/s12031-009-9217-4. July 25, 2009. View on PubMed.
A novel SACS gene mutation in a Tunisian family. Bouhlal Y, El Euch-Fayeche G, Hentati F, Amouri R J Mol Neurosci. 39(3):333-6. doi: 10.1007/s12031-009-9212-9. June 16, 2009. View on PubMed.
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family. Bouhlal Y, Zouari M, Kefi M, Ben Hamida C, Hentati F, Amouri R J Neurogenet. 22(2):139-48. doi: 10.1080/01677060802025233. 2008. View on PubMed.
Distinct phenotypes within autosomal recessive ataxias not linked to already known loci. Bouhlal Y, El-Euch-Fayeche G, Amouri R, Hentati F Acta Myol. 24(2):155-61. October 2005. View on PubMed.
Occurrence of Shiga toxin-producing Escherichia coli O157 in selected dairy and meat products marketed in the city of Rabat, Morocco. Benkerroum N, Bouhlal Y, El Attar A, Marhaben A J Food Prot. 67(6):1234-7. June 2004. View on PubMed.
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