Siwar Gargouri-Baklouti

Sfax, Tunisia

Last Updated: 09/26/2026

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Found 11 publications

Y-chromosome haplogroups and Azoospermia Factor (AZF) analysis in Tunisian infertile male.

Y-chromosome haplogroups and Azoospermia Factor (AZF) analysis in Tunisian infertile male.

Journal: Human fertility (Cambridge, England)

Published: January 02, 2023

gr/gr-DAZ2-DAZ4-CDY1b deletion is a high-risk factor for male infertility in Tunisian population.

gr/gr-DAZ2-DAZ4-CDY1b deletion is a high-risk factor for male infertility in Tunisian population.

Journal: Gene

Published: May 09, 2016

Evaluation of the effect of c.2946+1G>T mutation on splicing in the SCN1A gene.

Evaluation of the effect of c.2946+1G>T mutation on splicing in the SCN1A gene.

Journal: Computational biology and chemistry

Published: July 19, 2014

Deletion of CDY1b copy of Y chromosome CDY1 gene is a risk factor of male infertility in Tunisian men.

Deletion of CDY1b copy of Y chromosome CDY1 gene is a risk factor of male infertility in Tunisian men.

Journal: Gene

Published: April 02, 2014

Combined deletion of DAZ2 and DAZ4 copies of Y chromosome DAZ gene is associated with male infertility in Tunisian men.

Combined deletion of DAZ2 and DAZ4 copies of Y chromosome DAZ gene is associated with male infertility in Tunisian men.

Journal: Gene

Published: April 02, 2014

Identification of a novel m.9588G > a missense mutation in the mitochondrial COIII gene in asthenozoospermic Tunisian infertile men.

Identification of a novel m.9588G > a missense mutation in the mitochondrial COIII gene in asthenozoospermic Tunisian infertile men.

Journal: Journal of assisted reproduction and genetics

Published: July 22, 2013

First functional analysis of a novel splicing mutation in the B3GALTL gene by an ex vivo approach in Tunisian patients with typical Peters plus syndrome.

First functional analysis of a novel splicing mutation in the B3GALTL gene by an ex vivo approach in Tunisian patients with typical Peters plus syndrome.

Journal: Gene

Published: May 11, 2013

A novel m.6307A>G mutation in the mitochondrial COXI gene in asthenozoospermic infertile men.

A novel m.6307A>G mutation in the mitochondrial COXI gene in asthenozoospermic infertile men.

Journal: Molecular reproduction and development

Published: April 06, 2013

Pericentric inversion of chromosom 12 [Inv (12) (p12q12)] associated with idiopathic azoospermia in one infertile Tunisian man.

Pericentric inversion of chromosom 12 [Inv (12) (p12q12)] associated with idiopathic azoospermia in one infertile Tunisian man.

Journal: Biochemical and biophysical research communications

Published: January 22, 2013

Possible association of a novel missense mutation A6375G in the mitochondrial cytochrome C oxidase I gene with asthenospermia in the Tunisian population.

Possible association of a novel missense mutation A6375G in the mitochondrial cytochrome C oxidase I gene with asthenospermia in the Tunisian population.

Journal: Genetic testing and molecular biomarkers

Published: October 04, 2012

Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men.

Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men.

Journal: Molecular biology reports

Published: June 08, 2012

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Last Updated: 09/26/2026