List of works - Olfa Messaoud

A Tunisian patient with two rare syndromes: triple a syndrome and congenital hypogonadotropic hypogonadism

scientific article

A founder large deletion mutation in Xeroderma pigmentosum-Variant form in Tunisia: implication for molecular diagnosis and therapy

scientific article

A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa

scientific article published on 08 January 2021

A novel POLH gene mutation in a xeroderma pigmentosum-V Tunisian patient: phenotype-genotype correlation.

scientific article

Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia

scientific article published on 26 November 2015

Comorbidity in the Tunisian population

scientific article published on 22 May 2015

Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia

scientific article

Epidemiological trends and clinicopathological features of cutaneous melanoma in sporadic and xeroderma pigmentosum Tunisian patients.

scientific article

Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases.

scientific article

Further evidence of mutational heterogeneity of the XPC gene in Tunisian families: a spectrum of private and ethnic specific mutations.

scientific article

Genetic homogeneity of mutational spectrum of group-A xeroderma pigmentosum in Tunisian patients

scientific article

H syndrome: Clinical, histological and genetic investigation in Tunisian patients

scientific article published on 29 May 2018

High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.

scientific article published on 05 February 2014

Identification of a Novel Mutation of LAMB3 Gene in a Lybian Patient with Hereditary Epidermolysis Bullosa by Whole Exome Sequencing

scientific article published on 24 March 2017

Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family.

scientific article

Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: implication for diagnosis in North Africa

scientific article published on 25 June 2013

Mutational spectrum of Xeroderma pigmentosum group A in Egyptian patients

scientific article

Polymorphisms in the human cytochrome P450 and arylamine N-acetyltransferase: susceptibility to head and neck cancers

scientific article

Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity.

scientific article

Specific aspects of consanguinity: some examples from the Tunisian population

scientific article

The experience of a Tunisian referral centre in prenatal diagnosis of Xeroderma pigmentosum

scientific article published on 7 September 2013

Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis

scientific article published on 2 November 2017

c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.

scientific article

List of works by Olfa Messaoud

A Tunisian patient with two rare syndromes: triple a syndrome and congenital hypogonadotropic hypogonadism

A founder large deletion mutation in Xeroderma pigmentosum-Variant form in Tunisia: implication for molecular diagnosis and therapy

A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa

A novel POLH gene mutation in a xeroderma pigmentosum-V Tunisian patient: phenotype-genotype correlation.

Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia

Comorbidity in the Tunisian population

Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia

Epidemiological trends and clinicopathological features of cutaneous melanoma in sporadic and xeroderma pigmentosum Tunisian patients.

Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases.

Further evidence of mutational heterogeneity of the XPC gene in Tunisian families: a spectrum of private and ethnic specific mutations.

Genetic homogeneity of mutational spectrum of group-A xeroderma pigmentosum in Tunisian patients

H syndrome: Clinical, histological and genetic investigation in Tunisian patients

High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.

Identification of a Novel Mutation of LAMB3 Gene in a Lybian Patient with Hereditary Epidermolysis Bullosa by Whole Exome Sequencing

Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family.

Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: implication for diagnosis in North Africa

Mutational spectrum of Xeroderma pigmentosum group A in Egyptian patients

Polymorphisms in the human cytochrome P450 and arylamine N-acetyltransferase: susceptibility to head and neck cancers

Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity.

Specific aspects of consanguinity: some examples from the Tunisian population

The experience of a Tunisian referral centre in prenatal diagnosis of Xeroderma pigmentosum

Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis

c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.