TRIFI CHOGRANI Manel

RGS6: a novel gene associated with congenital cataract, mental retardation, and microcephaly in a Tunisian family, Investigative Ophthalmology and Visual Science, vol. 56, N° 2, Décembre 2014

KHARRAT Maher

The relationship between telomere length and clinicopathologic characteristics in colorectal cancers among Tunisian patients, Tumor Biology, vol. n, N° n, Juin 2015

KELMEMI Wided, CHELLY Imen, KHARRAT Maher

Consanguinity And Homozygosity Among Tunisian Patients With An Autosomal Recessive Disorder Journal of Biosocial Science, vol. 47, N° 6, Novembre 2015

KELMEMI Wided

Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome, BMC Medical Genetics, vol. 20, N° n, Juillet 2015

KELMEMI Wided, KHARRAT Maher

Estimating the total pathogenic allele frequency of autosomal recessive disorders in case of consanguinity, Human Heredity, vol. 80, N° n, Janvier 2015

TAJOURI Asma , KHARRAT Maher, M'RAD Ridha

In vitro functional characterization of the novel DHH mutations p.(Asn337Lysfs*24) and p.(Glu212Lys) associated with gonadal dysgenesis, Human Mutation, vol. 39, N° 12, pp. 2097-2109, Octobre 2018