Profil bibliographique

Insaf Rejeb

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7Publications signalées
110Citations signalées
2Affiliations récentes

Les institutions déclarées

Institut Pasteur de TunisTunis El Manar University

Les domaines associés

Diverse Scientific and Economic StudiesGenetic Associations and EpidemiologyGenomics and Rare DiseasesLegal Cases and CommentaryHuman auditory perception and evaluation

Les publications récentes

2016 article OpenAlex

Gender-specific associations of genetic variants with metabolic syndrome components in the Tunisian population

Sahar Elouej, Insaf Rejeb, Redha Attaoua, Majdi Nagara et autres

AIM OF THE STUDY: Recent genome-wide association studies (GWASs) have identified many genetic variants associated with metabolic syndrome (MetS). However, their contribution to MetS in ethnic groups in Tunisia is largely unexplored. In this study, we aim to examine the associations of …

Tunisie (code pays fourni par la source)

25 citations Endocrine Research
2015 article OpenAlex

Differential impact of consanguineous marriages on autosomal recessive diseases in T unisia

Nizar Ben Halim, Sana Hsouna, Khaled Lasram, Insaf Rejeb et autres

OBJECTIVES: Consanguinity is common in Tunisia. However, little information exists on its impact on recessive disorders. In this study, we evaluate the impact of consanguineous marriages on the occurrence of some specific autosomal recessive disorders and consider how other factors, such as …

Tunisie, ru (code pays fourni par la source)

31 citations American Journal of Human Biology
2014 article OpenAlex

Specific Aspects of Consanguinity: Some Examples from the Tunisian Population

Lilia Romdhane, Nizar Ben Halim, Insaf Rejeb, Rym Kéfi et autres

Located at the cross-road between Europe and Africa, Tunisia is a North African country of 11 million inhabitants. Throughout its history, it has been invaded by different ethnic groups. These historical events, and consanguinity, have impacted on the spectrum and frequency of …

Tunisie, fr, it (code pays fourni par la source)

25 citations Human Heredity
Notice OpenAlex

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