Leila Houti
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Explore the profile of Leila Houti including associated specialties, affiliations and a list of published articles.
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10
Citations
127
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Recent Articles
1.
Heroual N, Boukfoussa N, Houti L
Pan Afr Med J
. 2024 Aug;
47():183.
PMID: 39092017
Introduction: preterm births continue to be the main cause of infant and child mortality as well as sensory-motor disabilities and neurodevelopmental difficulties worldwide. The rate of preterm births has been...
2.
Boulenouar H, Hetraf S, Djellouli H, Meroufel D, Fodil F, Hammani-Medjaoui I, et al.
Afr Health Sci
. 2020 Nov;
20(2):735-744.
PMID: 33163038
Background: Coronary Heart Disease (CHD) is a major cause of morbidity and mortality over the world; intermediate traits associated with CHD commonly studied can be influenced by a combination of...
3.
Houti L, Hamani-Medjaoui I, Lardjam-Hetraf S, Ouhaibi-Djellouli H, Chougrani S, Goumidi L, et al.
Ethn Dis
. 2016 Feb;
26(1):99-106.
PMID: 26843802
Background: Aging and lifestyle changes had led to an epidemiological transition, with a significant impact on the incidence of cardiovascular diseases in North Africa. Objective: The aim of this study...
4.
Meroufel D, Mediene-Benchekor S, Lardjam-Hetraf S, Ouhaibi-Djellouli H, Boulenouar H, Hamani-Medjaoui I, et al.
Int J Clin Exp Pathol
. 2015 Aug;
8(6):7358-63.
PMID: 26261636
Genome-wide association studies have identified many lipid-associated loci primarily in European and Asian populations. In view of the differences between ethnic groups in terms of the frequency and impact of...
5.
Meroufel D, Ouhaibi-Djellouli H, Mediene-Benchekor S, Hermant X, Grenier-Boley B, Lardjam-Hetraf S, et al.
Gene
. 2015 May;
567(2):159-63.
PMID: 25934190
Background: In European populations, the NPPB rs198389 single nucleotide polymorphism (SNP) is associated with a reduced risk of type 2 diabetes mellitus (T2DM). We investigated the putative associations between NPPB...
6.
Ouhaibi-Djellouli H, Mediene-Benchekor S, Lardjam-Hetraf S, Hamani-Medjaoui I, Meroufel D, Boulenouar H, et al.
BMC Genet
. 2014 Dec;
15:134.
PMID: 25491720
Background: The transcription factor 7-like 2 (TCF7L2) gene is the most significant genetic risk factor for type 2 diabetes (T2D). Association analyses were performed on participants (n = 751, aged...
7.
Badsi M, Mediene-Benchekor S, Ouhaibi-Djellouli H, Lardjam-Hetraf S, Boulenouar H, Meroufel D, et al.
BMC Genet
. 2014 Nov;
15:128.
PMID: 25422053
Background: Genome-wide association studies have identified variants associated with BMI in populations of European descent. We sought to establish whether genetic variants that are robustly associated with BMI could modulate...
8.
Boulenouar H, Benchekor S, Meroufel D, Hetraf S, Djellouli H, Hermant X, et al.
Lipids Health Dis
. 2013 Oct;
12:155.
PMID: 24160669
Background: The importance of apolipoprotein E (APOE) in lipid and lipoprotein metabolism is well established. However, the impact of APOE polymorphisms has never been investigated in an Algerian population. This...
9.
Bounoua L, Kahime K, Houti L, Blakey T, Ebi K, Zhang P, et al.
Int J Environ Res Public Health
. 2013 Aug;
10(8):3172-91.
PMID: 23912199
Shifts in surface climate may have changed the dynamic of zoonotic cutaneous leishmaniasis (ZCL) in the pre-Saharan zones of North Africa. Caused by Leishmania major, this form multiplies in the...
10.
Bertherat E, Bekhoucha S, Chougrani S, Razik F, Duchemin J, Houti L, et al.
Emerg Infect Dis
. 2008 Feb;
13(10):1459-62.
PMID: 18257987
An outbreak of plague occurred in the region of Oran, Algeria, from June to July 2003. Algeria had not reported this disease for >50 years. Eighteen bubonic cases were identified,...