Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Houssein Khodjet El-khil"'
Autor:
Hocine Badache, Sami Boussetta, Amel Benammar Elgaaeid, Lotfi Cherni, Houssein Khodjet El-khil
Publikováno v:
Annals of Human Biology, Vol 46, Iss 2, Pp 150-159 (2019)
Background: In Algeria, as in all North Africa, Berbers constitute the old background of the population. Today, Berber speakers account for only ∼ 25% of Algerians. This decline is the product of a complex human settlement from pre-history to recen
Externí odkaz:
https://doaj.org/article/1c0a1593336c4bedbc4442bdefad6a93
Autor:
Shaza Alkhidir, Karen El-Akouri, Nader Al-Dewik, Houssein Khodjet-El-khil, Sarah Okashah, Nazmul Islam, Tawfeg Ben-Omran, Mashael Al-Shafai
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract Hearing loss is the most predominant sensory defect occurring in pediatrics, of which, 66% cases are attributed to genetic factors. The prevalence of hereditary hearing loss increases in consanguineous populations, and the prevalence of hear
Externí odkaz:
https://doaj.org/article/a5b78ae7fd3746b39dd5edc2d75c9ff8
Autor:
Sarra Elkamel, Sofia L. Marques, Luis Alvarez, Veronica Gomes, Sami Boussetta, Soufia Mourali-Chebil, Houssein Khodjet-El-Khil, Lotfi Cherni, Amel Benammar-Elgaaied, Maria J. Prata
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract To obtain refreshed insights into the paternal lineages of Tunisian populations, Y-chromosome diversity was assessed in two populations belonging to an Arab genealogical lineage, Kairouan and Wesletia, as well as in four Tunisian Andalusian
Externí odkaz:
https://doaj.org/article/749e912f28314418ba7aa6763a6b8601
Autor:
Mariem Sidenna, Houssein Khodjet-El-khil, Hajar Al Mulla, Mashael Al-Shafai, Hind Hassan Habish, Reem AL-Sulaiman, Salha Bujassoum Al-Bader
Publikováno v:
Genes; Volume 13; Issue 11; Pages: 2176
Lynch syndrome (LS) is the most common cause of hereditary colorectal cancers (CRC) and is associated with an increased risk for ovarian and endometrial cancers. There is lack of knowledge on the epidemiology of LS in the non-Caucasian populations es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d061ccee52d19792fa41e43ff9a25d36
https://pubmed.ncbi.nlm.nih.gov/36421850
https://pubmed.ncbi.nlm.nih.gov/36421850
Autor:
Sarah Okashah, Dhanya Vasudeva, Aya El Jerbi, Houssein Khodjet-El-khil, Mashael Al-Shafai, Najeeb Syed, Marios Kambouris, Sharda Udassi, Luis R. Saraiva, Hesham Al-Saloos, Jai Udassi, Kholoud N. Al-Shafai
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1369
Congenital heart disease (CHD) is one of the most common forms of birth defects worldwide, with a prevalence of 1–2% in newborns. CHD is a multifactorial disease partially caused by genetic defects, including chromosomal abnormalities and single ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff206244e831150a14b7d52051050544
https://pubmed.ncbi.nlm.nih.gov/36011280
https://pubmed.ncbi.nlm.nih.gov/36011280
Autor:
Sarra Elkamel, Amel Benammar Elgaaied, Houssein Khodjet-El-Khil, Kenneth K. Kidd, Nesrine Ben Salem, Andrew J. Pakstis, Sami Boussetta, Lotfi Cherni
Publikováno v:
Gene. 696:186-196
The COMT gene encodes for catechol-O-methyl-transferase, an enzyme playing a major role in regulation of synaptic catecholamine neurotransmitters. Investigating 4 markers of the COMT gene (rs2020917, rs4818, rs4680, rs9332377) in 6 Tunisian populatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b6e4b60c55c55d29a381309e51cef9c
https://doi.org/10.1016/j.gene.2019.02.021
https://doi.org/10.1016/j.gene.2019.02.021
Autor:
Sofia L. Marques, Luis Alvarez, Amel Benammar-Elgaaied, Soufia Mourali-Chebil, Maria João Prata, Verónica Gomes, Sarra Elkamel, Sami Boussetta, Houssein Khodjet-El-Khil, Lotfi Cherni
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
To obtain refreshed insights into the paternal lineages of Tunisian populations, Y-chromosome diversity was assessed in two populations belonging to an Arab genealogical lineage, Kairouan and Wesletia, as well as in four Tunisian Andalusian populatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55fecdcf56cb32ea98ae759ea48f7bad
https://pubmed.ncbi.nlm.nih.gov/34344940
https://pubmed.ncbi.nlm.nih.gov/34344940
Autor:
Nina Mjølsnes Salvo, Ozlem Bulbul, Sibte Hadi, Amel Benammar Elgaaied, Andrew J. Pakstis, Mustafa Dogan, Pavlos I. Neophytou, Kenneth K. Kidd, Vania Pereira, Serkan Dogan, Kirstin Janssen, Houssein Khodjet-El-Khil, Haseena Rajeevan, Hasan Emin Balkaya, Sami Boussetta, Cemal Gurkan, Eida Khalaf Almohammed, Gunn-Hege Olsen, Lotfi Cherni, Ditte Truelsen, Usha Soundararajan, Judith R. Kidd
Publikováno v:
Pakstis, A, Gurkan, C, Dogan, M, Balkaya, H E, Dogan, S, Neophytou, P I, Cherni, L, Boussetta, S, Khodjet-El-Khil, H, ElGaaied, A B A, Salvo, N M, Janssen, K, Olsen, G-H, Hadi, S, Almohammed, E K, Pereira, V, Truelsen, D M, Bulbul, O, Soundararajan, U, Rajeevan, H, Kidd, J R & Kidd, KK 2019, ' Genetic relationships of European, Mediterranean, and SW Asian populations using a panel of 55 AISNPs ', European Journal of Human Genetics, vol. 27, pp. 1885-1893 . https://doi.org/10.1038/s41431-019-0466-6
European Journal of Human Genetics
European Journal of Human Genetics
The set of 55 ancestry informative SNPs (AISNPs) originally developed by the Kidd Lab has been studied on a large numberof populations and continues to be applied to new population samples. The existing reference database of population samplesallows
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::091106bb89fdd299e85f2bb62265039d
https://hdl.handle.net/10037/17115
https://hdl.handle.net/10037/17115
Autor:
Amel Benammar Elgaaeid, Hocine Badache, Houssein Khodjet El-khil, Sami Boussetta, Lotfi Cherni
Publikováno v:
Annals of human biology. 46(2)
Background: In Algeria, as in all North Africa, Berbers constitute the old background of the population. Today, Berber speakers account for only ∼ 25% of Algerians. This decline is the product of a complex human settlement from pre-history to recen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b030eaad531ab73be04c9dfb990d846
https://pubmed.ncbi.nlm.nih.gov/30857436
https://pubmed.ncbi.nlm.nih.gov/30857436
Autor:
Maria João Prata, Amel Benammar-Elgaaied, Sofia L. Marques, Sami Boussetta, Sarra Elkamel, Lotfi Cherni, Houssein Khodjet-El-Khil, Luis Alvarez
Publikováno v:
Annals of Human Biology. 44:180-190
Recent genomic analyses suggest that the current North African gene pool was mainly influenced by population flow coming from the East that altered the genetic structure of autochthonous Berber populations. Such genetic flow has not been extensively
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1bb7531642dd77c02760e6df9038c54
https://doi.org/10.1080/03014460.2016.1205135
https://doi.org/10.1080/03014460.2016.1205135