New trend in the epidemiology of thalassaemia
CK Li - Best Practice & Research Clinical Obstetrics & …, 2017 - Elsevier
Highlights•Thalassaemia mutation is common in some ethnic groups.•Prenatal screening
and diagnosis can prevent severe cases.•Countries receiving migrants should establish …
and diagnosis can prevent severe cases.•Countries receiving migrants should establish …
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
Abstract The Greater Middle East (GME) has been a central hub of human migration and
population admixture. The tradition of consanguinity, variably practiced in the Persian Gulf …
population admixture. The tradition of consanguinity, variably practiced in the Persian Gulf …
Keratoconus in Africa: a systematic review and meta‐analysis
PK Akowuah, E Kobia‐Acquah… - Ophthalmic and …, 2021 - Wiley Online Library
Purpose The aim of this review is to evaluate the prevalence of and factors associated with
keratoconus in Africa. Method A systematic online literature search was conducted for …
keratoconus in Africa. Method A systematic online literature search was conducted for …
Qatar genome: Insights on genomics from the Middle East
Despite recent biomedical breakthroughs and large genomic studies growing momentum,
the Middle Eastern population, home to over 400 million people, is underrepresented in the …
the Middle Eastern population, home to over 400 million people, is underrepresented in the …
[HTML][HTML] Global distribution of consanguinity and their impact on complex diseases: Genetic disorders from an endogamous population
A Bener, RR Mohammad - Egyptian Journal of Medical Human Genetics, 2017 - Elsevier
Background Marriage between close relatives has been practised globally since the early
existence of human society. The role of consanguinity and inbreeding affecting human …
existence of human society. The role of consanguinity and inbreeding affecting human …
Thousands of Qatari genomes inform human migration history and improve imputation of Arab haplotypes
RM Razali, J Rodriguez-Flores, M Ghorbani… - Nature …, 2021 - nature.com
Arab populations are largely understudied, notably their genetic structure and history. Here
we present an in-depth analysis of 6,218 whole genomes from Qatar, revealing extensive …
we present an in-depth analysis of 6,218 whole genomes from Qatar, revealing extensive …
Consanguineous marriages and their association with women's reproductive health and fertility behavior in Pakistan: secondary data analysis from Demographic and …
Background Pakistan has been showing consistently the highest prevalence of
consanguinity. The popularity of consanguineous marriages is not declining in the country …
consanguinity. The popularity of consanguineous marriages is not declining in the country …
The Qatari population's genetic structure and gene flow as revealed by the Y chromosome
EK Almohammed, A Hadi, M Al-Asmakh, H Lazim - Plos one, 2023 - journals.plos.org
The Y-chromosome has been widely used in forensic genetic applications and human
population genetic studies due to its uniparental origins. A large database on the Qatari …
population genetic studies due to its uniparental origins. A large database on the Qatari …
The impact of recent demography on functional genetic variation in North African human groups
M Lucas-Sánchez, A Abdeli, A Bekada… - Molecular Biology …, 2024 - academic.oup.com
The strategic location of North Africa has made the region the core of a wide range of human
demographic events, including migrations, bottlenecks, and admixture processes. This has …
demographic events, including migrations, bottlenecks, and admixture processes. This has …
Exploring the global landscape of genetic variation in coagulation factor XI deficiency
R Asselta, EM Paraboschi, V Rimoldi… - Blood, The Journal …, 2017 - ashpublications.org
Factor XI (FXI) deficiency is an autosomal bleeding disorder, usually posttrauma or
postsurgery, characterized by reduced levels of coagulation FXI in plasma. The disease is …
postsurgery, characterized by reduced levels of coagulation FXI in plasma. The disease is …