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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Ancestry of the Timorese: Age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world

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Συγγραφέας
Morrison, M. A.; Magalhaes, T. R.; Ramke, J.; Smith, S. E.; Ennis, S.; Simpson, C. L.; Portas, L.; Murgia, F.; Ahn, J.; Dardenne, C.; Mayne, K.; Robinson, R.; Morgan, D. J.; Brian, G.; Lee, L.; Woo, S. J.; Zacharaki, F.; Tsironi, E. E.; Miller, J. W.; Kim, I. K.; Park, K. H.; Bailey-Wilson, J. E.; Farrer, L. A.; Stambolian, D.; DeAngelis, M. M.
Ημερομηνία
2015
DOI
10.3389/fgene.2015.00238
Λέξη-κλειδί
Age-related macular degeneration
Ancestry
Complex disease and epidemiology
Population genetics
DNA
hemoglobin A1c
mitochondrial DNA
adult
age related macular degeneration
allele
ancestry group
Article
Caucasian
chromosome 3
chromosome 6
exome
female
gene frequency
genetic variability
genotype
haplogroup
human
major clinical study
male
mitochondrial genome
ophthalmoscopy
principal component analysis
short tandem repeat
single nucleotide polymorphism
Timor-Leste
Εμφάνιση Μεταδεδομένων
Επιτομή
We observed that the third leading cause of blindness in the world, age-related macular degeneration (AMD), occurs at a very low documented frequency in a population-based cohort from Timor-Leste. Thus, we determined a complete catalog of the ancestry of the Timorese by analysis of whole exome chip data and haplogroup analysis of SNP genotypes determined by sequencing the Hypervariable I and II regions of the mitochondrial genome and 17 genotyped YSTR markers obtained from 535 individuals. We genotyped 20 previously reported AMD-associated SNPs in the Timorese to examine their allele frequencies compared to and between previously documented AMD cohorts of varying ethnicities. For those without AMD (average age > 55 years), genotype and allele frequencies were similar for most SNPs with a few exceptions. The major risk allele of HTRA1 rs11200638 (10q26) was at a significantly higher frequency in the Timorese, as well as 3 of the 5 protective CFH (1q32) SNPs (rs800292, rs2284664, and rs12066959). Additionally, the most commonly associated AMD-risk SNP, CFH rs1061170 (Y402H), was also seen at a much lower frequency in the Korean and Timorese populations than in the assessed Caucasian populations (C ~7 vs. ~40%, respectively). The difference in allele frequencies between the Timorese population and the other genotyped populations, along with the haplogroup analysis, also highlight the genetic diversity of the Timorese. Specifically, the most common ancestry groupings were Oceanic (Melanesian and Papuan) and Eastern Asian (specifically Han Chinese). The low prevalence of AMD in the Timorese population (2 of 535 randomly selected participants) may be due to the enrichment of protective alleles in this population at the 1q32 locus. © 2015 Morrison, Magalhaes, Ramke, Smith, Ennis, Simpson, Portas, Murgia, Ahn, Dardenne, Mayne, Robinson, Morgan, Brian, Lee, Woo, Zacharaki, Tsironi, Miller, Kim, Park, Bailey-Wilson, Farrer, Stambolian and DeAngelis.
URI
http://hdl.handle.net/11615/31134
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]
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