Results 51 to 60 of about 84,890 (266)

Geographic patterns of genome admixture in Latin American Mestizos. [PDF]

open access: yesPLoS Genetics, 2008
The large and diverse population of Latin America is potentially a powerful resource for elucidating the genetic basis of complex traits through admixture mapping.
Sijia Wang   +27 more
doaj   +1 more source

Laboratory colonisation and genetic bottlenecks in the tsetse fly Glossina pallidipes [PDF]

open access: yes, 2014
Background The IAEA colony is the only one available for mass rearing of Glossina pallidipes, a vector of human and animal African trypanosomiasis in eastern Africa. This colony is the source for Sterile Insect Technique (SIT) programs in East Africa.
Ciosi, Marc   +2 more
core   +3 more sources

Genetic continuity across a deeply divergent linguistic contact zone in North Maluku, Indonesia

open access: yesBMC Genetics, 2011
Background The islands of North Maluku, Indonesia occupy a central position in the major prehistoric dispersal streams that shaped the peoples of Island Southeast Asia and the Pacific. Within this region a linguistic contact zone exists where speakers of
Wilder Jason A   +6 more
doaj   +1 more source

Inference of population splits and mixtures from genome-wide allele frequency data [PDF]

open access: yes, 2012
Many aspects of the historical relationships between populations in a species are reflected in genetic data. Inferring these relationships from genetic data, however, remains a challenging task. In this paper, we present a statistical model for inferring
A Keinan   +66 more
core   +5 more sources

Interactions between genetic admixture, ethnic identity, APOE genotype and dementia prevalence in an admixed Cuban sample; a cross-sectional population survey and nested case-control study

open access: yesBMC Medical Genetics, 2011
Background The prevalence and incidence of dementia are low in Nigeria, but high among African-Americans. In these populations there is a high frequency of the risk-conferring APOE-e4 allele, but the risk ratio is less than in Europeans.
Hernandez Milagros   +9 more
doaj   +1 more source

Molecular footprints of the Holocene retreat of dwarf birch in Britain [PDF]

open access: yes, 2014
© 2014 The Authors. Molecular Ecology Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original ...
Atkinson MD   +14 more
core   +1 more source

The genetic structure and admixture of Manchus and Koreans in northeast China

open access: yesAnnals of Human Biology, 2023
Background The fine-scale genetic profiles and population history of Manchus and Koreans remain unclear. Aim To infer a fine-scale genetic structure and admixture of Manchu and Korean populations.
Na Sun   +5 more
doaj   +1 more source

Genomic Insights Into the Unique Demographic History and Genetic Structure of Five Hmong-Mien-Speaking Miao and Yao Populations in Southwest China

open access: yesFrontiers in Ecology and Evolution, 2022
Southern China was the original center of multiple ancestral populations related to modern Hmong-Mien, Tai-Kadai, Austroasiatic, and Austronesian people.
Meiqing Yang   +27 more
doaj   +1 more source

The Drosophila genome nexus: a population genomic resource of 623 Drosophila melanogaster genomes, including 197 from a single ancestral range population. [PDF]

open access: yes, 2015
Hundreds of wild-derived Drosophila melanogaster genomes have been published, but rigorous comparisons across data sets are precluded by differences in alignment methodology.
Cardeno, Charis M   +7 more
core   +1 more source

Mechanochemical Synthesis and Characterization of Nanostructured ErB4 and NdB4 Rare‐Earth Tetraborides

open access: yesAdvanced Engineering Materials, Volume 27, Issue 6, March 2025.
ErB4 and NdB4 nanostructured powders are produced by mechanochemical synthesis. 5 h mechanical alloying and 4 M HCl acid leaching are used in the production. ErB4 and NdB4 powders exhibit maximum magnetization of 0.4726 emu g−1 accompanied with an antiferromagnetic‐to‐paramagnetic phase transition at about TN = 18 K and 0.132 emu g−1 with a maximum at ...
Burçak Boztemur   +5 more
wiley   +1 more source

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