R
Rosalind M. Harding
Researcher at John Radcliffe Hospital
Publications - 20
Citations - 2356
Rosalind M. Harding is an academic researcher from John Radcliffe Hospital. The author has contributed to research in topics: Population & Haplotype. The author has an hindex of 14, co-authored 20 publications receiving 2323 citations.
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Journal Article
Origin and evolution of Native American mtDNA variation: a reappraisal.
TL;DR: Reappraising mtDNA control region sequences from aboriginal Siberians and Native Americans confirms in agreement with linguistic, archaeological and climatic evidence that the major wave of migration brought one population, ancestral to the Amerinds, from northeastern Siberia to America 20,000-25,000 years ago.
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The population genetics of the haemoglobinopathies.
TL;DR: It is argued that malaria selection has operated relatively recently on human populations (within the last 5000 years) and the present distribution of haemoglobinopathies is seen as the result of selection elevating sporadic mutations in local populations.
Journal Article
Archaic African and Asian lineages in the genetic ancestry of modern humans
Rosalind M. Harding,Stephanie M. Fullerton,Robert C. Griffiths,Jacquelyn Bond,Martin John Cox,Julie A. Schneider,Danielle S. Moulin,John B. Clegg +7 more
TL;DR: Patterns of beta-globin diversity suggest extensive worldwide late Pleistocene gene flow and are not easily reconciled with a unidirectional migration out of Africa 100,000 years ago and total replacement of archaic populations in Asia.
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Molecular Analysis of the β-Globin Gene Cluster in the Niokholo Mandenka Population Reveals a Recent Origin of the βS Senegal Mutation
Mathias Currat,Mathias Currat,G. Trabuchet,David C. Rees,Pascale Perrin,Rosalind M. Harding,John B. Clegg,André Langaney,Laurent Excoffier,Laurent Excoffier +9 more
TL;DR: A large and ethnically well-defined Mandenka sample from eastern Senegal was analyzed for the polymorphism of the β-globin gene cluster, showing the presence of four transversions, five transitions, and a composite microsatellite polymorphism.
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Why are some genetic diseases common ? Distinguishing selection from other processes by molecular analysis of globin gene variants
TL;DR: It is shown how for each disease it is possible to recognize a pattern of regionally specific mutations that is best explained as the result of selection, and it is concluded that although this combination of molecular and population genetics is successful when applied to the study of haemoglobinopathies, it may not be so easy to apply it to theStudy of other genetic diseases.