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All Outputs (9)

Mutation spectrum of PRPF31, genotype-phenotype correlation in retinitis pigmentosa, and opportunities for therapy (2020)
Journal Article

Pathogenic variants in pre-messenger RNA (pre-mRNA) splicing factor 31, PRPF31, are the second most common genetic cause of autosomal dominant retinitis pigmentosa (adRP) in most populations. This remains a completely untreatable and incurable form o... Read More about Mutation spectrum of PRPF31, genotype-phenotype correlation in retinitis pigmentosa, and opportunities for therapy.

Complex genetic patterns in human arise from a simple range-expansion model over continental landmasses (2018)
Journal Article

© 2018 Kanitz et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are cre... Read More about Complex genetic patterns in human arise from a simple range-expansion model over continental landmasses.

Relaxed observance of traditional marriage rules allows social connectivity without loss of genetic diversity (2015)
Journal Article

© 2015 The Author. Marriage rules, the community prescriptions that dictate who an individual can or cannot marry, are extremely diverse and universally present in traditional societies. A major focus of research in the early decades of modern anthro... Read More about Relaxed observance of traditional marriage rules allows social connectivity without loss of genetic diversity.