The human Y chromosome: an evolutionary marker comes of age

By M. Jobling, Chris Tyler-Smith. Nature reviews genetics, 2003

964 citations recorded by the source corpus.

Subfields: Genetics, Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/988259cad668e4229a5645f0e92f9bb574632fbb

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In Genetics

1. S. Rootsi
2. D. Fuller
3. J. Krause
4. Mark Stoneking

In Molecular Biology

1. J. Krause
2. S. Rootsi
3. D. Fuller

In Plant Science

1. S. Rootsi
2. D. Fuller
3. Robin G. Allaby

Citations in the corpus

• Human dispersal across diverse environments of Asia during the Upper Pleistocene (2013, background): “While studies of mtDNA (Richards et al., 1996; Krings et al., 1997; Handt et al., 1998; Serre et al., 2004; Green et al., 2008) and the Y-chromosome (Jobling and Tyler-Smith, 2003) have not indicated admixture, for example, it was widely recognized that autosomal DNA might tell a different story.”
• Human Y-chromosomal variation in European populations (2004, background): “One such example is a 2kb deletion in 12f2 marker (Casanova et al. 1985), used for defining haplogroup J according to the present nomenclature (YCC 2002).”
• Learning about human population history from ancient and modern genomes (2011, background): “Prior to the availability of genome-wide data, human population history studies relied largely on single genetic loci, such as mitochondrial DNA (mtDNA) or the non-recombining regions of the Y chromosome (NRY”
• New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree. (2008, background): “The geographic distribution of haplogroup H is almost entirely restricted to the Indian subcontinent (Jobling and Tyler-Smith 2003; Karafet et al. 2005; Sengupta et al. 2006).”
• Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation (2009, background): “…portions of the human genome have important applications in a wide range of fields including evolutionary anthropology and population history (Jobling and Tyler-Smith, 2003; Torroni et al., 2006; Underhill and Kivisild, 2007), medical genetics (Krausz et al., 2004; Taylor and Turnbull,…”