Three separate and parallel North American Carduelis evolutionary radiations have been identified. North American siskin radiation (starting about 2.7 million years ago) comprises siskin, Antillean siskin, black-capped siskin, pine siskin and pine siskin perplexus. C. spinus could have passed to America through the Beringia or Greenland coast and, during Pliocene Epoch, reached the Antilles and evolved into Antillean siskin (C. dominicensis), endemic to Hispaniola Island. It is ancestor of pine siskin. Pine Siskin, also a sister taxon of C. spinus, thrives in North America from Alaska to Guatemala since about 0.2 MYA. It lives below the Mexican Isthmus in the highlands from northern Chiapas (Mexico) to western Guatemala. Black-capped siskin (C. atriceps) is a sister species of C. spinus, with which it shares habitat and territory. C. pinus green-backed morphs may have been mistaken by C. atriceps which is a grey-backed finch. Mesoamerican goldfinch radiation (starting about 5 million years ago) includes C. tristis (American goldfinch), C. psaltria (lesser goldfinch) and C. lawrencei (Lawrence's goldfinch). They all thrive in western United States and Mexico, down to northern South America. C. psaltria is a North American bird that colonized South American habitats to North Peru and evolved into darker head and back while going southwards. South American siskin radiation started about 3.5 million years ago; parental C. notata thrives in Mexican mountains and successfully colonized South America, giving rise to this radiation. South American Carduelis radiation occurred only when mesothermal plants from the Rocky Mountains invaded the Andean spine after emergence of the Panama Isthmus.

Amerindian Mapuche (Araucanians) are now living in Chile and Argentina at both sides of Andean Mountains. They are anthropologically and genetically different from southernmost South America Patagonian Amerindians. Most of the HLA alleles found in our Mapuche sample are frequent or very frequent in North and South America Amerindians: (1) Class I: A*02:01, A*03:01, A*68:01, B*39:09, B*51:01, (2) Class II: DRB1*03:01, DRB1*04:03, DRB1*07:01, DRB1*08:02, DRB1*14:02, DRB1*16:02. One of the nine most frequent extended haplotypes seems to be from European origin, suggesting the existence of a degree of admixture with Europeans in our Mapuche sample. It has been calculated of about 11 % admixture. Three of the extended haplotypes are also found in other Amerindians and five of them are newly found in Mapuche Amerindians: A*68:01-B*39:09-DRB1*08:02-DQB1*04:02; A*68:01-B*51:01-DRB1*04:03-DQB1*03:02; A*29:01-B*08:01-DRB1*03:01-DQB1*02:01; A*02:01-B*15:01-DRB1*04:03-DQB1*03:02; A*33:01-B*14:02-DRB1*07:01-DQB1*03:03. The medical importance of calculating HLA profile is discussed on the diagnostic (HLA and disease) and therapeutical bases of HLA pharmacogenomics and on the construction of a virtual transplantation HLA list profile. Also, anthropological conclusions are drawn.

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Kurds from Iraq (Dohuk and Erbil Area, North Iraq) have been analyzed for HLA genes. Their HLA genetic profile has been compared with that of other Kurd groups from Iran and Tbilisi (Georgia, Caucasus) and also Worldwide populations. A total of 7,746 HLA chromosomes have been used. Genetic distances, NJ dendrograms and correspondence analyses have been carried out. Haplotype HLA-B*52—DRB1*15 is present in all three analyzed Kurd populations. HLA-A*02-B*51-DRB1*11 is present in Iraq and Georgia Kurds. Haplotypes common to Iran and Iraq Kurds are HLA DRB1*11—DQB1*03, HLA DRB1*03—DQB1*02 and others in a lower frequency. Our HLA study conclusions are that Kurds most probably belong to an ancient Mediterranean / Middle East / Caucasian genetic substratum and that present results and those previously obtained by us in Kurds may be useful for Medicine in future Kurd transplantation programs, HLA Epidemiology (HLA linked diseases) and Pharmacogenomics (HLA-associated drug side effects) and also for Anthropology. It is discussed that one of the most ancient Kurd ancestor groups is in Hurrians (2,000 years BC).

HLA-A, -B, -DQB1, and -DRB1 typing has been performed in a sample of Georgian population (South Caucasus). Allele frequencies, neighbour joining and correspondence relatedness analyses and extended HLA haplotypes have been obtained with comparison with other Middle East and Mediterranean populations. Our Georgian sample tends to be genetically related in these analyses with Eastern Mediterraneans and Middle East people. This is important for future regional transplant programs, and Georgian HLA and disease epidemiology and pharmacogenomics.