<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">O&#039;Bleness, M</style></author><author><style face="normal" font="default" size="100%">Searles, VB</style></author><author><style face="normal" font="default" size="100%">Ajit Varki</style></author><author><style face="normal" font="default" size="100%">Gagneux, P</style></author><author><style face="normal" font="default" size="100%">Sikela, JM</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evolution of genetic and genomic features unique to the human lineage</style></title><secondary-title><style face="normal" font="default" size="100%">Nat Rev Genet</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nature reviews. Genetics</style></alt-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">*Evolution</style></keyword><keyword><style  face="normal" font="default" size="100%">*Genome</style></keyword><keyword><style  face="normal" font="default" size="100%">Animals</style></keyword><keyword><style  face="normal" font="default" size="100%">Chromosomes</style></keyword><keyword><style  face="normal" font="default" size="100%">Comparative Genomic Hybridization</style></keyword><keyword><style  face="normal" font="default" size="100%">Genetic Speciation</style></keyword><keyword><style  face="normal" font="default" size="100%">Genomics/trends</style></keyword><keyword><style  face="normal" font="default" size="100%">Hominidae/genetics</style></keyword><keyword><style  face="normal" font="default" size="100%">Human</style></keyword><keyword><style  face="normal" font="default" size="100%">Human/genetics</style></keyword><keyword><style  face="normal" font="default" size="100%">Humans</style></keyword><keyword><style  face="normal" font="default" size="100%">Karyotyping</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenotype</style></keyword><keyword><style  face="normal" font="default" size="100%">Primates/genetics</style></keyword><keyword><style  face="normal" font="default" size="100%">Species Specificity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Dec</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/23154808</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">12</style></number><edition><style face="normal" font="default" size="100%">2012/11/17</style></edition><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">853-66</style></pages><isbn><style face="normal" font="default" size="100%">1471-0064 (Electronic)14</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Given the unprecedented tools that are now available for rapidly comparing genomes, the identification and study of genetic and genomic changes that are unique to our species have accelerated, and we are entering a golden age of human evolutionary genomics. Here we provide an overview of these efforts, highlighting important recent discoveries, examples of the different types of human-specific genomic and genetic changes identified, and salient trends, such as the localization of evolutionary adaptive changes to complex loci that are highly enriched for disease associations. Finally, we discuss the remaining challenges, such as the incomplete nature of current genome sequence assemblies and difficulties in linking human-specific genomic changes to human-specific phenotypic traits.&lt;/p&gt;
</style></abstract><work-type><style face="normal" font="default" size="100%">Comparative StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov&#039;tReview</style></work-type><notes><style face="normal" font="default" size="100%">&lt;p&gt;&lt;span role=&quot;menubar&quot;&gt;Nat Rev Genet.&lt;/span&gt;&amp;nbsp;2012 Dec;13(12):853-66. doi: 10.1038/nrg3336.&lt;/p&gt;
</style></notes><auth-address><style face="normal" font="default" size="100%">Department of Biochemistry and Molecular Genetics, Human Medical Genetics and Neuroscience Programs, University of Colorado School of Medicine, Aurora, Colorado 80045, USA.</style></auth-address></record></records></xml>