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Ten South American species are removed from the genus Odontocera Audinet-Serville (Coleoptera: Cerambycidae) and placed in Odontocroton Clarke new genus. The new genus is further organized into two informal groups. Group A includes Odontocroton flavicauda (Bates, 1873) new combination, Odontocroton flavirostris (Melzer, 1930) new combination, Odontocroton melzeri (Fisher, 1952) new combination and Odontocroton soror (Gounelle, 1911) new combination. Group B includes Odontocroton apicalis (Klug, 1825) new combination, Odontocroton quinquecallosus (Zajciw, 1963) new combination, Odontocroton sanguinolentus (Bates, 1873) new combination, Odontocroton septemtuberculatus (Zajciw, 1963) new combination, Odontocroton rufifrons (Fisher, 1937) new rank and new combination, and provisionally Odontocroton monnei (Zajciw, 1968), new combination. A monotypic new genus, Rhinobatesia Clarke, is described for the Central American species Rhinobatesia rugicollis (Bates, 1880) new combination, which was formerly in Odontocera. The Central American Odontocera nevermanni Fisher, 1930 is placed as a junior synonym of R. rugicollis, and Odontocera typhoeus Fisher, 1947 is placed as a junior synonym of Odontogracilis gracilis (Klug, 1825). A key to separate Odontocroton and Rhinobatesia as well as the species of the former is provided. All species are illustrated, including the tegmen of the aedeagus when available. Host flower records for the Bolivian species are also provided.
Background: Alzheimer's disease is a common debilitating dementia with known heritability, for which 20 late onset susceptibility loci have been identified, but more remain to be discovered. This study sought to identify new susceptibility genes, using an alternative gene-wide analytical approach which tests for patterns of association within genes, in the powerful genome-wide association dataset of the International Genomics of Alzheimer's Project Consortium, comprising over 7 m genotypes from 25,580 Alzheimer's cases and 48,466 controls.
Principal findings: In addition to earlier reported genes, we detected genome-wide significant loci on chromosomes 8 (TP53INP1, p = 1.4×10−6) and 14 (IGHV1-67 p = 7.9×10−8) which indexed novel susceptibility loci.
Significance: The additional genes identified in this study, have an array of functions previously implicated in Alzheimer's disease, including aspects of energy metabolism, protein degradation and the immune system and add further weight to these pathways as potential therapeutic targets in Alzheimer's disease.