Literature DB >> 31706744

Next generation sequencing and the classical HLA loci in full heritage Pima Indians of Arizona: Defining the core HLA variation for North American Paleo-Indians.

Robert C Williams1, William C Knowler2, Alan R Shuldiner3, Nehal Gosalia3, Cristopher Van Hout3, Robert L Hanson2, Clifton Bogardus2, Leslie J Baier2.   

Abstract

The Pima Indians of the Gila River Indian Community in Arizona have participated in a long-range study of type 2 diabetes mellitus since 1965 and have been the subject of HLA typing and population studies since the early days of serological assays. These data have been in numerous HLA workshops and conferences and have been the source of at least five novel alleles at the classical HLA loci. In recent time nearly the entire study group was subject to next generation sequencing by whole genome or exome technologies, which has allowed us to HLA type over 3000 full heritage persons with recently developed computer algorithms. We present here the results for the classical HLA Loci: HLA-A, B, C, DRA, DRB1, DRB3, DRB4, DRB5, DPA1, DPB1, DQA1, and DQB1 to the third field of resolution for synonymous alleles and type the likely four field resolution alleles from the subset of whole genome sequences. Allele frequencies, and haplotype frequencies at up to five loci, are presented as well as measures of population structure and heterozygosity. We define a core set of HLA variation that approximates the distribution for the Paleo-Indians and impute nine-locus, 4-field haplotypes that are expected to be common in full heritage peoples. Published by Elsevier Inc.

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Year:  2019        PMID: 31706744     DOI: 10.1016/j.humimm.2019.10.002

Source DB:  PubMed          Journal:  Hum Immunol        ISSN: 0198-8859            Impact factor:   2.850


  7 in total

1.  Next generation sequencing for HLA loci in full heritage Pima Indians of Arizona, Part II: HLA-A, -B, and -C with selected non-classical loci at 4-field resolution from whole genome sequences.

Authors:  Robert C Williams; Cigdem Koroglu; William C Knowler; Alan R Shuldiner; Nehal Gosalia; Cristopher Van Hout; Robert L Hanson; Clifton Bogardus; Leslie J Baier
Journal:  Hum Immunol       Date:  2021-04-17       Impact factor: 2.211

2.  Pharmacogenomic Study of Statin-Associated Muscle Symptoms in the ODYSSEY OUTCOMES Trial.

Authors:  William A Murphy; Nan Lin; Amy Damask; Gregory G Schwartz; P Gabriel Steg; Michael Szarek; Poulabi Banerjee; Sergio Fazio; Garen Manvelian; Robert Pordy; Alan R Shuldiner; Charles Paulding
Journal:  Circ Genom Precis Med       Date:  2022-05-11

3.  Pro-inflammatory dopamine-2 receptor-specific T cells in paediatric movement and psychiatric disorders.

Authors:  Deepti Pilli; Alicia Zou; Ruebena Dawes; Joseph A Lopez; Fiona Tea; Ganesha Liyanage; Fiona Xz Lee; Vera Merheb; Samuel D Houston; Aleha Pillay; Hannah F Jones; Sudarshini Ramanathan; Shekeeb Mohammad; Anthony D Kelleher; Stephen I Alexander; Russell C Dale; Fabienne Brilot
Journal:  Clin Transl Immunology       Date:  2020-12-17

4.  Thrombotic risk determined by rare and common SERPINA1 variants in a population-based cohort study.

Authors:  Eric Manderstedt; Christer Halldén; Christina Lind-Halldén; Johan Elf; Peter J Svensson; Gunnar Engström; Olle Melander; Aris Baras; Luca A Lotta; Bengt Zöller
Journal:  J Thromb Haemost       Date:  2022-03-19       Impact factor: 16.036

5.  Whole-exome sequencing uncovers new variants in GDF15 associated with hyperemesis gravidarum.

Authors:  Marlena S Fejzo; Kimber W MacGibbon; Olivia First; Courtney Quan; Patrick M Mullin
Journal:  BJOG       Date:  2022-03-16       Impact factor: 7.331

6.  Classic Thrombophilias and Thrombotic Risk Among Middle-Aged and Older Adults: A Population-Based Cohort Study.

Authors:  Eric Manderstedt; Christina Lind-Halldén; Christer Halldén; Johan Elf; Peter J Svensson; Björn Dahlbäck; Gunnar Engström; Olle Melander; Aris Baras; Luca A Lotta; Bengt Zöller
Journal:  J Am Heart Assoc       Date:  2022-02-03       Impact factor: 6.106

7.  Exome Sequencing of 21 Bardet-Biedl Syndrome (BBS) Genes to Identify Obesity Variants in 6,851 American Indians.

Authors:  Samantha E Day; Yunhua L Muller; Cigdem Koroglu; Sayuko Kobes; Kim Wiedrich; Darin Mahkee; Hye In Kim; Cris Van Hout; Nehal Gosalia; Bin Ye; Alan R Shuldiner; William C Knowler; Robert L Hanson; Clifton Bogardus; Leslie J Baier
Journal:  Obesity (Silver Spring)       Date:  2021-02-22       Impact factor: 5.002

  7 in total

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