Association of a haplotype in the NRG1 gene with schizophrenia: a case-control study

Schizophrenia (SZ) is a severe multifactorial disease. NRG1 is a gene acting in the development of SZ. A number of NRG1 single nucleotide polymorphisms (SNPs) and their haplotypes are associated with SZ. In the present study, we investigated the association of a NRG1 haplotype (G-C in rs6988339-rs37...

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Main Authors: Sözen Mustafa Mert, Kartalcı Şükrü
Format: Article
Language:English
Published: De Gruyter 2023-05-01
Series:Türk Biyokimya Dergisi
Subjects:
Online Access:https://doi.org/10.1515/tjb-2022-0233
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author Sözen Mustafa Mert
Kartalcı Şükrü
author_facet Sözen Mustafa Mert
Kartalcı Şükrü
author_sort Sözen Mustafa Mert
collection DOAJ
description Schizophrenia (SZ) is a severe multifactorial disease. NRG1 is a gene acting in the development of SZ. A number of NRG1 single nucleotide polymorphisms (SNPs) and their haplotypes are associated with SZ. In the present study, we investigated the association of a NRG1 haplotype (G-C in rs6988339-rs3757930 frame) which was reported to be associated with SZ, and two other SNPs in the same gene (rs74942016, rs80127039) whose rare missense alleles were found in SZ patients. Also, we analyzed disease associations of potential new haplotypes constructed by the variants of these SNPs.
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spelling doaj.art-5f953f91da9b4bde96e5e63f94f778de2023-07-24T11:19:38ZengDe GruyterTürk Biyokimya Dergisi1303-829X2023-05-0148324625610.1515/tjb-2022-0233Association of a haplotype in the NRG1 gene with schizophrenia: a case-control studySözen Mustafa Mert0Kartalcı Şükrü1Faculty of Science and Literature, Department of Molecular Biology and Genetics, Bioinformatics Section, Inonu University, Malatya, TürkiyeFaculty of Medicine, Department of Psychiatry, Inonu University, Malatya, TürkiyeSchizophrenia (SZ) is a severe multifactorial disease. NRG1 is a gene acting in the development of SZ. A number of NRG1 single nucleotide polymorphisms (SNPs) and their haplotypes are associated with SZ. In the present study, we investigated the association of a NRG1 haplotype (G-C in rs6988339-rs3757930 frame) which was reported to be associated with SZ, and two other SNPs in the same gene (rs74942016, rs80127039) whose rare missense alleles were found in SZ patients. Also, we analyzed disease associations of potential new haplotypes constructed by the variants of these SNPs.https://doi.org/10.1515/tjb-2022-0233associationdiplotypegenetic associationgeneticshaplotypeneuregulin-1nrg1schizophreniasnp
spellingShingle Sözen Mustafa Mert
Kartalcı Şükrü
Association of a haplotype in the NRG1 gene with schizophrenia: a case-control study
Türk Biyokimya Dergisi
association
diplotype
genetic association
genetics
haplotype
neuregulin-1
nrg1
schizophrenia
snp
title Association of a haplotype in the NRG1 gene with schizophrenia: a case-control study
title_full Association of a haplotype in the NRG1 gene with schizophrenia: a case-control study
title_fullStr Association of a haplotype in the NRG1 gene with schizophrenia: a case-control study
title_full_unstemmed Association of a haplotype in the NRG1 gene with schizophrenia: a case-control study
title_short Association of a haplotype in the NRG1 gene with schizophrenia: a case-control study
title_sort association of a haplotype in the nrg1 gene with schizophrenia a case control study
topic association
diplotype
genetic association
genetics
haplotype
neuregulin-1
nrg1
schizophrenia
snp
url https://doi.org/10.1515/tjb-2022-0233
work_keys_str_mv AT sozenmustafamert associationofahaplotypeinthenrg1genewithschizophreniaacasecontrolstudy
AT kartalcısukru associationofahaplotypeinthenrg1genewithschizophreniaacasecontrolstudy