{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Prasad S"],"funding":["NIMH NIH HHS"],"pagination":["28"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5577284"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["3(1)"],"pubmed_abstract":["Schizophrenia is a chronic, severe, heritable disorder. Genome-wide association studies, conducted predominantly among Caucasians, have indicated > 100 risk alleles, with most significant SNPs on chromosome 6. There is growing interest as to whether these risk alleles are relevant in other ethnic groups as well. Neither an Indian genome-wide association studies nor a systematic replication of GWAS findings from other populations are reported. Thus, we analyzed 32 SNPs, including those associated in the Caucasian ancestry GWAS and other candidate gene studies, in a north Indian schizophrenia cohort (n = 1009 patients; n = 1029 controls) using a Sequenom mass array. Cognitive functioning was also assessed using the Hindi version of the Penn Computerized Neuropsychological Battery in a subset"],"journal":["NPJ schizophrenia"],"pubmed_title":["Attempts to replicate genetic associations with schizophrenia in a cohort from north India."],"pmcid":["PMC5577284"],"funding_grant_id":["R01 MH063480"],"pubmed_authors":["Nimgaonkar VL","Kukshal P","Prasad S","Thelma BK","Deshpande SN","Bhatia T"],"additional_accession":[]},"is_claimable":false,"name":"Attempts to replicate genetic associations with schizophrenia in a cohort from north India.","description":"Schizophrenia is a chronic, severe, heritable disorder. Genome-wide association studies, conducted predominantly among Caucasians, have indicated > 100 risk alleles, with most significant SNPs on chromosome 6. There is growing interest as to whether these risk alleles are relevant in other ethnic groups as well. Neither an Indian genome-wide association studies nor a systematic replication of GWAS findings from other populations are reported. Thus, we analyzed 32 SNPs, including those associated in the Caucasian ancestry GWAS and other candidate gene studies, in a north Indian schizophrenia cohort (n = 1009 patients; n = 1029 controls) using a Sequenom mass array. Cognitive functioning was also assessed using the Hindi version of the Penn Computerized Neuropsychological Battery in a subset","dates":{"release":"2017-01-01T00:00:00Z","publication":"2017 Aug","modification":"2026-05-02T05:46:40.958Z","creation":"2019-03-27T02:54:58Z"},"accession":"S-EPMC5577284","cross_references":{"pubmed":["28855605"],"doi":["10.1038/s41537-017-0030-8"]}}