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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Rare GATA6 variants associated with risk of congenital heart disease phenotypes in 200,000 UK Biobank exomesJournal of human genetics, 2022-02, Vol.67 (2), p.123-125 [Peer Reviewed Journal]2021. The Author(s). ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-021-00976-0 ;PMID: 34493817Full text available |
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The pursuit of genome-wide association studies: where are we now?Journal of human genetics, 2010-04, Vol.55 (4), p.195-206 [Peer Reviewed Journal]The Japan Society of Human Genetics 2010. ;ISSN: 1434-5161 ;ISSN: 1435-232X ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2010.19 ;PMID: 20300123Full text available |
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A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki diseaseJournal of human genetics, 2017-12, Vol.62 (12), p.1023-1029 [Peer Reviewed Journal]Copyright Nature Publishing Group Dec 2017 ;The Japan Society of Human Genetics 2017. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2017.87 ;PMID: 28855716Full text available |
| 4 |
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NAT2 variants are associated with drug-induced liver injury caused by anti-tuberculosis drugs in Indonesian patients with tuberculosisJournal of human genetics, 2016-06, Vol.61 (6), p.533-537 [Peer Reviewed Journal]Copyright Nature Publishing Group Jun 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2016.10 ;PMID: 26911349Full text available |
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Genetic cluster of fragile X syndrome in a Colombian districtJournal of human genetics, 2018-04, Vol.63 (4), p.509-516 [Peer Reviewed Journal]Copyright Nature Publishing Group Apr 2018 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-017-0407-6 ;PMID: 29379191Full text available |
| 6 |
Material Type: Article
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Effect of genomics-related literacy on non-communicable diseasesJournal of human genetics, 2017-09, Vol.62 (9), p.839-846 [Peer Reviewed Journal]Copyright Nature Publishing Group Sep 2017 ;The Japan Society of Human Genetics 2017. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2017.50 ;PMID: 28490765Full text available |
| 7 |
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Logistic Bayesian LASSO for genetic association analysis of data from complex sampling designsJournal of human genetics, 2017-09, Vol.62 (9), p.819-829 [Peer Reviewed Journal]Copyright Nature Publishing Group Sep 2017 ;The Japan Society of Human Genetics 2017. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2017.43 ;PMID: 28424482Full text available |
| 8 |
Material Type: Article
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Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curseJournal of human genetics, 2009-11, Vol.54 (11), p.615-623 [Peer Reviewed Journal]The Japan Society of Human Genetics 2009. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2009.95 ;PMID: 19851339Full text available |
| 9 |
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Additive composite ABCG2, SLC2A9 and SLC22A12 scores of high-risk alleles with alcohol use modulate gout riskJournal of human genetics, 2016-09, Vol.61 (9), p.803-810 [Peer Reviewed Journal]Copyright Nature Publishing Group Sep 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2016.57 ;PMID: 27225847Full text available |
| 10 |
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Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populationsJournal of human genetics, 2008-04, Vol.53 (4), p.357-359 [Peer Reviewed Journal]The Japan Society of Human Genetics and Springer 2008. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1007/s10038-008-0248-4 ;PMID: 18264662Full text available |
| 11 |
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PAX4 R192H and P321H polymorphisms in type 2 diabetes and their functional defectsJournal of human genetics, 2016-11, Vol.61 (11), p.943-949 [Peer Reviewed Journal]Copyright Nature Publishing Group Nov 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2016.80 ;PMID: 27334367Full text available |
| 12 |
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A significant association between rs8067378 at 17q12 and invasive cervical cancer originally identified by a genome-wide association study in Han Chinese is replicated in a Japanese populationJournal of human genetics, 2016-09, Vol.61 (9), p.793-796 [Peer Reviewed Journal]Copyright Nature Publishing Group Sep 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2016.50 ;PMID: 27193219Full text available |
| 13 |
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SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern ChineseJournal of human genetics, 2012-04, Vol.57 (4), p.244-246 [Peer Reviewed Journal]The Japan Society of Human Genetics 2012. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2012.11 ;PMID: 22301463Full text available |
| 14 |
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Androgen receptor CAG polymorphism and sporadic and early-onset prostate cancer among Mexican menJournal of human genetics, 2016-09, Vol.61 (9), p.781-786 [Peer Reviewed Journal]Copyright Nature Publishing Group Sep 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2016.49 ;PMID: 27193223Full text available |
| 15 |
Material Type: Article
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Detecting multiple variants associated with disease based on sequencing data of case-parent triosJournal of human genetics, 2016-10, Vol.61 (10), p.851-860 [Peer Reviewed Journal]Copyright Nature Publishing Group Oct 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2016.63 ;PMID: 27278787Full text available |
| 16 |
Material Type: Article
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Identification of novel susceptibility markers for the risk of overall breast cancer as well as subtypes defined by hormone receptor status in the Chinese populationJournal of human genetics, 2016-12, Vol.61 (12), p.1027-1034 [Peer Reviewed Journal]Copyright Nature Publishing Group Dec 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2016.97 ;PMID: 27604554Full text available |
| 17 |
Material Type: Article
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Estimation of the risk of a qualitative phenotype: dependence on population riskJournal of human genetics, 2017-02, Vol.62 (2), p.191-198 [Peer Reviewed Journal]Copyright Nature Publishing Group Feb 2017 ;The Japan Society of Human Genetics 2017. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2016.106 ;PMID: 27557667Full text available |
| 18 |
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Investigation of associations between ten polymorphisms and the risk of coronary artery disease in Southern Han ChineseJournal of human genetics, 2016-05, Vol.61 (5), p.389-393 [Peer Reviewed Journal]Copyright Nature Publishing Group May 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2015.158 ;PMID: 26740236Full text available |
| 19 |
Material Type: Article
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Association of CDKAL1 nucleotide variants with the risk of non-syndromic cleft lip with or without cleft palateJournal of human genetics, 2018-04, Vol.63 (4), p.397-406 [Peer Reviewed Journal]Copyright Nature Publishing Group Apr 2018 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-017-0397-4 ;PMID: 29403086Full text available |
| 20 |
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Genome-wide association study reveals sex-specific selection signals against autosomal nucleotide variantsJournal of human genetics, 2016-05, Vol.61 (5), p.423-426 [Peer Reviewed Journal]Copyright Nature Publishing Group May 2016 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2015.169 ;PMID: 26763874Full text available |
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