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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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Comparison of effects of UGT1A16 and UGT1A128 on irinotecan-induced adverse reactions in the Japanese population: analysis of the Biobank Japan ProjectJournal of human genetics, 2019-12, Vol.64 (12), p.1195-1202 [Peer Reviewed Journal]Copyright Nature Publishing Group Dec 2019 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-019-0677-2 ;PMID: 31586129Full text available |
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Intronic LINE-1 insertion in SLCO1B3 as a highly prevalent cause of rotor syndrome in East Asian populationJournal of human genetics, 2022-02, Vol.67 (2), p.71-77 [Peer Reviewed Journal]2021. The Author(s), under exclusive licence to The Japan Society of Human Genetics. ;The Author(s), under exclusive licence to The Japan Society of Human Genetics 2021. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-021-00967-1 ;PMID: 34354231Full text available |
| 3 |
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Genetic association of MMP14 promoter variants and their functional significance in gallbladder cancer pathogenesisJournal of human genetics, 2021-10, Vol.66 (10), p.947-956 [Peer Reviewed Journal]2021. The Author(s), under exclusive licence to The Japan Society of Human Genetics. ;The Author(s), under exclusive licence to The Japan Society of Human Genetics 2021. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-021-00917-x ;PMID: 33727629Full text available |
| 4 |
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Importance of gastric cancer for the diagnosis and surveillance of Japanese Lynch syndrome patientsJournal of human genetics, 2019-12, Vol.64 (12), p.1187-1194 [Peer Reviewed Journal]Copyright Nature Publishing Group Dec 2019 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-019-0674-5 ;PMID: 31588121Full text available |
| 5 |
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Analysis of genetic risk factors in Japanese patients with Parkinson's diseaseJournal of human genetics, 2021-10, Vol.66 (10), p.957-964 [Peer Reviewed Journal]2021. The Author(s), under exclusive licence to The Japan Society of Human Genetics. ;The Author(s), under exclusive licence to The Japan Society of Human Genetics 2021. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-021-00910-4 ;PMID: 33742109Full text available |
| 6 |
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Screening of PCSK9 and LDLR genetic variants in Familial Hypercholesterolemia (FH) patients in IndiaJournal of human genetics, 2021-10, Vol.66 (10), p.983-993 [Peer Reviewed Journal]2021. The Author(s), under exclusive licence to The Japan Society of Human Genetics. ;The Author(s), under exclusive licence to The Japan Society of Human Genetics 2021. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-021-00924-y ;PMID: 33864011Full text available |
| 7 |
Material Type: Article
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Gene flow between Zhuang and Han populations in the China-Vietnam borderlandJournal of human genetics, 2010-11, Vol.55 (11), p.774-776 [Peer Reviewed Journal]The Japan Society of Human Genetics 2010. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2010.107 ;PMID: 20811387Full text available |
| 8 |
Material Type: Article
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Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's diseaseJournal of human genetics, 2011-09, Vol.56 (9), p.671-675 [Peer Reviewed Journal]The Japan Society of Human Genetics 2011. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2011.79 ;PMID: 21796139Full text available |
| 9 |
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Y chromosomal DNA variation in East Asian populations and its potential for inferring the peopling of KoreaJournal of human genetics, 2000-01, Vol.45 (2), p.76-83 [Peer Reviewed Journal]The Japanese Society of Human Genetics and Springer-Verlag Tokyo 2000. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1007/s100380050015 ;PMID: 10721667Full text available |
| 10 |
Material Type: Article
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Phylogenetic analysis of the Y-chromosome haplogroup C2b-F1067, a dominant paternal lineage in Eastern EurasiaJournal of human genetics, 2020-10, Vol.65 (10), p.823-829 [Peer Reviewed Journal]The Author(s), under exclusive licence to The Japan Society of Human Genetics 2020. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-020-0775-1 ;PMID: 32427951Full text available |
| 11 |
Material Type: Article
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Unique characteristics of the Ainu population in Northern JapanJournal of human genetics, 2015-10, Vol.60 (10), p.565-571 [Peer Reviewed Journal]Copyright Nature Publishing Group Oct 2015 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2015.79 ;PMID: 26178428Full text available |
| 12 |
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Japonica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individualsJournal of human genetics, 2015-10, Vol.60 (10), p.581-587 [Peer Reviewed Journal]Copyright Nature Publishing Group Oct 2015 ;Copyright © 2015 The Japan Society of Human Genetics 2015 The Japan Society of Human Genetics ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2015.68 ;PMID: 26108142Full text available |
| 13 |
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Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategiesJournal of human genetics, 2022-02, Vol.67 (2), p.87-93 [Peer Reviewed Journal]2021. The Author(s), under exclusive licence to The Japan Society of Human Genetics. ;The Author(s), under exclusive licence to The Japan Society of Human Genetics 2021. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-021-00968-0 ;PMID: 34376796Full text available |
| 14 |
Material Type: Article
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A partial nuclear genome of the Jomons who lived 3000 years ago in Fukushima, JapanJournal of human genetics, 2017-02, Vol.62 (2), p.213-221 [Peer Reviewed Journal]Copyright Nature Publishing Group Feb 2017 ;Copyright © 2017 The Author(s) 2017 The Author(s) ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2016.110 ;PMID: 27581845Full text available |
| 15 |
Material Type: Article
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GWA meta-analysis of personality in Korean cohortsJournal of human genetics, 2015-08, Vol.60 (8), p.455-460 [Peer Reviewed Journal]Copyright Nature Publishing Group Aug 2015 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2015.52 ;PMID: 25994864Full text available |
| 16 |
Material Type: Article
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Concurrence of novel mutations causing Gilbert's and Dubin-Johnson syndrome with poor clinical outcomes in a Han Chinese familyJournal of human genetics, 2023-01, Vol.68 (1), p.17-23 [Peer Reviewed Journal]2022. The Author(s). ;The Author(s) 2022. 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) 2022 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-022-01086-1 ;PMID: 36274106Full text available |
| 17 |
Material Type: Article
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A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndromeJournal of human genetics, 2018-12, Vol.63 (12), p.1269-1272 [Peer Reviewed Journal]Copyright Nature Publishing Group Dec 2018 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-018-0505-0 ;PMID: 30140060Full text available |
| 18 |
Material Type: Article
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Association studies of SEPS1 gene polymorphisms with Hashimoto's thyroiditis in Han ChineseJournal of human genetics, 2015-08, Vol.60 (8), p.427-433 [Peer Reviewed Journal]Copyright Nature Publishing Group Aug 2015 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2015.42 ;PMID: 26016409Full text available |
| 19 |
Material Type: Article
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A genome-wide association study of a coronary artery disease risk variantJournal of human genetics, 2013-03, Vol.58 (3), p.120-126 [Peer Reviewed Journal]The Japan Society of Human Genetics 2013. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2012.124 ;PMID: 23364394Full text available |
| 20 |
Material Type: Article
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Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort studyJournal of human genetics, 2014-05, Vol.59 (5), p.262-268 [Peer Reviewed Journal]The Author(s) 2014. This work is published under https://creativecommons.org/licenses/by-nc-sa/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2014 The Japan Society of Human Genetics 2014 The Japan Society of Human Genetics ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2014.12 ;PMID: 24599119Full text available |
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