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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Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populationsHereditas, 2018-04, Vol.155 (1), p.19-19, Article 19 [Peer Reviewed Journal]The Author(s) 2018 ;ISSN: 1601-5223 ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1186/s41065-018-0057-5 ;PMID: 29636655Full text available |
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2 |
Material Type: Article
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NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese populationCell reports (Cambridge), 2021-11, Vol.37 (7), p.110017-110017, Article 110017 [Peer Reviewed Journal]2021 The Authors ;Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved. ;ISSN: 2211-1247 ;EISSN: 2211-1247 ;DOI: 10.1016/j.celrep.2021.110017 ;PMID: 34788621Full text available |
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3 |
Material Type: Article
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Genetic Origins and Sex-Biased Admixture of the HuisMolecular biology and evolution, 2021-09, Vol.38 (9), p.3804-3819 [Peer Reviewed Journal]The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 2021 ;The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. ;COPYRIGHT 2021 Oxford University Press ;ISSN: 1537-1719 ;ISSN: 0737-4038 ;EISSN: 1537-1719 ;DOI: 10.1093/molbev/msab158 ;PMID: 34021754Full text available |
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4 |
Material Type: Article
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Association between RECQL5 genetic polymorphisms and susceptibility to breast cancerTumor biology, 2014-12, Vol.35 (12), p.12201-12204 [Peer Reviewed Journal]International Society of Oncology and BioMarkers (ISOBM) 2014 ;ISSN: 1010-4283 ;EISSN: 1423-0380 ;DOI: 10.1007/s13277-014-2528-2 ;PMID: 25394896Full text available |
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5 |
Material Type: Article
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Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han ChineseHereditas, 2019, Vol.156 (1), p.4-4, Article 4 [Peer Reviewed Journal]Copyright © 2019. This work is licensed 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) 2019 ;ISSN: 1601-5223 ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1186/s41065-018-0078-0 ;PMID: 30679935Full text available |
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6 |
Material Type: Article
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Confirming the TMEM232 gene associated with atopic dermatitis through targeted capture sequencingScientific reports, 2021-11, Vol.11 (1), p.21830-21830, Article 21830 [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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-01194-6 ;PMID: 34750414Full text available |
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7 |
Material Type: Article
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Polymorphism of rs12294045 in EAAT2 gene is potentially associated with schizophrenia in Chinese Han populationBMC psychiatry, 2022-03, Vol.22 (1), p.171-171, Article 171 [Peer Reviewed Journal]2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;The Author(s) 2022 ;ISSN: 1471-244X ;EISSN: 1471-244X ;DOI: 10.1186/s12888-022-03799-1 ;PMID: 35260124Full text available |
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8 |
Material Type: Article
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Polymorphism of the PPARD Gene and Dynamic Balance Performance in Han Chinese ChildrenHereditas, 2019-05, Vol.156 (1), p.15-15, Article 15 [Peer Reviewed Journal]2019. This work is licensed 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) 2019 ;ISSN: 1601-5223 ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1186/s41065-019-0092-x ;PMID: 31148953Full text available |
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9 |
Material Type: Article
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Effect of CYP2C19 polymorphisms on serum valproic level acid in Chinese Han patients with schizophreniaScientific reports, 2021-11, Vol.11 (1), p.23150-23150, Article 23150 [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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-02628-x ;PMID: 34848811Full text available |
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10 |
Material Type: Article
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Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axisGenetics in medicine, 2019-10, Vol.21 (10), p.2345-2354 [Peer Reviewed Journal]American College of Medical Genetics and Genomics 2019. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0507-0 ;PMID: 31000793Full text available |
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11 |
Material Type: Article
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Genetic variation of pharmacogenomic VIP variants in the Chinese Li population: an updated researchMolecular genetics and genomics : MGG, 2022-03, Vol.297 (2), p.407-417 [Peer Reviewed Journal]The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 ;2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. ;The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022. ;ISSN: 1617-4615 ;EISSN: 1617-4623 ;DOI: 10.1007/s00438-022-01855-9 ;PMID: 35146537Full text available |
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12 |
Material Type: Article
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Vitamin D Receptor Genetic Variations May Associate with the Risk of Developing Late Fracture-Related Infection in the Chinese Han PopulationJournal of immunology research, 2022-02, Vol.2022, p.9025354-8 [Peer Reviewed Journal]Copyright © 2022 Xing-qi Zhao et al. ;Copyright © 2022 Xing-qi Zhao et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0 ;Copyright © 2022 Xing-qi Zhao et al. 2022 ;ISSN: 2314-8861 ;EISSN: 2314-7156 ;DOI: 10.1155/2022/9025354 ;PMID: 35242885Full text available |
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13 |
Material Type: Article
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Association of lncRNA PVT1 Gene Polymorphisms with the Risk of Essential Hypertension in Chinese PopulationBioMed research international, 2022, Vol.2022, p.9976909-9 [Peer Reviewed Journal]Copyright © 2022 Rong Li et al. ;Copyright © 2022 Rong Li et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0 ;Copyright © 2022 Rong Li et al. 2022 ;ISSN: 2314-6133 ;EISSN: 2314-6141 ;DOI: 10.1155/2022/9976909 ;PMID: 35036445Full text available |
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14 |
Material Type: Article
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Genome-wide association study of survival in patients with pancreatic adenocarcinomaGut, 2014-01, Vol.63 (1), p.152-160 [Peer Reviewed Journal]Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Copyright: 2014 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 0017-5749 ;ISSN: 1468-3288 ;EISSN: 1468-3288 ;DOI: 10.1136/gutjnl-2012-303477 ;PMID: 23180869 ;CODEN: GUTTAKFull text available |
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15 |
Material Type: Article
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Effect of gene polymorphism on bleeding complications in Chinese Han patients taking warfarinEuropean journal of clinical pharmacology, 2022-02, Vol.78 (2), p.205-214 [Peer Reviewed Journal]The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021 ;2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. ;The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021. ;ISSN: 0031-6970 ;EISSN: 1432-1041 ;DOI: 10.1007/s00228-021-03204-y ;PMID: 34596727Full text available |
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16 |
Material Type: Article
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Genome-wide association study of serum tumor markers in Southern Chinese Han populationBMC cancer, 2022-02, Vol.22 (1), p.160-160, Article 160 [Peer Reviewed Journal]2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;2022. This work is licensed 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: 1471-2407 ;EISSN: 1471-2407 ;DOI: 10.1186/s12885-022-09236-6 ;PMID: 35144566Full text available |
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17 |
Material Type: Article
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Relationships of interleukin-17 polymorphisms with recurrent aphthous ulcer risk in a Han Chinese populationJournal of international medical research, 2020-12, Vol.48 (12), p.300060520976833-300060520976833 [Peer Reviewed Journal]The Author(s) 2020 ;The Author(s) 2020. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/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) 2020 2020 SAGE Publications ;ISSN: 0300-0605 ;EISSN: 1473-2300 ;DOI: 10.1177/0300060520976833 ;PMID: 33351682Full text available |
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18 |
Material Type: Article
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The rs9953490 polymorphism of DAL-1 gene is associated with gastric cancer risk in the Han population in Northeast ChinaBMC gastroenterology, 2021-09, Vol.21 (1), p.354-354, Article 354 [Peer Reviewed Journal]2021. The Author(s). ;COPYRIGHT 2021 BioMed Central Ltd. ;2021. This work is licensed 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: 1471-230X ;EISSN: 1471-230X ;DOI: 10.1186/s12876-021-01929-9 ;PMID: 34579655Full text available |
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19 |
Material Type: Article
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Glutathione S-transferase Omega 2 DD genotype is associated with an increased risk of sporadic amyotrophic lateral sclerosis in Chinese menJournal of international medical research, 2021-07, Vol.49 (7), p.3000605211033219-3000605211033219 [Peer Reviewed Journal]The Author(s) 2021 ;The Author(s) 2021. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/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 2021 SAGE Publications ;ISSN: 0300-0605 ;EISSN: 1473-2300 ;DOI: 10.1177/03000605211033219 ;PMID: 34311603Full text available |
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20 |
Material Type: Article
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Association of pigmentation related-genes polymorphisms and geographic environmental variables in the Chinese populationHereditas, 2021-07, Vol.158 (1), p.24-24, Article 24 [Peer Reviewed Journal]2021. This work is licensed 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: 1601-5223 ;ISSN: 0018-0661 ;EISSN: 1601-5223 ;DOI: 10.1186/s41065-021-00189-7 ;PMID: 34238381Full text available |