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Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expressionNature genetics, 2021-09, Vol.53 (9), p.1300-1310 [Peer Reviewed Journal]2021. The Author(s), under exclusive licence to Springer Nature America, Inc. ;COPYRIGHT 2021 Nature Publishing Group ;Copyright Nature Publishing Group Sep 2021 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-021-00913-z ;PMID: 34475573Full text available |
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Identification of common genetic risk variants for autism spectrum disorderNature genetics, 2019-03, Vol.51 (3), p.431-444 [Peer Reviewed Journal]COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2019 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-019-0344-8 ;PMID: 30804558Full text available |
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Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasetsAmerican journal of human genetics, 2023-04, Vol.110 (4), p.575-591 [Peer Reviewed Journal]2023 American Society of Human Genetics ;Copyright © 2023 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2023 American Society of Human Genetics. 2023 American Society of Human Genetics ;ISSN: 0002-9297 ;ISSN: 1537-6605 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2023.03.007 ;PMID: 37028392Full text available |
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Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translationNature genetics, 2022-05, Vol.54 (5), p.560-572 [Peer Reviewed Journal]2022. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group May 2022 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01058-3 ;PMID: 35551307Full text available |
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Material Type: Article
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Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association StudiesThe American journal of psychiatry, 2019-03, Vol.176 (3), p.217-227 [Peer Reviewed Journal]Copyright © 2019 by the American Psychiatric Association 2019 ;Copyright American Psychiatric Association Mar 2019 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-953X ;EISSN: 1535-7228 ;DOI: 10.1176/appi.ajp.2018.18070857 ;PMID: 30818990Full text available |
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Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in SingaporeCell, 2019-10, Vol.179 (3), p.736-749.e15 [Peer Reviewed Journal]2019 Elsevier Inc. ;Copyright © 2019 Elsevier Inc. All rights reserved. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2019.09.019 ;PMID: 31626772Full text available |
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Material Type: Article
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TOLLIP, MUC5B, and the Response to N-Acetylcysteine among Individuals with Idiopathic Pulmonary FibrosisAmerican journal of respiratory and critical care medicine, 2015-12, Vol.192 (12), p.1475-1482 [Peer Reviewed Journal]Copyright American Thoracic Society Dec 15, 2015 ;Copyright © 2015 by the American Thoracic Society 2015 ;ISSN: 1073-449X ;EISSN: 1535-4970 ;DOI: 10.1164/rccm.201505-1010OC ;PMID: 26331942Full text available |
8 |
Material Type: Article
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New genetic loci link adipose and insulin biology to body fat distributionNature (London), 2015-02, Vol.518 (7538), p.187-196 [Peer Reviewed Journal]COPYRIGHT 2015 Nature Publishing Group ;COPYRIGHT 2015 Nature Publishing Group ;Copyright Nature Publishing Group Feb 12, 2015 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/nature14132 ;PMID: 25673412 ;CODEN: NATUASFull text available |
9 |
Material Type: Article
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DrugBank 5.0: a major update to the DrugBank database for 2018Nucleic acids research, 2018-01, Vol.46 (D1), p.D1074-D1082 [Peer Reviewed Journal]The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. 2018 ;The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. ;ISSN: 0305-1048 ;EISSN: 1362-4962 ;DOI: 10.1093/nar/gkx1037 ;PMID: 29126136Full text available |
10 |
Material Type: Article
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GAPIT Version 3: Boosting Power and Accuracy for Genomic Association and PredictionGenomics, proteomics & bioinformatics, 2021-08, Vol.19 (4), p.629-640 [Peer Reviewed Journal]2021 The Authors ;Copyright © Wanfang Data Co. Ltd. All Rights Reserved. ;2021 The Authors 2021 ;ISSN: 1672-0229 ;EISSN: 2210-3244 ;DOI: 10.1016/j.gpb.2021.08.005 ;PMID: 34492338Full text available |
11 |
Material Type: Article
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An Expanded View of Complex Traits: From Polygenic to OmnigenicCell, 2017-06, Vol.169 (7), p.1177-1186 [Peer Reviewed Journal]2017 Elsevier Inc. ;Copyright © 2017 Elsevier Inc. All rights reserved. ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2017.05.038 ;PMID: 28622505Full text available |
12 |
Material Type: Article
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Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence DataCirculation research, 2014-10, Vol.115 (10), p.884-896 [Peer Reviewed Journal]2014 American Heart Association, Inc. ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.115.304458 ;PMID: 25205790Full text available |
13 |
Material Type: Article
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Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial)Circulation (New York, N.Y.), 2016-03, Vol.133 (12), p.1181-1188 [Peer Reviewed Journal]2016 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2016 American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.115.020109 ;PMID: 26915630Full text available |
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Material Type: Article
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PANTHER version 11: expanded annotation data from Gene Ontology and Reactome pathways, and data analysis tool enhancementsNucleic acids research, 2017-01, Vol.45 (D1), p.D183-D189 [Peer Reviewed Journal]The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. ;The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. 2017 ;ISSN: 0305-1048 ;EISSN: 1362-4962 ;DOI: 10.1093/nar/gkw1138 ;PMID: 27899595Full text available |
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Material Type: Article
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Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individualsNature genetics, 2020-12, Vol.52 (12), p.1314-1332 [Peer Reviewed Journal]COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Dec 2020 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-020-00713-x ;PMID: 33230300Full text available |
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Material Type: Article
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Estimating and interpreting FST: the impact of rare variantsGenome research, 2013-09, Vol.23 (9), p.1514-1521 [Peer Reviewed Journal]2013 ;ISSN: 1088-9051 ;EISSN: 1549-5469 ;DOI: 10.1101/gr.154831.113 ;PMID: 23861382Full text available |
17 |
Material Type: Article
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15 years of GWAS discovery: Realizing the promiseAmerican journal of human genetics, 2023-02, Vol.110 (2), p.179-194 [Peer Reviewed Journal]2022 American Society of Human Genetics ;Copyright © 2022 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2022 American Society of Human Genetics. 2022 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2022.12.011 ;PMID: 36634672Full text available |
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Material Type: Article
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Discordant calls across genotype discovery approaches elucidate variants with systematic errorsGenome research, 2023-06, Vol.33 (6), p.999-1005 [Peer Reviewed Journal]2023 Atkinson et al.; Published by Cold Spring Harbor Laboratory Press. ;2023 ;ISSN: 1088-9051 ;EISSN: 1549-5469 ;DOI: 10.1101/gr.277908.123 ;PMID: 37253541Full text available |
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Material Type: Article
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Assessing the suitability of summary data for two-sample Mendelian randomization analyses using MR-Egger regression: the role of the I2 statisticInternational journal of epidemiology, 2016-12, Vol.45 (6), p.1961-1974 [Peer Reviewed Journal]The Author 2016. Published by Oxford University Press on behalf of the International Epidemiological Association. ;The Author 2016. Published by Oxford University Press on behalf of the International Epidemiological Association. 2016 ;ISSN: 0300-5771 ;EISSN: 1464-3685 ;DOI: 10.1093/ije/dyw220 ;PMID: 27616674Full text available |
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Material Type: Article
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Identification of common variants associated with human hippocampal and intracranial volumesNature genetics, 2012-05, Vol.44 (5), p.552-561 [Peer Reviewed Journal]2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;Distributed under a Creative Commons Attribution 4.0 International License ;2012 Nature America, Inc. All rights reserved. 2012 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.2250 ;PMID: 22504417 ;CODEN: NGENECFull text available |