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1
Unraveling the mystery of oligogenic inheritance under way?
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Unraveling the mystery of oligogenic inheritance under way?

Molecules and cells, 2024-01, Vol.47 (1), p.100003-100003, Article 100003 [Peer Reviewed Journal]

2023 The Author(s) ;2023 The Author(s) 2023 ;ISSN: 1016-8478 ;EISSN: 0219-1032 ;DOI: 10.1016/j.mocell.2023.10.002 ;PMID: 38376484

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2
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
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Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Nature genetics, 2022, Vol.54 (4), p.437-449 [Peer Reviewed Journal]

2022. The Author(s). ;Copyright Nature Publishing Group Apr 2022 ;The Author(s) 2022 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01016-z ;PMID: 35361970

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3
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
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Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

Nature 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: 34475573

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4
Identification of common genetic risk variants for autism spectrum disorder
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Identification of common genetic risk variants for autism spectrum disorder

Nature 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: 30804558

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5
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
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Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

Nature genetics, 2021-06, Vol.53 (6), p.817-829 [Peer Reviewed Journal]

COPYRIGHT 2021 Nature Publishing Group ;Copyright Nature Publishing Group Jun 2021 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-021-00857-4 ;PMID: 34002096

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6
The trans-ancestral genomic architecture of glycemic traits
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The trans-ancestral genomic architecture of glycemic traits

Nature genetics, 2021-06, Vol.53 (6), p.840-860 [Peer Reviewed Journal]

COPYRIGHT 2021 Nature Publishing Group ;Copyright Nature Publishing Group Jun 2021 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-021-00852-9 ;PMID: 34059833

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7
Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association
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Article
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Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2022-08, Vol.146 (8), p.e93-e118 [Peer Reviewed Journal]

ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/cir.0000000000001077 ;PMID: 35862132

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8
Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies
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Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

The 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: 30818990

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9
Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative
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Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative

American journal of human genetics, 2018-06, Vol.102 (6), p.1048-1061 [Peer Reviewed Journal]

2018 American Society of Human Genetics ;Copyright © 2018 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2018 American Society of Human Genetics. 2018 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2018.04.001 ;PMID: 29779563

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10
Making the Most of Clumping and Thresholding for Polygenic Scores
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Making the Most of Clumping and Thresholding for Polygenic Scores

American journal of human genetics, 2019-12, Vol.105 (6), p.1213-1221 [Peer Reviewed Journal]

2019 American Society of Human Genetics ;Copyright © 2019 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Attribution - NonCommercial ;2019 American Society of Human Genetics. 2019 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2019.11.001 ;PMID: 31761295

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11
Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease
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Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease

Nature genetics, 2021-06, Vol.53 (6), p.787-793 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jun 2021 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-021-00847-6 ;PMID: 33958783

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12
Patterns and rates of exonic de novo mutations in autism spectrum disorders
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Article
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Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature (London), 2012-05, Vol.485 (7397), p.242-245 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group May 10, 2012 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature11011 ;PMID: 22495311 ;CODEN: NATUAS

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13
Potential corporate uses of polygenic indexes: Starting a conversation about the associated ethics and policy issues
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Article
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Potential corporate uses of polygenic indexes: Starting a conversation about the associated ethics and policy issues

American journal of human genetics, 2024-05, Vol.111 (5), p.833-840 [Peer Reviewed Journal]

2024 American Society of Human Genetics ;Copyright © 2024 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2024.03.010 ;PMID: 38701744

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14
10 Years of GWAS Discovery: Biology, Function, and Translation
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Article
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10 Years of GWAS Discovery: Biology, Function, and Translation

American journal of human genetics, 2017-07, Vol.101 (1), p.5-22 [Peer Reviewed Journal]

2017 American Society of Human Genetics ;Copyright © 2017 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2017 American Society of Human Genetics. 2017 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2017.06.005 ;PMID: 28686856

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15
An Expanded View of Complex Traits: From Polygenic to Omnigenic
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Article
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An Expanded View of Complex Traits: From Polygenic to Omnigenic

Cell, 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: 28622505

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16
Hundreds of variants clustered in genomic loci and biological pathways affect human height
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Article
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Hundreds of variants clustered in genomic loci and biological pathways affect human height

Nature (London), 2010-10, Vol.467 (7317), p.832-838 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Oct 14, 2010 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/nature09410 ;PMID: 20881960 ;CODEN: NATUAS

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17
15 years of GWAS discovery: Realizing the promise
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Article
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15 years of GWAS discovery: Realizing the promise

American 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: 36634672

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18
The genetics of obesity: from discovery to biology
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Article
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The genetics of obesity: from discovery to biology

Nature reviews. Genetics, 2022-02, Vol.23 (2), p.120-133 [Peer Reviewed Journal]

2021. Springer Nature Limited. ;Springer Nature Limited 2021. ;Springer Nature Limited 2021 ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-021-00414-z ;PMID: 34556834

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19
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
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Article
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Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions

Nature neuroscience, 2019-03, Vol.22 (3), p.343-352 [Peer Reviewed Journal]

2019© The Author(s), under exclusive licence to Springer Nature America, Inc. 2019 ;ISSN: 1097-6256 ;ISSN: 1546-1726 ;EISSN: 1546-1726 ;DOI: 10.1038/s41593-018-0326-7 ;PMID: 30718901

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20
Widespread signatures of natural selection across human complex traits and functional genomic categories
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Widespread signatures of natural selection across human complex traits and functional genomic categories

Nature communications, 2021-02, Vol.12 (1), p.1164-1164, Article 1164 [Peer Reviewed Journal]

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: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-021-21446-3 ;PMID: 33608517

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