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1
NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants
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NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants

Genome medicine, 2019-10, Vol.11 (1), p.64-64, Article 64 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;The Author(s). 2019 ;ISSN: 1756-994X ;EISSN: 1756-994X ;DOI: 10.1186/s13073-019-0677-z ;PMID: 31640730

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2
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
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Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Nature genetics, 2018-06, Vol.50 (6), p.834-848 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Jun 2018 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0127-7 ;PMID: 29808027

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3
Genetic variants underlying differences in facial morphology in East Asian and European populations
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Genetic variants underlying differences in facial morphology in East Asian and European populations

Nature genetics, 2022-04, Vol.54 (4), p.403-411 [Peer Reviewed Journal]

2022. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group Apr 2022 ;Attribution ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01038-7 ;PMID: 35393595

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4
Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populations
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Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populations

Hereditas, 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: 29636655

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5
Amino acid signatures of HLA Class-I and II molecules are strongly associated with SLE susceptibility and autoantibody production in Eastern Asians
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Amino acid signatures of HLA Class-I and II molecules are strongly associated with SLE susceptibility and autoantibody production in Eastern Asians

PLoS genetics, 2019-04, Vol.15 (4), p.e1008092 [Peer Reviewed Journal]

COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Molineros et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 Molineros et al 2019 Molineros et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1008092 ;PMID: 31022184

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6
HIBAG--HLA genotype imputation with attribute bagging
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HIBAG--HLA genotype imputation with attribute bagging

The pharmacogenomics journal, 2014-04, Vol.14 (2), p.192-200 [Peer Reviewed Journal]

COPYRIGHT 2014 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2014 ;Copyright © 2014 Macmillan Publishers Limited 2014 Macmillan Publishers Limited ;ISSN: 1470-269X ;EISSN: 1473-1150 ;DOI: 10.1038/tpj.2013.18 ;PMID: 23712092

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7
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
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A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

Nature genetics, 2011-04, Vol.43 (4), p.339-344 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2011 Nature Publishing Group ;COPYRIGHT 2011 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2011 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.782 ;PMID: 21378988 ;CODEN: NGENEC

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8
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
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Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci

Nature genetics, 2011-10, Vol.43 (10), p.984-989 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2011 Nature Publishing Group ;COPYRIGHT 2011 Nature Publishing Group ;Copyright Nature Publishing Group Oct 2011 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.921 ;PMID: 21874001 ;CODEN: NGENEC

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9
Meta-analysis identifies multiple loci associated with kidney function―related traits in east Asian populations
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Meta-analysis identifies multiple loci associated with kidney function―related traits in east Asian populations

Nature genetics, 2012-08, Vol.44 (8), p.904-909 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.2352 ;PMID: 22797727 ;CODEN: NGENEC

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10
FTO genetic variants, dietary intake and body mass index: insights from 177,330 individuals
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FTO genetic variants, dietary intake and body mass index: insights from 177,330 individuals

Human molecular genetics, 2014-12, Vol.23 (25), p.6961-6972 [Peer Reviewed Journal]

The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2014 ;ISSN: 0964-6906 ;ISSN: 1460-2083 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddu411 ;PMID: 25104851

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11
Genetic Origins and Sex-Biased Admixture of the Huis
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Genetic Origins and Sex-Biased Admixture of the Huis

Molecular 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: 34021754

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12
Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error
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Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error

American journal of human genetics, 2013-08, Vol.93 (2), p.264-277 [Peer Reviewed Journal]

2013 The American Society of Human Genetics ;Copyright © 2013 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Aug 8, 2013 ;2013 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2013 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2013.06.016 ;PMID: 24144296

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13
Large-scale gene-centric analysis identifies novel variants for coronary artery disease
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Large-scale gene-centric analysis identifies novel variants for coronary artery disease

PLoS genetics, 2011-09, Vol.7 (9), p.e1002260-e1002260 [Peer Reviewed Journal]

COPYRIGHT 2011 Public Library of Science ;COPYRIGHT 2011 Public Library of Science ;Butterworth et al. 2011 ;2011 Butterworth et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: The IBC 50K CAD Consortium (2011) Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease. PLoS Genet 7(9): e1002260. doi:10.1371/journal.pgen.1002260 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002260 ;PMID: 21966275

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14
Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People
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Article
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Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People

Molecular biology and evolution, 2021-10, Vol.38 (10), p.4149-4165 [Peer Reviewed Journal]

The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 2020 ;The Author(s) 2020. 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/msaa276 ;PMID: 33170928

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15
Genome-wide association studies identify two novel loci conferring susceptibility to diabetic retinopathy in Japanese patients with type 2 diabetes
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Genome-wide association studies identify two novel loci conferring susceptibility to diabetic retinopathy in Japanese patients with type 2 diabetes

Human molecular genetics, 2021-05, Vol.30 (8), p.716-726 [Peer Reviewed Journal]

The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2021 ;The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddab044 ;PMID: 33607655

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16
The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent
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The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent

PLoS genetics, 2013-11, Vol.9 (11), p.e1003912-e1003912 [Peer Reviewed Journal]

COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Basu Mallick et al 2013 Basu Mallick et al ;2013 Basu Mallick et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Basu Mallick C, Iliescu FM, Möls M, Hill S, Tamang R, et al. (2013) The Light Skin Allele of SLC24A5 in South Asians and Europeans Shares Identity by Descent. PLoS Genet 9(11): e1003912. doi:10.1371/journal.pgen.1003912 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1003912 ;PMID: 24244186

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17
Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability
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Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2012-05, Vol.90 (5), p.856-863 [Peer Reviewed Journal]

2012 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press May 4, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.03.023 ;PMID: 22541562 ;CODEN: AJHGAG

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18
Genome-wide identification of cis DNA methylation quantitative trait loci in three Southeast Asian Populations
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Genome-wide identification of cis DNA methylation quantitative trait loci in three Southeast Asian Populations

Human molecular genetics, 2021-05, Vol.30 (7), p.603-618 [Peer Reviewed Journal]

The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2021 ;The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddab038 ;PMID: 33547791

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19
Dysfunction of VIPR2 leads to myopia in humans and mice
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Article
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Dysfunction of VIPR2 leads to myopia in humans and mice

Journal of medical genetics, 2022-01, Vol.59 (1), p.88-100 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ. ;2022 Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2020-107220 ;PMID: 33318135

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20
Resolving the ancestry of Austronesian-speaking populations
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Resolving the ancestry of Austronesian-speaking populations

Human genetics, 2016-03, Vol.135 (3), p.309-326 [Peer Reviewed Journal]

The Author(s) 2016 ;COPYRIGHT 2016 Springer ;Springer-Verlag Berlin Heidelberg 2016 ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-015-1620-z ;PMID: 26781090

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