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1
DrugBank 5.0: a major update to the DrugBank database for 2018
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DrugBank 5.0: a major update to the DrugBank database for 2018

Nucleic 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: 29126136

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2
Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data
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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 Data

Circulation 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: 25205790

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3
Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial)
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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: 26915630

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4
Variant Review with the Integrative Genomics Viewer
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Variant Review with the Integrative Genomics Viewer

Cancer research (Chicago, Ill.), 2017-11, Vol.77 (21), p.e31-e34 [Peer Reviewed Journal]

2017 American Association for Cancer Research. ;Copyright American Association for Cancer Research, Inc. Nov 1, 2017 ;ISSN: 0008-5472 ;EISSN: 1538-7445 ;DOI: 10.1158/0008-5472.CAN-17-0337 ;PMID: 29092934

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5
Estimating and interpreting FST: the impact of rare variants
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Estimating and interpreting FST: the impact of rare variants

Genome 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: 23861382

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6
Discordant calls across genotype discovery approaches elucidate variants with systematic errors
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Discordant calls across genotype discovery approaches elucidate variants with systematic errors

Genome 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: 37253541

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7
Improving the visualization, interpretation and analysis of two-sample summary data Mendelian randomization via the Radial plot and Radial regression
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Improving the visualization, interpretation and analysis of two-sample summary data Mendelian randomization via the Radial plot and Radial regression

International journal of epidemiology, 2018-08, Vol.47 (4), p.1264-1278 [Peer Reviewed Journal]

The Author(s) 2018. Published by Oxford University Press on behalf of the International Epidemiological Association. 2018 ;ISSN: 0300-5771 ;EISSN: 1464-3685 ;DOI: 10.1093/ije/dyy101 ;PMID: 29961852

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8
Efficient CRISPR/Cas9 Gene Editing in Uncultured Naive Mouse T Cells for In Vivo Studies
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Efficient CRISPR/Cas9 Gene Editing in Uncultured Naive Mouse T Cells for In Vivo Studies

The Journal of immunology (1950), 2020-04, Vol.204 (8), p.2308-2315 [Peer Reviewed Journal]

Copyright © 2020 by The American Association of Immunologists, Inc. ;ISSN: 0022-1767 ;EISSN: 1550-6606 ;DOI: 10.4049/jimmunol.1901396 ;PMID: 32152070

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9
Mechanistic basis for impaired ferroptosis in cells expressing the African-centric S47 variant of p53
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Article
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Mechanistic basis for impaired ferroptosis in cells expressing the African-centric S47 variant of p53

Proceedings of the National Academy of Sciences - PNAS, 2019-04, Vol.116 (17), p.8390-8396 [Peer Reviewed Journal]

Copyright National Academy of Sciences Apr 23, 2019 ;2019 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1821277116 ;PMID: 30962386

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10
fastSTRUCTURE: variational inference of population structure in large SNP data sets
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fastSTRUCTURE: variational inference of population structure in large SNP data sets

Genetics (Austin), 2014-06, Vol.197 (2), p.573-589 [Peer Reviewed Journal]

Copyright © 2014 by the Genetics Society of America. ;Copyright Genetics Society of America Jun 2014 ;Copyright © 2014 by the Genetics Society of America 2014 ;ISSN: 1943-2631 ;ISSN: 0016-6731 ;EISSN: 1943-2631 ;DOI: 10.1534/genetics.114.164350 ;PMID: 24700103 ;CODEN: GENTAE

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11
Evaluating the potential role of pleiotropy in Mendelian randomization studies
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Evaluating the potential role of pleiotropy in Mendelian randomization studies

Human molecular genetics, 2018-08, Vol.27 (R2), p.R195-R208 [Peer Reviewed Journal]

The Author(s) 2018. Published by Oxford University Press. 2018 ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddy163 ;PMID: 29771313

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12
lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs
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lncRNASNP2: an updated database of functional SNPs and mutations in human and mouse lncRNAs

Nucleic acids research, 2018-01, Vol.46 (D1), p.D276-D280 [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/gkx1004 ;PMID: 29077939

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13
Genomic epidemiology of the Escherichia coli O104:H4 outbreaks in Europe, 2011
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Genomic epidemiology of the Escherichia coli O104:H4 outbreaks in Europe, 2011

Proceedings of the National Academy of Sciences - PNAS, 2012-02, Vol.109 (8), p.3065-3070 [Peer Reviewed Journal]

copyright © 1993-2008 National Acadamy of Sciences of the United States of America ;Copyright National Academy of Sciences Feb 21, 2012 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1121491109 ;PMID: 22315421

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14
Naturally occurring ERAP1 haplotypes encode functionally distinct alleles with fine substrate specificity
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Naturally occurring ERAP1 haplotypes encode functionally distinct alleles with fine substrate specificity

The Journal of immunology (1950), 2013-07, Vol.191 (1), p.35-43 [Peer Reviewed Journal]

ISSN: 0022-1767 ;EISSN: 1550-6606 ;DOI: 10.4049/jimmunol.1300598 ;PMID: 23733883

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15
Basset: learning the regulatory code of the accessible genome with deep convolutional neural networks
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Basset: learning the regulatory code of the accessible genome with deep convolutional neural networks

Genome research, 2016-07, Vol.26 (7), p.990-999 [Peer Reviewed Journal]

2016 Kelley et al.; Published by Cold Spring Harbor Laboratory Press. ;2016 ;ISSN: 1088-9051 ;EISSN: 1549-5469 ;DOI: 10.1101/gr.200535.115 ;PMID: 27197224

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16
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease
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Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease

Circulation research, 2018-02, Vol.122 (3), p.433-443 [Peer Reviewed Journal]

2018 American Heart Association, Inc. ;2017 The Authors. ;2017 The Authors. 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.117.312086 ;PMID: 29212778

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17
Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption
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Article
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Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption

International journal of epidemiology, 2019-06, Vol.48 (3), p.728-742 [Peer Reviewed Journal]

The Author(s) 2018. Published by Oxford University Press on behalf of the International Epidemiological Association. 2018 ;The Author(s) 2018. Published by Oxford University Press on behalf of the International Epidemiological Association. ;ISSN: 0300-5771 ;EISSN: 1464-3685 ;DOI: 10.1093/ije/dyy258 ;PMID: 30561657

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18
NONCODEV5: a comprehensive annotation database for long non-coding RNAs
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NONCODEV5: a comprehensive annotation database for long non-coding RNAs

Nucleic acids research, 2018-01, Vol.46 (D1), p.D308-D314 [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/gkx1107 ;PMID: 29140524

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19
Evolutionary history of tuberculosis shaped by conserved mutations in the PhoPR virulence regulator
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Evolutionary history of tuberculosis shaped by conserved mutations in the PhoPR virulence regulator

Proceedings of the National Academy of Sciences - PNAS, 2014-08, Vol.111 (31), p.11491-11496 [Peer Reviewed Journal]

copyright © 1993—2008 National Academy of Sciences of the United States of America ;Copyright National Academy of Sciences Aug 5, 2014 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1406693111 ;PMID: 25049399

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20
Invited Commentary: Detecting Individual and Global Horizontal Pleiotropy in Mendelian Randomization—A Job for the Humble Heterogeneity Statistic?
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Invited Commentary: Detecting Individual and Global Horizontal Pleiotropy in Mendelian Randomization—A Job for the Humble Heterogeneity Statistic?

American journal of epidemiology, 2018-12, Vol.187 (12), p.2681-2685 [Peer Reviewed Journal]

The Author(s) 2018. Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health. 2018 ;The Author(s) 2018. Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health. ;ISSN: 0002-9262 ;EISSN: 1476-6256 ;DOI: 10.1093/aje/kwy185 ;PMID: 30188969

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