skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index

Results 1 - 20 of 492  for All Library Resources

Results 1 2 3 4 5 next page
Show only
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Using electronic patient records to discover disease correlations and stratify patient cohorts
Material Type:
Article
Add to My Research

Using electronic patient records to discover disease correlations and stratify patient cohorts

PLoS computational biology, 2011-08, Vol.7 (8), p.e1002141-e1002141 [Peer Reviewed Journal]

Roque et al. 2011 ;2011 Roque 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: Roque FS, Jensen PB, Schmock H, Dalgaard M, Andreatta M, et al. (2011) Using Electronic Patient Records to Discover Disease Correlations and Stratify Patient Cohorts. PLoS Comput Biol 7(8): e1002141. doi:10.1371/journal.pcbi.1002141 ;ISSN: 1553-7358 ;ISSN: 1553-734X ;EISSN: 1553-7358 ;DOI: 10.1371/journal.pcbi.1002141 ;PMID: 21901084

Full text available

2
Methods of integrating data to uncover genotype-phenotype interactions
Material Type:
Article
Add to My Research

Methods of integrating data to uncover genotype-phenotype interactions

Nature reviews. Genetics, 2015-02, Vol.16 (2), p.85-97 [Peer Reviewed Journal]

COPYRIGHT 2015 Nature Publishing Group ;COPYRIGHT 2015 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2015 ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/nrg3868 ;PMID: 25582081

Full text available

3
From GWAS to Gene: Transcriptome-Wide Association Studies and Other Methods to Functionally Understand GWAS Discoveries
Material Type:
Article
Add to My Research

From GWAS to Gene: Transcriptome-Wide Association Studies and Other Methods to Functionally Understand GWAS Discoveries

Frontiers in genetics, 2021-09, Vol.12, p.713230-713230 [Peer Reviewed Journal]

Copyright © 2021 Li and Ritchie. 2021 Li and Ritchie ;ISSN: 1664-8021 ;EISSN: 1664-8021 ;DOI: 10.3389/fgene.2021.713230 ;PMID: 34659337

Full text available

4
Electronic health records and polygenic risk scores for predicting disease risk
Material Type:
Article
Add to My Research

Electronic health records and polygenic risk scores for predicting disease risk

Nature reviews. Genetics, 2020-08, Vol.21 (8), p.493-502 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Springer Nature Limited 2020. ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-020-0224-1 ;PMID: 32235907

Full text available

5
The success of pharmacogenomics in moving genetic association studies from bench to bedside: study design and implementation of precision medicine in the post-GWAS era
Material Type:
Article
Add to My Research

The success of pharmacogenomics in moving genetic association studies from bench to bedside: study design and implementation of precision medicine in the post-GWAS era

Human genetics, 2012-10, Vol.131 (10), p.1615-1626 [Peer Reviewed Journal]

The Author(s) 2012 ;COPYRIGHT 2012 Springer ;Springer-Verlag 2012 ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-012-1221-z ;PMID: 22923055

Full text available

6
Defining the role of common variation in the genomic and biological architecture of adult human height
Material Type:
Article
Add to My Research

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature genetics, 2014-11, Vol.46 (11), p.1173-1186 [Peer Reviewed Journal]

COPYRIGHT 2014 Nature Publishing Group ;COPYRIGHT 2014 Nature Publishing Group ;Wageningen University & Research ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3097 ;PMID: 25282103

Full text available

7
Pacific Symposium on Biocomputing 2023: Kohala Coast, Hawaii, USA, 3 – 7 January 2023
Material Type:
Book
Add to My Research

Pacific Symposium on Biocomputing 2023: Kohala Coast, Hawaii, USA, 3 – 7 January 2023

ISBN: 9789811270604 ;ISBN: 9811270600 ;DOI: 10.1142/13257

Digital Resources/Online E-Resources

8
A first update on mapping the human genetic architecture of COVID-19
Material Type:
Article
Add to My Research

A first update on mapping the human genetic architecture of COVID-19

Nature (London), 2022-08, Vol.608 (7921), p.E1-E10 [Peer Reviewed Journal]

Copyright Nature Publishing Group Aug 4, 2022 ;This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022 ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-022-04826-7 ;PMID: 35922517

Full text available

9
The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies
Material Type:
Article
Add to My Research

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies

BMC genomics, 2011-01, Vol.4 (1), p.13-13, Article 13 [Peer Reviewed Journal]

COPYRIGHT 2011 BioMed Central Ltd. ;COPYRIGHT 2011 BioMed Central Ltd. ;2011 McCarty et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright ©2011 McCarty et al; licensee BioMed Central Ltd. 2011 McCarty et al; licensee BioMed Central Ltd. ;ISSN: 1755-8794 ;ISSN: 1471-2164 ;EISSN: 1755-8794 ;EISSN: 1471-2164 ;DOI: 10.1186/1755-8794-4-13 ;PMID: 21269473

Full text available

10
Genetics of height and risk of atrial fibrillation: A Mendelian randomization study
Material Type:
Article
Add to My Research

Genetics of height and risk of atrial fibrillation: A Mendelian randomization study

PLoS medicine, 2020-10, Vol.17 (10), p.e1003288-e1003288 [Peer Reviewed Journal]

COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Levin 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. ;2020 Levin et al 2020 Levin et al ;ISSN: 1549-1676 ;ISSN: 1549-1277 ;EISSN: 1549-1676 ;DOI: 10.1371/journal.pmed.1003288 ;PMID: 33031386

Full text available

11
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations
Material Type:
Article
Add to My Research

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations

Bioinformatics, 2010-05, Vol.26 (9), p.1205-1210 [Peer Reviewed Journal]

The Author(s) 2010. Published by Oxford University Press. 2010 ;ISSN: 1367-4803 ;EISSN: 1460-2059 ;EISSN: 1367-4811 ;DOI: 10.1093/bioinformatics/btq126 ;PMID: 20335276

Full text available

12
Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease
Material Type:
Article
Add to My Research

Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease

The New England journal of medicine, 2016-03, Vol.374 (12), p.1123-1133 [Peer Reviewed Journal]

Copyright © 2016 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1510926 ;PMID: 26933753

Full text available

13
Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study
Material Type:
Article
Add to My Research

Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study

PLoS biology, 2013-09, Vol.11 (9), p.e1001661-e1001661 [Peer Reviewed Journal]

2013 ;2013 Public Library of Science. 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: Citation: Carlson CS, Matise TC, North KE, Haiman CA, Fesinmeyer MD, et al. (2013) Generalization and Dilution of Association Results from European GWAS in Populations of Non-European Ancestry: The PAGE Study. PLoS Biol 11(9): e1001661. doi:10.1371/journal.pbio.1001661 ;ISSN: 1545-7885 ;ISSN: 1544-9173 ;EISSN: 1545-7885 ;DOI: 10.1371/journal.pbio.1001661 ;PMID: 24068893

Full text available

14
Disrupting upstream translation in mRNAs is associated with human disease
Material Type:
Article
Add to My Research

Disrupting upstream translation in mRNAs is associated with human disease

Nature communications, 2021-03, Vol.12 (1), p.1515-14, Article 1515 [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/s41467-021-21812-1 ;PMID: 33750777

Full text available

15
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future
Material Type:
Article
Add to My Research

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

Genetics in medicine, 2013-10, Vol.15 (10), p.761-771 [Peer Reviewed Journal]

2013 The Author(s) ;The Author(s) 2013. This work is published under http://creativecommons.org/licenses/by-nc-nd/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2013 American College of Medical Genetics and Genomics 2013 American College of Medical Genetics and Genomics ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2013.72 ;PMID: 23743551

Full text available

16
Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network
Material Type:
Article
Add to My Research

Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

American journal of human genetics, 2019-09, Vol.105 (3), p.588-605 [Peer Reviewed Journal]

2019 American Society of Human Genetics ;Copyright © 2019 American Society of Human Genetics. All rights reserved. ;2019 American Society of Human Genetics. 2019 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2019.07.018 ;PMID: 31447099

Full text available

17
Using Biological Knowledge to Uncover the Mystery in the Search for Epistasis in Genome‐Wide Association Studies
Material Type:
Article
Add to My Research

Using Biological Knowledge to Uncover the Mystery in the Search for Epistasis in Genome‐Wide Association Studies

Annals of human genetics, 2011-01, Vol.75 (1), p.172-182 [Peer Reviewed Journal]

2010 The Author Annals of Human Genetics © 2010 Blackwell Publishing Ltd/University College London ;2010 The Author Annals of Human Genetics © 2010 Blackwell Publishing Ltd/University College London. ;ISSN: 0003-4800 ;EISSN: 1469-1809 ;DOI: 10.1111/j.1469-1809.2010.00630.x ;PMID: 21158748

Full text available

18
Genetic Determinants of Response to Warfarin during Initial Anticoagulation
Material Type:
Article
Add to My Research

Genetic Determinants of Response to Warfarin during Initial Anticoagulation

The New England journal of medicine, 2008-03, Vol.358 (10), p.999-1008 [Peer Reviewed Journal]

Copyright © 2008 Massachusetts Medical Society. All rights reserved. ;2008 INIST-CNRS ;Copyright 2008 Massachusetts Medical Society. ;Copyright © 2008 Massachusetts Medical Society. 2008 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa0708078 ;PMID: 18322281 ;CODEN: NEJMAG

Full text available

19
Estimating the effect size of a hidden causal factor between SNPs and a continuous trait: a mediation model approach
Material Type:
Article
Add to My Research

Estimating the effect size of a hidden causal factor between SNPs and a continuous trait: a mediation model approach

BMC bioinformatics, 2022-10, Vol.23 (1), p.420-420, Article 420 [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: 1471-2105 ;EISSN: 1471-2105 ;DOI: 10.1186/s12859-022-04977-4 ;PMID: 36229773

Full text available

20
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes
Material Type:
Article
Add to My Research

Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes

PLoS genetics, 2014-08, Vol.10 (8), p.e1004517-e1004517 [Peer Reviewed Journal]

COPYRIGHT 2014 Public Library of Science ;COPYRIGHT 2014 Public Library of Science ;2014 ;2014 Public Library of Science. 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: Ng MCY, Shriner D, Chen BH, Li J, Chen W-M, Guo X, et al. (2014) Meta-Analysis of Genome-Wide Association Studies in African Americans Provides Insights into the Genetic Architecture of Type 2 Diabetes. PLoS Genet 10(8): e1004517. doi:10.1371/journal.pgen.1004517 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1004517 ;PMID: 25102180

Full text available

Results 1 - 20 of 492  for All Library Resources

Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Show only

  1. Peer-reviewed Journals (360)

Refine My Results

Creation Date 

From To
  1. Before 2005  (12)
  2. 2005 To 2008  (34)
  3. 2009 To 2012  (64)
  4. 2013 To 2017  (183)
  5. After 2017  (202)
  6. More options open sub menu

Language 

  1. English  (491)
  2. Japanese  (54)
  3. Norwegian  (2)
  4. More options open sub menu

Searching Remote Databases, Please Wait