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 189  for All Library Resources

Sorted by: Sorted by: RelevanceOr hit Enter to replace sort method
Results 1 2 3 4 5 next page
Refined by: language: Norwegian remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
New insights into the genetic etiology of Alzheimer's disease and related dementias
New insights into the genetic etiology of Alzheimer's disease and related dementias
Material Type:
Article 		Add to My Research

New insights into the genetic etiology of Alzheimer's disease and related dementias

Nature genetics, 2022, Vol.54 (4), p.412-436 [Peer Reviewed Journal]

2022. The Author(s). ;Copyright Nature Publishing Group Apr 2022 ;info:eu-repo/semantics/openAccess ;Attribution ;The Author(s) 2022 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01024-z ;PMID: 35379992

Full text available

Citations Cited by
2
Two-view digital breast tomosynthesis versus digital mammography in a population-based breast cancer screening programme (To-Be): a randomised, controlled trial
Two-view digital breast tomosynthesis versus digital mammography in a population-based breast cancer screening programme (To-Be): a randomised, controlled trial
Material Type:
Article 		Add to My Research

Two-view digital breast tomosynthesis versus digital mammography in a population-based breast cancer screening programme (To-Be): a randomised, controlled trial

The lancet oncology, 2019-06, Vol.20 (6), p.795-805 [Peer Reviewed Journal]

2019 Elsevier Ltd ;Copyright © 2019 Elsevier Ltd. All rights reserved. ;2019. Elsevier Ltd ;info:eu-repo/semantics/openAccess ;ISSN: 1470-2045 ;EISSN: 1474-5488 ;DOI: 10.1016/S1470-2045(19)30161-5 ;PMID: 31078459

Full text available

Citations Cited by
3
Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
Material Type:
Article 		Add to My Research

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

Gut, 2018-07, Vol.67 (7), p.1306-1316 [Peer Reviewed Journal]

Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;Copyright: 2018 © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;info:eu-repo/semantics/openAccess ;Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. 2018 ;ISSN: 0017-5749 ;ISSN: 1468-3288 ;EISSN: 1468-3288 ;DOI: 10.1136/gutjnl-2017-314057 ;PMID: 28754778

Full text available

Citations Cited by
4
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Material Type:
Article 		Add to My Research

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Genetics in medicine, 2020-01, Vol.22 (1), p.15-25 [Peer Reviewed Journal]

2019. This work is published under http://creativecommons.org/licenses/by-nc-sa/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;info:eu-repo/semantics/openAccess ;The Author(s) 2019 ;ISSN: 1098-3600 ;ISSN: 1530-0366 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0596-9 ;PMID: 31337882

Full text available

Citations Cited by
5
Re-definition of claudin-low as a breast cancer phenotype
Re-definition of claudin-low as a breast cancer phenotype
Material Type:
Article 		Add to My Research

Re-definition of claudin-low as a breast cancer phenotype

Nature communications, 2020-04, Vol.11 (1), p.1787-1787, Article 1787 [Peer Reviewed Journal]

The Author(s) 2020. 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. ;info:eu-repo/semantics/openAccess ;The Author(s) 2020 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-15574-5 ;PMID: 32286297

Full text available

Citations Cited by
6
Body mass index and all cause mortality in HUNT and UK Biobank studies: linear and non-linear mendelian randomisation analyses
Body mass index and all cause mortality in HUNT and UK Biobank studies: linear and non-linear mendelian randomisation analyses
Material Type:
Article 		Add to My Research

Body mass index and all cause mortality in HUNT and UK Biobank studies: linear and non-linear mendelian randomisation analyses

BMJ (Online), 2019-03, Vol.364, p.l1042-l1042 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go tohttp://group.bmj.com/group/rights-licensing/permissions2019BMJThis is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See:http://creativecommons.org/licenses/by/4.0/. ;info:eu-repo/semantics/openAccess ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to 2019 BMJ ;ISSN: 0959-8138 ;ISSN: 1756-1833 ;EISSN: 1756-1833 ;DOI: 10.1136/bmj.l1042 ;PMID: 30957776

Full text available

Citations Cited by
7
Homocysteine and Dementia: An International Consensus Statement
Homocysteine and Dementia: An International Consensus Statement
Material Type:
Article 		Add to My Research

Homocysteine and Dementia: An International Consensus Statement

Journal of Alzheimer's disease, 2018-01, Vol.62 (2), p.561 [Peer Reviewed Journal]

info:eu-repo/semantics/openAccess ;ISSN: 1387-2877 ;ISSN: 1875-8908 ;EISSN: 1875-8908 ;DOI: 10.3233/JAD-171042

Digital Resources/Online E-Resources

Citations Cited by
8
Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study
Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study
Material Type:
Article 		Add to My Research

Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study

BMJ (Online), 2018-08, Vol.362, p.k3225-k3225 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions 2018 BMJ This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;info:eu-repo/semantics/openAccess ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to 2018 BMJ ;ISSN: 0959-8138 ;ISSN: 1756-1833 ;EISSN: 1756-1833 ;DOI: 10.1136/bmj.k3225 ;PMID: 30158200

Full text available

Citations Cited by
9
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Material Type:
Article 		Add to My Research

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

Nature genetics, 2020-12, Vol.52 (12), p.1303-1313 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Dec 2020 ;info:eu-repo/semantics/openAccess ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-020-00725-7 ;PMID: 33199917

Full text available

Citations Cited by
10
Stroke genetics informs drug discovery and risk prediction across ancestries
Stroke genetics informs drug discovery and risk prediction across ancestries
Material Type:
Article 		Add to My Research

Stroke genetics informs drug discovery and risk prediction across ancestries

Nature (London), 2022, Vol.611 (7934), p.115-123 [Peer Reviewed Journal]

2022. The Author(s). ;Copyright Nature Publishing Group Nov 3, 2022 ;info:eu-repo/semantics/openAccess ;Attribution ;The Author(s) 2022 ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-022-05165-3 ;PMID: 36180795

Full text available

Citations Cited by
11
Identification of nine new susceptibility loci for endometrial cancer
Identification of nine new susceptibility loci for endometrial cancer
Material Type:
Article 		Add to My Research

Identification of nine new susceptibility loci for endometrial cancer

Nature communications, 2018-08, Vol.9 (1), p.3166-12, Article 3166 [Peer Reviewed Journal]

2018. 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. ;info:eu-repo/semantics/openAccess ;The Author(s) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-05427-7 ;PMID: 30093612

Full text available

Citations Cited by
12
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes
Material Type:
Article 		Add to My Research

Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes

Nature communications, 2019-08, Vol.10 (1), p.3503-12, Article 3503 [Peer Reviewed Journal]

2019. 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. ;info:eu-repo/semantics/openAccess ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-11456-7 ;PMID: 31409809

Full text available

Citations Cited by
13
Post-transplant diabetes mellitus in patients with solid organ transplants
Post-transplant diabetes mellitus in patients with solid organ transplants
Material Type:
Article 		Add to My Research

Post-transplant diabetes mellitus in patients with solid organ transplants

Nature reviews. Endocrinology, 2019-03, Vol.15 (3), p.172-188 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;2018© Springer Nature Limited 2018 ;info:eu-repo/semantics/openAccess ;ISSN: 1759-5029 ;EISSN: 1759-5037 ;DOI: 10.1038/s41574-018-0137-7 ;PMID: 30622369

Full text available

Citations Cited by
14
Efficacy and Safety of Empagliflozin in Renal Transplant Recipients With Posttransplant Diabetes Mellitus
Efficacy and Safety of Empagliflozin in Renal Transplant Recipients With Posttransplant Diabetes Mellitus
Material Type:
Article 		Add to My Research

Efficacy and Safety of Empagliflozin in Renal Transplant Recipients With Posttransplant Diabetes Mellitus

Diabetes care, 2019-06, Vol.42 (6), p.1067-1074 [Peer Reviewed Journal]

2019 by the American Diabetes Association. ;Copyright American Diabetes Association Jun 1, 2019 ;info:eu-repo/semantics/openAccess ;ISSN: 0149-5992 ;EISSN: 1935-5548 ;DOI: 10.2337/dc19-0093 ;PMID: 30862658

Full text available

Citations Cited by
15
Prenatal fever and autism risk
Prenatal fever and autism risk
Material Type:
Article 		Add to My Research

Prenatal fever and autism risk

Molecular psychiatry, 2018-03, Vol.23 (3), p.759-766 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2018 ;info:eu-repo/semantics/openAccess ;Copyright © 2018 The Author(s) 2018 The Author(s) ;ISSN: 1359-4184 ;EISSN: 1476-5578 ;DOI: 10.1038/mp.2017.119 ;PMID: 28607458

Full text available

Citations Cited by
16
Cerebral small vessel disease genomics and its implications across the lifespan
Cerebral small vessel disease genomics and its implications across the lifespan
Material Type:
Article 		Add to My Research

Cerebral small vessel disease genomics and its implications across the lifespan

Nature communications, 2020-12, Vol.11 (1), p.6285-6285, Article 6285 [Peer Reviewed Journal]

The Author(s) 2020. 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. ;info:eu-repo/semantics/openAccess ;Attribution ;The Author(s) 2020 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-19111-2 ;PMID: 33293549

Full text available

Citations Cited by
17
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Material Type:
Article 		Add to My Research

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Nature communications, 2019-04, Vol.10 (1), p.1741-18, Article 1741 [Peer Reviewed Journal]

The Author(s) 2019. 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. ;info:eu-repo/semantics/openAccess ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-08053-5 ;PMID: 30988301

Full text available

Citations Cited by
18
Polygenic overlap and shared genetic loci between loneliness, severe mental disorders, and cardiovascular disease risk factors suggest shared molecular mechanisms
Polygenic overlap and shared genetic loci between loneliness, severe mental disorders, and cardiovascular disease risk factors suggest shared molecular mechanisms
Material Type:
Article 		Add to My Research

Polygenic overlap and shared genetic loci between loneliness, severe mental disorders, and cardiovascular disease risk factors suggest shared molecular mechanisms

Translational psychiatry, 2021-01, Vol.11 (1), p.3-3, Article 3 [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. ;info:eu-repo/semantics/openAccess ;The Author(s) 2021 ;ISSN: 2158-3188 ;EISSN: 2158-3188 ;DOI: 10.1038/s41398-020-01142-4 ;PMID: 33414458

Full text available

Citations Cited by
19
Genome-wide association study identifies RNF123 locus as associated with chronic widespread musculoskeletal pain
Genome-wide association study identifies RNF123 locus as associated with chronic widespread musculoskeletal pain
Material Type:
Article 		Add to My Research

Genome-wide association study identifies RNF123 locus as associated with chronic widespread musculoskeletal pain

Annals of the rheumatic diseases, 2021-09, Vol.80 (9), p.1227-1235 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;info:eu-repo/semantics/openAccess ;Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. 2021 ;ISSN: 0003-4967 ;EISSN: 1468-2060 ;DOI: 10.1136/annrheumdis-2020-219624 ;PMID: 33926923

Full text available

Citations Cited by
20
Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort
Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort
Material Type:
Article 		Add to My Research

Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort

Nature communications, 2020-10, Vol.11 (1), p.5404-12, Article 5404 [Peer Reviewed Journal]

The Author(s) 2020. 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. ;info:eu-repo/semantics/openAccess ;The Author(s) 2020 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-19257-z ;PMID: 33106479

Full text available

Citations Cited by

Results 1 - 20 of 189  for All Library Resources

Sorted by: Sorted by: RelevanceOr hit Enter to replace sort method
Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Refine My Results

Creation Date 

From To
Refine
  1. Before 2013  (2)
  2. 2013 To 2014  (2)
  3. 2015 To 2016  (3)
  4. 2017 To 2019  (119)
  5. After 2019  (64)
  6. More options open sub menu

Language 

  1. Japanese  (22)
  2. Swedish  (4)
  3. Danish  (3)
  4. German  (2)
  5. French  (1)
  6. More options open sub menu
INSPIRE LIBRARY - TON DUC THANG UNIVERSITY (84-028) 37 755 057 Feedback
19 Nguyen Huu Tho St. Dist.7, HCM thuvien@tdtu.edu.vn

Copyright © 2017 INSPIRE LIBRARY - TON DUC THANG UNIVERSITY

Searching Remote Databases, Please Wait