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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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SNP Selection in genome-wide and candidate gene studies via penalized logistic regressionGenetic epidemiology, 2010-12, Vol.34 (8), p.879-891 [Peer Reviewed Journal]2010 Wiley‐Liss, Inc. ;2010 Wiley-Liss, Inc. ;2010 Wiley-Liss, Inc. 2010 ;ISSN: 0741-0395 ;ISSN: 1098-2272 ;EISSN: 1098-2272 ;DOI: 10.1002/gepi.20543 ;PMID: 21104890Full text available |
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Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease: A Mendelian Randomization StudyNeurology, 2022-01, Vol.98 (4), p.e343-e351 [Peer Reviewed Journal]2021 American Academy of Neurology. ;ISSN: 0028-3878 ;EISSN: 1526-632X ;DOI: 10.1212/WNL.0000000000013120 ;PMID: 34845052Full text available |
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A composite biomarker of neutrophil-lymphocyte ratio and hemoglobin level correlates with clinical response to PD-1 and PD-L1 inhibitors in advanced non-small cell lung cancersBMC cancer, 2021-04, Vol.21 (1), p.441-441, Article 441 [Peer Reviewed Journal]COPYRIGHT 2021 BioMed Central Ltd. ;COPYRIGHT 2021 BioMed Central Ltd. ;2021. 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) 2021 ;ISSN: 1471-2407 ;EISSN: 1471-2407 ;DOI: 10.1186/s12885-021-08194-9 ;PMID: 33882890Full text available |
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Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical HeterogeneityStroke (1970), 2023-03, Vol.54 (3), p.810-818 [Peer Reviewed Journal]info:eu-repo/semantics/openAccess ;Attribution ;2023 The Authors. 2023 ;ISSN: 0039-2499 ;ISSN: 1524-4628 ;EISSN: 1524-4628 ;DOI: 10.1161/STROKEAHA.122.040715 ;PMID: 36655558Full text available |
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Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitisPLoS genetics, 2018-12, Vol.14 (12), p.e1007833 [Peer Reviewed Journal]COPYRIGHT 2018 Public Library of Science ;COPYRIGHT 2018 Public Library of Science ;2018 Darlay 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. ;2018 Darlay et al 2018 Darlay et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1007833 ;PMID: 30507971Full text available |
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Human GPR17 missense variants identified in metabolic disease patients have distinct downstream signaling profilesThe Journal of biological chemistry, 2021-07, Vol.297 (1), p.100881-100881, Article 100881 [Peer Reviewed Journal]2021 The Authors ;Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved. ;2021 The Authors 2021 ;ISSN: 0021-9258 ;EISSN: 1083-351X ;DOI: 10.1016/j.jbc.2021.100881 ;PMID: 34144038Full text available |
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Targeted Next-Generation Sequencing Reveals Exceptionally High Rates of Molecular Driver Mutations in Never-Smokers With Lung AdenocarcinomaThe oncologist (Dayton, Ohio), 2022-06, Vol.27 (6), p.476-486 [Peer Reviewed Journal]The Author(s) 2022. Published by Oxford University Press. ;COPYRIGHT 2022 Oxford University Press ;The Author(s) 2022. Published by Oxford University Press. 2022 ;ISSN: 1083-7159 ;EISSN: 1549-490X ;DOI: 10.1093/oncolo/oyac035 ;PMID: 35298662Full text available |
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Melanocortin 4 Receptor Pathway Dysfunction in Obesity: Patient Stratification Aimed at MC4R Agonist TreatmentThe journal of clinical endocrinology and metabolism, 2018-07, Vol.103 (7), p.2601-2612 [Peer Reviewed Journal]Copyright © Oxford University Press 2015 ;Copyright © 2018 Endocrine Society ;Copyright © 2018 Endocrine Society 2018 ;ISSN: 0021-972X ;EISSN: 1945-7197 ;DOI: 10.1210/jc.2018-00258 ;PMID: 29726959Full text available |
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Analysis of Real‐World Data to Investigate the Impact of Race and Ethnicity on Response to Programmed Cell Death‐1 and Programmed Cell Death‐Ligand 1 Inhibitors in Advanced Non‐Small Cell Lung CancersThe oncologist (Dayton, Ohio), 2021-07, Vol.26 (7), p.e1226-e1239 [Peer Reviewed Journal]2021 Mount Sinai Genomics, Inc., DBA Sema4 and Icahn School of Medicine at Mount Sinai. The Oncologist published by Wiley Periodicals LLC on behalf of AlphaMed Press. ;COPYRIGHT 2021 Oxford University Press ;ISSN: 1083-7159 ;EISSN: 1549-490X ;DOI: 10.1002/onco.13780 ;PMID: 33829580Full text available |
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Comparative analyses of population-scale phenomic data in electronic medical records reveal race-specific disease networksBioinformatics, 2016-06, Vol.32 (12), p.i101-i110 [Peer Reviewed Journal]The Author 2016. Published by Oxford University Press. ;The Author 2016. Published by Oxford University Press. 2016 ;ISSN: 1367-4803 ;EISSN: 1367-4811 ;EISSN: 1460-2059 ;DOI: 10.1093/bioinformatics/btw282 ;PMID: 27307606Full text available |
| 11 |
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A loss of function variant in CASP7 protects against Alzheimer's disease in homozygous APOE ε4 allele carriersBMC genomics, 2016-06, Vol.17 Suppl 2 (S2), p.445-445, Article 445 [Peer Reviewed Journal]Ayers et al. 2016 ;ISSN: 1471-2164 ;EISSN: 1471-2164 ;DOI: 10.1186/s12864-016-2725-z ;PMID: 27358062Full text available |
| 12 |
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Identification of Grouped Rare and Common Variants via Penalized Logistic RegressionGenetic epidemiology, 2013-09, Vol.37 (6), p.592-602 [Peer Reviewed Journal]2013 The Authors. * published by Wiley Periodicals, Inc. ;2013 WILEY PERIODICALS, INC. ;2013 WILEY PERIODICALS, INC. 2013 ;ISSN: 0741-0395 ;EISSN: 1098-2272 ;DOI: 10.1002/gepi.21746 ;PMID: 23836590Full text available |
| 13 |
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Penalized estimation of haplotype frequenciesBioinformatics, 2008-07, Vol.24 (14), p.1596-1602 [Peer Reviewed Journal]The Author 2008. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2008 ;2008 INIST-CNRS ;ISSN: 1367-4803 ;EISSN: 1460-2059 ;EISSN: 1367-4811 ;DOI: 10.1093/bioinformatics/btn236 ;PMID: 18487240 ;CODEN: BOINFPFull text available |
| 14 |
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Correction to: Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traitsBMC medical genomics, 2019-11, Vol.12 (1), p.154-154, Article 154 [Peer Reviewed Journal]COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;The Author(s). 2019 ;ISSN: 1755-8794 ;EISSN: 1755-8794 ;DOI: 10.1186/s12920-019-0573-9 ;PMID: 31684948Full text available |
| 15 |
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Analysis of Genetic Analysis Workshop 18 data with gene-based penalized regressionBMC proceedings, 2014, Vol.8 (Suppl 1), p.S43-S43, Article S43 [Peer Reviewed Journal]2014 Ayers and Cordell; 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. ;Copyright © 2014 Ayers and Cordell; licensee BioMed Central Ltd. 2014 Ayers and Cordell; licensee BioMed Central Ltd. ;ISSN: 1753-6561 ;EISSN: 1753-6561 ;DOI: 10.1186/1753-6561-8-S1-S43 ;PMID: 25519325Full text available |
| 16 |
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traitsNature genetics, 2018-10, Vol.50 (10), p.1412-1425 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Oct 2018 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0205-x ;PMID: 30224653Full text available |
| 17 |
Material Type: Article
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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular riskNature genetics, 2017-03, Vol.49 (3), p.403-415 [Peer Reviewed Journal]COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2017 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3768 ;PMID: 28135244Full text available |
| 18 |
Material Type: Article
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A meta-analysis of genome-wide association studies identifies multiple longevity genesNature communications, 2019-08, Vol.10 (1), p.3669-14, Article 3669 [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. ;The Author(s) 2019. corrected publication 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. ;Attribution ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-11558-2 ;PMID: 31413261Full text available |
| 19 |
Material Type: Article
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Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the KidneyHypertension (Dallas, Tex. 1979), 2017-09, Vol.70 (3), p.e4 [Peer Reviewed Journal]2017 American Heart Association, Inc ;ISSN: 0194-911X ;ISSN: 1524-4563 ;EISSN: 1524-4563 ;DOI: 10.1161/HYPERTENSIONAHA.117.09438 ;PMID: 28739976Full text available |
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Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of ageHuman molecular genetics, 2014-08, Vol.23 (16), p.4420-4432 [Peer Reviewed Journal]The Author 2014. Published by Oxford University Press. ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author 2014. Published by Oxford University Press. 2014 ;ISSN: 0964-6906 ;ISSN: 1460-2083 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddu139 ;PMID: 24688116Full text available |
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