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Results 1 - 20 of 30  for All Library Resources

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1
Machine learning of native T1 mapping radiomics for classification of hypertrophic cardiomyopathy phenotypes
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Machine learning of native T1 mapping radiomics for classification of hypertrophic cardiomyopathy phenotypes

Scientific reports, 2021-12, Vol.11 (1), p.23596-23596, Article 23596 [Peer Reviewed Journal]

2021. The Author(s). ;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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-02971-z ;PMID: 34880319

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2
A Chinese multicenter retrospective study of isolated increased nuchal translucency associated chromosome anomaly and prenatal diagnostic suggestions
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A Chinese multicenter retrospective study of isolated increased nuchal translucency associated chromosome anomaly and prenatal diagnostic suggestions

Scientific reports, 2021-03, Vol.11 (1), p.5596-5596, Article 5596 [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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-85108-6 ;PMID: 33692422

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3
Dynamics and implications of circulating anti-angiogenic VEGF-A165b isoform in patients with ST-elevation myocardial infarction
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Dynamics and implications of circulating anti-angiogenic VEGF-A165b isoform in patients with ST-elevation myocardial infarction

Scientific reports, 2017-08, Vol.7 (1), p.1-14, Article 9962 [Peer Reviewed Journal]

2017. 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) 2017 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-017-10505-9 ;PMID: 28855597

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4
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
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Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders

Nature communications, 2019-10, Vol.10 (1), p.4897-10, Article 4897 [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 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-12869-0 ;PMID: 31653860

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5
Triple X syndrome: a review of the literature
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Triple X syndrome: a review of the literature

European journal of human genetics : EJHG, 2010-03, Vol.18 (3), p.265-271 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Mar 2010 ;Copyright © 2010 Macmillan Publishers Limited 2010 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2009.109 ;PMID: 19568271

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6
Association between chronic obstructive pulmonary disease and in-hospital mortality after percutaneous coronary intervention: a retrospective cohort study in Germany
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Association between chronic obstructive pulmonary disease and in-hospital mortality after percutaneous coronary intervention: a retrospective cohort study in Germany

Scientific reports, 2024-03, Vol.14 (1), p.6044-6044 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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) 2024 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-56255-3 ;PMID: 38472246

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7
Risk of stroke in patients with rheumatism: a nationwide longitudinal population-based study
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Risk of stroke in patients with rheumatism: a nationwide longitudinal population-based study

Scientific reports, 2014-06, Vol.4 (1), p.5110-5110, Article 5110 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jun 2014 ;Copyright © 2014, Macmillan Publishers Limited. All rights reserved 2014 Macmillan Publishers Limited. All rights reserved ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep05110 ;PMID: 24898360

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8
Morbidity in 47,XYY syndrome: a nationwide epidemiological study of hospital diagnoses and medication use
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Morbidity in 47,XYY syndrome: a nationwide epidemiological study of hospital diagnoses and medication use

Genetics in medicine, 2020-09, Vol.22 (9), p.1542-1551 [Peer Reviewed Journal]

American College of Medical Genetics and Genomics 2020. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-020-0837-y ;PMID: 32475987

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9
Risk factors analysis of COVID-19 patients with ARDS and prediction based on machine learning
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Risk factors analysis of COVID-19 patients with ARDS and prediction based on machine learning

Scientific reports, 2021-02, Vol.11 (1), p.2933-12, Article 2933 [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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-82492-x ;PMID: 33536460

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10
Limited ability of increased sequencing depth in detecting cases missed by noninvasive prenatal testing: a comparative analysis of 3 clinical cases
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Limited ability of increased sequencing depth in detecting cases missed by noninvasive prenatal testing: a comparative analysis of 3 clinical cases

Scientific reports, 2024-01, Vol.14 (1), p.2304-2304, Article 2304 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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) 2024 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-52767-0 ;PMID: 38280905

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11
Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach
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Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach

Genetics in medicine, 2016-09, Vol.18 (9), p.940-948 [Peer Reviewed Journal]

Copyright Nature Publishing Group Sep 2016 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2015.199 ;PMID: 26820068

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12
Distinct composition of the oral indigenous microbiota in South Korean and Japanese adults
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Distinct composition of the oral indigenous microbiota in South Korean and Japanese adults

Scientific reports, 2014-11, Vol.4 (1), p.6990-6990, Article 6990 [Peer Reviewed Journal]

Copyright Nature Publishing Group Nov 2014 ;Copyright © 2014, Macmillan Publishers Limited. All rights reserved 2014 Macmillan Publishers Limited. All rights reserved ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep06990 ;PMID: 25384884

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13
Gene-environment interactions and their impact on human health
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Gene-environment interactions and their impact on human health

Genes and immunity, 2023-02, Vol.24 (1), p.1-11 [Peer Reviewed Journal]

2022. The Author(s). ;The Author(s) 2022. 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. ;ISSN: 1476-5470 ;ISSN: 1466-4879 ;EISSN: 1476-5470 ;DOI: 10.1038/s41435-022-00192-6 ;PMID: 36585519

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14
Spatio-temporal prediction of the COVID-19 pandemic in US counties: modeling with a deep LSTM neural network
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Spatio-temporal prediction of the COVID-19 pandemic in US counties: modeling with a deep LSTM neural network

Scientific reports, 2021-11, Vol.11 (1), p.21715-21715, Article 21715 [Peer Reviewed Journal]

2021. The Author(s). ;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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-01119-3 ;PMID: 34741093

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15
Implications of germline copy-number variations in psychiatric disorders: review of large-scale genetic studies
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Implications of germline copy-number variations in psychiatric disorders: review of large-scale genetic studies

Journal of human genetics, 2021-01, Vol.66 (1), p.25-37 [Peer Reviewed Journal]

The Author(s), under exclusive licence to The Japan Society of Human Genetics 2020. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-020-00838-1 ;PMID: 32958875

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16
Comorbidity landscape of the Danish patient population affected by chromosome abnormalities
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Comorbidity landscape of the Danish patient population affected by chromosome abnormalities

Genetics in medicine, 2019-11, Vol.21 (11), p.2485-2495 [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. ;The Author(s) 2019 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0519-9 ;PMID: 31019277

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17
The impact of lifestyle, measured with the HLPCQ questionnaire on the prevalence of metabolic syndrome in Poland: a multicenter study
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The impact of lifestyle, measured with the HLPCQ questionnaire on the prevalence of metabolic syndrome in Poland: a multicenter study

Scientific reports, 2024-05, Vol.14 (1), p.10070-10070 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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. ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-60866-1 ;PMID: 38698159

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18
X inactivation in triploidy and trisomy : the search for autosomal transfactors that choose the active X
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X inactivation in triploidy and trisomy : the search for autosomal transfactors that choose the active X

European journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.153-162 [Peer Reviewed Journal]

2008 INIST-CNRS ;Copyright Nature Publishing Group Feb 2008 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5201944 ;PMID: 17971834

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19
Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities
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Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities

European journal of human genetics : EJHG, 2013-07, Vol.21 (7), p.725-730 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 2013 ;Copyright © 2013 Macmillan Publishers Limited 2013 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2012.253 ;PMID: 23211699

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20
Survival among people with Down syndrome: a nationwide population-based study in Denmark
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Survival among people with Down syndrome: a nationwide population-based study in Denmark

Genetics in medicine, 2013-01, Vol.15 (1), p.64-69 [Peer Reviewed Journal]

American College of Medical Genetics and Genomics 2013. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2012.93 ;PMID: 22878506

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