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Results 1 - 20 of 1,857  for All Library Resources

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1
Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland
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Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland

European journal of human genetics : EJHG, 2020-12, Vol.28 (12), p.1656-1661 [Peer Reviewed Journal]

The Author(s), under exclusive licence to European Society of Human Genetics 2020. ;The Author(s), under exclusive licence to European Society of Human Genetics 2020 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-020-0665-1 ;PMID: 32523053

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2
The Global State of the Genetic Counseling Profession
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The Global State of the Genetic Counseling Profession

European journal of human genetics : EJHG, 2019-02, Vol.27 (2), p.183-197 [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 Copyright © The Author(s) 2018. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/ ;The Author(s) 2018 ;ISSN: 1018-4813 ;ISSN: 1476-5438 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-018-0252-x ;PMID: 30291341

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3
Evaluation of telephone genetic counselling to facilitate germline BRCA1/2 testing in women with high-grade serous ovarian cancer
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Evaluation of telephone genetic counselling to facilitate germline BRCA1/2 testing in women with high-grade serous ovarian cancer

European journal of human genetics : EJHG, 2019-08, Vol.27 (8), p.1186-1196 [Peer Reviewed Journal]

European Society of Human Genetics 2019. ;European Society of Human Genetics 2019 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-019-0390-9 ;PMID: 30962500

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4
Telegenetics use in presymptomatic genetic counselling: patient evaluations on satisfaction and quality of care
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Telegenetics use in presymptomatic genetic counselling: patient evaluations on satisfaction and quality of care

European journal of human genetics : EJHG, 2016-04, Vol.24 (4), p.513-520 [Peer Reviewed Journal]

Copyright Nature Publishing Group Apr 2016 ;Copyright © 2016 Macmillan Publishers Limited 2016 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2015.164 ;PMID: 26173963

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5
Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics
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Article
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Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

European journal of human genetics : EJHG, 2019-02, Vol.27 (2), p.169-182 [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. ;The Author(s) 2018 ;ISSN: 1018-4813 ;ISSN: 1476-5438 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-018-0285-1 ;PMID: 30310124

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6
BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study
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BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.881-888 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jun 2016 ;The Author(s) 2016. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2016 Macmillan Publishers Limited 2016 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2015.196 ;PMID: 26350514

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7
Decision making and experiences of young adults undergoing presymptomatic genetic testing for familial cancer: a longitudinal grounded theory study
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Decision making and experiences of young adults undergoing presymptomatic genetic testing for familial cancer: a longitudinal grounded theory study

European journal of human genetics : EJHG, 2018-01, Vol.26 (1), p.44-53 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jan 2018 ;European Society of Human Genetics 2017 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-017-0030-1 ;PMID: 29162934

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8
Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow
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Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow

European journal of human genetics : EJHG, 2011-12, Vol.19 (12), p.1230-1237 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Dec 2011 ;Distributed under a Creative Commons Attribution 4.0 International License ;Copyright © 2011 Macmillan Publishers Limited 2011 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2011.119 ;PMID: 21694736

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9
Attitudes, knowledge and consequences of uncertain genetic findings in hypertrophic cardiomyopathy
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Attitudes, knowledge and consequences of uncertain genetic findings in hypertrophic cardiomyopathy

European journal of human genetics : EJHG, 2017-06, Vol.25 (7), p.809-815 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jun 2017 ;Copyright © 2017 Macmillan Publishers Limited, part of Springer Nature. 2017 Macmillan Publishers Limited, part of Springer Nature. ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2017.66 ;PMID: 28594412

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10
Quality issues concerning genetic counselling for presymptomatic testing: a European Delphi study
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Article
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Quality issues concerning genetic counselling for presymptomatic testing: a European Delphi study

European journal of human genetics : EJHG, 2015-11, Vol.23 (11), p.1468-1472 [Peer Reviewed Journal]

Copyright Nature Publishing Group Nov 2015 ;Copyright © 2015 Macmillan Publishers Limited 2015 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2015.23 ;PMID: 25689925

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11
A systematic review of factors that act as barriers to patient referral to genetic services
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Article
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A systematic review of factors that act as barriers to patient referral to genetic services

European journal of human genetics : EJHG, 2015-06, Vol.23 (6), p.739-745 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jun 2015 ;Copyright © 2015 Macmillan Publishers Limited 2015 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2014.180 ;PMID: 25205405

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12
Mainstream genetic testing for breast cancer patients: early experiences from the Parkville Familial Cancer Centre
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Article
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Mainstream genetic testing for breast cancer patients: early experiences from the Parkville Familial Cancer Centre

European journal of human genetics : EJHG, 2021-05, Vol.29 (5), p.872-880 [Peer Reviewed Journal]

The Author(s), under exclusive licence to European Society of Human Genetics 2021. ;The Author(s), under exclusive licence to European Society of Human Genetics 2021 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-021-00848-3 ;PMID: 33723355

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13
A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial
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Article
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A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial

European journal of human genetics : EJHG, 2022-02, Vol.30 (2), p.203-210 [Peer Reviewed Journal]

2021. The Author(s), under exclusive licence to European Society of Human Genetics. ;The Author(s), under exclusive licence to European Society of Human Genetics 2021. ;The Author(s), under exclusive licence to European Society of Human Genetics 2021 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-021-00993-9 ;PMID: 34815540

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14
Genetic Counselling for the Laboratory: building bridges between disciplines
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Article
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Genetic Counselling for the Laboratory: building bridges between disciplines

European Journal of Human Genetics, 2019-03, Vol.27 (3), p.503-504 [Peer Reviewed Journal]

Copyright Nature Publishing Group Mar 2019 ;European Society of Human Genetics 2018 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-018-0278-0 ;PMID: 30349064

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15
Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes
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Article
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Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes

European journal of human genetics : EJHG, 2010-12, Vol.18 (12), p.1271-1273 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Dec 2010 ;Copyright © 2010 Macmillan Publishers Limited 2010 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2010.129 ;PMID: 20736974

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16
Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery
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Article
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Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.794-802 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jun 2016 ;The Author(s) 2016. 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. ;Copyright © 2016 Macmillan Publishers Limited 2016 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2015.215 ;PMID: 26443265

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17
Patient experience and utility of genetic information: a cross-sectional study among patients tested for cancer susceptibility and thrombophilia
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Article
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Patient experience and utility of genetic information: a cross-sectional study among patients tested for cancer susceptibility and thrombophilia

European journal of human genetics : EJHG, 2018-04, Vol.26 (4), p.518-526 [Peer Reviewed Journal]

2018. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Authors 2018 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-017-0083-1 ;PMID: 29374276

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18
A randomized experimental study to test the effects of discussing uncertainty during cancer genetic counseling: different strategies, different outcomes?
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Article
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A randomized experimental study to test the effects of discussing uncertainty during cancer genetic counseling: different strategies, different outcomes?

European journal of human genetics : EJHG, 2021-05, Vol.29 (5), p.789-799 [Peer Reviewed Journal]

The Author(s), under exclusive licence to European Society of Human Genetics 2021. ;The Author(s), under exclusive licence to European Society of Human Genetics 2021 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-020-00799-1 ;PMID: 33437034

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19
Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?
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Article
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Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?

European journal of human genetics : EJHG, 2011-11, Vol.19 (11), p.1122-1126 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Nov 2011 ;Copyright © 2011 Macmillan Publishers Limited 2011 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2011.94 ;PMID: 21629297

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20
Couples' experiences with expanded carrier screening: evaluation of a university hospital screening offer
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Article
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Couples' experiences with expanded carrier screening: evaluation of a university hospital screening offer

European journal of human genetics : EJHG, 2021-08, Vol.29 (8), p.1252-1258 [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: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-021-00923-9 ;PMID: 34155360

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