About: Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort

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scientific article published on 01 January 2004

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rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2004 (fr) 2004 թվականին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована у квітні 2004 (uk) im Jahr 2004 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 2004 (ast) artikull shkencor i botuar më 01 janar 2004 (sq) scientific article published on 01 January 2004 (en)
publication date	wds:Q57266769-60C19812-B414-4852-8EEF-34BD2A07E1DA
publication date	2004-01-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q57266769-0DAB6988-38AA-41E7-81F1-A3CB9446D0A3 wds:Q57266769-1A02E318-DBB0-4EE9-999F-D0D91606E2A3 wds:Q57266769-294215B3-BB9F-46ED-B85C-FC43DD47475C wds:Q57266769-3449BA57-A885-45E8-AACE-21CA59D808A0 wds:Q57266769-58715172-38C1-4D81-A5D9-E30F11E4066E wds:Q57266769-6E076B0B-B5DE-4979-A55A-D7DFC9427E9D wds:Q57266769-7562A17A-BE39-4555-BCAE-EF4A0AE2E429 wds:Q57266769-C4DBDF2B-9643-46E8-9134-636B2FBE7C7D wds:Q57266769-DB3DBF2C-50CE-49C8-B549-AB9AF3C474EE
author name string	Gregory H Ashley S Davidson R Cole T Mackay J Watson M Morrison PJ Cook J Brooks L
rdfs:label	Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort (en) Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort (nl) Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort (sq)
skos:prefLabel	Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort (en) Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort (nl) Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort (sq)
name	Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort (en) Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort (nl) Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort (sq)
author	wds:Q57266769-280BC324-320D-410D-ACF9-8E09E91F1374 wds:Q57266769-6514BB86-8A7A-4D0C-926C-60796FAB451F wds:Q57266769-88639E40-FF3A-459F-AAFD-3A638F7DD2C1 wds:Q57266769-EFDC0EB8-5399-4C5F-B888-00537A72AE4D
author	Gareth Evans Rosalind Eeles Diana Eccles Claire Foster
title	wds:Q57266769-44573C0E-F169-4E68-8EDD-B42493608D51
title	Non-uptake of predictive genetic testing for BRCA1/2 among relatives of known carriers: attributes, cancer worry, and barriers to testing in a multicenter clinical cohort (en)
page(s)	wds:Q57266769-6829E13B-8366-4A6E-8A7C-645C07CCD4CB
page(s)	23-29
instance of	wds:Q57266769-24D0B6EA-AB7F-4D8D-802F-5C8DDD82AACF
instance of	scholarly article
PubMed ID	wds:Q57266769-FFD77A3E-7D2E-4BCC-9CA1-AA2D228D5829
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15140371
PubMed ID	15140371
published in	wds:Q57266769-A77B421E-3425-4E16-AB35-0A925643007E
published in	Genetic Testing and Molecular Biomarkers
issue	wds:Q57266769-8A3D024E-61B2-46D8-AFC5-7A95BCCAAC66
volume	wds:Q57266769-7EE7BC26-2128-459A-A023-0317CDC67306
issue	1
volume	8
DOI	wds:Q57266769-00DE6B05-82D7-40D9-86BF-EA8E48BDFB50
DOI	http://dx.doi.org/10.1089/109065704323016003
DOI	10.1089/109065704323016003
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57266769
is cites work of	Clinical implications of genomics for cancer risk genetics Familial testicular cancer: interest in genetic testing among high-risk family members The role of distress in uptake and response to predisposition genetic testing: the BMPR2 experience Withdrawal from genetic counselling for cancer Genetic testing for melanoma risk: a prospective cohort study of uptake and outcomes among Australian families Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National Society of Genetic Counselors Incidental findings in genetics research using archived DNA Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer Comparing family members' motivations and attitudes towards genetic testing for hereditary breast and ovarian cancer: a qualitative analysis Improving mutation notification when new genetic information is identified in research: a trial of two strategies in familial breast cancer. Genetic risk, perceived risk, and cancer worry in daughters of breast cancer patients All in the Family: Barriers and Motivators to the Use of Cancer Family History Questionnaires and the Impact on Attendance Rates Psychosocial impact of breast/ovarian (BRCA1/2) cancer-predictive genetic testing in a UK multi-centre clinical cohort The effect of BRCA gene testing on family relationships: A thematic analysis of qualitative interviews Predictors of genetic testing decisions: a systematic review and critique of the literature Psychiatric implications of cancer genetic testing Facilitators and Challenges in Psychosocial Adaptation to Being at Increased Familial Risk of Breast Cancer. Factors associated with an individuals' decision to withdraw from genetic counseling for BRCA1 and BRCA2 genes mutations: are personality traits involved? Written pretest information and germline BRCA1/2 pathogenic variant testing in unselected breast cancer patients: predictors of testing uptake Family Communication in Inherited Cardiovascular Conditions in Ireland Uptake of testing for BRCA1/2 mutations in South East Scotland Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium. Why Is Cancer Genetic Counseling Underutilized by Women Identified as at Risk for Hereditary Breast Cancer? Patient Perceptions of Barriers Following a Referral Letter Deaf genetic testing and psychological well-being in deaf adults Public Views on Genetics and Genetic Testing: A Survey of the General Public in Belgium Impact of free cancer predisposition cascade genetic testing on uptake in Singapore Distress and family functioning in oncogenetic counselling for hereditary and familial breast and/or ovarian cancers Distress in unaffected individuals who decline, delay or remain ineligible for genetic testing for hereditary diseases: a systematic review Genetic testing for Lynch syndrome: family communication and motivation Perceptions and attitudes about HFE genotyping among college-age adults. The use of family history questionnaires: an examination of genetic risk estimates and genetic testing eligibility in the non-responder population. Uptake of BRCA1 rearrangement panel testing: in individuals previously tested for BRCA1/2 mutations Familial breast cancer genetic testing in the West of Ireland.
is cites work of	wds:Q33721583-8B9C2F60-4CA1-4742-B039-3B576812B568 wds:Q84170924-AE4BDEC9-B3C4-4C19-B06D-EA5E98583EDF

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