Výsledky vyhledávání - "Aisha S. Sie"

Lifestyle Risk Factors for Breast Cancer in BRCA1/2-Mutation Carriers Around Childbearing Age

Autor: L. Derks, A. van Erkelens, Nicoline Hoogerbrugge, Judith B. Prins, G.H. Woldringh, Aisha S. Sie, L. Egbers, Peggy Manders

Publikováno v: Journal of Genetic Counseling, 26, 4, pp. 785-791
Journal of Genetic Counseling, 26, 785-791
Europe PubMed Central
Journal of Genetic Counseling

Contains fulltext : 177380.pdf (Publisher’s version ) (Open Access) BRCA1/2-mutation carriers are at high risk of breast cancer (BC) and ovarian cancer. Physical inactivity, overweight (body mass index >/=25, BMI), smoking, and alcohol consumption

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11b45bf9e8c985815ba0c18c3ae92e7f
https://doi.org/10.1007/s10897-016-0049-4

Zobrazit plný text záznamu

An online self-test added to colorectal cancer screening can increase the effectiveness of familial cancer risk assessment without increasing distress

Autor: A. van Erkelens, M. B. W. Spanier, Judith B. Prins, Aisha S. Sie, A. Visser, M. C. A. van Kouwen, Nicoline Hoogerbrugge

Publikováno v: Colorectal Disease, 20, 897-904
Colorectal Disease, 20, 10, pp. 897-904

AIM Most people who are at increased familial colorectal cancer (FCRC) risk are not identified, despite the need for enhanced surveillance colonoscopy for effective CRC prevention. An online self-test may enhance this identification. We assessed whet

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49c71bf6da367876ba23302588781273
http://hdl.handle.net/2066/196645

Zobrazit plný text záznamu

High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic Counseling

Autor: Judith B. Prins, Arjen R. Mensenkamp, Han G. Brunner, Liesbeth Spruijt, Wendy A. G. van Zelst-Stams, Aisha S. Sie, Marjolijn J. L. Ligtenberg, Nicoline Hoogerbrugge

Publikováno v: Journal of Genetic Counseling, 25, 3, pp. 504-14
Journal of Genetic Counseling, 25, 504-14
Journal of Genetic Counseling

Contains fulltext : 167845.pdf (Publisher’s version ) (Open Access) According to standard practice following referral to clinical genetics, most high risk breast cancer (BC) patients in many countries receive face-to-face genetic counseling prior t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d244afd489903a34af17154e7ef8eae
https://doi.org/10.1007/s10897-015-9899-4

Zobrazit plný text záznamu

Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas

Autor: Marcel R. Nelen, Aisha S. Sie, Michiel Simons, Marjolijn J. L. Ligtenberg, Encarna B. Gomez-Garcia, Johan Bulten, Alexander Hoischen, Hicham Ouchene, Marinus J. Blok, Nicoline Hoogerbrugge, Arjen R. Mensenkamp, Joanne A. de Hullu, Bastiaan B J Tops, Monique van Asseldonk, Robbert D.A. Weren, Astrid Eijkelenboom

Publikováno v: Human Mutation, 38(2), 226-235. Wiley
Human Mutation, 38, 226-235
Human Mutation
Human Mutation, 38, 2, pp. 226-235

With the recent introduction of Poly(ADP‐ribose) polymerase inhibitors, a promising novel therapy has become available for ovarian carcinoma (OC) patients with inactivating BRCA1 or BRCA2 mutations in their tumor. To select patients who may benefit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d6a4636858a82c5e90e5385671f4c59
https://cris.maastrichtuniversity.nl/en/publications/3fbdaaf0-2158-4279-9942-17585eb83be5

Zobrazit plný text záznamu

Online self-test identifies women at high familial breast cancer risk in population-based breast cancer screening without inducing anxiety or distress

Autor: Aisha S. Sie, M.A. Ten Voorde, Ritse M. Mann, H. Kroeze, A. van Erkelens, A. Visser, Nicoline Hoogerbrugge, Judith B. Prins, L.E.M. Duijm, Peggy Manders

Publikováno v: European Journal of Cancer, 78, pp. 45-52
European Journal of Cancer, 78, 45-52

Item does not contain fulltext INTRODUCTION: Identifying high familial breast cancer (FBC) risk improves detection of yet unknown BRCA1/2-mutation carriers, for whom BC risk is both highly likely and potentially preventable. We assessed whether a new

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::882fc9f58546ab573b595c9d120e3d00
https://doi.org/10.1016/j.ejca.2017.03.014

Zobrazit plný text záznamu

Patient experiences with gene panels based on exome sequencing in clinical diagnostics: high acceptance and low distress

Autor: Nicoline Hoogerbrugge, Ilse Feenstra, Aisha S. Sie, W. A. G. van Zelst-Stams, Judith B. Prins, Joris A. Veltman

Publikováno v: Clinical Genetics. 87:319-326

The Radboud University Medical Center was among the first to implement two-step exome sequencing in clinical genetic diagnostics. This study is the first to evaluate patient experiences with gene panels based on exome sequencing, using quantified psy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9cdbf49f0c56aeb5c4d8822b21788aa9
https://doi.org/10.1111/cge.12433

Zobrazit plný text záznamu

Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes

Autor: C. Marleen Kets, Liesbeth Spruijt, Judith B. Prins, Aisha S. Sie, Nicoline Hoogerbrugge

Publikováno v: Familial Cancer, 12, 675-82
Familial Cancer, 12, 4, pp. 675-82

Item does not contain fulltext DNA-testing for BRCA1/2 or Lynch syndrome is possible from the age of 18 years, although surveillance usually starts at 25. Some patients regret their decision of testing before age 25. This retrospective study evaluate

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40fe23d70100977fe207c01af89d6908
https://doi.org/10.1007/s10689-013-9644-9

Zobrazit plný text záznamu

Stopping ovarian cancer screening in BRCA1/2 mutation carriers: effects on risk management decisionsoutcome of risk-reducing salpingo-oophorectomy specimens

Autor: Harry Hollema, Henriette J. G. Arts, Aisha S. Sie, Jan C. Oosterwijk, Geertruida H. de Bock, Marian J.E. Mourits, Catheleine van Driel

Publikováno v: Maturitas, 80(3), 318-322. ELSEVIER IRELAND LTD

Objective: Ovarian cancer screening (OCS) for BRCA1/2 mutation carriers was stopped in our family cancer clinic in 2009 because of its ineffectiveness. The study objective was to investigate the effect of stopping OCS on the timing and uptake of risk

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecb294d4a4d3893534e1be9bdbd18f64
https://pubmed.ncbi.nlm.nih.gov/25600260

Zobrazit plný text záznamu

Fourfold increased detection of Lynch syndrome by raising age limit for tumour genetic testing from 50 to 70 years is cost-effective

Autor: Arjen R. Mensenkamp, M.J.L. Ligtenberg, Aisha S. Sie, Eddy M. M. Adang, Nicoline Hoogerbrugge

Publikováno v: Annals of Oncology, 25, 2001-7
Annals of Oncology, 25, 10, pp. 2001-7
ResearcherID

Item does not contain fulltext BACKGROUND: Recognising colorectal cancer (CRC) patients with Lynch syndrome (LS) can increase life expectancy of these patients and their close relatives. To improve identification of this under-diagnosed disease, expe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea580e86c6ddb1c0400abc7d6ca968a7
https://pubmed.ncbi.nlm.nih.gov/25081898

Zobrazit plný text záznamu

DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-direct

Autor: Aisha S. Sie, Judith B. Prins, Wendy A. G. van Zelst-Stams, Han G. Brunner, Marjolijn J L Ligtenberg, Arjen R. Mensenkamp, Nicoline Hoogerbrugge, Liesbeth Spruijt

Publikováno v: BMC Women's Health, 12, pp. 12-12
BMC Women's Health
BMC Women's Health, 12, 12-12
BMC Women's Health, Vol 12, Iss 1, p 12 (2012)

Background Current practice for patients with breast cancer referred for genetic counseling, includes face-to-face consultations with a genetic counselor prior to and following DNA-testing. This is based on guidelines regarding Huntington’s disease

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61a632a01e6ee81e3160cde0ea08d3dc
https://hdl.handle.net/2066/110772

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání