Literature DB >> 15537575

Identifying and testing for hereditary susceptibility to common cancers.

Randa Sifri1, Sarita Gangadharappa, Louise S Acheson.   

Abstract

Hereditary cancer syndromes account for an estimated 5% of breast, ovarian, and colon cancers. The rapid discovery of cancer-related genes in the last 15 years has propelled the field of cancer genetic risk assessment forward. With patients becoming increasingly aware of available genetic testing options, it is important that various health professionals become knowledgeable in identifying and advising patients at increased risk for a hereditary cancer syndrome. This article will outline the components of providing a hereditary cancer risk assessment with a focus on hereditary breast and ovarian cancer syndrome and hereditary colon cancer.

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Year:  2004        PMID: 15537575     DOI: 10.3322/canjclin.54.6.309

Source DB:  PubMed          Journal:  CA Cancer J Clin        ISSN: 0007-9235            Impact factor:   508.702


  9 in total

1.  Family matters: examining a multi-family group intervention for women with BRCA mutations in the scope of genetic counselling.

Authors:  Alvaro Mendes; Raquel Chiquelho; Teresa Almeida Santos; Liliana Sousa
Journal:  J Community Genet       Date:  2010-10-05

2.  Risk-reduction surgery decisions in high-risk women seen for genetic counseling.

Authors:  Jessica A Ray; Lois J Loescher; Molly Brewer
Journal:  J Genet Couns       Date:  2005-12       Impact factor: 2.537

3.  Electrochemical DNA biosensors for label-free breast cancer gene marker detection.

Authors:  Mehmet Senel; Muamer Dervisevic; Firdevs Kokkokoğlu
Journal:  Anal Bioanal Chem       Date:  2019-04-08       Impact factor: 4.142

4.  From observation to intervention: development of a psychoeducational intervention to increase uptake of BRCA genetic counseling among high-risk breast cancer survivors.

Authors:  Susan T Vadaparampil; Teri L Malo; Kelli M Nam; Alison Nelson; Cara Z de la Cruz; Gwendolyn P Quinn
Journal:  J Cancer Educ       Date:  2014-12       Impact factor: 2.037

5.  Missed opportunities: family history and behavioral risk factors in breast cancer risk assessment among a multiethnic group of women.

Authors:  Leah S Karliner; Anna Napoles-Springer; Karla Kerlikowske; Jennifer S Haas; Steven E Gregorich; Celia Patricia Kaplan
Journal:  J Gen Intern Med       Date:  2007-03       Impact factor: 5.128

6.  Factors for the Primary Prevention of Breast Cancer: A Meta-Analysis of Prospective Cohort Studies.

Authors:  Jalal Poorolajal; Fatemeh Heidarimoghis; Manoochehr Karami; Zahra Cheraghi; Fatemeh Gohari-Ensaf; Fatemeh Shahbazi; Bushra Zareie; Pegah Ameri; Fatemeh Sahraee
Journal:  J Res Health Sci       Date:  2021-07-20

7.  Patient interest in recording family histories of cancer via the Internet.

Authors:  Christian Simon; Louise Acheson; Christopher Burant; Nancy Gerson; Sarah Schramm; Susan Lewis; Georgia Wiesner
Journal:  Genet Med       Date:  2008-12       Impact factor: 8.822

8.  Do Breast Cancer Patients Tested in the Oncology Care Setting Share BRCA Mutation Results with Family Members and Health Care Providers?

Authors:  Susan T Vadaparampil; Teri Malo; Cara de la Cruz; Juliette Christie
Journal:  J Cancer Epidemiol       Date:  2012-07-15

Review 9.  Graphene: The Missing Piece for Cancer Diagnosis?

Authors:  Sandra M A Cruz; André F Girão; Gil Gonçalves; Paula A A P Marques
Journal:  Sensors (Basel)       Date:  2016-01-21       Impact factor: 3.576

  9 in total

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