Lista de obras - Chris Jacobs - Dominio Público Uruguay

Accuracy of recall of information about a cancer-predisposing BRCA1/2 gene mutation among patients and relatives

artículo científico publicado en 2014

Australian human research ethics committee members’ confidence in reviewing genomic research applications

artículo científico publicado en 2021

Cancer genetics

artículo científico publicado en 2010

Cancer patients' views and understanding of genome sequencing: a qualitative study

artículo científico publicado en 2020

Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations

artículo científico publicado en 2016

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

artículo científico publicado en 2012

Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2012

Communicating BRCA1/2 genetic test results within the family: a qualitative analysis

artículo científico publicado en 2011

Communication about genetic testing with breast and ovarian cancer patients: a scoping review

scientific article published on 20 December 2018

Comparing family members' motivations and attitudes towards genetic testing for hereditary breast and ovarian cancer: a qualitative analysis

artículo científico publicado en 2010

Cost-effectiveness of population screening for BRCA mutations in Ashkenazi jewish women compared with family history-based testing

artículo científico publicado en 2014

Current detection rates and time-to-detection of all identifiable BRCA carriers in the Greater London population

artículo científico publicado en 2018

Doing the right thing for one's children: deciding whether to take the genetic test for Huntington's disease as a moral dilemma.

artículo científico publicado en 2013

Genetic Testing for Rare Cancer: The Wider Issues.

artículo científico publicado en 2016

Genetics in palliative care: too much to ask?

scientific article published on 01 May 2019

Genetics in palliative oncology: a missing agenda? A review of the literature and future directions

artículo científico publicado en 2017

Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk

artículo científico publicado en 2013

Identification of germline missense mutations and rare allelic variants in theATM gene in early-onset breast cancer

article

Identifying individuals who might benefit from genetic services and information

artículo científico publicado en 2013

Key messages for communicating information about BRCA1 and BRCA2 to women with breast or ovarian cancer: Consensus across health professionals and service users

artículo científico publicado en 2017

No news is (not necessarily) good news: impact of preliminary results for BRCA1 mutation searches

artículo científico publicado en 2002

Novel one-stop multidisciplinary follow-up clinic for BRCA1/2 carriers: patient satisfaction and decision making

scientific article published on 03 October 2010

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2012

Patient perspectives on molecular tumor profiling: "Why wouldn't you?"

artículo científico publicado en 2019

Population testing for cancer predisposing BRCA1/BRCA2 mutations in the Ashkenazi-Jewish community: a randomized controlled trial

artículo científico publicado en 2014

Preparing the genetic counseling workforce for the future in Australasia

artículo científico publicado en 2020

Providing a community-based cancer risk assessment service for a socially and ethnically diverse population

artículo científico publicado en 2007

Risk reducing salpingectomy and delayed oophorectomy in high risk women: views of cancer geneticists, genetic counsellors and gynaecological oncologists in the UK.

artículo científico publicado en 2015

The Angelina Jolie effect: how high celebrity profile can have a major impact on provision of cancer related services

artículo científico publicado en 2014

The PiGeOn project: protocol of a longitudinal study examining psychosocial and ethical issues and outcomes in germline genomic sequencing for cancer.

artículo científico publicado en 2018

The development of a methodology for examining the process of family communication of genetic test results

artículo científico publicado en 2010

Lista de obras de Chris Jacobs

Accuracy of recall of information about a cancer-predisposing BRCA1/2 gene mutation among patients and relatives

Australian human research ethics committee members’ confidence in reviewing genomic research applications

Cancer genetics

Cancer patients' views and understanding of genome sequencing: a qualitative study

Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

Communicating BRCA1/2 genetic test results within the family: a qualitative analysis

Communication about genetic testing with breast and ovarian cancer patients: a scoping review

Comparing family members' motivations and attitudes towards genetic testing for hereditary breast and ovarian cancer: a qualitative analysis

Cost-effectiveness of population screening for BRCA mutations in Ashkenazi jewish women compared with family history-based testing

Current detection rates and time-to-detection of all identifiable BRCA carriers in the Greater London population

Doing the right thing for one's children: deciding whether to take the genetic test for Huntington's disease as a moral dilemma.

Genetic Testing for Rare Cancer: The Wider Issues.

Genetics in palliative care: too much to ask?

Genetics in palliative oncology: a missing agenda? A review of the literature and future directions

Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk

Identification of germline missense mutations and rare allelic variants in theATM gene in early-onset breast cancer

Identifying individuals who might benefit from genetic services and information

Key messages for communicating information about BRCA1 and BRCA2 to women with breast or ovarian cancer: Consensus across health professionals and service users

No news is (not necessarily) good news: impact of preliminary results for BRCA1 mutation searches

Novel one-stop multidisciplinary follow-up clinic for BRCA1/2 carriers: patient satisfaction and decision making

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

Patient perspectives on molecular tumor profiling: "Why wouldn't you?"

Population testing for cancer predisposing BRCA1/BRCA2 mutations in the Ashkenazi-Jewish community: a randomized controlled trial

Preparing the genetic counseling workforce for the future in Australasia

Providing a community-based cancer risk assessment service for a socially and ethnically diverse population

Risk reducing salpingectomy and delayed oophorectomy in high risk women: views of cancer geneticists, genetic counsellors and gynaecological oncologists in the UK.

The Angelina Jolie effect: how high celebrity profile can have a major impact on provision of cancer related services

The PiGeOn project: protocol of a longitudinal study examining psychosocial and ethical issues and outcomes in germline genomic sequencing for cancer.

The development of a methodology for examining the process of family communication of genetic test results