Lista de obras -

Assessing patient readiness for personalized genomic medicine.

artículo científico publicado en 2018

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

artículo científico publicado en 2019

Association of Prepubertal and Adolescent Androgen Concentrations With Timing of Breast Development and Family History of Breast Cancer

article

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

artículo científico publicado en 2016

Breast Cancer Family History and Allele-Specific DNA Methylation in the Legacy Girls Study

artículo científico publicado en 2018

Comparison of Clinical, Maternal, and Self Pubertal Assessments: Implications for Health Studies

artículo científico publicado en 2016

Comparison of methods to assess onset of breast development in the LEGACY Girls Study: methodological considerations for studies of breast cancer

artículo científico publicado en 2018

Correlation of DNA methylation levels in blood and saliva DNA in young girls of the LEGACY Girls study

artículo científico publicado en 2014

Detailed phenotyping reveals distinct trajectories of cardiovascular function and symptoms with exposure to modern breast cancer therapy

scientific article published on 01 May 2019

Development of a communication protocol for telephone disclosure of genetic test results for cancer predisposition

artículo científico publicado en 2014

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

artículo científico publicado en 2017

Governance of a Learning Health Care System for Oncology: Patient Recommendations

artículo científico publicado en 2020

Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

artículo científico publicado en 2019

Human subjects protection: an event monitoring committee for research studies of girls from breast cancer families

artículo científico publicado en 2014

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

artículo científico publicado en 2017

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

artículo científico publicado en 2017

Longitudinal follow-up after telephone disclosure in the randomized COGENT study

scientific article published on 07 May 2020

Longitudinal outcomes with cancer multigene panel testing in previously tested BRCA1/2 negative patients

artículo científico publicado en 2020

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

scientific article published on 19 June 2019

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

artículo científico publicado en 2018

Non-invasive optical spectroscopic monitoring of breast development during puberty

artículo científico publicado en 2017

Patient Experiences, Trust, and Preferences for Health Data Sharing

scientific article published in 2022

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

artículo científico publicado en 2020

Preferences for in-person disclosure: Patients declining telephone disclosure characteristics and outcomes in the multicenter Communication Of GENetic Test Results by Telephone study

artículo científico publicado en 2018

Proceedings from the 9th annual conference on the science of dissemination and implementation: Washington, DC, USA. 14-15 December 2016.

artículo científico publicado en 2017

Proceedings of the 8th Annual Conference on the Science of Dissemination and Implementation : Washington, DC, USA. 14-15 December 2015

article by David Chambers et al published 1 August 2016 in Implementation Science

Psychosocial Adjustment in School-age Girls With a Family History of Breast Cancer

artículo científico publicado en 2015

Pubertal development in girls by breast cancer family history: the LEGACY girls cohort

artículo científico publicado en 2017

Research participants' experiences with return of genetic research results and preferences for web-based alternatives

scientific article published on 03 August 2019

The LEGACY Girls Study: Growth and Development in the Context of Breast Cancer Family History

artículo científico publicado en 2016

Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study

artículo científico publicado en 2016

Lista de obras de

Assessing patient readiness for personalized genomic medicine.

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

Association of Prepubertal and Adolescent Androgen Concentrations With Timing of Breast Development and Family History of Breast Cancer

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

Breast Cancer Family History and Allele-Specific DNA Methylation in the Legacy Girls Study

Comparison of Clinical, Maternal, and Self Pubertal Assessments: Implications for Health Studies

Comparison of methods to assess onset of breast development in the LEGACY Girls Study: methodological considerations for studies of breast cancer

Correlation of DNA methylation levels in blood and saliva DNA in young girls of the LEGACY Girls study

Detailed phenotyping reveals distinct trajectories of cardiovascular function and symptoms with exposure to modern breast cancer therapy

Development of a communication protocol for telephone disclosure of genetic test results for cancer predisposition

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

Governance of a Learning Health Care System for Oncology: Patient Recommendations

Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

Human subjects protection: an event monitoring committee for research studies of girls from breast cancer families

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Longitudinal follow-up after telephone disclosure in the randomized COGENT study

Longitudinal outcomes with cancer multigene panel testing in previously tested BRCA1/2 negative patients

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

Non-invasive optical spectroscopic monitoring of breast development during puberty

Patient Experiences, Trust, and Preferences for Health Data Sharing

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Preferences for in-person disclosure: Patients declining telephone disclosure characteristics and outcomes in the multicenter Communication Of GENetic Test Results by Telephone study

Proceedings from the 9th annual conference on the science of dissemination and implementation: Washington, DC, USA. 14-15 December 2016.

Proceedings of the 8th Annual Conference on the Science of Dissemination and Implementation : Washington, DC, USA. 14-15 December 2015

Psychosocial Adjustment in School-age Girls With a Family History of Breast Cancer

Pubertal development in girls by breast cancer family history: the LEGACY girls cohort

Research participants' experiences with return of genetic research results and preferences for web-based alternatives

The LEGACY Girls Study: Growth and Development in the Context of Breast Cancer Family History

Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study