Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project

por Sanderson, Saskia C, Hill, Melissa, Patch, Christine, Searle, Beverly, Lewis, Celine, Chitty, Lyn S
Publicado 2019

Implementation and utilization of genetic testing in personalized medicine

por Abul-Husn, Noura S, Owusu Obeng, Aniwaa, Sanderson, Saskia C, Gottesman, Omri, Scott, Stuart A
Publicado 2014

Opening the “black box” of informed consent appointments for genome sequencing: a multisite observational study

por Sanderson, Saskia C., Lewis, Celine, Patch, Christine, Hill, Melissa, Bitner-Glindzicz, Maria, Chitty, Lyn S.
Publicado 2018

Development of a measure of genome sequencing knowledge for young people: The kids‐KOGS

por Lewis, Celine, Loe, Bao S., Sidey‐Gibbons, Chris, Patch, Christine, Chitty, Lyn S., Sanderson, Saskia C.
Publicado 2019

Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public

por Sanderson, Saskia C., Suckiel, Sabrina A., Zweig, Micol, Bottinger, Erwin P., Jabs, Ethylin Wang, Richardson, Lynne D.
Publicado 2016

Development and mixed-methods evaluation of an online animation for young people about genome sequencing

por Lewis, Celine, Sanderson, Saskia C., Hammond, Jennifer, Hill, Melissa, Searle, Beverly, Hunter, Amy, Patch, Christine, Chitty, Lyn S.
Publicado 2020

Knowledge, attitudes and decision regret: a longitudinal survey study of participants offered genome sequencing in the 100,000 Genomes Project

por Peter, Michelle, Hammond, Jennifer, Sanderson, Saskia C., Gurasashvili, Jana, Hunter, Amy, Searle, Beverly, Patch, Christine, Chitty, Lyn S., Hill, Melissa, Lewis, Celine
Publicado 2023

Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project

por Sanderson, Saskia C, Linderman, Michael D, Suckiel, Sabrina A, Zinberg, Randi, Wasserstein, Melissa, Kasarskis, Andrew, Diaz, George A, Schadt, Eric E
Publicado 2017

Awareness, knowledge, perceptions, and attitudes towards genetic testing for cancer risk among ethnic minority groups: a systematic review

por Hann, Katie E. J., Freeman, Madeleine, Fraser, Lindsay, Waller, Jo, Sanderson, Saskia C., Rahman, Belinda, Side, Lucy, Gessler, Sue, Lanceley, Anne
Publicado 2017

Health care professionals’ attitudes towards population-based genetic testing and risk-stratification for ovarian cancer: a cross-sectional survey

por Hann, Katie E. J., Fraser, Lindsay, Side, Lucy, Gessler, Sue, Waller, Jo, Sanderson, Saskia C., Freeman, Madeleine, Jacobs, Ian, Lanceley, Anne
Publicado 2017

Attitudes towards a programme of risk assessment and stratified management for ovarian cancer: a focus group study of UK South Asians’ perspectives

por Hann, Katie E J, Ali, Nasreen, Gessler, Sue, Fraser, Lindsay Sarah Macduff, Side, Lucy, Waller, Jo, Sanderson, Saskia C, Lanceley, Anne
Publicado 2018

Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study

por Peter, Michelle, Hammond, Jennifer, Sanderson, Saskia C., Gurasashvili, Jana, Hunter, Amy, Searle, Beverly, Patch, Christine, Chitty, Lyn S., Hill, Melissa, Lewis, Celine
Publicado 2022

Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project

por Sanderson, Saskia C, Linderman, Michael D, Suckiel, Sabrina A, Diaz, George A, Zinberg, Randi E, Ferryman, Kadija, Wasserstein, Melissa, Kasarskis, Andrew, Schadt, Eric E
Publicado 2016

Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years

por Linderman, Michael D., Sanderson, Saskia C., Bashir, Ali, Diaz, George A., Kasarskis, Andrew, Zinberg, Randi, Mahajan, Milind, Suckiel, Sabrina A., Zweig, Micol, Schadt, Eric E.
Publicado 2018

A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States

por Garrison, Nanibaa' A., Sathe, Nila A., Antommaria, Armand H. Matheny, Holm, Ingrid A., Sanderson, Saskia C., Smith, Maureen E., McPheeters, Melissa L., Clayton, Ellen W.
Publicado 2016

Preparing the next generation of genomicists: a laboratory-style course in medical genomics

por Linderman, Michael D., Bashir, Ali, Diaz, George A., Kasarskis, Andrew, Sanderson, Saskia C., Zinberg, Randi E., Mahajan, Milind, Shah, Hardik, Suckiel, Sabrina, Zweig, Micol, Schadt, Eric E.
Publicado 2015

Informed decision-making among students analyzing their personal genomes on a whole genome sequencing course: a longitudinal cohort study

por Sanderson, Saskia C, Linderman, Michael D, Kasarskis, Andrew, Bashir, Ali, Diaz, George A, Mahajan, Milind C, Shah, Hardik, Wasserstein, Melissa, Zinberg, Randi E, Zweig, Micol, Schadt, Eric E
Publicado 2013

Impact of a decision aid about stratified ovarian cancer risk-management on women’s knowledge and intentions: a randomised online experimental survey study

por Meisel, Susanne F., Freeman, Maddie, Waller, Jo, Fraser, Lindsay, Gessler, Sue, Jacobs, Ian, Kalsi, Jatinderpal, Manchanda, Ranjit, Rahman, Belinda, Side, Lucy, Wardle, Jane, Lanceley, Anne, Sanderson, Saskia C.
Publicado 2017

Return of results in the genomic medicine projects of the eMERGE network

por Kullo, Iftikhar J., Haddad, Ra'ad, Prows, Cynthia A., Holm, Ingrid, Sanderson, Saskia C., Garrison, Nanibaa' A., Sharp, Richard R., Smith, Maureen E., Kuivaniemi, Helena, Bottinger, Erwin P., Connolly, John J., Keating, Brendan J., McCarty, Catherine A., Williams, Marc S., Jarvik, Gail P.
Publicado 2014

Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium

por Zoltick, Emilie S., Linderman, Michael D., McGinniss, Molly A., Ramos, Erica, Ball, Madeleine P., Church, George M., Leonard, Debra G. B., Pereira, Stacey, McGuire, Amy L., Caskey, C. Thomas, Sanderson, Saskia C., Schadt, Eric E., Nielsen, Daiva E., Crawford, Scott D., Green, Robert C.
Publicado 2019