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Author Details

Saskia C Sanderson
University College London
2001
85
32
PMIDPaper TitleJournal TitlePublished Year
34758513Jewish cultural and religious factors and uptake of population-based BRCA testing across denominations: a cohort study.BJOG2022
35772452Multi-cancer early detection tests for cancer screening: a behavioural science perspective.Lancet Oncol2022
35626184Unselected Population Genetic Testing for Personalised Ovarian Cancer Risk Prediction: A Qualitative Study Using Semi-Structured Interviews.Diagnostics (Basel)2022
35244702Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial.JAMA Netw Open2022
34906473Decision-making, attitudes, and understanding among patients and relatives invited to undergo genome sequencing in the 100,000 Genomes Project: A multisite survey study.Genet Med2022
35264738Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study.Eur J Hum Genet2022
33678496Animation or leaflet: Does it make a difference when educating young people about genome sequencing?Patient Educ Couns2021
32429029Population Study of Ovarian Cancer Risk Prediction for Targeted Screening and Prevention.Cancers (Basel)2020
32001839Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study.Eur J Hum Genet2020
31701797Attitudes towards risk-stratified breast cancer screening among women in England: A cross-sectional survey.J Med Screen2020
31896776Development and mixed-methods evaluation of an online animation for young people about genome sequencing.Eur J Hum Genet2020
33260928Women's Intentions to Engage in Risk-Reducing Behaviours after Receiving Personal Ovarian Cancer Risk Information: An Experimental Survey Study.Cancers (Basel)2020
32835846Young people's understanding, attitudes and involvement in decision-making about genome sequencing for rare diseases: A qualitative study with participants in the UK 100, 000 Genomes Project.Eur J Med Genet2020
30270361Opening the "black box" of informed consent appointments for genome sequencing: a multisite observational study.Genet Med2019
31685495Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project.BMJ Open2019
30214064Increasing genomic literacy among adolescents.Genet Med2019
31323115Development of a measure of genome sequencing knowledge for young people: The kids-KOGS.Clin Genet2019
30808425Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium.Genome Med2019
31104772The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.Am J Hum Genet2019
29382336Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years.BMC Med Genomics2018
30240342Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey.AJOB Empir Bioeth2018
30021754Attitudes towards a programme of risk assessment and stratified management for ovarian cancer: a focus group study of UK South Asians' perspectives.BMJ Open2018
30031711Development of the Knowledge of Genome Sequencing (KOGS) questionnaire.Patient Educ Couns2018
28051073Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.Eur J Hum Genet2017
28190457Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.Am J Hum Genet2017
29145813Impact of a decision aid about stratified ovarian cancer risk-management on women's knowledge and intentions: a randomised online experimental survey study.BMC Public Health2017
29246147Health care professionals' attitudes towards population-based genetic testing and risk-stratification for ovarian cancer: a cross-sectional survey.BMC Womens Health2017
28545429Awareness, knowledge, perceptions, and attitudes towards genetic testing for cancer risk among ethnic minority groups: a systematic review.BMC Public Health2017
26036856Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.Eur J Hum Genet2016
26334178Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public.Genet Med2016
26508568Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.Eur J Hum Genet2016
26583683A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.Genet Med2016
27881091Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions.BMC Med Res Methodol2016
27595545Experiences and concerns of patients with recurrent attacks of acute hepatic porphyria: A qualitative study.Mol Genet Metab2016
26993268Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations.J Med Genet2016
26898680Impact of Genomic Counseling on Informed Decision-Making among ostensibly Healthy Individuals Seeking Personal Genome Sequencing: the HealthSeq Project.J Genet Couns2016
25634025How do students react to analyzing their own genomes in a whole-genome sequencing course?: outcomes of a longitudinal cohort study.Genet Med2015
26264128Preparing the next generation of genomicists: a laboratory-style course in medical genomics.BMC Med Genomics2015
25634646Factors affecting recall of different types of personal genetic information about Alzheimer's disease risk: the REVEAL study.Public Health Genomics2015
24222509Contemplating genetic feedback regarding lung cancer susceptibility.Ann Behav Med2014
25435542Cost-effectiveness of population screening for BRCA mutations in Ashkenazi jewish women compared with family history-based testing.J Natl Cancer Inst2014
25435541Population testing for cancer predisposing BRCA1/BRCA2 mutations in the Ashkenazi-Jewish community: a randomized controlled trial.J Natl Cancer Inst2014
25264176Practical guidance on informed consent for pediatric participants in a biorepository.Mayo Clin Proc2014
25206309Implementation and utilization of genetic testing in personalized medicine.Pharmgenomics Pers Med2014
24814192Return of genomic results to research participants: the floor, the ceiling, and the choices in between.Am J Hum Genet2014
24615004Article does not prove that smoking cessation has an "effect" on mental health.BMJ2014
24556984Young smokers' interpretations of the estimated lung cancer risk associated with a common genetic variant of low penetrance.Public Health Genomics2014
24723935Return of results in the genomic medicine projects of the eMERGE network.Front Genet2014
22888806Testing different communication formats on responses to imagined risk of having versus missing the GSTM1 gene.J Health Commun2013
24373383Informed decision-making among students analyzing their personal genomes on a whole genome sequencing course: a longitudinal cohort study.Genome Med2013
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Collaborators

Middlebury College
Co-authored papers 9
Queen Mary University of London, United Kingdom Society and Ethics Research
Co-authored papers 9
Icahn School of Medicine at Mount Sinai
Co-authored papers 9
Institute for Health Equity Research, Icahn School of Medicine at Mount Sinai
Co-authored papers 9
Rollins School of Public Health, Emory University
Co-authored papers 9
UCL Institute of Child Health and Great Ormond Street NHS Foundation Trust
Co-authored papers 9
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 8
Icahn School of Medicine at Mount Sinai
Co-authored papers 8
Co-authored papers 7
Harvard Medical School
Co-authored papers 7
University of Minnesota Medical School, 1035 University Drive duluth
Co-authored papers 7
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers 7
University of Washington Medical Center
Co-authored papers 7
Institute for Society and Genetics, University of California los angeles
Co-authored papers 6
University of Washington School of Medicine
Co-authored papers 6
Norton Children's Research Institute Affiliated with the University of Louisville
Co-authored papers 6
College of Nursing, University of South Florida
Co-authored papers 6
Marshfield Clinic Research Institute
Co-authored papers 5
University of Washington Medical Center
Co-authored papers 5
Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 5
Cincinnati Children's Hospital Medical Center
Co-authored papers 5
Penn State College of Medicine
Co-authored papers 5
Mayo Clinic
Co-authored papers 4
Hasso Plattner Institute for Digital Health at Mount Sinai
Co-authored papers 4
Northwestern University, Center for Genetic Medicine
Co-authored papers 4
Google Accelerated Science Team, Google Inc
Co-authored papers 4
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 4
Genomic Medicine Institute
Co-authored papers 4
Co-authored papers 3
Vanderbilt University Medical Center
Co-authored papers 3