P. Marshall

发表

A second generation human haplotype map of over 3.1 million SNPs

Zhaohui S. Qin, Gudmundur A. Thorisson, L. M. Sung, 2007, Nature.

Integrating common and rare genetic variation in diverse human populations

Sharon R Grossman, Pardis C Sabeti, P. Deloukas, 2010, Nature.

Enabling Genomic Revolution in Africa

Faisal M. Fadlelmola, Dan J Stein, Ebony B Madden, 2019, The Genetics of African Populations in Health and Disease.

Developing the science and methods of community engagement for genomic research and biobanking in Africa

P. Marshall, J. Seeley, K. Littler, 2017, Global health, epidemiology and genomics.

The translational potential of research on the ethical, legal, and social implications of genomics

P. Marshall, P. Appelbaum, R. Sharp, 2014, Genetics in Medicine.

Next-generation disadvantages: identifying potential barriers to integrating genomics into underserved medical settings.

P. Marshall, R. Sharp, A. Goldenberg, 2013, Personalized medicine.

Guideline for feedback of individual genetic research findings for genomics research in Africa

Ebony B Madden, Ebony B. Madden, P. Marshall, 2022, BMJ Global Health.

How Patients View Probiotics: Findings From a Multicenter Study of Patients With Inflammatory Bowel Disease and Irritable Bowel Syndrome

Jennifer B. McCormick, P. Marshall, G. Geller, 2012, Journal of clinical gastroenterology.

Tailoring the process of informed consent in genetic and genomic research

C. Rotimi, P. Marshall, 2010, Genome Medicine.

Translational Science, DNA Commercialization, and Informed Consent: The Need for Specific Terminology, Insights from a Review of H3Africa Projects

P. Marshall, C. Royal, R. Chadwick, 2022, Public Health Genomics.

Exploring how a genetic attribution to disease relates to stigma experiences of Xhosa patients with schizophrenia in South Africa

Dan J Stein, P. Marshall, P. Appelbaum, 2020, Social Psychiatry and Psychiatric Epidemiology.

Photo-documentation in the community: reflections on genetics, health and health disparities.

P. Marshall, Kari Colón-Zimmermann, A. Goldenberg, 2017, International journal of epidemiology.

Informed Consent in International Health Research

P. Marshall, 2006, Journal of empirical research on human research ethics : JERHRE.

Accounting for Culture in a Globalized Bioethics

P. Marshall, B. Koenig, 2004, The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics.

A perpetual source of DNA or something really different: ethical issues in the creation of cell lines for African genomics research

Ebony B Madden, Ebony B. Madden, P. Marshall, 2014, BMC medical ethics.

Gene–environment interactions and health inequalities: views of underserved communities

P. Marshall, Kari Colón-Zimmermann, A. Goldenberg, 2013, Journal of Community Genetics.

Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents

D. Stein, P. Marshall, J. Seeley, 2015, Journal of Medical Ethics.

Including all voices in international data-sharing governance

P. Marshall, Kazuto Kato, S. Terry, 2018, Human Genomics.

“A rising tide lifts all boats”: establishing a multidisciplinary genomic tumor board for breast cancer patients with advanced disease

Michelle L. McGowan, Lyndsay N. Harris, P. Marshall, 2016, BMC Medical Genomics.

Community engagement strategies for genomic studies in Africa: a review of the literature

P. Marshall, J. Seeley, V. Alibu, 2015, BMC medical ethics.

Genetic research and health disparities.

Celeste M Condit, Mildred K Cho, Paul Spicer, 2004, JAMA.

ELSI 2.0 for Genomics and Society

Clement Adebamowo, Kelly Edwards, Eric M Meslin, 2012, Science.

The role of causal knowledge in stigma considerations in African genomics research: Views of South African Xhosa people.

Dan J Stein, D. Stein, P. Marshall, 2021, Social science & medicine.

Is There a Space for Place in Family History Assessment? Underserved Community Views on the Impact of Neighborhood Factors on Health and Prevention

P. Marshall, A. Goldenberg, Christopher D. Hartmann, 2015, The Journal of Primary Prevention.

Does genetics matter for disease-related stigma? The impact of genetic attribution on stigma associated with rheumatic heart disease in the Western Cape, South Africa.

Dan J Stein, P. Marshall, P. Appelbaum, 2019, Social science & medicine.

Lessons learned from the translation of the Internalised Stigma of Mental Illness (ISMI) scale into isiXhosa for use with South African Xhosa people with schizophrenia.

P. Marshall, D. Stein, P. Appelbaum, 2023, Transcultural psychiatry.

Ethical Challenges in Community‐Based Research

P. Marshall, C. Rotimi, 2001, The American journal of the medical sciences.

Informed consent process for patient participation in rare disease registries linked to biorepositories.

Yaffa R Rubinstein, Vanessa Rangel Miller, Jack Schwartz, 2012, Contemporary clinical trials.

Integrating common and rare genetic variation in diverse human populations

Joshua M. Korn, Pardis C Sabeti, P. Deloukas, 2010, Nature.

How Patients View Probiotics: Findings From a Multicenter Study of Patients With Inflammatory Bowel Disease and Irritable Bowel Syndrome

Jennifer B. McCormick, P. Marshall, G. Geller, 2012, Journal of clinical gastroenterology.

‘Someone should oversee it’: patient perspectives on the ethical issues arising with the regulation of probiotics

Jennifer B. McCormick, P. Marshall, G. Geller, 2015, Health expectations : an international journal of public participation in health care and health policy.

Informed Consent in International Health Research

P. Marshall, 2006, Journal of empirical research on human research ethics : JERHRE.