Pages that link to "Q2885924"
Jump to navigation
Jump to search
The following pages link to Bartha Knoppers (Q2885924):
Displaying 50 items.
- Research ethics recommendations for whole-genome research: consensus statement (Q21145862) (← links)
- An integrated map of genetic variation from 1,092 human genomes (Q22122153) (← links)
- Genome-wide detection and characterization of positive selection in human populations (Q23000444) (← links)
- Towards a data sharing Code of Conduct for international genomic research (Q24264066) (← links)
- International network of cancer genome projects (Q24611474) (← links)
- A second generation human haplotype map of over 3.1 million SNPs (Q24651939) (← links)
- Special Issue - From Biobanks to the Clinic (Q24658616) (← links)
- Prepublication data sharing (Q26283296) (← links)
- Data Safe Havens in health research and healthcare (Q26827422) (← links)
- Recommendations for returning genomic incidental findings? We need to talk! (Q26995124) (← links)
- Genomic medicine: considerations for health professionals and the public (Q27499767) (← links)
- Streamlining ethical review of data intensive research (Q27797589) (← links)
- A review of the key issues associated with the commercialization of biobanks (Q28554316) (← links)
- Sharing health-related data: a privacy test? (Q28586853) (← links)
- Facilitating a culture of responsible and effective sharing of cancer genome data (Q28597289) (← links)
- Towards an ethics safe harbor for global biomedical research (Q28598421) (← links)
- Identifiability and privacy in pluripotent stem cell research (Q28601541) (← links)
- Consent Codes: Upholding Standard Data Use Conditions (Q28602211) (← links)
- International Charter of principles for sharing bio-specimens and data (Q28602512) (← links)
- Framework for responsible sharing of genomic and health-related data (Q28603879) (← links)
- RESEARCH ETHICS. Ethics review for international data-intensive research (Q28604024) (← links)
- The ethics weathervane (Q28608069) (← links)
- Where Next for Genetics and Genomics? (Q28645977) (← links)
- From the principles of genomic data sharing to the practices of data access committees (Q28647502) (← links)
- DataSHIELD: taking the analysis to the data, not the data to the analysis (Q28649310) (← links)
- Building a data sharing model for global genomic research (Q28652801) (← links)
- Stem cell research funding policies and dynamic innovation: a survey of open access and commercialization requirements (Q28654693) (← links)
- A human rights approach to an international code of conduct for genomic and clinical data sharing (Q28658438) (← links)
- Data sharing in large research consortia: experiences and recommendations from ENGAGE (Q28659060) (← links)
- Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting (Q28659644) (← links)
- A P3G generic access agreement for population genomic studies (Q28686896) (← links)
- Emerging issues in paediatric health research consent forms in Canada: working towards best practices (Q28708977) (← links)
- Toward a roadmap in global biobanking for health (Q28716151) (← links)
- Data sharing in the post-genomic world: the experience of the International Cancer Genome Consortium (ICGC) Data Access Compliance Office (DACO) (Q28727215) (← links)
- Power to the people: a wiki-governance model for biobanks (Q28727712) (← links)
- Publishing SNP genotypes of human embryonic stem cell lines: policy statement of the International Stem Cell Forum Ethics Working Party (Q28742548) (← links)
- The commercialization of genomic research in Canada (Q28743681) (← links)
- DataSHIELD: resolving a conflict in contemporary bioscience--performing a pooled analysis of individual-level data without sharing the data (Q28748614) (← links)
- Rationale for an integrated approach to genetic epidemiology. (Q30329077) (← links)
- Framing genomics, public health research and policy: points to consider (Q30388137) (← links)
- Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics (Q30391597) (← links)
- Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics (Q30391601) (← links)
- Currents in contemporary bioethics. Open access as benefit sharing? The example of publicly funded large-scale genomic databases (Q30485412) (← links)
- A decision tool to guide the ethics review of a challenging breed of emerging genomic projects (Q30488808) (← links)
- Registered access: a 'Triple-A' approach (Q30489911) (← links)
- An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. (Q30581758) (← links)
- Rare diseases and now rare data? (Q30652877) (← links)
- Human genetic research, DNA banking and consent: a question of 'form'? (Q30664023) (← links)
- Maelstrom Research guidelines for rigorous retrospective data harmonization (Q30847112) (← links)
- Data sharing, year 1--access to data from industry-sponsored clinical trials (Q30860404) (← links)