Bartha Maria M Knoppers


Ontology type: schema:Person     


Person Info

NAME

Bartha Maria M

SURNAME

Knoppers

Publications in SciGraph latest 50 shown

  • 2022-05-03 How to ensure the Human Cell Atlas benefits humanity in NATURE
  • 2022-02-24 Women’s perceptions of PERSPECTIVE: a breast cancer risk stratification e-platform in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2022-01-13 Author Correction: Computational tools for genomic data de-identification: facilitating data protection law compliance in NATURE COMMUNICATIONS
  • 2021-11-29 Computational tools for genomic data de-identification: facilitating data protection law compliance in NATURE COMMUNICATIONS
  • 2021-10-28 The impact of reporting magnetic resonance imaging incidental findings in the Canadian alliance for healthy hearts and minds cohort in BMC MEDICAL ETHICS
  • 2021-09-07 Frontline Ethico-Legal Issues in Childhood Cancer Genetics Research in THE HEREDITARY BASIS OF CHILDHOOD CANCER
  • 2021-07-20 ISSCR guidelines uphold human right to science for benefit of all in NATURE
  • 2021-07-15 An international policy on returning genomic research results in GENOME MEDICINE
  • 2021-06-09 A policy Delphi study to validate the key implications of data sharing (KIDS) framework for pediatric genomics in Canada in BMC MEDICAL ETHICS
  • 2021-01-19 In Memoriam: Gertjan van Ommen (1947–2020) in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2021-01-07 Toward better governance of human genomic data in NATURE GENETICS
  • 2020-07-13 Correction to: Pandemics, privacy, and public health research in CANADIAN JOURNAL OF PUBLIC HEALTH
  • 2020-06-26 Pandemics, privacy, and public health research in CANADIAN JOURNAL OF PUBLIC HEALTH
  • 2020-02-05 Genomics: data sharing needs an international code of conduct in NATURE
  • 2019-08-01 Model consent clauses for rare disease research in BMC MEDICAL ETHICS
  • 2019-04-11 Letter: Relearning the 3 R’s? Reinterpretation, recontact, and return of genetic variants in GENETICS IN MEDICINE
  • 2019-02-28 Health professionals’ perspectives on breast cancer risk stratification: understanding evaluation of risk versus screening for disease in PUBLIC HEALTH REVIEWS
  • 2019-02-27 A response to “Personalised medicine and population health: breast and ovarian cancer” in HUMAN GENETICS
  • 2019-01-08 Return of individual genomic research results: are laws and policies keeping step? in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-11-08 Overcoming barriers to facilitate the regulation of multi-centre regenerative medicine clinical trials in STEM CELL RESEARCH & THERAPY
  • 2018-09-04 Correction to: Accelerating evidence gathering and approval of precision medicine therapies: the FDA takes aim at rare mutations in GENETICS IN MEDICINE
  • 2018-08-10 Introduction: the why and whither of genomic data sharing in HUMAN GENETICS
  • 2018-08-02 Registered access: authorizing data access in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-07-23 Responsible sharing of biomedical data and biospecimens via the “Automatable Discovery and Access Matrix” (ADA-M) in NPJ GENOMIC MEDICINE
  • 2018-07-10 Accelerating evidence gathering and approval of precision medicine therapies: the FDA takes aim at rare mutations in GENETICS IN MEDICINE
  • 2018-06-13 Broaden human-rights focus for health data under GDPR in NATURE
  • 2018-06-13 Development of a consent resource for genomic data sharing in the clinical setting in GENETICS IN MEDICINE
  • 2018-06-12 Genome-wide sequencing in acutely ill infants: genomic medicine’s critical application? in GENETICS IN MEDICINE
  • 2018-02-27 Epigenome-based cancer risk prediction: rationale, opportunities and challenges in NATURE REVIEWS CLINICAL ONCOLOGY
  • 2017-11-28 Points to consider for laboratories reporting results from diagnostic genomic sequencing in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-09-14 Criminal Prohibition of Wrongful Re‑identification: Legal Solution or Minefield for Big Data? in JOURNAL OF BIOETHICAL INQUIRY
  • 2017-06-07 Population Biobanks and the Principle of Reciprocity in BIOBANKING OF HUMAN BIOSPECIMENS
  • 2017-06-07 P3G: Towards an International Policy Platform for Population Genomics in BIOBANKING OF HUMAN BIOSPECIMENS
  • 2017-05-31 Reply to C Harling in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-04-13 Erratum: Legal approaches regarding health-care decisions involving minors: implications for next-generation sequencing in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-03-06 Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder in NATURE NEUROSCIENCE
  • 2017-01-05 Human gene editing: revisiting Canadian policy in NPJ REGENERATIVE MEDICINE
  • 2016-12-15 Public variant databases: liability? in GENETICS IN MEDICINE
  • 2016-11-23 Reply to Kranendonk et al in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-11-08 The discombobulation of de-identification in NATURE BIOTECHNOLOGY
  • 2016-09-28 Registered access: a ‘Triple-A’ approach in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-08-17 Sharing health-related data: a privacy test? in NPJ GENOMIC MEDICINE
  • 2016-07-27 Rationale, design, and methods for Canadian alliance for healthy hearts and minds cohort study (CAHHM) – a Pan Canadian cohort study in BMC PUBLIC HEALTH
  • 2016-06-16 Erratum: International Charter of principles for sharing bio-specimens and data in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-06-15 Legal approaches regarding health-care decisions involving minors: implications for next-generation sequencing in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-05-26 Human genome meeting 2016 in HUMAN GENOMICS
  • 2016-05-05 Facilitating a culture of responsible and effective sharing of cancer genome data in NATURE MEDICINE
  • 2016-01-20 A decision tool to guide the ethics review of a challenging breed of emerging genomic projects in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-10-20 Population genetic testing for cancer susceptibility: founder mutations to genomes in NATURE REVIEWS CLINICAL ONCOLOGY
  • 2015-09-04 The ethics weathervane in BMC MEDICAL ETHICS
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