Emilia Niemiec

Emilia Niemic

Postdoc

Emilia Niemiec är postdocforskare hos CRB och arbetar med etiska, sociala och legala aspekter av genteknik och genomforskning.

E-post: emilia.niemiec@crb.uu.se

Senaste publikationerna

  • Niemiec, Emilia; Howard, Heidi Carmen

    “Genethics” and Public Health Genomics

    Ingår i Applied Genomics and Public Health, s. 243-257, 2020.

  • Niemiec, Emilia; Howard, Heidi Carmen

    Germline Genome Editing Research: What Are Gamete Donors (Not) Informed About in Consent Forms?

    Ingår i The CRISPR Journal, s. 52-63, 2020.

    Open access
  • Middleton, Anna; Milne, Richard; Thorogood, Adrian; Kleiderman, Erika et al.

    Attitudes of publics who are unwilling to donate DNA data for research.

    Ingår i European Journal of Medical Genetics, s. 316-323, 2019.

    Open access
  • Niemiec, Emilia; Howard, Heidi Carmen

    Consenting Patients to Genome Sequencing

    Ingår i Clinical Genome Sequencing: Psychological Considerations, 2019.

  • Niemiec, Emilia; Howard, Heidi Carmen

    Include egg donors in CRISPR gene-editing debate

    Ingår i Nature, s. 51-51, 2019.

  • Middleton, Anna; Milne, Richard; Howard, Heidi; Niemiec, Emilia et al.

    Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data

    Ingår i European Journal of Human Genetics, 2019.

    Open access
  • Płociński, Przemysław; Macios, Maria; Houghton, Joanna; Niemiec, Emilia et al.

    Proteomic and transcriptomic experiments reveal an essential role of RNA degradosome complexes in shaping the transcriptome of Mycobacterium tuberculosis.

    Ingår i Nucleic Acids Research, 2019.

    Open access
  • Milne, Richard; Morley, Katherine I.; Howard, Heidi; Niemiec, Emilia et al.

    Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia

    Ingår i Human Genetics, s. 1237-1246, 2019.

    Open access
  • Vears, Danya F.; Niemiec, Emilia; Howard, Heidi Carmen; Borry, Pascal

    Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms

    Ingår i European Journal of Human Genetics, s. 1743-1751, 2018.

    Open access
  • Vears, D. F.; Niemiec, Emilia; Howard, Heidi Carmen; Borry, P.

    How do consent forms for diagnostic high-throughput sequencing address unsolicited and secondary findings?: A content analysis

    Ingår i Clinical Genetics, s. 321-329, 2018.

    Open access