Detailansicht

Wissensnetz

Person

Bartha Maria Knoppers

Name	Bartha Maria Knoppers
Zeit	1972- (Wirkungsdaten)
Ort	Kanada
Geschlecht	weiblich
Variante	B. M. Knoppers
Weitere Angaben	M.A. in vergl. Literaturwissenschaft, Dr. jur.; Prof. an den Fakultäten für Recht u. Medizin in Montreal. Arbeitet auf dem Gebiet rechtlicher, ethischer u. polit. Fragen im Bereich Humangenetik u. Reproduktionstechnologie; Kanad. Juristin
Quelle	LoC-NA
Datensatztyp	Person
GND-Nummer	124367097
Datensatz-ID	124367097
Beteiligt an alle anzeigen Data sharing ethics toolkit: The Human Cell Atlas The commitment of the human cell atlas to humanity Defining and pursuing diversity in human genetic studies Toward better governance of human genomic data Model consent clauses for rare disease research Letter: Relearning the 3 R’s? Reinterpretation, recontact, and return of genetic variants Return of individual genomic research results: are laws and policies keeping step? Responsible sharing of biomedical data and biospecimens via the “Automatable Discovery and Access Matrix” (ADA-M) From the principles of genomic data sharing to the practices of data access committees An implementation framework for the feedback of individual research results and incidental findings in research The Human Genome Organisation: towards next-generation ethics Special issue on the art and science of biobanking Blurring lines : The research activities of direct‐to‐consumer genetic testing companies raise questions about consumers as research subjects

Hinweis

Die Betaversion beinhaltet noch nicht alle Funktionen und Informationen des Katalogs des DNB-Portals. Falls Sie Informationen vermissen oder ein Medium bestellen wollen, besuchen Sie bitte die entsprechende Seite im Katalog des DNB-Portals über folgenden Link:

Katalog der Deutschen Nationalbibliothek

Bartha Maria Knoppers

Data sharing ethics toolkit: The Human Cell Atlas

The commitment of the human cell atlas to humanity

Defining and pursuing diversity in human genetic studies

Toward better governance of human genomic data

Model consent clauses for rare disease research

Letter: Relearning the 3 R’s? Reinterpretation, recontact, and return of genetic variants

Return of individual genomic research results: are laws and policies keeping step?

Responsible sharing of biomedical data and biospecimens via the “Automatable Discovery and Access Matrix” (ADA-M)

From the principles of genomic data sharing to the practices of data access committees

An implementation framework for the feedback of individual research results and incidental findings in research

The Human Genome Organisation: towards next-generation ethics

Special issue on the art and science of biobanking

Blurring lines : The research activities of direct‐to‐consumer genetic testing companies raise questions about consumers as research subjects