List of works - Francesca Forzano

A response to the forensic genetics policy initiative’s report “Establishing Best Practice for Forensic DNA Databases”

article

Delineation of dominant and recessive forms of LZTR1-associated Noonan syndrome.

scientific article published on 3 April 2019

Developing a policy for paediatric biobanks: principles for good practice

scientific article

ESHG PPPC Comments on postmortem use of genetic data for research purposes

scientific article published on 08 October 2019

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

article published in 2019

Human germline gene editing. Recommendations of ESHG and ESHRE

scientific article published on 12 January 2018

Human germline gene editing: Recommendations of ESHG and ESHRE.

scientific article published on 12 January 2018

Italian appeal court: a genetic predisposition to commit murder?

scientific article published on 10 March 2010

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

scientific article

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

article

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations

One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans

scientific article published on 30 November 2017

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

scientific article published on 22 November 2020

Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe.

scientific article published on 23 April 2018

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

Reply to Bombard and Mighton

scientific article published on 18 January 2019

Responsible implementation of expanded carrier screening

scientific article published on 16 March 2016

Responsible implementation of expanded carrier screening

scientific article published on November 2017

Responsible innovation in human germline gene editing. Background document to the recommendations of ESHG and ESHRE

scientific article published on 12 January 2018

Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHRE.

scientific article

The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity

scientific article

List of works by Francesca Forzano

A response to the forensic genetics policy initiative’s report “Establishing Best Practice for Forensic DNA Databases”

Delineation of dominant and recessive forms of LZTR1-associated Noonan syndrome.

Developing a policy for paediatric biobanks: principles for good practice

ESHG PPPC Comments on postmortem use of genetic data for research purposes

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

Human germline gene editing. Recommendations of ESHG and ESHRE

Human germline gene editing: Recommendations of ESHG and ESHRE.

Italian appeal court: a genetic predisposition to commit murder?

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations

One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe.

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

Reply to Bombard and Mighton

Responsible implementation of expanded carrier screening

Responsible implementation of expanded carrier screening

Responsible innovation in human germline gene editing. Background document to the recommendations of ESHG and ESHRE

Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHRE.

The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity