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List of works by Anneke Lucassen

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Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas

scientific article
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

article
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33

scientific article
Missed threads. The impact of pre-mRNA splicing defects on clinical practice.

scientific article published on August 2009
Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer

article
Revealing false paternity: some ethical considerations

scientific article published in The Lancet
Health-care professionals' responsibility to patients' relatives in genetic medicine: a systematic review and synthesis of empirical research.

scientific article published on 25 June 2015
Common hereditary cancers and implications for primary care

scientific article
RNA analysis reveals splicing mutations and loss of expression defects in MLH1 and BRCA1.

scientific article
Evaluation of the impact of two educational interventions on GP management of familial breast/ovarian cancer cases: a cluster randomised controlled trial

scientific article published on October 1, 2001
Deciphering the genetics of hereditary non-syndromic colorectal cancer

scientific article published on 16 July 2008
Next generation diagnostics in inherited arrhythmia syndromes : a comparison of two approaches.

scientific article published on 7 September 2012
Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom

scientific article published on 18 February 2016
Confidentiality and serious harm in genetics - preserving the confidentiality of one patient and preventing harm to relatives.

scientific article
Confidentiality and sharing genetic information with relatives

scientific article published in May 2010
Consent and confidentiality in clinical genetic practice: guidance on genetic testing and sharing genetic information

scientific article published on 01 February 2012
Working towards ethical management of genetic testing

scientific article
Limitations and Pitfalls of Using Family Letters to Communicate Genetic Risk: a Qualitative Study with Patients and Healthcare Professionals

scientific article published on November 1, 2017
Telemedicine uptake among Genetics Professionals in Europe: room for expansion

scientific article published on April 22, 2015
Genetic Testing of Children: The Need for a Family Perspective

journal article; published in The American Journal of Bioethics in 2014
Using a genetic test result in the care of family members: how does the duty of confidentiality apply?

scientific article published on 27 April 2018
Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?

scientific article published on 23 May 2019
Feasibility of couple-based expanded carrier screening offered by general practitioners

scientific article published on 11 February 2019
The Insulin Gene Region and Susceptibility to Insulin-Dependent Diabetes Mellitus in Four Races; New Insights from Afro-Caribbean Race-Specific Haplotypes

scientific article published on 01 January 1997
Genomic variant sharing: a position statement

scientific article published on 05 February 2019
Disclosure of genetic information to relatives: balancing confidentiality and relatives’ interests

scientific article published on November 10, 2017
Prenatal diagnosis of chromosomal imbalances

scientific article published on 05 March 2014
Erratum: Responsible implementation of expanded carrier screening

scientific article published on November 1, 2017
European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

article published in 2019
Genome sequencing in healthcare: understanding the UK general public's views and implications for clinical practice

scientific article published on 16 September 2019
The impact of cancer pathology confirmation on clinical management of a family history of cancer

scientific article published on June 1, 2011
Fostering trust in healthcare: Participants' experiences, views, and concerns about the 100,000 genomes project

article
Ethical implications of new genetic technologies

scientific article published on January 3, 2012
Cognitive and affective outcomes of genetic counselling in the Netherlands at group and individual level: a personalized approach seems necessary

scientific article published on 27 April 2020
I Had Genetic Testing for Alzheimer’s Disease Without My Consent

scientific article published on January 1, 2015
Is it acceptable to contact an anonymous egg donor to facilitate diagnostic genetic testing for the donor-conceived child?

scientific article published on 12 June 2019
Predictive genetic testing in a young child: a case report

scientific article published on 12 August 2009
A validated PROM in genetic counselling: the psychometric properties of the Dutch version of the Genetic Counselling Outcome Scale

scientific article published on 25 January 2019
GP-provided couple-based expanded preconception carrier screening in the Dutch general population: who accepts the test-offer and why?

scientific article published on 30 September 2019
Exploring broad consent in the context of the 100,000 Genomes Project: a mixed methods study

scientific article published on 09 January 2020
Genetic testing from different angles. Introduction

scientific article published on 01 March 2010
Legal implications of tissue.

scientific article published on April 2010
The moral argument for heritable genome editing requires an inappropriately deterministic view of genetics

scientific article published on 12 March 2019
Using biomarkers in acute medicine to prevent hearing loss: should this require specific consent?

scientific article published on 13 July 2020
Beyond regulatory approaches to ethics: making space for ethical preparedness in healthcare research

scientific article published in 2022
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

scientific article published in July 2014
Using a biomarker acutely to identify babies at risk of serious adverse effects from antibiotics: where is the 'Terrible Moral and Medical Dilemma'?

scientific article published on 17 December 2020
What is the meaning of a 'genomic result' in the context of pregnancy?

scientific article published on 14 September 2020
Ethicolegal aspects of genetics in surgical practice.

scientific article
Genomic testing in healthcare: a hybrid space where clinical practice and research need to co-exist

scientific article published on 11 October 2019

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