Author details

Full Name

A Cecile J W Janssens

Affiliation

ORCID

Career Start Year

2003

Papers

193

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36097155	Societal implications of expanded universal carrier screening: a scoping review.	Eur J Hum Genet	2023
33587168	Do we measure or compute polygenic risk scores? Why language matters.	Human Genetics	2022
32853342	Personalizing Breast Cancer Screening Based on Polygenic Risk and Family History.	J Natl Cancer Inst	2021
33595827	Critical examination of current response shift methods and proposal for advancing new methods.	Quality of Life Research	2021
31967640	Reflection on modern methods: Revisiting the area under the ROC Curve.	International Journal of Epidemiology	2020
32028894	Novel citation-based search method for scientific literature: a validation study.	BMC Med Res Methodol	2020
31200546	Proprietary Algorithms for Polygenic Risk: Protecting Scientific Innovation or Hiding the Lack of It?	Genes	2019
32025627	Cost-Effectiveness of Risk-Stratified Colorectal Cancer Screening Based on Polygenic Risk: Current Status and Future Potential.	JNCI Cancer Spectr	2019
29895851	Evaluation of polygenic risk models using multiple performance measures: a critical assessment of discordant results.	Genetics in Medicine	2019
31504522	Validity of polygenic risk scores: are we measuring what we think we are?	Human Molecular Genetics	2019
30193269	Lowering the P Value Threshold.	JAMA - Journal of the American Medical Association	2018
28964749	Cost Effectiveness of Age-Specific Screening Intervals for People With Family Histories of Colorectal Cancer.	Gastroenterology	2018
30311678	Finding Wealth in Waste: Irreplicability Re-Examined.	BioEssays	2018
30071015	A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health.	PLoS Med	2018
30114233	Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health.	PLoS Med	2018
28273476	Predicting Polygenic Obesity Using Genetic Information.		2017
28645363	Response to letter Dr Gail.	Journal of Clinical Epidemiology	2017
28488677	Uninformed consent in nutrigenomic research.	Eur J Hum Genet	2017
28968388	A critical evaluation of the algorithm behind the Relative Citation Ratio (RCR).	PLoS Biol	2017
27168098	Assessment of pharmacogenetic tests: presenting measures of clinical validity and potential population impact in association studies.	Pharmacogenomics J	2017
21547703	Value of EUS in Determining Curative Resectability in Reference to CT and FDG-PET: The Optimal Sequence in Preoperative Staging of Esophageal Cancer?	Ann Surg Oncol	2016
25726454	External validation is only needed when prediction models are worth it (Letter commenting on: J Clin Epidemiol. 2015;68:25-34).	Journal of Clinical Epidemiology	2016
27023073	Constructing Hypothetical Risk Data from the Area under the ROC Curve: Modelling Distributions of Polygenic Risk.	PLoS ONE	2016
27430730	Small improvement in the area under the receiver operating characteristic curve indicated small changes in predicted risks.	Journal of Clinical Epidemiology	2016
27054708	Designing babies through gene editing: science or science fiction?	Genetics in Medicine	2016
27487404	An Electrocardiogram-Based Risk Equation for Incident Cardiovascular Disease From the National Health and Nutrition Examination Survey.	JAMA Cardiology	2016
26762807	Risk Analysis of Prostate Cancer in PRACTICAL Consortium-Letter.	Cancer Epidemiology Biomarkers and Prevention	2016
26119889	Prediction impact curve is a new measure integrating intervention effects in the evaluation of risk models.	J Clin Epidemiol	2016
24872596	Personal utility in genomic testing: is there such a thing?	Journal of Medical Ethics	2015
25590981	Family history and the natural history of colorectal cancer: systematic review.	Genet Med	2015
25412399	The hidden harm behind the return of results from personal genome services: a need for rigorous and responsible evaluation.	Genetics in Medicine	2015
25950734	Returning pharmacogenetic secondary findings from genome sequencing: let's not put the cart before the horse.	Genet Med	2015
26554355	Erratum to: Novel citation-based search method for scientific literature: application to meta-analyses.	BMC Med Res Methodol	2015
26462491	Novel citation-based search method for scientific literature: application to meta-analyses.	BMC Med Res Methodol	2015
26384276	The Prediction of Radiotherapy Toxicity Using Single Nucleotide Polymorphism-Based Models: A Step Toward Prevention.	Seminars in Radiation Oncology	2015
26542756	Predictive or not predictive: understanding the mixed messages from the patient's DNA sequence.	J Clin Nurs	2015
24946154	A systematic review and critical assessment of 11 discordant meta-analyses on reduced-function CYP2C19 genotype and risk of adverse clinical outcomes in clopidogrel users.	Genet Med	2015
25117528	Quality criteria for health checks: development of a European consensus agreement.	Preventive Medicine	2014
25399713	Useless until proven effective: the clinical utility of preemptive pharmacogenetic testing.	Clin Pharmacol Ther	2014
24411311	Scientific reporting is suboptimal for aspects that characterize genetic risk prediction studies: a review of published articles based on the Genetic RIsk Prediction Studies statement.	J Clin Epidemiol	2014
23807614	Variations in predicted risks in personal genome testing for common complex diseases.	Genet Med	2014
24485561	Naming and framing in genomic testing.	Trends in Molecular Medicine	2014
24472337	[Biobanks and the return of results to donors].	Nederlands Tijdschrift voor Geneeskunde	2014
23962456	Prediction model for knee osteoarthritis incidence, including clinical, genetic and biochemical risk factors.	Ann Rheum Dis	2014
23137034	Informed consent in direct-to-consumer personal genome testing: the outline of a model between specific and generic consent.	Bioethics	2014
25037055	B-type natriuretic peptide and C-reactive protein in the prediction of atrial fibrillation risk: the CHARGE-AF Consortium of community-based cohort studies.	Europace	2014
24982668	Estimating the predictive ability of genetic risk models in simulated data based on published results from genome-wide association studies.	Frontiers in Genetics	2014
24578562	Raw data: access to inaccuracy.	Science	2014
22105623	A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.	Mol Psychiatry	2013
22415036	Heritability of dietary food intake patterns.	Acta Diabetol	2013