929 results on '"Borry, Pascal"'
Search Results
202. The role of pharmacogenomics in contemporary cardiovascular therapy: a position statement from the European Society of Cardiology Working Group on Cardiovascular Pharmacotherapy
203. Challenges in cardiovascular pharmacogenomics implementation: a viewpoint from the European Society of Cardiology Working Group on Cardiovascular Pharmacotherapy
204. Return of Results in Population Studies: How Do Participants Perceive Them?
205. Should minors and young adults qualify as potential live kidney donors? The views of international transplant professionals
206. Consent insufficient for data release
207. The athlete biological passport: challenges and possibilities
208. Reproductive autonomy in expanded carrier screening: more than meets the eye?
209. Old Challenges or New Issues? Genetic Health Professionals' Experiences Obtaining Informed Consent in Diagnostic Genomic Sequencing.
210. Psychosocial impact of pediatric living-donor kidney and liver transplantation on recipients, donors, and the family: a systematic review
211. How international is bioethics? A quantitative retrospective study
212. Genetic health professionals' experiences returning results from diagnostic genomic sequencing to patients.
213. CAREGIVERS' ATTITUDE TOWARDS FAMILY PLANNING AND TIMING OF DIAGNOSIS IN AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE
214. Expanded carrier screening in a reproductive context. Towards a responsible implementation in the healthcare system
215. Living Organ Donation by Minors: An Analysis of the Regulations in EU Member States
216. Interest in expanded carrier screening among individuals and couples in the general population: systematic review of the literature.
217. Forensic Epigenetic Age Estimation and Beyond: Ethical and Legal Considerations
218. Do athletes have a right to access data in their Athlete Biological Passport?
219. The author who wasn’t there? Fairness and attribution in publications following access to population biobanks
220. Geolocalisation of athletes for out-of-competition drug testing: ethical considerations. Position statement by the WADA Ethics Panel
221. Raw Genomic Data: Storage, Access, and Sharing
222. Noninvasive prenatal testing: a survey of young (future) parents in Flanders
223. A systematic analysis of online marketing materials used by providers of expanded carrier screening
224. Rules for processing genetic data for research purposes in view of the new EU General Data Protection Regulation
225. Research ethics review for the use of anonymized samples and data: A systematic review of normative documents
226. Participants’ decision to enroll in cohort studies with biobanks: quantitative insights from two German studies
227. Time out: ethical reflections on medical disqualification of athletes in the context of mandated pre-participation cardiac screening
228. Reporting practices for variants of uncertain significance from next generation sequencing technologies
229. Oversight of Genomic Data Sharing: What Roles for Ethics and Data Access Committees?
230. Growing complexity of (expanded) carrier screening: Direct-to-consumer, physician-mediated, and clinic-based offers
231. Toward better governance of human genomic data
232. Avis n° 66 du 9 mai 2016 relatif aux défis éthiques posés par le diagnostic prénatal non–invasif (NIPT) pour les trisomies 21, 13 et 18
233. Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes
234. Quality Assessment of Genetic Counseling Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities
235. Clinicians’ attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney disease
236. The challenges of the expanded availability of genomic information: an agenda-setting paper
237. Readability of informed consent forms for whole-exome and whole-genome sequencing
238. Third party interpretation of raw genetic data: an ethical exploration
239. Pre- and post-testing counseling considerations for the provision of expanded carrier screening: exploration of European geneticists’ views
240. Expanded carrier screening for monogenic disorders: where are we now?
241. Regulating the advertising of genetic tests in Europe: a balancing act
242. Newspaper coverage of human-pig chimera research: A qualitative study on select media coverage of scientific breakthrough
243. Reporting practices for unsolicited and secondary findings from next‐generation sequencing technologies: Perspectives of laboratory personnel
244. Reply to C Harling
245. Ethical considerations for genetic testing in the context of mandated cardiac screening before athletic participation
246. Erratum: Legal approaches regarding health-care decisions involving minors: implications for next-generation sequencing
247. Paternity testing under the cloak of recreational genetics
248. Public Views on Genetics and Genetic Testing: A Survey of the General Public in Belgium
249. Unsolved challenges in pediatric whole-exome sequencing: A literature analysis
250. Attitudes of European Geneticists Regarding Expanded Carrier Screening
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