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European Journal of Human Genetics : EJHG|March 5, 2009
Genetic horoscopes: is it all in the genes? Points for regulatory control of direct-to-consumer genetic testingChristine Patch, Jorge Sequeiros, Martina C CornelJournal of Community Genetics|March 31, 2012
Using a community of practice to develop standards of practice and education for genetic counsellors in EuropeHeather Skirton, Christine Patch, Marie-Antoinette VoelckelInternational Journal of Nursing Studies|July 25, 2016
Living a normal life in an extraordinary way: A systematic review investigating experiences of families of young people's transition into adulthood when affected by a genetic and chronic childhood conditionVeronika Waldboth, Christine Patch, Romy Mahrer-Imhof, et al.Journal of Clinical Nursing|November 7, 2015
Predictive or not predictive: understanding the mixed messages from the patient's DNA sequenceA Cecile J W Janssens, Christine Patch, Heather SkirtonJournal of Advanced Nursing|January 12, 2021
The family transition experience when living with childhood neuromuscular disease: A grounded theory studyVeronika Waldboth, Christine Patch, Romy Mahrer-Imhof, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 5, 2011
Use of antihypertensive medications and mortality of patients with autosomal dominant polycystic kidney disease: a population-based studyChristine Patch, Judith Charlton, Paul J Roderick, et al.Ebiomedicine|February 14, 2022
Towards equitable and trustworthy genomics researchJerome Atutornu, Richard Milne, Alesia Costa, et al.Journal of Genetic Counseling|June 10, 2023
International genetic counseling: What do genetic counselors actually do?Kelly E Ormond, Laura Hayward, Tina-Marié Wessels, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2005
How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United KingdomSimon Sanderson, Ron Zimmern, Mark Kroese, et al.F1000 Medicine Reports|October 16, 2010
Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics?David A Collier, Evangelos Vassos, Simon Holden, et al.Pageof 6