Recent developments in genetic/genomic medicine von Horton, Rachel H, Lucassen, Anneke M

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Interventions to support patients with sharing genetic test results with at-risk relatives: a synthesis without meta-analysis (SWiM) von Ballard, Lisa Marie, Band, Rebecca, Lucassen, Anneke M

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What is the meaning of a 'genomic result' in the context of pregnancy? von Shkedi-Rafid, Shiri, Horton, Rachel, Lucassen, Anneke

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Exploring broad consent in the context of the 100,000 Genomes Project: a mixed methods study von Ballard, Lisa M., Horton, Rachel H., Dheensa, Sandi, Fenwick, Angela, Lucassen, Anneke M.

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Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives? von Dove, Edward S, Chico, Vicky, Fay, Michael, Laurie, Graeme, Lucassen, Anneke M, Postan, Emily

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Responsible implementation of expanded carrier screening von Henneman, Lidewij, Borry, Pascal, Chokoshvili, Davit, Cornel, Martina C, van El, Carla G, Forzano, Francesca, Hall, Alison, Howard, Heidi C, Janssens, Sandra, Kayserili, Hülya, Lakeman, Phillis, Lucassen, Anneke, Metcalfe, Sylvia A, Vidmar, Lovro, de Wert, Guido, Dondorp, Wybo J, Peterlin, Borut

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Old consent and new developments: health professionals should ask and not presume von Horton, Rachel, Fenwick, Angela, Lucassen, Anneke M

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Towards a national genomics medicine service: the challenges facing clinical-research hybrid practices and the case of the 100 000 genomes project von Dheensa, Sandi, Samuel, Gabrielle, Lucassen, Anneke M, Farsides, Bobbie

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Genome sequencing in healthcare: understanding the UK general public's views and implications for clinical practice von Ballard, Lisa M., Horton, Rachel H., Fenwick, Angela, Lucassen, Anneke M.

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The moral argument for heritable genome editing requires an inappropriately deterministic view of genetics von Horton, Rachel, Lucassen, Anneke M

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"A very big challenge": a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England von Friedrich, Bettina, Vindrola-Padros, Cecilia, Lucassen, Anneke M, Patch, Chris, Clarke, Angus, Lakhanpaul, Monica, Lewis, Celine

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The environmental impact of data-driven precision medicine initiatives von Samuel, Gabrielle, Lucassen, Anneke M

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Ethical issues raised by new genomic technologies: the case study of newborn genome screening von Horton, Rachel, Lucassen, Anneke

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Defining and managing incidental findings in genetic and genomic practice von Shkedi-Rafid, Shiri, Dheensa, Sandi, Crawford, Gillian, Fenwick, Angela, Lucassen, Anneke

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Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature von Otten, Ellen, Plantinga, Mirjam, Birnie, Erwin, Verkerk, Marian A., Lucassen, Anneke M., Ranchor, Adelita V., Van Langen, Irene M.

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Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics von Carrieri, Daniele, Howard, Heidi C, Benjamin, Caroline, Clarke, Angus J, Dheensa, Sandi, Doheny, Shane, Hawkins, Naomi, Halbersma-Konings, Tanya F, Jackson, Leigh, Kayserili, Hülya, Kelly, Susan E, Lucassen, Anneke M, Mendes, Álvaro, Rial-Sebbag, Emmanuelle, Stefánsdóttir, Vigdís, Turnpenny, Peter D, van El, Carla G, van Langen, Irene M, Cornel, Martina C, Forzano, Francesca

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Is it acceptable to contact an anonymous egg donor to facilitate diagnostic genetic testing for the donor-conceived child? von Horton, Rachel, Bell, Benjamin, Fenwick, Angela, Lucassen, Anneke M

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Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases von Plantinga, Mirjam, Birnie, Erwin, Abbott, Kristin M, Sinke, Richard J, Lucassen, Anneke M, Schuurmans, Juliette, Kaplan, Seyma, Verkerk, Marian A, Ranchor, Adelita V, van Langen, Irene M

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Feasibility of couple-based expanded carrier screening offered by general practitioners von Schuurmans, Juliette, Birnie, Erwin, van den Heuvel, Lieke M, Plantinga, Mirjam, Lucassen, Anneke, van der Kolk, Dorina M, Abbott, Kristin M, Ranchor, Adelita V, Diemers, Agnes D, van Langen, Irene M

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Systematic reanalysis of genomic data by diagnostic laboratories: a scoping review of ethical, economic, legal and (psycho)social implications von van der Geest, Marije A, Maeckelberghe, Els L M, van Gijn, Marielle E, Lucassen, Anneke M, Swertz, Morris A, van Langen, Irene M, Plantinga, Mirjam

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