Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries by Milne, Richard, Morley, Katherine I, Almarri, Mohamed A, Anwer, Shamim, Atutornu, Jerome, Baranova, Elena E, Bevan, Paul, Cerezo, Maria, Cong, Yali, Costa, Alessia, Critchley, Christine, Fernow, Josepine, Goodhand, Peter, Hasan, Qurratulain, Hibino, Aiko, Houeland, Gry, Howard, Heidi C, Hussain, S Zakir, Malmgren, Charlotta Ingvoldstad, Izhevskaya, Vera L, Jędrzejak, Aleksandra, Jinhong, Cao, Kimura, Megumi, Kleiderman, Erika, Leach, Brandi, Liu, Keying, Mascalzoni, Deborah, Mendes, Álvaro, Minari, Jusaku, Nicol, Dianne, Niemiec, Emilia, Patch, Christine, Pollard, Jack, Prainsack, Barbara, Rivière, Marie, Robarts, Lauren, Roberts, Jonathan, Romano, Virginia, Sheerah, Haytham A, Smith, James, Soulier, Alexandra, Steed, Claire, Stefànsdóttir, Vigdis, Tandre, Cornelia, Thorogood, Adrian, Voigt, Torsten H, Wang, Nan, West, Anne V, Yoshizawa, Go, Middleton, Anna

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Opportunistic genomic screening. Recommendations of the European Society of Human Genetics by de Wert, Guido, Dondorp, Wybo, Clarke, Angus, Dequeker, Elisabeth M C, Cordier, Christophe, Deans, Zandra, van El, Carla G, Fellmann, Florence, Hastings, Ros, Hentze, Sabine, Howard, Heidi, Macek, Milan, Mendes, Alvaro, Patch, Chris, Rial-Sebbag, Emmanuelle, Stefansdottir, Vigdis, Cornel, Martina C, Forzano, Francesca

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Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice by Forzano, Francesca, Antonova, Olga, Clarke, Angus, de Wert, Guido, Hentze, Sabine, Jamshidi, Yalda, Moreau, Yves, Perola, Markus, Prokopenko, Inga, Read, Andrew, Reymond, Alexandre, Stefansdottir, Vigdis, van El, Carla, Genuardi, Maurizio

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Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data? by Middleton, Anna, Milne, Richard, Almarri, Mohamed A., Anwer, Shamim, Atutornu, Jerome, Baranova, Elena E., Bevan, Paul, Cerezo, Maria, Cong, Yali, Critchley, Christine, Fernow, Josepine, Goodhand, Peter, Hasan, Qurratulain, Hibino, Aiko, Houeland, Gry, Howard, Heidi C., Hussain, S. Zakir, Malmgren, Charlotta Ingvoldstad, Izhevskaya, Vera L., Jędrzejak, Aleksandra, Jinhong, Cao, Kimura, Megumi, Kleiderman, Erika, Leach, Brandi, Liu, Keying, Mascalzoni, Deborah, Mendes, Álvaro, Minari, Jusaku, Wang, Nan, Nicol, Dianne, Niemiec, Emilia, Patch, Christine, Pollard, Jack, Prainsack, Barbara, Rivière, Marie, Robarts, Lauren, Roberts, Jonathan, Romano, Virginia, Sheerah, Haytham A., Smith, James, Soulier, Alexandra, Steed, Claire, Stefànsdóttir, Vigdís, Tandre, Cornelia, Thorogood, Adrian, Voigt, Torsten H., West, Anne V., Yoshizawa, Go, Morley, Katherine I.

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Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals by Hill, Melissa, Johnson, Jo-Ann, Langlois, Sylvie, Lee, Hyun, Winsor, Stephanie, Dineley, Brigid, Horniachek, Marisa, Lalatta, Faustina, Ronzoni, Luisa, Barrett, Angela N, Advani, Henna V, Choolani, Mahesh, Rabinowitz, Ron, Pajkrt, Eva, van Schendel, Rachèl V, Henneman, Lidewij, Rommers, Wieke, Bilardo, Caterina M, Rendeiro, Paula, Ribeiro, Maria João, Rocha, José, Bay Lund, Ida Charlotte, Petersen, Olav B, Becher, Naja, Vogel, Ida, Stefánsdottir, Vigdis, Ingvarsdottir, Sigrun, Gottfredsdottir, Helga, Morris, Stephen, Chitty, Lyn S

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Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland by Stefansdottir, Vigdis, Thorolfsdottir, Eirny, Hognason, Hakon B, Patch, Christine, van El, Carla, Hentze, Sabine, Cordier, Christophe, Mendes, Álvaro, Jonsson, Jon J

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Reply to Bombard and Mighton by Carrieri, Daniele, Howard, Heidi C, Clarke, Angus J, Stefansdottir, Vigdis, Cornel, Martina C, van El, Carla G, Forzano, Francesca

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Experience of Social Media Support Group for BRCA Carriers by Stefansdottir, Vigdis

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Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics by 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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Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries by Milne, Richard, Morley, Katherine I, Almarri, Mohamed A, Anwer, Shamim, Atutornu, Jerome, Baranova, Elena E, Bevan, Paul, Cerezo, Maria, Cong, Yali, Costa, Alessia, Critchley, Christine, Fernow, Josepine, Goodhand, Peter, Hasan, Qurratulain, Hibino, Aiko, Houeland, Gry, Howard, Heidi C, Hussain, S Zakir, Malmgren, Charlotta Ingvoldstad, Izhevskaya, Vera L, Jędrzejak, Aleksandra, Jinhong, Cao, Kimura, Megumi, Kleiderman, Erika, Leach, Brandi, Liu, Keying, Mascalzoni, Deborah, Mendes, Álvaro, Minari, Jusaku, Nicol, Dianne, Niemiec, Emilia, Patch, Christine, Pollard, Jack, Prainsack, Barbara, Rivière, Marie, Robarts, Lauren, Roberts, Jonathan, Romano, Virginia, Sheerah, Haytham A, Smith, James, Soulier, Alexandra, Steed, Claire, Stefànsdóttir, Vigdis, Tandre, Cornelia, Thorogood, Adrian, Voigt, Torsten H, Wang, Nan, West, Anne V, Yoshizawa, Go, Middleton, Anna

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The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice by Forzano, Francesca, Antonova, Olga, Clarke, Angus, de Wert, Guido, Hentze, Sabine, Jamshidi, Yalda, Moreau, Yves, Perola, Markus, Prokopenko, Inga, Read, Andrew, Reymond, Alexandre, Stefansdottir, Vigdis, van El, Carla, Genuardi, Maurizio

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Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers by Page, Elizabeth C., Bancroft, Elizabeth K., Brook, Mark N., Assel, Melissa, Hassan Al Battat, Mona, Thomas, Sarah, Taylor, Natalie, Raghallaigh, Holly Ni, Evans, D. Gareth, Maehle, Lovise, Grindedal, Eli Marie, James, Paul, Mascarenhas, Lyon, McKinley, Joanne, Thomas, Tessy, van Asperen, Christi, Vasen, Hans, Kiemeney, Lambertus A., Ringelberg, Janneke, Jensen, Thomas Dyrsø, Osther, Palle J.S., Helfand, Brian T., Genova, Elena, Oldenburg, Rogier A., Cybulski, Cezary, Ong, Kai-Ren, Lam, Jimmy, Taylor, Louise, Feliubadaló, Lidia, van Zelst-Stams, Wendy, Rosario, Derek J., Domchek, Susan, Powers, Jacquelyn, Buys, Saundra, O'Toole, Karen, Ausems, Margreet G.E.M., Schmutzler, Rita K., Rhiem, Kerstin, Izatt, Louise, Cardoso, Marta, Aprikian, Armen, van Randeraad, Heleen, Davidson, Rosemarie, Longmuir, Mark, Helderman van den Enden, Apollonia T.J.M., Adank, Muriel, Williams, Rachel, Andrews, Lesley, Murphy, Declan G., Halliday, Dorothy, Walker, Lisa, Liljegren, Annelie, Carlsson, Stefan, Morton, Catherine, Snape, Katie, Hanson, Helen, Tischkowitz, Marc, Taylor, Amy, Kirk, Judy, Susman, Rachel, Chen-Shtoyerman, Rakefet, Spigelman, Allan, Pachter, Nicholas, Ahmed, Munaza, Ramon y Cajal, Teresa, Brewer, Carole, Gadea, Neus, van Os, Theo, Gallagher, David, Johannsson, Oskar, Barwell, Julian, Nicolai, Nicola, Friedman, Eitan, Greenhalgh, Lynn, Murthy, Vedang, Saya, Sibel, McGrath, John, Rønlund, Karina, Teo, Soo H., Kast, Karin, Aaronson, Neil K., Ardern-Jones, Audrey, Bangma, Chris H., Dearnaley, David, Tricker, Karen, Eyfjord, Jorunn, Falconer, Alison, Foster, Christopher, Gronberg, Henrik, Hamdy, Freddie C., Stefansdottir, Vigdis, Khoo, Vincent, Lindeman, Geoffrey J., Lubinski, Jan, Mikropoulos, Christos, Mitra, Anita, Moynihan, Clare, Wilson, Penny, Dudderidge, Tim, Offman, Judith

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Ethical issues in precision medicine by Jonsson, Jon J, Stefansdottir, Vigdis

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Molecular genetics of inherited retinal degenerations in Icelandic patients by Thorsteinsson, Daniel A., Stefansdottir, Vigdis, Eysteinsson, Thor, Thorisdottir, Sigridur, Jonsson, Jon J.

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Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study by Bancroft, Elizabeth K, Page, Elizabeth C, Castro, Elena, Lilja, Hans, Vickers, Andrew, Sjoberg, Daniel, Assel, Melissa, Foster, Christopher S, Drew, Kate, Mæhle, Lovise, Axcrona, Karol, Evans, D. Gareth, Bulman, Barbara, Eccles, Diana, van Asperen, Christi, Vasen, Hans, Kiemeney, Lambertus A, Ringelberg, Janneke, Cybulski, Cezary, Wokolorczyk, Dominika, Selkirk, Christina, Hulick, Peter J, Bojesen, Anders, Skytte, Anne-Bine, Lam, Jimmy, Taylor, Louise, Oldenburg, Rogier, Verhaegh, Gerald, van Zelst-Stams, Wendy A, Oosterwijk, Jan C, Blanco, Ignacio, Salinas, Monica, Cook, Jackie, Rosario, Derek J, Buys, Saundra, Conner, Tom, Ausems, Margreet G, Ong, Kai-ren, Hoffman, Jonathan, Domchek, Susan, Teixeira, Manuel R, Maia, Sofia, Foulkes, William D, Taherian, Nassim, Ruijs, Marielle, den Enden, Apollonia T. Helderman-van, Izatt, Louise, Davidson, Rosemarie, Adank, Muriel A, Walker, Lisa, Schmutzler, Rita, Tucker, Kathy, Kirk, Judy, Hodgson, Shirley, Harris, Marion, Douglas, Fiona, Lindeman, Geoffrey J, Zgajnar, Janez, Tischkowitz, Marc, Susman, Rachel, Ramón y Cajal, Teresa, Patcher, Nicholas, Spigelman, Allan, Liljegren, Annelie, Side, Lucy, Brewer, Carole, Donaldson, Alan, Stefansdottir, Vigdis, Chen-Shtoyerman, Rakefet, Amor, David J, Barwell, Julian, Giri, Veda N, Murthy, Vedang, Nicolai, Nicola, Teo, Soo-Hwang, Greenhalgh, Lynn, Strom, Sara, Henderson, Alex, McGrath, John, Gallagher, David, Aaronson, Neil, Ardern-Jones, Audrey, Bangma, Chris, Dearnaley, David, Eyfjord, Jorunn, Rothwell, Jeanette, Falconer, Alison, Gronberg, Henrik, Johannsson, Oskar, Kote-Jarai, Zsofia, Axcrona, Ulrika, Melia, Jane, McKinley, Joanne, Mitra, Anita V, Moynihan, Clare, Rennert, Gad, Suri, Mohnish, Wilson, Penny, Killick, Emma, Moss, Sue

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European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death by Fellmann, Florence, van El, Carla G, Charron, Philippe, Michaud, Katarzyna, Howard, Heidi C, Boers, Sarah N, Clarke, Angus J, Duguet, Anne-Marie, Forzano, Francesca, Kauferstein, Silke, Kayserili, Hülya, Lucassen, Anneke, Mendes, Álvaro, Patch, Christine, Radojkovic, Dragica, Rial-Sebbag, Emmanuelle, Sheppard, Mary N, Tassé, Anne-Marie, Temel, Sehime G, Sajantila, Antti, Basso, Cristina, Wilde, Arthur A M, Cornel, Martina C

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A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome by Klemenzdottir, Elin Ola, Arnadottir, Gudny Anna, Jensson, Brynjar Orn, Jonasdottir, Adalbjorg, Katrinardottir, Hildigunnur, Fridriksdottir, Run, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Gudjonsson, Sigurjon Axel, Jonsson, Jon Johannes, Stefansdottir, Vigdis, Danielsen, Ragnar, Palsdottir, Astridur, Jonsson, Hakon, Helgason, Agnar, Magnusson, Olafur Thor, Thorsteinsdottir, Unnur, Bjornsson, Hans Tomas, Stefansson, Kari, Sulem, Patrick

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Oestrogen receptor status, treatment and breast cancer prognosis in Icelandic BRCA2 mutation carriers by Jonasson, Jon G, Stefansson, Olafur A, Johannsson, Oskar T, Sigurdsson, Helgi, Agnarsson, Bjarni A, Olafsdottir, Gudridur H, Alexiusdottir, Kristin K, Stefansdottir, Hrefna, Munoz Mitev, Rodrigo, Olafsdottir, Katrin, Olafsdottir, Kristrun, Arason, Adalgeir, Stefansdottir, Vigdis, Olafsdottir, Elinborg J, Barkardottir, Rosa B, Eyfjord, Jorunn E, Narod, Steven A, Tryggvadóttir, Laufey

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Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection' by Forzano, Francesca, Antonova, Olga, Clarke, Angus, de Wert, Guido, Hentze, Sabine, Jamshidi, Yalda, Moreau, Yves, Perola, Markus, Prokopenko, Inga, Read, Andrew, Reymond, Alexandre, Stefansdottir, Vigdis, van El, Carla, Genuardi, Maurizio

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Comparing prenatal screening experiences of Icelandic women who received false‐positive and true‐negative first‐trimester combined screening results in Iceland in 2012–2016 by Thorolfsdottir, Eirny, Lunde, Åshild, Stefansdottir, Vigdis, Hjartardottir, Hulda, Rut Haraldsdottir, Kristin

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