32
TÍTULO: Correction to: Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’ (European Journal of Human Genetics, (2022), 10.1038/s41431-022-01241-4)  Full Text
AUTORES: Forzano, F; Antonova, O; Clarke, A; de Wert, G; Hentze, S; Jamshidi, Y; Moreau, Y; Perola, M; Prokopenko, I; Read, A; Reymond, A; Stefansdottir, V; van El, C; Genuardi, M; Genuardi, M; Peterlin, B; Oliveira, C; Writzl, K; Houge, GD; Cordier, C; Howard, H; Macek, M; Melegh, B; Mendes, A; Radojkovic, D; Rial Sebbag, E; Ulph, F; Committee of the European Society of Human Genetics Executive; and Professional Policy Committee of the European Society of Human Genetics Public; ...Mais
PUBLICAÇÃO: 2022, FONTE: European Journal of Human Genetics, VOLUME: 31, NÚMERO: 3
INDEXADO EM: Scopus CrossRef
NO MEU: ORCID
33
TÍTULO: Multifamily interventions in the context of inherited genetic conditions: A scoping review
AUTORES: Guerra, Sara; Oliveira, Carla; Seidi, Catarina; Sousa, Liliana; Mendes, Alvaro;
PUBLICAÇÃO: 2022, FONTE: JOURNAL OF FAMILY THERAPY, VOLUME: 45, NÚMERO: 1
INDEXADO EM: Scopus WOS CrossRef: 3
NO MEU: ORCID
34
TÍTULO: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice
AUTORES: Francesca Forzano; Olga Antonova; Angus Clarke; Guido de Wert; Sabine Hentze; Yalda Jamshidi; Yalda Jamshidi; Yves Moreau; Markus Perola; Inga Prokopenko; Andrew Read; Alexandre Reymond; Vigdis Stefansdottir; Carla van El; Maurizio Genuardi; Borut Peterlin; Carla Oliveira; Karin Writzl; Gunnar Douzgos Houge; Christophe Cordier; Heidi Howard; Milan Macek; Béla Melegh; Alvaro Mendes; Dragica Radojkovic; Emmanuelle Rial Sebbag; Fiona Ulph; ...Mais
PUBLICAÇÃO: 2022, FONTE: European Journal of Human Genetics, VOLUME: 30, NÚMERO: 5
INDEXADO EM: Scopus CrossRef: 45
NO MEU: ORCID
35
TÍTULO: Role of older generations in the family's adjustment to Huntington disease
AUTORES: Oliveira, CR; Mendes, A; Sequeiros, J ; Sousa, L;
PUBLICAÇÃO: 2021, FONTE: JOURNAL OF COMMUNITY GENETICS, VOLUME: 12, NÚMERO: 3
INDEXADO EM: Scopus WOS CrossRef: 4
NO MEU: ORCID
36
TÍTULO: Between responsibility and desire: Accounts of reproductive decisions from those at risk for or affected by late-onset neurological diseases  Full Text
AUTORES: Mendes, A; Sequeiros, J ; Clarke, AJ;
PUBLICAÇÃO: 2021, FONTE: JOURNAL OF GENETIC COUNSELING, VOLUME: 30, NÚMERO: 5
INDEXADO EM: Scopus WOS CrossRef: 5
NO MEU: ORCID
37
TÍTULO: Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries
AUTORES: Milne, R; Morley, KI; Almarri, MA; Anwer, S; Atutornu, J; Baranova, EE; Bevan, P; Cerezo, M; Cong, YL; Costa, A; Critchley, C; Fernow, J; Goodhand, P; Hasan, Q; Hibino, A; Houeland, G; Howard, HC; Hussain, SZ; Malmgren, CI; Izhevskaya, VL; Jedrzejak, A; Cao, JH; Kimura, M; Kleiderman, E; Leach, B; Liu, KY; Mascalzoni, D; Mendes, A; Minari, J; Nicol, D; Niemiec, E; Patch, C; Pollard, J; Prainsack, B; Riviere, M; Robarts, L; Roberts, J; Romano, V; Sheerah, HA; Smith, J; Soulier, A; Steed, C; Stefansdottir, V; Tandre, C; Thorogood, A; Voigt, TH; Wang, N; West, AV; Yoshizawa, G; Middleton, A; ...Mais
PUBLICAÇÃO: 2021, FONTE: GENOME MEDICINE, VOLUME: 13, NÚMERO: 1
INDEXADO EM: Scopus WOS CrossRef: 36
NO MEU: ORCID
38
TÍTULO: Management of information within Portuguese families with Huntington disease: a transgenerational process for putting the puzzle together  Full Text
AUTORES: Oliveira, CR; Mendes, A; Sequeiros, J; Sousa, L ;
PUBLICAÇÃO: 2020, FONTE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 28, NÚMERO: 9
INDEXADO EM: Scopus WOS CrossRef: 9
NO MEU: ORCID
39
TÍTULO: Web-based return ofBRCA2research results: one-year genetic counselling experience in Iceland
AUTORES: Stefansdottir, V; Thorolfsdottir, E; Hognason, HB; Patch, C; van El, C; Hentze, S; Cordier, C; Mendes, A; Jonsson, JJ;
PUBLICAÇÃO: 2020, FONTE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 28, NÚMERO: 12
INDEXADO EM: Scopus WOS CrossRef: 13
NO MEU: ORCID
40
TÍTULO: Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
AUTORES: Middleton, A; Milne, R; Almarri, MA; Anwer, S; Atutornu, J; Baranova, EE; Bevan, P; Cerezo, M; Cong, YL; Critchley, C; Fernow, J; Goodhand, P; Hasan, Q; Hibino, A; Houeland, G; Howard, HC; Hussain, SZ; Malmgren, CI; Izhevskaya, VL; Jedrzejak, A; Cao, JH; Kimura, M; Kleiderman, E; Leach, B; Liu, KY; Mascalzoni, D; Mendes, A; Minari, J; Wang, N; Nicol, D; Niemiec, E; Patch, C; Pollard, J; Prainsack, B; Riviere, M; Robarts, L; Roberts, J; Romano, V; Sheerah, HA; Smith, J; Soulier, A; Steed, C; Stefansdottir, V; Tandre, C; Thorogood, A; Voigt, TH; West, AV; Yoshizawa, G; Morley, KI; ...Mais
PUBLICAÇÃO: 2020, FONTE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 107, NÚMERO: 4
INDEXADO EM: Scopus WOS CrossRef: 84
NO MEU: ORCID
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