ProfileOfResearchers

Identificadas 34

TÃTULO: 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

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TÃTULO: 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

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TÃTULO: 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

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TÃTULO: 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

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TÃTULO: Opportunistic genomic screening. Recommendations of the European Society of Human Genetics
AUTORES: de Wert, G; Dondorp, W; Clarke, A; Dequeker, EMC; Cordier, C; Deans, Z; van El, CG; Fellmann, F; Hastings, R; Hentze, S; Howard, H; Macek, M; Mendes, A; Patch, C; Rial Sebbag, E; Stefansdottir, V; Cornel, MC; Forzano, F;
PUBLICAÇÃO: 2020, FONTE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 29, NÚMERO: 3

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TÃTULO: Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics
AUTORES: Carrieri, D; Howard, HC; Benjamin, C; Clarke, AJ; Dheensa, S; Doheny, S; Hawkins, N; Halbersma Konings, TF; Jackson, L; Kayserili, H; Kelly, SE; Lucassen, AM; Mendes, A; Rial Sebbag, E; Stefansdottir, V; Turnpenny, PD; van El, CG; van Langen, IM; Cornel, MC; Forzano, F;
PUBLICAÇÃO: 2019, FONTE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27, NÚMERO: 2

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TÃTULO: Twenty Years of a Pre-Symptomatic Testing Protocol for Late-Onset Neurological Diseases in Portugal Full Text
AUTORES: Paneque, M ; Felix, J; Mendes, A; Lemos, C ; Ledo, S; Silva, J; Sequeiros, J;
PUBLICAÇÃO: 2019, FONTE: ACTA MEDICA PORTUGUESA, VOLUME: 32, NÚMERO: 4

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TÃTULO: Choosing not to know: accounts of non-engagement with pre-symptomatic testing for late onset-neurological disorders
AUTORES: Mendes, A; Paneque, M ; Clarke, A; Sequeiros, J;
PUBLICAÇÃO: 2019, FONTE: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27

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TÃTULO: A diabetes não dói, não se sente, mas está cá dentro!
AUTORES: Alvaro Mendes; Carmen Elisa Travieso; Liliana Sousa;
PUBLICAÇÃO: 2019, FONTE: Psychologica, VOLUME: 62, NÚMERO: 2

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