ProfileOfResearchers

Identificadas 52

TÃTULO: RESTRICTIONS IN CARE FOLLOWING THE COVID-19 PANDEMIC SEVERELY IMPACTED MACHADO-JOSEPH DISEASE PATIENTS: A STUDY IN SAO MIGUEL, THE AZORES Full Text
AUTORES: Couto, Daniela; Sousa, Liliana ; Sequeiros, Jorge; Lima, Manuela; Mendes, Alvaro;
PUBLICAÇÃO: 2023, FONTE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, NÚMERO: 13

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WOS

TÃTULO: A An online genetic counselling narrative group as a tool for supporting patients with hereditary ataxias in Portugal Full Text
AUTORES: Paneque, Milena ; Policarpo, Mariana; Barbosa, Maria; Lemos, Marina; Mendes, Alvaro;
PUBLICAÇÃO: 2023, FONTE: 55th European-Society-of-Human-Genetics (ESHG) Conference in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 31

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TÃTULO: Intergenerational relations matter: exploring health-related roles in families with transthyretin-related familial amyloid polyneuropathy (TTR-FAP) and Huntington disease (HD) Full Text
AUTORES: Oliveira, Carla ; Mendes, Alvaro; Sequeiros, Jorge; Sousa, Liliana ;
PUBLICAÇÃO: 2023, FONTE: 55th European-Society-of-Human-Genetics (ESHG) Conference in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 31

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TÃTULO: Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’ Full Text
AUTORES: Francesca Forzano; Olga Antonova; Angus Clarke; Guido de Wert; Sabine Hentze; Yalda Jamshidi; Yves Moreau; Markus Perola; Inga Prokopenko; Andrew Read; Alexandre Reymond; Vigdis Stefansdottir; Carla van El; Maurizio Genuardi; 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: 2023, FONTE: European Journal of Human Genetics, VOLUME: 31, NÚMERO: 3

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Scopus

CrossRef: 1

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ORCID

TÃTULO: Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries
AUTORES: Milne, Richard; Morley, Katherine, I; Almarri, Mohamed A.; Atutornu, Jerome; Baranova, Elena E.; Bevan, Paul; Cerezo, Maria; Cong, Yali; Costa, Alessia; Feijao, Carolina; de Freitas, Claudia ; Fernow, Josepine; Goodhand, Peter; Hasan, Qurratulain; Hibino, Aiko; Houeland, Gry; Howard, Heidi C.; Sheikh, Zakir Hussain; Malmgren, Charlotta Ingvoldstad; Izhevskaya, Vera L.; Jedrzejak, Aleksandra; Cao, JH; Kimura, Megumi; Kleiderman, Erika; Liu, Keying; Mascalzoni, Deborah; Mendes, Alvaro; Minari, Jusaku; Nicol, Dianne; Niemiec, Emilia; Patch, Christine; Prainsack, Barbara; Riviere, Marie; Robarts, Lauren; Roberts, Jonathan; Romano, Virginia; Sheerah, Haytham A.; Smith, James; Soulier, Alexandra; Steed, Claire; Stefansdottir, Vigdis; Tandre, Cornelia; Thorogood, Adrian; Voigt, Torsten H.; Wang, Nan; Yoshizawa, Go; Middleton, Anna; ...Mais
PUBLICAÇÃO: 2022, FONTE: GENETICS IN MEDICINE, VOLUME: 24, NÚMERO: 5

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CrossRef: 3

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ORCID

TÃTULO: The Experience of Receiving and Transmitting a Genetic Disease Full Text
AUTORES: Seidi, C; Patrao, M ; Guerra, S; Oliveira, CR; Mendes, A; Sousa, L;
PUBLICAÇÃO: 2022, FONTE: JOURNAL OF CONSTRUCTIVIST PSYCHOLOGY, VOLUME: 36, NÚMERO: 2

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CrossRef: 2

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ORCID

TÃTULO: Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice (European Journal of Human Genetics, (2021), 10.1038/s41431-021-01000-x) 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; Maurizio, G; Peterlin, B; Oliveira, C; Writzl, K; Houge, GD; Cordier, C; de Wert, G; Howard, H; Macek, M; Melegh, B; Mendes, A; Radojkovic, D; Rial Sebbag, E; Stefánsdottir, V; Ulph, F; van El, C; on behalf of the Executive Committee of the European Society of Human Genetics; the Public and Professional Policy Committee of the European Society of Human Genetics; ...Mais
PUBLICAÇÃO: 2022, FONTE: European Journal of Human Genetics, VOLUME: 30, NÚMERO: 5

INDEXADO EM:

Scopus

CrossRef: 3

NO MEU:

ORCID