Milena Paneque Herrera


AuthID: R-000-JG5

Confirmed Publications: 95



31
TITLE: Developing a national certification pathway for genetic counselors in Sweden-a short report
AUTHORS: Rebecka Pestoff; Karin Svensson; Milena Paneque ; Charlotta Ingvoldstad Malmgren;
PUBLISHED: 2020, SOURCE: JOURNAL OF COMMUNITY GENETICS, VOLUME: 11, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID | CIÊNCIAVITAE
32
TITLE: A Portuguese Tool for Quality Assessment of Genetic Counselling by Genetics Healthcare Professionals  Full Text
AUTHORS: Catarina Costa; Marina S Lemos; Carolina Lemos ; Miguel Alves Ferreira; Jorge Sequeiros; Milena Paneque ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
33
TITLE: Choosing not to know: accounts of non-engagement with pre-symptomatic testing for late onset-neurological disorders
AUTHORS: Mendes, A; Paneque, M ; Clarke, A; Sequeiros, J;
PUBLISHED: 2019, SOURCE: 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
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
34
TITLE: Choosing not to know: accounts of non-engagement with pre-symptomatic testing for Machado-Joseph disease
AUTHORS: Alvaro Mendes ; Milena Paneque ; Angus Clarke; Jorge Sequeiros;
PUBLISHED: 2019, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 10
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
35
TITLE: Complementariness between medical geneticists and genetic counsellors: its added value in genetics services in Europe
AUTHORS: Paneque P Herrera ; Serra Juhe, C; Pestoff, R; Cordier, C; Silva, J; Moldovan, R; Ingvoldstad, C;
PUBLISHED: 2019, SOURCE: 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
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
36
TITLE: Patients' views: a new tool for quality assessment of genetic counselling  Full Text
AUTHORS: Marcia Carvalho; Milena Paneque ; Fidjy Rodrigues; Jorge Saraiva; Alexandra Leonardo; Ana B Sousa; Vania Machado; Renata Oliveira; Miguel Rocha; Jorge Sequeiros; Marina S Lemos;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
37
TITLE: Patients' Voices in Portugal - when rare becomes common  Full Text
AUTHORS: Catarina Costa; Isabel Alonso; Jorge Sequeiros; Milena Paneque ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
38
TITLE: Psychiatric genetic counseling: A mapping exercise  Full Text
AUTHORS: Ramona Moldovan; Kevin A McGhee; Domenico Coviello; Anniken Hamang; Angela Inglis; Charlotta I Ingvoldstad Malmgren; Maria Johansson Soller; Mercy Laurino; Bettina Meiser; Lauren Murphy; Milena Paneque ; Oleg Papsuev; Joanna Pawlak; Eulalia R Rovira Moreno; Clara Serra Juhe; Shiri Shkedi Rafid; Nakita Laing; Marie Antoinette Voelckel; Melanie Watson; Jehannine C Austin;
PUBLISHED: 2019, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, VOLUME: 180, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 21
IN MY: ORCID | CIÊNCIAVITAE
39
TITLE: Psychosocial experiences of young adults at risk for transthyretin familial amyloid polyneuropathy: early versus late-onset Portuguese case report  Full Text
AUTHORS: Jose D Pereira; Marina S Lemos; Milena Paneque ;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
40
TITLE: The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages
AUTHORS: Jackson, L; O'Connor, A; Paneque, M ; Curtisova, V; Lunt, PW; Pourova, RK; Macek, M; Stefansdottir, V; Turchetti, D; Campos, M; Henneman, L; Godino, L; Skirton, H; Cornel, MC;
PUBLISHED: 2019, SOURCE: GENETICS IN MEDICINE, VOLUME: 21, ISSUE: 3
INDEXED IN: WOS
IN MY: ORCID | CIÊNCIAVITAE
Page 4 of 10. Total results: 95.

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