Maria João Prata Martins Ribeiro


AuthID: R-000-BXM

Confirmed Publications: 149



71
TITLE: Patterns of pharmacogenetic diversity in African populations: role of ancient and recent history
AUTHORS: Elisabete Oliveira; Rui Pereira ; Amorim, Antonio ; Howard McLeod; Maria Joao Prata ;
PUBLISHED: 2009, SOURCE: PHARMACOGENOMICS, VOLUME: 10, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef: 9
IN MY: ORCID | ResearcherID
72
TITLE: Polymorphisms in one-carbon metabolism pathway genes and risk for bladder cancer in a Tunisian population  Full Text
AUTHORS: Kamel Rouissi; Slah Ouerhani; Elisabete Oliveira; Raja Marrakchi; Lotfi Cherni; Fethi Ben Othman; Mohamed R Ben Slama; Mohamed Sfaxi; Mohsen Ayed; Mohamed Chebil; Amorim, Antonio ; Maria Joao Prata ; Amel Benammar Elgaaied;
PUBLISHED: 2009, SOURCE: CANCER GENETICS AND CYTOGENETICS, VOLUME: 195, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 22
IN MY: ORCID | ResearcherID
73
74
TITLE: The Karimojong from Uganda: Genetic characterization using an X-STR decaplex system  Full Text
AUTHORS: Iva Gomes; Vania Pereira; Veronica Gomes ; Maria Joao Prata ; Nadia Pinto ; Angel Carracedo; Amorim, Antonio ; Leonor Gusmao ;
PUBLISHED: 2009, SOURCE: FORENSIC SCIENCE INTERNATIONAL-GENETICS, VOLUME: 3, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 19
IN MY: ORCID
75
76
TITLE: Evidence for the founder origin of 117delC MSUD mutation in Portugese gypsies  Full Text
AUTHORS: Quental, S ; Gusmao, A; Vilarinho, L; Amorim, Antonio ; Prata, MJ ;
PUBLISHED: 2008, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 31
INDEXED IN: WOS
IN MY: ResearcherID
77
TITLE: Maple syrup urine disease due to a new large deletion at BCKDHA caused by non-homologous recombination  Full Text
AUTHORS: Quental, S ; Martins, E ; Vilarinho, L; Amorim, Antonio ; Joao Prata, MJ ;
PUBLISHED: 2008, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 31, ISSUE: S2
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID | ResearcherID
78
TITLE: Molecular analysis of mucopolysaccharidosis type IIIB in Portugal: evidence of a single origin for a common mutation (R234C) in the Iberian Peninsula  Full Text
AUTHORS: Mangas, M; Nogueira, C; Prata, MJ ; Lacerda, L; Coll, MJ; Soares, G; Ribeiro, G; Amaral, O; Ferreira, C; Alves, C; Coutinho, MF; Alves, S;
PUBLISHED: 2008, SOURCE: CLINICAL GENETICS, VOLUME: 73, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 14
IN MY: ORCID | ResearcherID
79
TITLE: Molecular and structural analyses of maple syrup urine disease and identification of a founder mutation in a Portuguese Gypsy community  Full Text
AUTHORS: Sofia Quental ; Sandra Macedo Ribeiro ; Raquel Matos; Laura Vilarinho; Esmeralda Martins ; Elisa Leao Teles; Esmeralda Rodrigues; Luisa Diogo; Paula Garcia; Filomena Eusebio; Ana Gaspar; Silvia Sequeira; Fatima Furtado; Isabel Lanca; Amorim, Antonio ; Maria Joao Prata ;
PUBLISHED: 2008, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 94, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 25
IN MY: ORCID | ResearcherID
80
TITLE: Molecular characterization of Portuguese patients with mucopolysaccharidosis IIIC: two novel mutations in the HGSNAT gene  Full Text
AUTHORS: Coutinho, MF; Lacerda, L; Prata, MJ ; Ribeiro, H; Lopes, L; Ferreira, C; Alves, S;
PUBLISHED: 2008, SOURCE: CLINICAL GENETICS, VOLUME: 74, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 13
IN MY: ORCID | ResearcherID
Page 8 of 15. Total results: 149.

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