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Mafalda Matos
Mafalda Matos
Instituto Gulbenkian de Ciência
Single-nucleotide polymorphism
Biology
Genetics
Genotyping
SNP array
4
Papers
70
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IL10 low-frequency variants in Behçet's disease patients
2017
International Journal of Rheumatic Diseases
Mafalda Matos
Joana M. Xavier
Patricia Abrantes
Inês Sousa
Nádia Rei
Fereydoun Davatchi
Farhad Shahram
Gorete Jesus
F. Barcelos
Joana Vedes
Manuel Salgado
Bahar Sadeghi-Abdollahi
Abdolhadi Nadji
Maria Francisca Moraes-Fontes
Niloofar Mojarad Shafiee
Fahmida Ghaderibarmi
José Vaz Patto
Jorge Crespo
Sofia A. Oliveira
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Citations (2)
FUT2: filling the gap between genes and environment in Behçet's disease?
2015
Annals of the Rheumatic Diseases
Joana M. Xavier
Farhad Shahram
Inês Sousa
Fereydoun Davatchi
Mafalda Matos
Bahar Sadeghi-Abdollahi
João Sobral
Abdolhadi Nadji
Manuela M. Oliveira
Fahmida Ghaderibarim
Niloofar Mojarad Shafiee
Sofia A. Oliveira
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Citations (53)
Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal.
2015
PLOS ONE
Patrícia Abrantes
Maria M. M. Santos
Inês Sousa
Joana M. Xavier
Vânia Francisco
Tiago Krug
João Sobral
Mafalda Matos
Madalena Martins
Antonio Jacinto
Domingos Coiteiro
Sofia A. Oliveira
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Citations (15)
A2.4 Are protein tyrosine phosphatase-n1 polymorphisms associated with ankylosing spondylitis? – a pilot study
2014
Annals of the Rheumatic Diseases
Ana Luísa Cartaxo
Inês Godet
Dário Ligeiro
Mafalda Matos
Jaime Branco
Fernando M. Pimentel-Santos
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