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Identification

Personal identification

Full name
Marisa Silva

Author identifiers

Ciência ID
5B1F-0DD7-493E
Outputs

Publications

Journal article
  1. Nicolau, Marta; Vargas, Sofia; Silva, Marisa; Coelho, Andreia; Ferreira, Emanuel; Mendonça, Joana; Vieira, Luís; et al. "Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia". Annals of Hematology (2019): http://dx.doi.org/10.1007/s00277-019-03783-y.
    Published • 10.1007/s00277-019-03783-y
  2. Silva, Marisa; de Leeuw, Nicole; Mann, Kathy; Schuring-Blom, Heleen; Morgan, Sian; Giardino, Daniela; Rack, Katrina; Hastings, Ros. "European guidelines for constitutional cytogenomic analysis". European Journal of Human Genetics 27 1 (2018): 1-16. http://dx.doi.org/10.1038/s41431-018-0244-x.
    Published • 10.1038/s41431-018-0244-x
  3. Ferrão, José; Silva, Marisa; Gonçalves, Lúcia; Gomes, Susana; Loureiro, Pedro; Coelho, Andreia; Miranda, Armandina; et al. "Widening the spectrum of deletions and molecular mechanisms underlying alpha-thalassemia". Annals of Hematology 96 11 (2017): 1921-1929. http://dx.doi.org/10.1007/s00277-017-3090-y.
    10.1007/s00277-017-3090-y
  4. Silva, Marisa; Vargas, Sofia; Coelho, Andreia; Dias, Alexandra; Ferreira, Teresa; Morais, Anabela; Maia, Raquel; et al. "Hemorheological alterations in sickle cell anemia and their clinical consequences – The role of genetic modulators". Clinical Hemorheology and Microcirculation 64 4 (2017): 859-866. http://dx.doi.org/10.3233/ch-168048.
    10.3233/ch-168048
  5. Silva, Marisa; Alves, Cristina; Pedro, Sónia; Marques, Bárbara; Ferreira, Cristina; Furtado, José; Martins, Ana Teresa; et al. "Trisomy 15 mosaicism: Challenges in prenatal diagnosis". American Journal of Medical Genetics Part A 167 11 (2015): 2847-2850. http://dx.doi.org/10.1002/ajmg.a.37229.
    10.1002/ajmg.a.37229
  6. Silva, Marisa; Caetano, Paula; Olival, Vanessa; Alves, Cristina; Simão, Laurentino; Ferreira, Cristina; Marques, Bárbara; et al. "Discordant chromosome placental mosaicism in a dichorionic twin pregnancy". American Journal of Medical Genetics Part A 6 (2013): 1498-1500. http://dx.doi.org/10.1002/ajmg.a.35902.
    Published • 10.1002/ajmg.a.35902
  7. Veitia, R.A.; Nunes, M.; Quintana-Murci, L.; Rappaport, R.; Thibaud, E.; Jaubert, F.; Fellous, M.; et al. "Swyer Syndrome and 46,XY Partial Gonadal Dysgenesis Associated with 9p Deletions in the Absence of Monosomy-9p Syndrome". The American Journal of Human Genetics 63 3 (1998): 901-905. http://dx.doi.org/10.1086/302023.
    10.1086/302023
Distinctions

Other distinction

2008 Menção Honrosa para Comunicação Livre
Associação Portuguesa de Diagnóstico Pré-Natal, Portugal
1998 1º Prémio para a melhor Comunicação Livre.
Sociedade Portuguesa de Medicina da Reprodução, Portugal