TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia

Por Sandbacka, Maria, Laivuori, Hannele, Freitas, Érika, Halttunen, Mervi, Jokimaa, Varpu, Morin-Papunen, Laure, Rosenberg, Carla, Aittomäki, Kristiina
Publicado em 2013

A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family

Por Uehara, Daniela T, Freitas, Érika L, Alves, Leandro U, Mazzeu, Juliana F, Auricchio, Maria TBM, Tabith, Alfredo, Monteiro, Mário LR, Rosenberg, Carla, Mingroni-Netto, Regina C
Publicado no Hum Genome Var (2015)

Zinc Status Biomarkers and Cardiometabolic Risk Factors in Metabolic Syndrome: A Case Control Study

Por Freitas, Erika P. S., Cunha, Aline T. O., Aquino, Sephora L. S., Pedrosa, Lucia F. C., Lima, Severina C. V. C., Lima, Josivan G., Almeida, Maria G., Sena-Evangelista, Karine C. M.
Publicado no Nutrients (2017)

Maternally Inherited Partial Monosomy 9p (pter → p24.1) and Partial Trisomy 20p (pter → p12.1) Characterized by Microarray Comparative Genomic Hybridization

Por Freitas, Érika L., Gribble, Susan M., Simioni, Milena, Vieira, Társis P., Silva-Grecco, Roseane L., Balarin, Marly A. S., Prigmore, Elena, Krepischi-Santos, Ana C., Rosenberg, Carla, Szuhai, Karoly, van Haeringen, Arie, Carter, Nigel P., Gil-da-Silva-Lopes, Vera Lúcia
Publicado em 2011

Partial 1q Duplications and Associated Phenotype

Por Morris, Marcos L.M., Baroneza, José E., Teixeira, Patricia, Medina, Cristina T.N., Cordoba, Mara S., Versiani, Beatriz R., Roese, Liege L., Freitas, Erika L., Fonseca, Ana C.S., dos Santos, Maria C.G., Pic-Taylor, Aline, Rosenberg, Carla, Oliveira, Silviene F., Ferrari, Iris, Mazzeu, Juliana F.
Publicado no Mol Syndromol (2016)