Fundación Pública Galega de Medicina Xenómica
Centro de investigación
Publicacións nas que colabora con Noa Carrera Cachaza (7)
2023
-
Genetic testing in focal segmental glomerulosclerosis: in whom and when?
Clinical Kidney Journal, Vol. 16, Núm. 11, pp. 2011-2022
2022
-
Genetic Kidney Diseases (GKDs) Modeling Using Genome Editing Technologies
Cells, Vol. 11, Núm. 9
2018
-
Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples
European Archives of Psychiatry and Clinical Neuroscience, Vol. 268, Núm. 6, pp. 585-592
2016
-
Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia
Translational Psychiatry, Vol. 6, Núm. 3
2015
-
An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders
Clinica Chimica Acta, Vol. 445, pp. 34-40
2009
-
A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia
Human Genetics, Vol. 124, Núm. 6, pp. 607-613
-
Recent adaptive selection at MAOB and ancestral susceptibility to schizophrenia
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 150, Núm. 3, pp. 369-374