A. Nishimura

Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene.

M. Zatz, J. S. Schwartzman, A. Bernardino, 2001, Neuropediatrics.

Analysis of the disease risk locus DXS1047 polymorphism in Brazilian Alzheimer patients

M. Zatz, J. R. Oliveira, V. Bahia, 2000, Molecular Psychiatry.

A new locus for recessive distal spinal muscular atrophy at Xq13.1–q21

M. Passos-Bueno, M. Zatz, A. Nishimura, 2004, Journal of Medical Genetics.

Analysis of the serotonin transporter polymorphism (5-HTTLPR) in Brazilian patients affected by dysthymia, major depression and bipolar disorder

M. Passos-Bueno, M. Zatz, H. Vallada, 2000, Molecular Psychiatry.

The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case

P. Trillenberg, M. Zatz, J. Weis, 2010, Clinical genetics.