G. O. Diaz

Autosomal dominant cerebellar ataxia

G. Auburger, G. O. Diaz, A. Fleites, 1990, Neurology.

Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population.

M. Farrall, R. Williamson, G. Auburger, 1990, American journal of human genetics.

Extended pathoanatomical studies point to a consistent affection of the thalamus in spinocerebellar ataxia type 2

H. Braak, L. Schöls, J. Bohl, 2005, Neuropathology and applied neurobiology.

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

S. Cichon, M. Rietschel, M. Nöthen, 2018, bioRxiv.

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

S. Cichon, M. Rietschel, M. Nöthen, 2005, American journal of human genetics.

Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3

H. Braak, L. Schöls, U. Rüb, 2004, Neurology.

A new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3

S. Cichon, M. Rietschel, M. Nöthen, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2)

H. Braak, L. Schöls, U. Rüb, 2005, Acta Neuropathologica.