F. Poustka

Serotonin transporter (5-HTT) gene variants associated with autism?

A Benner, S. Klauck, A. Poustka, 1997, Human molecular genetics.

Fragile-X carrier females: evidence for a distinct psychopathological phenotype?

M. Hautzinger, S. Schwab, P. Franke, 1996, American journal of medical genetics.

Clinical evidence for genomic imprinting in bipolar I disorder

P. Propping, M. Nothen, M. Grigoroiu-Serbanescu, 1995, Acta psychiatrica Scandinavica.

Variants of the CNTNAP2 5′ promoter as risk factors for autism spectrum disorders: a genetic and functional approach

E. Duketis, C. Freitag, S. Klauck, 2014, Molecular Psychiatry.

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q

Rodney Cotterill, Annemarie Poustka, Chantal Kemner, 2005, European Journal of Human Genetics.

Mutation and expression analyses of the ribosomal protein gene RPL10 in an extended German sample of patients with autism spectrum disorder

E. Duketis, S. Klauck, A. Poustka, 2011, American journal of medical genetics. Part A.

Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism

S. Klauck, A. Poustka, F. Poustka, 2006, Molecular Psychiatry.

The 5-HT transporter gene-linked polymorphic region (5-HTTLPR) in evolutionary perspective: Alternative biallelic variation in rhesus monkeys

Annemarie Poustka, Johannes Hebebrand, Klaus-Peter Lesch, 2005, Journal of Neural Transmission.