Gabriele Schmötzer

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.

C. Francks, A. Bailey, G. Baird, 1998, Human molecular genetics.

Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders

R. Anney, S. Bölte, T. Bourgeron, 2014, Human Genetics.

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

Stephen J. Guter, A. Bailey, G. Baird, 2001, American journal of human genetics.

The standardized diagnosis of autism, Autism Diagnostic Interview-Revised: interrater reliability of the German form of the interview.

F. Poustka, D. Rühl, G. Schmötzer, 1996, Psychopathology.

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

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

FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome

Axel Benner, Annemarie Poustka, Sven Bölte, 2009, American journal of medical genetics. Part A.

A 15q13.3 microdeletion segregating with autism

Jiannis Ragoussis, Annemarie Poustka, Sven Bölte, 2009, European Journal of Human Genetics.

Pilot evaluation of the Frankfurt Social Skills Training for children and adolescents with autism spectrum disorder

S. Bölte, E. Duketis, F. Poustka, 2009, European Child & Adolescent Psychiatry.

Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders

R. Anney, S. Bölte, T. Bourgeron, 2014, Human Genetics.