U. Fischer

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

K. Friend, M. Shaw, E. Haan, 2015, Molecular Psychiatry.

Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes

D. Rujescu, A. Hartmann, H. Völzke, 2015, EMBO molecular medicine.

The X-chromosome-linked intellectual disability protein PQBP1 is a component of neuronal RNA granules and regulates the appearance of stress granules.

E. Wanker, V. Kalscheuer, E. Müller, 2011, Human molecular genetics.

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

J. Rosenfeld, M. Shaw, E. Haan, 2016, Molecular Psychiatry.

In utero gene therapy rescues microcephaly caused by Pqbp1-hypofunction in neural stem progenitor cells

C. Romano, S. Miyano, E. Wanker, 2014, Molecular Psychiatry.

EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO

S. Haas, E. Leshinsky‐Silver, M. Skopkova, 2018, Yearbook of Paediatric Endocrinology.

Evidence that fragile X mental retardation protein is a negative regulator of translation.

A. Ostareck-Lederer, D. Ostareck, U. Fischer, 2001, Human molecular genetics.