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

Author:

Stepniak Beata1,Kästner Anne12,Poggi Giulia1,Mitjans Marina1,Begemann Martin1,Hartmann Annette3,Van der Auwera Sandra4,Sananbenesi Farahnaz5,Krueger‐Burg Dilja6,Matuszko Gabriela7,Brosi Cornelia8,Homuth Georg9,Völzke Henry10,Benseler Fritz6,Bagni Claudia1112,Fischer Utz8,Dityatev Alexander7,Grabe Hans‐Jörgen4,Rujescu Dan3,Fischer Andre513,Ehrenreich Hannelore12

Affiliation:

1. Clinical Neuroscience Max Planck Institute of Experimental Medicine Göttingen Germany

2. DFG Research Center for Nanoscale Microscopy and Molecular Physiology of the Brain (CNMPB) Göttingen Germany

3. Department of Psychiatry and Psychotherapy University of Halle Halle Germany

4. Department of Psychiatry and Psychotherapy University Medicine Greifswald Greifswald Germany

5. Epigenetics in Neurodegenerative Diseases German Center for Neurodegenerative Diseases (DZNE) Göttingen Germany

6. Molecular Neurobiology Max Planck Institute of Experimental Medicine Göttingen Germany

7. Molecular Neuroplasticity German Center for Neurodegenerative Diseases (DZNE) Magdeburg Germany

8. Department of Biochemistry University of Würzburg Würzburg Germany

9. Interfaculty Institute for Genetics and Functional Genomics University Medicine Greifswald Greifswald Germany

10. Institute for Community Medicine University Medicine Greifswald Greifswald Germany

11. KU Leuven Center for Human Genetics and Leuven Institute for Neurodegenerative Diseases Leuven Belgium

12. Department of Biomedicine and Prevention University of Rome “Tor Vergata” Rome Italy

13. Department of Psychiatry & Psychotherapy University of Göttingen Göttingen Germany

Publisher

EMBO

Subject

Molecular Medicine

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