1. A genetic locus for paranoia. (17th January 2018) Authors: Crespi, Bernard; Read, Silven; Salminen, Iiro; Hurd, Peter Journal: Biology letters Issue: Volume 14:Number 1(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A genetic locus for paranoia. (31st January 2018) Authors: Crespi, Bernard; Read, Silven; Salminen, Iiro; Hurd, Peter Journal: Biology letters Issue: Volume 14:Number 1(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. AMBRA1, Autophagy, and the Extreme Male Brain Theory of Autism. (10th October 2019) Authors: Crespi, Bernard; Read, Silven; Ly, Amy; Hurd, Peter Other Names: Canitano Roberto Academic Editor. Journal: Autism research and treatment Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Does SNORD116 mediate aspects of psychosis in Prader-Willi syndrome? Evidence from a non-clinical population. (April 2020) Authors: Salminen, Iiro; Read, Silven; Hurd, Pete; Crespi, Bernard Journal: Psychiatry research Issue: Volume 286(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic variation of UBE3A is associated with schizotypy in a population of typical individuals. (May 2019) Authors: Salminen, Iiro; Read, Silven; Hurd, Pete; Crespi, Bernard Journal: Psychiatry research Issue: Volume 275(2019) Page Start: 94 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Segregating polymorphism in the NMDA receptor gene GRIN2A, schizotypy, and mental rotation among healthy individuals. (August 2018) Authors: Jha, Siddharth; Read, Silven; Hurd, Peter; Crespi, Bernard Journal: Neuropsychologia Issue: Volume 117(2018) Page Start: 347 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. SHANK3 Genotype Mediates Speech and Language Phenotypes in a Nonclinical Population. (4th June 2021) Authors: Manning, Christina; Hurd, Peter L.; Read, Silven; Crespi, Bernard Other Names: Canitano Roberto Academic Editor. Journal: Autism research and treatment Issue: Volume 2021(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The PCSK6 gene is associated with handedness, the autism spectrum, and magical ideation in a non-clinical population. (April 2016) Authors: Robinson, Kelsey J.; Hurd, Peter L.; Read, Silven; Crespi, Bernard J. Journal: Neuropsychologia Issue: Volume 84(2016) Page Start: 205 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. The PCSK6 gene is associated with handedness, the autism spectrum, and magical ideation in a non-clinical population. (April 2016) Authors: Robinson, Kelsey J.; Hurd, Peter L.; Read, Silven; Crespi, Bernard J. Journal: Neuropsychologia Issue: Volume 84(2016) Page Start: 205 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The SETDB2 locus: evidence for a genetic link between handedness and atopic disease. (January 2018) Authors: Crespi, Bernard; Read, Silven; Hurd, Peter Journal: Heredity Issue: Volume 120:Number 1(2018) Page Start: 77 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗