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Silven Read

Showing results (1-10 of 19) with videos related to

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Brain and Language|June 14, 2017
Segregating polymorphisms of FOXP2 are associated with measures of inner speech, speech fluency and strength of handedness in a healthy populationBernard Crespi, Silven Read, Peter Hurd
Heredity|December 14, 2017
The SETDB2 locus: evidence for a genetic link between handedness and atopic diseaseBernard Crespi, Silven Read, Peter Hurd
Frontiers in Genetics|December 12, 2022
Do the diverse phenotypes of Prader-Willi syndrome reflect extremes of covariation in typical populations?Iiro Salminen, Silven Read, Bernard Crespi
Psychiatry Research|February 18, 2020
Does SNORD116 mediate aspects of psychosis in Prader-Willi syndrome? Evidence from a non-clinical populationIiro Salminen, Silven Read, Pete Hurd, et al.
Autism Research and Treatment|November 6, 2019
AMBRA1, Autophagy, and the Extreme Male Brain Theory of AutismBernard Crespi, Silven Read, Amy Ly, et al.
Biology Letters|January 19, 2018
A genetic locus for paranoiaBernard Crespi, Silven Read, Iiro Salminen, et al.
Plos One|March 9, 2019
Spirituality, dimensional autism, and schizotypal traits: The search for meaningBernard Crespi, Natalie Dinsdale, Silven Read, et al.
Psychiatry Research|March 22, 2019
Genetic variation of UBE3A is associated with schizotypy in a population of typical individualsIiro Salminen, Silven Read, Pete Hurd, et al.
Neuropsychologia|July 1, 2018
Segregating polymorphism in the NMDA receptor gene GRIN2A, schizotypy, and mental rotation among healthy individualsSiddharth Jha, Silven Read, Peter Hurd, et al.
Frontiers in Psychiatry|April 19, 2021
Cognitive Empathy as Imagination: Evidence From Reading the Mind in the Eyes in Autism and SchizotypyPriya Nahal, Peter L Hurd, Silven Read, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Brain and Language|June 14, 2017
Segregating polymorphisms of FOXP2 are associated with measures of inner speech, speech fluency and strength of handedness in a healthy populationBernard Crespi, Silven Read, Peter Hurd
Heredity|December 14, 2017
The SETDB2 locus: evidence for a genetic link between handedness and atopic diseaseBernard Crespi, Silven Read, Peter Hurd
Frontiers in Genetics|December 12, 2022
Do the diverse phenotypes of Prader-Willi syndrome reflect extremes of covariation in typical populations?Iiro Salminen, Silven Read, Bernard Crespi
Psychiatry Research|February 18, 2020
Does SNORD116 mediate aspects of psychosis in Prader-Willi syndrome? Evidence from a non-clinical populationIiro Salminen, Silven Read, Pete Hurd, et al.
Autism Research and Treatment|November 6, 2019
AMBRA1, Autophagy, and the Extreme Male Brain Theory of AutismBernard Crespi, Silven Read, Amy Ly, et al.
Biology Letters|January 19, 2018
A genetic locus for paranoiaBernard Crespi, Silven Read, Iiro Salminen, et al.
Plos One|March 9, 2019
Spirituality, dimensional autism, and schizotypal traits: The search for meaningBernard Crespi, Natalie Dinsdale, Silven Read, et al.
Psychiatry Research|March 22, 2019
Genetic variation of UBE3A is associated with schizotypy in a population of typical individualsIiro Salminen, Silven Read, Pete Hurd, et al.
Neuropsychologia|July 1, 2018
Segregating polymorphism in the NMDA receptor gene GRIN2A, schizotypy, and mental rotation among healthy individualsSiddharth Jha, Silven Read, Peter Hurd, et al.
Frontiers in Psychiatry|April 19, 2021
Cognitive Empathy as Imagination: Evidence From Reading the Mind in the Eyes in Autism and SchizotypyPriya Nahal, Peter L Hurd, Silven Read, et al.
Pageof 2