scispace - formally typeset
P

Peter Kirsch

Researcher at Heidelberg University

Publications -  236
Citations -  16149

Peter Kirsch is an academic researcher from Heidelberg University. The author has contributed to research in topics: Functional magnetic resonance imaging & Cognition. The author has an hindex of 62, co-authored 223 publications receiving 14145 citations. Previous affiliations of Peter Kirsch include University of Wuppertal & British Antarctic Survey.

Papers
More filters
Journal ArticleDOI

Oxytocin Modulates Neural Circuitry for Social Cognition and Fear in Humans

TL;DR: It is shown that human amygdala function is strongly modulated by oxytocin, and this results indicate a neural mechanism for the effects of Oxytocin in social cognition in the human brain and provide a methodology and rationale for exploring therapeutic strategies in disorders in which abnormal amygdala function has been implicated, such as social phobia or autism.
Journal ArticleDOI

Oxytocin and vasopressin in the human brain: social neuropeptides for translational medicine

TL;DR: OXT and AVP are emerging as targets for novel treatment approaches — particularly in synergistic combination with psychotherapy — for mental disorders characterized by social dysfunction, such as autism, social anxiety disorder, borderline personality disorder and schizophrenia.
Journal ArticleDOI

City living and urban upbringing affect neural social stress processing in humans.

TL;DR: It is shown that urban upbringing and city living have dissociable impacts on social evaluative stress processing in humans, and distinct neural mechanisms for an established environmental risk factor are identified.
Journal ArticleDOI

Neural substrates of pleiotropic action of genetic variation in COMT: a meta-analysis

TL;DR: A meta-analysis of all available neuroimaging studies of rs4680 shows significant association between the COMT genotype and prefrontal activation, and meta-analytical evidence for a neural substrate for the pleiotropic behavioral effects of COMT genetic variation is found.