Rixt van der Veen
- Position:
- Postdoctoral researcher
- Telephone number
- +31 (0)71 527 6301
- E-mail address
- veenrvander@lacdr.leidenuniv.nl
- Faculty/Unit
- Faculty of Science, Leiden/Amsterdam Center for Drug Research, Medical Pharmacology
- Office address
- Gorlaeus Laboratories
Einsteinweg 55
2333 CC Leiden
roomnumber HB908
- 2011
Behavioral Responses to Combinations of Timed Light, Food Availability, and Ultradian Rhythms in the Common Vole (Microtus arvalis),
Chronobiol Int, vol. 28, no. 7, pp. 563-571.
Development of individual differences in stress responsiveness: an overview of factors mediating the outcome of early life experiences,
Psychopharmacology, vol. 214, no. 1, pp. 141-154.
- 2010
Brain development under stress: hypotheses of glucocorticoid actions revisited,
Neurosci Biobehav Rev, vol. 34, no. 6, pp. 853-866.
- 2009
Stress and addiction: glucocorticoid receptor in dopaminoceptive neurons facilitates cocaine seeking,
Nature Neuroscience, vol. 12, no. 3, pp. 247-249.
- 2008
Impact of intra- and interstrain cross-fostering on mouse maternal care,
Genes Brain Behav, vol. 7, no. 2, pp. 184-192.
Gene-environment interactions in early life and adulthood. Implications for cocaine intake,
, vol. PhD, Leiden, Leiden University.
Maternal environment influences cocaine intake in adulthood in a genotype-dependent manner,
PLoS One, vol. 3, no. 5, pp. 1-9.
- 2007
Gene-environment interactions in vulnerability to cocaine intravenous self-administration: a brief social experience affects intake in DBA/2J but not in C57BL/6J mice,
Psychopharmacology, vol. 193, no. 2, pp. 179-186.
- 2002
17 beta-estradiol enhances cortical cholinergic innervation and preserves synaptic density following excitotoxic lesions to the rat nucleus basalis magnocellularis,
Neuroscience, vol. 110, no. 3, pp. 489-504.
Novel susceptibility pathways and drug targets for psychosis
Researcher:
Rixt van der VeenPostdoc on the TI-Pharma project “Novel susceptibility pathways and drug targets for psychosis”
In this project, rodent ‘psychosis’ models are used displaying differences in susceptibility to acute or chronic dopamine receptor stimulation. We try to identify novel pathways affected in key brain areas of susceptible and resistant individuals.



