Susanne R. Haadsma‐Svensson

Author

W.E. Upjohn Institute for Employment Research

Also Known As

S R Haadsma-Svensson, S. Haadsma-Svensson, S. R. HAADSMA‐SVENSSON, S. R. Haadsma-Svensson, Susanne R. Haadsma-Svensson, Susanne R. Haadsma‐Svensson

Publications

535

Citations

H-Index

Concepts

All Affiliations

W.E. Upjohn Institute for Employment Research University of Gothenburg

About

Susanne R. Haadsma‐Svensson is an author at W.E. Upjohn Institute for Employment Research specializing in medicine, neuropharmacology, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	401
2	Natural Sciences	4	4	78
3	Health Sciences	1	1	256
4	Social Sciences	1	1	67
5	Behavioral Sciences	1	1	67

Susanne R. Haadsma‐Svensson

Publications

502

Citations

H-Index

Page 1

	Year	Citations
The dopamine D3-receptor: A postsynaptic receptor inhibitory on rat locomotor activity Nicholas Waters, Kjell Svensson, Susanne R. Haadsma‐Svensson, Journal of Neural Transmission Health SciencesPostsynaptic Receptor InhibitoryFunctional SelectivityPhysiologyNeurotransmitter	1993	256
Differential effects of dopamine D2 and D3 receptor antagonists in regard to dopamine release, in vivo receptor displacement and behaviour Nicholas Waters, L. L�fberg, Susanne R. Haadsma‐Svensson, Journal of Neural Transmission Behavioral SciencesNeuropsychologyBehavioral NeuroscienceFunctional SelectivityBehavioural Pharmacology	1994	67
Dopamine D<sub>3</sub> Receptor Antagonists. 1. Synthesis and Structure−Activity Relationships of 5,6-Dimethoxy-<i>N</i>-alkyl- and <i>N</i>-Alkylaryl-Substituted 2-Aminoindans Susanne R. Haadsma‐Svensson, Kerry A. Cleek, Dac M. Dinh, Journal of Medicinal Chemistry Molecular PharmacologyMedicinal ChemistryBiochemistryNitrogen SubstitutionMedicine	2001	41
PNU‐99194A: A Preferential Dopamine D<sub>3</sub>Receptor Antagonist Susanne R. Haadsma‐Svensson, Kjell Svensson CNS Drug Reviews	1998	31
Comparison of 5-HT1A and dopamine D2 pharmacophores. X-ray structures and affinities of conformationally constrained ligands Connie G. Chidester, Chiu Hong Lin, Robert A. Lahti, Journal of Medicinal Chemistry	1993	30
Centrally acting serotonergic and dopaminergic agents. 2. Synthesis and structure-activity relationships of 2,3,3a,4,9,9a-hexahydro-1H-benz[f]indole derivatives Chiu Hong Lin, Susanne R. Haadsma‐Svensson, Gillian Phillips, Journal of Medicinal Chemistry	1993	20
Common discriminative stimulus properties in rats of muscarinic antagonists, clozapine and the D 3 preferring antagonist PNU-99194A: an analysis of possible mechanisms Andrew J. Goudie, Lisa E. Baker, Judith A. Smith, Behavioural Pharmacology	2001	20
Structure-Activity Relationships in the 8-Amino-6,7,8,9-tetrahydro-3H-benz[e]indole Ring System. Part 2: Effect of 8-Amino Nitrogen Substitution on Serotonin Receptor Binding and Pharmacology Michael D. Ennis, P. STJERNLOEF, Robert L. Hoffman, Journal of Medicinal Chemistry Serotonin Receptor BindingPharmacotherapyExperimental PharmacologyMedicinal Chemistry5-Htp Brain Levels	1995	13
Centrally acting serotonergic and dopaminergic agents. 1. Synthesis and structure-activity relationships of 2,3,3a,4,5,9b-hexahydro-1H-benz[e]indole derivatives Chiu Hong Lin, Susanne R. Haadsma‐Svensson, Robert A. Lahti, Journal of Medicinal Chemistry Molecular PharmacologyBiochemistryMedicineNatural SciencesMonoamine Neurotransmitters	1993	13
Synthesis and biological activity of C-5 modified derivatives of (+)-AJ76 and (+)-UH232: Increased dopamine D3 receptor preference and improved pharmacokinetic properties Susanne R. Haadsma‐Svensson, Martin Smith, Chiu‐Hong Lin, Bioorganic & Medicinal Chemistry Letters Biological ActivityMolecular PharmacologyBiochemistryFunctional SelectivityMedicine	1994	11

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