Susann Haraldsson

Publications

Author

Title

Year sorteringsordning

Fulltext

Andre, Kadri
Kampman, Olli
Illi, Ari; et al.

SERT and NET polymorphisms, temperament and antidepressant response
Nordic Journal of Psychiatry, 69(7): 531-538

2015

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Kautto, Mervi
Kampman, Olli
Mononen, Nina; et al.

Serotonin transporter (5-HTTLPR) and norepinephrine transporter (NET) gene polymorphisms: Susceptibility and treatment response of electroconvulsive therapy in treatment resistant depression
Neuroscience Letters, 590: 116-120

2015

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Degerman, Sofie
Domellöf, Magdalena
Landfors, Mattias; et al.

Long Leukocyte Telomere Length at Diagnosis Is a Risk Factor for Dementia Progression in Idiopathic Parkinsonism
PLoS ONE, 9(12)

2014

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Illi, Ari
Poutanen, Outi
Setala-Soikkeli, Eija; et al.

Is 5-HTTLPR linked to the response of selective serotonin reuptake inhibitors in MDD?
European Archives of Psychiatry and Clinical Neuroscience, 261(2): 95-102

2011

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Köhn, Linda
Kadzhaev, Konstantin
Burstedt, Marie S I; et al.

Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families.
Recent Advances in Retinal Degeneration: 229-234

2008

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Köhn, Linda
Kadzhaev, Konstantin
Burstedt, Marie SI; et al.

Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families
European Journal of Human Genetics, 15(6): 664-671

2007

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Malmer, Beatrice
Haraldsson, Susann
Einarsdottir, Elisabet; et al.

Homozygosity mapping of familial glioma in Northern Sweden
Acta Oncol, 44(2): 114-119

2005

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Einarsdottir, Elisabet
Söderström, Ingegerd
Löfgren-Burström, Anna; et al.

The CTLA4 region as a general autoimmunity factor: an extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto's thyroiditis and Graves' disease
European Journal of Human Genetics, 11(1): 81-84

2003

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