Information till studenter och medarbetare med anledning av covid-19 (Uppdaterad: 18 januari 2021)

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Umeå universitet
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Personalbild Susann Haraldsson

Susann Haraldsson

Kontakt

E-post
susann.haraldsson@umu.se
Telefon
090-785 44 02

Verksam vid

Anknytning
Laboratorieassistent vid Institutionen för medicinsk biovetenskap Enhet: Patologi
Plats
By 6M, vån 3, Sjukhusområdet Umeå universitet, 901 85 Umeå
2015
SERT and NET polymorphisms, temperament and antidepressant response
Nordic Journal of Psychiatry, Vol. 69, (7) : 531-538
Andre, Kadri; Kampman, Olli; Illi, Ari; et al.
2015
Serotonin transporter (5-HTTLPR) and norepinephrine transporter (NET) gene polymorphisms: Susceptibility and treatment response of electroconvulsive therapy in treatment resistant depression
Neuroscience Letters, Vol. 590 : 116-120
Kautto, Mervi; Kampman, Olli; Mononen, Nina; et al.
2014
Long Leukocyte Telomere Length at Diagnosis Is a Risk Factor for Dementia Progression in Idiopathic Parkinsonism
PLoS ONE, Vol. 9, (12)
Degerman, Sofie; Domellöf, Magdalena; Landfors, Mattias; et al.
2011
Is 5-HTTLPR linked to the response of selective serotonin reuptake inhibitors in MDD?
European Archives of Psychiatry and Clinical Neuroscience, Vol. 261, (2) : 95-102
Illi, Ari; Poutanen, Outi; Setala-Soikkeli, Eija; et al.
2008
Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families.
Recent Advances in Retinal Degeneration, Springer 2008 : 229-234
Köhn, Linda; Kadzhaev, Konstantin; Burstedt, Marie S I; et al.
2007
Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families
European Journal of Human Genetics, Nature publishing group 2007, Vol. 15, (6) : 664-671
Köhn, Linda; Kadzhaev, Konstantin; Burstedt, Marie SI; et al.
2005
Homozygosity mapping of familial glioma in Northern Sweden
Acta Oncol, Vol. 44, (2) : 114-119
Malmer, Beatrice; Haraldsson, Susann; Einarsdottir, Elisabet; et al.
2003
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, Nature Publishing Group 2003, Vol. 11, (1) : 81-84
Einarsdottir, Elisabet; Söderström, Ingegerd; Löfgren-Burström, Anna; et al.
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