Susann Haraldsson

Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families

Linda M. Kohn, Konstantin Kadzhaev, Marie Burstedt et al. · European Journal of Human Genetics · 2007 · 64 citations

Life Sciences, Genetics, Molecular Genetics +4

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

Elísabet Einarsdóttir, Ingegerd Söderström, Anna Löfgren‐Burström et al. · European Journal of Human Genetics · 2003 · 64 citations

Life Sciences, Genetics, Molecular Genetics +17

Long Leukocyte Telomere Length at Diagnosis Is a Risk Factor for Dementia Progression in Idiopathic Parkinsonism

Sofie Degerman, Mattias Landfors, Jan Linder et al. · PLoS ONE · 2014 · 32 citations · Full text

Medicine, Neurology, Neuroscience +17

Is 5-HTTLPR linked to the response of selective serotonin reuptake inhibitors in MDD?

Ari Illi, Outi Poutanen, Eija Setälä-Soikkeli et al. · European Archives of Psychiatry and Clinical Neuroscience · 2010 · 30 citations

Medicine, Pharmacology, Psychiatry +12

Homozygosity mapping of familial glioma in Northern Sweden

Beatrice Malmer, Susann Haraldsson, Elísabet Einarsdóttir et al. · Acta Oncologica · 2005 · 21 citations · Full text

Life Sciences, Genetics, Oncology +17