Stefanie Binzer

ORCID: 0000-0002-0998-0952
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About
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Research Areas
  • Multiple Sclerosis Research Studies
  • Intracerebral and Subarachnoid Hemorrhage Research
  • Acute Ischemic Stroke Management
  • Mycobacterium research and diagnosis
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Systemic Lupus Erythematosus Research
  • Plant Pathogens and Resistance
  • Skin and Cellular Biology Research
  • Medicine and Dermatology Studies History
  • Genetic Mapping and Diversity in Plants and Animals
  • Powdery Mildew Fungal Diseases
  • RNA regulation and disease
  • Peripheral Neuropathies and Disorders
  • T-cell and Retrovirus Studies
  • Colorectal Cancer Screening and Detection
  • Cytokine Signaling Pathways and Interactions
  • Plant Virus Research Studies
  • T-cell and B-cell Immunology
  • Body Image and Dysmorphia Studies
  • Plant Disease Resistance and Genetics
  • Intracranial Aneurysms: Treatment and Complications
  • Systemic Sclerosis and Related Diseases
  • Autoimmune and Inflammatory Disorders Research
  • Wheat and Barley Genetics and Pathology
  • RNA Research and Splicing

Karolinska Institutet
2019-2024

Kolding Hospital
2021-2024

Lillebaelt Hospital
2020

Karolinska University Hospital
2019

Odense University Hospital
2015-2019

Instituto de Neurologia Y Neurocirugia
2018

Sygehus Sønderjylland
2009-2015

University of Southern Denmark
2014-2015

Brighton and Sussex Medical School
2009-2010

Depression is common in multiple sclerosis (MS), but its impact on disability worsening has not yet been determined. We explored the risk of associated with depression a nationwide longitudinal cohort.This retrospective cohort study used linked data from 3 Swedish registries: MS Register, National Patient and Prescribed Drug Register. Two incident cohorts were developed: 1 included all registered cases Registry (2001-2014) defined as ≥1 ICD-10 code for depression; 2 comprised (2005-2014)...

10.1212/wnl.0000000000008617 article EN cc-by Neurology 2019-11-09

Background: Large population-based genome-wide association studies have identified several multiple sclerosis (MS) genetic risk variants, but the existing missing heritability warrants different strategies. Isolated populations offer an alternative way of searching for rare variants and evaluating possible role consanguinity in development MS. Studies MS yielded conflicting results. Objectives: In this study we investigated on relatively isolated Faroe Islands, which a presumed high level...

10.1177/1352458514557305 article EN Multiple Sclerosis Journal 2014-11-12

To establish the validity of intracerebral hemorrhage (ICH) diagnoses in Danish Stroke Registry (DSR) and National Patient (DNPR).Based on discharge summaries brain imaging reports, we estimated positive predictive value (PPV) a first-ever diagnosis code for ICH (ICD-10, I61) all patients Region Southern Denmark (1.2 million) during 2009-2017 according to either DNPR or DSR. We PPVs any non-traumatic (a-ICH) spontaneous (s-ICH) alone (ie, without underlying structural cause). also calculated...

10.2147/clep.s267583 article EN cc-by-nc Clinical Epidemiology 2020-11-30

Depression is common in multiple sclerosis (MS); however, the underlying mechanism for relationship remains unknown. In this study, we examined a putative causal between depression and MS using bidirectional Mendelian randomisation (MR) framework. Using latest genome-wide association study data available, 168 non-major histocompatibility complex (MHC) independent variants associated with 96 genetic susceptibility were used. Maximum likelihood, weighted median, inverse variance method...

10.1177/1352458521996601 article EN cc-by Multiple Sclerosis Journal 2021-02-19

In search of the missing heritability in multiple sclerosis (MS), additional approaches adding to genetic discoveries large genome-wide association studies are warranted.The objective this research paper is for rare MS risk variants genetically homogenous population isolated Faroe Islands.Twenty-nine Faroese cases and 28 controls were genotyped with HumanOmniExpressExome-chip. The individuals make up 1596 pair-combinations which we searched identical-by-descent shared segments using...

10.1177/1352458515602338 article EN Multiple Sclerosis Journal 2015-09-11

John Kurtzke has proposed that multiple sclerosis (MS) on the Faroe Islands occurred as a result of spread transmittable agent brought to country during World War II.Kurtzke's theory been opposed earlier and in this study, we present family from containing total 14 members with MS which show further inconsistencies theory. The study is our knowledge, first description familial incidences Islands.Medical histories were gathered 12 6 8 living cases human leukocyte antigen (HLA)-typed.Seven had...

10.1111/j.1600-0404.2009.01291.x article EN Acta Neurologica Scandinavica 2009-11-17

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10.2139/ssrn.4683900 preprint EN 2024-01-01

Few studies have examined the effect of concomitant autoimmune diseases on multiple sclerosis (MS) disability worsening. We set out to examine whether Crohn's Disease (CD), Ulcerative Colitis (UC), or Type 1 Diabetes (T1D) affect MS worsening in a nationwide cohort patients as defined by reaching expanded scale status (EDSS) scores 3.0, 4.0 and 6.0. Patients with onset between January 2004 2019 were identified from Swedish registry National Patient Register. Kaplan-Meier analysis was used...

10.1016/j.msard.2024.105637 article EN cc-by Multiple Sclerosis and Related Disorders 2024-05-01

OBJECTIVE: In this study we performed a segmental sharing analysis of multiple sclerosis (MS) cases and controls in order to identify segments shared more frequently among case-pairs than control-pairs, which may suggest presence MS risk loci. BACKGROUND: Studies have shown that heritability might be as high 70[percnt]. So far approximately 30[percnt] the has been accounted for. Isolated populations studies offer an alternative large-scale genome wide association search for missing...

10.1212/wnl.84.14_supplement.p2.220 article EN Neurology 2015-04-06

OBJECTIVE: In this study we investigated the role of consanguinity on MS risk in relatively isolated Faroe Islands, which have presumed high level inbreeding. BACKGROUND:Large population based genome-wide-association-studies identified several multiple sclerosis (MS) genetic variants, but existing missing heritability warrants different strategies. Isolated populations offer an alternative way searching for rare variants and evaluating possible development MS. Studies yielded conflicting...

10.1212/wnl.84.14_supplement.p2.215 article EN Neurology 2015-04-06
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