Staffan Nilsson
Visar 280 publikationer
Normal neonatal TREC and KREC levels in early onset juvenile idiopathic arthritis
Axonal injury in asymptomatic individuals preceding onset of multiple sclerosis
Dynamics of the normal gut microbiota: A longitudinal one-year population study in Sweden
Developmental trajectory of the healthy human gut microbiota during the first 5 years of life
Low Incidence of Reinfection With Endemic Coronaviruses Diagnosed by Real-Time PCR
Effects of assistive technology for students with reading and writing disabilities
Validation of DIGIROP decision support tool on a contemporary Swedish cohort
Effect of antiretroviral treatment on blood-brain barrier integrity in HIV-1 infection
Viral interference cannot be concluded from datasets containing only symptomatic patients
Higher plasma drug levels in elderly people living with HIV treated with darunavir
MYO5B Mutations in Pheochromocytoma/Paraganglioma Promote Cancer Progression
Neurochemical evidence of astrocytic and neuronal injury commonly found in COVID-19
Serum neopterin levels in relation to mild and severe COVID-19
Item-based analysis of the effects of duloxetine in depression: a patient-level post hoc study
MYO5B mutations in pheochromocytoma/paraganglioma promote cancer progression
Circulating neurofilament light in ischemic stroke: temporal profile and outcome prediction
Anthracycline-based consolidation may determine outcome of post-consolidation immunotherapy in AML
How do we determine whether antidepressants are useful or not? – Authors' reply
Somatic MYO5Bmutations in adrenal neural tumors promote cancer progression
Fibrinogen concentrations predict long-term cognitive outcome in young ischemic stroke patients
The Effect of Reading Interventions among Poor Readers at a Forensic Psychiatric Clinic
Association between Plasma Homocysteine Levels and Neuronal Injury in HIV Infection
Blood-brain barrier integrity, intrathecal immunoactivation, and neuronal injury in HIV.
GREM1 and POLE variants in hereditary colorectal cancer syndromes
Antecedents of cerebral palsy according to severity of motor impairment.
A Genetic Variant of the Sortilin 1 Gene is Associated with Reduced Risk of Alzheimer's Disease
Oestradiol levels and superoxide dismutase activity in age-related cataract: a case-control study.
Serotonin Depletion-Induced Maladaptive Aggression Requires the Presence of Androgens
Association analysis of GWAS and candidate gene loci in a Pakistani population with psoriasis.
Expression of inflammatory markers in a genetic rodent model of depression
Estrogen-related polymorphisms in Estonian patients with age-related cataract.
The role of IL-17A and IFN gamma in vaccine-induced protection against Helicobacter pylori infection
A mutation in POLE predisposing to a multi-tumour phenotype
Biomarker Evidence of Axonal Injury in Neuroasymptomatic HIV-1 Patients
Association of NFE2L2 and KEAP1 haplotypes with amyotrophic lateral sclerosis.
Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson's disease: a multicenter study
Genetic Variation of Superoxide Dismutases in Patients with Primary Open-angle Glaucoma
Real-time PCR Identification of Agents Causing Diarrhea in Rwandan Children Less Than 5 Years of Age
Persisting hypoxaemia is an insufficient measure of adverse lung function in very immature infants.
Superoxide dismutase gene polymorphisms in patients with age-related cataract
Genetic Variation of the Ghrelin Signalling System in Individuals with Amphetamine Dependence
Complement Gene Single Nucleotide Polymorphisms and Biomarker Endophenotypes of Alzheimer's Disease
Functional Mannose-Binding Lectin Haplotype Variants are Associated with Alzheimer's Disease
Genetic variation of superoxide dismutases in patients with primary open-angle glaucoma
A possible association between panic disorder and a polymorphism in the preproghrelin gene
Cerebrospinal fluid biomarkers in patients with varicella-zoster virus CNS infections.
Spectrum of chronic lung disease in a population of newborns with extremely low gestational age.
The recurrent Guillain-Barre syndrome: a long-term population-based study
A novel ARC gene polymorphism is associated with reduced risk of Alzheimer's disease
Plasma factor VII-activating protease antigen levels and activity are increased in ischemic stroke.
Myelin glycosphingolipid immunoreactivity and CSF levels in multiple sclerosis.
Glial fibrillary acidic protein: a potential biomarker for progression in multiple sclerosis.
Familial Dyslexia in a Large Swedish Family: A Whole Genome Linkage Scan
Continuous glucose monitoring system during physical exercise in adolescents with type 1 diabetes
A 6-gene signature identifies four molecular subgroups of neuroblastoma
Perinatal lack of maternal IL-6 promotes increased adiposity during adulthood in mice.
Plasma levels of von Willebrand factor in the etiologic subtypes of ischemic stroke
Inflammatory cytokines in gastric fluid at birth and the development of bronchopulmonary dysplasia
Hepatitis C treatment response kinetics and impact of baseline predictors.
Identification of epigenetically regulated genes that predict patient outcome in neuroblastoma
Leukocyte oxygen radical production determines disease severity in the recurrent Guillain-Barré
HIV-1 viral escape in cerebrospinal fluid of subjects on suppressive antiretroviral treatment.
Association of the RAGE G82S polymorphism with Alzheimer's disease
Parents' views of their child's health and family function in paediatric inflammatory bowel disease.
A variant near the interleukin-6 gene is associated with fat mass in Caucasian men
Kinesin Light Chain 1 Gene Haplotypes in Three Conformational Diseases.
Association of Nrf2-encoding NFE2L2 haplotypes with Parkinson's disease.
Molecular classification of spontaneous endometrial adenocarcinomas in BDII rats.
Association between genetic variation at the ADAMTS13 locus and ischemic stroke
Association of nAChR gene haplotypes with heavy alcohol use and body mass.
Association between genetic variation at the ADAMTS13 locus and ischemic stroke.
Influence of androgen receptor repeat polymorphisms on personality traits in men
Breast cancer incidence after hormonal infertility treatment in Sweden: a cohort study
Variants of the interleukin-1 receptor antagonist gene are associated with fat mass in men.
Mice chronically fed high-fat diet have increased mortality and disturbed immune response in sepsis.
Oxygen radical production in leukocytes and disease severity in multiple sclerosis.
Association of genetic variants in ADAMTS13 with ischemic stroke.
Association Between Genotypes and Phenotypes in Coeliac Disease.
Searching for genes influencing a complex disease: the case of coeliac disease.
Association between Gm allotypes and asthma severity from childhood to young middle age.
Detecting two-locus gene-gene effects using monotonisation of the penetrance matrix
Inflammatory bowel disease and self-esteem in adolescence.
Oxygen radical production and severity of the Guillain--Barré syndrome.
Serum C-reactive protein concentration and genotype in relation to ischemic stroke subtype
Interleukin-1 system gene polymorphisms are associated with fat mass in young men.
Pubertal timing predicts previous fractures and BMD in young adult men: the GOOD study.
Sex steroid-related genes and male-to-female transsexualism
Fibrinolytic gene polymorphism and ischemic stroke
Investigation of genes coding for inflammatory components in Parkinson's disease.
Genetiska tester och personförsäkringar. En analys. (Bilaga 3)
The risk of celiac disease in 107 families with at least two affected siblings.
Analysis of 6 genetic loci for disease susceptibility in psoriatic arthritis.
Association between the estrogen receptor beta gene and age of onset of Parkinson's disease.
Meta and pooled analysis of European coeliac disease data
The HCR gene on 6p21 is unlikely to be a psoriasis susceptibility gene
Which Genes are Involved? - Statistical Planning and Analysis of Human Genetic Samples
Incidence of CSF abnormalities in siblings of multiple sclerosis patients and unrelated controls.
Serum concentrations of VEGF and b-FGF in renal cell, prostate and urinary bladder carcinomas.
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