Caroline Ran
occupation: researcher
Articles 28
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Calcitonin Gene-Related Peptide (CGRP) and Cluster Headache
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Analysis of NOS Gene Polymorphisms in Relation to Cluster Headache and Predisposing Factors in Sweden
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Analysis of HCRTR2 Gene Variants and Cluster Headache in Sweden
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Genetic Screening of Plasticity Regulating Nogo-Type Signaling Genes in Migraine
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Anoctamin 3: A Possible Link between Cluster Headache and Ca2+ Signaling
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S100B polymorphisms are associated with age of onset of Parkinson's disease.
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Analysis of shared heritability in common disorders of the brain
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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families
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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families
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Implications for the migraine SNP rs1835740 in a Swedish cluster headache population
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Genetic Variations and mRNA Expression of NRF2 in Parkinson's Disease
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A genetic CLOCK variant associated with cluster headache causing increased mRNA levels
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Screening of genetic variants in ADCYAP1R1, MME and 14q21 in a Swedish cluster headache cohort
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Cluster headache - clinical pattern and a new severity scale in a Swedish cohort.
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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden
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No Association Between rs7077361 in ITGA8 and Parkinson's Disease in Sweden
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Screening of Two ADH4 Variations in a Swedish Cluster Headache Case-Control Material.
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Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample
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The HLA-DRA variation rs3129882 is not associated with Parkinson's disease in Sweden
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Genetic Screening of the Mitochondrial Rho GTPases MIRO1 and MIRO2 in Parkinson's Disease
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Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease
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DJ-1 Mutations are Rare in a Swedish Parkinson Cohort
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Genetic studies of the protein kinase AKT1 in Parkinson's disease.
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Adh1 and Adh1/4 knockout mice as possible rodent models for presymptomatic Parkinson's disease.
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Possible involvement of a mitochondrial translation initiation factor 3 variant causing decreased mRNA levels in Parkinson's disease
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Lrrk2 and alpha-synuclein are co-regulated in rodent striatum.
Human - wd:Q42408302