Pages that link to "Q24622472"
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The following pages link to Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study (Q24622472):
Displaying 50 items.
- Behavioral variant frontotemporal lobar degeneration with amyotrophic lateral sclerosis with a chromosome 9p21 hexanucleotide repeat (Q21129431) (← links)
- Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study (Q24600803) (← links)
- The genetics and neuropathology of frontotemporal lobar degeneration (Q24615201) (← links)
- Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS (Q24633692) (← links)
- A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD (Q24634583) (← links)
- Asparaginase treatment side-effects may be due to genes with homopolymeric Asn codons (Review-Hypothesis) (Q26801165) (← links)
- Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis (Q26863439) (← links)
- State of play in amyotrophic lateral sclerosis genetics (Q26864816) (← links)
- TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia (Q28294001) (← links)
- ALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the disease (Q28392297) (← links)
- Searching for Grendel: origin and global spread of the C9ORF72 repeat expansion (Q28608607) (← links)
- NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases (Q28650457) (← links)
- A High-Density Genome-Wide Association Screen of Sporadic ALS in US Veterans (Q28730882) (← links)
- Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. (Q29417029) (← links)
- What causes amyotrophic lateral sclerosis? (Q30234813) (← links)
- Global epidemiology of amyotrophic lateral sclerosis: a systematic review of the published literature (Q30580165) (← links)
- XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome (Q30987029) (← links)
- A powerful and efficient set test for genetic markers that handles confounders (Q31115587) (← links)
- Age-related penetrance of the C9orf72 repeat expansion (Q33704777) (← links)
- C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis (Q34063137) (← links)
- Principal component analysis characterizes shared pathogenetics from genome-wide association studies (Q34165673) (← links)
- Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. (Q34235637) (← links)
- Gene ontology analysis of pairwise genetic associations in two genome-wide studies of sporadic ALS (Q34290691) (← links)
- Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants (Q34299422) (← links)
- Genome wide assessment of young onset Parkinson's disease from Finland (Q34388219) (← links)
- Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases (Q34639949) (← links)
- Progress in therapy development for amyotrophic lateral sclerosis (Q34640800) (← links)
- Genome-wide association studies in neurology (Q34658391) (← links)
- Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population (Q35086781) (← links)
- Understanding the role of TDP-43 and FUS/TLS in ALS and beyond. (Q35587208) (← links)
- Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study (Q35671414) (← links)
- Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72 (Q35752001) (← links)
- Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p (Q35776895) (← links)
- Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations (Q35776901) (← links)
- Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72. (Q35776914) (← links)
- Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. (Q35776923) (← links)
- Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study (Q35859698) (← links)
- Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p (Q35878727) (← links)
- Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion (Q36035170) (← links)
- Accurate Non-parametric Estimation of Recent Effective Population Size from Segments of Identity by Descent (Q36045113) (← links)
- Controversies and priorities in amyotrophic lateral sclerosis (Q36045826) (← links)
- Genome-wide analysis of the heritability of amyotrophic lateral sclerosis (Q36051575) (← links)
- Genome-wide association study of neocortical Lewy-related pathology (Q36072427) (← links)
- Identification of pharmacological targets in amyotrophic lateral sclerosis through genomic analysis of deregulated genes and pathways. (Q36087937) (← links)
- Fast admixture analysis and population tree estimation for SNP and NGS data (Q36320258) (← links)
- TARDBP mutations are not a frequent cause of ALS in Finnish patients (Q36334443) (← links)
- UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study (Q36354384) (← links)
- Extensive genetics of ALS: a population-based study in Italy (Q36359631) (← links)
- Expanding the genetics of amyotrophic lateral sclerosis and frontotemporal dementia (Q36424852) (← links)
- Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene (Q36441637) (← links)