Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data (Q28943361)

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Sampath Arepalli

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John Anthony Hardy

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ALS: life and death in a bad neighborhood

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Incidence and prevalence of ALS in Ireland, 1995-1997: a population-based study.

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7 January 2021

Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study.

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7 January 2021

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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7 January 2021

Mutant dynactin in motor neuron disease.

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7 January 2021

Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.

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7 January 2021

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

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7 January 2021

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

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7 January 2021

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

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7 January 2021

A novel candidate region for ALS on chromosome 14q11.2.

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7 January 2021

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.

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7 January 2021

The International HapMap Project

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7 January 2021

A haplotype map of the human genome

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7 January 2021

Highly parallel genomic assays

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7 January 2021

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

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7 January 2021

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

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7 January 2021

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

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7 January 2021

Epstein-Barr virus: transformation, cytopathic changes, and viral antigens in squirrel monkey and marmoset leukocytes

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7 January 2021

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

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7 January 2021

The Association Between H63D Mutations in HFE and Amyotrophic Lateral Sclerosis in a Dutch Population

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7 January 2021

Association of the H63D polymorphism in the hemochromatosis gene with sporadic ALS

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7 January 2021

Assessing the impact of population stratification on genetic association studies

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7 January 2021

The role of Self-Defined Race/Ethnicity in Population Structure Control

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7 January 2021

Genetic structure of human populations

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7 January 2021

A worldwide survey of haplotype variation and linkage disequilibrium in the human genome

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7 January 2021

Isolates and their potential use in complex gene mapping efforts

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7 January 2021

Genomic screening and replication using the same data set in family-based association testing

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7 January 2021

Shroom, a PDZ domain-containing actin-binding protein, is required for neural tube morphogenesis in mice

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7 January 2021

RhoG activates Rac1 by direct interaction with the Dock180-binding protein Elmo

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7 January 2021

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

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7 January 2021

Sporadic ALS is not associated with VAPB gene mutations in Southern Italy

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7 January 2021

Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis

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7 January 2021

SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study

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7 January 2021

Complement factor H polymorphism in age-related macular degeneration

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7 January 2021

High-resolution whole-genome association study of Parkinson disease.

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7 January 2021

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

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7 January 2021

Genomewide association, Parkinson disease, and PARK10

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7 January 2021

No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

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7 January 2021

A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan

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7 January 2021