Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis

[1]  B. S. Weir,et al.  Exact tests for association between alleles at arbitrary numbers of loci , 2005, Genetica.

[2]  J. Haines,et al.  Apolipoprotein E controls the risk and age at onset of Parkinson disease , 2004, Neurology.

[3]  E R Martin,et al.  Genotype‐based association test for general pedigrees: The genotype‐PDT , 2003, Genetic epidemiology.

[4]  C. Lewis,et al.  Two families with familial amyotrophic lateral sclerosis are linked to a novel locus on chromosome 16q. , 2003, American journal of human genetics.

[5]  John Mitchell,et al.  A new familial amyotrophic lateral sclerosis locus on chromosome 16q12.1-16q12.2. , 2003, American journal of human genetics.

[6]  J. Haines,et al.  Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis. , 2003, American journal of human genetics.

[7]  J. Haines,et al.  Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis. , 2002, American journal of human genetics.

[8]  Robert H. Brown,et al.  A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q. , 2002, American journal of human genetics.

[9]  V. Drory,et al.  Association of APOE ε4 allele with survival in amyotrophic lateral sclerosis , 2001, Journal of the Neurological Sciences.

[10]  E R Martin,et al.  Letter to the Editor Correcting for a Potential Bias in the Pedigree Disequilibrium Test , 2022 .

[11]  R C Elston,et al.  Transmission/disequilibrium tests for quantitative traits , 2001, Genetic epidemiology.

[12]  V. Drory,et al.  Association of APOE epsilon4 allele with survival in amyotrophic lateral sclerosis. , 2001, Journal of the neurological sciences.

[13]  J. Haines,et al.  Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. , 2000, JAMA.

[14]  E. Martin,et al.  A test for linkage and association in general pedigrees: the pedigree disequilibrium test. , 2000, American journal of human genetics.

[15]  G. Abecasis,et al.  A general test of association for quantitative traits in nuclear families. , 2000, American journal of human genetics.

[16]  M. Pericak-Vance,et al.  Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers , 1998, Neurogenetics.

[17]  J. Haines,et al.  Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33 , 1998, Neurogenetics.

[18]  A. Wilbourn.  Clinical neurophysiology in the diagnosis of amyotrophic lateral sclerosis: The Lambert and the El Escorial criteria , 1998, Journal of the Neurological Sciences.

[19]  J R O'Connell,et al.  PedCheck: a program for identification of genotype incompatibilities in linkage analysis. , 1998, American journal of human genetics.

[20]  J. Haines,et al.  Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis , 1998, Neurogenetics.

[21]  G. Schellenberg,et al.  Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes , 1997, Annals of neurology.

[22]  D Rabinowitz,et al.  A transmission disequilibrium test for quantitative trait loci. , 1997, Human heredity.

[23]  A. Ludolph,et al.  Lack of association of apolipoprotein E ϵ4 allele with bulbar‐onset motor neuron disease , 1997 .

[24]  A. Ludolph,et al.  Lack of association of apolipoprotein E epsilon 4 allele with bulbar-onset motor neuron disease. , 1997, Annals of neurology.

[25]  L. Haverkamp,et al.  Apolipoprotein E ɛ4 in bulbar-onset motor neuron disease , 1996, The Lancet.

[26]  L. Haverkamp,et al.  Apolipoprotein E epsilon 4 in bulbar-onset motor neuron disease. , 1996, The Lancet.

[27]  A. Malafosse,et al.  Apolipoprotein E genotyping in sporadic amyotrophic lateral sclerosis: evidence for a major influence on the clinical presentation and prognosis , 1996, Journal of the Neurological Sciences.

[28]  J. Powell,et al.  Association of apolipoprotein E ∈4 allele with bulbar-onset motor neuron disease , 1996, The Lancet.

[29]  Robert H. Brown,et al.  Apolipoprotein E ϵ4 allele is not associated with earlier age at onset in amyotrophic lateral sclerosis , 1995 .

[30]  B. Hyman,et al.  Apolipoprotein E epsilon 4 allele is not associated with earlier age at onset in amyotrophic lateral sclerosis. , 1995, Annals of neurology.

[31]  J. Haines,et al.  Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35 , 1994, Nature Genetics.

[32]  J. Haines,et al.  Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. , 1993, Science.

[33]  J. Haines,et al.  Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis , 1993, Nature.

[34]  J. Haines,et al.  Linkage analysis in familial Alzheimer disease: Description of the Duke and Boston data sets , 1993, Genetic epidemiology.

[35]  M A Pericak-Vance,et al.  Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease. , 1993, Neurology.

[36]  J. Haines,et al.  Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity. , 1991, The New England journal of medicine.

[37]  C C Li,et al.  Population subdivision with respect to multiple alleles , 1969, Annals of human genetics.