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SNP association studies in Alzheimer's disease highlight problems for complex disease analysis

Trends in Genetics, 2001-07, Vol.17 (7), p.407-413

2001

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Two genes encoding immune-regulatory molecules ( and ) confer susceptibility to multiple sclerosis

Genes and immunity, 2005-03, Vol.6 (2), p.145-152

2005

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Genetic linkage analysis of collagen‐induced arthritis in the mouse

European journal of immunology, 1998-10, Vol.28 (10), p.3321-3328

1998

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Identification of 167 polymorphisms in 88 genes from candidate neurodegeneration pathways

Gene, 1999-10, Vol.238 (2), p.315-324

1999

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Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism

BMC genomics, 2014-12, Vol.15 (1), p.1090-1090

2014

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No association between the α2-macroglobulin (A2M) deletion and Alzheimer's disease, and no change in A2M mRNA, protein, or protein expression

JOURNAL OF NEURAL TRANSMISSION, 2000, Vol.107 (8-9), p.1065-1079

2000

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Robust and accurate single nucleotide polymorphism genotyping by dynamic allele-specific hybridization (DASH): design criteria and assay validation

Genome research, 2001-01, Vol.11 (1), p.152-162

2001

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The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q

Journal of medical genetics, 1997-05, Vol.34 (5), p.360-365

1997

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No association between the alpha 2-macroglobulin (A2M) deletion and Alzheimer's disease, and no change in A2M mRNA, protein, or protein expression

Journal of Neural Transmission, 2000-08, Vol.107 (8/9), p.1065-1079

2000

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Mapping 1 of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping

Cytogenetic and genome research, 1998-12, Vol.82 (1-2), p.114-114

1998

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Apolipoprotein-E dependent role for the FAS receptor in early onset Alzheimer's disease : finding of a positive association for a polymorphism in the TNFRSF6 gene

Human genetics, 2000-10, Vol.107 (4), p.391-396

2000

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Mapping of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping

Cytogenetics and cell genetics, 1998, Vol.82 (1-2), p.114

1998

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Intron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain

Cytogenetics and cell genetics, 1998, Vol.82 (1-2), p.115

1998

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lntron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain

Cytogenetic and genome research, 1998-12, Vol.82 (1-2), p.115-119

1998

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No association between the alpha2-macroglobulin (A2M) deletion and Alzheimer's disease, and no change in A2M mRNA, protein, or protein expression

Journal of Neural Transmission, 2000, Vol.107 (8-9), p.1065-1079

2000

Volltextzugriff (PDF)

Generation of a Ni(II) binding site by introduction of a histidine cluster in the structure of human glutathione transferase A1-1

Protein engineering, 1995-11, Vol.8 (11), p.1163

1995

Volltextzugriff (PDF)

Generation of a Ni(II) binding site by introduction of a histidine cluster in the structure of human glutathione transferase Al-1

Protein engineering, design and selection, 1995-11, Vol.8 (11), p.1163-1169

1995

Volltextzugriff (PDF)

Genomic strategies towards the dissection of human complex disease

Emahazion, Tesfai

2001

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Genomic strategies towards the dissection of human complex disease

Emahazion, Tesfai

2001

Volltextzugriff (PDF)

SNP association studies in Alzheimer' disease highlight problems for complex disease analysis

Trends in genetics, 2001, Vol.17 (7), p.407-413

2001

Volltextzugriff (PDF)

cDNA Sequencing of Nuclear NADH Dehydrogenase Subunit Genes in Complex I Deficient Myopathic Patients

Gene function & disease, 2000-05, Vol.1 (1), p.21-27

2000

Volltextzugriff (PDF)

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SNP association studies in Alzheimer's disease highlight problems for complex disease analysis

Two genes encoding immune-regulatory molecules ( and ) confer susceptibility to multiple sclerosis

Genetic linkage analysis of collagen‐induced arthritis in the mouse

Identification of 167 polymorphisms in 88 genes from candidate neurodegeneration pathways

Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism

No association between the α2-macroglobulin (A2M) deletion and Alzheimer's disease, and no change in A2M mRNA, protein, or protein expression

Robust and accurate single nucleotide polymorphism genotyping by dynamic allele-specific hybridization (DASH): design criteria and assay validation

The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q

No association between the alpha 2-macroglobulin (A2M) deletion and Alzheimer's disease, and no change in A2M mRNA, protein, or protein expression

Mapping 1 of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping

Apolipoprotein-E dependent role for the FAS receptor in early onset Alzheimer's disease : finding of a positive association for a polymorphism in the TNFRSF6 gene

Mapping of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping

Intron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain

lntron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain

No association between the alpha2-macroglobulin (A2M) deletion and Alzheimer's disease, and no change in A2M mRNA, protein, or protein expression

Generation of a Ni(II) binding site by introduction of a histidine cluster in the structure of human glutathione transferase A1-1

Generation of a Ni(II) binding site by introduction of a histidine cluster in the structure of human glutathione transferase Al-1

Genomic strategies towards the dissection of human complex disease

Genomic strategies towards the dissection of human complex disease

SNP association studies in Alzheimer' disease highlight problems for complex disease analysis

cDNA Sequencing of Nuclear NADH Dehydrogenase Subunit Genes in Complex I Deficient Myopathic Patients

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