Human Molecular Genetics · 1999 · 794 citations · 17 references
Life SciencesGeneticsNeurologyHuman GeneticsMedical GeneticsNeurogeneticsGenetic SusceptibilityGenotype-phenotype CorrelationHaplotype AnalysisNeurodegenerative Disease GeneticsNeurogenetic DisordersNeuropsychiatric GeneticsHaplotype MappingHaplotype-based Association AnalysisTauopathy Genetics
We describe two extended haplotypes that cover the human tau gene. In a total of approximately 200 unrelated caucasian individuals there is complete disequilibrium between polymorphisms which span the gene (which covers approximately 100 kb of DNA). This suggests that the establishment of the two haplotypes was an ancient event and either that recombination is suppressed in this region, or that recombinant genes are selected against. Furthermore, we show that the more common haplotype (H1) is significantly over-represented in patients with progressive supranuclear palsy (PSP), extending earlier reports of an association between an intronic dinucleotide polymorphism and PSP.
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The American Journal of Human Genetics
J. S. · Population · 1950 · 5.1K citations
Life Sciences, Biology, Genetics +4
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
Mike Hutton, Corinne Lendon, Patrizia Rizzu et al. · Nature · 1998 · 3.5K citations
Life Sciences, Genetics, Neurology +14
Tau is a candidate gene for chromosome 17 frontotemporal dementia
Parvoneh Poorkaj, Thomas D. Bird, Ellen M. Wijsman et al. · Annals of Neurology · 1998 · 1.4K citations
Life Sciences, Genetics, Neurology +13