All Comments by John Hardy
- Next-Generation Sequencing: Boldly Going Where No Geneticist...
- Genetic signatures of exceptional longevity in humans.
- Good Gene, Bad Gene?—New APP Variant May Be Both
- SORLA Soars—Large Study Links Gene to Late-onset AD
- Haplotype-specific expression of exon 10 at the human MAPT locus.
- Highs and Lows: Overactive Synuclein Promoter Linked to Parkinson’s, Tau Loss to Mental Retardation
- Birds of a Feather…Mutations in Tau Gene Neighbor Progranulin Cause FTD
- Charting Genetic Diversity—First Haplotype Map Appears
- Beta amyloid gene duplication in Alzheimer's disease and karyotypically normal Down syndrome.
- Alzheimer’s Vaccine: In Some Patients, at Least, It Might Just Work
- Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease.
- A patient with dementia with Lewy bodies and codon 232 mutation of PRNP.
- BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein.
- D90A-SOD1 mediated amyotrophic lateral sclerosis: a single founder for all cases with evidence for a Cis-acting disease modifier in the recessive haplotype.
- The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility.