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Molecular Psychiatry|October 17, 2012
Molecular evidence of N-methyl-D-aspartate receptor hypofunction in schizophreniaC S Weickert, S J Fung, V S Catts, et al.
Mechanisms of Ageing and Development|June 12, 2018
Review and meta-analysis of genetic polymorphisms associated with exceptional human longevityMary Revelas, Anbupalam Thalamuthu, Christopher Oldmeadow, et al.
Age (Dordrecht, Netherlands)|July 2, 2014
Impact of the AGTR1 A1166C polymorphism on subcortical hyperintensities and cognition in healthy older adultsLauren E Salminen, Peter R Schofield, Kerrie D Pierce, et al.
Behavioural Brain Research|May 2, 2017
Vulnerability of white matter tracts and cognition to the SOD2 polymorphism: A preliminary study of antioxidant defense genes in brain agingLauren E Salminen, Peter R Schofield, Kerrie D Pierce, et al.
Neuroreport|November 27, 1998
Two novel presenilin-1 mutations (Ser169Leu and Pro436Gln) associated with very early onset Alzheimer's diseaseK Taddei, J B Kwok, J J Kril, et al.
Scientific Reports|November 27, 2015
Physiologically generated presenilin 1 lacking exon 8 fails to rescue brain PS1-/- phenotype and forms complexes with wildtype PS1 and nicastrinHannah Brautigam, Cesar L Moreno, John W Steele, et al.
Annals of Neurology|November 11, 2008
Glycogen synthase kinase-3beta and tau genes interact in Alzheimer's diseaseJohn B J Kwok, Clement T Loy, Gillian Hamilton, et al.
Annals of Neurology|February 24, 2001
Variable phenotype of Alzheimer's disease with spastic paraparesisM J Smith, J B Kwok, C A McLean, et al.
Genes|March 21, 2019
Exceptional Longevity and Polygenic Risk for Cardiovascular HealthMary Revelas, Anbupalam Thalamuthu, Christopher Oldmeadow, et al.
Diagnosis (Berlin, Germany)|June 4, 2026
Progress in mast cell activation syndrome: the global consensus-2 diagnostic criteria at six yearsLawrence B Afrin, Svetlana Blitshteyn, Linda S Bluestein, et al.
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