Extreme cerebrospinal fluid amyloid β levels identify family with late-onset Alzheimer's disease presenilin 1 mutationKAUWE, John S. K; JACQUART, Sarah; CHAKRAVERTY, Sumi et al.Annals of neurology. 2007, Vol 61, Num 5, pp 446-453, issn 0364-5134, 8 p.Article

Novel presenilin 1 mutation (S170F) causing Alzheimer disease with lewy bodies in the third decade of lifeSNIDER, B. Joy; NORTON, Joanne; COATS, Mary A et al.Archives of neurology (Chicago). 2005, Vol 62, Num 12, pp 1821-1830, issn 0003-9942, 10 p.Article

Neuropathologic heterogeneity in HDDD1 : A familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and Progranulin mutationBEHRENS, Maria I; MUKHERJEE, Odity; CHAKRAVERTY, Sumi et al.Alzheimer disease and associated disorders. 2007, Vol 21, Num 1, pp 1-7, issn 0893-0341, 7 p.Article

Novel haplotypes in 17q21 are associated with progressive supranuclear palsyPASTOR, Pau; EZQUERRA, Mario; PEREZ, J. Christian et al.Annals of neurology. 2004, Vol 56, Num 2, pp 249-258, issn 0364-5134, 10 p.Article

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulinMUKHERJEE, Odity; PASTOR, Pau; LEVITCH, Denise et al.Annals of neurology. 2006, Vol 60, Num 3, pp 314-322, issn 0364-5134, 9 p.Article

No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been foundJOHNSON, Janel; OSTOJIC, Jovanka; PASTOR, Pau et al.Neuroscience letters. 2004, Vol 363, Num 2, pp 99-101, issn 0304-3940, 3 p.Article

Apolipoprotein Eε4 modifies Alzheimer's disease onset in an E280A PS1 kindredPASTOR, Pau; ROE, Catherine M; KOSIK, Kenneth S et al.Annals of neurology. 2003, Vol 54, Num 2, pp 163-169, issn 0364-5134, 7 p.Article

Novel presenilin 1 variant (P117A) causing Alzheimer's disease in the fourth decade of lifeKAUWE, John S. K; JUN WANG; CHAKRAVERTY, Sumi et al.Neuroscience letters. 2008, Vol 438, Num 2, pp 257-259, issn 0304-3940, 3 p.Article

TDP-43 A315T Mutation in Familial Motor Neuron DiseaseGITCHO, Michael A; BALOH, Robert H; BAKER, Matt et al.Annals of neurology. 2008, Vol 63, Num 4, pp 535-538, issn 0364-5134, 4 p.Article

Association studies using novel polymorphisms in BACEI and BACE2NOWOTNY, Petra; KWON, Jennifer M; CHAKRAVERTY, Sumi et al.Neuroreport (Oxford). 2001, Vol 12, Num 9, pp 1799-1802, issn 0959-4965Article