Alzheimer's Disease
Genetics Consortium

ADGC Publications

Found 4 results

Filters: Keyword is Mutation, Missense [Clear All Filters]

2018

Ikezu T, Chen CD, DeLeo AM, Zeldich E, M Fallin D, Kanaan NM, Lunetta KL, Abraham CR, Logue MW, Farrer LA. 2018. Tau Phosphorylation is Impacted by Rare AKAP9 Mutations Associated with Alzheimer Disease in African Americans.. J Neuroimmune Pharmacol. 13(2):254-264.

2015

Nho K, Kim S, Risacher SL, Shen L, Corneveaux JJ, Swaminathan S, Lin H, Ramanan VK, Liu Y, Foroud TM et al.. 2015. Protective variant for hippocampal atrophy identified by whole exome sequencing.. Ann Neurol. 77(3):547-52.

2014

Carney RM, Kohli MA, Kunkle BW, Naj AC, Gilbert JR, Züchner S, Pericak-Vance MA. 2014. Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.. Alzheimers Dement. 10(3):360-5.

2013

Reitz C, Mayeux R. 2013. TREM2 and neurodegenerative disease.. N Engl J Med. 369(16):1564-5.