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Neurology. Genetics|May 9, 2017
African American exome sequencing identifies potential risk variants at Alzheimer disease lociAurelie N'Songo, Minerva M Carrasquillo, Xue Wang, et al.
Brain : a Journal of Neurology|January 23, 2009
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family membersNiCole Finch, Matt Baker, Richard Crook, et al.
Alzheimer'S Research & Therapy|October 18, 2014
Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levelsMariet Allen, Michaela Kachadoorian, Zachary Quicksall, et al.
The New Phytologist|October 20, 2022
Diversity and divergence: evolution of secondary metabolism in the tropical tree genus IngaDale L Forrister, María-José Endara, Abrianna J Soule, et al.
Human Molecular Genetics|November 5, 1997
A new pathogenic mutation in the APP gene (I716V) increases the relative proportion of A beta 42(43)C B Eckman, N D Mehta, R Crook, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 7, 2017
Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseasesMariet Allen, Xue Wang, Jeremy D Burgess, et al.
Blood|April 4, 2002
Longitudinal changes in brain magnetic resonance imaging findings in children with sickle cell diseaseCharles H Pegelow, Eric A Macklin, Franklin G Moser, et al.
Plos Genetics|June 12, 2012
Brain expression genome-wide association study (eGWAS) identifies human disease-associated variantsFanggeng Zou, High Seng Chai, Curtis S Younkin, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 13, 2016
A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expressionMinerva M Carrasquillo, Mariet Allen, Jeremy D Burgess, et al.
Neurology|May 30, 2008
Biochemical markers in persons with preclinical familial Alzheimer diseaseJ M Ringman, S G Younkin, D Pratico, et al.
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