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Beach, Thomas G
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2020
Reiman EM
,
Arboleda-Velasquez JF
,
Quiroz YT
,
Huentelman MJ
,
Beach TG
,
Caselli RJ
,
Chen Y
,
Su Y
,
Myers AJ
,
Hardy J
et al.
. 2020.
Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study.
.
Nat Commun. 11(1):667.
2015
Beecham GW
,
Dickson DW
,
Scott WK
,
Martin ER
,
Schellenberg GD
,
Nuytemans K
,
Larson EB
,
Buxbaum JD
,
Trojanowski JQ
,
Van Deerlin VM
et al.
. 2015.
PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease.
.
Neurology. 84(10):972-80.
Wang L-S
,
Naj AC
,
Graham RR
,
Crane PK
,
Kunkle BW
,
Cruchaga C
,
Murcia JDGonzalez
,
Cannon-Albright L
,
Baldwin CT
,
Zetterberg H
et al.
. 2015.
Rarity of the Alzheimer disease-protective APP A673T variant in the United States.
.
JAMA Neurol. 72(2):209-16.
2014
Naj AC
,
Jun G
,
Reitz C
,
Kunkle BW
,
Perry W
,
Park YSon
,
Beecham GW
,
Rajbhandary RA
,
Hamilton-Nelson KL
,
Wang L-S
et al.
. 2014.
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.
.
JAMA Neurol. 71(11):1394-404.
2012
Coppola G
,
Chinnathambi S
,
Lee JJiYong
,
Dombroski BA
,
Baker MC
,
Soto-Ortolaza AI
,
Lee SE
,
Klein E
,
Huang AY
,
Sears R
et al.
. 2012.
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.
.
Hum Mol Genet. 21(15):3500-12.
2011
Chen-Plotkin AS
,
Martinez-Lage M
,
Sleiman PMA
,
Hu W
,
Greene R
,
Wood EMcCarty
,
Bing S
,
Grossman M
,
Schellenberg GD
,
Hatanpaa KJ
et al.
. 2011.
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.
.
Arch Neurol. 68(4):488-97.
2010
Van Deerlin VM
,
Sleiman PMA
,
Martinez-Lage M
,
Chen-Plotkin A
,
San Wang L-
,
Graff-Radford NR
,
Dickson DW
,
Rademakers R
,
Boeve BF
,
Grossman M
et al.
. 2010.
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
.
Nat Genet. 42(3):234-9.