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Found 5 results
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2017
Kunkle BW
,
Vardarajan BN
,
Naj AC
,
Whitehead PL
,
Rolati S
,
Slifer S
,
Carney RM
,
Cuccaro ML
,
Vance JM
,
Gilbert JR
et al.
. 2017.
Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport.
.
JAMA Neurol. 74(9):1113-1122.
2016
Jakobsdottir J
,
van der Lee SJ
,
Bis JC
,
Chouraki V
,
Li-Kroeger D
,
Yamamoto S
,
Grove ML
,
Naj A
,
Vronskaya M
,
Salazar JL
et al.
. 2016.
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.
.
PLoS Genet. 12(10):e1006327.
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
Samocha KE
,
Robinson EB
,
Sanders SJ
,
Stevens C
,
Sabo A
,
McGrath LM
,
Kosmicki JA
,
Rehnström K
,
Mallick S
,
Kirby A
et al.
. 2014.
A framework for the interpretation of de novo mutation in human disease.
.
Nat Genet. 46(9):944-50.
2013
Schafer CM
,
Campbell NG
,
Cai G
,
Yu F
,
Makarov V
,
Yoon S
,
Daly MJ
,
Gibbs RA
,
Schellenberg GD
,
Devlin B
et al.
. 2013.
Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.
.
Genomics. 102(4):270-7.