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Found 9 results
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Keyword
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Genetic Variation
and
Author
is
Gerard D Schellenberg
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2018
Blue EE
,
Bis JC
,
Dorschner MO
,
Tsuang DW
,
Barral SM
,
Beecham G
,
Below JE
,
Bush WS
,
Butkiewicz M
,
Cruchaga C
et al.
. 2018.
Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.
.
Dement Geriatr Cogn Disord. 45(1-2):1-17.
2017
Rehker J
,
Rodhe J
,
Nesbitt RR
,
Boyle EA
,
Martin BK
,
Lord J
,
Karaca I
,
Naj A
,
Jessen F
,
Helisalmi S
et al.
. 2017.
Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants.
.
PLoS One. 12(10):e0185777.
Naj AC
,
Schellenberg GD
. 2017.
Genomic variants, genes, and pathways of Alzheimer's disease: An overview.
.
Am J Med Genet B Neuropsychiatr Genet. 174(1):5-26.
2016
Ridge PG
,
Hoyt KB
,
Boehme K
,
Mukherjee S
,
Crane PK
,
Haines JL
,
Mayeux R
,
Farrer LA
,
Pericak-Vance MA
,
Schellenberg GD
et al.
. 2016.
Assessment of the genetic variance of late-onset Alzheimer's disease.
.
Neurobiol Aging. 41:200.e13-200.e20.
2015
Escott-Price V
,
Sims R
,
Bannister C
,
Harold D
,
Vronskaya M
,
Majounie E
,
Badarinarayan N
,
Morgan K
,
Passmore P
,
Holmes C
et al.
. 2015.
Common polygenic variation enhances risk prediction for Alzheimer's disease.
.
Brain. 138(Pt 12):3673-84.
2013
Reitz C
,
Jun G
,
Naj A
,
Rajbhandary R
,
Vardarajan BNarayan
,
Wang L-S
,
Valladares O
,
Lin C-F
,
Larson EB
,
Graff-Radford NR
et al.
. 2013.
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.
.
JAMA. 309(14):1483-92.
2012
Whitcomb DC
,
LaRusch J
,
Krasinskas AM
,
Klei L
,
Smith JP
,
Brand RE
,
Neoptolemos JP
,
Lerch MM
,
Tector M
,
Sandhu BS
et al.
. 2012.
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.
.
Nat Genet. 44(12):1349-54.
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
Naj AC
,
Jun G
,
Beecham GW
,
Wang L-S
,
Vardarajan BNarayan
,
Buros J
,
Gallins PJ
,
Buxbaum JD
,
Jarvik GP
,
Crane PK
et al.
. 2011.
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
.
Nat Genet. 43(5):436-41.