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2020
Miller JB
,
Ward E
,
Staley LA
,
Stevens J
,
Teerlink CC
,
Tavana JP
,
Cloward M
,
Page M
,
Dayton L
,
Cannon-Albright LA
et al.
. 2020.
Identification and genomic analysis of pedigrees with exceptional longevity identifies candidate rare variants.
.
Neurobiol Dis. 143:104972.
2018
Nafikov RA
,
Nato AQ
,
Sohi H
,
Wang B
,
Brown L
,
Horimoto AR
,
Vardarajan BN
,
Barral SM
,
Tosto G
,
Mayeux RP
et al.
. 2018.
Analysis of Pedigree Data in Populations with Multiple Ancestries: Strategies for Dealing with Admixture in Caribbean Hispanic Families from the ADSP.
.
Genet Epidemiol. 42(6):500-515.
2016
Kunkle BW
,
Jaworski J
,
Barral S
,
Vardarajan B
,
Beecham GW
,
Martin ER
,
Cantwell LS
,
Partch A
,
Bird TD
,
Raskind WH
et al.
. 2016.
Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease.
.
Alzheimers Dement. 12(1):2-10.
2015
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
Barral S
,
Cosentino S
,
Christensen K
,
Newman AB
,
Perls TT
,
Province MA
,
Mayeux R
. 2014.
Common genetic variants on 6q24 associated with exceptional episodic memory performance in the elderly.
.
JAMA Neurol. 71(12):1514-9.
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.
Jun G
,
Asai H
,
Zeldich E
,
Drapeau E
,
Chen CD
,
Chung J
,
Park J-H
,
Kim S
,
Haroutunian V
,
Foroud T
et al.
. 2014.
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation.
.
Ann Neurol. 76(3):379-92.
2013
Kalimo H
,
Lalowski M
,
Bogdanovic N
,
Philipson O
,
Bird TD
,
Nochlin D
,
Schellenberg GD
,
Brundin R
,
Olofsson T
,
Soliymani R
et al.
. 2013.
The Arctic AβPP mutation leads to Alzheimer's disease pathology with highly variable topographic deposition of differentially truncated Aβ.
.
Acta Neuropathol Commun. 1:60.
Nuytemans K
,
Bademci G
,
Kohli MM
,
Beecham GW
,
Wang L-S
,
Young JI
,
Nahab F
,
Martin ER
,
Gilbert JR
,
Benatar M
et al.
. 2013.
C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease.
.
Ann Hum Genet. 77(5):351-63.