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Bis, Joshua C
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2021
de Rojas I
,
Moreno-Grau S
,
Tesi N
,
Grenier-Boley B
,
Andrade V
,
Jansen IE
,
Pedersen NL
,
Stringa N
,
Zettergren A
,
Hernández I
et al.
. 2021.
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
.
Nat Commun. 12(1):3417.
PubMed
Madrid L
,
Moreno-Grau S
,
Ahmad S
,
González-Perez A
,
de Rojas I
,
Xia R
,
Adami PVMartino
,
García-González P
,
Kleineidam L
,
Yang Q
et al.
. 2021.
Multiomics integrative analysis identifies allele-specific blood biomarkers associated to Alzheimer's disease etiopathogenesis.
.
Aging (Albany NY). 13(7):9277-9329.
PubMed
2020
Pase MP
,
Himali JJ
,
Beiser AS
,
DeCarli C
,
McGrath ER
,
Satizabal CL
,
Aparicio HJ
,
Adams HHH
,
Reiner AP
,
Longstreth WT
et al.
. 2020.
Association of CD14 with incident dementia and markers of brain aging and injury.
.
Neurology. 94(3):e254-e266.
PubMed
Grasby KL
,
Jahanshad N
,
Painter JN
,
Colodro-Conde L
,
Bralten J
,
Hibar DP
,
Lind PA
,
Pizzagalli F
,
Ching CRK
,
McMahon MAgnes B
et al.
. 2020.
The genetic architecture of the human cerebral cortex.
.
Science. 367(6484)
PubMed
Hofer E
,
Roshchupkin GV
,
Adams HHH
,
Knol MJ
,
Lin H
,
Li S
,
Zare H
,
Ahmad S
,
Armstrong NJ
,
Satizabal CL
et al.
. 2020.
Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.
.
Nat Commun. 11(1):4796.
PubMed
2019
Ma Y
,
Jun GR
,
Zhang X
,
Chung J
,
Naj AC
,
Chen Y
,
Bellenguez C
,
Hamilton-Nelson K
,
Martin ER
,
Kunkle BW
et al.
. 2019.
Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype.
.
JAMA Neurol.
PubMed
Mishra A
,
Chauhan G
,
Violleau M-H
,
Vojinovic D
,
Jian X
,
Bis JC
,
Li S
,
Saba Y
,
Grenier-Boley B
,
Yang Q
et al.
. 2019.
Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects.
.
Brain. 142(4):1009-1023.
PubMed
Chauhan G
,
Adams HHH
,
Satizabal CL
,
Bis JC
,
Teumer A
,
Sargurupremraj M
,
Hofer E
,
Trompet S
,
Hilal S
,
Smith AVernon
et al.
. 2019.
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting.
.
Neurology.
PubMed
Satizabal CL
,
Adams HHH
,
Hibar DP
,
White CC
,
Knol MJ
,
Stein JL
,
Scholz M
,
Sargurupremraj M
,
Jahanshad N
,
Roshchupkin GV
et al.
. 2019.
Genetic architecture of subcortical brain structures in 38,851 individuals.
.
Nat Genet. 51(11):1624-1636.
PubMed
Kunkle BW
,
Grenier-Boley B
,
Sims R
,
Bis JC
,
Damotte V
,
Naj AC
,
Boland A
,
Vronskaya M
,
van der Lee SJ
,
Amlie-Wolf A
et al.
. 2019.
Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.
.
Nat Genet. 51(3):414-430.
PubMed
van der Lee SJ
,
Knol MJ
,
Chauhan G
,
Satizabal CL
,
Smith AVernon
,
Hofer E
,
Bis JC
,
Hibar DP
,
Hilal S
,
van den Akker EB
et al.
. 2019.
A genome-wide association study identifies genetic loci associated with specific lobar brain volumes.
.
Commun Biol. 2:285.
PubMed
Wolters FJ
,
Yang Q
,
Biggs ML
,
Jakobsdottir J
,
Li S
,
Evans DS
,
Bis JC
,
Harris TB
,
Vasan RS
,
Zilhao NR
et al.
. 2019.
The impact of APOE genotype on survival: Results of 38,537 participants from six population-based cohorts (E2-CHARGE).
.
PLoS One. 14(7):e0219668.
PubMed
Kowalski MH
,
Qian H
,
Hou Z
,
Rosen JD
,
Tapia AL
,
Shan Y
,
Jain D
,
Argos M
,
Arnett DK
,
Avery C
et al.
. 2019.
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
.
PLoS Genet. 15(12):e1008500.
PubMed
2018
Jian X
,
Satizabal CL
,
Smith AV
,
Wittfeld K
,
Bis JC
,
Smith JA
,
Hsu F-C
,
Nho K
,
Hofer E
,
Hagenaars SP
et al.
. 2018.
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging.
.
Stroke. 49(8):1812-1819.
PubMed
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.
PubMed
Naj AC
,
Lin H
,
Vardarajan BN
,
White S
,
Lancour D
,
Ma Y
,
Schmidt M
,
Sun F
,
Butkiewicz M
,
Bush WS
et al.
. 2018.
Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.
.
Genomics.
PubMed
Bis JC
,
Jian X
,
Kunkle BW
,
Chen Y
,
Hamilton-Nelson KL
,
Bush WS
,
Salerno WJ
,
Lancour D
,
Ma Y
,
Renton AE
et al.
. 2018.
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.
.
Mol Psychiatry.
PubMed
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