Vardarajan, BN
19  Ergebnisse:
Personensuche X
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2

Genetic meta-analysis of diagnosed Alzheimer's disease iden..:

Kunkle, BW ; Grenier-Boley, B ; Sims, R...
https://discovery.ucl.ac.uk/id/eprint/10071668/1/IGAP_GWAS_Article_revision.pdf.  , 2019
 
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4

CpG-related SNPs in the MS4A region have a dose-dependent e..:

Ma, Y ; Jun, GR ; Chung, J...
https://discovery.ucl.ac.uk/id/eprint/10082322/1/Hardy_CpG-related%20SNPs%20in%20the%20MS4A%20region%20have%20a%20dose-dependent%20effect%20on%20risk%20of%20late-onset%20Alzheimer%20disease_VoR.pdf.  , 2019
 
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5

Association of Rare Coding Mutations With Alzheimer Disease..:

Patel, D ; Mez, J ; Vardarajan, BN...
Patel , D , Mez , J , Vardarajan , BN , Staley , L , Chung , J , Zhang , XK , Ahmad , S , Amin , N , Ikram , A , van der Lee , S , Duijn , C , van der Spek , A , Waligorski , J & Wilson , RK 2019 , ' Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry ' , JAMA network open , vol. 2 , no. 3 , e191350 . https://doi.org/10.1001/jamanetworkopen.2019.1350.  , 2019
 
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6

A statistical framework for cross-tissue transcriptome-wide..:

Hu, Y ; Li, M ; Lu, Q...
https://discovery.ucl.ac.uk/id/eprint/10084678/1/Hu_NG_2019.pdf.  , 2019
 
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8

Genetically elevated high-density lipoprotein cholesterol t..:

Peloso, GM ; van der Lee, SJ ; Sims, R...
https://discovery.ucl.ac.uk/id/eprint/10078370/1/1-s2.0-S2352872918300605-main.pdf.  , 2018
 
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11

A rare loss-of-function variant of ADAM17 is associated wit..:

Hartl, D ; May, P ; Gu, W...
https://discovery.ucl.ac.uk/id/eprint/10053021/1/Hartl_Rare%20loss-of-function.pdf.  , 2018
 
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12

Analysis of shared heritability in common disorders of the ..:

Anttila, V ; Bulik-Sullivan, B ; Finucane, HK...
https://discovery.ucl.ac.uk/id/eprint/10052781/1/Wood_aap8757_MainText.pdf.  , 2018
 
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13

Transethnic genome-wide scan identifies novel Alzheimer's d..:

Jun, GR ; Chung, J ; Mez, J...
https://discovery.ucl.ac.uk/id/eprint/10025982/1/1-s2.0-S1552526017300031-main.pdf.  , 2017
 
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14

Rare coding variants in PLCG2, ABI3, and TREM2 implicate mi..:

Sims, R ; van der Lee, SJ ; Naj, AC...
https://discovery.ucl.ac.uk/id/eprint/1566558/1/Mead_NGLE43635R_Manuscript_170124.pdf.  , 2017
 
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