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1.
Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes.
Proc Natl Acad Sci U S A
; 120(36): e2302720120, 2023 09 05.
Article
in English
| MEDLINE | ID: mdl-37643212
2.
CADPS functional mutations in patients with bipolar disorder increase the sensitivity to stress.
Mol Psychiatry
; 27(2): 1145-1157, 2022 02.
Article
in English
| MEDLINE | ID: mdl-35169262
3.
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis.
Ann Neurol
; 85(4): 470-481, 2019 04.
Article
in English
| MEDLINE | ID: mdl-30723964
4.
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
Am J Hum Genet
; 98(3): 500-513, 2016 Mar 03.
Article
in English
| MEDLINE | ID: mdl-26942284
5.
Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease.
Ann Neurol
; 84(2): 191-199, 2018 08.
Article
in English
| MEDLINE | ID: mdl-30014513
6.
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.
Hum Mol Genet
; 25(24): 5483-5489, 2016 12 15.
Article
in English
| MEDLINE | ID: mdl-27798102
7.
Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study.
PLoS Med
; 14(6): e1002314, 2017 Jun.
Article
in English
| MEDLINE | ID: mdl-28609445
8.
Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease.
JAMA Netw Open
; 6(5): e2313734, 2023 05 01.
Article
in English
| MEDLINE | ID: mdl-37195665
9.
Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease.
JAMA Neurol
; 79(7): 652-663, 2022 07 01.
Article
in English
| MEDLINE | ID: mdl-35639372
10.
A Meta-Analysis of the Transferability of Bone Mineral Density Genetic Loci Associations From European to African Ancestry Populations.
J Bone Miner Res
; 36(3): 469-479, 2021 03.
Article
in English
| MEDLINE | ID: mdl-33249669
11.
Genetic discovery and risk characterization in type 2 diabetes across diverse populations.
HGG Adv
; 2(2)2021 Apr 08.
Article
in English
| MEDLINE | ID: mdl-34604815
12.
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Neuron
; 97(6): 1268-1283.e6, 2018 03 21.
Article
in English
| MEDLINE | ID: mdl-29566793
13.
Genome-Wide Association Analysis of the Sense of Smell in U.S. Older Adults: Identification of Novel Risk Loci in African-Americans and European-Americans.
Mol Neurobiol
; 54(10): 8021-8032, 2017 Dec.
Article
in English
| MEDLINE | ID: mdl-27878761
14.
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases.
Neurobiol Aging
; 57: 247.e9-247.e13, 2017 09.
Article
in English
| MEDLINE | ID: mdl-28602509
15.
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease.
Neurol Genet
; 1(1): e9, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-27066548
16.
Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study.
Lancet Neurol
; 14(10): 1002-9, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26271532
17.
Common and rare variant analysis in early-onset bipolar disorder vulnerability.
PLoS One
; 9(8): e104326, 2014.
Article
in English
| MEDLINE | ID: mdl-25111785
18.
De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
Nat Genet
; 46(6): 640-5, 2014 Jun.
Article
in English
| MEDLINE | ID: mdl-24747641
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