Adrian J Ivinson
Overview
Explore the profile of Adrian J Ivinson including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
26
Citations
3447
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Lauwers E, Lalli G, Brandner S, Collinge J, Compernolle V, Duyckaerts C, et al.
Lancet Neurol
. 2020 Sep;
19(10):872-878.
PMID: 32949547
Studies in experimental animals show transmissibility of amyloidogenic proteins associated with prion diseases, Alzheimer's disease, Parkinson's disease, and other neurodegenerative diseases. Although these data raise potential concerns for public health,...
2.
Moutsianas L, Jostins L, Beecham A, Dilthey A, Xifara D, Ban M, et al.
Nat Genet
. 2015 Sep;
47(10):1107-1113.
PMID: 26343388
Association studies have greatly refined the understanding of how variation within the human leukocyte antigen (HLA) genes influences risk of multiple sclerosis. However, the extent to which major effects are...
3.
Doss S, Wandinger K, Hyman B, Panzer J, Synofzik M, Dickerson B, et al.
Ann Clin Transl Neurol
. 2014 Dec;
1(10):822-32.
PMID: 25493273
Objective: To retrospectively determine the frequency of N-Methyl-D-Aspartate (NMDA) receptor (NMDAR) autoantibodies in patients with different forms of dementia. Methods: Clinical characterization of 660 patients with dementia, neurodegenerative disease without...
4.
Ivinson A
Neuron
. 2014 Dec;
84(3):521-5.
PMID: 25442928
Neurological and psychiatric disorders present an immediate and growing challenge. The scale and complexity of this unmet need calls for a concomitantly large and sophisticated response. Here the author discusses...
5.
Das S, McCaffrey P, Talkington M, Andrews N, Corlosquet S, Ivinson A, et al.
Front Neuroinform
. 2014 Mar;
8:21.
PMID: 24653693
Background: Social media has the potential to accelerate the pace of biomedical research through online collaboration, discussions, and faster sharing of information. Focused web-based scientific social collaboratories such as the...
6.
Beecham A, Patsopoulos N, Xifara D, Davis M, Kemppinen A, Cotsapas C, et al.
Nat Genet
. 2013 Oct;
45(11):1353-60.
PMID: 24076602
Using the ImmunoChip custom genotyping array, we analyzed 14,498 subjects with multiple sclerosis and 24,091 healthy controls for 161,311 autosomal variants and identified 135 potentially associated regions (P < 1.0...
7.
Wright P, Wightman N, Huang M, Weiss A, Sapp P, Cuny G, et al.
Front Biosci (Elite Ed)
. 2012 Jun;
4(8):2701-8.
PMID: 22652679
Amyotrophic lateral sclerosis (ALS) is a fatal degenerative motor neuron disease. Approximately 20 percent of familial ALS cases are caused by mutations in the Cu/Zn superoxide dismutase (SOD1) gene. Rodents...
8.
Pankratz N, Beecham G, DeStefano A, Dawson T, Doheny K, Factor S, et al.
Ann Neurol
. 2012 Mar;
71(3):370-84.
PMID: 22451204
Objective: Genome-wide association (GWAS) methods have identified genes contributing to Parkinson's disease (PD); we sought to identify additional genes associated with PD susceptibility. Methods: A 2-stage design was used. First,...
9.
van Blitterswijk M, Gulati S, Smoot E, Jaffa M, Maher N, Hyman B, et al.
Amyotroph Lateral Scler
. 2011 Oct;
12(6):430-8.
PMID: 22023190
Our objective was to test the hypothesis that aberrantly modified forms of superoxide dismutase (SOD1) influence the disease course for sporadic amyotrophic lateral sclerosis (SALS). We probed for anti-SOD1 antibodies...
10.
Association of SNCA with Parkinson: replication in the Harvard NeuroDiscovery Center Biomarker Study
Ding H, Sarokhan A, Roderick S, Bakshi R, Maher N, Ashourian P, et al.
Mov Disord
. 2011 Sep;
26(12):2283-6.
PMID: 21953863
Background: Mutations in the α-synuclein gene (SNCA) cause autosomal dominant forms of Parkinson's disease, but the substantial risk conferred by this locus to the common sporadic disease has only recently...