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Author Details
Full Name
Adrian J Ivinson
Affiliation
Brigham and Women's Hospital
ORCID
Career Start Year
1987
Papers
49
H Index
22
Expertise
CM4AI Collaborator
Timothy Clark (CM4AI)
PMID
Paper Title
Journal Title
Published Year
26220939
Association between α-synuclein blood transcripts and early, neuroimaging-supported Parkinson's disease.
Brain
2015
26220939
Association between α-synuclein blood transcripts and early, neuroimaging-supported Parkinson's disease.
Brain
2015
26343388
Class II HLA interactions modulate genetic risk for multiple sclerosis.
Nat Genet
2015
26343388
Class II HLA interactions modulate genetic risk for multiple sclerosis.
Nat Genet
2015
24653693
Pain Research Forum: application of scientific social media frameworks in neuroscience.
Front Neuroinform
2014
25493273
High prevalence of NMDA receptor IgA/IgM antibodies in different dementia types.
Ann Clin Transl Neurol
2014
25442928
Collaboration in translational neuroscience: a call to arms.
Neuron
2014
24653693
Pain Research Forum: application of scientific social media frameworks in neuroscience.
Front Neuroinform
2014
25442928
Collaboration in translational neuroscience: a call to arms.
Neuron
2014
25493273
High prevalence of NMDA receptor IgA/IgM antibodies in different dementia types.
Ann Clin Transl Neurol
2014
24076602
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
Nat Genet
2013
24076602
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
Nat Genet
2013
22652679
A high-throughput screen to identify inhibitors of SOD1 transcription.
Front Biosci (Elite Ed)
2012
22652679
A high-throughput screen to identify inhibitors of SOD1 transcription.
Front Biosci (Elite Ed)
2012
22451204
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
Ann Neurol
2012
22451204
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
Ann Neurol
2012
21653641
Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.
Hum Mol Genet
2011
22190364
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
Ann Neurol
2011
21953863
Association of SNCA with Parkinson: replication in the Harvard NeuroDiscovery Center Biomarker Study.
Mov Disord
2011
21833088
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature
2011
21653641
Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.
Hum Mol Genet
2011
22023190
Anti-superoxide dismutase antibodies are associated with survival in patients with sporadic amyotrophic lateral sclerosis.
Amyotroph Lateral Scler
2011
21635769
Untapped ethical resources for neurodegeneration research.
BMC Med Ethics
2011
22023190
Anti-superoxide dismutase antibodies are associated with survival in patients with sporadic amyotrophic lateral sclerosis.
Amyotroph Lateral Scler
2011
22190364
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
Ann Neurol
2011
21833088
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature
2011
21953863
Association of SNCA with Parkinson: replication in the Harvard NeuroDiscovery Center Biomarker Study.
Mov Disord
2011
21635769
Untapped ethical resources for neurodegeneration research.
BMC Med Ethics
2011
20211854
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.
Hum Mol Genet
2010
20699326
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.
Hum Mol Genet
2010
20574445
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.
Genes Immun
2010
20522537
Variation within DNA repair pathway genes and risk of multiple sclerosis.
Am J Epidemiol
2010
20211854
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.
Hum Mol Genet
2010
20502484
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis.
Nat Genet
2010
20699326
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.
Hum Mol Genet
2010
20522537
Variation within DNA repair pathway genes and risk of multiple sclerosis.
Am J Epidemiol
2010
20502484
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis.
Nat Genet
2010
20574445
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.
Genes Immun
2010
19293837
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor.
Eur J Hum Genet
2009
19451621
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.
Proc Natl Acad Sci U S A
2009
19293837
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor.
Eur J Hum Genet
2009
19237575
The role of the CD58 locus in multiple sclerosis.
Proc Natl Acad Sci U S A
2009
19451621
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.
Proc Natl Acad Sci U S A
2009
19237575
The role of the CD58 locus in multiple sclerosis.
Proc Natl Acad Sci U S A
2009
18631952
Partnership between academia and industry for drug discovery in Alzheimer's disease.
Alzheimers Dement
2008
18631952
Partnership between academia and industry for drug discovery in Alzheimer's disease.
Alzheimers Dement
2008
17252545
A second major histocompatibility complex susceptibility locus for multiple sclerosis.
Ann Neurol
2007
17660530
Risk alleles for multiple sclerosis identified by a genomewide study.
N Engl J Med
2007
17252545
A second major histocompatibility complex susceptibility locus for multiple sclerosis.
Ann Neurol
2007
17660530
Risk alleles for multiple sclerosis identified by a genomewide study.
N Engl J Med
2007
1 - 50 of 98
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