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Author Details
Full Name
Olena Korvatska
Affiliation
University of Washington
ORCID
Career Start Year
2009
Papers
16
H Index
12
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37115208
Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation.
Acta Neuropathol
2023
37598468
NOTCH3 C201R variant causes cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) that can be confused with early-onset Alzheimer's disease.
J Neurol Sci
2023
35779466
Reduced gene dosage is a common mechanism of neuropathologies caused by ATP6AP2 splicing mutations.
Parkinsonism Relat Disord
2022
34061398
Novel TREM2 splicing isoform that lacks the V-set immunoglobulin domain is abundant in the human brain.
J Leukoc Biol
2021
33101276
Triggering Receptor Expressed on Myeloid Cell 2 R47H Exacerbates Immune Response in Alzheimer's Disease Brain.
Front Immunol
2020
26076170
R47H Variant of TREM2 Associated With Alzheimer Disease in a Large Late-Onset Family: Clinical, Genetic, and Neuropathological Study.
JAMA Neurol
2015
26537056
ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.
Neurology
2015
23553203
Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families.
JAMA Psychiatry
2013
23595882
Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS).
Hum Mol Genet
2013
21478475
ABCB1 genotype and CSF beta-amyloid in Alzheimer disease.
J Geriatr Psychiatry Neurol
2011
21438139
Mutations in the TSGA14 gene in families with autism spectrum disorders.
Am J Med Genet B Neuropsychiatr Genet
2011
19401682
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
Mol Psychiatry
2010
20531469
Functional impact of global rare copy number variation in autism spectrum disorders.
Nature
2010
20663923
A genome-wide scan for common alleles affecting risk for autism.
Hum Mol Genet
2010
19404256
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Nature
2009
19404257
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Nature
2009
1 - 16 of 16
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