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Janis Blevins
Janis Blevins
MSM-Healthcare, Case Western Reserve University
Verified email at techtoaster.com
Title
Cited by
Cited by
Year
Quantifying prion disease penetrance using large population control cohorts
EV Minikel, SM Vallabh, M Lek, K Estrada, KE Samocha, ...
Science translational medicine 8 (322), 322ra9-322ra9, 2016
3602016
Treatable neurological disorders misdiagnosed as Creutzfeldt‐Jakob disease
N Chitravas, RS Jung, DM Kofskey, JE Blevins, P Gambetti, RJ Leigh, ...
Annals of neurology 70 (3), 437-444, 2011
2282011
Diagnostic and prognostic value of human prion detection in cerebrospinal fluid
A Foutz, BS Appleby, C Hamlin, X Liu, S Yang, Y Cohen, W Chen, ...
Annals of neurology 81 (1), 79-92, 2017
2092017
Rapidly progressive Alzheimer’s disease features distinct structures of amyloid-β
ML Cohen, C Kim, T Haldiman, M ElHag, P Mehndiratta, T Pichet, ...
Brain 138 (4), 1009-1022, 2015
1962015
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics
I Cali, R Castellani, A Alshekhlee, Y Cohen, J Blevins, J Yuan, ...
Brain 132 (10), 2643-2658, 2009
1532009
Small Protease Sensitive Oligomers of PrPSc in Distinct Human Prions Determine Conversion Rate of PrPC
C Kim, T Haldiman, K Surewicz, Y Cohen, W Chen, J Blevins, MS Sy, ...
Public Library of Science 8 (8), e1002835, 2012
862012
Protease-Sensitive Conformers in Broad Spectrum of Distinct PrPSc Structures in Sporadic Creutzfeldt-Jakob Disease Are Indicator of Progression Rate
C Kim, T Haldiman, Y Cohen, W Chen, J Blevins, MS Sy, M Cohen, ...
PLoS pathogens 7 (9), e1002242, 2011
852011
Diagnosis of prion diseases by RT-QuIC results in improved surveillance
DD Rhoads, A Wrona, A Foutz, J Blevins, K Glisic, M Person, RA Maddox, ...
Neurology 95 (8), e1017-e1026, 2020
822020
Evaluation of a new criterion for detecting prion disease with diffusion magnetic resonance imaging
A Bizzi, R Pascuzzo, J Blevins, M Grisoli, R Lodi, MEM Moscatelli, ...
JAMA neurology 77 (9), 1141-1149, 2020
592020
Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selection
T Haldiman, C Kim, Y Cohen, W Chen, J Blevins, L Qing, ML Cohen, ...
Journal of Biological Chemistry 288 (41), 29846-29861, 2013
592013
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
E Jones, H Hummerich, E Viré, J Uphill, A Dimitriadis, H Speedy, ...
The Lancet Neurology 19 (10), 840-848, 2020
502020
Prion disease incidence in the United States: 2003–2015
RA Maddox, MK Person, JE Blevins, JY Abrams, BS Appleby, ...
Neurology 94 (2), e153-e157, 2020
402020
Subtype diagnosis of sporadic Creutzfeldt–Jakob disease with diffusion magnetic resonance imaging
A Bizzi, R Pascuzzo, J Blevins, MEM Moscatelli, M Grisoli, R Lodi, ...
Annals of Neurology 89 (3), 560-572, 2021
342021
Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt–Jakob disease
R Pascuzzo, NP Oxtoby, AL Young, J Blevins, G Castelli, S Garbarino, ...
Acta neuropathologica 140, 169-181, 2020
312020
A low-molecular-weight ferroxidase is increased in the CSF of sCJD cases: CSF ferroxidase and transferrin as diagnostic biomarkers for sCJD
S Haldar, AJ Beveridge, J Wong, A Singh, D Galimberti, B Borroni, X Zhu, ...
Antioxidants & Redox Signaling 19 (14), 1662-1675, 2013
272013
Daly MJ, MacArthur DG
EV Minikel, SM Vallabh, M Lek, K Estrada, KE Samocha, ...
Quantifying prion disease penetrance using large population control cohorts …, 2016
162016
019 neurogenic persistent genital arousal disorder (PGAD) secondary to radiculopathy of sacral spinal nerve roots (SSNR): treatment outcome following spine surgery
C Kim, J Blevins, J Hanley, S Goldstein, B Komisaruk, I Goldstein
The Journal of Sexual Medicine 16 (Supplement_3), S9-S9, 2019
112019
Human prion disease surveillance in Washington State, 2006-2017
L Sánchez-González, RA Maddox, LC Lewis, JE Blevins, EJ Harker, ...
JAMA Network Open 3 (10), e2020690-e2020690, 2020
62020
Improving Creutzfeldt-Jakob disease incidence estimates by incorporating results of neuropathological analyses, United States, 2003-2011
R Maddox, M Person, A Minino, J Blevins, L Schonberger, E Belay
Prion 9, S55-S56, 2015
52015
The co-existence of PrPSc type 1 and 2 in Sporadic Creutzfeldt-Jakob Disease affects the phenotype and PrPSc conformation
I Cali, I Cohen, J Blevins, R Castellani, A Al-Shekhlee, J Yuan, P Parchi, ...
Journal of Neuropathology and Experimental Neurology 68 (5), 553-553, 2009
52009
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