| Year |
Citation |
Score |
| 2024 |
İş Ö, Wang X, Reddy JS, Min Y, Yilmaz E, Bhattarai P, Patel T, Bergman J, Quicksall Z, Heckman MG, Tutor-New FQ, Can Demirdogen B, White L, Koga S, Krause V, ... ... Kouri N, et al. Gliovascular transcriptional perturbations in Alzheimer's disease reveal molecular mechanisms of blood brain barrier dysfunction. Nature Communications. 15: 4758. PMID 38902234 DOI: 10.1038/s41467-024-48926-6 |
0.563 |
|
| 2024 |
Morderer D, Wren MC, Liu F, Kouri N, Maistrenko A, Khalil B, Pobitzer N, Salemi M, Phinney BS, Dickson DW, Murray ME, Rossoll W. Probe-dependent Proximity Profiling (ProPPr) Uncovers Similarities and Differences in Phospho-Tau-Associated Proteomes Between Tauopathies. Biorxiv : the Preprint Server For Biology. PMID 38585836 DOI: 10.1101/2024.03.25.585597 |
0.334 |
|
| 2023 |
Shir D, Thu Pham NT, Botha H, Koga S, Kouri N, Ali F, Knopman DS, Petersen RC, Boeve BF, Kremers WK, Nguyen AT, Murray ME, Reichard RR, Dickson DW, Graff-Radford N, et al. Clinicoradiologic and Neuropathologic Evaluation of Corticobasal Syndrome. Neurology. PMID 37268436 DOI: 10.1212/WNL.0000000000207397 |
0.568 |
|
| 2021 |
Kouri N, Murray ME, Reddy JS, Serie DJ, Soto-Beasley A, Allen M, Carrasquillo MM, Wang X, Castanedes MC, Baker MC, Rademakers R, Uitti RJ, Graff-Radford NR, Wszolek ZK, Schellenberg GD, et al. Latent trait modeling of tau neuropathology in progressive supranuclear palsy. Acta Neuropathologica. PMID 33635380 DOI: 10.1007/s00401-021-02289-0 |
0.372 |
|
| 2020 |
Valentino RR, Koga S, Walton RL, Soto-Beasley AI, Kouri N, DeTure MA, Murray ME, Johnson PW, Petersen RC, Boeve BF, Uitti RJ, Wszolek ZK, Dickson DW, Ross OA, Heckman MG. MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features. Acta Neuropathologica Communications. 8: 218. PMID 33287913 DOI: 10.1186/s40478-020-01097-z |
0.698 |
|
| 2018 |
Allen M, Wang X, Serie DJ, Strickland SL, Burgess JD, Koga S, Younkin CS, Nguyen TT, Malphrus KG, Lincoln SJ, Alamprese M, Zhu K, Chang R, Carrasquillo MM, Kouri N, et al. Divergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsy. Acta Neuropathologica. PMID 30136084 DOI: 10.1007/S00401-018-1900-5 |
0.725 |
|
| 2018 |
Sanchez-Contreras MY, Kouri N, Cook CN, Serie DJ, Heckman MG, Finch NA, Caselli RJ, Uitti RJ, Wszolek ZK, Graff-Radford N, Petrucelli L, Wang LS, Schellenberg GD, Dickson DW, Rademakers R, et al. Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci. Molecular Neurodegeneration. 13: 37. PMID 29986742 DOI: 10.1186/S13024-018-0267-3 |
0.532 |
|
| 2018 |
Koga S, Kouri N, Walton RL, Ebbert MTW, Josephs KA, Litvan I, Graff-Radford N, Ahlskog JE, Uitti RJ, van Gerpen JA, Boeve BF, Parks A, Ross OA, Dickson DW. Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtype. Acta Neuropathologica. PMID 29926172 DOI: 10.1007/S00401-018-1878-Z |
0.678 |
|
| 2018 |
Karch CM, Wen N, Fan CC, Yokoyama JS, Kouri N, Ross OA, Höglinger G, Müller U, Ferrari R, Hardy J, Schellenberg GD, Sleiman PM, Momeni P, Hess CP, Miller BL, et al. Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum. Jama Neurology. PMID 29630712 DOI: 10.1001/Jamaneurol.2018.0372 |
0.365 |
|
| 2018 |
Broce I, Karch CM, Wen N, Fan CC, Wang Y, Hong Tan C, Kouri N, Ross OA, Höglinger GU, Muller U, Hardy J, Momeni P, Hess CP, Dillon WP, et al. Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies. Plos Medicine. 15: e1002487. PMID 29315334 DOI: 10.1371/Journal.Pmed.1002487 |
0.375 |
|
| 2017 |
Yokoyama JS, Karch CM, Fan CC, Bonham LW, Kouri N, Ross OA, Rademakers R, Kim J, Wang Y, Höglinger GU, Müller U, Ferrari R, Hardy J, Momeni P, et al. Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia. Acta Neuropathologica. PMID 28271184 DOI: 10.1007/S00401-017-1693-Y |
0.572 |
|
| 2017 |
DeTure M, Tacik P, Kouri N, Carlomagno Y, Ross K, Murray ME, Dickson DW. [P4-106]: GENETIC MUTATIONS IN MAPT AND SIGNIFICANT VARIABILITY IN TAU PROTEIN MODIFICATIONS INDICATE THE EXISTANCE OF A WIDE ARRAY OF STRAINS WITHIN AND ACROSS PRIMARY AND SECONDARY TAUOPATHIES Alzheimer's & Dementia. 13: P1298-P1298. DOI: 10.1016/J.Jalz.2017.06.1972 |
0.605 |
|
| 2017 |
Allen M, Wang X, Younkin CS, Serie D, Burgess JD, Nguyen T, Lincoln SJ, Malphrus KG, Carrasquillo MM, Kouri N, Murray ME, Schellenberg GD, Younkin SG, Crook JE, Asmann YW, et al. [P4-074]: INTEGRATIVE SYSTEMS BIOLOGY APPROACH TO IDENTIFY NOVEL RISK FACTORS FOR PSP Alzheimer's & Dementia. 13: P1286-P1286. DOI: 10.1016/J.Jalz.2017.06.1939 |
0.554 |
|
| 2016 |
Tacik P, DeTure MA, Yari C, Lin WL, Murray ME, Baker MC, Josephs KA, Boeve BF, Wszolek ZK, Graff-Radford NR, Parisi JE, Petrucelli L, Rademakers R, Isaacson RS, Heilman KM, ... ... Kouri N, et al. FTDP-17 with pick body-like inclusions associated with a novel tau mutation, p.E372G. Brain Pathology (Zurich, Switzerland). PMID 27529406 DOI: 10.1111/Bpa.12428 |
0.648 |
|
| 2016 |
Allen M, Burgess JD, Ballard T, Serie D, Wang X, Younkin CS, Sun Z, Kouri N, Baheti S, Wang C, Carrasquillo MM, Nguyen T, Lincoln S, Malphrus K, Murray M, et al. Gene expression, methylation and neuropathology correlations at progressive supranuclear palsy risk loci. Acta Neuropathologica. PMID 27115769 DOI: 10.1007/S00401-016-1576-7 |
0.611 |
|
| 2016 |
Allen M, Wang X, Younkin CS, Serie D, Sun Z, Burgess JD, Baheti S, Kouri N, Nguyen T, Lincoln S, Malphrus KG, Carrasquillo MM, Zou F, Chai H, Murray ME, et al. P4-048: Convergent Analysis of Endophenotypes in Progressive Supranuclear Palsy Alzheimer's & Dementia. 12: P1032-P1033. DOI: 10.1016/J.Jalz.2016.06.2137 |
0.583 |
|
| 2015 |
Kouri N, Ross OA, Dombroski B, Younkin CS, Serie DJ, Soto-Ortolaza A, Baker M, Finch NC, Yoon H, Kim J, Fujioka S, McLean CA, Ghetti B, Spina S, Cantwell LB, et al. Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. Nature Communications. 6: 7247. PMID 26077951 DOI: 10.1038/Ncomms8247 |
0.504 |
|
| 2015 |
Tacik P, DeTure M, Lin WL, Sanchez Contreras M, Wojtas A, Hinkle KM, Fujioka S, Baker MC, Walton RL, Carlomagno Y, Brown PH, Strongosky AJ, Kouri N, Murray ME, Petrucelli L, et al. A novel tau mutation, p.K317N, causes globular glial tauopathy. Acta Neuropathologica. 130: 199-214. PMID 25900293 DOI: 10.1007/S00401-015-1425-0 |
0.647 |
|
| 2014 |
Murray ME, Kouri N, Lin WL, Jack CR, Dickson DW, Vemuri P. Clinicopathologic assessment and imaging of tauopathies in neurodegenerative dementias. Alzheimer's Research & Therapy. 6: 1. PMID 24382028 DOI: 10.1186/Alzrt231 |
0.643 |
|
| 2014 |
Kouri N, Carlomagno Y, Baker M, Liesinger AM, Caselli RJ, Wszolek ZK, Petrucelli L, Boeve BF, Parisi JE, Josephs KA, Uitti RJ, Ross OA, Graff-Radford NR, DeTure MA, Dickson DW, et al. Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration. Acta Neuropathologica. 127: 271-82. PMID 24121548 DOI: 10.1007/S00401-013-1193-7 |
0.571 |
|
| 2013 |
Murray ME, Bieniek KF, Banks Greenberg M, DeJesus-Hernandez M, Rutherford NJ, van Blitterswijk M, Niemantsverdriet E, Ash PE, Gendron TF, Kouri N, Baker M, Goodman IJ, Petrucelli L, Rademakers R, Dickson DW. Progressive amnestic dementia, hippocampal sclerosis, and mutation in C9ORF72. Acta Neuropathologica. 126: 545-54. PMID 23922030 DOI: 10.1007/S00401-013-1161-2 |
0.74 |
|
| 2013 |
Lincoln S, Allen M, Cox CL, Walker LP, Malphrus K, Qiu Y, Nguyen T, Rowley C, Kouri N, Crook J, Pankratz VS, Younkin S, Younkin L, Carrasquillo M, Zou F, et al. LRRTM3 interacts with APP and BACE1 and has variants associating with late-onset Alzheimer's disease (LOAD). Plos One. 8: e64164. PMID 23750206 DOI: 10.1371/Journal.Pone.0064164 |
0.521 |
|
| 2013 |
Kouri N, Oshima K, Takahashi M, Murray ME, Ahmed Z, Parisi JE, Yen SH, Dickson DW. Corticobasal degeneration with olivopontocerebellar atrophy and TDP-43 pathology: an unusual clinicopathologic variant of CBD. Acta Neuropathologica. 125: 741-52. PMID 23371366 DOI: 10.1007/S00401-013-1087-8 |
0.64 |
|
| 2012 |
Zou F, Chai HS, Younkin CS, Allen M, Crook J, Pankratz VS, Carrasquillo MM, Rowley CN, Nair AA, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus KG, Palusak R, ... ... Kouri N, et al. Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants. Plos Genetics. 8: e1002707. PMID 22685416 DOI: 10.1371/Journal.Pgen.1002707 |
0.565 |
|
| 2012 |
Rademakers R, Baker M, Nicholson AM, Rutherford NJ, Finch N, Soto-Ortolaza A, Lash J, Wider C, Wojtas A, DeJesus-Hernandez M, Adamson J, Kouri N, Sundal C, Shuster EA, Aasly J, et al. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids. Nature Genetics. 44: 200-5. PMID 22197934 DOI: 10.1038/Ng.1027 |
0.467 |
|
| 2012 |
Taner N, Zou F, Chai HS, Younkin C, Crook J, Pankratz V, Allen M, Carrasquillo M, Rowley C, Nair A, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus K, ... ... Kouri N, et al. Novel Progressive Supranuclear Palsy (PSP) Risk Loci Variants Associate with Brain Gene Expression Levels (S54.002) Neurology. 78: S54.002-S54.002. DOI: 10.1212/Wnl.78.1_Meetingabstracts.S54.002 |
0.405 |
|
| 2012 |
Taner N, Zou F, Chai HS, Younkin C, Crook J, Pankratz V, Allen M, Carrasquillo M, Rowley C, Nair A, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus K, ... ... Kouri N, et al. Brain Expression Genome-Wide Association Study (eGWAS) Identifies Human Disease-Associated Variants (P05.069) Neurology. 78: P05.069-P05.069. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P05.069 |
0.418 |
|
| 2012 |
Ertekin-Taner N, Zou F, Chai HS, Younkin C, Crook J, Pankratz V, Allen M, Carrasquillo M, Rowley C, Nair A, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus K, ... ... Kouri N, et al. Identification of human disease-associated variants in a brain expression genome-wide association study (eGWAS) Alzheimers & Dementia. 8: 178. DOI: 10.1016/J.Jalz.2012.05.480 |
0.491 |
|
| 2012 |
Ertekin-Taner N, Allen M, Murray M, Crook J, Serie D, Zou F, Chai HS, Younkin C, Pankratz V, Carrasquillo M, Rowley C, Nair A, Middha S, Maharjan S, Nguyen T, ... ... Kouri N, et al. O5-03-03: Genetic association of progressive supranuclear palsy (PSP) risk loci variants with brain gene expression and neuropathology endophenotypes Alzheimer's & Dementia. 8: P735-P735. DOI: 10.1016/J.Jalz.2012.05.1983 |
0.612 |
|
| 2011 |
Kocerha J, Kouri N, Baker M, Finch N, DeJesus-Hernandez M, Gonzalez J, Chidamparam K, Josephs KA, Boeve BF, Graff-Radford NR, Crook J, Dickson DW, Rademakers R. Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations. Bmc Genomics. 12: 527. PMID 22032330 DOI: 10.1186/1471-2164-12-527 |
0.429 |
|
| 2011 |
DeJesus-Hernandez M, Mackenzie IR, Boeve BF, Boxer AL, Baker M, Rutherford NJ, Nicholson AM, Finch NA, Flynn H, Adamson J, Kouri N, Wojtas A, Sengdy P, Hsiung GY, Karydas A, et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron. 72: 245-56. PMID 21944778 DOI: 10.1016/J.Neuron.2011.09.011 |
0.482 |
|
| 2011 |
Kouri N, Murray ME, Hassan A, Rademakers R, Uitti RJ, Boeve BF, Graff-Radford NR, Wszolek ZK, Litvan I, Josephs KA, Dickson DW. Neuropathological features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndrome. Brain : a Journal of Neurology. 134: 3264-75. PMID 21933807 DOI: 10.1093/Brain/Awr234 |
0.605 |
|
| 2011 |
Dickson DW, Kouri N, Murray ME, Josephs KA. Neuropathology of frontotemporal lobar degeneration-tau (FTLD-tau). Journal of Molecular Neuroscience : Mn. 45: 384-9. PMID 21720721 DOI: 10.1007/S12031-011-9589-0 |
0.636 |
|
| 2011 |
Kouri N, Whitwell JL, Josephs KA, Rademakers R, Dickson DW. Corticobasal degeneration: a pathologically distinct 4R tauopathy. Nature Reviews. Neurology. 7: 263-72. PMID 21487420 DOI: 10.1038/Nrneurol.2011.43 |
0.567 |
|
| 2010 |
Zou F, Carrasquillo MM, Pankratz VS, Belbin O, Morgan K, Allen M, Wilcox SL, Ma L, Walker LP, Kouri N, Burgess JD, Younkin LH, Younkin SG, Younkin CS, Bisceglio GD, et al. Gene expression levels as endophenotypes in genome-wide association studies of Alzheimer disease. Neurology. 74: 480-6. PMID 20142614 DOI: 10.1212/Wnl.0B013E3181D07654 |
0.513 |
|
| 2009 |
Delledonne A, Kouri N, Reinstatler L, Sahara T, Li L, Zhao J, Dickson DW, Ertekin-Taner N, Leissring MA. Development of monoclonal antibodies and quantitative ELISAs targeting insulin-degrading enzyme. Molecular Neurodegeneration. 4: 39. PMID 19835587 DOI: 10.1186/1750-1326-4-39 |
0.402 |
|
| 2008 |
Younkin SG, Carrasquillo M, Younkin S, Zou F, Walker LP, Wilcox S, Younkin C, Pishotta FT, Ma L, Bisceglio G, Kouri N, Pankratz VS, Cunningham JM, Petersen RC, Graff-Radford NR, et al. P3-275: Genome-wide association study for Braak neurofibrillary tangle (NFT) staging Alzheimer's & Dementia. 4: T602-T603. DOI: 10.1016/J.Jalz.2008.05.1843 |
0.465 |
|
| 2008 |
Walker L, Allen M, Cox C, Younkin S, Younkin L, Carrasquillo M, Zou F, Ma L, Kouri N, Pankratz VS, Dickson D, Boeve B, Petersen RC, Graff-Radford NR, Younkin SG, et al. P3-271: Association of candidate gene susceptibility alleles on chromosome 10 with Alzheimer's disease risk and endophenotypes Alzheimer's & Dementia. 4: T601-T601. DOI: 10.1016/J.Jalz.2008.05.1839 |
0.527 |
|
| 2008 |
Ertekin-Taner N, Zou F, Carrasquillo M, Younkin S, Ma L, Walker LP, Wilcox S, Bisceglio G, Kouri N, Pankratz VS, Cunningham JM, Dickson D, Petersen RC, Graff-Radford NR, Younkin SG. P3-216: Identification of CIS
variants associating with expression levels of 12 late-onset Alzheimer's disease (LOAD) candidate genes in a Genome-Wide Association Study (GWAS) Alzheimer's & Dementia. 4: T584-T584. DOI: 10.1016/J.Jalz.2008.05.1783 |
0.531 |
|
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