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Letter
2020

Prevalence of GBA p.K198E mutation in Colombian and Hispanic populations

Tipton, P. W., Soto-Beasley, A. I., Walton, R. L., Soler-Rangel, S., Romero-Osorio, Ó., Díaz, C., Moreno-López, C. L., Ross, O. A., Wszolek, Z. K. & Cerquera-Cleves, C., Apr 2020, In : Parkinsonism and Related Disorders. 73, p. 16-18 3 p.

Research output: Contribution to journalLetter

2019

Dipeptide repeat (DPR) pathology in the skeletal muscle of ALS patients with C9ORF72 repeat expansion

Cykowski, M. D., Dickson, D. W., Powell, S. Z., Arumanayagam, A. S., Rivera, A. L. & Appel, S. H., Oct 1 2019, In : Acta neuropathologica. 138, 4, p. 667-670 4 p.

Research output: Contribution to journalLetter

1 Scopus citations

Reply: LATE to the PART-y

Nelson, P. T., Dickson, D. W., Trojanowski, J. Q., Jack, C. R., Boyle, P. A., Arfanakis, K., Rademakers, R., Alafuzoff, I., Attems, J., Brayne, C., Coyle-Gilchrist, I. T. S., Fardo, D. W., Flanagan, M. E., Halliday, G., Hunter, S., Jicha, G. A., Katsumata, Y., Kawas, C. H., Dirk Keene, C., Kovacs, G. G. & 10 others, Kukull, W. A., Levey, A. I., Makkinejad, N., Montine, T. J., Murray, M. E., Nag, S., Seeley, W. W., Sperling, R. A., White, C. L. & Schneider, J. A., Sep 1 2019, In : Brain. 142, 9, p. 1-3 3 p.

Research output: Contribution to journalLetter

Revisiting the utility of TDP-43 immunoreactive (TDP-43-ir) pathology to classify FTLD-TDP subtypes

Nishihira, Y., Gefen, T., Mao, Q., Appin, C., Kohler, M., Walker, J., Rademakers, R., Rademaker, A., Rogalski, E., Weintraub, S., Geula, C., Mesulam, M. M. & Bigio, E. H., Jul 1 2019, In : Acta neuropathologica. 138, 1, p. 167-169 3 p.

Research output: Contribution to journalLetter

3 Scopus citations
2018

LRP10 in α-synucleinopathies

MSA Exome Consortium, Dec 1 2018, In : The Lancet Neurology. 17, 12, p. 1033-1034 2 p.

Research output: Contribution to journalLetter

3 Scopus citations

LRP10 in α-synucleinopathies

International DLB Genetics Consortium, Dec 1 2018, In : The Lancet Neurology. 17, 12, p. 1032-1033 2 p.

Research output: Contribution to journalLetter

3 Scopus citations

Regenerative Medicine in the State of Florida: Letter Outlining the Florida Organization for Regenerative Medicine

Bruce, C. J., Bu, G. D., Centanni, J. M., Davis, M. D., Dobson, J., Hare, J. M., Fields, G. B., Jove, R., Kenyon, N., Khan, A., March, K., Matosevic, S., Mahmood, A., Pepine, C. J., Ricordi, C., Shapiro, S. A., Zylberberg, C. & Zylberberg, E., Jul 1 2018, In : Stem cells translational medicine. 7, 7, p. 511-512 2 p.

Research output: Contribution to journalLetter

Tau mutations as a novel risk factor for cancer—letter

the LEFFTDS Consortium, Nov 15 2018, In : Cancer Research. 78, 22, p. 6523-6524 2 p.

Research output: Contribution to journalLetter

1 Scopus citations
2017

Occurrence of Crohn's disease with Parkinson's disease

Fujioka, S., Curry, S. E., Kennelly, K., Tacik, P., Heckman, M. G., Tsuboi, Y., Strongosky, A. J., Van Gerpen, J. A., Uitti, R. J., Ross, O. A., Ikezu, T. & Wszolek, Z. K., Apr 1 2017, In : Parkinsonism and Related Disorders. 37, p. 116-117 2 p.

Research output: Contribution to journalLetter

13 Scopus citations

Reply: Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder

Puschmann, A., Fiesel, F., Caulfield, T., Hudec, R., Ando, M., Truban, D., Hou, X., Ogaki, K., Heckman, M. G., James, E. D., Swanberg, M., Jimenez-Ferrer, I., Hansson, O., Opala, G., Siuda, J., Boczarska-Jedynak, M., Friedman, A., Koziorowski, D., Rudzińska-Bar, M., Aasly, J. O. & 13 others, Lynch, T., Mellick, G. D., Mohan, M., Silburn, P. A., Sanotsky, Y., Vilarinõ-Güell, C., Farrer, M. J., Chen, L., Dawson, V. L., Dawson, T. M., Wszolek, Z. K., Ross, O. A. & Springer, W., 2017, In : Brain. 140, 6, p. e33

Research output: Contribution to journalLetter

1 Scopus citations
2015

CHCHD2 and Parkinson's disease

Puschmann, A., Dickson, D. W., Englund, E., Wszolek, Z. K. & Ross, O. A., Jul 1 2015, In : The Lancet Neurology. 14, 7, 1 p.

Research output: Contribution to journalLetter

9 Scopus citations
2 Scopus citations

Concurrent neurodegenerative pathologies in periventricular nodular heterotopia

Bieniek, K. F. & Dickson, D. W., Dec 1 2015, In : Acta neuropathologica. 130, 6, p. 895-897 3 p.

Research output: Contribution to journalLetter

2 Scopus citations

PART, a distinct tauopathy, different from classical sporadic Alzheimer disease

Jellinger, K. A., Alafuzoff, I., Attems, J., Beach, T. G., Cairns, N. J., Crary, J. F., Dickson, D. W., Hof, P. R., Hyman, B. T., Jack, C. R., Jicha, G. A., Knopman, D. S., Kovacs, G. G., Mackenzie, I. R., Masliah, E., Montine, T. J., Nelson, P. T., Schmitt, F., Schneider, J. A., Serrano-Pozo, A. & 6 others, Thal, D. R., Toledo, J. B., Trojanowski, J. Q., Troncoso, J. C., Vonsattel, J. P. & Wisniewski, T., May 1 2015, In : Acta neuropathologica. 129, 5, p. 757-762 6 p.

Research output: Contribution to journalLetter

84 Scopus citations
2014

Asymmetrical leg atrophy in levodopa-responsive dystonia due to a novel GTP cyclohydrolase mutation

Mulroy, E., McCarthy, A., Lynch, T., Costello, D. & Ross, O. A., Mar 2014, In : Movement Disorders. 29, 3, p. 425-426 2 p.

Research output: Contribution to journalLetter

1 Scopus citations
1 Scopus citations

Concurrent variably protease-sensitive prionopathy and amyotrophic lateral sclerosis

Cannon, A., Bieniek, K. F., Lin, W. L., Notari, S., Zou, W. Q., Gambetti, P., Pedraza, O., Graff-Radford, N. R., Ferman, T. J. & Dickson, D. W., Jan 1 2014, In : Acta neuropathologica. 128, 2, p. 313-315 3 p.

Research output: Contribution to journalLetter

3 Scopus citations

Latin America's first case of Perry syndrome and a new treatment option for respiratory insufficiency

Pretelt, F., Castañeda Cardona, C., Tacik, P., Ross, O. A. & Wszolek, Z. K., Mar 2014, In : Journal of Neurology. 261, 3, p. 620-621 2 p.

Research output: Contribution to journalLetter

6 Scopus citations

Neurotensin agonists in the regulation of food intake

Fredrickson, P., Boules, M. & Richelson, E., Mar 2014, In : International Journal of Obesity. 38, 3, 1 p.

Research output: Contribution to journalLetter

The blood glucose-lowering effect of racecadotril is not attributable to inhibition of insulin-degrading enzyme

Kurklinsky, S., Abdul-Hay, S. O., McGuire, M. P., Howard, E. A., Knight, J. & Leissring, M. A., Jan 1 2014, In : Hormone and Metabolic Research. 46, 1, p. 73-74 2 p.

Research output: Contribution to journalLetter

2013

An adult-onset leukoencephalopathy with axonal spheroids and pigmented glia accompanied by brain calcifications: A case report and a literature review of brain calcifications disorders

Fujioka, S., Broderick, D. F., Sundal, C., Baker, M. C., Rademakers, R. & Wszolek, Z. K., Oct 1 2013, In : Journal of Neurology. 260, 10, p. 2665-2668 4 p.

Research output: Contribution to journalLetter

16 Scopus citations

In reply

Sheeler, R. D., Ackerman, M. J., Richelson, E., Nelson, T. K., Staab, J. P., Tangalos, E. G., Dieser, L. M. & Cunningham, J. L., Apr 2013, In : Mayo Clinic proceedings. 88, 4, 1 p.

Research output: Contribution to journalLetter

6 Scopus citations

Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients

Bardien, S., Blanckenberg, J., van der Merwe, L., Farrer, M. J. & Ross, O. A., Dec 1 2013, In : Movement Disorders. 28, 14, p. 2039-2040 2 p.

Research output: Contribution to journalLetter

Proteotoxicity and cardiac dysfunction [9]

Ebrahimi-Fakhari, D., McLean, P. J. & Wahlster, L., Jan 1 2013, In : New England Journal of Medicine. 368, 18, p. 1754-1755 2 p.

Research output: Contribution to journalLetter

2 Scopus citations
2012

Angiogenin variation and Parkinson disease

Rayaprolu, S., Soto-Ortolaza, A., Rademakers, R., Uitti, R. J., Wszolek, Z. K. & Ross, O. A., May 1 2012, In : Annals of neurology. 71, 5, p. 725-727 3 p.

Research output: Contribution to journalLetter

17 Scopus citations

A novel de novo pathogenic mutation in the CACNA1A gene

Fujioka, S., Rayaprolu, S., Sundal, C., Broderick, D. F., Langley, W. A., Shoffner, J., Hyams, L. C., Rademakers, R., Graff-Radford, N. R., Tatum, W., Ross, O. A. & Wszolek, Z. K., Oct 1 2012, In : Movement Disorders. 27, 12, p. 1578-1579 2 p.

Research output: Contribution to journalLetter

2 Scopus citations

C9orf72 repeat expansions in patients with ALS and FTD

Rademakers, R., Apr 1 2012, In : The Lancet Neurology. 11, 4, p. 297-298 2 p.

Research output: Contribution to journalLetter

31 Scopus citations

Hippocampal-sparing Alzheimer's disease presenting as corticobasal syndrome

Malkani, R. G., Dickson, D. W. & Simuni, T., Jun 1 2012, In : Parkinsonism and Related Disorders. 18, 5, p. 683-685 3 p.

Research output: Contribution to journalLetter

5 Scopus citations

Mutations in the TRPV4 gene are not associated with sporadic progressive muscular atrophy.

Vlam, L., Schelhaas, H. J., van Blitterswijk, M., van Vught, P. W. J., de Visser, M., van der Kooi, A. J., van der Pol, W. L. & van den Berg, L. H., Jun 1 2012, In : Archives of neurology. 69, 6, p. 790-791 2 p.

Research output: Contribution to journalLetter

4 Scopus citations

To the editor: Rapidly progressive dementia in a Chinese patient due to C9ORF72 mutation

Kandiah, N., Sengdy, P., MacKenzie, I. R. A., Hsiung, G. Y. R., DeJesus-Hernandez, M. & Rademakers, R., Sep 1 2012, In : Canadian Journal of Neurological Sciences. 39, 5, p. 676-677 2 p.

Research output: Contribution to journalLetter

9 Scopus citations
2011

No effect on SOD1 splicing by TARDP or FUS mutations

Belzil, V. V., Daoud, H., Dion, P. A. & Rouleau, G. A., Mar 1 2011, In : Archives of neurology. 68, 3, p. 395-396 2 p.

Research output: Contribution to journalLetter

Open Access
3 Scopus citations
2010

Association of pyridoxal kinase and parkinson disease

Vilariño-Güell, C., Wider, C., Aasly, J. O., White, L. R., Rajput, A., Rajput, A. H., Lynch, T., Krygowska-Wajs, A., Jasinska-Myga, B., Opala, G., Barcikowska, M., Czyzewski, K., Wu, R. M., Uitti, R. J., Wszolek, Z. K., Farrer, M. J. & Ross, O. A., Mar 1 2010, In : Annals of neurology. 67, 3, p. 409-411 3 p.

Research output: Contribution to journalLetter

7 Scopus citations

Chromosome 9p21 in amyotrophic lateral sclerosis: The plot thickens

Daoud, H., Belzil, V., Dion, P. A. & Rouleau, G. A., Oct 2010, In : The Lancet Neurology. 9, 10, p. 945-947 3 p.

Research output: Contribution to journalLetter

2 Scopus citations

Does mitochondrial DNA have a protective role in stroke?

Meschia, J. F. & Ross, O. A., May 1 2010, In : The Lancet Neurology. 9, 5, p. 453-454 2 p.

Research output: Contribution to journalLetter

2 Scopus citations

Psychometric evaluation of personality in a patient with FTDP-17

Sitek, E. J., Narozańska, E., Sławek, J., Wójcik, J., Wieczorek, D., Robowski, P., Schinwelski, M., Jasińska-Myga, B., Baker, M., Rademakers, R. & Wszołek, Z. K., Apr 1 2010, In : Psychiatry and Clinical Neurosciences. 64, 2, p. 211-212 2 p.

Research output: Contribution to journalLetter

3 Scopus citations

Reply to: SNCA variants are associated with increased risk of multiple system atrophy

Ross, O. A., Vilariño-Güell, C., Wszolek, Z. K., Farrer, M. J. & Dickson, D. W., Mar 1 2010, In : Annals of neurology. 67, 3, p. 414-415 2 p.

Research output: Contribution to journalLetter

31 Scopus citations
2009

Brainstem atrophy on routine MR study in pallidopontonigral degeneration

Slowinski, J. L., Schweitzer, K. J., Imamura, A., Uitti, R. J., Strongosky, A. J., Dickson, D. W., Broderick, D. F. & Wszolek, Z. K., May 1 2009, In : Journal of Neurology. 256, 5, p. 827-829 3 p.

Research output: Contribution to journalLetter

3 Scopus citations

Corticobasal syndrome with Alzheimer's disease pathology

Imamura, A., Wszolek, Z. K., Lucas, J. A. & Dickson, D. W., Jan 15 2009, In : Movement Disorders. 24, 1, p. 152-153 2 p.

Research output: Contribution to journalLetter

14 Scopus citations

Familial idiopathic basal ganglia calcification: A challenging clinical-pathological correlation

Wider, C., Dickson, D. W., Schweitzer, K. J., Broderick, D. F. & Wszolek, Z. K., May 1 2009, In : Journal of Neurology. 256, 5, p. 839-842 4 p.

Research output: Contribution to journalLetter

29 Scopus citations

FGF20 and Parkinson's disease: No evidence of association or pathogenicity via α-synuclein expression

Wider, C., Dachsel, J. C., Soto, A. I., Heckman, M. G., Diehl, N. N., Yue, M., Lincoln, S., Aasly, J. O., Haugarvoll, K., Trojanowski, J. Q., Papapetropoulos, S., Mash, D., Rajput, A., Rajput, A. H., Gibson, J. M., Lynch, T., Dickson, D. W., Uitti, R. J., Wszolek, Z. K., Farrer, M. J. & 1 others, Ross, O. A., Feb 15 2009, In : Movement Disorders. 24, 3, p. 455-459 5 p.

Research output: Contribution to journalLetter

36 Scopus citations

Reply: GIGYF2 variants are not associated with Parkinson's disease in Italy

Vilariño-Güell, C., Ross, O. A. & Farrer, M. J., Sep 15 2009, In : Movement Disorders. 24, 12, p. 1868-1869 2 p.

Research output: Contribution to journalLetter

2 Scopus citations

Reported mutations in GIGYF2 are not a common cause of Parkinson's disease

Vilariño-Güell, C., Ross, O. A., Soto, A. I., Farrer, M. J., Haugarvoll, K., Aasly, J. O. & Uitti, R. J., Mar 15 2009, In : Movement Disorders. 24, 4, p. 619-620 2 p.

Research output: Contribution to journalLetter

25 Scopus citations
2008

Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations

Ross, O. A., Toft, M. & Haugarvoll, K., Jul 22 2008, In : Neurology. 71, 4, 1 p.

Research output: Contribution to journalLetter

1 Scopus citations

In dementia with lewy bodies, braak stage determines phenotype, not lewy body distribution

Dickson, D. W. & Fujishiro, H., May 2008, In : Neurology. 70, 22, p. 2087-2088 2 p.

Research output: Contribution to journalLetter

2 Scopus citations

Lrrk2 R1628P in non-Chinese Asian races

Tan, E. K., Tang, M., Tan, L. C., Wu, Y. R., Wu, R. M., Ross, O. A. & Zhao, Y., Oct 1 2008, In : Annals of neurology. 64, 4, p. 472-473 2 p.

Research output: Contribution to journalLetter

20 Scopus citations

Neuropsychological findings in clinically atypical autopsy confirmed corticobasal degeneration and progressive supranuclear palsy

VanVoorst, W. A., Greenaway, M. C., Boeve, B. F., Ivnik, R. J., Parisi, J. E., Eric Ahlskog, J., Knopman, D. S., Dickson, D. W., Petersen, R. C., Smith, G. E. & Josephs, K. A., May 1 2008, In : Parkinsonism and Related Disorders. 14, 4, p. 376-378 3 p.

Research output: Contribution to journalLetter

22 Scopus citations
2007

Common variants in Parkinson's disease [2]

Ross, O. A., Farrer, M. J. & Wu, R. M., Apr 30 2007, In : Movement Disorders. 22, 6, p. 899-900 2 p.

Research output: Contribution to journalLetter

2 Scopus citations

Global distribution and reduced penetrance: Lrrk2 R1441C in an Irish Parkinson's disease kindred [9]

Gosal, D., Lynch, T., Ross, O. A., Haugarvoll, K., Farrer, M. J. & Gibson, J. M., Jan 15 2007, In : Movement Disorders. 22, 2, p. 291-292 2 p.

Research output: Contribution to journalLetter

10 Scopus citations