• 26667 Citations
  • 79 Scopus h-Index
19992020

Research output per year

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Research Output

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Letter
2019

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

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
2015
2 Scopus citations
2014
1 Scopus citations
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
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

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
2010

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
2006

Visualization of MAPT inversion on stretched chromosomes of tau-negative frontotemporal dementia patients

Gijselinck, I., Bogaerts, V., Rademakers, R., Van Der Zee, J., Van Broeckhoven, C. & Cruts, M., Oct 1 2006, In : Human mutation. 27, 10, p. 1057-1059 3 p.

Research output: Contribution to journalLetter

9 Scopus citations
2004

Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia family [2]

Rademakers, R., Van Den Broeck, M., Sleegers, K., Van Duijn, C., Van Broeckhoven, C. & Cruts, M., Feb 1 2004, In : Neurogenetics. 5, 1, p. 79-80 2 p.

Research output: Contribution to journalLetter

2 Scopus citations
2003

Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family [2]

Cruts, M., Dermaut, B., Rademakers, R., Van Den Broeck, M., Stögbauer, F. & Van Broeckhoven, C., Nov 1 2003, In : Journal of Neurology. 250, 11, p. 1374-1375 2 p.

Research output: Contribution to journalLetter

15 Scopus citations

Tau (MAPT) Mutation Arg406Trp Presenting Clinically with Alzheimer Disease Does Not Share a Common Founder in Western Europe [1]

Rademakers, R., Dermaut, B., Peeters, K., Cruts, M., Heutink, P., Goate, A. & Van Broeckhoven, C., Nov 11 2003, In : Human mutation. 22, 5, p. 409-411 3 p.

Research output: Contribution to journalLetter

58 Scopus citations