• 28307 Citations
  • 81 Scopus h-Index
20012020

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Article
2001

Amyloid β secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease

Cruts, M., Dermaut, B., Rademakers, R., Roks, G., Van den Broeck, M., Munteanu, G., Van Duijn, C. M. & Van Broeckhoven, C., Nov 2 2001, In : Neuroscience Letters. 313, 1-2, p. 105-107 3 p.

Research output: Contribution to journalArticle

36 Scopus citations

Variable expression of presenilin 1 is not a major determinant of risk for late-onset Alzheimer's disease

Dermaut, B., Roks, G., Theuns, J., Rademakers, R., Houwing-Duistermaat, J. J., Serneels, S., Hofman, A., Breteler, M. M. B., Cruts, M., Van Broeckhoven, C. & Van Duijn, C. M., Dec 1 2001, In : Journal of Neurology. 248, 11, p. 935-939 5 p.

Research output: Contribution to journalArticle

14 Scopus citations
2002

Tau negative frontal lobe dementia at 17q21: Significant finemapping of the candidate region to a 4.8 cM interval

Rademakers, R., Cruts, M., Dermaut, B., Sleegers, K., Rosso, S. M., Van den Broeck, M., Backhovens, H., Van Swieten, J., Van Duijn, C. M. & Van Broeckhoven, C., Dec 1 2002, In : Molecular Psychiatry. 7, 10, p. 1064-1074 11 p.

Research output: Contribution to journalArticle

102 Scopus citations
2003

PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease

Dermaut, B., Croes, E. A., Rademakers, R., Van den Broeck, M. V., Cruts, M., Hofman, A., Van Duijn, C. M. & Van Broeckhoven, C., Mar 1 2003, In : Annals of neurology. 53, 3, p. 409-412 4 p.

Research output: Contribution to journalArticle

72 Scopus citations
2004

A Novel Presenilin 1 Mutation Associated with Pick's Disease but Not β-Amyloid Plaques

Dermaut, B., Kumar-Singh, S., Engelborghs, S., Theuns, J., Rademakers, R., Saerens, J., Pickut, B. A., Peeters, K., Van Den Broeck, M., Vennekens, K., Claes, S., Cruts, M., Cras, P., Martin, J. J., Van Broeckhoven, C. & De Deyn, P. P., May 1 2004, In : Annals of neurology. 55, 5, p. 617-626 10 p.

Research output: Contribution to journalArticle

165 Scopus citations

Familial clustering and genetic risk for dementia in a genetically isolated Dutch population

Sleegers, K., Roks, G., Theuns, J., Aulchenko, Y. S., Rademakers, R., Cruts, M., Van Gool, W. A., Van Broeckhoven, C., Heutink, P., Oostra, B. A., Van Swieten, J. C. & Van Duijn, C. M., Jul 2004, In : Brain. 127, 7, p. 1641-1649 9 p.

Research output: Contribution to journalArticle

56 Scopus citations
2005

Association of cyclin-dependent kinase 5 and neuronal activators p35 and p39 complex in early-onset Alzheimer's disease

Rademakers, R., Sleegers, K., Theuns, J., Van Den Broeck, M., Bel Kacem, S., Nilsson, L. G., Adolfsson, R., Van Duijn, C. M., Van Broeckhoven, C. & Cruts, M., Aug 1 2005, In : Neurobiology of aging. 26, 8, p. 1145-1151 7 p.

Research output: Contribution to journalArticle

20 Scopus citations

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

Cruts, M., Rademakers, R., Gijselinck, I., van der Zee, J., Dermaut, B., de Pooter, T., de Rijk, P., Del-Favero, J. & van Broeckhoven, C., Jul 1 2005, In : Human molecular genetics. 14, 13, p. 1753-1762 10 p.

Research output: Contribution to journalArticle

75 Scopus citations

High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

Rademakers, R., Melquist, S., Cruts, M., Theuns, J., Del-Favero, J., Poorkaj, P., Baker, M., Sleegers, K., Crook, R., De Pooter, T., Kacem, S. B., Adamson, J., Van den Bossche, D., Van den Broeck, M., Gass, J., Corsmit, E., De Rijk, P., Thomas, N., Engelborghs, S., Heckman, M. & 7 others, Litvan, I., Crook, J., De Deyn, P. P., Dickson, D., Schellenberg, G. D., Van Broeckhoven, C. & Hutton, M. L., Nov 1 2005, In : Human molecular genetics. 14, 21, p. 3281-3292 12 p.

Research output: Contribution to journalArticle

127 Scopus citations

Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample

Rademakers, R., Cruts, M., Sleegers, K., Dermaut, B., Theuns, J., Aulchenko, Y., Weckx, S., De Pooter, T., Van Den Broeck, M., Corsmit, E., De Rijk, P., Del-Favero, J., Van Swieten, J., Van Duijn, C. M. & Van Broeckhoven, C., Oct 2005, In : American journal of human genetics. 77, 4, p. 643-652 10 p.

Research output: Contribution to journalArticle

40 Scopus citations

novoSNP, a novel computational tool for sequence variation discovery

Weckx, S., Del-Favero, J., Rademakers, R., Claes, L., Cruts, M., De Jonghe, P., Van Broeckhoven, C. & De Rijk, P., Mar 2005, In : Genome Research. 15, 3, p. 436-442 7 p.

Research output: Contribution to journalArticle

190 Scopus citations
2006

A Belgian ancestral haplotype harbours a highly prevalent mutation for I7q21-linked tau-negative FTLD

Van Der Zee, J., Rademakers, R., Engelborghs, S., Gijselinck, I., Bogaerts, V., Vandenberghe, R., Santens, P., Caekebeke, J., De Pooter, T., Peeters, K., Lübke, U., Van Den Broeck, M., Martin, J. J., Cruts, M., De Deyn, P. P., Van Broeckhoven, C. & Dermaut, B., Apr 2006, In : Brain. 129, 4, p. 841-852 12 p.

Research output: Contribution to journalArticle

77 Scopus citations

Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family

Pirici, D., Vandenberghe, R., Rademakers, R., Dermaut, B., Cruts, M., Vennekens, K., Cuijt, I., Lübke, U., Ceuterick, C., Martin, J. J., Van Broeckhoven, C. & Kumar-Singh, S., Mar 1 2006, In : Journal of Neuropathology and Experimental Neurology. 65, 3, p. 289-301 13 p.

Research output: Contribution to journalArticle

47 Scopus citations

Dose dependent effect of APOE ε4 on behavioral symptoms in frontal lobe dementia

Engelborghs, S., Dermaut, B., Mariën, P., Symons, A., Vloeberghs, E., Maertens, K., Somers, N., Goeman, J., Rademakers, R., Van Den Broeck, M., Pickut, B., Cruts, M., Van Broeckhoven, C. & De Deyn, P. P., Feb 1 2006, In : Neurobiology of aging. 27, 2, p. 285-292 8 p.

Research output: Contribution to journalArticle

56 Scopus citations

Frontotemporal dementia and parkinsonism associated with the IVS1+1G→A mutation in progranulin: A clinicopathologic study

Boeve, B. F., Baker, M., Dickson, D. W., Parisi, J. E., Giannini, C., Josephs, K. A., Hutton, M., Pickering-Brown, S. M., Rademakers, R., Tang-Wai, D., Jack, C. R., Kantarci, K., Shiung, M. M., Golde, T., Smith, G. E., Geda, Y. E., Knopman, D. S. & Petersen, R. C., Nov 2006, In : Brain. 129, 11, p. 3103-3114 12 p.

Research output: Contribution to journalArticle

85 Scopus citations

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

Gass, J., Cannon, A., Mackenzie, I. R., Boeve, B., Baker, M., Adamson, J., Crook, R., Melquist, S., Kuntz, K., Petersen, R., Josephs, K., Pickering-Brown, S. M., Graff-Radford, N., Uitti, R., Dickson, D., Wszolek, Z., Gonzalez, J., Beach, T. G., Bigio, E., Johnson, N. & 10 others, Weintraub, S., Mesulam, M., White, C. L., Woodruff, B., Caselli, R., Hsiung, G. Y., Feldman, H., Knopman, D., Hutton, M. & Rademakers, R., Oct 15 2006, In : Human molecular genetics. 15, 20, p. 2988-3001 14 p.

Research output: Contribution to journalArticle

431 Scopus citations

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Baker, M., Mackenzie, I. R., Pickering-Brown, S. M., Gass, J., Rademakers, R., Lindholm, C., Snowden, J., Adamson, J., Sadovnick, A. D., Rollinson, S., Cannon, A., Dwosh, E., Neary, D., Melquist, S., Richardson, A., Dickson, D., Berger, Z., Eriksen, J., Robinson, T., Zehr, C. & 7 others, Dickey, C. A., Crook, R., McGowan, E., Mann, D., Boeve, B., Feldman, H. & Hutton, M., Aug 24 2006, In : Nature. 442, 7105, p. 916-919 4 p.

Research output: Contribution to journalArticle

1361 Scopus citations

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Cruts, M., Gijselinck, I., Van Der Zee, J., Engelborghs, S., Wils, H., Pirici, D., Rademakers, R., Vandenberghe, R., Dermaut, B., Martin, J. J., Van Duijn, C., Peeters, K., Sciot, R., Santens, P., De Pooter, T., Mattheijssens, M., Van Den Broeck, M., Cuijt, I., Vennekens, K., De Deyn, P. P. & 2 others, Kumar-Singh, S. & Van Broeckhoven, C., Aug 24 2006, In : Nature. 442, 7105, p. 920-924 5 p.

Research output: Contribution to journalArticle

1083 Scopus citations

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene

Mackenzie, I. R. A., Baker, M., Pickering-Brown, S., Hsiung, G. Y. R., Lindholm, C., Dwosh, E., Gass, J., Cannon, A., Rademakers, R., Hutton, M. & Feldman, H. H., Nov 1 2006, In : Brain. 129, 11, p. 3081-3090 10 p.

Research output: Contribution to journalArticle

224 Scopus citations
2007

Clinicopathologic correlation in PGRN mutations

Davion, S., Johnson, N., Weintraub, S., Mesulam, M. M., Engberg, A., Mishra, M., Baker, M., Adamson, J., Hutton, M., Rademakers, R. & Bigio, E. H., Sep 2007, In : Neurology. 69, 11, p. 1113-1121 9 p.

Research output: Contribution to journalArticle

44 Scopus citations

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations

Josephs, K. A., Ahmed, Z., Katsuse, O., Parisi, J. F., Boeve, B. F., Knopman, D. S., Petersen, R. C., Davies, P., Duara, R., Graff-Radford, N. R., Uitti, R. J., Rademakers, R., Adamson, J., Baker, M., Hutton, M. L. & Dickson, D. W., Feb 1 2007, In : Journal of Neuropathology and Experimental Neurology. 66, 2, p. 142-151 10 p.

Research output: Contribution to journalArticle

147 Scopus citations

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative

Rademakers, R., Baker, M., Gass, J., Adamson, J., Huey, E. D., Momeni, P., Spina, S., Coppola, G., Karydas, A. M., Stewart, H., Johnson, N., Hsiung, G. Y., Kelley, B., Kuntz, K., Steinbart, E., Wood, E. M. C., Yu, C. E., Josephs, K., Sorenson, E., Womack, K. B. & 30 others, Weintraub, S., Pickering-Brown, S. M., Schofield, P. R., Brooks, W. S., Van Deerlin, V. M., Snowden, J., Clark, C. M., Kertesz, A., Boylan, K., Ghetti, B., Neary, D., Schellenberg, G. D., Beach, T. G., Mesulam, M., Mann, D., Grafman, J., Mackenzie, I. R., Feldman, H., Bird, T., Petersen, R., Knopman, D., Boeve, B., Geschwind, D. H., Miller, B., Wszolek, Z., Lippa, C., Bigio, E. H., Dickson, D., Graff-Radford, N. & Hutton, M., Oct 2007, In : Lancet Neurology. 6, 10, p. 857-868 12 p.

Research output: Contribution to journalArticle

169 Scopus citations

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes

Schymick, J. C., Yang, Y., Andersen, P. M., Vonsattel, J. P., Greenway, M., Momeni, P., Elder, J., Chiò, A., Restagno, G., Robberecht, W., Dahlberg, C., Mukherjee, O., Goate, A., Graff-Radford, N., Caselli, R. J., Hutton, M., Gass, J., Cannon, A., Rademakers, R., Singleton, A. B. & 4 others, Hardiman, O., Rothstein, J., Hardy, J. & Traynor, B. J., Jul 2007, In : Journal of Neurology, Neurosurgery and Psychiatry. 78, 7, p. 754-756 3 p.

Research output: Contribution to journalArticle

101 Scopus citations

Progressive supranuclear palsy: Pathology and genetics

Dickson, D. W., Rademakers, R. & Hutton, M. L., Jan 1 2007, In : Brain Pathology. 17, 1, p. 74-82 9 p.

Research output: Contribution to journalArticle

151 Scopus citations
68 Scopus citations
2008

A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro

Winton, M. J., Van Deerlin, V. M., Kwong, L. K., Yuan, W., Wood, E. M. C., Yu, C. E., Schellenberg, G. D., Rademakers, R., Caselli, R., Karydas, A., Trojanowski, J. Q., Miller, B. L. & Lee, V. M. Y., Jun 25 2008, In : FEBS Letters. 582, 15, p. 2252-2256 5 p.

Research output: Contribution to journalArticle

68 Scopus citations

Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotype

Josephs, K. A., Whitwell, J. L., Knopman, D. S., Hu, W. T., Stroh, D. A., Baker, M., Rademakers, R., Boeve, B. F., Parisi, J. E., Smith, G. E., Ivnik, R. J., Petersen, R. C., Jack, C. R. & Dickson, D. W., May 2008, In : Neurology. 70, 19 PART 2, p. 1850-1857 8 p.

Research output: Contribution to journalArticle

135 Scopus citations

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

Rademakers, R., Eriksen, J. L., Baker, M., Robinson, T., Ahmed, Z., Lincoln, S. J., Finch, N., Rutherford, N. J., Crook, R. J., Josephs, K. A., Boeve, B. F., Knopman, D. S., Petersen, R. C., Parisi, J. E., Caselli, R. J., Wszolek, Z. K., Uitti, R. J., Feldman, H., Hutton, M. L., Mackenzie, I. R. & 2 others, Graff-Radford, N. R. & Dickson, D. W., 2008, In : Human molecular genetics. 17, 23, p. 3631-3642 12 p.

Research output: Contribution to journalArticle

209 Scopus citations

Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients

Nuytemans, K., Rademakers, R., Theuns, J., Pals, P., Engelborghs, S., Pickut, B., de Pooter, T., Peeters, K., Mattheijssens, M., Van den Broeck, M., Cras, P., De Deyn, P. P. & van Broeckhoven, C., Apr 1 2008, In : European Journal of Human Genetics. 16, 4, p. 471-479 9 p.

Research output: Contribution to journalArticle

36 Scopus citations

Gene expression study on peripheral blood identifies progranulin mutations

Coppola, G., Karyda, A., Rademakers, R., Wang, Q., Baker, M., Hutton, M., Miller, B. L. & Geschwind, D. H., Jul 1 2008, In : Annals of neurology. 64, 1, p. 92-96 5 p.

Research output: Contribution to journalArticle

75 Scopus citations

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

Haugarvoll, K., Rademakers, R., Kachergus, J. M., Nuytemans, K., Ross, O. A., Gibson, J. M., Tan, E. K., Gaig, C., Tolosa, E., Goldwurm, S., Guidi, M., Riboldazzi, G., Brown, L., Walter, U., Benecke, R., Berg, D., Gasser, T., Theuns, J., Pals, P., Cras, P. & 14 others, De Deyn, P. P., Engelborghs, S., Pickut, B., Uitti, R. J., Foroud, T., Nichols, W. C., Hagenah, J., Klein, C., Samii, A., Zabetian, C. P., Bonifati, V., Van Broeckhoven, C., Farrer, M. J. & Wszolek, Z. K., Apr 2008, In : Neurology. 70, 16 PART 2, p. 1456-1460 5 p.

Research output: Contribution to journalArticle

93 Scopus citations

Novel mutations in TARDBP(TDP-43) in patients with familial amyotrophic lateral sclerosis

Rutherford, N. J., Zhang, Y. J., Baker, M., Gass, J. M., Finch, N. C. A., Xu, Y. F., Stewart, H., Kelley, B. J., Kuntz, K., Crook, R. J. P., Sreedharan, J., Vance, C., Sorenson, E., Lippa, C., Bigio, E. H., Geschwind, D. H., Knopman, D. S., Mitsumoto, H., Petersen, R. C., Cashman, N. R. & 11 others, Hutton, M., Shaw, C. E., Boylan, K. B., Boeve, B., Graff-Radford, N. R., Wszolek, Z. K., Caselli, R. J., Dickson, D. W., Mackenzie, I. R., Petrucelli, L. & Rademakers, R., Sep 2008, In : PLoS genetics. 4, 9, e1000193.

Research output: Contribution to journalArticle

305 Scopus citations

Progranulin gene mutation with an unusual clinical and neuropathologic presentation

Wider, C., Uitti, R. J., Wszolek, Z. K., Fang, J. Y., Josephs, K. A., Baker, M. C., Rademakers, R., Hutton, M. L. & Dickson, D. W., Jun 15 2008, In : Movement Disorders. 23, 8, p. 1168-1173 6 p.

Research output: Contribution to journalArticle

13 Scopus citations

TDP-43 A315T mutation in familial motor neuron disease

Gitcho, M. A., Baloh, R. H., Chakraverty, S., Mayo, K., Norton, J. B., Levitch, D., Hatanpaa, K. J., White, C. L., Bigio, E. H., Caselli, R., Baker, M., Al-Lozi, M. T., Morris, J. C., Pestronk, A., Rademakers, R., Goate, A. M. & Cairns, N. J., Apr 1 2008, In : Annals of neurology. 63, 4, p. 535-538 4 p.

Research output: Contribution to journalArticle

467 Scopus citations
2009

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

Neumann, M., Roeber, S., Kretzschmar, H. A., Rademakers, R., Baker, M. & MacKenzie, I. R. A., Nov 1 2009, In : Acta neuropathologica. 118, 5, p. 605-616 12 p.

Research output: Contribution to journalArticle

200 Scopus citations

A new subtype of frontotemporal lobar degeneration with FUS pathology

Neumann, M., Rademakers, R., Roeber, S., Baker, M., Kretzschmar, H. A. & MacKenzie, I. R. A., Nov 2009, In : Brain. 132, 11, p. 2922-2931 10 p.

Research output: Contribution to journalArticle

456 Scopus citations

Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations

Whitwell, J. L., Jack, C. R., Boeve, B. F., Senjem, M. L., Baker, M., Ivnik, R. J., Knopman, D. S., Wszolek, Z. K., Petersen, R. C., Rademakers, R. & Josephs, K. A., Sep 2009, In : Neurology. 73, 13, p. 1058-1065 8 p.

Research output: Contribution to journalArticle

48 Scopus citations

Characterization of DCTN1 genetic variability in neurodegeneration

Vilariño-Güell, C., Wider, C., Soto-Ortolaza, A. I., Cobb, S. A., Kachergus, J. M., Keeling, B. H., Dachsel, J. C., Hulihan, M. M., Dickson, D. W., Wszolek, Z. K., Uitti, R. J., Graff-Radford, N. R., Boeve, B. F., Josephs, K. A., Miller, B., Boylan, K. B., Gwinn, K., Adler, C. H., Aasly, J. O., Hentati, F. & 6 others, Destée, A., Krygowska-Wajs, A., Chartier-Harlin, M. C., Ross, O. A., Rademakers, R. & Farrer, M. J., Jun 9 2009, In : Neurology. 72, 23, p. 2024-2028 5 p.

Research output: Contribution to journalArticle

37 Scopus citations

GRN 3′UTR+78 C>T is not associated with risk for Parkinson's disease

Jasinska-Myga, B., Wider, C., Opala, G., Krygowska-Wajs, A., Barcikowska, M., Czyzewski, K., Baker, M., Rademakers, R., Uitti, R. J., Farrer, M. J., Ross, O. A. & Wszolek, Z. K., Aug 1 2009, In : European Journal of Neurology. 16, 8, p. 909-911 3 p.

Research output: Contribution to journalArticle

8 Scopus citations

Longitudinal modeling of age-related memory decline and the APOE ε4 effect

Caselli, R. J., Dueck, A. C., Osborne, D., Sabbagh, M. N., Connor, D. J., Ahern, G. L., Baxter, L. C., Rapcsak, S. Z., Shi, J., Woodruff, B. K., Locke, D. E. C., Snyder, C. H., Alexander, G. E., Rademakers, R. & Reiman, E. M., Jul 16 2009, In : New England Journal of Medicine. 361, 3, p. 255-263 9 p.

Research output: Contribution to journalArticle

319 Scopus citations

Pallidonigral TDP-43 pathology in Perry syndrome

Wider, C., Dickson, D. W., Stoessl, A. J., Tsuboi, Y., Chapon, F., Gutmann, L., Lechevalier, B., Calne, D. B., Personett, D. A., Hulihan, M., Kachergus, J., Rademakers, R., Baker, M. C., Grantier, L. L., Sujith, O. K., Brown, L., Calne, S., Farrer, M. J. & Wszolek, Z. K., May 1 2009, In : Parkinsonism and Related Disorders. 15, 4, p. 281-286 6 p.

Research output: Contribution to journalArticle

55 Scopus citations

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

Finch, N., Baker, M., Crook, R., Swanson, K., Kuntz, K., Surtees, R., Bisceglio, G., Rovelet-Lecrux, A., Boeve, B., Petersen, R. C., Dickson, D. W., Younkin, S. G., Deramecourt, V., Crook, J., Graff-Radford, N. R. & Rademakers, R., Mar 2009, In : Brain. 132, 3, p. 583-591 9 p.

Research output: Contribution to journalArticle

270 Scopus citations

Prominent phenotypic variability associated with mutations in Progranulin

Kelley, B. J., Haidar, W., Boeve, B. F., Baker, M., Graff-Radford, N. R., Krefft, T., Frank, A. R., Jack, C. R., Shiung, M., Knopman, D. S., Josephs, K. A., Parashos, S. A., Rademakers, R., Hutton, M., Pickering-Brown, S., Adamson, J., Kuntz, K. M., Dickson, D. W., Parisi, J. E., Smith, G. E. & 2 others, Ivnik, R. J. & Petersen, R. C., May 1 2009, In : Neurobiology of aging. 30, 5, p. 739-751 13 p.

Research output: Contribution to journalArticle

118 Scopus citations

TARDBP 3′-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

Gitcho, M. A., Bigio, E. H., Mishra, M., Johnson, N., Weintraub, S., Mesulam, M., Rademakers, R., Chakraverty, S., Cruchaga, C., Morris, J. C., Goate, A. M. & Cairns, N. J., Nov 1 2009, In : Acta neuropathologica. 118, 5, p. 633-645 13 p.

Research output: Contribution to journalArticle

95 Scopus citations

Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration

Rollinson, S., Rizzu, P., Sikkink, S., Baker, M., Halliwell, N., Snowden, J., Traynor, B. J., Ruano, D., Cairns, N., Rohrer, J. D., Mead, S., Collinge, J., Rossor, M., Akay, E., Guerreiro, R., Rademakers, R., Morrison, K. E., Pastor, P., Alonso, E., Martinez-Lage, P. & 6 others, Graff-Radford, N., Neary, D., Heutink, P., Mann, D. M. A., Van Swieten, J. & Pickering-Brown, S. M., Apr 2009, In : Neurobiology of aging. 30, 4, p. 656-665 10 p.

Research output: Contribution to journalArticle

30 Scopus citations

Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN

Josephs, K. A., Whitwell, J. L., Jack, C. R., Boeve, B. F., Senjem, M. L., Baker, M., Rademakers, R., Ivnik, R. J., Knopman, D. S., Wszolek, Z. K. & Petersen, R. C., Mar 3 2009, In : Neurology. 72, 9, p. 813-820 8 p.

Research output: Contribution to journalArticle

93 Scopus citations
2010

Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin

Kelley, B. J., Haidar, W., Boeve, B. F., Baker, M., Shiung, M., Knopman, D. S., Rademakers, R., Hutton, M., Adamson, J., Kuntz, K. M., Dickson, D. W., Parisi, J. E., Smith, G. E. & Petersen, R. C., Feb 1 2010, In : Archives of neurology. 67, 2, p. 171-177 7 p.

Research output: Contribution to journalArticle

47 Scopus citations

Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly

Dickson, D. W., Baker, M. & Rademakers, R., Apr 1 2010, In : Neurodegenerative Diseases. 7, 1-3, p. 170-174 5 p.

Research output: Contribution to journalArticle

60 Scopus citations

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

Van Deerlin, V. M., Sleiman, P. M. A., Martinez-Lage, M., Chen-Plotkin, A., Wang, L. S., Graff-Radford, N. R., Dickson, D. W., Rademakers, R., Boeve, B. F., Grossman, M., Arnold, S. E., Mann, D. M. A., Pickering-Brown, S. M., Seelaar, H., Heutink, P., Van Swieten, J. C., Murrell, J. R., Ghetti, B., Spina, S., Grafman, J. & 80 others, Hodges, J., Spillantini, M. G., Gilman, S., Lieberman, A. P., Kaye, J. A., Woltjer, R. L., Bigio, E. H., Mesulam, M., Al-Sarraj, S., Troakes, C., Rosenberg, R. N., White, C. L., Ferrer, I., Lladó, A., Neumann, M., Kretzschmar, H. A., Hulette, C. M., Welsh-Bohmer, K. A., Miller, B. L., Alzualde, A., De Munain, A. L., McKee, A. C., Gearing, M., Levey, A. I., Lah, J. J., Hardy, J., Rohrer, J. D., Lashley, T., MacKenzie, I. R. A., Feldman, H. H., Hamilton, R. L., Dekosky, S. T., Van Der Zee, J., Kumar-Singh, S., Van Broeckhoven, C., Mayeux, R., Vonsattel, J. P. G., Troncoso, J. C., Kril, J. J., Kwok, J. B. J., Halliday, G. M., Bird, T. D., Ince, P. G., Shaw, P. J., Cairns, N. J., Morris, J. C., McLean, C. A., Decarli, C., Ellis, W. G., Freeman, S. H., Frosch, M. P., Growdon, J. H., Perl, D. P., Sano, M., Bennett, D. A., Schneider, J. A., Beach, T. G., Reiman, E. M., Woodruff, B. K., Cummings, J., Vinters, H. V., Miller, C. A., Chui, H. C., Alafuzoff, I., Hartikainen, P., Seilhean, D., Galasko, D., Masliah, E., Cotman, C. W., Tũón, M. T., Martínez, M. C. C., Munoz, D. G., Carroll, S. L., Marson, D., Riederer, P. F., Bogdanovic, N., Schellenberg, G. D., Hakonarson, H., Trojanowski, J. Q. & Lee, V. M. Y., Mar 2010, In : Nature Genetics. 42, 3, p. 234-239 6 p.

Research output: Contribution to journalArticle

297 Scopus citations

De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis

DeJesus-Hernandez, M., Kocerha, J., Finch, N., Crook, R., Baker, M., Desaro, P., Johnston, A., Rutherford, N., Wojtas, A., Kennelly, K., Wszolek, Z. K., Graff-Radford, N., Boylan, K. & Rademakers, R., May 1 2010, In : Human mutation. 31, 5, p. E1377-E1389

Research output: Contribution to journalArticle

102 Scopus citations