Grant Detail
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GENETICS AND MOLECULAR BIOLOGY OF PARKINSONISM
30 September 1999 - 31 July 2004
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
Total Funding: $ 3,886,270
This grant has a simple philosophy: a powerful method to approach neurodegenerative disease is (1) use molecular genetics to identify the genes involved in their etiology, with the expectation that these genes will mark a biochemical pathway to disease (2) use the techniques of cell biology and transgenics to try and dissect this pathway and to try and develop cellular and animal models of elements of the disease process. In this proposal, we apply these techniques (predominantly) to Lewy Body Parkinson's disease. It is clear that there are more than three genes involved in the etiology: first, the alpha-synuclein gene, second, an as-yet-unidentified gene on chromosomes 2p and third, an as yet unidentified gene on chromosome 4p: both of these latter two genes have been "linked" by this group. In addition to these known and localized genes, many families do not show linkage to any of the known loci, implying that there are others to be found. With this philosophy and progress as "background", we have the following major aims: Project, to clone the gene on chromosome 4p: Project, to clone the gene on chromosome 2p: Project, to make overexpressing wild type and mutant alpha-synuclein mice with the longterm goal of mimicking parts of the human disease process, and "knockout" mice to aid in the understanding of synuclein function. Projects will encompass similar analyses of the ch4p and ch2p genes and their products as they are identified. These projects will be co-ordinated through an Administrative Core and grouped around a Clinical/pathological Core, which will be responsible for family ascertainment and human blood and brain sample collection and for the pathological verification of diagnosis in both family members and in transgenic animals and a Linkage Core which will be responsible for distributing human family material into four "bins": "mutation Known", "ch4p linked" "ch2p linked and "presently unlinked".
132 Resulting Publications
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1.
2012D C Perry; J L Whitwell; B F Boeve; V S Pankratz; D S Knopman; R C Petersen; C R Jack; K A Josephs
European journal of neurology : the official journal of the European Federation of Neurological Societies 2012;19(6):911-7. -
2.
2011Marie-Christine Chartier-Harlin; Justus C Dachsel; Carles Vilariño-Güell; Sarah J Lincoln; Frédéric Leprêtre; Mary M Hulihan; Jennifer Kachergus; Austen J Milnerwood; Lucia Tapia; Mee-Sook Song; et al.
Translation initiator EIF4G1 mutations in familial Parkinson disease.
American journal of human genetics 2011;89(3):398-406. -
3.
2011Roberta Frigerio; Hiroshige Fujishiro; Tae-Beom Ahn; Keith A Josephs; Demetrius M Maraganore; Anthony DelleDonne; Joseph E Parisi; Kevin J Klos; Bradley F Boeve; Dennis W Dickson; et al.
Neurobiology of aging 2011;32(5):857-63. -
4.
2011Rejko Krüger; Manu Sharma; Olaf Riess; Thomas Gasser; Christine Van Broeckhoven; Jessie Theuns; Jan Aasly; Grazia Annesi; Anna Rita Bentivoglio; Alexis Brice; et al.
Neurobiology of aging 2011;32(3):548.e9-18. -
5.
2011C Vilariño-Güell; A I Soto-Ortolaza; A Rajput; D C Mash; S Papapetropoulos; R Pahwa; K E Lyons; R J Uitti; Z K Wszolek; D W Dickson; et al.
MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy.
Neurology 2011;76(7):670-2. -
6.
2011N Finch; M M Carrasquillo; M Baker; N J Rutherford; G Coppola; M Dejesus-Hernandez; R Crook; T Hunter; R Ghidoni; L Benussi; et al.
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.
Neurology 2011;76(5):467-74. -
7.
2011Kenya Nishioka; Owen A Ross; Carles Vilariño-Güell; Stephanie A Cobb; Jennifer M Kachergus; David M A Mann; Julie Snowden; Anna M T Richardson; David Neary; Christopher A Robinson; et al.
Glucocerebrosidase mutations in diffuse Lewy body disease.
Parkinsonism & related disorders 2011;17(1):55-7. -
8.
2010H L Melrose; J C Dächsel; B Behrouz; S J Lincoln; M Yue; K M Hinkle; C B Kent; E Korvatska; J P Taylor; L Witten; et al.
Neurobiology of disease 2010;40(3):503-17. -
9.
2010J L Whitwell; C R Jack; B F Boeve; J E Parisi; J E Ahlskog; D A Drubach; M L Senjem; D S Knopman; R C Petersen; D W Dickson; et al.
Imaging correlates of pathology in corticobasal syndrome.
Neurology 2010;75(21):1879-87. -
10.
2010Brittany N Dugger; Dennis W Dickson
Acta neuropathologica 2010;120(5):633-9. -
11.
2010K Kantarci; B F Boeve; Z K Wszolek; R Rademakers; J L Whitwell; M C Baker; M L Senjem; A R Samikoglu; D S Knopman; R C Petersen; et al.
MRS in presymptomatic MAPT mutation carriers: a potential biomarker for tau-mediated pathology.
Neurology 2010;75(9):771-8. -
12.
2010Dennis W Dickson; Zeshan Ahmed; Avi A Algom; Yoshio Tsuboi; Keith A Josephs
Neuropathology of variants of progressive supranuclear palsy.
Current opinion in neurology 2010;23(4):394-400. -
13.
2010Kenya Nishioka; Christian Wider; Carles Vilariño-Güell; Alexandra I Soto-Ortolaza; Sarah J Lincoln; Jennifer M Kachergus; Barbara Jasinska-Myga; Owen A Ross; Alex Rajput; Christopher A Robinson; et al.
Association of alpha-, beta-, and gamma-Synuclein with diffuse lewy body disease.
Archives of neurology 2010;67(8):970-5. -
14.
2010Keith A Josephs; Jennifer L Whitwell; Bradley F Boeve; David S Knopman; Ronald C Petersen; William T Hu; Joseph E Parisi; Dennis W Dickson; Clifford R Jack
Anatomical differences between CBS-corticobasal degeneration and CBS-Alzheimer's disease.
Movement disorders : official journal of the Movement Disorder Society 2010;25(9):1246-52. -
15.
2010Anna Wypijewska; Jolanta Galazka-Friedman; Erika R Bauminger; Zbigniew K Wszolek; Katherine J Schweitzer; Dennis W Dickson; Andrzej Jaklewicz; Danek Elbaum; Andrzej Friedman
Iron and reactive oxygen species activity in parkinsonian substantia nigra.
Parkinsonism & related disorders 2010;16(5):329-33. -
16.
2010K J Schweitzer; P Foroutan; D W Dickson; D F Broderick; U Klose; D Berg; Z K Wszolek; S C Grant
A novel approach to dementia: high-resolution 1H MRI of the human hippocampus performed at 21.1 T.
Neurology 2010;74(20):1654. -
17.
2010J L Whitwell; R Avula; M L Senjem; K Kantarci; S D Weigand; A Samikoglu; H A Edmonson; P Vemuri; D S Knopman; B F Boeve; et al.
Gray and white matter water diffusion in the syndromic variants of frontotemporal dementia.
Neurology 2010;74(16):1279-87. -
18.
2010Anhar Hassan; Jennifer L Whitwell; Bradley F Boeve; Clifford R Jack; Joseph E Parisi; Dennis W Dickson; Keith A Josephs
Symmetric corticobasal degeneration (S-CBD).
Parkinsonism & related disorders 2010;16(3):208-14. -
19.
2010Justus C Dachsel; Kenya Nishioka; Carles Vilariño-Güell; Sarah J Lincoln; Alexandra I Soto-Ortolaza; Jennifer Kachergus; Kelly M Hinkle; Michael G Heckman; Barbara Jasinska-Myga; Julie P Taylor; et al.
Heterodimerization of Lrrk1-Lrrk2: Implications for LRRK2-associated Parkinson disease.
Mechanisms of ageing and development 2010;131(3):210-4. -
20.
2010Owen A Ross; Carles Vilariño-Güell; Zbigniew K Wszolek; Matthew J Farrer; Dennis W Dickson
Reply to: SNCA variants are associated with increased risk of multiple system atrophy.
Annals of neurology 2010;67(3):414-5. -
21.
2010Christian Wider; Justus C Dachsel; Matthew J Farrer; Dennis W Dickson; Yoshio Tsuboi; Zbigniew K Wszolek
Elucidating the genetics and pathology of Perry syndrome.
Journal of the neurological sciences 2010;289(1-2):149-54. -
22.
2010Jennifer Molano; Bradley Boeve; Tanis Ferman; Glenn Smith; Joseph Parisi; Dennis Dickson; David Knopman; Neill Graff-Radford; Yonas Geda; John Lucas; et al.
Brain : a journal of neurology 2010;133(Pt 2):540-56. -
23.
2010Dennis W Dickson; Hirotake Uchikado; Hiroshige Fujishiro; Yoshio Tsuboi
Evidence in favor of Braak staging of Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2010;25 Suppl 1():S78-82. -
24.
2010Dennis W Dickson; Matthew Baker; Rosa Rademakers
Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly.
Neuro-degenerative diseases 2010;7(1-3):170-4. -
25.
2010Christian Wider; Dennis W Dickson; Zbigniew K Wszolek
Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation.
Neuro-degenerative diseases 2010;7(1-3):175-9. -
26.
2010Wen-Lang Lin; Zbigniew K Wszolek; Dennis W Dickson
International journal of clinical and experimental pathology 2010;3(7):665-74. -
27.
2009Dennis W Dickson; Hiroshige Fujishiro; Carolyn Orr; Anthony DelleDonne; Keith A Josephs; Roberta Frigerio; Melinda Burnett; Joseph E Parisi; Kevin J Klos; J Eric Ahlskog
Neuropathology of non-motor features of Parkinson disease.
Parkinsonism & related disorders 2009;15 Suppl 3():S1-5. -
28.
2009K A Josephs; J L Whitwell; D S Knopman; B F Boeve; P Vemuri; M L Senjem; J E Parisi; R J Ivnik; D W Dickson; R C Petersen; et al.
Two distinct subtypes of right temporal variant frontotemporal dementia.
Neurology 2009;73(18):1443-50. -
29.
2009Wen-Lang Lin; Monica Castanedes-Casey; Dennis W Dickson
Journal of neuropathology and experimental neurology 2009;68(11):1167-76. -
30.
2009Christian Wider; Sarah Lincoln; Justus C Dachsel; Gregory Kapatos; Michael G Heckman; Nancy N Diehl; Spiridon Papapetropoulos; Deborah Mash; Alex Rajput; Ali H Rajput; et al.
GCH1 expression in human cerebellum from healthy individuals is not gender dependent.
Neuroscience letters 2009;462(1):73-5. -
31.
2009Keith A Josephs; Alex Stroh; Brittany Dugger; Dennis W Dickson
Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes.
Acta neuropathologica 2009;118(3):349-58. -
32.
2009Roberta Frigerio; Hiroshige Fujishiro; Demetrius M Maraganore; Kevin J Klos; Anthony DelleDonne; Michael G Heckman; Julia E Crook; Keith A Josephs; Joseph E Parisi; Bradley F Boeve; et al.
Comparison of risk factor profiles in incidental Lewy body disease and Parkinson disease.
Archives of neurology 2009;66(9):1114-9. -
33.
2009Matthew J Farrer; Lindsey N Williams; Avi A Algom; Jennifer Kachergus; Mary M Hulihan; Owen A Ross; Alex Rajput; Spiridon Papapetropoulos; Deborah C Mash; Dennis W Dickson
Glucosidase-beta variations and Lewy body disorders.
Parkinsonism & related disorders 2009;15(6):414-6. -
34.
2009C Vilariño-Güell; C Wider; A I Soto-Ortolaza; S A Cobb; J M Kachergus; B H Keeling; J C Dachsel; M M Hulihan; D W Dickson; Z K Wszolek; et al.
Characterization of DCTN1 genetic variability in neurodegeneration.
Neurology 2009;72(23):2024-8. -
35.
2009C Wider; J A Van Gerpen; S DeArmond; E A Shuster; D W Dickson; Z K Wszolek
Leukoencephalopathy with spheroids (HDLS) and pigmentary leukodystrophy (POLD): a single entity?
Neurology 2009;72(22):1953-9. -
36.
2009Christian Wider; Dennis W Dickson; A Jon Stoessl; Yoshio Tsuboi; Françoise Chapon; Ludwig Gutmann; Bernard Lechevalier; Donald B Calne; David A Personett; Mary Hulihan; et al.
Pallidonigral TDP-43 pathology in Perry syndrome.
Parkinsonism & related disorders 2009;15(4):281-6. -
37.
2009Christian Wider; Dennis W Dickson; Katherine J Schweitzer; Daniel F Broderick; Zbigniew K Wszolek
Familial idiopathic basal ganglia calcification: a challenging clinical-pathological correlation.
Journal of neurology 2009;256(5):839-42. -
38.
2009J L Whitwell; C R Jack; B F Boeve; M L Senjem; M Baker; R Rademakers; R J Ivnik; D S Knopman; Z K Wszolek; R C Petersen; et al.
Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN.
Neurology 2009;72(9):813-20. -
39.
2009Carles Vilariño-Güell; Alexandra I Soto; Sarah J Lincoln; Samia Ben Yahmed; Mounir Kefi; Michael G Heckman; Mary M Hulihan; Hua Chai; Nancy N Diehl; Rim Amouri; et al.
ATP13A2 variability in Parkinson disease.
Human mutation 2009;30(3):406-10. -
40.
2009A C Ludolph; J Kassubek; B G Landwehrmeyer; E Mandelkow; E-M Mandelkow; D J Burn; D Caparros-Lefebvre; K A Frey; J G de Yebenes; T Gasser; et al.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2009;16(3):297-309. -
41.
2009Christian Wider; Justus C Dachsel; Alexandra I Soto; Michael G Heckman; Nancy N Diehl; Mei Yue; Sarah Lincoln; Jan O Aasly; Kristoffer Haugarvoll; John Q Trojanowski; et al.
Movement disorders : official journal of the Movement Disorder Society 2009;24(3):455-9. -
42.
2009Matthew J Farrer; Mary M Hulihan; Jennifer M Kachergus; Justus C Dächsel; A Jon Stoessl; Linda L Grantier; Susan Calne; Donald B Calne; Bernard Lechevalier; Francoise Chapon; et al.
DCTN1 mutations in Perry syndrome.
Nature genetics 2009;41(2):163-5. -
43.
2009Dennis W Dickson
Neuropathology of non-Alzheimer degenerative disorders.
International journal of clinical and experimental pathology 2009;3(1):1-23. -
44.
2008Rosa Rademakers; Jason L Eriksen; Matt Baker; Todd Robinson; Zeshan Ahmed; Sarah J Lincoln; Nicole Finch; Nicola J Rutherford; Richard J Crook; Keith A Josephs; et al.
Human molecular genetics 2008;17(23):3631-42. -
45.
2008J A Van Gerpen; C Wider; D F Broderick; D W Dickson; L A Brown; Z K Wszolek
Insights into the dynamics of hereditary diffuse leukoencephalopathy with axonal spheroids.
Neurology 2008;71(12):925-9. -
46.
2008Peizhou Jiang; Li-wen Ko; Karen R Jansen; Todd E Golde; Shu-Hui Yen
Using leucine zipper to facilitate alpha-synuclein assembly.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2008;22(9):3165-74. -
47.
2008Hiroshige Fujishiro; Tae-Beom Ahn; Roberta Frigerio; Anthony DelleDonne; Keith A Josephs; Joseph E Parisi; J Eric Ahlskog; Dennis W Dickson
Glial cytoplasmic inclusions in neurologically normal elderly: prodromal multiple system atrophy?
Acta neuropathologica 2008;116(3):269-75. -
48.
2008Wen-Lang Lin; Dennis W Dickson
Acta neuropathologica 2008;116(2):205-13. -
49.
2008Anthony DelleDonne; Kevin J Klos; Hiroshige Fujishiro; Zeshan Ahmed; Joseph E Parisi; Keith A Josephs; Roberta Frigerio; Melinda Burnett; Zbigniew K Wszolek; Ryan J Uitti; et al.
Incidental Lewy body disease and preclinical Parkinson disease.
Archives of neurology 2008;65(8):1074-80. -
50.
2008K Markopoulou; D W Dickson; R D McComb; Z K Wszolek; L Katechalidou; L Avery; M S Stansbury; B A Chase
Acta neuropathologica 2008;116(1):25-35. -
51.
2008Hiroshige Fujishiro; Yoshio Tsuboi; Wen-Lang Lin; Hirotake Uchikado; Dennis W Dickson
Acta neuropathologica 2008;116(1):17-24. -
52.
2008Leslie A Rudzinski; Rita M Fletcher; Dennis W Dickson; Richard Crook; Michael L Hutton; Jennifer Adamson; Neill R Graff-Radford
Alzheimer disease and associated disorders 2008;22(3):299-307. -
53.
2008Hiroshige Fujishiro; Tanis J Ferman; Bradley F Boeve; Glenn E Smith; Neill R Graff-Radford; Ryan J Uitti; Zbigniew K Wszolek; David S Knopman; Ronald C Petersen; Joseph E Parisi; et al.
Journal of neuropathology and experimental neurology 2008;67(7):649-56. -
54.
2008Hiroshige Fujishiro; Roberta Frigerio; Melinda Burnett; Kevin J Klos; Keith A Josephs; Anthony Delledonne; Joseph E Parisi; J Eric Ahlskog; Dennis W Dickson
Movement disorders : official journal of the Movement Disorder Society 2008;23(8):1085-92. -
55.
2008K A Josephs; J L Whitwell; D S Knopman; W T Hu; D A Stroh; M Baker; R Rademakers; B F Boeve; J E Parisi; G E Smith; et al.
Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotype.
Neurology 2008;70(19 Pt 2):1850-7. -
56.
2008K Haugarvoll; R Rademakers; J M Kachergus; K Nuytemans; O A Ross; J M Gibson; E-K Tan; C Gaig; E Tolosa; S Goldwurm; et al.
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.
Neurology 2008;70(16 Pt 2):1456-60. -
57.
2008Dennis W Dickson; Hiroshige Fujishiro; Anthony DelleDonne; Joshua Menke; Zeshan Ahmed; Kevin J Klos; Keith A Josephs; Roberta Frigerio; Melinda Burnett; Joseph E Parisi; et al.
Evidence that incidental Lewy body disease is pre-symptomatic Parkinson's disease.
Acta neuropathologica 2008;115(4):437-44. -
58.
2008Zeshan Ahmed; Keith A Josephs; John Gonzalez; Anthony DelleDonne; Dennis W Dickson
Brain : a journal of neurology 2008;131(Pt 2):460-72. -
59.
2008Dennis W Dickson
TDP-43 immunoreactivity in neurodegenerative disorders: disease versus mechanism specificity.
Acta neuropathologica 2008;115(1):147-9. -
60.
2008Catalina Amador-Ortiz; Dennis W Dickson
Neuropathology of hippocampal sclerosis.
Handbook of clinical neurology 2008;89():569-72. -
61.
2008Nicola J Rutherford; Yong-Jie Zhang; Matt Baker; Jennifer M Gass; Nicole A Finch; Ya-Fei Xu; Heather Stewart; Brendan J Kelley; Karen Kuntz; Richard J P Crook; et al.
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.
PLoS genetics 2008;4(9):e1000193. -
62.
2007Keith A Josephs; Dennis W Dickson
Hippocampal sclerosis in tau-negative frontotemporal lobar degeneration.
Neurobiology of aging 2007;28(11):1718-22. -
63.
2007B F Boeve; M H Silber; C B Saper; T J Ferman; D W Dickson; J E Parisi; E E Benarroch; J E Ahlskog; G E Smith; R C Caselli; et al.
Pathophysiology of REM sleep behaviour disorder and relevance to neurodegenerative disease.
Brain : a journal of neurology 2007;130(Pt 11):2770-88. -
64.
2007Rosa Rademakers; Matt Baker; Jennifer Gass; Jennifer Adamson; Edward D Huey; Parastoo Momeni; Salvatore Spina; Giovanni Coppola; Anna M Karydas; Heather Stewart; et al.
Lancet neurology 2007;6(10):857-68. -
65.
2007Veerle Bogaerts; Sebastiaan Engelborghs; Samir Kumar-Singh; Dirk Goossens; Barbara Pickut; Julie van der Zee; Kristel Sleegers; Karin Peeters; Jean-Jacques Martin; Jurgen Del-Favero; et al.
A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder.
Brain : a journal of neurology 2007;130(Pt 9):2277-91. -
66.
2007Sarah J Lincoln; Owen A Ross; Nicole M Milkovic; Dennis W Dickson; Alex Rajput; Christopher A Robinson; Spiridon Papapetropoulos; Deborah C Mash; Matthew J Farrer
Quantitative PCR-based screening of alpha-synuclein multiplication in multiple system atrophy.
Parkinsonism & related disorders 2007;13(6):340-2. -
67.
2007Kristoffer Haugarvoll; Zbigniew K Wszolek; Michael Hutton
The genetics of frontotemporal dementia.
Neurologic clinics 2007;25(3):697-715, vi. -
68.
2007H L Melrose; C B Kent; J P Taylor; J C Dachsel; K M Hinkle; S J Lincoln; S S Mok; J G Culvenor; C L Masters; G M Tyndall; et al.
Neuroscience 2007;147(4):1047-58. -
69.
2007Zeshan Ahmed; Gerry Shaw; Ved P Sharma; Cui Yang; Eileen McGowan; Dennis W Dickson
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2007;55(7):687-700. -
70.
2007Dennis W Dickson; Keith A Josephs; Catalina Amador-Ortiz
TDP-43 in differential diagnosis of motor neuron disorders.
Acta neuropathologica 2007;114(1):71-9. -
71.
2007Justus C Dächsel; Owen A Ross; Ignacio F Mata; Jennifer Kachergus; Mathias Toft; Ashley Cannon; Matt Baker; Jennifer Adamson; Mike Hutton; Dennis W Dickson; et al.
Acta neuropathologica 2007;113(5):601-6. -
72.
2007Catalina Amador-Ortiz; Wen-Lang Lin; Zeshan Ahmed; David Personett; Peter Davies; Ranjan Duara; Neill R Graff-Radford; Michael L Hutton; Dennis W Dickson
TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease.
Annals of neurology 2007;61(5):435-45. -
73.
2007Zdenek Berger; Hanno Roder; Amanda Hanna; Aaron Carlson; Vijayaraghavan Rangachari; Mei Yue; Zbigniew Wszolek; Karen Ashe; Joshua Knight; Dennis Dickson; et al.
Accumulation of pathological tau species and memory loss in a conditional model of tauopathy.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2007;27(14):3650-62. -
74.
2007Chad A Dickey; Adeela Kamal; Karen Lundgren; Natalia Klosak; Rachel M Bailey; Judith Dunmore; Peter Ash; Sareh Shoraka; Jelena Zlatkovic; Christopher B Eckman; et al.
The Journal of clinical investigation 2007;117(3):648-58. -
75.
2007Keith A Josephs; Zeshan Ahmed; Omi Katsuse; Joseph F Parisi; Bradley F Boeve; David S Knopman; Ronald C Petersen; Peter Davies; Ranjan Duara; Neill R Graff-Radford; et al.
Journal of neuropathology and experimental neurology 2007;66(2):142-51. -
76.
2007Jerzy Slowinski; Jake Dominik; Ryan J Uitti; Zeshan Ahmed; Dennis D Dickson; Zbigniew K Wszolek
Frontotemporal dementia and Parkinsonism linked to chromosome 17 with the N279K tau mutation.
Neuropathology : official journal of the Japanese Society of Neuropathology 2007;27(1):73-80. -
77.
2007B F Boeve; D W Dickson; E J Olson; J W Shepard; M H Silber; T J Ferman; J E Ahlskog; E E Benarroch
Sleep medicine 2007;8(1):60-4. -
78.
2007Dennis W Dickson
Linking selective vulnerability to cell death mechanisms in Parkinson's disease.
The American journal of pathology 2007;170(1):16-9. -
79.
2007Zeshan Ahmed; Ian R A Mackenzie; Michael L Hutton; Dennis W Dickson
Progranulin in frontotemporal lobar degeneration and neuroinflammation.
Journal of neuroinflammation 2007;4():7. -
80.
2007Dennis W Dickson; Rosa Rademakers; Michael L Hutton
Progressive supranuclear palsy: pathology and genetics.
Brain pathology (Zurich, Switzerland) 2007;17(1):74-82. -
81.
2007Thomas Kukar; Sonya Prescott; Jason L Eriksen; Vallie Holloway; M Paul Murphy; Edward H Koo; Todd E Golde; Michelle M Nicolle
BMC neuroscience 2007;8():54. -
82.
2006Yona Levites; Karen Jansen; Lisa A Smithson; Rachel Dakin; Vallie M Holloway; Pritam Das; Todd E Golde
The Journal of neuroscience : the official journal of the Society for Neuroscience 2006;26(46):11923-8. -
83.
2006Keith A Josephs; Jennifer L Whitwell; Clifford R Jack; Joseph E Parisi; Dennis W Dickson
Frontotemporal lobar degeneration without lobar atrophy.
Archives of neurology 2006;63(11):1632-8. -
84.
2006A Rajput; D W Dickson; C A Robinson; O A Ross; J C Dächsel; S J Lincoln; S A Cobb; M L Rajput; M J Farrer
Parkinsonism, Lrrk2 G2019S, and tau neuropathology.
Neurology 2006;67(8):1506-8. -
85.
2006Jennifer Gass; Ashley Cannon; Ian R Mackenzie; Bradley Boeve; Matt Baker; Jennifer Adamson; Richard Crook; Stacey Melquist; Karen Kuntz; Ron Petersen; et al.
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
Human molecular genetics 2006;15(20):2988-3001. -
86.
2006John P Anderson; Donald E Walker; Jason M Goldstein; Rian de Laat; Kelly Banducci; Russell J Caccavello; Robin Barbour; Jiping Huang; Kristin Kling; Michael Lee; et al.
The Journal of biological chemistry 2006;281(40):29739-52. -
87.
2006Yasuhiko Baba; John D Putzke; Yoshio Tsuboi; Keith A Josephs; Natalie Thomas; Zbigniew K Wszolek; Dennis W Dickson
Effect of MAPT and APOE on prognosis of progressive supranuclear palsy.
Neuroscience letters 2006;405(1-2):116-9. -
88.
2006Hirotake Uchikado; Wen-Lang Lin; Michael W DeLucia; Dennis W Dickson
Alzheimer disease with amygdala Lewy bodies: a distinct form of alpha-synucleinopathy.
Journal of neuropathology and experimental neurology 2006;65(7):685-97. -
89.
2006Chad A Dickey; Mei Yue; Wen-Lang Lin; Dennis W Dickson; Judith H Dunmore; Wing C Lee; Cynthia Zehr; Gemma West; Songsong Cao; Amber M K Clark; et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2006;26(26):6985-96. -
90.
2006K J Klos; J E Ahlskog; K A Josephs; H Apaydin; J E Parisi; B F Boeve; M W DeLucia; D W Dickson
Alpha-synuclein pathology in the spinal cords of neurologically asymptomatic aged individuals.
Neurology 2006;66(7):1100-2. -
91.
2006Yasuhiko Baba; Bernardino Ghetti; Matthew C Baker; Ryan J Uitti; Michael L Hutton; Keiji Yamaguchi; Thomas Bird; Wenlang Lin; Michael W DeLucia; Dennis W Dickson; et al.
Acta neuropathologica 2006;111(4):300-11. -
92.
2006Hirotake Uchikado; Anthony DelleDonne; Zeshan Ahmed; Dennis W Dickson
Lewy bodies in progressive supranuclear palsy represent an independent disease process.
Journal of neuropathology and experimental neurology 2006;65(4):387-95. -
93.
2006Keith A Josephs; Jayawant N Mandrekar; Dennis W Dickson
Parkinsonism & related disorders 2006;12(2):109-12. -
94.
2006O A Ross; A J Whittle; S A Cobb; M M Hulihan; S J Lincoln; M Toft; M J Farrer; D W Dickson
Lrrk2 R1441 substitution and progressive supranuclear palsy.
Neuropathology and applied neurobiology 2006;32(1):23-5. -
95.
2006Owen A Ross; Mathias Toft; Andrew J Whittle; Joseph L Johnson; Spiridon Papapetropoulos; Deborah C Mash; Irene Litvan; Mark F Gordon; Zbigniew K Wszolek; Matthew J Farrer; et al.
Annals of neurology 2006;59(2):388-93. -
96.
2006Hirotake Uchikado; Anthony DelleDonne; Ryan Uitti; Dennis W Dickson
Coexistence of PSP and MSA: a case report and review of the literature.
Acta neuropathologica 2006;111(2):186-92. -
97.
2006Bradley F Boeve; Siong-Chi Lin; Audrey Strongosky; Dennis W Dickson; Zbigniew K Wszolek
Archives of neurology 2006;63(2):268-72. -
98.
2005Dennis W Dickson; Matthew J Farrer
Tau kinases and Parkinson's disease: guilt by association?
Annals of neurology 2005;58(6):819-20. -
99.
2005A M Pittman; A J Myers; P Abou-Sleiman; H C Fung; M Kaleem; L Marlowe; J Duckworth; D Leung; D Williams; L Kilford; et al.
Journal of medical genetics 2005;42(11):837-46. -
100.
2005Omi Katsuse; Dennis W Dickson
Alzheimer disease and associated disorders 2005;19 Suppl 1():S37-43. -
101.
2005Wendy Noble; Emmanuel Planel; Cindy Zehr; Vicki Olm; Jordana Meyerson; Farhana Suleman; Kate Gaynor; Lili Wang; John LaFrancois; Boris Feinstein; et al.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(19):6990-5. -
102.
2005Hirotake Uchikado; Gerry Shaw; Deng-Shun Wang; Dennis W Dickson
Screening for neurofilament inclusion disease using alpha-internexin immunohistochemistry.
Neurology 2005;64(9):1658-9. -
103.
2005Deng-Shun Wang; Richard B Lipton; Mindy J Katz; Peter Davies; Herman Buschke; Gail Kuslansky; Joe Verghese; Steven G Younkin; Chris Eckman; Dennis W Dickson
Decreased neprilysin immunoreactivity in Alzheimer disease, but not in pathological aging.
Journal of neuropathology and experimental neurology 2005;64(5):378-85. -
104.
2005Yasuhiro Fujino; Deng-Shun Wang; Natalie Thomas; Marisol Espinoza; Peter Davies; Dennis W Dickson
Journal of neuropathology and experimental neurology 2005;64(3):209-14. -
105.
2005Dennis W Dickson
Acta neuropathologica 2005;109(1):14-24. -
106.
2005Zbigniew K Wszołek; Jerzy Słowiński; Maciej Golan; Dennis W Dickson
Frontotemporal dementia and parkinsonism linked to chromosome 17.
Folia neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences 2005;43(4):258-70. -
107.
2004Y Fujino; M W Delucia; P Davies; D W Dickson
Neuropathology and applied neurobiology 2004;30(6):676-82. -
108.
2004M Martinez; A Brice; J R Vaughan; A Zimprich; M M B Breteler; G Meco; A Filla; M J Farrer; C Bétard; J Hardy; et al.
Journal of medical genetics 2004;41(12):900-7. -
109.
2004Alexander Zimprich; Saskia Biskup; Petra Leitner; Peter Lichtner; Matthew Farrer; Sarah Lincoln; Jennifer Kachergus; Mary Hulihan; Ryan J Uitti; Donald B Calne; et al.
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Neuron 2004;44(4):601-7. -
110.
2004Keith A Josephs; Yoshio Tsuboi; Natalie Cookson; Hilary Watt; Dennis W Dickson
Archives of neurology 2004;61(10):1579-84. -
111.
2004H Ohtake; P Limprasert; Y Fan; O Onodera; A Kakita; H Takahashi; L T Bonner; D W Tsuang; I V J Murray; V M-Y Lee; et al.
Beta-synuclein gene alterations in dementia with Lewy bodies.
Neurology 2004;63(5):805-11. -
112.
2004Matt Farrer; Jennifer Kachergus; Lysia Forno; Sarah Lincoln; Deng-Shun Wang; Mary Hulihan; Demetrius Maraganore; Katrina Gwinn-Hardy; Zbigniew Wszolek; Dennis Dickson; et al.
Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications.
Annals of neurology 2004;55(2):174-9. -
113.
2004Alexander Zimprich; Bertram Müller-Myhsok; Matthew Farrer; Petra Leitner; Manu Sharma; Mary Hulihan; Paul Lockhart; Audrey Strongosky; Jennifer Kachergus; Donald B Calne; et al.
American journal of human genetics 2004;74(1):11-9. -
114.
2003Y Tsuboi; Z K Wszolek; N R Graff-Radford; N Cookson; D W Dickson
Neuropathology and applied neurobiology 2003;29(5):503-10. -
115.
2003Keith A Josephs; Dennis W Dickson
Movement disorders : official journal of the Movement Disorder Society 2003;18(9):1018-26. -
116.
2003Demetrius M Maraganore; Mariza de Andrade; Timothy G Lesnick; Matthew J Farrer; James H Bower; John A Hardy; Walter A Rocca
Complex interactions in Parkinson's disease: a two-phased approach.
Movement disorders : official journal of the Movement Disorder Society 2003;18(6):631-6. -
117.
2003Melisa J Baptista; Casey O'Farrell; Sneha Daya; Rili Ahmad; David W Miller; John Hardy; Matthew J Farrer; Mark R Cookson
Journal of neurochemistry 2003;85(4):957-68. -
118.
2003Haydeh Payami; John Nutt; Steven Gancher; Thomas Bird; Melissa Gonzales McNeal; William K Seltzer; Jennifer Hussey; Paul Lockhart; Katrina Gwinn-Hardy; Amanda A Singleton; et al.
SCA2 may present as levodopa-responsive parkinsonism.
Movement disorders : official journal of the Movement Disorder Society 2003;18(4):425-9. -
119.
2003Takashi Ishizawa; Petri Mattila; Peter Davies; Dengshun Wang; Dennis W Dickson
Colocalization of tau and alpha-synuclein epitopes in Lewy bodies.
Journal of neuropathology and experimental neurology 2003;62(4):389-97. -
120.
2003Yoshio Tsuboi; Keith A Josephs; Natalie Cookson; Dennis W Dickson
APOE E4 is a determinant for Alzheimer type pathology in progressive supranuclear palsy.
Neurology 2003;60(2):240-5. -
121.
2002Leonard Petrucelli; Casey O'Farrell; Paul J Lockhart; Melisa Baptista; Kathryn Kehoe; Liselot Vink; Peter Choi; Benjamin Wolozin; Matthew Farrer; John Hardy; et al.
Neuron 2002;36(6):1007-19. -
122.
2002Takashi Ishizawa; Li-wen Ko; Natalie Cookson; Peter Davias; Marisol Espinoza; Dennis W Dickson
Journal of neuropathology and experimental neurology 2002;61(12):1040-7. -
123.
2002John L Goudreau; Demetrius M Maraganore; Matthew J Farrer; Timothy G Lesnick; Andrew B Singleton; James H Bower; John A Hardy; Walter A Rocca
Movement disorders : official journal of the Movement Disorder Society 2002;17(6):1305-11. -
124.
2002Andrew B West; Demetrius Maraganore; Julia Crook; Tim Lesnick; Paul J Lockhart; Kristen M Wilkes; Gregory Kapatos; John A Hardy; Matt J Farrer
Functional association of the parkin gene promoter with idiopathic Parkinson's disease.
Human molecular genetics 2002;11(22):2787-92. -
125.
2002Keith A Josephs; Takashi Ishizawa; Yoshio Tsuboi; Natalie Cookson; Dennis W Dickson
Archives of neurology 2002;59(10):1597-601. -
126.
2002Demetrius M Maraganore; Matthew J Farrer; Shannon K McDonnell; Alexis Elbaz; Daniel J Schaid; John A Hardy; Walter A Rocca
Case-control study of estrogen receptor gene polymorphisms in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2002;17(3):509-12. -
127.
2002Matt Farrer; Lisa Skipper; Marianne Berg; Gina Bisceglio; Melissa Hanson; John Hardy; Amanda Adam; Katrina Gwinn-Hardy; Jan Aasly
The tau H1 haplotype is associated with Parkinson's disease in the Norwegian population.
Neuroscience letters 2002;322(2):83-6. -
128.
2002Hulya Apaydin; J Eric Ahlskog; Joseph E Parisi; Bradley F Boeve; Dennis W Dickson
Parkinson disease neuropathology: later-developing dementia and loss of the levodopa response.
Archives of neurology 2002;59(1):102-12. -
129.
2001C O'Farrell; D D Murphy; L Petrucelli; A B Singleton; J Hussey; M Farrer; J Hardy; D W Dickson; M R Cookson
Transfected synphilin-1 forms cytoplasmic inclusions in HEK293 cells.
Brain research. Molecular brain research 2001;97(1):94-102. -
130.
2001D M Maraganore; D G Hernandez; A B Singleton; M J Farrer; S K McDonnell; M L Hutton; J A Hardy; W A Rocca
Case-Control study of the extended tau gene haplotype in Parkinson's disease.
Annals of neurology 2001;50(5):658-61. -
131.
2001M Farrer; P Chan; R Chen; L Tan; S Lincoln; D Hernandez; L Forno; K Gwinn-Hardy; L Petrucelli; J Hussey; et al.
Lewy bodies and parkinsonism in families with parkin mutations.
Annals of neurology 2001;50(3):293-300. -
132.
2001M Farrer; A Destée; C Levecque; A Singleton; S Engelender; E Becquet; V Mouroux; F Richard; L Defebvre; R Crook; et al.
Genetic analysis of synphilin-1 in familial Parkinson's disease.
Neurobiology of disease 2001;8(2):317-23.
Scientific Context
This section shows information that has been computed by using the fingerprint of the grant, including related publications, related experts and related grants - all with fingerprints representing significant amounts of overlap between their fingerprint and this grant. The red dots indicate whether those experts or terms actually appear within this grant, showing potential and actual connections.
Related Grants
-
1.
Dickson, Dennis W
GENETICS AND MOLECULAR BIOLOGY OF PARKINSONISM
30 September 1999 - 29 September 2004
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
Total Funding: $ 2,454,521
-
2.
Dickson, Dennis William
Genetics and Molecular Biology of Parkinsonism
30 September 1999 - 31 August 2009
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
Total Funding: $ 8,904,777
-
3.
DICKSON, DENNIS WILLIAM
Genetics and Molecular Biology Parkinsonism
1 September 2010 - 31 August 2011
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
Total Funding: $ 116,250
Related Publications
-
1.
1999M Farrer; K Gwinn-Hardy; M Muenter; F W DeVrieze; R Crook; J Perez-Tur; S Lincoln; D Maraganore; C Adler; S Newman; et al.
A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor.
Human molecular genetics 1999;8(1):81-5. -
2.
1994T Lynch; M Sano; K S Marder; K L Bell; N L Foster; R F Defendini; A A Sima; C Keohane; T G Nygaard; S Fahn
Neurology 1994;44(10):1878-84. -
3.
2001V Bonifati; G De Michele; C B Lücking; A Dürr; E Fabrizio; G Ambrosio; N Vanacore; M De Mari; R Marconi; L Capus; et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2001;22(1):51-2.


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