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/vufind/Search/Results?lookfor=%22Valentino%2C+Rebecca+R%22&type=Person&sort=year
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PubPharm (27)
1
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium : a genetic association study
enthalten in:
The Lancet. Neurology
| 2024
von
Valentino, R.
|
Scotton, W.
|
Roemer, S.
| +153
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2
Genome-wide association study identifies
APOE
and
ZMIZ1
variants as mitophagy modifiers in Lewy body disease
enthalten in:
bioRxiv.org
| 2023
von
Hou, X.
|
Heckman, M.
|
Fiesel, F.
| +16
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3
Genome-wide association study identifies APOE and ZMIZ1 variants as mitophagy modifiers in Lewy body disease
enthalten in:
medRxiv : the preprint server for health sciences
| 2023
von
Hou, X.
|
Heckman, M.
|
Fiesel, F.
| +16
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4
Creating the Pick’s disease International Consortium: Association study of
MAPT
H2 haplotype with risk of Pick’s disease
enthalten in:
bioRxiv.org
| 2023
von
Valentino, R.
|
Scotton, W.
|
Roemer, S.
| +138
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5
Creating the Pick's disease International Consortium : Association study of MAPT H2 haplotype with risk of Pick's disease
enthalten in:
medRxiv : the preprint server for health sciences
| 2023
von
Valentino, R.
|
Scotton, W.
|
Roemer, S.
| +98
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6
Mitochondrial haplogroups and cognitive progression in Parkinson's disease
enthalten in:
Brain : a journal of neurology
| 2023
von
Liu, G.
|
Ni, C.
|
Zhan, J.
| +70
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7
Mitochondrial genomic variation in dementia with Lewy bodies : association with disease risk and neuropathological measures
enthalten in:
Acta neuropathologica communications
| 2022
von
Valentino, R.
|
Ramnarine, C.
|
Heckman, M.
| +25
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8
Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures
enthalten in:
Acta Neuropathologica Communications
| 2022
von
Valentino, R.
|
Ramnarine, C.
|
Heckman, M.
| +25
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9
Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures
enthalten in:
Acta Neuropathologica Communications
| 2022
von
Valentino, R.
|
Ramnarine, C.
|
Heckman, M.
| +25
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10
Investigating ELOVL7 coding variants in multiple system atrophy
enthalten in:
Neuroscience letters
| 2021
von
Wernick, A.
|
Walton, R.
|
Soto-Beasley, A.
| +11
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Acta Neuropathologica Communications
4
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3
Acta neuropathologica communications
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3
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The Lancet. Neurology
2
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1
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13
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12
Research Support, N.I.H., Extramural
11
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9
Genetics
8
Neuropathology
7
Research Support, U.S. Gov't, Non-P.H.S.
6
Mitochondrial haplogroups
6
Multiple system atrophy
5
Corticobasal degeneration
4
DNA, Mitochondrial
4
Spinocerebellar ataxia
4
mtDNA
4
tau Proteins
3
Dementia with Lewy-bodies
3
Lewy body disease
3
MAPT
3
MAPT protein, human
3
Mitochondrial DNA
3
Progressive supranuclear palsy
3
Tauopathy
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2024
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2020
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