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/vufind/Search/Results?lookfor=%22Norsworthy%2C+Penny+J%22&type=Person&sort=year
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PubPharm (25)
1
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease
enthalten in:
Nature genetics
| 2022
von
Holstege, H.
|
Hulsman, M.
|
Charbonnier, C.
| +98
CommentIn: Nat Rev Neurol. 2023 Jan;19(1):3. - PMID 36477429
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2
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as novel risk factors for Alzheimer’s Disease
enthalten in:
bioRxiv.org
| 2022
von
Holstege, H.
|
Hulsman, M.
|
Charbonnier, C.
| +104
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3
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis
enthalten in:
bioRxiv.org
| 2021
von
Norsworthy, P.
|
Thompson, A.
|
Mok, T.
| +8
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4
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis
enthalten in:
Nature communications
| 2020
von
Norsworthy, P.
|
Thompson, A.
|
Mok, T.
| +8
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5
Genetic, physiological and comparative genomic studies of hypertension and insulin resistance in the spontaneously hypertensive rat
enthalten in:
Disease models & mechanisms
| 2017
von
Coan, P.
|
Hummel, O.
|
Garcia Diaz, A.
| +7
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6
Genetic analysis of the cardiac methylome at single nucleotide resolution in a model of human cardiovascular disease
enthalten in:
PLoS genetics
| 2014
von
Johnson, M.
|
Mueller, M.
|
Adamowicz-Brice, M.
| +14
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7
Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing : a population-based study
enthalten in:
BMC medical genetics
| 2014
von
Norsworthy, P.
|
Vandrovcova, J.
|
Thomas, E.
| +11
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8
Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing: a population-based study
enthalten in:
BMC medical genetics
| 2014
von
Norsworthy, P.
|
Vandrovcova, J.
|
Thomas, E.
| +11
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9
Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing: a population-based study
enthalten in:
BMC medical genetics
| 2014
von
Norsworthy, P.
|
Vandrovcova, J.
|
Thomas, E.
| +11
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10
The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemia
enthalten in:
Genetics in medicine : official journal of the American College of Medical Genetics
| 2013
von
Vandrovcova, J.
|
Thomas, E.
|
Atanur, S.
| +9
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Antigens, CD
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