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/vufind/Search/Results?lookfor=%22Whitfield%2C+Jerome%22&type=Person&sort=year
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PubPharm (34)
1
Population structure and migration in the Eastern Highlands of Papua New Guinea, a region impacted by the kuru epidemic
enthalten in:
American journal of human genetics
| 2024
von
Quinn, L.
|
Whitfield, J.
|
Alpers, M.
| +9
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2
Robert Hertz, Anthropophagic Practices and Traditional South Fore Mortuary Rites in Papua New Guinea
enthalten in:
Omega
| 2024
von
Whitfield, J.
|
Pako, W.
|
Alpers, M.
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3
Population Structure and Migration in the Eastern Highlands of Papua New Guinea; a Region Impacted by the kuru Epidemic
enthalten in:
bioRxiv.org
| 2022
von
Quinn, L.
|
Moltke, I.
|
Whitfield, J.
| +9
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4
Genome-wide association study identifies risk variants for sporadic Creutzfeldt-Jakob disease in STX6 and GAL3ST1
enthalten in:
bioRxiv.org
| 2020
von
Jones, E.
|
Hummerich, H.
|
Viré, E.
| +62
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5
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease : a genome-wide association study
enthalten in:
The Lancet. Neurology
| 2020
von
Jones, E.
|
Hummerich, H.
|
Viré, E.
| +62
CommentIn: Nat Rev Neurol. 2021 Jan;17(1):5-6. - PMID 33173159
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6
A naturally occurring variant of the human prion protein completely prevents prion disease
enthalten in:
Nature
| 2015
von
Asante, E.
|
Smidak, M.
|
Grimshaw, A.
| +13
CommentIn: Nature. 2015 Jun 25;522(7557):423-4. - PMID 26061767
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7
Rare structural genetic variation in human prion diseases
enthalten in:
Neurobiology of aging
| 2015
von
Lukic, A.
|
Uphill, J.
|
Brown, C.
| +11
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8
Rare structural genetic variation in human prion diseases
enthalten in:
Neurobiology of aging
| 2015
von
Lukic, A.
|
Uphill, J.
|
Brown, C.
| +11
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9
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
enthalten in:
Human molecular genetics
| 2012
von
Mead, S.
|
Uphill, J.
|
Beck, J.
| +18
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10
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
enthalten in:
Human molecular genetics
| 2012
von
Mead, S.
|
Uphill, J.
|
Beck, J.
| +18
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