1933-6896

Prion

Landes Bioscience

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High impact774 DOIs
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DOIs for this ISSN

Showing the top 5 of 773 DOIs, ordered by correction priority.

# Title Missing Priority Citations
1 Amyloid fibrils (10.4161/pri.2.3.7488)
Abstract ORCID License
200.68 473
2 Silks produced by insect labial glands (10.4161/pri.2.4.7489)
Abstract References ORCID License
199.56 98
3 The elaborate structure of spider silk (10.4161/pri.2.4.7490)
Abstract ORCID License
190.99 351
4 Structural polymorphism of Alzheimer Aβ and other amyloid fi… (10.4161/pri.3.2.8859)
Abstract ORCID License
179.58 247
5 The therapeutic potential of chemical chaperones in protein… (10.4161/pri.28938)
Abstract ORCID License
177.69 233
6 The yeast prions [PSI+] and [URE3] are molecular degenerativ… (10.4161/pri.17748)
Abstract References ORCID License
174.82 55
7 Apoptosis Versus Cell Differentiation (10.4161/pri.1.1.4059)
Abstract ORCID License
173.22 203
8 Tunneling nanotubes: A possible highway in the spreading of… (10.1080/19336896.2016.1223003)
Abstract ORCID License
171.75 194
9 Real-time quaking-induced conversion (10.4161/pri.5.3.16893)
Abstract ORCID License
167.85 172
10 Modeling Huntington disease in yeast: Perspectives and futur… (10.4161/pri.18005)
Abstract References ORCID License
167.21 46
11 Dysregulation of neural calcium signaling in Alzheimer disea… (10.4161/pri.21767)
Abstract ORCID License
167.09 168
12 RNA-binding proteins with prion-like domains in ALS and FTLD… (10.4161/pri.5.3.17230)
Abstract ORCID License
163.42 150
13 The Prion Protein Knockout Mouse (10.4161/pri.1.2.4346)
Abstract ORCID License
161.19 140
14 Prion transmission (10.4161/pri.4.4.13678)
Abstract ORCID License
158.80 130
15 Self Assembly of Short Aromatic Peptides into Amyloid Fibril… (10.4161/pri.1.1.4095)
Abstract ORCID License
157.79 126
16 Modulation and elimination of yeast prions by protein chaper… (10.4161/pri.17749)
Abstract References ORCID License
156.82 36
17 <i>E. coli </i>chaperones DnaK, Hsp33 and Spy inhibit bacter… (10.4161/pri.18555)
Abstract References ORCID License
155.63 35
18 The role of genetics in chronic wasting disease of North Ame… (10.4161/pri.19640)
Abstract ORCID License
154.27 113
19 Fibril fragmentation in amyloid assembly and cytotoxicity (10.4161/pri.4.1.11378)
Abstract ORCID License
154.27 113
20 Detection of protease-resistant cervid prion protein in wate… (10.4161/pri.3.3.9819)
Abstract ORCID License
153.40 110
21 Amyloid-β induced signaling by cellular prion protein and Fy… (10.4161/pri.22212)
Abstract ORCID License
152.81 108
22 Alzheimer disease (10.4161/pri.22118)
Abstract ORCID License
151.90 105
23 Grey matter damage in multiple sclerosis (10.4161/pri.23499)
Abstract ORCID License
151.90 105
24 The aggregation of mutant p53 produces prion-like properties… (10.4161/pri.27776)
Abstract ORCID License
148.67 95
25 Functional amyloid (10.4161/pri.4.4.13676)
Abstract ORCID License
147.98 93
26 Variant CJD (10.4161/pri.29237)
Abstract ORCID License
147.28 91
27 New generation QuIC assays for prion seeding activity (10.4161/pri.19430)
Abstract ORCID License
146.93 90
28 Prions in the environment (10.4161/pri.2.4.7951)
Abstract ORCID License
145.09 85
29 The [ <i>RNQ</i> +]… (10.4161/pri.18213)
Abstract References ORCID License
144.72 27
30 The complexity and implications of yeast prion domains (10.4161/pri.18304)
Abstract References ORCID License
144.72 27
31 Early detection of chronic wasting disease prions in urine o… (10.4161/pri.24430)
Abstract ORCID License
143.93 82
32 Implications of the prion-related Q/N domains in TDP-43 and… (10.4161/pri.5.1.14265)
Abstract ORCID License
143.54 81
33 Influence of prion variant and yeast strain variation on pri… (10.4161/pri.17818)
Abstract References ORCID License
143.14 26
34 In vitro aggregation assays for the characterization of α-sy… (10.4161/pri.28125)
Abstract ORCID License
142.32 78
35 The structure of the infectious prion protein (10.4161/pri.28368)
Abstract ORCID License
142.32 78
36 Prion Propagation: The Role of Protein Dynamics (10.4161/pri.1.1.3992)
Abstract References ORCID License
141.50 25
37 Therapy for prion diseases: Insights from the use of RNA int… (10.4161/pri.3.3.9289)
Abstract References ORCID License
141.50 25
38 Prion formation by a yeast GLFG nucleoporin (10.4161/pri.20199)
Abstract ORCID License
141.49 76
39 Prion aggregates transfer through tunneling nanotubes in end… (10.1080/19336896.2015.1025189)
Abstract ORCID License
141.06 75
40 Tunnelling nanotubes (10.4161/pri.3.2.8917)
Abstract ORCID License
141.06 75
41 Prions, prionoids and pathogenic proteins in Alzheimer disea… (10.4161/pri.23061)
Abstract ORCID License
140.19 73
42 Engineering enhanced protein disaggregases for neurodegenera… (10.1080/19336896.2015.1020277)
Abstract ORCID License
139.75 72
43 The metazoan protein disaggregase and amyloid depolymerase s… (10.4161/pri.27531)
Abstract ORCID License
139.30 71
44 Protein Misfolding and Aggregation in Ageing and Disease (10.4161/pri.1.2.4651)
Abstract References ORCID License
138.02 23
45 Modeling ALS and FTLD proteinopathies in yeast: An efficient… (10.4161/pri.17229)
Abstract References ORCID License
138.02 23
46 Grey matter lesions in MS (10.4161/pri.22580)
Abstract ORCID License
137.91 68
47 H-Type Bovine Spongiform Encephalopathy (10.4161/pri.1.1.3828)
Abstract ORCID License
137.44 67
48 The pathology roadmap in Parkinson disease (10.4161/pri.23582)
Abstract ORCID License
137.44 67
49 Prion protein and Alzheimer disease (10.4161/pri.3.4.9980)
Abstract ORCID License
135.97 64
50 Multimodal fluorescence microscopy of prion strain specific… (10.4161/pri.29239)
Abstract ORCID License
135.46 63