2376-7839

Neurology Genetics

Ovid Technologies (Wolters Kluwer) - American Academy of Neurology

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Your prioritized action plan

Ordered by how many DOIs each fix touches — start here, not with every error at once.

1

Add abstracts to 1033 articles

Abstracts are what surface your work in Google Scholar, Dimensions, and OpenAlex.

High impact1033 DOIs
2

Add license metadata to 1033 records

License metadata tells indexers and readers how each article may be reused.

High impact1033 DOIs
3

Attach ORCID iDs across 496 articles

ORCID iDs strengthen author disambiguation and institutional reporting.

Medium impact496 DOIs

DOIs for this ISSN

Showing the top 5 of 1033 DOIs, ordered by correction priority.

# Title Missing Priority Citations
1 <i>KCNQ2</i> encephalopathy (10.1212/nxg.0000000000000096)
Abstract ORCID License
174.48 211
2 The Alzheimer's Disease Sequencing Project: Study design and… (10.1212/nxg.0000000000000194)
Abstract ORCID License
172.25 197
3 Mendelian randomization shows a causal effect of low vitamin… (10.1212/nxg.0000000000000097)
Abstract ORCID License
171.25 191
4 Antisense oligonucleotides (10.1212/nxg.0000000000000323)
Abstract ORCID License
170.56 187
5 Late-onset vs nonmendelian early-onset Alzheimer disease (10.1212/nxg.0000000000000512)
Abstract ORCID License
166.31 164
6 Germline and somatic mutations in the <i>MTOR</i… (10.1212/nxg.0000000000000118)
Abstract ORCID License
162.33 145
7 Diagnostic odyssey of patients with mitochondrial disease (10.1212/nxg.0000000000000230)
Abstract ORCID License
152.20 106
8 <i>GNAO1</i> encephalopathy (10.1212/nxg.0000000000000143)
Abstract ORCID License
150.00 99
9 Homozygous deletion in <i>MICU1</i>… (10.1212/nxg.0000000000000059)
Abstract ORCID License
149.67 98
10 <i>ABCA7</i> frameshift deletion associated with… (10.1212/nxg.0000000000000079)
Abstract ORCID License
148.67 95
11 The Clinical Outcome Study for dysferlinopathy (10.1212/nxg.0000000000000089)
Abstract ORCID License
147.64 92
12 <i>GBA</i> p.T369M substitution in Parkinson dis… (10.1212/nxg.0000000000000104)
Abstract ORCID License
147.64 92
13 Psychometric properties of the Friedreich Ataxia Rating Scal… (10.1212/nxg.0000000000000371)
Abstract ORCID License
147.28 91
14 Clinical and genetic study of hereditary spastic paraplegia… (10.1212/nxg.0000000000000122)
Abstract ORCID License
146.57 89
15 Mutation in <i>POLR3K</i>… (10.1212/nxg.0000000000000289)
Abstract ORCID License
145.84 87
16 Loss-of-function mutations in <i>RAB39B</i>… (10.1212/nxg.0000000000000009)
Abstract ORCID License
145.46 86
17 Multiple sclerosis risk loci and disease severity in 7,125 i… (10.1212/nxg.0000000000000087)
Abstract ORCID License
145.09 85
18 Loss-of-function variants of <i>SCN8A</i>… (10.1212/nxg.0000000000000170)
Abstract ORCID License
144.32 83
19 <i>CHCHD10</i> variant p.(Gly66Val) causes axona… (10.1212/nxg.0000000000000003)
Abstract ORCID License
143.54 81
20 <i>SORL1</i> mutations in early- and late-onset… (10.1212/nxg.0000000000000116)
Abstract ORCID License
140.63 74
21 Brain somatic mutations in <i>SLC35A2</i>… (10.1212/nxg.0000000000000294)
Abstract ORCID License
140.63 74
22 Redefining the phenotype of ALSP and <i>AARS2</i… (10.1212/nxg.0000000000000135)
Abstract ORCID License
140.19 73
23 <i>CDKL5</i> variants (10.1212/nxg.0000000000000200)
Abstract ORCID License
140.19 73
24 Delineating <i>FOXG1</i> syndrome (10.1212/nxg.0000000000000281)
Abstract ORCID License
139.75 72
25 Genome-wide brain DNA methylation analysis suggests epigenet… (10.1212/nxg.0000000000000342)
Abstract ORCID License
139.75 72
26 Epileptic spasms are a feature of <i>DEPDC5</i>… (10.1212/nxg.0000000000000016)
Abstract ORCID License
138.84 70
27 Loss of MUNC13-1 function causes microcephaly, cortical hype… (10.1212/nxg.0000000000000105)
Abstract ORCID License
138.84 70
28 Late-onset Alzheimer disease risk variants mark brain regula… (10.1212/nxg.0000000000000012)
Abstract ORCID License
138.38 69
29 Phenotypic and molecular analyses of primary lateral scleros… (10.1212/01.nxg.0000464294.88607.dd)
Abstract ORCID License
136.96 66
30 Genetic analysis for a shared biological basis between migra… (10.1212/nxg.0000000000000010)
Abstract ORCID License
136.96 66
31 Research conference summary from the 2014 International Task… (10.1212/nxg.0000000000000139)
Abstract ORCID License
136.47 65
32 Clinical features and outcome of 6 new patients carrying de… (10.1212/nxg.0000000000000206)
Abstract ORCID License
134.95 62
33 Defining the spectrum of frontotemporal dementias associated… (10.1212/nxg.0000000000000080)
Abstract ORCID License
133.36 59
34 Expanding genotype/phenotype of neuromuscular diseases by co… (10.1212/nxg.0000000000000015)
Abstract ORCID License
132.81 58
35 Novel genotype-phenotype and MRI correlations in a large coh… (10.1212/nxg.0000000000000279)
Abstract ORCID License
132.26 57
36 Epilepsy with auditory features (10.1212/nxg.0000000000000005)
Abstract ORCID License
131.69 56
37 <i>ANXA11</i> mutations prevail in Chinese ALS p… (10.1212/nxg.0000000000000237)
Abstract ORCID License
131.69 56
38 Practical guidelines to manage discordant situations of… (10.1212/nxg.0000000000000530)
Abstract ORCID License
131.69 56
39 <i>MME</i> mutation in dominant spinocerebellar… (10.1212/nxg.0000000000000094)
Abstract ORCID License
131.11 55
40 Two definite cases of sudden unexpected death in epilepsy in… (10.1212/nxg.0000000000000028)
Abstract ORCID License
129.93 53
41 Clinical and imaging findings in Parkinson disease associate… (10.1212/nxg.0000000000000027)
Abstract ORCID License
129.32 52
42 Epileptic encephalopathy-causing mutations in <i… (10.1212/01.nxg.0000464295.65736.da)
Abstract ORCID License
128.70 51
43 Clinical and genetic features of cervical dystonia in a larg… (10.1212/nxg.0000000000000069)
Abstract ORCID License
128.07 50
44 <i>PURA-</i> Related Developmental and Epileptic… (10.1212/nxg.0000000000000613)
Abstract ORCID License
127.42 49
45 Genotype-structure-phenotype relationships diverge in paralo… (10.1212/nxg.0000000000000303)
Abstract ORCID License
126.76 48
46 Precision therapy for a new disorder of AMPA receptor recycl… (10.1212/nxg.0000000000000130)
Abstract ORCID License
126.09 47
47 Diagnostic utility of exome sequencing in the evaluation of… (10.1212/nxg.0000000000000212)
Abstract ORCID License
126.09 47
48 A gain-of-function mutation in the <i>GRIK2</i>… (10.1212/nxg.0000000000000129)
Abstract ORCID License
125.41 46
49 Germline and somatic mutations in <i>STXBP1</i>… (10.1212/nxg.0000000000000199)
Abstract ORCID License
125.41 46
50 Atrial fibrillation genetic risk differentiates cardioemboli… (10.1212/nxg.0000000000000293)
Abstract ORCID License
125.41 46