1866-1947

Journal of Neurodevelopmental Disorders

Springer-Verlag

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

1

Attach ORCID iDs across 97 articles

ORCID iDs strengthen author disambiguation and institutional reporting.

High impact97 DOIs
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Medium impact33 DOIs
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DOIs for this ISSN

Showing the top 5 of 97 DOIs, ordered by correction priority.

# Title Missing Priority Citations
1 Clinical assessment of DSM-IV anxiety disorders in fragile X… (10.1007/s11689-010-9067-y)
Abstract ORCID License
182.95 274
2 The genetic basis of non-syndromic intellectual disability:… (10.1007/s11689-010-9055-2)
Abstract ORCID License
175.68 219
3 Convergent genetic linkage and associations to language, spe… (10.1007/s11689-009-9031-x)
Abstract ORCID License
150.65 101
4 Aging in fragile X syndrome (10.1007/s11689-010-9047-2)
Abstract ORCID License
135.97 64
5 Regulation of molecular pathways in the Fragile X Syndrome:… (10.1007/s11689-011-9087-2)
Abstract ORCID License
135.97 64
6 Language development after cochlear implantation: an epigene… (10.1007/s11689-011-9098-z)
Abstract ORCID License
135.97 64
7 How might stress contribute to increased risk for schizophre… (10.1007/s11689-010-9069-9)
Abstract ORCID License
126.76 48
8 Role for TGF-β superfamily signaling in telencephalic GABAer… (10.1007/s11689-009-9035-6)
Abstract ORCID License
122.51 42
9 A family with autism and rare copy number variants disruptin… (10.1007/s11689-011-9076-5)
Abstract ORCID License
119.33 38
10 Adult reversal of cognitive phenotypes in neurodevelopmental… (10.1007/s11689-009-9018-7)
Abstract ORCID License
117.62 36
11 Does bilateral damage to the human amygdala produce autistic… (10.1007/s11689-010-9056-1)
Abstract ORCID License
111.85 30
12 Enhanced prefrontal serotonin 5-HT1A currents in a mouse mod… (10.1007/s11689-010-9044-5)
Abstract ORCID License
109.68 28
13 Dissection of genetic associations with language-related tra… (10.1007/s11689-011-9091-6)
Abstract ORCID License
109.68 28
14 Regional cortical volumes and congenital heart disease: a MR… (10.1007/s11689-010-9061-4)
Abstract ORCID License
107.35 26
15 Atypical development of the executive attention network in c… (10.1007/s11689-010-9070-3)
Abstract ORCID License
103.52 23
16 Novel method for combined linkage and genome-wide associatio… (10.1007/s11689-011-9072-9)
Abstract ORCID License
97.58 19
17 Rightward hemispheric asymmetries in auditory language corte… (10.1007/s11689-009-9010-2)
Abstract ORCID
88.54 58
18 Maladaptive behaviors are linked with inefficient sleep in i… (10.1007/s11689-010-9048-1)
Abstract ORCID License
78.10 10
19 Reduced conditioned fear response in mice that lack Dlx1 and… (10.1007/s11689-009-9025-8)
Abstract ORCID
75.26 31
20 Combined linkage and linkage disequilibrium analysis of a mo… (10.1007/s11689-010-9063-2)
Abstract ORCID License
75.00 9
21 Common circuit defect of excitatory-inhibitory balance in mo… (10.1007/s11689-009-9023-x)
ORCID
68.57 552
22 Developmental malformation of the corpus callosum: a review… (10.1007/s11689-010-9059-y)
ORCID
58.61 220
23 Somatosensory processing in neurodevelopmental disorders (10.1007/s11689-010-9046-3)
ORCID
58.16 211
24 The pathophysiology of restricted repetitive behavior (10.1007/s11689-009-9019-6)
ORCID
57.14 192
25 A solution to limitations of cognitive testing in children w… (10.1007/s11689-008-9001-8)
ORCID
55.70 168
26 Development and validation of the Arizona Cognitive Test Bat… (10.1007/s11689-010-9054-3)
ORCID
55.10 159
27 Speech delays and behavioral problems are the predominant fe… (10.1007/s11689-009-9037-4)
ORCID
54.97 157
28 Association of oxytocin receptor (OXTR) gene variants with m… (10.1007/s11689-010-9071-2)
ORCID
54.40 149
29 Synaptic Wnt signaling—a contributor to major psychiatric di… (10.1007/s11689-011-9083-6)
ORCID
53.01 131
30 The benefit of directly comparing autism and schizophrenia f… (10.1007/s11689-010-9068-x)
ORCID
52.76 128
31 Prader–Willi syndrome and autism spectrum disorders: an evol… (10.1007/s11689-011-9092-5)
ORCID
50.73 106
32 Replication of CNTNAP2 association with nonword repetition a… (10.1007/s11689-010-9065-0)
ORCID
49.56 95
33 Modulation of dendritic spine development and plasticity by… (10.1007/s11689-009-9027-6)
ORCID
49.33 93
34 Teasing apart the heterogeneity of autism: Same behavior, di… (10.1007/s11689-009-9009-8)
ORCID
48.86 89
35 Targeted treatments for fragile X syndrome (10.1007/s11689-011-9074-7)
ORCID
48.49 86
36 FMR1 premutation and full mutation molecular mechanisms rela… (10.1007/s11689-011-9084-5)
ORCID
47.02 75
37 Choline transporter gene variation is associated with attent… (10.1007/s11689-009-9033-8)
ORCID
45.15 63
38 Anxiety disorders in children with Williams syndrome, their… (10.1007/s11689-009-9003-1)
ORCID
43.90 56
39 DNA methylation, the early-life social environment and behav… (10.1007/s11689-011-9079-2)
ORCID
43.31 53
40 Glutathione pathway gene variation and risk of autism spectr… (10.1007/s11689-011-9077-4)
ORCID
43.11 52
41 Deficient maternal care resulting from immunological stress… (10.1007/s11689-008-9000-9)
ORCID
42.90 51
42 Genetic approaches to understanding the causes of stuttering (10.1007/s11689-011-9090-7)
ORCID
42.47 49
43 Autistic behavior in boys with fragile X syndrome: social ap… (10.1007/s11689-009-9028-5)
ORCID
42.25 48
44 Hippocampus specific iron deficiency alters competition and… (10.1007/s11689-010-9049-0)
ORCID
42.25 48
45 Functional magnetic resonance imaging outcomes from a compre… (10.1007/s11689-009-9004-0)
ORCID
42.03 47
46 Using animal models of enriched environments to inform resea… (10.1007/s11689-010-9053-4)
ORCID
42.03 47
47 Prenatal exposure to β2-adrenergic receptor agonists and ris… (10.1007/s11689-011-9093-4)
ORCID
41.57 45
48 Is theory of mind related to social dysfunction and emotiona… (10.1007/s11689-011-9082-7)
ORCID
41.33 44
49 Modeling rare gene variation to gain insight into the oldest… (10.1007/s11689-009-9020-0)
ORCID
40.84 42
50 Role of MeCP2, DNA methylation, and HDACs in regulating syna… (10.1007/s11689-011-9078-3)
ORCID
40.84 42