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DOIs for this ISSN

Showing the top 5 of 627 DOIs, ordered by correction priority.

#	Title	Missing	Priority	Citations
1	Heterogeneity in clinical sequencing tests marketed for auti… (10.1038/s41525-018-0066-3)	Abstract ORCID	69.90	24
2	Whole-genome sequencing expands diagnostic utility and impro… (10.1038/npjgenmed.2015.12)	ORCID	62.11	304
3	PD-1 transcriptomic landscape across cancers and implication… (10.1038/s41525-025-00465-9)	Abstract ORCID	60.21	15
4	Erratum: Constellation: a tool for rapid, automated phenotyp… (10.1038/npjgenmed.2016.39)	References ORCID	58.80	14
5	Genome-wide characteristics of de novo mutations in autism (10.1038/npjgenmed.2016.27)	ORCID	56.32	178
6	The landscape of driver mutations in cutaneous squamous cell… (10.1038/s41525-021-00226-4)	ORCID	52.07	120
7	Metastatic basal cell carcinoma with amplification of PD-L1:… (10.1038/npjgenmed.2016.37)	ORCID	50.73	106
8	Constellation: a tool for rapid, automated phenotype assignm… (10.1038/npjgenmed.2015.7)	ORCID	50.53	104
9	Please give me a copy of my child’s raw genomic data (10.1038/s41525-021-00175-y)	Abstract ORCID	50.00	9
10	Publisher Correction: Rapid whole genome sequencing impacts… (10.1038/s41525-021-00206-8)	Abstract References	50.00	9
11	Cracking rare disorders: a new minimally invasive RNA-seq pr… (10.1038/s41525-025-00502-7)	Abstract ORCID	50.00	9
12	Quantum computing and the implementation of precision medici… (10.1038/s41525-025-00537-w)	Abstract ORCID	50.00	9
13	Mechanistic signatures of HPV insertions in cervical carcino… (10.1038/npjgenmed.2016.4)	ORCID	49.78	97
14	New insights into structural features and optimal detection… (10.1038/s41525-018-0069-0)	ORCID	48.36	85
15	Preparing for genomic medicine: a real world demonstration o… (10.1038/s41525-017-0017-4)	ORCID	47.98	82
16	Lead toxicity and genetics in Flint, MI (10.1038/npjgenmed.2016.18)	Abstract ORCID	47.71	8
17	Copy number variant analysis improves diagnostic yield in a… (10.1038/s41525-025-00478-4)	Abstract ORCID	47.71	8
18	The importance of copy number variation in congenital heart… (10.1038/npjgenmed.2016.31)	ORCID	47.02	75
19	Phenotypic profiling of CFTR modulators in patient-derived r… (10.1038/s41525-017-0015-6)	ORCID	46.88	74
20	Functional assays provide a robust tool for the clinical ann… (10.1038/npjgenmed.2016.1)	ORCID	46.73	73
21	Targeted long-read sequencing enables higher diagnostic yiel… (10.1038/s41525-025-00477-5)	Abstract ORCID	45.15	7
22	Machine-learning approach identifies a pattern of gene expre… (10.1038/npjgenmed.2016.38)	ORCID	44.81	61
23	The special considerations of gene therapy for mitochondrial… (10.1038/s41525-020-0116-5)	ORCID	44.09	57
24	Incorporating epilepsy genetics into clinical practice: a 36… (10.1038/s41525-018-0052-9)	ORCID	43.51	54
25	Mutation load estimation model as a predictor of the respons… (10.1038/s41525-018-0051-x)	ORCID	43.31	53
26	Inherited breast cancer predisposition in Asians: multigene… (10.1038/npjgenmed.2015.3)	ORCID	42.47	49
27	Noninvasive prenatal testing complicated by maternal maligna… (10.1038/npjgenmed.2015.2)	Abstract ORCID	42.25	6
28	Genome sequencing provides high diagnostic yield and new eti… (10.1038/s41525-025-00521-4)	Abstract ORCID	42.25	6
29	Precision medicine in heritable cancer: when somatic tumour… (10.1038/npjgenmed.2015.6)	ORCID	42.03	47
30	Pathogenic landscape of idiopathic male infertility: new ins… (10.1038/npjgenmed.2016.23)	ORCID	42.03	47
31	Precision drugging of the MAPK pathway in head and neck canc… (10.1038/s41525-022-00293-1)	ORCID	42.03	47
32	Missense-depleted regions in population exomes implicate ras… (10.1038/npjgenmed.2016.36)	ORCID	41.33	44
33	Identification of an immune gene expression signature associ… (10.1038/s41525-018-0054-7)	ORCID	41.33	44
34	Synaptosome microRNAs regulate synapse functions in Alzheime… (10.1038/s41525-022-00319-8)	ORCID	41.33	44
35	User considerations in assessing pharmacogenomic tests and t… (10.1038/s41525-018-0065-4)	ORCID	40.84	42
36	RNA sequencing identifies clonal structure of T-cell reperto… (10.1038/s41525-019-0084-9)	ORCID	40.58	41
37	Responsible sharing of biomedical data and biospecimens via… (10.1038/s41525-018-0057-4)	ORCID	40.32	40
38	Exome-wide study of ankylosing spondylitis demonstrates addi… (10.1038/npjgenmed.2016.8)	ORCID	40.05	39
39	Sharing health-related data: a privacy test? (10.1038/npjgenmed.2016.24)	ORCID	39.49	37
40	FetalQuantSD: accurate quantification of fetal DNA fraction… (10.1038/npjgenmed.2016.13)	ORCID	38.91	35
41	Author Correction: Rapid whole genome sequencing impacts car… (10.1038/s41525-021-00205-9)	Abstract References	38.91	5
42	Distinguishing benign from pathogenic duplications involving… (10.1038/s41525-025-00548-7)	Abstract ORCID	38.91	5
43	A community effort to protect genomic data sharing, collabor… (10.1038/s41525-017-0036-1)	ORCID	37.96	32
44	FDA guidance for next generation sequencing-based testing: b… (10.1038/s41525-018-0067-2)	Abstract	37.96	32
45	The role of genetics in neurodegenerative dementia: a large… (10.1038/s41525-021-00235-3)	ORCID	36.93	29
46	Assessment of clinical workload for general and specialty ge… (10.1038/npjgenmed.2016.10)	ORCID	36.56	28
47	Base resolution maps reveal the importance of 5-hydroxymeth… (10.1038/s41525-017-0007-6)	ORCID	36.56	28
48	HHV-6 encoded small non-coding RNAs define an intermediate a… (10.1038/s41525-018-0064-5)	ORCID	36.56	28
49	Characterizing the pathogenicity of genetic variants: the co… (10.1038/s41525-023-00386-5)	Abstract	36.18	27
50	Genomic medicine in the military (10.1038/npjgenmed.2015.8)	ORCID	35.78	26