PubMed Central (PMC) Search Page
Table representation of search results timeline featuring number of search results per year.
| Year | Number of Results |
|---|---|
| 2001 | 1 |
| 2002 | 1 |
| 2004 | 2 |
| 2005 | 4 |
| 2006 | 10 |
| 2007 | 8 |
| 2008 | 33 |
| 2009 | 61 |
| 2010 | 69 |
| 2011 | 72 |
| 2012 | 66 |
| 2013 | 68 |
| 2014 | 58 |
| 2015 | 74 |
| 2016 | 52 |
| 2017 | 88 |
| 2018 | 88 |
| 2019 | 114 |
| 2020 | 61 |
| 2021 | 51 |
| 2022 | 89 |
| 2023 | 34 |
| 2024 | 38 |
| 2025 | 95 |
| 2026 | 279 |
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Publication date
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Publication stage
These filters represent the three primary types of content included in the PMC archive: 1) content published in a scholarly journal 2) peer-reviewed author manuscripts accepted for publication in a journal and 3) preprint versions of articles collected through the NIH Preprint Pilot, made public prior to peer review
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Collections
The PMC Open Access Subset includes journal articles and preprints that are made available under license terms that allow reuse. Historical back issues refers to digitized content from print journals made available in PMC through the Biomedical Journal Digitization Projects.
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"Hum Mutat"[Journal]
The embargo is the time during which the publisher retains exclusive rights to distribute articles. Those articles are made freely available on the PMC website after the embargo period has ended. Citations for articles under an embargo period will still display in the PMC results list by default. Choose “Exclude” to prevent embargoed articles from displaying in your results.
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Partial Loss of FITM2 Function Causes Hereditary Spastic Paraplegia.
- Salazar-Villacorta A, Bond LM, Kim L, Anagnostopoulou K, Scardamaglia A, Filippakopoulou E, Ververi A, Efthymiou S, Dinopoulos A, Murphy D, Kartanou C, Vrachnos DM, Loupis T, Makrythanasis P, Stefanis L, Karadima G, Koutsis G, Kaliakatsos M, Houlden H, Walther TC, Farese RV.
- Hum Mutat. 2026 Oct 22;2026:5893503. doi: 10.1155/humu/5893503.
- PMCID: PMC13691184
Salazar-Villacorta A, et al.Hum Mutat. 2026.PMCID: PMC13691184 -
CCR5, CD163, CSF1R, and FCGR3A as Candidate Biomarkers Associated With Mitophagy in Atherosclerosis.
- Fu J, Dong Y.
- Hum Mutat. 2026 Oct 22;2026:3810886. doi: 10.1155/humu/3810886.
- PMCID: PMC13689538
Fu J, et al.Hum Mutat. 2026.PMCID: PMC13689538 -
Identification of Immuno-Diagnostic and Therapeutic Markers in Tumors and Inflammatory Diseases Based on Single-Cell and Machine Learning Methods.
- Tang J, Yuan D, Wu Z, Xie Y, Xu J.
- Hum Mutat. 2026 Oct 21;2026:5519367. doi: 10.1155/humu/5519367.
- PMCID: PMC13685496
Tang J, et al.Hum Mutat. 2026.PMCID: PMC13685496 -
Insights Into RP2-Associated Retinopathy: From Molecular Basis to Clinical Translation.
- Bögershausen N, Döring P, Gerhardt M, Fedorenko A, Strohmeyer C, Bayati R, Li Y, Yigit G, Kaygusuz E, Gutiérrez-Gutiérrez O, Gaubert M, Javanmardi B, Boss K, Kowallick A, Krawitz P, Michalakis S, Ueffing M, Zimmermann WH, Hoerauf H, Büning H, Feltgen N, Cyganek L, Wollnik B.
- Hum Mutat. 2026 Oct 17;2026:1839164. doi: 10.1155/humu/1839164.
- PMCID: PMC13676036
Bögershausen N, et al.Hum Mutat. 2026.PMCID: PMC13676036 -
Next-Generation Sequencing to Identify Genetic Causes of Chinese Patients Affected With Non-retinal Developmental Eye Disorders.
- Liu X, Jia R, Zhao Y, Yu S, Xu B, Yang L, Hong J.
- Hum Mutat. 2026 Oct 16;2026:4035027. doi: 10.1155/humu/4035027.
- PMCID: PMC13673294
Liu X, et al.Hum Mutat. 2026.PMCID: PMC13673294 -
Rapid and Sensitive Detection of USP26 Cluster Variants Based on CRISPR/Cas12a.
- Li N, Huo Y, Zhao Y, Liu C, Zhang Z, Chen K, Chen L, Liu X, Lin Z, Sun L, Jiang H, Wang X, Li W.
- Hum Mutat. 2026 Oct 13;2026:5152235. doi: 10.1155/humu/5152235.
- PMCID: PMC13662412
Li N, et al.Hum Mutat. 2026.PMCID: PMC13662412 -
VarSim: A Python Toolkit for HGVS Variant Description Validation, Normalization, and Representation Conversion.
- Sun L, Wang R, Yang J.
- Hum Mutat. 2026 Oct 9;2026:6006096. doi: 10.1155/humu/6006096.
- PMCID: PMC13653078
Sun L, et al.Hum Mutat. 2026.PMCID: PMC13653078 -
Somatic Mutation-Informed Transcriptional Architecture of Hepatocellular Carcinoma: A Multiomics Study Centered on TP53.
- Zhang S, Zhang G, Wang W, Luo H, Chen H.
- Hum Mutat. 2026 Oct 9;2026:2377057. doi: 10.1155/humu/2377057.
- PMCID: PMC13653071
Zhang S, et al.Hum Mutat. 2026.PMCID: PMC13653071 -
Pathogenic Mechanisms of Two Novel Variants in the GJB1 Gene.
- Xiao F, Xu M, Li W, Xu Z, Jiang H, Qu S.
- Hum Mutat. 2026 Oct 9;2026:7388252. doi: 10.1155/humu/7388252.
- PMCID: PMC13651715
Xiao F, et al.Hum Mutat. 2026.PMCID: PMC13651715 -
Xeroderma Pigmentosum Monozygotic Twins: Same Mutation Divergent Clinical Outcomes.
- Dos Santos Júnior JP, Dos Santos MCFC, da Silva LG, da Silva Júnior WJ, Corradi C, Munford V, de Queiroz Balbino V, de Lima Campos T, Menck CFM, de Azevêdo Silva J.
- Hum Mutat. 2026 Oct 7;2026:7247751. doi: 10.1155/humu/7247751.
- PMCID: PMC13643933
Dos Santos Júnior JP, et al.Hum Mutat. 2026.PMCID: PMC13643933