PubMed Central (PMC) Search Page
Table representation of search results timeline featuring number of search results per year.
| Year | Number of Results |
|---|---|
| 1987 | 1 |
| 1988 | 1 |
| 1990 | 2 |
| 1996 | 1 |
| 1999 | 1 |
| 2002 | 1 |
| 2004 | 1 |
| 2005 | 9 |
| 2006 | 12 |
| 2007 | 9 |
| 2008 | 51 |
| 2009 | 51 |
| 2010 | 64 |
| 2011 | 85 |
| 2012 | 59 |
| 2013 | 65 |
| 2014 | 64 |
| 2015 | 45 |
| 2016 | 69 |
| 2017 | 49 |
| 2018 | 57 |
| 2019 | 65 |
| 2020 | 65 |
| 2021 | 79 |
| 2022 | 47 |
| 2023 | 60 |
| 2024 | 52 |
| 2025 | 41 |
| 2026 | 44 |
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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 Genet"[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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A genome-wide association study of cognitive impairment in a Chinese cohort of 1,040 individuals.
- Wang MH, Zhang Y, Sun R, Li F, Zhang T, Gu X, Lou J, Cao L, Su S, Zheng H, Liu C, Chong MKC, Wu WKK, Yu J, Zee BC, Lin J.
- Hum Genet. 2026 Oct 17;145(1):87. doi: 10.1007/s00439-026-02887-6.
- PMCID: PMC13675299
Wang MH, et al.Hum Genet. 2026.PMCID: PMC13675299 -
Gene-based association analysis of depression risk among European ancestry Parkinson's disease patients.
- Wang H, Paul K, Kusters C, Lill CM, Zhou J, Bronstein J, Ritz B.
- Hum Genet. 2026 Oct 17;145(1):88. doi: 10.1007/s00439-026-02877-8.
- PMCID: PMC13675371
Wang H, et al.Hum Genet. 2026.PMCID: PMC13675371 -
Geographic barrier contributed to the diversity of maternal and paternal lineages in New Guinea Island.
- Isshiki M, Soemantri A, Ohtsuka R, Nakazawa M, Ishida T, Ohashi J.
- Hum Genet. 2026 Oct 9;145(1):85. doi: 10.1007/s00439-026-02869-8.
- PMCID: PMC13652891
Isshiki M, et al.Hum Genet. 2026.PMCID: PMC13652891 -
Annual average exposure to ambient air pollution, polygenic risk, and incidence of major chronic diseases: a large-scale prospective cohort study.
- Tian J, Wang S, Chang X, Han Y.
- Hum Genet. 2026 Oct 5;145(1):83. doi: 10.1007/s00439-026-02875-w.
- PMCID: PMC13638686
Tian J, et al.Hum Genet. 2026.PMCID: PMC13638686 -
Mitochondrial dysfunction drives metabolic reprogramming in Gitelman syndrome: insights from proteomics and isogenic modeling.
- Zhang H, Zhao W, Ma L, Yang X, Gao J, Liu X, Xie YG, Hu Y, Luo H, Han J.
- Hum Genet. 2026 Sep 21;145(1):79. doi: 10.1007/s00439-026-02880-z.
- PMCID: PMC13593708
Zhang H, et al.Hum Genet. 2026.PMCID: PMC13593708 -
The Russian FSHD registry: a first look at the cohort.
- Kuchina A, Sherstyukova D, Borovikov A, Soloshenko M, Zernov N, Subbotin D, Dadali E, Sharkova I, Rudenskaya G, Kutsev S, Skoblov M, Murtazina A.
- Hum Genet. 2026 Aug 8;145(1):67. doi: 10.1007/s00439-026-02865-y.
- PMCID: PMC13582244
Kuchina A, et al.Hum Genet. 2026.PMCID: PMC13582244 -
Optical genome mapping improves structural variant detection and characterization in syndromic and neurogenetic disorders.
- Lederbogen RC, Hoffjan S, Köhler C, Thiels C, Mau-Holzmann UA, Singer S, Schreiber S, Purczeld A, Buchert R, Yusenko MV, Nguyen HHP, Gerding WM.
- Hum Genet. 2026 Sep 10;145(1):76. doi: 10.1007/s00439-026-02856-z.
- PMCID: PMC13562348
Lederbogen RC, et al.Hum Genet. 2026.PMCID: PMC13562348 -
Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.
- Hull S, Mero M, Hankey W, Lee K, Sullivan LS, Ayyagari R, Benson MD, Haer-Wigman L, Hufnagel RB, Hussain HMJ, Kämpjärvi K, Sieving PA, Wang M, Wang G, Zeitz C, Lewis RA, Chen R, Worley KC; ClinGen X-linked Inherited Retinal Disease Variant Curation Expert Panel.
- Hum Genet. 2026 Sep 4;145(1):75. doi: 10.1007/s00439-026-02871-0.
- PMCID: PMC13545035
Hull S, et al.Hum Genet. 2026.PMCID: PMC13545035 -
Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.
- Vlaming M, Kiemeney LALM, Koole W, van Oort IM, Bleiker EMA, Ausems MGEM, Frederix GWJ.
- Hum Genet. 2026 Aug 29;145(1):73. doi: 10.1007/s00439-026-02854-1.
- PMCID: PMC13526062
Vlaming M, et al.Hum Genet. 2026.PMCID: PMC13526062 -
From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.
- Szalai R, Till A, Galimurka K, Banfai Z, Zsigmond A, Hadzsiev K.
- Hum Genet. 2026 Aug 29;145(1):72. doi: 10.1007/s00439-026-02867-w.
- PMCID: PMC13526097
Szalai R, et al.Hum Genet. 2026.PMCID: PMC13526097