PubMed Central (PMC) Search Page
Table representation of search results timeline featuring number of search results per year.
| Year | Number of Results |
|---|---|
| 1993 | 1 |
| 1994 | 1 |
| 1996 | 1 |
| 1997 | 2 |
| 1999 | 2 |
| 2001 | 2 |
| 2002 | 4 |
| 2003 | 7 |
| 2004 | 9 |
| 2005 | 15 |
| 2006 | 23 |
| 2007 | 32 |
| 2008 | 218 |
| 2009 | 285 |
| 2010 | 310 |
| 2011 | 311 |
| 2012 | 277 |
| 2013 | 356 |
| 2014 | 367 |
| 2015 | 337 |
| 2016 | 253 |
| 2017 | 276 |
| 2018 | 255 |
| 2019 | 250 |
| 2020 | 214 |
| 2021 | 202 |
| 2022 | 229 |
| 2023 | 218 |
| 2024 | 134 |
| 2025 | 130 |
| 2026 | 92 |
-
Publication date
-
-
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
-
-
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.
-
"Hum Mol 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.
-
KATNAL2 dysfunction impairs microtubule dynamics and contributes to syndromic neurodevelopmental disease.
- Sönmezler E, Hız Kurul S, Erez O, Ekinci B, Yaraş T, Binokay L, Karakülah G, Lochmüller H, Horvath R, Yaramış A, Cakan-Akdogan G, Oktay Y.
- Hum Mol Genet. 2026 Oct 13;35(21):ddag102. doi: 10.1093/hmg/ddag102.
- PMCID: PMC13685775
Sönmezler E, et al.Hum Mol Genet. 2026.PMCID: PMC13685775 -
Droplet digital PCR as a first-line detection tool in the genetic diagnosis of vascular anomalies.
- Lane TK, Brown NJ, Green TE, Garza D, de Silva MG, Bennett MF, Tubb C, Macdonald SMW, Gascoigne A, Phillips RJ, Slavin J, D'Arcy C, MacGregor D, Clifford A, Pathmanathan L, Robertson SJ, Bekhor P, Simpson J, Gooley S, Scheffer IE, Berkovic SF, Penington AJ, Hildebrand MS.
- Hum Mol Genet. 2026 Oct 13;35(21):ddag109. doi: 10.1093/hmg/ddag109.
- PMCID: PMC13682581
Lane TK, et al.Hum Mol Genet. 2026.PMCID: PMC13682581 -
The monogenic forms of obesity in Saudi families.
- Almolafikh ST, Alshatwi AA, Orfali R, AlSaud H.
- Hum Mol Genet. 2026 Oct 13;35(21):ddag054. doi: 10.1093/hmg/ddag054.
- PMCID: PMC13679745
Almolafikh ST, et al.Hum Mol Genet. 2026.PMCID: PMC13679745 -
Gene regulatory behaviors of mutant CRX proteins demonstrated with late-stage human retinal organoids.
- Mullin NK, Voigt AP, Lamba DA, Chirco KR.
- Hum Mol Genet. 2026 Oct 13;35(21):ddag107. doi: 10.1093/hmg/ddag107.
- PMCID: PMC13669955
Mullin NK, et al.Hum Mol Genet. 2026.PMCID: PMC13669955 -
Mitochondrial dysfunction, metabolic quiescence and premature senescence in CMT4B3 fibroblasts.
- Zanfardino P, Amati A, Cox S, Agrimi G, Doccini S, Fernández-Silva P, Tullo A, Rosati J, Santorelli FM, Petruzzella V.
- Hum Mol Genet. 2026 Aug 10;35(17):ddag080. doi: 10.1093/hmg/ddag080.
- PMCID: PMC13648011
Zanfardino P, et al.Hum Mol Genet. 2026.PMCID: PMC13648011 -
CRISPR/dCas9-mediated tuning of DMPK transcription reveals a quantitative relationship between toxic repeat RNA expression and MBNL1 activity in myotonic dystrophy.
- Ripken L, Hoekman TD, Willemse M, Troost ML, Kenyon AN, van den Broek WJAA, Wansink DG.
- Hum Mol Genet. 2026 Aug 10;35(17):ddag079. doi: 10.1093/hmg/ddag079.
- PMCID: PMC13648012
Ripken L, et al.Hum Mol Genet. 2026.PMCID: PMC13648012 -
Zebrafish knockout models of atxn1a, atxn1b, and atxn1l reveal distinct and shared phenotypic and transcriptomic alterations.
- Karim A, Keerthisinghe P, Sarasamma S, Ciaburri NA, Giraldez MG, Naidoo K, Orengo JP.
- Hum Mol Genet. 2026 Aug 10;35(17):ddag078. doi: 10.1093/hmg/ddag078.
- PMCID: PMC13648013
Karim A, et al.Hum Mol Genet. 2026.PMCID: PMC13648013 -
N-acetylcysteine suppresses retinal defects in Drosophila models of SNRNP200-associated retinitis pigmentosa.
- Mayer SK, Christensen QH, McCoy-Munger H, Mohar NP, Botero V, Tomchik SM, Rong Y, Drack AV, Wallrath LL.
- Hum Mol Genet. 2026 Aug 10;35(17):ddag077. doi: 10.1093/hmg/ddag077.
- PMCID: PMC13648025
Mayer SK, et al.Hum Mol Genet. 2026.PMCID: PMC13648025 -
A patient-derived mouse model reproduces molecular, neurological, and sleep symptoms of SHINE syndrome.
- Tamir S, Paulose J, Nguyen A, Gadara D, Witt RM, Prasad B, Hogenesch JB.
- Hum Mol Genet. 2026 Jul 28;35(16):ddag065. doi: 10.1093/hmg/ddag065.
- PMCID: PMC13648028
Tamir S, et al.Hum Mol Genet. 2026.PMCID: PMC13648028 -
Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.
- Ehn E, Thonberg H, Nennesmo I, Lindstrand A, Kvarnung M, Graff C.
- Hum Mol Genet. 2026 Jul 28;35(16):ddag072. doi: 10.1093/hmg/ddag072.
- PMCID: PMC13648039
Ehn E, et al.Hum Mol Genet. 2026.PMCID: PMC13648039