PubMed Central (PMC) Search Page
Results by year
Table representation of search results timeline featuring number of search results per year.
| Year | Number of Results |
|---|---|
| 1999 | 1 |
| 2000 | 3 |
| 2001 | 4 |
| 2002 | 1 |
| 2003 | 2 |
| 2004 | 1 |
| 2005 | 3 |
| 2006 | 10 |
| 2007 | 7 |
| 2008 | 29 |
| 2009 | 34 |
| 2010 | 35 |
| 2011 | 42 |
| 2012 | 85 |
| 2013 | 74 |
| 2014 | 78 |
| 2015 | 63 |
| 2016 | 84 |
| 2017 | 100 |
| 2018 | 156 |
| 2019 | 148 |
| 2020 | 152 |
| 2021 | 184 |
| 2022 | 96 |
| 2023 | 61 |
| 2024 | 55 |
| 2025 | 53 |
| 2026 | 37 |
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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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"Genet Med"[Journal]
1,598
results
Embargoed Articles:
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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Optical mapping in Black genomes: Distinct LCR22 structures and 22q11.2 deletion syndrome mechanisms.
- Pastor S, Tran O, Lapointe R, Olali AZ, Wallace DC, Morrow B, Zackai EH, McDonald-McGinn DM, Emanuel BS.
- Genet Med. Author manuscript. 2025 Oct 21;28(1):101614. doi: 10.1016/j.gim.2025.101614.
- PMCID: PMC12645408
Pastor S, et al.Genet Med. Author manuscript. 2025.PMCID: PMC12645408 -
Uncovering phenotypic expansion in AXIN2-related disorders through precision animal modeling.
- Aceves-Ewing NM, Lanza DG, Marcogliese PC, Lu D, Hsu CW, Hashimoto H, Gonzalez M, Christiansen AE, Rasmussen TL, Ho AJ, Gaspero A, Sha C, Dickinson ME, Yuan B, Shayota BJ, Pachter S, Hu X, Day-Salvatore DL, Mackay L, Kanca O, Wangler MF, Potocki L, Rosenfeld JA, Lewis RA, Chao HT, Lee B, Blieden L, Wasserman BN, Bax DA, Ragge NK, Lee S; Undiagnosed Diseases Network; Baylor College of Medicine Center for Precision Medicine Models; Yamamoto S, Bellen HJ, Burrage LC, Heaney JD.
- Genet Med. Author manuscript. 2026 Jul 9;28(9):102648. doi: 10.1016/j.gim.2026.102648.
- PMCID: PMC13678866
Aceves-Ewing NM, et al.Genet Med. Author manuscript. 2026.PMCID: PMC13678866 -
Awareness, knowledge, and attitudes toward polygenic risk scores for breast cancer in multiethnic high-risk cohorts of women.
- Freeman JQ, Sun Y, Guo W, Aschebrook-Kilfoy B, Essling C, McEvilly JM, Siljander I, Basdag H, Olopade OI, Huo D.
- Genet Med. Author manuscript. 2025 Oct 10;27(12):101603. doi: 10.1016/j.gim.2025.101603.
- PMCID: PMC12574554
Freeman JQ, et al.Genet Med. Author manuscript. 2025.PMCID: PMC12574554 -
Arriving at a diagnosis: Effective strategies used by the Undiagnosed Diseases Network.
- Hwang S, Brown RM, Baldridge D, Baldwin EE, Beggs AH, Bernstein JA, Blue E, Borja NA, Botto LD, Briere LC, Cassini T, Esteves C, Fieg EL, Jarvik GP, Kobren SN, Levanto MP, Martínez-Agosto JA, Marwaha S, Nelson SF, Rosenfeld JA, Schedl T, Truong TK, Wambach JA, Wheeler MT, Yamamoto S; Undiagnosed Diseases Network; Shashi V, McCray AT, Adams DR, LeBlanc K.
- Genet Med. Author manuscript. 2026 Sep 9;28(11):102718. doi: 10.1016/j.gim.2026.102718. Online ahead of print.
- PMCID: PMC13644579
Hwang S, et al.Genet Med. Author manuscript. 2026.PMCID: PMC13644579 -
A scalable new model of germline cancer genomic care delivery: Assessing psychological outcomes.
- Solomon IB, Boyd P, Xiao Y, Dang KR, Mochizuki A, Currey M, Garcia M, Luong M, Cheung F, Gruber SB, Hampel H, Labib S, Mak A, Qiao R, Tang S, Davey S, Gray SW.
- Genet Med. Author manuscript. 2026 Feb 12;28(5):102537. doi: 10.1016/j.gim.2026.102537.
- PMCID: PMC13638032
Solomon IB, et al.Genet Med. Author manuscript. 2026.PMCID: PMC13638032 -
P-KNN: Joint calibration of multiple pathogenicity prediction tools streamlines variant classification.
- Lin PY, Brandes N.
- Genet Med. Author manuscript. 2026 Aug 26;28(11):102692. doi: 10.1016/j.gim.2026.102692. Online ahead of print.
- PMCID: PMC13587846
Lin PY, et al.Genet Med. Author manuscript. 2026.PMCID: PMC13587846 -
Decision-making criteria in polygenic embryo screening: A survey of reproductive medicine physicians.
- Furrer RA, Gandhi A, Barlevy D, Carmi S, Lencz T, Pereira S, Lázaro-Muñoz G.
- Genet Med. Author manuscript. 2026 Jun 16;28(8):102631. doi: 10.1016/j.gim.2026.102631.
- PMCID: PMC13573636
Furrer RA, et al.Genet Med. Author manuscript. 2026.PMCID: PMC13573636 -
Cost-effectiveness of BRCA1/BRCA2 variant reclassification and recontact for hereditary breast and ovarian cancer in the United States.
- Guzauskas GF, Berger SM, O'Connor R, Kim S, Topper S, Chao E, Horton C, Hoang L, Veenstra DL, Chung WK.
- Genet Med. Author manuscript. 2026 Aug 26;28(11):102697. doi: 10.1016/j.gim.2026.102697. Online ahead of print.
- PMCID: PMC13548783
Guzauskas GF, et al.Genet Med. Author manuscript. 2026.PMCID: PMC13548783 -
Polygenic risk scores in the clinic: Health-system leaders and primary care providers weigh in.
- Trinidad SB, Fullerton SM, Cohn B, Crosslin DR, Jarvik GP.
- Genet Med. Author manuscript. 2025 Sep 4;27(11):101575. doi: 10.1016/j.gim.2025.101575.
- PMCID: PMC12457071
Trinidad SB, et al.Genet Med. Author manuscript. 2025.PMCID: PMC12457071 -
Implementing secondary findings analysis in a genetic and environmental research study.
- Johnston JJ, Sapp JC, Yoo S, Wermers Z, Hernandez S, Motsinger-Reif A, Burkholder A, Fargo D, Emerson JL, Hall JE, Biesecker LG.
- Genet Med. Author manuscript. 2025 Jul 1;27(9):101515. doi: 10.1016/j.gim.2025.101515.
- PMCID: PMC13366468
Johnston JJ, et al.Genet Med. Author manuscript. 2025.PMCID: PMC13366468