Cited In for PMID: 27729835

Year	Number of Results
2016	1
2017	4
2018	5
2019	8
2020	6
2021	4
2022	9
2023	9
2024	3
2025	0

1

Structural Variation of Alu Element and Human Disease.

Kim S, Cho CS, Han K, Lee J. Kim S, et al. Genomics Inform. 2016 Sep;14(3):70-77. doi: 10.5808/GI.2016.14.3.70. Epub 2016 Sep 30. Genomics Inform. 2016. PMID: 27729835 Free PMC article. Review.

2

[Molecular pathological analysis through the ages].

Walker M, Mayr EM, Koppermann ML, Terron A, Wagner Y, Kling C, Pfarr N. Walker M, et al. Pathologie (Heidelb). 2024 May;45(3):173-179. doi: 10.1007/s00292-024-01326-5. Epub 2024 Apr 15. Pathologie (Heidelb). 2024. PMID: 38619582 Free PMC article. Review. German.

3

Long-read sequencing identified a causal structural variant in an exome-negative case and enabled preimplantation genetic diagnosis.

Miao H, Zhou J, Yang Q, Liang F, Wang D, Ma N, Gao B, Du J, Lin G, Wang K, Zhang Q. Miao H, et al. Hereditas. 2018 Sep 28;155:32. doi: 10.1186/s41065-018-0069-1. eCollection 2018. Hereditas. 2018. PMID: 30279644 Free PMC article.

4

An evolving view of copy number variants.

Lauer S, Gresham D. Lauer S, et al. Curr Genet. 2019 Dec;65(6):1287-1295. doi: 10.1007/s00294-019-00980-0. Epub 2019 May 10. Curr Genet. 2019. PMID: 31076843 Review.

5

Novel Gross Deletion Mutations in NTRK1 Gene Associated With Congenital Insensitivity to Pain With Anhidrosis.

Li L, Jia C, Tang Y, Kong Y, Xia Y, Ma L. Li L, et al. Front Pediatr. 2021 Mar 4;9:638190. doi: 10.3389/fped.2021.638190. eCollection 2021. Front Pediatr. 2021. PMID: 33748046 Free PMC article.

6

A Novel Whole Gene Deletion of BCKDHB by Alu-Mediated Non-allelic Recombination in a Chinese Patient With Maple Syrup Urine Disease.

Liu G, Ma D, Hu P, Wang W, Luo C, Wang Y, Sun Y, Zhang J, Jiang T, Xu Z. Liu G, et al. Front Genet. 2018 Apr 24;9:145. doi: 10.3389/fgene.2018.00145. eCollection 2018. Front Genet. 2018. PMID: 29740478 Free PMC article.

7

The Roles of Epigenetics Regulation in Bone Metabolism and Osteoporosis.

Xu F, Li W, Yang X, Na L, Chen L, Liu G. Xu F, et al. Front Cell Dev Biol. 2021 Jan 25;8:619301. doi: 10.3389/fcell.2020.619301. eCollection 2020. Front Cell Dev Biol. 2021. PMID: 33569383 Free PMC article. Review.

8

Human Retrotransposons and Effective Computational Detection Methods for Next-Generation Sequencing Data.

Lee H, Min JW, Mun S, Han K. Lee H, et al. Life (Basel). 2022 Oct 12;12(10):1583. doi: 10.3390/life12101583. Life (Basel). 2022. PMID: 36295018 Free PMC article. Review.

9

DNA methylation of individual repetitive elements in hepatitis C virus infection-induced hepatocellular carcinoma.

Zheng Y, Hlady RA, Joyce BT, Robertson KD, He C, Nannini DR, Kibbe WA, Achenbach CJ, Murphy RL, Roberts LR, Hou L. Zheng Y, et al. Clin Epigenetics. 2019 Oct 21;11(1):145. doi: 10.1186/s13148-019-0733-y. Clin Epigenetics. 2019. PMID: 31639042 Free PMC article.

10

Identification and Mapping of a 2,009-bp DNA Deletion in SERPING1 of a Hereditary Angioedema Patient.

Wong WY, Wong H, Au E, Chan E. Wong WY, et al. Case Rep Genet. 2019 Feb 24;2019:7052062. doi: 10.1155/2019/7052062. eCollection 2019. Case Rep Genet. 2019. PMID: 30923640 Free PMC article.

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Cited In for PMID: 27729835

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