Similar articles for PMID: 28415132

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1

Genetic alterations in mesiodens as revealed by targeted next-generation sequencing and gene co-occurrence network analysis.

Kim YY, Hwang J, Kim HS, Kwon HJ, Kim S, Lee JH, Lee JH. Kim YY, et al. Oral Dis. 2017 Oct;23(7):966-972. doi: 10.1111/odi.12680. Epub 2017 May 16. Oral Dis. 2017. PMID: 28415132

2

Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve.

Bonachea EM, Zender G, White P, Corsmeier D, Newsom D, Fitzgerald-Butt S, Garg V, McBride KL. Bonachea EM, et al. BMC Med Genomics. 2014 Sep 26;7:56. doi: 10.1186/1755-8794-7-56. BMC Med Genomics. 2014. PMID: 25260786 Free PMC article.

3

Isolated and Sporadic Human Mesiodens Is Associated with a Synonymous Variant in the ACVR2A Gene.

Jo CW, Lee JH, Song JS, Park MK, Cho SW, Lee JH, Lee HS. Jo CW, et al. Pediatr Dent. 2021 Jan 15;43(1):39-43. Pediatr Dent. 2021. PMID: 33662249

4

Comparison and evaluation of two exome capture kits and sequencing platforms for variant calling.

Zhang G, Wang J, Yang J, Li W, Deng Y, Li J, Huang J, Hu S, Zhang B. Zhang G, et al. BMC Genomics. 2015 Aug 5;16(1):581. doi: 10.1186/s12864-015-1796-6. BMC Genomics. 2015. PMID: 26242175 Free PMC article.

5

Clinical evaluation of panel testing by next-generation sequencing (NGS) for gene mutations in myeloid neoplasms.

Au CH, Wa A, Ho DN, Chan TL, Ma ES. Au CH, et al. Diagn Pathol. 2016 Jan 22;11:11. doi: 10.1186/s13000-016-0456-8. Diagn Pathol. 2016. PMID: 26796102 Free PMC article.

6

Lack of association between PAX6/SOSTDC1/FAM20B gene polymorphisms and mesiodens.

Liu S, Li J, Xu J, Liao S, Chen Y, Zhang R, Tian R, Zhang K. Liu S, et al. BMC Oral Health. 2019 May 27;19(1):90. doi: 10.1186/s12903-019-0788-3. BMC Oral Health. 2019. PMID: 31133012 Free PMC article.

7

Identification of novel mutations of PKD1 gene in Chinese patients with autosomal dominant polycystic kidney disease by targeted next-generation sequencing.

Yang T, Meng Y, Wei X, Shen J, Zhang M, Qi C, Wang C, Liu J, Ma M, Huang S. Yang T, et al. Clin Chim Acta. 2014 Jun 10;433:12-9. doi: 10.1016/j.cca.2014.02.011. Epub 2014 Feb 26. Clin Chim Acta. 2014. PMID: 24582653

8

Integration of Technical, Bioinformatic, and Variant Assessment Approaches in the Validation of a Targeted Next-Generation Sequencing Panel for Myeloid Malignancies.

Thomas M, Sukhai MA, Zhang T, Dolatshahi R, Harbi D, Garg S, Misyura M, Pugh T, Stockley TL, Kamel-Reid S. Thomas M, et al. Arch Pathol Lab Med. 2017 Jun;141(6):759-775. doi: 10.5858/arpa.2016-0547-RA. Epub 2017 Mar 9. Arch Pathol Lab Med. 2017. PMID: 28557600 Free article.

9

Bioinformatic Challenges in Clinical Diagnostic Application of Targeted Next Generation Sequencing: Experience from Pheochromocytoma.

Crona J, Ljungström V, Welin S, Walz MK, Hellman P, Björklund P. Crona J, et al. PLoS One. 2015 Jul 31;10(7):e0133210. doi: 10.1371/journal.pone.0133210. eCollection 2015. PLoS One. 2015. PMID: 26230854 Free PMC article.

10

Clinical validation of targeted next-generation sequencing for inherited disorders.

Yohe S, Hauge A, Bunjer K, Kemmer T, Bower M, Schomaker M, Onsongo G, Wilson J, Erdmann J, Zhou Y, Deshpande A, Spears MD, Beckman K, Silverstein KA, Thyagarajan B. Yohe S, et al. Arch Pathol Lab Med. 2015 Feb;139(2):204-10. doi: 10.5858/arpa.2013-0625-OA. Arch Pathol Lab Med. 2015. PMID: 25611102 Free article.

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