Cited In for PMID: 21305653

Year	Number of Results
1987	1
2011	3
2012	5
2013	2
2014	2
2015	3
2016	5
2017	5
2018	2
2019	2
2021	1
2024	0

1

Massive parallel amplicon sequencing of the breast cancer genes BRCA1 and BRCA2: opportunities, challenges, and limitations.

De Leeneer K, Hellemans J, De Schrijver J, Baetens M, Poppe B, Van Criekinge W, De Paepe A, Coucke P, Claes K. De Leeneer K, et al. Hum Mutat. 2011 Mar;32(3):335-44. doi: 10.1002/humu.21428. Epub 2011 Feb 8. Hum Mutat. 2011. PMID: 21305653

2

Dealing with Pseudogenes in Molecular Diagnostics in the Next Generation Sequencing Era.

Claes KBM, Rosseel T, De Leeneer K. Claes KBM, et al. Methods Mol Biol. 2021;2324:363-381. doi: 10.1007/978-1-0716-1503-4_22. Methods Mol Biol. 2021. PMID: 34165726 Review.

3

Next-generation sequencing of BRCA1 and BRCA2 genes for rapid detection of germline mutations in hereditary breast/ovarian cancer.

Nicolussi A, Belardinilli F, Mahdavian Y, Colicchia V, D'Inzeo S, Petroni M, Zani M, Ferraro S, Valentini V, Ottini L, Giannini G, Capalbo C, Coppa A. Nicolussi A, et al. PeerJ. 2019 Apr 22;7:e6661. doi: 10.7717/peerj.6661. eCollection 2019. PeerJ. 2019. PMID: 31065452 Free PMC article.

4

Whole-Genome Sequencing in Cancer.

Zhao EY, Jones M, Jones SJM. Zhao EY, et al. Cold Spring Harb Perspect Med. 2019 Mar 1;9(3):a034579. doi: 10.1101/cshperspect.a034579. Cold Spring Harb Perspect Med. 2019. PMID: 29844223 Free PMC article. Review.

5

Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing.

Soares BL, Brant AC, Gomes R, Pastor T, Schneider NB, Ribeiro-Dos-Santos Â, de Assumpção PP, Achatz MIW, Ashton-Prolla P, Moreira MAM. Soares BL, et al. Fam Cancer. 2018 Jul;17(3):387-394. doi: 10.1007/s10689-017-0043-5. Fam Cancer. 2018. PMID: 28932927

6

Comparison of Ion Personal Genome Machine Platforms for the Detection of Variants in BRCA1 and BRCA2.

Hwang SM, Lee KC, Lee MS, Park KU. Hwang SM, et al. Cancer Res Treat. 2018 Jan;50(1):255-264. doi: 10.4143/crt.2017.062. Epub 2017 Apr 7. Cancer Res Treat. 2018. PMID: 28392550 Free PMC article.

7

A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscape.

Castellanos E, Gel B, Rosas I, Tornero E, Santín S, Pluvinet R, Velasco J, Sumoy L, Del Valle J, Perucho M, Blanco I, Navarro M, Brunet J, Pineda M, Feliubadaló L, Capellá G, Lázaro C, Serra E. Castellanos E, et al. Sci Rep. 2017 Jan 4;7:39348. doi: 10.1038/srep39348. Sci Rep. 2017. PMID: 28051113 Free PMC article.

8

Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer.

Feliubadaló L, Tonda R, Gausachs M, Trotta JR, Castellanos E, López-Doriga A, Teulé À, Tornero E, Del Valle J, Gel B, Gut M, Pineda M, González S, Menéndez M, Navarro M, Capellá G, Gut I, Serra E, Brunet J, Beltran S, Lázaro C. Feliubadaló L, et al. Sci Rep. 2017 Jan 4;7:37984. doi: 10.1038/srep37984. Sci Rep. 2017. PMID: 28050010 Free PMC article.

9

Flexible and Scalable Full-Length CYP2D6 Long Amplicon PacBio Sequencing.

Buermans HP, Vossen RH, Anvar SY, Allard WG, Guchelaar HJ, White SJ, den Dunnen JT, Swen JJ, van der Straaten T. Buermans HP, et al. Hum Mutat. 2017 Mar;38(3):310-316. doi: 10.1002/humu.23166. Epub 2017 Jan 18. Hum Mutat. 2017. PMID: 28044414 Free PMC article.

10

Clinical Applications of Next-Generation Sequencing in Cancer Diagnosis.

Sabour L, Sabour M, Ghorbian S. Sabour L, et al. Pathol Oncol Res. 2017 Apr;23(2):225-234. doi: 10.1007/s12253-016-0124-z. Epub 2016 Oct 8. Pathol Oncol Res. 2017. PMID: 27722982 Free article. Review.

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