Zhang L - Search Results

1

Toward automation of germline variant curation in clinical cancer genetics.

Ravichandran V, Shameer Z, Kemel Y, Walsh M, Cadoo K, Lipkin S, Mandelker D, Zhang L, Stadler Z, Robson M, Offit K, Vijai J. Ravichandran V, et al. Among authors: zhang l. Genet Med. 2019 Sep;21(9):2116-2125. doi: 10.1038/s41436-019-0463-8. Epub 2019 Feb 21. Genet Med. 2019. PMID: 30787465 Free PMC article.

2

cDNA analysis demonstrates that the BRCA2 intronic variant IVS4-12del5 is a deleterious mutation.

Zhang L, Bacares R, Boyar S, Hudis C, Nafa K, Offit K. Zhang L, et al. Mutat Res. 2009 Apr 26;663(1-2):84-9. doi: 10.1016/j.mrfmmm.2008.11.010. Epub 2008 Nov 25. Mutat Res. 2009. PMID: 19070627

3

A rapid and reliable test for BRCA1 and BRCA2 founder mutation analysis in paraffin tissue using pyrosequencing.

Zhang L, Kirchhoff T, Yee CJ, Offit K. Zhang L, et al. J Mol Diagn. 2009 May;11(3):176-81. doi: 10.2353/jmoldx.2009.080137. Epub 2009 Mar 26. J Mol Diagn. 2009. PMID: 19324993 Free PMC article.

4

Germline PALB2 mutation analysis in breast-pancreas cancer families.

Stadler ZK, Salo-Mullen E, Sabbaghian N, Simon JA, Zhang L, Olson SH, Kurtz R, Offit K, Foulkes WD, Robson ME, Tischkowitz M. Stadler ZK, et al. Among authors: zhang l. J Med Genet. 2011 Aug;48(8):523-5. doi: 10.1136/jmg.2010.087379. Epub 2011 Mar 17. J Med Genet. 2011. PMID: 21415078

5

Assessment of the prevalence of de novo mutations in the BRCA1 and BRCA2 genes.

Zhang L, Fleischut MH, Kohut K, Spencer S, Wong K, Stadler ZK, Kauff ND, Offit K, Robson ME. Zhang L, et al. Clin Genet. 2011 Jul;80(1):97-8. doi: 10.1111/j.1399-0004.2011.01691.x. Clin Genet. 2011. PMID: 21649643 No abstract available.

6

De novo CDH1 mutation in a family presenting with early-onset diffuse gastric cancer.

Shah MA, Salo-Mullen E, Stadler Z, Ruggeri JM, Mirander M, Pristyazhnyuk Y, Zhang L. Shah MA, et al. Among authors: zhang l. Clin Genet. 2012 Sep;82(3):283-7. doi: 10.1111/j.1399-0004.2011.01744.x. Epub 2011 Aug 2. Clin Genet. 2012. PMID: 21696387

7

BRCA1 R71K missense mutation contributes to cancer predisposition by increasing alternative transcript levels.

Zhang L, Chen L, Bacares R, Ruggeri JM, Somar J, Kemel Y, Stadler ZK, Offit K. Zhang L, et al. Breast Cancer Res Treat. 2011 Dec;130(3):1051-6. doi: 10.1007/s10549-011-1732-7. Epub 2011 Aug 24. Breast Cancer Res Treat. 2011. PMID: 21863257

8

Unusual DNA mismatch repair-deficient tumors in Lynch syndrome: a report of new cases and review of the literature.

Karamurzin Y, Zeng Z, Stadler ZK, Zhang L, Ouansafi I, Al-Ahmadie HA, Sempoux C, Saltz LB, Soslow RA, O'Reilly EM, Paty PB, Coit DG, Shia J, Klimstra DS. Karamurzin Y, et al. Among authors: zhang l. Hum Pathol. 2012 Oct;43(10):1677-87. doi: 10.1016/j.humpath.2011.12.012. Epub 2012 Apr 17. Hum Pathol. 2012. PMID: 22516243 Review.

9

Juvenile polyposis syndrome presenting with familial gastric cancer and massive gastric polyposis.

Stadler ZK, Salo-Mullen E, Zhang L, Shia J, Bacares R, Power DG, Weiser M, Coit D, Robson ME, Offit K, Schattner M. Stadler ZK, et al. Among authors: zhang l. J Clin Oncol. 2012 Sep 1;30(25):e229-32. doi: 10.1200/JCO.2012.41.7949. Epub 2012 Jul 23. J Clin Oncol. 2012. PMID: 22826269 No abstract available.

10

Secondary mutation in a coding mononucleotide tract in MSH6 causes loss of immunoexpression of MSH6 in colorectal carcinomas with MLH1/PMS2 deficiency.

Shia J, Zhang L, Shike M, Guo M, Stadler Z, Xiong X, Tang LH, Vakiani E, Katabi N, Wang H, Bacares R, Ruggeri J, Boland CR, Ladanyi M, Klimstra DS. Shia J, et al. Among authors: zhang l. Mod Pathol. 2013 Jan;26(1):131-8. doi: 10.1038/modpathol.2012.138. Epub 2012 Aug 24. Mod Pathol. 2013. PMID: 22918162 Free PMC article.

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