King MC - Search Results

1

Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.

Lewinsohn M, Brown AL, Weinel LM, Phung C, Rafidi G, Lee MK, Schreiber AW, Feng J, Babic M, Chong CE, Lee Y, Yong A, Suthers GK, Poplawski N, Altree M, Phillips K, Jaensch L, Fine M, D'Andrea RJ, Lewis ID, Medeiros BC, Pollyea DA, King MC, Walsh T, Keel S, Shimamura A, Godley LA, Hahn CN, Churpek JE, Scott HS. Lewinsohn M, et al. Among authors: king mc. Blood. 2016 Feb 25;127(8):1017-23. doi: 10.1182/blood-2015-10-676098. Epub 2015 Dec 28. Blood. 2016. PMID: 26712909 Free PMC article.

2

Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1.

Smith TM, Lee MK, Szabo CI, Jerome N, McEuen M, Taylor M, Hood L, King MC. Smith TM, et al. Among authors: king mc. Genome Res. 1996 Nov;6(11):1029-49. doi: 10.1101/gr.6.11.1029. Genome Res. 1996. PMID: 8938427 Free article.

3

BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance, and the possibility of families whose cancer is not attributable to BRCA1 or BRCA2.

Schubert EL, Lee MK, Mefford HC, Argonza RH, Morrow JE, Hull J, Dann JL, King MC. Schubert EL, et al. Among authors: king mc. Am J Hum Genet. 1997 May;60(5):1031-40. Am J Hum Genet. 1997. PMID: 9150150 Free PMC article.

4

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.

Lynch ED, Ostermeyer EA, Lee MK, Arena JF, Ji H, Dann J, Swisshelm K, Suchard D, MacLeod PM, Kvinnsland S, Gjertsen BT, Heimdal K, Lubs H, Møller P, King MC. Lynch ED, et al. Among authors: king mc. Am J Hum Genet. 1997 Dec;61(6):1254-60. doi: 10.1086/301639. Am J Hum Genet. 1997. PMID: 9399897 Free PMC article.

5

SeqHelp: a program to analyze molecular sequences utilizing common computational resources.

Lee MK, Lynch ED, King MC. Lee MK, et al. Among authors: king mc. Genome Res. 1998 Mar;8(3):306-12. doi: 10.1101/gr.8.3.306. Genome Res. 1998. PMID: 9521933 Free PMC article.

6

Single nucleotide polymorphisms (SNPs) in the estrogen receptor gene and breast cancer susceptibility.

Schubert EL, Lee MK, Newman B, King MC. Schubert EL, et al. Among authors: king mc. J Steroid Biochem Mol Biol. 1999 Nov;71(1-2):21-7. doi: 10.1016/s0960-0760(99)00126-0. J Steroid Biochem Mol Biol. 1999. PMID: 10619354

7

A novel sodium bicarbonate cotransporter-like gene in an ancient duplicated region: SLC4A9 at 5q31.

Lipovich L, Lynch ED, Lee MK, King MC. Lipovich L, et al. Among authors: king mc. Genome Biol. 2001;2(4):RESEARCH0011. doi: 10.1186/gb-2001-2-4-research0011. Epub 2001 Mar 22. Genome Biol. 2001. PMID: 11305939 Free PMC article.

8

Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.

Young TL, Ives E, Lynch E, Person R, Snook S, MacLaren L, Cater T, Griffin A, Fernandez B, Lee MK, King MC. Young TL, et al. Among authors: king mc. Hum Mol Genet. 2001 Oct 15;10(22):2509-14. doi: 10.1093/hmg/10.22.2509. Hum Mol Genet. 2001. PMID: 11709538

9

Tamoxifen and breast cancer incidence among women with inherited mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention Trial.

King MC, Wieand S, Hale K, Lee M, Walsh T, Owens K, Tait J, Ford L, Dunn BK, Costantino J, Wickerham L, Wolmark N, Fisher B; National Surgical Adjuvant Breast and Bowel Project. King MC, et al. JAMA. 2001 Nov 14;286(18):2251-6. doi: 10.1001/jama.286.18.2251. JAMA. 2001. PMID: 11710890 Clinical Trial.

10

Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East.

Shahin H, Walsh T, Sobe T, Lynch E, King MC, Avraham KB, Kanaan M. Shahin H, et al. Among authors: king mc. Hum Genet. 2002 Mar;110(3):284-9. doi: 10.1007/s00439-001-0674-2. Epub 2002 Feb 8. Hum Genet. 2002. PMID: 11935342

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