Whelan AJ - Search Results

1

MSI in endometrial carcinoma: absence of MLH1 promoter methylation is associated with increased familial risk for cancers.

Whelan AJ, Babb S, Mutch DG, Rader J, Herzog TJ, Todd C, Ivanovich JL, Goodfellow PJ. Whelan AJ, et al. Int J Cancer. 2002 Jun 10;99(5):697-704. doi: 10.1002/ijc.10429. Int J Cancer. 2002. PMID: 12115503

2

Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.

Buttin BM, Powell MA, Mutch DG, Babb SA, Huettner PC, Edmonston TB, Herzog TJ, Rader JS, Gibb RK, Whelan AJ, Goodfellow PJ. Buttin BM, et al. Among authors: whelan aj. Am J Hum Genet. 2004 Jun;74(6):1262-9. doi: 10.1086/421332. Epub 2004 Apr 19. Am J Hum Genet. 2004. PMID: 15098177 Free PMC article.

3

Clustering of Lynch syndrome malignancies with no evidence for a role of DNA mismatch repair.

Case AS, Zighelboim I, Mutch DG, Babb SA, Schmidt AP, Whelan AJ, Thibodeau SN, Goodfellow PJ. Case AS, et al. Among authors: whelan aj. Gynecol Oncol. 2008 Feb;108(2):438-44. doi: 10.1016/j.ygyno.2007.09.036. Epub 2007 Nov 26. Gynecol Oncol. 2008. PMID: 18022218 Free PMC article.

4

Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for Lynch syndrome.

Zighelboim I, Powell MA, Babb SA, Whelan AJ, Schmidt AP, Clendenning M, Senter L, Thibodeau SN, de la Chapelle A, Goodfellow PJ. Zighelboim I, et al. Among authors: whelan aj. Fam Cancer. 2009;8(4):501-4. doi: 10.1007/s10689-009-9276-2. Epub 2009 Aug 12. Fam Cancer. 2009. PMID: 19672700 Free PMC article.

5

Evaluation of the family history collection process and the accuracy of cancer reporting among a series of women with endometrial cancer.

Ivanovich J, Babb S, Goodfellow P, Mutch D, Herzog T, Rader J, Whelan A. Ivanovich J, et al. Clin Cancer Res. 2002 Jun;8(6):1849-56. Clin Cancer Res. 2002. PMID: 12060627

6

Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability.

Herfarth KK, Kodner IJ, Whelan AJ, Ivanovich JL, Bracamontes JR, Wells SA Jr, Goodfellow PJ. Herfarth KK, et al. Among authors: whelan aj. Genes Chromosomes Cancer. 1997 Jan;18(1):42-9. doi: 10.1002/(sici)1098-2264(199701)18:1<42::aid-gcc5>3.0.co;2-1. Genes Chromosomes Cancer. 1997. PMID: 8993979

7

Atypical clustering of gynecologic malignancies: A family study including molecular analysis of candidate genes.

Cohn DE, Babb S, Whelan AJ, Mutch DG, Herzog TJ, Rader JS, Elbendary A, Goodfellow PJ. Cohn DE, et al. Among authors: whelan aj. Gynecol Oncol. 2000 Apr;77(1):18-25. doi: 10.1006/gyno.1999.5709. Gynecol Oncol. 2000. PMID: 10739686

8

Low frequency of CDKN2 mutation in endometrial carcinomas.

Peiffer SL, Bartsch D, Whelan AJ, Mutch DG, Herzog TJ, Goodfellow PJ. Peiffer SL, et al. Among authors: whelan aj. Mol Carcinog. 1995 Aug;13(4):210-2. doi: 10.1002/mc.2940130403. Mol Carcinog. 1995. PMID: 7646759

9

A practical approach to familial and hereditary colorectal cancer.

Ivanovich JL, Read TE, Ciske DJ, Kodner IJ, Whelan AJ. Ivanovich JL, et al. Among authors: whelan aj. Am J Med. 1999 Jul;107(1):68-77. doi: 10.1016/s0002-9343(99)00168-0. Am J Med. 1999. PMID: 10403355 Review.

10

Cancer and Peutz-Jeghers Syndrome: A Review.

Ivanovich JL, Whelan AJ. Ivanovich JL, et al. Among authors: whelan aj. J Genet Couns. 1997 Jun;6(2):193-206. doi: 10.1023/A:1025616203564. J Genet Couns. 1997. PMID: 26142097

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