Monaghan KG - Search Results

1

Associations between smoking, polymorphisms in polycyclic aromatic hydrocarbon (PAH) metabolism and conjugation genes and PAH-DNA adducts in prostate tumors differ by race.

Nock NL, Tang D, Rundle A, Neslund-Dudas C, Savera AT, Bock CH, Monaghan KG, Koprowski A, Mitrache N, Yang JJ, Rybicki BA. Nock NL, et al. Among authors: monaghan kg. Cancer Epidemiol Biomarkers Prev. 2007 Jun;16(6):1236-45. doi: 10.1158/1055-9965.EPI-06-0736. Cancer Epidemiol Biomarkers Prev. 2007. PMID: 17548691 Free PMC article.

2

SRD5A2 and HSD3B2 polymorphisms are associated with prostate cancer risk and aggressiveness.

Neslund-Dudas C, Bock CH, Monaghan K, Nock NL, Yang JJ, Rundle A, Tang D, Rybicki BA. Neslund-Dudas C, et al. Prostate. 2007 Nov 1;67(15):1654-63. doi: 10.1002/pros.20625. Prostate. 2007. PMID: 17823934 Free PMC article.

3

Prostate cancer risk from occupational exposure to polycyclic aromatic hydrocarbons interacting with the GSTP1 Ile105Val polymorphism.

Rybicki BA, Neslund-Dudas C, Nock NL, Schultz LR, Eklund L, Rosbolt J, Bock CH, Monaghan KG. Rybicki BA, et al. Among authors: monaghan kg. Cancer Detect Prev. 2006;30(5):412-22. doi: 10.1016/j.cdp.2006.09.004. Epub 2006 Oct 25. Cancer Detect Prev. 2006. PMID: 17067754 Free PMC article.

4

Mutation analysis of the HFE gene associated with hereditary hemochromatosis in African Americans.

Monaghan KG, Rybicki BA, Shurafa M, Feldman GL. Monaghan KG, et al. Am J Hematol. 1998 Jul;58(3):213-7. doi: 10.1002/(sici)1096-8652(199807)58:3<213::aid-ajh9>3.0.co;2-u. Am J Hematol. 1998. PMID: 9662273 Free article.

5

Cystic Fibrosis testing among Arab-Americans.

Wei S, Feldman GL, Monaghan KG. Wei S, et al. Among authors: monaghan kg. Genet Med. 2006 Apr;8(4):255-8. doi: 10.1097/01.gim.0000214453.74456.f3. Genet Med. 2006. PMID: 16617247 Free article.

6

Cytogenetic and clinical findings in a patient with a deletion of 16q23.1: first report of bilateral cataracts and a 16q deletion.

Monaghan KG, Van Dyke DL, Wiktor A, Feldman GL. Monaghan KG, et al. Am J Med Genet. 1997 Dec 12;73(2):180-3. doi: 10.1002/(sici)1096-8628(1997)73:2<180::aid-ajmg13>3.0.co;2-q. Am J Med Genet. 1997. PMID: 9409869 Review.

7

Prader-Willi-like syndrome in a patient with an Xq23q25 duplication.

Monaghan KG, Van Dyke DL, Feldman GL. Monaghan KG, et al. Am J Med Genet. 1998 Nov 16;80(3):227-31. doi: 10.1002/(sici)1096-8628(19981116)80:3<227::aid-ajmg10>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9843044

8

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.

Crawford DC, Schwartz CE, Meadows KL, Newman JL, Taft LF, Gunter C, Brown WT, Carpenter NJ, Howard-Peebles PN, Monaghan KG, Nolin SL, Reiss AL, Feldman GL, Rohlfs EM, Warren ST, Sherman SL. Crawford DC, et al. Among authors: monaghan kg. Am J Hum Genet. 2000 Feb;66(2):480-93. doi: 10.1086/302762. Am J Hum Genet. 2000. PMID: 10677308 Free PMC article.

9

Mutation analysis of the cystic fibrosis and cationic trypsinogen genes in patients with alcohol-related pancreatitis.

Monaghan KG, Jackson CE, KuKuruga DL, Feldman GL. Monaghan KG, et al. Am J Med Genet. 2000 Sep 11;94(2):120-4. doi: 10.1002/1096-8628(20000911)94:2<120::aid-ajmg4>3.0.co;2-n. Am J Med Genet. 2000. PMID: 10982968

10

Frequency and clinical significance of the S1235R mutation in the cystic fibrosis transmembrane conductance regulator gene: results from a collaborative study.

Monaghan KG, Feldman GL, Barbarotto GM, Manji S, Desai TK, Snow K. Monaghan KG, et al. Am J Med Genet. 2000 Dec 11;95(4):361-5. Am J Med Genet. 2000. PMID: 11186891

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