Eng C - Search Results

1

Investigating the Link between Lynch Syndrome and Breast Cancer.

Sheehan M, Heald B, Yanda C, Kelly ED, Grobmyer S, Eng C, Kalady M, Pederson H. Sheehan M, et al. Among authors: eng c. Eur J Breast Health. 2020 Apr 1;16(2):106-109. doi: 10.5152/ejbh.2020.5198. eCollection 2020 Apr. Eur J Breast Health. 2020. PMID: 32285031 Free PMC article.

2

Severe TMD/AMKL with GATA1 mutation in a stillborn fetus with Down syndrome.

Heald B, Hilden JM, Zbuk K, Norton A, Vyas P, Theil KS, Eng C. Heald B, et al. Among authors: eng c. Nat Clin Pract Oncol. 2007 Jul;4(7):433-8. doi: 10.1038/ncponc0876. Nat Clin Pract Oncol. 2007. PMID: 17597708

3

Familial adenomatous polyposis in a patient with unexplained mental retardation.

Heald B, Moran R, Milas M, Burke C, Eng C. Heald B, et al. Among authors: eng c. Nat Clin Pract Neurol. 2007 Dec;3(12):694-700. doi: 10.1038/ncpneuro0658. Nat Clin Pract Neurol. 2007. PMID: 18046442

4

Frequent gastrointestinal polyps and colorectal adenocarcinomas in a prospective series of PTEN mutation carriers.

Heald B, Mester J, Rybicki L, Orloff MS, Burke CA, Eng C. Heald B, et al. Among authors: eng c. Gastroenterology. 2010 Dec;139(6):1927-33. doi: 10.1053/j.gastro.2010.06.061. Epub 2010 Jun 27. Gastroenterology. 2010. PMID: 20600018 Free PMC article.

5

A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands.

Tan MH, Mester J, Peterson C, Yang Y, Chen JL, Rybicki LA, Milas K, Pederson H, Remzi B, Orloff MS, Eng C. Tan MH, et al. Among authors: eng c. Am J Hum Genet. 2011 Jan 7;88(1):42-56. doi: 10.1016/j.ajhg.2010.11.013. Epub 2010 Dec 30. Am J Hum Genet. 2011. PMID: 21194675 Free PMC article.

6

Defining phenotypes and cancer risk in hyperplastic polyposis syndrome.

Kalady MF, Jarrar A, Leach B, LaGuardia L, O'Malley M, Eng C, Church JM. Kalady MF, et al. Among authors: eng c. Dis Colon Rectum. 2011 Feb;54(2):164-70. doi: 10.1007/DCR.0b013e3181fd4c15. Dis Colon Rectum. 2011. PMID: 21228663

7

Germline mutations in MSR1, ASCC1, and CTHRC1 in patients with Barrett esophagus and esophageal adenocarcinoma.

Orloff M, Peterson C, He X, Ganapathi S, Heald B, Yang YR, Bebek G, Romigh T, Song JH, Wu W, David S, Cheng Y, Meltzer SJ, Eng C. Orloff M, et al. Among authors: eng c. JAMA. 2011 Jul 27;306(4):410-9. doi: 10.1001/jama.2011.1029. JAMA. 2011. PMID: 21791690 Free PMC article.

8

Prospective comparison of family medical history with personal genome screening for risk assessment of common cancers.

Heald B, Edelman E, Eng C. Heald B, et al. Among authors: eng c. Eur J Hum Genet. 2012 May;20(5):547-51. doi: 10.1038/ejhg.2011.224. Epub 2012 Jan 4. Eur J Hum Genet. 2012. PMID: 22215421 Free PMC article.

9

Characterization of the colorectal cancer-associated enhancer MYC-335 at 8q24: the role of rs67491583.

Tuupanen S, Yan J, Turunen M, Gylfe AE, Kaasinen E, Li L, Eng C, Culver DA, Kalady MF, Pennison MJ, Pasche B, Manne U, de la Chapelle A, Hampel H, Henderson BE, Marchand LL, Hautaniemi S, Askhtorab H, Smoot D, Sandler RS, Keku T, Kupfer SS, Ellis NA, Haiman CA, Taipale J, Aaltonen LA. Tuupanen S, et al. Among authors: eng c. Cancer Genet. 2012 Jan-Feb;205(1-2):25-33. doi: 10.1016/j.cancergen.2012.01.005. Cancer Genet. 2012. PMID: 22429595 Free PMC article.

10

The prevalence of hereditary hemorrhagic telangiectasia in juvenile polyposis syndrome.

O'Malley M, LaGuardia L, Kalady MF, Parambil J, Heald B, Eng C, Church J, Burke CA. O'Malley M, et al. Among authors: eng c. Dis Colon Rectum. 2012 Aug;55(8):886-92. doi: 10.1097/DCR.0b013e31825aad32. Dis Colon Rectum. 2012. PMID: 22810475

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