Cohen Z - Search Results

1

Family history and molecular features of children, adolescents, and young adults with colorectal carcinoma.

Durno C, Aronson M, Bapat B, Cohen Z, Gallinger S. Durno C, et al. Among authors: cohen z. Gut. 2005 Aug;54(8):1146-50. doi: 10.1136/gut.2005.066092. Epub 2005 Apr 21. Gut. 2005. PMID: 15845562 Free PMC article.

2

A truncated hMSH2 transcript occurs as a common variant in the population: implications for genetic diagnosis.

Xia L, Shen W, Ritacca F, Mitri A, Madlensky L, Berk T, Cohen Z, Gallinger S, Bapat B. Xia L, et al. Among authors: cohen z. Cancer Res. 1996 May 15;56(10):2289-92. Cancer Res. 1996. PMID: 8625301

3

A preventive registry for hereditary nonpolyposis colorectal cancer.

Madlensky L, Berk TC, Bapat BV, McLeod RS, Couture J, Baron D, Hiruki T, Redston M, Cohen Z, Gallinger S. Madlensky L, et al. Among authors: cohen z. Can J Oncol. 1995 Jul;5(2):355-60. Can J Oncol. 1995. PMID: 8853507

4

Using genetic information to make surgical decisions: report of a case of a 13-year-old boy with colon cancer.

Madlensky L, Bapat B, Redston M, Pearl R, Gallinger S, Cohen Z. Madlensky L, et al. Among authors: cohen z. Dis Colon Rectum. 1997 Feb;40(2):240-3. doi: 10.1007/BF02054995. Dis Colon Rectum. 1997. PMID: 9075764

5

Familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC): a review of clinical, genetic and therapeutic aspects.

Soravia C, Bapat B, Cohen Z. Soravia C, et al. Among authors: cohen z. Schweiz Med Wochenschr. 1997 Apr 19;127(16):682-90. Schweiz Med Wochenschr. 1997. PMID: 9140167 Review.

6

Genotype-phenotype correlations in attenuated adenomatous polyposis coli.

Soravia C, Berk T, Madlensky L, Mitri A, Cheng H, Gallinger S, Cohen Z, Bapat B. Soravia C, et al. Among authors: cohen z. Am J Hum Genet. 1998 Jun;62(6):1290-301. doi: 10.1086/301883. Am J Hum Genet. 1998. PMID: 9585611 Free PMC article.

7

Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer.

Bapat BV, Madlensky L, Temple LK, Hiruki T, Redston M, Baron DL, Xia L, Marcus VA, Soravia C, Mitri A, Shen W, Gryfe R, Berk T, Chodirker BN, Cohen Z, Gallinger S. Bapat BV, et al. Among authors: cohen z. Hum Genet. 1999 Feb;104(2):167-76. doi: 10.1007/s004390050931. Hum Genet. 1999. PMID: 10190329

8

Cost comparison of predictive genetic testing versus conventional clinical screening for familial adenomatous polyposis.

Bapat B, Noorani H, Cohen Z, Berk T, Mitri A, Gallie B, Pritzker K, Gallinger S, Detsky AS. Bapat B, et al. Among authors: cohen z. Gut. 1999 May;44(5):698-703. doi: 10.1136/gut.44.5.698. Gut. 1999. PMID: 10205208 Free PMC article.

9

STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients.

Jiang CY, Esufali S, Berk T, Gallinger S, Cohen Z, Tobi M, Redston M, Bapat B. Jiang CY, et al. Among authors: cohen z. Clin Genet. 1999 Aug;56(2):136-41. doi: 10.1034/j.1399-0004.1999.560207.x. Clin Genet. 1999. PMID: 10517250

10

Characterization of two novel adenomatous polyposis coli (APC) gene mutations in patients with familial adenomatous polyposis (FAP).

Bapat B, Berk T, Mitri A, Cohen Z, Gallinger S, Stern H. Bapat B, et al. Among authors: cohen z. Hum Mutat. 1994;4(4):253-6. doi: 10.1002/humu.1380040404. Hum Mutat. 1994. PMID: 7866403

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