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Items: 14

1.

The National Cancer Institute R25 Cancer Education Grants Program: A Workshop Report.

Korczak JF, Chung DW, Rosemond E, Von Hoff DD, Haspel RL, Waterbor JW, Chang S, Ramirez AG, Perkins S, Wiest J, Lei M.

J Cancer Educ. 2017 Mar;32(1):3-10. doi: 10.1007/s13187-016-1161-8. Review.

2.

African American-preponderant single nucleotide polymorphisms (SNPs) and risk of breast cancer.

Kato I, Cichon M, Yee CL, Land S, Korczak JF.

Cancer Epidemiol. 2009 Jul;33(1):24-30. doi: 10.1016/j.canep.2009.04.009. Epub 2009 May 14.

3.

Breast cancer risk estimates for relatives of white and African American women with breast cancer in the Women's Contraceptive and Reproductive Experiences Study.

Simon MS, Korczak JF, Yee CL, Malone KE, Ursin G, Bernstein L, McDonald JA, Deapen D, Strom BL, Press MF, Marchbanks PA, Burkman RT, Weiss LK, Schwartz AG.

J Clin Oncol. 2006 Jun 1;24(16):2498-504.

PMID:
16735703
4.

Pancreatic cancer genetic epidemiology consortium.

Petersen GM, de Andrade M, Goggins M, Hruban RH, Bondy M, Korczak JF, Gallinger S, Lynch HT, Syngal S, Rabe KG, Seminara D, Klein AP.

Cancer Epidemiol Biomarkers Prev. 2006 Apr;15(4):704-10.

5.

Racial differences in the familial aggregation of breast cancer and other female cancers.

Simon MS, Korczak JF, Yee CL, Daling JR, Malone KE, Bernstein L, Marchbanks PA, Folger SG, McDonald JA, Norman SA, Strom BL, Deapen D, Ursin G, Burkman RT, Press MF, Schwartz AG, Spirtas R.

Breast Cancer Res Treat. 2005 Feb;89(3):227-35.

PMID:
15754120
6.

Familial chordoma, a tumor of notochordal remnants, is linked to chromosome 7q33.

Kelley MJ, Korczak JF, Sheridan E, Yang X, Goldstein AM, Parry DM.

Am J Hum Genet. 2001 Aug;69(2):454-60. Epub 2001 Jul 10.

7.

Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly.

Kelley MJ, Jawien W, Ortel TL, Korczak JF.

Nat Genet. 2000 Sep;26(1):106-8.

PMID:
10973260
8.

Autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly) is linked to chromosome 22q12-13.

Kelley MJ, Jawien W, Lin A, Hoffmeister K, Pugh EW, Doheny KF, Korczak JF.

Hum Genet. 2000 May;106(5):557-64.

PMID:
10914687
9.

Sib-pair linkage analyses of alcoholism: dichotomous and quantitative measures.

Korczak JF, Bergen AW, Goldstein AM, Weissbecker KA.

Genet Epidemiol. 1999;17 Suppl 1:S205-10.

PMID:
10597437
10.

A genome-wide search for loci contributing to smoking and alcoholism.

Bergen AW, Korczak JF, Weissbecker KA, Goldstein AM.

Genet Epidemiol. 1999;17 Suppl 1:S55-60.

PMID:
10597412
11.

Nevoid basal cell carcinoma syndrome with medulloblastoma in an African-American boy: a rare case illustrating gene-environment interaction.

Korczak JF, Brahim JS, DiGiovanna JJ, Kase RG, Wexler LH, Goldstein AM.

Am J Med Genet. 1997 Mar 31;69(3):309-14.

PMID:
9096762
12.

Detecting gene-environment interactions using a case-control design.

Goldstein AM, Falk RT, Korczak JF, Lubin JH.

Genet Epidemiol. 1997;14(6):1085-9.

PMID:
9433628
13.
14.

Effects of marker information on sib-pair linkage analysis of a rare disease.

Korczak JF, Pugh EW, Premkumar S, Guo X, Elston RC, Bailey-Wilson JE.

Genet Epidemiol. 1995;12(6):625-30.

PMID:
8787984

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