Thibodeau SN - Search Results

1

Human SULT1A1 gene: copy number differences and functional implications.

Hebbring SJ, Adjei AA, Baer JL, Jenkins GD, Zhang J, Cunningham JM, Schaid DJ, Weinshilboum RM, Thibodeau SN. Hebbring SJ, et al. Among authors: thibodeau sn. Hum Mol Genet. 2007 Mar 1;16(5):463-70. doi: 10.1093/hmg/ddl468. Epub 2006 Dec 22. Hum Mol Genet. 2007. PMID: 17189289

2

Current status of adjuvant chemotherapy for colorectal cancer. Can molecular markers play a role in predicting prognosis?

O'Connell MJ, Schaid DJ, Ganju V, Cunningham J, Kovach JS, Thibodeau SN. O'Connell MJ, et al. Among authors: thibodeau sn. Cancer. 1992 Sep 15;70(6 Suppl):1732-9. doi: 10.1002/1097-0142(19920915)70:4+<1732::aid-cncr2820701614>3.0.co;2-#. Cancer. 1992. PMID: 1516028

3

Expression of p53 and 17p allelic loss in colorectal carcinoma.

Cunningham J, Lust JA, Schaid DJ, Bren GD, Carpenter HA, Rizza E, Kovach JS, Thibodeau SN. Cunningham J, et al. Among authors: thibodeau sn. Cancer Res. 1992 Apr 1;52(7):1974-80. Cancer Res. 1992. PMID: 1551126

4

Exclusion of calcitonin/alpha-CGRP gene defect in a family with autosomal dominant supravalvular aortic stenosis.

Pastores GM, Michels VV, Schaid DJ, Driscoll DJ, Feldt RH, Thibodeau SN. Pastores GM, et al. Among authors: thibodeau sn. J Med Genet. 1992 Jan;29(1):56-7. doi: 10.1136/jmg.29.1.56. J Med Genet. 1992. PMID: 1552547 Free PMC article. No abstract available.

5

Linkage of nonspecific X-linked mental retardation to Xq21.31.

Jedele KB, Michels VV, Schaid DJ, Schowalter KV, Thibodeau SN. Jedele KB, et al. Among authors: thibodeau sn. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):436-42. doi: 10.1002/ajmg.1320430166. Am J Med Genet. 1992. PMID: 1605223

6

Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.

Khosla S, Patel VM, Hay ID, Schaid DJ, Grant CS, van Heerden JA, Thibodeau SN. Khosla S, et al. Among authors: thibodeau sn. J Clin Invest. 1991 May;87(5):1691-9. doi: 10.1172/JCI115186. J Clin Invest. 1991. PMID: 2022740 Free PMC article.

7

The location of the Philadelphia chromosomal breakpoint site and prognosis in chronic granulocytic leukemia.

Tefferi A, Bren GD, Wagner KV, Schaid DJ, Ash RC, Thibodeau SN. Tefferi A, et al. Among authors: thibodeau sn. Leukemia. 1990 Dec;4(12):839-42. Leukemia. 1990. PMID: 2173804

8

Carrier identification of cystic fibrosis by recombinant DNA techniques.

Dawson DB, Cummins LA, Schaid DJ, Michels VV, Gordon H, O'Connell EJ, Thibodeau SN. Dawson DB, et al. Among authors: thibodeau sn. Mayo Clin Proc. 1989 Mar;64(3):325-34. doi: 10.1016/s0025-6196(12)65252-5. Mayo Clin Proc. 1989. PMID: 2564899 Review.

9

An intronic region within the human factor VIII gene is duplicated within Xq28 and is homologous to the polymorphic locus DXS115 (767).

Patterson M, Gitschier J, Bloomfield J, Bell M, Dorkins H, Froster-Iskenius U, Sommer S, Sobell J, Schaid D, Thibodeau S, et al. Patterson M, et al. Am J Hum Genet. 1989 May;44(5):679-85. Am J Hum Genet. 1989. PMID: 2565080 Free PMC article.

10

Apolipoprotein E status as a predictor of the development of Alzheimer's disease in memory-impaired individuals.

Petersen RC, Smith GE, Ivnik RJ, Tangalos EG, Schaid DJ, Thibodeau SN, Kokmen E, Waring SC, Kurland LT. Petersen RC, et al. Among authors: thibodeau sn. JAMA. 1995 Apr 26;273(16):1274-8. JAMA. 1995. PMID: 7646655

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