Thibodeau SN - Search Results

1

Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus.

Johanneson B, McDonnell SK, Karyadi DM, Quignon P, McIntosh L, Riska SM, FitzGerald LM, Johnson G, Deutsch K, Williams G, Tillmans LS, Stanford JL, Schaid DJ, Thibodeau SN, Ostrander EA. Johanneson B, et al. Among authors: thibodeau sn. Hum Mol Genet. 2010 Oct 1;19(19):3852-62. doi: 10.1093/hmg/ddq283. Epub 2010 Jul 14. Hum Mol Genet. 2010. PMID: 20631155 Free PMC article.

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

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.

4

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

5

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.

6

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.

7

Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.

Snow K, Tester DJ, Kruckeberg KE, Schaid DJ, Thibodeau SN. Snow K, et al. Among authors: thibodeau sn. Hum Mol Genet. 1994 Sep;3(9):1543-51. doi: 10.1093/hmg/3.9.1543. Hum Mol Genet. 1994. PMID: 7833909

8

Confirmation of linkage of supravalvular aortic stenosis to the elastin gene on chromosome 7q.

Kumar A, Olson TM, Thibodeau SN, Michels VV, Schaid DJ, Wallace MR. Kumar A, et al. Among authors: thibodeau sn. Am J Cardiol. 1994 Dec 15;74(12):1281-3. doi: 10.1016/0002-9149(94)90567-3. Am J Cardiol. 1994. PMID: 7977109 No abstract available.

9

Apolipoprotein E: risk factor for Alzheimer disease.

Tsai MS, Tangalos EG, Petersen RC, Smith GE, Schaid DJ, Kokmen E, Ivnik RJ, Thibodeau SN. Tsai MS, et al. Among authors: thibodeau sn. Am J Hum Genet. 1994 Apr;54(4):643-9. Am J Hum Genet. 1994. PMID: 8128961 Free PMC article.

10

Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7.

Olson TM, Michels VV, Lindor NM, Pastores GM, Weber JL, Schaid DJ, Driscoll DJ, Feldt RH, Thibodeau SN. Olson TM, et al. Among authors: thibodeau sn. Hum Mol Genet. 1993 Jul;2(7):869-73. doi: 10.1093/hmg/2.7.869. Hum Mol Genet. 1993. PMID: 8364568

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