Thibodeau SN - Search Results

1

Mendelian Randomization Study of Body Mass Index and Colorectal Cancer Risk.

Thrift AP, Gong J, Peters U, Chang-Claude J, Rudolph A, Slattery ML, Chan AT, Locke AE, Kahali B, Justice AE, Pers TH, Gallinger S, Hayes RB, Baron JA, Caan BJ, Ogino S, Berndt SI, Chanock SJ, Casey G, Haile RW, Du M, Harrison TA, Thornquist M, Duggan DJ, Le Marchand L, Lindor NM, Seminara D, Song M, Wu K, Thibodeau SN, Cotterchio M, Win AK, Jenkins MA, Hopper JL, Ulrich CM, Potter JD, Newcomb PA, Hoffmeister M, Brenner H, White E, Hsu L, Campbell PT. Thrift AP, et al. Among authors: thibodeau sn. Cancer Epidemiol Biomarkers Prev. 2015 Jul;24(7):1024-31. doi: 10.1158/1055-9965.EPI-14-1309. Epub 2015 May 14. Cancer Epidemiol Biomarkers Prev. 2015. PMID: 25976416 Free PMC article.

2

A genetic review of complete and partial hydatidiform moles and nonmolar triploidy.

Lindor NM, Ney JA, Gaffey TA, Jenkins RB, Thibodeau SN, Dewald GW. Lindor NM, et al. Among authors: thibodeau sn. Mayo Clin Proc. 1992 Aug;67(8):791-9. doi: 10.1016/s0025-6196(12)60805-2. Mayo Clin Proc. 1992. PMID: 1434919 Review.

3

Mutations in the RET protooncogene in sporadic pheochromocytomas.

Lindor NM, Honchel R, Khosla S, Thibodeau SN. Lindor NM, et al. Among authors: thibodeau sn. J Clin Endocrinol Metab. 1995 Feb;80(2):627-9. doi: 10.1210/jcem.80.2.7852530. J Clin Endocrinol Metab. 1995. PMID: 7852530

4

Eight novel polymorphisms in the dystrophin gene of African-Americans: the rate of polymorphism is high.

Lindor NM, Sommer SS, Sobell J, Heston L, Thibodeau SN. Lindor NM, et al. Among authors: thibodeau sn. Hum Mutat. 1993;2(6):485-8. doi: 10.1002/humu.1380020610. Hum Mutat. 1993. PMID: 7906594 No abstract available.

5

Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenics.

Lindor NM, Sobell JL, Heston LL, Thibodeau SN, Sommer SS. Lindor NM, et al. Among authors: thibodeau sn. Am J Med Genet. 1994 Mar 15;54(1):1-4. doi: 10.1002/ajmg.1320540102. Am J Med Genet. 1994. PMID: 7909988

6

Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II.

Ledger GA, Khosla S, Lindor NM, Thibodeau SN, Gharib H. Ledger GA, et al. Among authors: thibodeau sn. Ann Intern Med. 1995 Jan 15;122(2):118-24. doi: 10.7326/0003-4819-122-2-199501150-00008. Ann Intern Med. 1995. PMID: 7992986 Review.

7

Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16.

Lindor NM, Jalal SM, Thibodeau SN, Bonde D, Sauser KL, Karnes PS. Lindor NM, et al. Among authors: thibodeau sn. Clin Genet. 1993 Oct;44(4):185-9. doi: 10.1111/j.1399-0004.1993.tb03876.x. Clin Genet. 1993. PMID: 8261647

8

Uniparental disomy in congenital disorders: a prospective study.

Lindor NM, Karnes PS, Michels VV, Dewald GW, Goerss J, Jalal S, Jenkins RB, Vockley G, Thibodeau SN. Lindor NM, et al. Among authors: thibodeau sn. Am J Med Genet. 1995 Aug 28;58(2):143-6. doi: 10.1002/ajmg.1320580210. Am J Med Genet. 1995. PMID: 8533805

9

Tumor necrosis factor-alpha allelic frequency and chromosome 6 allelic imbalance in patients with colorectal cancer.

Honchel R, McDonnell S, Schaid DJ, Thibodeau SN. Honchel R, et al. Among authors: thibodeau sn. Cancer Res. 1996 Jan 1;56(1):145-9. Cancer Res. 1996. PMID: 8548754

10

Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism.

Lindor NM, Devries EM, Michels VV, Schad CR, Jalal SM, Donovan KM, Smithson WA, Kvols LK, Thibodeau SN, Dewald GW. Lindor NM, et al. Among authors: thibodeau sn. Clin Genet. 1996 Mar;49(3):124-9. doi: 10.1111/j.1399-0004.1996.tb03270.x. Clin Genet. 1996. PMID: 8737976

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