Schaid D - Search Results

1

Evidence for a prostate cancer susceptibility locus on the X chromosome.

Xu J, Meyers D, Freije D, Isaacs S, Wiley K, Nusskern D, Ewing C, Wilkens E, Bujnovszky P, Bova GS, Walsh P, Isaacs W, Schleutker J, Matikainen M, Tammela T, Visakorpi T, Kallioniemi OP, Berry R, Schaid D, French A, McDonnell S, Schroeder J, Blute M, Thibodeau S, Grönberg H, Emanuelsson M, Damber JE, Bergh A, Jonsson BA, Smith J, Bailey-Wilson J, Carpten J, Stephan D, Gillanders E, Amundson I, Kainu T, Freas-Lutz D, Baffoe-Bonnie A, Van Aucken A, Sood R, Collins F, Brownstein M, Trent J. Xu J, et al. Among authors: schaid d. Nat Genet. 1998 Oct;20(2):175-9. doi: 10.1038/2477. Nat Genet. 1998. PMID: 9771711

2

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: schaid dj. 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.

3

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: schaid dj. 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

4

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: schaid dj. Mayo Clin Proc. 1989 Mar;64(3):325-34. doi: 10.1016/s0025-6196(12)65252-5. Mayo Clin Proc. 1989. PMID: 2564899 Review.

5

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. Among authors: schaid d. Am J Hum Genet. 1989 May;44(5):679-85. Am J Hum Genet. 1989. PMID: 2565080 Free PMC article.

6

Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome.

Patterson MN, Bell MV, Bloomfield J, Flint T, Dorkins H, Thibodeau SN, Schaid D, Bren G, Schwartz CE, Wieringa B, et al. Patterson MN, et al. Among authors: schaid d. Genomics. 1989 May;4(4):570-8. doi: 10.1016/0888-7543(89)90281-4. Genomics. 1989. PMID: 2744766

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: schaid dj. 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: schaid dj. 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: schaid dj. 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: schaid dj. 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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