Baysal BE - Search Results

1

Analysis of CHEK2 gene for ovarian cancer susceptibility.

Baysal BE, DeLoia JA, Willett-Brozick JE, Goodman MT, Brady MF, Modugno F, Lynch HT, Conley YP, Watson P, Gallion HH. Baysal BE, et al. Gynecol Oncol. 2004 Oct;95(1):62-9. doi: 10.1016/j.ygyno.2004.07.015. Gynecol Oncol. 2004. PMID: 15385111

2

High-resolution methylation analysis of the BRCA1 promoter in ovarian tumors.

Wilcox CB, Baysal BE, Gallion HH, Strange MA, DeLoia JA. Wilcox CB, et al. Among authors: baysal be. Cancer Genet Cytogenet. 2005 Jun;159(2):114-22. doi: 10.1016/j.cancergencyto.2004.12.017. Cancer Genet Cytogenet. 2005. PMID: 15899382

3

Coordinate up-regulation of TMEM97 and cholesterol biosynthesis genes in normal ovarian surface epithelial cells treated with progesterone: implications for pathogenesis of ovarian cancer.

Wilcox CB, Feddes GO, Willett-Brozick JE, Hsu LC, DeLoia JA, Baysal BE. Wilcox CB, et al. Among authors: baysal be. BMC Cancer. 2007 Dec 11;7:223. doi: 10.1186/1471-2407-7-223. BMC Cancer. 2007. PMID: 18070364 Free PMC article.

4

Relationship between ERCC1 polymorphisms, disease progression, and survival in the Gynecologic Oncology Group Phase III Trial of intraperitoneal versus intravenous cisplatin and paclitaxel for stage III epithelial ovarian cancer.

Krivak TC, Darcy KM, Tian C, Armstrong D, Baysal BE, Gallion H, Ambrosone CB, DeLoia JA; Gynecologic Oncology Group Phase III Trial. Krivak TC, et al. Among authors: baysal be. J Clin Oncol. 2008 Jul 20;26(21):3598-606. doi: 10.1200/JCO.2008.16.1323. J Clin Oncol. 2008. PMID: 18640939 Free PMC article. Clinical Trial.

5

Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect.

Astrom K, Cohen JE, Willett-Brozick JE, Aston CE, Baysal BE. Astrom K, et al. Among authors: baysal be. Hum Genet. 2003 Aug;113(3):228-37. doi: 10.1007/s00439-003-0969-6. Epub 2003 Jun 17. Hum Genet. 2003. PMID: 12811540

6

Common variations in ALG9 are not associated with bipolar I disorder: a family-based study.

Baysal BE, Willett-Brozick JE, Bacanu SA, Detera-Wadleigh S, Nimgaonkar VL. Baysal BE, et al. Behav Brain Funct. 2006 Jul 21;2:25. doi: 10.1186/1744-9081-2-25. Behav Brain Funct. 2006. PMID: 16859551 Free PMC article.

7

A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family.

Baysal BE, Willett-Brozick JE, Badner JA, Corona W, Ferrell RE, Nimgaonkar VL, Detera-Wadleigh SD. Baysal BE, et al. Neurogenetics. 2002 Mar;4(1):43-53. doi: 10.1007/s10048-001-0129-x. Neurogenetics. 2002. PMID: 12030331

8

Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation.

Willett-Brozick JE, Savul SA, Richey LE, Baysal BE. Willett-Brozick JE, et al. Among authors: baysal be. Hum Genet. 2001 Aug;109(2):216-23. doi: 10.1007/s004390100564. Hum Genet. 2001. PMID: 11511928

9

A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region.

Baysal BE, Willett-Brozick JE, Taschner PE, Dauwerse JG, Devilee P, Devlin B. Baysal BE, et al. Eur J Hum Genet. 2001 Feb;9(2):121-9. doi: 10.1038/sj.ejhg.5200585. Eur J Hum Genet. 2001. PMID: 11313745

10

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.

Baysal BE, Ferrell RE, Willett-Brozick JE, Lawrence EC, Myssiorek D, Bosch A, van der Mey A, Taschner PE, Rubinstein WS, Myers EN, Richard CW 3rd, Cornelisse CJ, Devilee P, Devlin B. Baysal BE, et al. Science. 2000 Feb 4;287(5454):848-51. doi: 10.1126/science.287.5454.848. Science. 2000. PMID: 10657297

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