Willett-Brozick JE - 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. Among authors: willett brozick je. Gynecol Oncol. 2004 Oct;95(1):62-9. doi: 10.1016/j.ygyno.2004.07.015. Gynecol Oncol. 2004. PMID: 15385111

2

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: willett brozick je. BMC Cancer. 2007 Dec 11;7:223. doi: 10.1186/1471-2407-7-223. BMC Cancer. 2007. PMID: 18070364 Free PMC article.

3

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: willett brozick je. Hum Genet. 2003 Aug;113(3):228-37. doi: 10.1007/s00439-003-0969-6. Epub 2003 Jun 17. Hum Genet. 2003. PMID: 12811540

4

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. Among authors: willett brozick je. Behav Brain Funct. 2006 Jul 21;2:25. doi: 10.1186/1744-9081-2-25. Behav Brain Funct. 2006. PMID: 16859551 Free PMC article.

5

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. Among authors: willett brozick je. Neurogenetics. 2002 Mar;4(1):43-53. doi: 10.1007/s10048-001-0129-x. Neurogenetics. 2002. PMID: 12030331

6

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. Hum Genet. 2001 Aug;109(2):216-23. doi: 10.1007/s004390100564. Hum Genet. 2001. PMID: 11511928

7

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

8

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

9

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.

Baysal BE, Willett-Brozick JE, Lawrence EC, Drovdlic CM, Savul SA, McLeod DR, Yee HA, Brackmann DE, Slattery WH 3rd, Myers EN, Ferrell RE, Rubinstein WS. Baysal BE, et al. Among authors: willett brozick je. J Med Genet. 2002 Mar;39(3):178-83. doi: 10.1136/jmg.39.3.178. J Med Genet. 2002. PMID: 11897817 Free PMC article.

10

Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria.

Janecke AR, Willett-Brozick JE, Karas C, Hasipek M, Loeffler-Ragg J, Baysal BE. Janecke AR, et al. Among authors: willett brozick je. J Hum Genet. 2010 Mar;55(3):182-5. doi: 10.1038/jhg.2009.142. Epub 2010 Jan 29. J Hum Genet. 2010. PMID: 20111059

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