Publications by authors named "Wendy Roeb"

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Response to DNA damage of CHEK2 missense mutations in familial breast cancer.
Wendy Roeb, Jake Higgins, Mary-Claire King

Hum Mol Genet· June 2012

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Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing.
Tom Walsh, Silvia Casadei, Ming K Lee, Christopher C Pennil, Alex S Nord, Wendy Roeb

Proc Natl Acad Sci U S A· November 2011

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Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.
Alex S Nord, Wendy Roeb, Diane E Dickel, Tom Walsh, Mary Kusenda

Eur J Hum Genet· June 2011

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Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.
Tom Walsh, Hashem Shahin, Tal Elkan-Miller, Ming K Lee, Anne M Thornton, Wendy Roeb

Am J Hum Genet· July 2010

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Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.
Tom Walsh, Sarah B Pierce, Danielle R Lenz, Zippora Brownstein, Orit Dagan-Rosenfeld, Wendy Roeb

Am J Hum Genet· July 2010

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Guilt by association: PAX3-FOXO1 regulates gene expression through selective destabilization of the EGR1 transcription factor.
Wendy Roeb, Antonia Boyer, Webster K Cavenee, Karen C Arden

Cell Cycle· April 2008

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PAX3-FOXO1 controls expression of the p57Kip2 cell-cycle regulator through degradation of EGR1.
Wendy Roeb, Antonia Boyer, Webster K Cavenee, Karen C Arden

Proc Natl Acad Sci U S A· November 2007

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