Publications by authors named "Anne Thornton"

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Inherited predisposition to breast cancer among African American women.
Jane E Churpek, Tom Walsh, Yonglan Zheng, Zakiya Moton, Anne M Thornton

Breast Cancer Res Treat· January 2015

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Transcriptional analysis of four family 4 P450s in a Puerto Rico strain of Aedes aegypti (Diptera: Culicidae) compared with an Orlando strain and their possible functional roles in permethrin resistance.
William R Reid, Anne Thornton, Julia W Pridgeon, James J Becnel, Fang Tang

J Med Entomol· May 2014

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Germline and somatic mutations in homologous recombination genes predict platinum response and survival in ovarian, fallopian tube, and peritoneal carcinomas.
Kathryn P Pennington, Tom Walsh, Maria I Harrell, Ming K Lee, Christopher C Pennil, Anne Thornton

Clin Cancer Res· February 2014

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Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
Suleyman Gulsuner, Tom Walsh, Amanda C Watts, Ming K Lee, Anne M Thornton

Cell· August 2013

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Characteristics of women with ovarian carcinoma who have BRCA1 and BRCA2 mutations not identified by clinical testing.
Barbara M Norquist, Kathryn P Pennington, Kathy J Agnew, Maria I Harrell, Christopher C Pennil, Anne M Thornton

Gynecol Oncol· March 2013

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BRCA1, TP53, and CHEK2 germline mutations in uterine serous carcinoma.
Kathryn P Pennington, Tom Walsh, Ming Lee, Christopher Pennil, Akiva P Novetsky, Anne Thornton

Cancer· January 2013

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ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.
Colin C Pritchard, Christina Smith, Stephen J Salipante, Ming K Lee, Anne M Thornton

J Mol Diagn· July 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, Anne M Thornton

Proc Natl Acad Sci U S A· November 2011

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Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome.
Sarah B Pierce, Tom Walsh, Karen M Chisholm, Ming K Lee, Anne M Thornton

Am J Hum Genet· August 2010

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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

Am J Hum Genet· July 2010

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Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing.
Tom Walsh, Ming K Lee, Silvia Casadei, Anne M Thornton, Sunday M Stray

Proc Natl Acad Sci U S A· July 2010

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