Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

Por Walsh, Tom, Lee, Ming K., Casadei, Silvia, Thornton, Anne M., Stray, Sunday M., Pennil, Christopher, Nord, Alex S., Mandell, Jessica B., Swisher, Elizabeth M., King, Mary-Claire
Publicado em 2010

Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82

Por Walsh, Tom, Shahin, Hashem, Elkan-Miller, Tal, Lee, Ming K., Thornton, Anne M., Roeb, Wendy, Abu Rayyan, Amal, Loulus, Suheir, Avraham, Karen B., King, Mary-Claire, Kanaan, Moien
Publicado em 2010

Mutations in the DBP-Deficiency Protein HSD17B4 Cause Ovarian Dysgenesis, Hearing Loss, and Ataxia of Perrault Syndrome

Por Pierce, Sarah B., Walsh, Tom, Chisholm, Karen M., Lee, Ming K., Thornton, Anne M., Fiumara, Agata, Opitz, John M., Levy-Lahad, Ephrat, Klevit, Rachel E., King, Mary-Claire
Publicado em 2010

Characteristics of Women with Ovarian Carcinoma who have BRCA1 and BRCA2 Mutations not Identified by Clinical Testing

Por Norquist, Barbara M., Pennington, Kathryn P., Agnew, Kathy J., Harrell, Maria I., Pennil, Christopher C., Lee, Ming K., Casadei, Silvia, Thornton, Anne M., Garcia, Rochelle L., Walsh, Tom, Swisher, Elizabeth M.
Publicado em 2012

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

Por Walsh, Tom, Casadei, Silvia, Lee, Ming K., Pennil, Christopher C., Nord, Alex S., Thornton, Anne M., Roeb, Wendy, Agnew, Kathy J., Stray, Sunday M., Wickramanayake, Anneka, Norquist, Barbara, Pennington, Kathryn P., Garcia, Rochelle L., King, Mary-Claire, Swisher, Elizabeth M.
Publicado em 2011

Spatial and Temporal Mapping of De novo Mutations in Schizophrenia To a Fetal Prefrontal Cortical Network

Por Gulsuner, Suleyman, Walsh, Tom, Watts, Amanda C., Lee, Ming K., Thornton, Anne M., Casadei, Silvia, Rippey, Caitlin, Shahin, Hashem, Nimgaonkar, Vishwajit L., Go, Rodney C. P., Savage, Robert M., Swerdlow, Neal R., Gur, Raquel E., Braff, David L., King, Mary-Claire, McClellan, Jon M.
Publicado em 2013

Inherited predisposition to breast cancer among African American women

Por Churpek, Jane E., Walsh, Tom, Zheng, Yonglan, Moton, Zakiya, Thornton, Anne M., Lee, Ming K., Casadei, Silvia, Watts, Amanda, Neistadt, Barbara, Churpek, Matthew M., Huo, Dezheng, Zvosec, Cecilia, Liu, Fang, Niu, Qun, Marquez, Rafael, Zhang, Jing, Fackenthal, James, King, Mary-Claire, Olopade, Olufunmilayo I.
Publicado no Breast Cancer Res Treat (2014)

ColoSeq Provides Comprehensive Lynch and Polyposis Syndrome Mutational Analysis Using Massively Parallel Sequencing

Por Pritchard, Colin C., Smith, Christina, Salipante, Stephen J., Lee, Ming K., Thornton, Anne M., Nord, Alex S., Gulden, Cassandra, Kupfer, Sonia S., Swisher, Elizabeth M., Bennett, Robin L., Novetsky, Akiva P., Jarvik, Gail P., Olopade, Olufunmilayo I., Goodfellow, Paul J., King, Mary-Claire, Tait, Jonathan F., Walsh, Tom
Publicado em 2012