Genetic Heterogeneity in Human Disease von McClellan, Jon, King, Mary-Claire

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"The Race" to Clone BRCA1 von King, Mary-Claire

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Population-Based Screening for BRCA1 and BRCA2: 2014 Lasker Award von King, Mary-Claire, Levy-Lahad, Ephrat, Lahad, Amnon

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2020 William Allan Award address: genetics as a way of thinking—cultural inheritance from our teachers von King, Mary-Claire

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A tipping point in neuropsychiatric genetics von McClellan, Jon M, King, Mary-Claire

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Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy‐related leukemia von Churpek, Jane E., Marquez, Rafael, Neistadt, Barbara, Claussen, Kimberly, Lee, Ming K., Churpek, Matthew M., Huo, Dezheng, Weiner, Howard, Bannerjee, Mekhala, Godley, Lucy A., Le Beau, Michelle M., Pritchard, Colin C., Walsh, Tom, King, Mary‐Claire, Olopade, Olufunmilayo I., Larson, Richard A.

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Accurate and exact CNV identification from targeted high-throughput sequence data von Nord, Alex S, Lee, Ming, King, Mary-Claire, Walsh, Tom

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The phenotypic spectrum of SCN2A-related epilepsy von Reynolds, Claire, King, Mary D., Gorman, Kathleen M.

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Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas von PENNINGTON, Kathryn P, WALSH, Tom, AGNEW, Kathy J, PRITCHARD, Colin C, SCROGGINS, Sheena, GARCIA, Rochelle L, KING, Mary-Claire, SWISHER, Elizabeth M, HARRELL, Maria I, LEE, Ming K, PENNIL, Christopher C, RENDI, Mara H, THORNTON, Anne, NORQUIST, Barbara M, CASADEI, Silvia, NORD, Alexander S

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Inherited predisposition to malignant mesothelioma and overall survival following platinum chemotherapy von Hassan, Raffit, Morrow, Betsy, Thomas, Anish, Walsh, Tom, Lee, Ming K., Gulsuner, Suleyman, Gadiraju, Meghana, Panou, Vasiliki, Gao, Shaojian, Mian, Idrees, Khan, Javed, Raffeld, Mark, Patel, Snehal, Xi, Liqiang, Wei, Jun S., Hesdorffer, Mary, Zhang, Jingli, Calzone, Kathleen, Desai, Arpita, Padiernos, Emerson, Alewine, Christine, Schrump, David S., Steinberg, Seth M., Kindler, Hedy L., King, Mary-Claire, Churpek, Jane E.

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Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2 von Gabai-Kapara, Efrat, Lahad, Amnon, Kaufman, Bella, Friedman, Eitan, Segev, Shlomo, Renbaum, Paul, Beeri, Rachel, Gal, Moran, Grinshpun-Cohen, Julia, Djemal, Karen, Mandell, Jessica B., Lee, Ming K., Beller, Uziel, Catane, Raphael, King, Mary-Claire, Levy-Lahad, Ephrat

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Triage of Scarce Critical Care Resources in COVID-19 An Implementation Guide for Regional Allocation: An Expert Panel Report of the Task Force for Mass Critical Care and the Americ... von Maves, Ryan C, Downar, James, Dichter, Jeffrey R, Hick, John L, Devereaux, Asha, Geiling, James A, Kissoon, Niranjan, Hupert, Nathaniel, Niven, Alexander S, King, Mary A, Rubinson, Lewis L, Hanfling, Dan, Hodge, Jr, James G, Marshall, Mary Faith, Fischkoff, Katherine, Evans, Laura E, Tonelli, Mark R, Wax, Randy S, Seda, Gilbert, Parrish, John S, Truog, Robert D, Sprung, Charles L, Christian, Michael D

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

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Ten Genes for Inherited Breast Cancer von Walsh, Tom, King, Mary-Claire

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Hiding in Plain Sight — Somatic Mutation in Human Disease von Levy-Lahad, Ephrat, King, Mary-Claire

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Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management von Baxter, Sarah K., Walsh, Tom, Casadei, Silvia, Eckert, Mary M., Allenspach, Eric J., Hagin, David, Segundo, Gesmar, Lee, Ming K., Gulsuner, Suleyman, Shirts, Brian H., Sullivan, Kathleen E., Keller, Michael D., Torgerson, Troy R., King, Mary-Claire

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Response to DNA damage of CHEK2 missense mutations in familial breast cancer von ROEB, Wendy, HIGGINS, Jake, KING, Mary-Claire

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Status dystonicus: a practice guide von Allen, Nicholas M, Lin, Jean‐Pierre, Lynch, Tim, King, Mary D

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Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients von Keel, Siobán B, Scott, Angela, Sanchez-Bonilla, Marilyn, Ho, Phoenix A, Gulsuner, Suleyman, Pritchard, Colin C, Abkowitz, Janis L, King, Mary-Claire, Walsh, Tom, Shimamura, Akiko

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Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion von Allen, Nicholas M., Conroy, Judith, Shahwan, Amre, Lynch, Bryan, Correa, Raony G., Pena, Sergio D. J., McCreary, Dara, Magalhães, Tiago R., Ennis, Sean, Lynch, Sally A., King, Mary D.

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