The Bcr-Abl Leukemia Oncogene Activates Jun Kinase and Requires Jun for Transformation von Raitano, Arthur B., Halpern, Jocelyn R., Hambuch, Tina M., Sawyers, Charles L.

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Patterns of Synonymous Codon Usage in Drosophila melanogaster Genes With Sex-Biased Expression von Hambuch, Tina M, Parsch, John

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Sherloc: a comprehensive refinement of the ACMG–AMP variant classification criteria von Nykamp, Keith, Anderson, Michael, Powers, Martin, Garcia, John, Herrera, Blanca, Ho, Yuan-Yuan, Kobayashi, Yuya, Patil, Nila, Thusberg, Janita, Westbrook, Marjorie, Topper, Scott

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Twenty-Five Years of Germline Genetic Testing and What May Lie Ahead von Pratt, Victoria M., Akhavanfard, Sara, Houldsworth, Jane, Laffin, Jennifer J., Moyer, Ann M., Reddi, Honey V., Scott, Stuart A., Lebo, Matthew S., Lebo, Matthew S., Akhavanfard, Sara, Du, Xiaoli, Hawks, Tina Hambuch, Houldsworth, Jane, Laffin, Jennifer J., Moyer, Ann M., Pratt, Victoria M., Reddi, Honey V., Scott, Stuart A., Williams, Eli

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Deep sequencing multi-gene panel analysis is a useful first-tier test with a high diagnostic yield and broad mutation spectrum detection in childhood epilepsy von Aradhya, S., Patil, N., Truty, R., Riethmaier, D., Elias, L., Entezam, A., Fuller, A., Hambuch, T., Hogue, M., Khouzam, A., Kobayashi, Y., Lewis, R., Nykamp, K., Rabideau, M., Westbrook, J., Zeman, M., Nussbaum, R.

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Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study von Lane, William J, Westhoff, Connie M, Gleadall, Nicholas S, Aguad, Maria, Smeland-Wagman, Robin, Vege, Sunitha, Simmons, Daimon P, Mah, Helen H, Lebo, Matthew S, Walter, Klaudia, Soranzo, Nicole, Di Angelantonio, Emanuele, Danesh, John, Roberts, David J, Watkins, Nick A, Ouwehand, Willem H, Butterworth, Adam S, Kaufman, Richard M, Rehm, Heidi L, Silberstein, Leslie E, Green, Robert C, Bates, David W., Blout, Carrie, Christensen, Kurt D., Cirino, Allison L., Ho, Carolyn Y., Krier, Joel B., Lehmann, Lisa S., MacRae, Calum A., Morton, Cynthia C., Perry, Denise L., Seidman, Christine E., Sunyaev, Shamil R., Vassy, Jason L., Schonman, Erica, Nguyen, Tiffany, Steffens, Eleanor, Betting, Wendi Nicole, Aronson, Samuel J., Ceyhan-Birsoy, Ozge, Machini, Kalotina, McLaughlin, Heather M., Azzariti, Danielle R., Tsai, Ellen A., Blumenthal-Barby, Jennifer, Feuerman, Lindsay Z., McGuire, Amy L., Lee, Kaitlyn, Robinson, Jill O., Slashinski, Melody J., Diamond, Pamela M., Davis, Kelly, Ubel, Peter A., Kraft, Peter, Roberts, J. Scott, Garber, Judy E., Hambuch, Tina, Murray, Michael F., Kohane, Isaac, Kong, Sek Won

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Molecular evolution of sex-biased genes in Drosophila von Zhang, Zhi, Hambuch, Tina M, Parsch, John

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The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine von Vassy, Jason L, Lautenbach, Denise M, McLaughlin, Heather M, Kong, Sek Won, Christensen, Kurt D, Krier, Joel, Kohane, Isaac S, Feuerman, Lindsay Z, Blumenthal-Barby, Jennifer, Roberts, J Scott, Lehmann, Lisa Soleymani, Ho, Carolyn Y, Ubel, Peter A, MacRae, Calum A, Seidman, Christine E, Murray, Michael F, McGuire, Amy L, Rehm, Heidi L, Green, Robert C

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Comprehensive red blood cell and platelet antigen prediction from whole genome sequencing: proof of principle von Lane, William J., Westhoff, Connie M., Uy, Jon Michael, Aguad, Maria, Smeland-Wagman, Robin, Kaufman, Richard M., Rehm, Heidi L., Green, Robert C., Silberstein, Leslie E.

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A systematic approach to the reporting of medically relevant findings from whole genome sequencing von McLaughlin, Heather M, Ceyhan-Birsoy, Ozge, Christensen, Kurt D, Kohane, Isaac S, Krier, Joel, Lane, William J, Lautenbach, Denise, Lebo, Matthew S, Machini, Kalotina, MacRae, Calum A, Azzariti, Danielle R, Murray, Michael F, Seidman, Christine E, Vassy, Jason L, Green, Robert C, Rehm, Heidi L

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A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg a von Lane, William J, Aguad, Maria, Smeland-Wagman, Robin, Vege, Sunitha, Mah, Helen H, Joseph, Abigail, Blout, Carrie L, Nguyen, Tiffany T, Lebo, Matthew S, Sidhu, Manpreet, Lomas-Francis, Christine, Kaufman, Richard M, Green, Robert C, Westhoff, Connie M

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Summarizing polygenic risks for complex diseases in a clinical whole-genome report von Kong, Sek Won, Lee, In-Hee, Leshchiner, Ignaty, Krier, Joel, Kraft, Peter, Rehm, Heidi L., Green, Robert C., Kohane, Isaac S., MacRae, Calum A.

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Correction: Sherloc: a comprehensive refinement of the ACMG–AMP variant classification criteria von Nykamp, Keith, Anderson, Michael, Powers, Martin, Garcia, John, Herrera, Blanca, Ho, Yuan-Yuan, Kobayashi, Yuya, Patil, Nila, Thusberg, Janita, Westbrook, Marjorie, Topper, Scott

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The role of the F508C mutation in congenital bilateral absence of the vas deferens von Havasi, Viktoria, Keiles, Steven, Hambuch, Tina, Sorscher, Eric J., Kammesheidt, Anja

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Whole Genome Sequencing in the Clinical Laboratory von Laurent, M., Sickler, B., Liao, A., Cotter, P., Jain, S., Lyan, Y., Bernd, J., Daniel, J.O., Poggio, P., Ross, M., Bentley, D., Hambuch, T.

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Enhanced Selection For MHC Diversity In Social Tuco-tucos von Hambuch, T M, Lacey, E A

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ENHANCED SELECTION FOR MHC DIVERSITY IN SOCIAL TUCO-TUCOS von Hambuch, Tina M, Lacey, Eileen A

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The Association for Molecular Pathology's Approach to Supporting a Global Agenda to Embrace Personalized Genomic Medicine

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Population Genetic Analysis of Bartonella bacilliformis Isolates from Areas of Peru Where Carrion's Disease Is Endemic and Epidemic von HAMBUCH, Tina M, HANDLEY, Scott A, ELLIS, Barbara, CHAMBERLIN, Judith, ROMERO, Sofia, REGNERY, Russell

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Ways of Seeing Nujoom Alghanem’s Nearby Sky (سماء قريبة) and Sharp Tools (آلات حادة) as Docupoetry von Hambuch, Doris

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