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

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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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Successful Application of Whole Genome Sequencing in a Medical Genetics Clinic von Bick, David, Fraser, Pamela C., Gutzeit, Michael F., Harris, Jeremy M., Hambuch, Tina M., Helbling, Daniel C., Jacob, Howard J., Kersten, Juliet N., Leuthner, Steven R., May, Thomas, North, Paula E., Prisco, Sasha Z., Schuler, Bryce A., Shimoyama, Mary, Strong, Kimberly A., Van Why, Scott K., Veith, Regan, Verbsky, James, Weborg, Arthur M., Wilk, Brandon M., Willoughby, Rodney E., Worthey, Elizabeth A., Dimmock, David P.

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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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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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ENHANCED SELECTION FOR MHC DIVERSITY IN SOCIAL TUCO-TUCOS von Hambuch, Tina M, Lacey, Eileen 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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One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementation von Lincoln, Stephen E., Hambuch, Tina, Zook, Justin M., Bristow, Sara L., Hatchell, Kathryn, Truty, Rebecca, Kennemer, Michael, Shirts, Brian H., Fellowes, Andrew, Chowdhury, Shimul, Klee, Eric W., Mahamdallie, Shazia, Cleveland, Megan H., Vallone, Peter M., Ding, Yan, Seal, Sheila, DeSilva, Wasanthi, Tomson, Farol L., Huang, Catherine, Garlick, Russell K., Rahman, Nazneen, Salit, Marc, Kingsmore, Stephen F., Ferber, Matthew J., Aradhya, Swaroop, Nussbaum, Robert L.

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Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease von Gross, Andrew M., Ajay, Subramanian S., Rajan, Vani, Brown, Carolyn, Bluske, Krista, Burns, Nicole J., Chawla, Aditi, Coffey, Alison J., Malhotra, Alka, Scocchia, Alicia, Thorpe, Erin, Dzidic, Natasa, Hovanes, Karine, Sahoo, Trilochan, Dolzhenko, Egor, Lajoie, Bryan, Khouzam, Amirah, Chowdhury, Shimul, Belmont, John, Roller, Eric, Ivakhno, Sergii, Tanner, Stephen, McEachern, Julia, Hambuch, Tina, Eberle, Michael, Hagelstrom, R. Tanner, Bentley, David R., Perry, Denise L., Taft, Ryan J.

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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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Assuring the quality of next-generation sequencing in clinical laboratory practice von Gargis, Amy S, Kalman, Lisa, Berry, Meredith W, Bick, David P, Dimmock, David P, Hambuch, Tina, Lu, Fei, Lyon, Elaine, Voelkerding, Karl V, Zehnbauer, Barbara A, Agarwala, Richa, Bennett, Sarah F, Chen, Bin, Chin, Ephrem L H, Compton, John G, Das, Soma, Farkas, Daniel H, Ferber, Matthew J, Funke, Birgit H, Furtado, Manohar R, Ganova-Raeva, Lilia M, Geigenmüller, Ute, Gunselman, Sandra J, Hegde, Madhuri R, Johnson, Philip L F, Kasarskis, Andrew, Kulkarni, Shashikant, Lenk, Thomas, Liu, C S Jonathan, Manion, Megan, Manolio, Teri A, Mardis, Elaine R, Merker, Jason D, Rajeevan, Mangalathu S, Reese, Martin G, Rehm, Heidi L, Simen, Birgitte B, Yeakley, Joanne M, Zook, Justin M, Lubin, Ira M

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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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Whole exome sequencing in patients with white matter abnormalities von Vanderver, Adeline, Simons, Cas, Helman, Guy, Crawford, Joanna, Wolf, Nicole I., Bernard, Geneviève, Pizzino, Amy, Schmidt, Johanna L., Takanohashi, Asako, Miller, David, Khouzam, Amirah, Rajan, Vani, Ramos, Erica, Chowdhury, Shimul, Hambuch, Tina, Ru, Kelin, Baillie, Gregory J., Grimmond, Sean M., Caldovic, Ljubica, Devaney, Joseph, Bloom, Miriam, Evans, Sarah H., Murphy, Jennifer L. P., McNeill, Nathan, Fogel, Brent L., Schiffmann, Raphael, van der Knaap, Marjo S., Taft, Ryan J.

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Good laboratory practice for clinical next-generation sequencing informatics pipelines von Gargis, Amy S, Kalman, Lisa, Bick, David P, da Silva, Cristina, Dimmock, David P, Funke, Birgit H, Gowrisankar, Sivakumar, Hegde, Madhuri R, Kulkarni, Shashikant, Mason, Christopher E, Nagarajan, Rakesh, Voelkerding, Karl V, Worthey, Elizabeth A, Aziz, Nazneen, Barnes, John, Bennett, Sarah F, Bisht, Himani, Church, Deanna M, Dimitrova, Zoya, Gargis, Shaw R, Hafez, Nabil, Hambuch, Tina, Hyland, Fiona C L, Luna, Ruth Ann, MacCannell, Duncan, Mann, Tobias, McCluskey, Megan R, McDaniel, Timothy K, Ganova-Raeva, Lilia M, Rehm, Heidi L, Reid, Jeffrey, Campo, David S, Resnick, Richard B, Ridge, Perry G, Salit, Marc L, Skums, Pavel, Wong, Lee-Jun C, Zehnbauer, Barbara A, Zook, Justin M, Lubin, Ira M

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A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories von O’Daniel, Julianne M., McLaughlin, Heather M., Amendola, Laura M., Bale, Sherri J., Berg, Jonathan S., Bick, David, Bowling, Kevin M., Chao, Elizabeth C., Chung, Wendy K., Conlin, Laura K., Cooper, Gregory M., Das, Soma, Deignan, Joshua L., Dorschner, Michael O., Evans, James P., Ghazani, Arezou A., Goddard, Katrina A., Gornick, Michele, Farwell Hagman, Kelly D., Hambuch, Tina, Hegde, Madhuri, Hindorff, Lucia A., Holm, Ingrid A., Jarvik, Gail P., Knight Johnson, Amy, Mighion, Lindsey, Morra, Massimo, Plon, Sharon E., Punj, Sumit, Richards, C. Sue, Santani, Avni, Shirts, Brian H., Spinner, Nancy B., Tang, Sha, Weck, Karen E., Wolf, Susan M., Yang, Yaping, Rehm, Heidi L.

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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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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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Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology von Schrijver, Iris, Aziz, Nazneen, Farkas, Daniel H, Furtado, Manohar, Gonzalez, Andrea Ferreira, Greiner, Timothy C, Grody, Wayne W, Hambuch, Tina, Kalman, Lisa, Kant, Jeffrey A, Klein, Roger D, Leonard, Debra G B, Lubin, Ira M, Mao, Rong, Nagan, Narasimhan, Pratt, Victoria M, Sobel, Mark E, Voelkerding, Karl V, Gibson, Jane S

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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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