Characterizing the Major Structural Variant Alleles of the Human Genome von Audano, Peter A., Sulovari, Arvis, Graves-Lindsay, Tina A., Cantsilieris, Stuart, Sorensen, Melanie, Welch, AnneMarie E., Dougherty, Max L., Nelson, Bradley J., Shah, Ankeeta, Dutcher, Susan K., Warren, Wesley C., Magrini, Vincent, McGrath, Sean D., Li, Yang I., Wilson, Richard K., Eichler, Evan E.

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Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain von Wang, Xu, Sun, Qi, McGrath, Sean D, Mardis, Elaine R, Soloway, Paul D, Clark, Andrew G

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Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects von Mertens, Jerome, Paquola, Apuã C.M., Ku, Manching, Hatch, Emily, Böhnke, Lena, Ladjevardi, Shauheen, McGrath, Sean, Campbell, Benjamin, Lee, Hyungjun, Herdy, Joseph R., Gonçalves, J. Tiago, Toda, Tomohisa, Kim, Yongsung, Winkler, Jürgen, Yao, Jun, Hetzer, Martin W., Gage, Fred H.

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BreakDancer: an algorithm for high-resolution mapping of genomic structural variation von Chen, Ken, Wallis, John W, McLellan, Michael D, Larson, David E, Kalicki, Joelle M, Pohl, Craig S, McGrath, Sean D, Wendl, Michael C, Zhang, Qunyuan, Locke, Devin P, Shi, Xiaoqi, Fulton, Robert S, Ley, Timothy J, Wilson, Richard K, Ding, Li, Mardis, Elaine R

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Segmental Duplications and Copy-Number Variation in the Human Genome von Sharp, Andrew J., Locke, Devin P., McGrath, Sean D., Cheng, Ze, Bailey, Jeffrey A., Vallente, Rhea U., Pertz, Lisa M., Clark, Royden A., Schwartz, Stuart, Segraves, Rick, Oseroff, Vanessa V., Albertson, Donna G., Pinkel, Daniel, Eichler, Evan E.

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Addressing treatment switching in the ALTA-1L trial with g-methods: exploring the impact of model specification von Al Tawil, Amani, McGrath, Sean, Ristl, Robin, Mansmann, Ulrich

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Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms within Duplicated Regions of the Human Genome von Locke, Devin P., Sharp, Andrew J., McCarroll, Steven A., McGrath, Sean D., Newman, Tera L., Cheng, Ze, Schwartz, Stuart, Albertson, Donna G., Pinkel, Daniel, Altshuler, David M., Eichler, Evan E.

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Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing von Ding, Li, Ley, Timothy J., Larson, David E., Miller, Christopher A., Koboldt, Daniel C., Welch, John S., Ritchey, Julie K., Young, Margaret A., Lamprecht, Tamara, McLellan, Michael D., McMichael, Joshua F., Wallis, John W., Lu, Charles, Shen, Dong, Harris, Christopher C., Dooling, David J., Fulton, Robert S., Fulton, Lucinda L., Chen, Ken, Schmidt, Heather, Kalicki-Veizer, Joelle, Magrini, Vincent J., Cook, Lisa, McGrath, Sean D., Vickery, Tammi L., Wendl, Michael C., Heath, Sharon, Watson, Mark A., Link, Daniel C., Tomasson, Michael H., Shannon, William D., Payton, Jacqueline E., Kulkarni, Shashikant, Westervelt, Peter, Walter, Matthew J., Graubert, Timothy A., Mardis, Elaine R., Wilson, Richard K., DiPersio, John F.

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Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content von Hughes, Jennifer F., Skaletsky, Helen, Pyntikova, Tatyana, Graves, Tina A., van Daalen, Saskia K. M., Minx, Patrick J., Fulton, Robert S., McGrath, Sean D., Locke, Devin P., Friedman, Cynthia, Trask, Barbara J., Mardis, Elaine R., Warren, Wesley C., Repping, Sjoerd, Rozen, Steve, Wilson, Richard K., Page, David C.

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Can we predict the severe course of COVID-19 - a systematic review and meta-analysis of indicators of clinical outcome? von Katzenschlager, Stephan, Zimmer, Alexandra J, Gottschalk, Claudius, Grafeneder, Jürgen, Schmitz, Stephani, Kraker, Sara, Ganslmeier, Marlene, Muth, Amelie, Seitel, Alexander, Maier-Hein, Lena, Benedetti, Andrea, Larmann, Jan, Weigand, Markus A, McGrath, Sean, Denkinger, Claudia M

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A Sequence Motif within Chromatin Entry Sites Directs MSL Establishment on the Drosophila X Chromosome von Alekseyenko, Artyom A., Peng, Shouyong, Larschan, Erica, Gorchakov, Andrey A., Lee, Ok-Kyung, Kharchenko, Peter, McGrath, Sean D., Wang, Charlotte I., Mardis, Elaine R., Park, Peter J., Kuroda, Mitzi I.

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Genome remodelling in a basal-like breast cancer metastasis and xenograft von Ding, Li, Ellis, Matthew J., Li, Shunqiang, Larson, David E., Chen, Ken, Wallis, John W., Harris, Christopher C., McLellan, Michael D., Fulton, Robert S., Fulton, Lucinda L., Abbott, Rachel M., Hoog, Jeremy, Dooling, David J., Koboldt, Daniel C., Schmidt, Heather, Kalicki, Joelle, Zhang, Qunyuan, Chen, Lei, Lin, Ling, Wendl, Michael C., McMichael, Joshua F., Magrini, Vincent J., Cook, Lisa, McGrath, Sean D., Vickery, Tammi L., Appelbaum, Elizabeth, DeSchryver, Katherine, Davies, Sherri, Guintoli, Therese, Lin, Li, Crowder, Robert, Tao, Yu, Snider, Jacqueline E., Smith, Scott M., Dukes, Adam F., Sanderson, Gabriel E., Pohl, Craig S., Delehaunty, Kim D., Fronick, Catrina C., Pape, Kimberley A., Reed, Jerry S., Robinson, Jody S., Hodges, Jennifer S., Schierding, William, Dees, Nathan D., Shen, Dong, Locke, Devin P., Wiechert, Madeline E., Eldred, James M., Peck, Josh B., Oberkfell, Benjamin J., Lolofie, Justin T., Du, Feiyu, Hawkins, Amy E., O’Laughlin, Michelle D., Bernard, Kelly E., Cunningham, Mark, Elliott, Glendoria, Mason, Mark D., Thompson Jr, Dominic M., Ivanovich, Jennifer L., Goodfellow, Paul J., Perou, Charles M., Weinstock, George M., Aft, Rebecca, Watson, Mark, Ley, Timothy J., Wilson, Richard K., Mardis, Elaine R.

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Cave hominem: Critical Reflections on the Treatment of Domestic Animals in Pseudo-Oppian’s Cynegetica von McGrath, Sean E.

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Cave hominem von McGrath, Sean E

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Identification of difficult laryngoscopy using an optimized hybrid architecture von Liu, XiaoXiao, Flanagan, Colin, Li, Gang, Lei, Yiming, Zeng, Liaoyuan, Fang, Jingchao, Guo, Xiangyang, McGrath, Sean, Han, Yongzheng

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Optimizing Cancer Genome Sequencing and Analysis von Griffith, Malachi, Miller, Christopher A., Griffith, Obi L., Krysiak, Kilannin, Skidmore, Zachary L., Ramu, Avinash, Walker, Jason R., Dang, Ha X., Trani, Lee, Larson, David E., Demeter, Ryan T., Wendl, Michael C., McMichael, Joshua F., Austin, Rachel E., Magrini, Vincent, McGrath, Sean D., Ly, Amy, Kulkarni, Shashikant, Cordes, Matthew G., Fronick, Catrina C., Fulton, Robert S., Maher, Christopher A., Ding, Li, Klco, Jeffery M., Mardis, Elaine R., Ley, Timothy J., Wilson, Richard K.

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Impact of molecular diagnostic tests on diagnostic and treatment delays in tuberculosis: a systematic review and meta-analysis von Lee, Jae Hyoung, Garg, Tushar, Lee, Jungsil, McGrath, Sean, Rosman, Lori, Schumacher, Samuel G, Benedetti, Andrea, Qin, Zhi Zhen, Gore, Genevieve, Pai, Madhukar, Sohn, Hojoon

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Long‐read whole genome sequencing reveals HOXD13 alterations in synpolydactyly von Melas, Marilena, Kautto, Esko A., Franklin, Samuel J., Mori, Mari, McBride, Kim L., Mosher, Theresa Mihalic, Pfau, Ruthann B., Hernandez‐Gonzalez, Maria Elena, McGrath, Sean D., Magrini, Vincent J., White, Peter, Samora, Julie Balch, Koboldt, Daniel C., Wilson, Richard K.

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Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome–Based Resolution of Isoform Complexity von Miller, Anthony R., Wijeratne, Saranga, McGrath, Sean D., Schieffer, Kathleen M., Miller, Katherine E., Lee, Kristy, Mathew, Mariam, LaHaye, Stephanie, Fitch, James R., Kelly, Benjamin J., White, Peter, Mardis, Elaine R., Wilson, Richard K., Cottrell, Catherine E., Magrini, Vincent

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Gastroblastoma with a novel EWSR1‐CTBP1 fusion presenting in adolescence von Koo, Selene C., LaHaye, Stephanie, Kovari, Bence P., Schieffer, Kathleen M., Ranalli, Mark A., Aldrink, Jennifer H., Michalsky, Marc P., Colace, Susan, Miller, Katherine E., Bedrosian, Tracy A., Leraas, Kristen M., Voytovich, Kyle, Wheeler, Gregory, Brennan, Patrick, Fitch, James, Kelly, Benjamin J., McGrath, Sean D., Miller, Anthony R., White, Peter, Magrini, Vincent, Wilson, Richard K., Mardis, Elaine R., Lauwers, Gregory Y., Baker, Peter B., Cottrell, Catherine E.

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