未登录 Feasibility of institution-agnostic, EHR-integrated regional clinical trial matching 与机构无关，EHR集成的区域临床试验匹配的可行性 Shriver, Sharon P.; Arafat, Waddah; Potteiger, Caroline; Butler, Dorothy L.; Beg, Muhammad S.; Hullings, Melanie; Semy, Salim; Lister, Zach; Khosama, Leticia; Armstrong, Susan; Hadley, David; Pappa, John; Fleury, Mark E. 分享 收藏
Morphology-Predicted Large-Scale Transition Number in Circulating Tumor Cells Identifies a Chromosomal Instability Biomarker Associated with Poor Outcome in Castration-Resistant Prostate Cancer Schonhoft, Joseph D.; Zhao, Jimmy L.; Jendrisak, Adam; Carbone, Emily A.; Barnett, Ethan S.; Hullings, Melanie A.; Gill, Audrey; Sutton, Ramsay; Lee, Jerry; Dago, Angel E.; Landers, Mark; Bakhoum, Samuel F.; Wang, Yipeng; Gonen, Mithat; Dittamore, Ryan; Scher, Howard I. 分享 收藏
Oncogenic Genomic Alterations, Clinical Phenotypes, and Outcomes in Metastatic Castration-Sensitive for Prostate Cancer 转移性去势敏感性前列腺癌的致癌基因组改变，临床表型和结局 Stopsack, Konrad H.; Nandakumar, Subhiksha; Wibmer, Andreas G.; Haywood, Samuel; Weg, Emily S.; Barnett, Ethan S.; Kim, Chloe J.; Carbone, Emily A.; Vasselman, Samantha E.; Nguyen, Bastien; Hullings, Melanie A.; Scher, Howard I.; Morris, Michael J.; Solit, David B.; Schultz, Nikolaus; Kantoff, Philip W.; Abida, Wassim 分享 收藏
Minimum Technical Data Elements for Liquid Biopsy Data Submitted to Public Databases 提交给公共数据库的液体活检数据的最低技术数据元素 Febbo, Phillip G.; Martin, Anne-Marie; Scher, Howard I.; Barrett, J. Carl; Beaver, Julia A.; Beresford, Paul J.; Blumenthal, Gideon M.; Bramlett, Kelli; Compton, Carolyn; Dittamore, Ryan; Eberhard, David A.; Edelstein, Daniel; Godsey, James; Gruen, Andrew; Hanlon, Sean E.; Hicks, James; Hovelson, Daniel; Hullings, Melanie; Johann, Donald; Johnson, Justin; Kolatkar, Anand; Kuhn, Peter; Levine, Rebecca; Martini, Jean-Francois; Miller, Daniel P.; Moore, Carissa; Moy, Bryan; Pathak, Anand; Philip, Reena; Reese, David; Royalty, Wendy; Ryder, Matthew; Sakul, Hakan; Salvatore, Lea M.; Schade, Andrew; Silvestro, Angela; Simmons, John K.; Simons, Jonathan; Bhan, Seema Singh; Smalley, Matthew D.; Somiari, Stella B.; Talasaz, AmirAli; Tewari, Muneesh; Tseng, Hsian-Rong; Vinson, Jake; Wells, Walt; Welsh, Allison; Grossman, Robert L.; Lee, Jerry S. H.; Leiman, Lauren C. 分享 收藏
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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance Kaiser, Frank J.; Ansari, Morad; Braunholz, Diana; Gil-Rodriguez, Maria Concepcion; Decroos, Christophe; Wilde, Jonathan J.; Fincher, Christopher T.; Kaur, Maninder; Bando, Masashige; Amor, David J.; Atwal, Paldeep S.; Bahlo, Melanie; Bowman, Christine M.; Bradley, Jacquelyn J.; Brunner, Han G.; Clark, Dinah; Del Campo, Miguel; Di Donato, Nataliya; Diakumis, Peter; Dubbs, Holly; Dyment, David A.; Eckhold, Juliane; Ernst, Sarah; Ferreira, Jose C.; Francey, Lauren J.; Gehlken, Ulrike; Guillen-Navarro, Encarna; Gyftodimou, Yolanda; Hall, Bryan D.; Hennekam, Raoul; Hudgins, Louanne; Hullings, Melanie; Hunter, Jennifer M.; Yntema, Helger; Innes, A. Micheil; Kline, Antonie D.; Krumina, Zita; Lee, Hane; Leppig, Kathleen; Lynch, Sally Ann; Mallozzi, Mark B.; Mannini, Linda; Mckee, Shane; Mehta, Sarju G.; Micule, Ieva; Mohammed, Shehla; Moran, Ellen; Mortier, Geert R.; Moser, Joe-Ann S.; Noon, Sarah E.; Nozaki, Naohito; Nunes, Luis; Pappas, John G.; Penney, Lynette S.; Perez-Aytes, Antonio; Petersen, Michael B.; Puisac, Beatriz; Revencu, Nicole; Roeder, Elizabeth; Saitta, Sulagna; Scheuerle, Angela E.; Schindeler, Karen L.; Siu, Victoria M.; Stark, Zornitza; Strom, Samuel P.; Thiese, Heidi; Vater, Inga; Willems, Patrick; Williamson, Kathleen; Wilson, Louise C.; Hakonarson, Hakon; Quintero-Rivera, Fabiola; Wierzba, Jolanta; Musio, Antonio; Gillessen-Kaesbach, Gabriele; Ramos, Feliciano J.; Jackson, Laird G.; Shirahige, Katsuhiko; Pie, Juan; Christianson, David W.; Krantz, Ian D.; Fitzpatrick, David R.; Deardorff, Matthew A. 分享 收藏
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Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (vol 20, pg 271, 2012) Braunholz, Diana; Hullings, Melanie; Gil-Rodriguez, Maria Concepcion; Fincher, Christopher T.; Mallozzi, Mark B.; Loy, Elizabeth; Albrecht, Melanie; Kaur, Maninder; Limon, Janusz; Rampuria, Abhinav; Clark, Dinah; Kline, Antonie; Dalski, Andreas; Eckhold, Juliane; Tzschach, Andreas; Hennekam, Raoul; Gillessen-Kaesbach, Gabriele; Wierzba, Jolanta; Krantz, Ian D.; Deardorff, Matthew A.; Kaiser, Frank J. 分享 收藏
Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction Braunholz, Diana; Hullings, Melanie; Concepcion Gil-Rodriguez, Maria; Fincher, Christopher T.; Mallozzi, Mark B.; Loy, Elizabeth; Albrecht, Melanie; Kaur, Maninder; Limon, Janusz; Rampuria, Abhinav; Clark, Dinah; Kline, Antonie; Dalski, Andreas; Eckhold, Juliane; Tzschach, Andreas; Hennekam, Raoul; Gillessen-Kaesbach, Gabriele; Wierzba, Jolanta; Krantz, Ian D.; Deardorff, Matthew A.; Kaiser, Frank J. 分享 收藏
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