Comprehensive profiling of metaplastic breast carcinomas reveals frequent overexpression of programmed death-ligand 1 von Joneja, Upasana, Vranic, Semir, Swensen, Jeffrey, Feldman, Rebecca, Chen, Wangjuh, Kimbrough, Jeffrey, Xiao, Nianqing, Reddy, Sandeep, Palazzo, Juan, Gatalica, Zoran

Volltext

High microsatellite instability (MSI-H) colorectal carcinoma: a brief review of predictive biomarkers in the era of personalized medicine von Gatalica, Zoran, Vranic, Semir, Xiu, Joanne, Swensen, Jeffrey, Reddy, Sandeep

Volltext

NUTM1-rearranged neoplasia: a multi-institution experience yields novel fusion partners and expands the histologic spectrum von Stevens, Todd M., Morlote, Diana, Xiu, Joanne, Swensen, Jeffrey, Brandwein-Weber, Margaret, Miettinen, Markku M., Gatalica, Zoran, Bridge, Julia A.

Volltext

Comprehensive molecular profiling of advanced/metastatic olfactory neuroblastomas von Topcagic, Jasmina, Feldman, Rebecca, Ghazalpour, Anatole, Swensen, Jeffrey, Gatalica, Zoran, Vranic, Semir

Volltext

Pan-tumor survey of ROS1 fusions detected by next-generation RNA and whole transcriptome sequencing von Nagasaka, Misako, Zhang, Shannon S, Baca, Yasmine, Xiu, Joanne, Nieva, Jorge, Vanderwalde, Ari, Swensen, Jeffrey J, Spetzler, David, Korn, Wolfgang Michael, Raez, Luis E, Liu, Stephen V, Ou, Sai-Hong Ignatius

Volltext

Potential Novel Therapy Targets in Neuroendocrine Carcinomas of the Breast von Vranic, Semir, Palazzo, Juan, Sanati, Souzan, Florento, Elena, Contreras, Elma, Xiu, Joanne, Swensen, Jeffrey, Gatalica, Zoran

Volltext

Molecular Profiling of the Metaplastic Spindle Cell Carcinoma of the Breast Reveals Potentially Targetable Biomarkers von Vranic, Semir, Stafford, Phillip, Palazzo, Juan, Skenderi, Faruk, Swensen, Jeffrey, Xiu, Joanne, Spetzler, David, Gatalica, Zoran

Volltext

Novel therapeutic targets in salivary duct carcinoma uncovered by comprehensive molecular profiling von Gargano, Stacey M., Senarathne, Wijendra, Feldman, Rebecca, Florento, Elena, Stafford, Phillip, Swensen, Jeffrey, Vranic, Semir, Gatalica, Zoran

Volltext

Pan-tumor survey of RET fusions as detected by next-generation RNA sequencing identified RET fusion positive colorectal carcinoma as a unique molecular subset von Nagasaka, Misako, Brazel, Danielle, Baca, Yasmine, Xiu, Joanne, Al-Hallak, Mohammed Najeeb, Kim, Chul, Nieva, Jorge, Swensen, Jeffrey J., Spetzler, David, Korn, Wolfgang Michael, Socinski, Mark A., Raez, Luis E., Halmos, Balazs, Ou, Sai-Hong Ignatius

Volltext

Disseminated histiocytoses biomarkers beyond BRAFV600E: frequent expression of PD-L1 von Gatalica, Zoran, Bilalovic, Nurija, Palazzo, Juan P, Bender, Ryan P, Swensen, Jeffrey, Millis, Sherri Z, Vranic, Semir, Von Hoff, Daniel, Arceci, Robert J

Volltext

Molecular characterization of cancers with NTRK gene fusions von Gatalica, Zoran, Xiu, Joanne, Swensen, Jeffrey, Vranic, Semir

Volltext

Clinical analysis of PMS2: mutation detection and avoidance of pseudogenes von Vaughn, Cecily P, Robles, Jorge, Swensen, Jeffrey J, Miller, Christine E, Lyon, Elaine, Mao, Rong, Bayrak-Toydemir, Pinar, Samowitz, Wade S

Volltext

Avoidance of pseudogene interference in the detection of 3′ deletions in PMS2 von Vaughn, Cecily P., Hart, Kimberly J., Samowitz, Wade S., Swensen, Jeffrey J.

Volltext

Using VAAST to Identify an X-Linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency von Rope, Alan F., Wang, Kai, Evjenth, Rune, Xing, Jinchuan, Johnston, Jennifer J., Swensen, Jeffrey J., Johnson, W. Evan, Moore, Barry, Huff, Chad D., Bird, Lynne M., Carey, John C., Opitz, John M., Stevens, Cathy A., Jiang, Tao, Schank, Christa, Fain, Heidi Deborah, Robison, Reid, Dalley, Brian, Chin, Steven, South, Sarah T., Pysher, Theodore J., Jorde, Lynn B., Hakonarson, Hakon, Lillehaug, Johan R., Biesecker, Leslie G., Yandell, Mark, Arnesen, Thomas, Lyon, Gholson J.

Volltext

Identification of Novel CDH1-NRG2α and F11R-NRG2α Fusions in NSCLC Plus Additional Novel NRG2α Fusions in Other Solid Tumors by Whole Transcriptome Sequencing von Ou, Sai-Hong Ignatius, Xiu, Joanne, Nagasaka, Misako, Xia, Bing, Zhang, Shannon S., Zhang, Qing, Swensen, Jeffrey J., Spetzler, David, Korn, Wolfgang Michael, Zhu, Viola W., Liu, Stephen V.

Volltext

The frequency of previously undetectable deletions involving 3′ Exons of the PMS2 gene von Vaughn, Cecily P., Baker, Christine L., Samowitz, Wade S., Swensen, Jeffrey J.

Volltext

Constitutional mismatch repair deficiency presenting in childhood as three simultaneous malignancies von Walter, Andrew W., Ennis, Sara, Best, Hunter, Vaughn, Cecily P., Swensen, Jeffrey J., Openshaw, Amanda, Gripp, Karen W.

Volltext

Noncontinuously Binding Loop-Out Primers for Avoiding Problematic DNA Sequences in PCR and Sanger Sequencing von Sumner, Kelli, Swensen, Jeffrey J, Procter, Melinda, Jama, Mohamed, Wooderchak-Donahue, Whitney, Lewis, Tracey, Fong, Michael, Hubley, Lindsey, Schwarz, Monica, Ha, Youna, Paul, Eleri, Brulotte, Benjamin, Lyon, Elaine, Bayrak-Toydemir, Pinar, Mao, Rong, Pont-Kingdon, Genevieve, Best, D. Hunter

Volltext

Using VAAST to Identify an X-linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency von Rope, Alan F., Wang, Kai, Evjenth, Rune, Xing, Jinchuan, Johnston, Jennifer J., Swensen, Jeffrey J., Johnson, W. Evan, Moore, Barry, Huff, Chad D., Bird, Lynne M., Carey, John C., Opitz, John M., Stevens, Cathy A., Jiang, Tao, Schank, Christa, Fain, Heidi Deborah, Robison, Reid, Dalley, Brian, Chin, Steven, South, Sarah T., Pysher, Theodore J., Jorde, Lynn B., Hakonarson, Hakon, Lillehaug, Johan R., Biesecker, Leslie G., Yandell, Mark, Arnesen, Thomas, Lyon, Gholson J.

Volltext

Sickle cell disease resulting from uniparental disomy in a child who inherited sickle cell trait von Swensen, Jeffrey J., Agarwal, Archana M., Esquilin, Jose M., Swierczek, Sabina, Perumbeti, Ajay, Hussey, Dottie, Lee, Margaret, Joiner, Clinton H., Pont-Kingdon, Genevieve, Lyon, Elaine, Prchal, Josef T.

Volltext