Compliance and Falsification of Duty Hours: Reports From Residents and Program Directors

von Drolet, Brian C., Schwede, Matthew, Bishop, Kenneth D., Fischer, Staci A.
Veröffentlicht 2013

An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma

von Minhas, Hassan M., Pescosolido, Matthew F., Schwede, Matthew, Piasecka, Justyna, Gaitanis, John, Tantravahi, Umadevi, Morrow, Eric M.
Veröffentlicht 2013

Stem Cell-Like Gene Expression in Ovarian Cancer Predicts Type II Subtype and Prognosis

von Schwede, Matthew, Spentzos, Dimitrios, Bentink, Stefan, Hofmann, Oliver, Haibe-Kains, Benjamin, Harrington, David, Quackenbush, John, Culhane, Aedín C.
Veröffentlicht 2013

Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex

von Schwede, Matthew, Nagpal, Shailender, Gandal, Michael J., Parikshak, Neelroop N., Mirnics, Karoly, Geschwind, Daniel H., Morrow, Eric M.
Veröffentlicht in J Neurodev Disord (2018)

Effects of bone marrow‐derived mesenchymal stromal cells on gene expression in human alveolar type II cells exposed to TNF‐α, IL‐1β, and IFN‐γ

von Schwede, Matthew, Wilfong, Erin M., Zemans, Rachel L., Lee, Patty J., dos Santos, Claudia, Fang, Xiaohui, Matthay, Michael A.
Veröffentlicht in Physiol Rep (2018)

Proinflammatory cytokines and ARDS pulmonary edema fluid induce CD40 on human mesenchymal stromal cells—A potential mechanism for immune modulation

von Wilfong, Erin M., Croze, Roxanne, Fang, Xiaohui, Schwede, Matthew, Niemi, Erene, López, Giselle Y., Lee, Jae-Woo, Nakamura, Mary C., Matthay, Michael A.
Veröffentlicht in PLoS One (2020)

Clinician recognition of the acute respiratory distress syndrome: Risk factors for under-recognition and trends over time

von Schwede, Matthew, Lee, Robert Y., Zhuo, Hanjing, Kangelaris, Kirsten N., Jauregui, Alejandra, Vessel, Kathryn, Belzer, Annika, Deiss, Thomas, Matthay, Michael A., Liu, Kathleen D., Calfee, Carolyn S.
Veröffentlicht in Crit Care Med (2020)

Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein

von Pescosolido, Matthew F, Schwede, Matthew, Johnson Harrison, Ashley, Schmidt, Michael, Gamsiz, Ece D, Chen, Wendy S, Donahue, John P, Shur, Natasha, Jerskey, Beth A, Phornphutkul, Chanika, Morrow, Eric M
Veröffentlicht 2014

The impact of stroma admixture on molecular subtypes and prognostic gene signatures in serous ovarian cancer

von Schwede, Matthew, Waldron, Levi, Mok, Samuel C., Wei, Wei, Basunia, Azfar, Merritt, Melissa A., Mitsiades, Constantine S., Parmigiani, Giovanni, Harrington, David, Quackenbush, John, Birrer, Michael J., Culhane, Aedín C.
Veröffentlicht in Cancer Epidemiol Biomarkers Prev (2019)

Gene Expression Signature of Normal Cell-of-Origin Predicts Ovarian Tumor Outcomes

von Merritt, Melissa A., Bentink, Stefan, Schwede, Matthew, Iwanicki, Marcin P., Quackenbush, John, Woo, Terri, Agoston, Elin S., Reinhardt, Ferenc, Crum, Christopher P., Berkowitz, Ross S., Mok, Samuel C., Witt, Abigail E., Jones, Michelle A., Wang, Bin, Ince, Tan A.
Veröffentlicht 2013

Taxonomy of breast cancer based on normal cell phenotype predicts outcome

von Santagata, Sandro, Thakkar, Ankita, Ergonul, Ayse, Wang, Bin, Woo, Terri, Hu, Rong, Harrell, J. Chuck, McNamara, George, Schwede, Matthew, Culhane, Aedin C., Kindelberger, David, Rodig, Scott, Richardson, Andrea, Schnitt, Stuart J., Tamimi, Rulla M., Ince, Tan A.
Veröffentlicht 2014

Profiles of Genomic Instability in High-Grade Serous Ovarian Cancer Predict Treatment Outcome

von Wang, Zhigang C., Birkbak, Nicolai Juul, Culhane, Aedín C., Drapkin, Ronny, Fatima, Aquila, Tian, Ruiyang, Schwede, Matthew, Alsop, Kathryn, Daniels, Kathryn E., Piao, Huiying, Liu, Joyce, Etemadmoghadam, Dariush, Miron, Alexander, Salvesen, Helga B., Mitchell, Gillian, DeFazio, Anna, Quackenbush, John, Berkowitz, Ross S., Iglehart, J. Dirk, Bowtell, David D.L., Matulonis, Ursula A.
Veröffentlicht 2012

Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features

von Ouyang, Qing, Nakayama, Tojo, Baytas, Ozan, Davidson, Shawn M., Yang, Chendong, Schmidt, Michael, Lizarraga, Sofia B., Mishra, Sasmita, EI-Quessny, Malak, Niaz, Saima, Gul Butt, Mirrat, Imran Murtaza, Syed, Javed, Afzal, Chaudhry, Haroon Rashid, Vaughan, Dylan J., Hill, R. Sean, Partlow, Jennifer N., Yoo, Seung-Yun, Lam, Anh-Thu N., Nasir, Ramzi, Al-Saffar, Muna, Barkovich, A. James, Schwede, Matthew, Nagpal, Shailender, Rajab, Anna, DeBerardinis, Ralph J., Housman, David E., Mochida, Ganeshwaran H., Morrow, Eric M.
Veröffentlicht in Proc Natl Acad Sci U S A (2016)