Cohesin Mutations in Human Cancer

per Hill, Victoria K., Kim, Jung-Sik, Waldman, Todd
Publicat a Biochim Biophys Acta (2016)

Tumor-Specific Hypermethylation of Epigenetic Biomarkers, Including SFRP1, Predicts for Poorer Survival in Patients from the TCGA Kidney Renal Clear Cell Carcinoma (KIRC) Project

per Ricketts, Christopher J., Hill, Victoria K., Linehan, W. Marston
Publicat 2014

Correction of PTEN mutations in glioblastoma cell lines via AAV-mediated gene editing

per Hill, Victoria K., Kim, Jung-Sik, James, C. David, Waldman, Todd
Publicat a PLoS One (2017)

Frequent epigenetic inactivation of KIBRA, an upstream member of the Salvador/Warts/Hippo (SWH) tumor suppressor network, is associated with specific genetic event in B-cell acute...

per Hill, Victoria K, Dunwell, Thomas, Catchpoole, Daniel, Krex, Dietmar, Brini, Anna T, Griffiths, Mike, Craddock, Charles, Maher, Eamonn R, Latif, Farida
Publicat 2011

DNA methylation profiles of long- and short-term glioblastoma survivors

per Shinawi, Thoraia, Hill, Victoria K., Krex, Dietmar, Schackert, Gabriele, Gentle, Dean, Morris, Mark R., Wei, Wenbin, Cruickshank, Garth, Maher, Eamonn R., Latif, Farida
Publicat 2013

Stability of the CpG island methylator phenotype during glioma progression and identification of methylated loci in secondary glioblastomas

per Hill, Victoria K, Shinawi, Thoraia, Ricketts, Christopher J, Krex, Dietmar, Schackert, Gabriele, Bauer, Julien, Wei, Wenbin, Cruickshank, Garth, Maher, Eamonn R, Latif, Farida
Publicat a BMC Cancer (2014)

Somatic mutation of GRIN2A in malignant melanoma results in loss of tumor suppressor activity via aberrant NMDAR complex formation

per Prickett, Todd D., Zerlanko, Brad J., Hill, Victoria K., Gartner, Jared J., Qutob, Nouar, Jiang, Jiji, Simaan, May, Wunderlich, John, Gutkind, J. Silvio, Rosenberg, Steven A., Samuels, Yardena
Publicat 2014

Identification of 5 novel genes methylated in breast and other epithelial cancers

per Hill, Victoria K, Hesson, Luke B, Dansranjavin, Temuujin, Dallol, Ashraf, Bieche, Ivan, Vacher, Sophie, Tommasi, Stella, Dobbins, Timothy, Gentle, Dean, Euhus, David, Lewis, Cheryl, Dammann, Reinhard, Ward, Robyn L, Minna, John, Maher, Eammon R, Pfeifer, Gerd P, Latif, Farida
Publicat 2010

RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells

per Qutob, Nouar, Masuho, Ikuo, Alon, Michal, Emmanuel, Rafi, Cohen, Isadora, Di Pizio, Antonella, Madore, Jason, Elkahloun, Abdel, Ziv, Tamar, Levy, Ronen, Gartner, Jared J., Hill, Victoria K., Lin, Jimmy C., Hevroni, Yael, Greenberg, Polina, Brodezki, Alexandra, Rosenberg, Steven A., Kosloff, Mickey, Hayward, Nicholas K., Admon, Arie, Niv, Masha Y., Scolyer, Richard A., Martemyanov, Kirill A., Samuels, Yardena
Publicat a Sci Rep (2018)

Author Correction: RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells

per Qutob, Nouar, Masuho, Ikuo, Alon, Michal, Emmanuel, Rafi, Cohen, Isadora, Di Pizio, Antonella, Madore, Jason, Elkahloun, Abdel, Ziv, Tamar, Levy, Ronen, Gartner, Jared J., Hill, Victoria K., Lin, Jimmy C., Hevroni, Yael, Greenberg, Polina, Brodezki, Alexandra, Rosenberg, Steven A., Kosloff, Mickey, Hayward, Nicholas K., Admon, Arie, Niv, Masha Y., Scolyer, Richard A., Martemyanov, Kirill A., Samuels, Yardena
Publicat a Sci Rep (2019)

Recurrent inactivating RASA2 mutations in melanoma

per Arafeh, Rand, Qutob, Nouar, Emmanuel, Rafi, Keren-Paz, Alona, Madore, Jason, Elkahloun, Abdel, Wilmott, James S., Gartner, Jared J., Di Pizio, Antonella, Winograd-Katz, Sabina, Sindiri, Sivasish, Rotkopf, Ron, Dutton-Regester, Ken, Johansson, Peter, Pritchard, Antonia, Waddell, Nicola, Hill, Victoria K., Lin, Jimmy C., Hevroni, Yael, Rosenberg, Steven A., Khan, Javed, Ben-Dor, Shifra, Niv, Masha Y., Ulitsky, Igor, Mann, Graham J, Scolyer, Richard A., Hayward, Nicholas K., Samuels, Yardena
Publicat a Nat Genet (2015)