RE: BRCA1 and BRCA2 Gene Mutations and Colorectal Cancer Risk: Systematic Review and Meta-analysis

nork Katona, Bryson W, Stadler, Zsofia K, Robson, Mark E, Domchek, Susan M
Argitaratua izan da J Natl Cancer Inst (2019)

Cancer Genomics and Inherited Risk

nork Stadler, Zsofia K., Schrader, Kasmintan A., Vijai, Joseph, Robson, Mark E., Offit, Kenneth
Argitaratua izan da J Clin Oncol (2014)

Insertion of an Alu‐like element in MLH1 intron 7 as a novel cause of Lynch syndrome

nork Li, Yirong, Salo‐Mullen, Erin, Varghese, Anna, Trottier, Magan, Stadler, Zsofia K., Zhang, Liying
Argitaratua izan da Mol Genet Genomic Med (2020)

Immunotherapy in colorectal cancer: rationale, challenges and potential

nork Ganesh, Karuna, Stadler, Zsofia K., Cercek, Andrea, Mendelsohn, Robin B., Shia, Jinru, Segal, Neil H., Diaz, Luis A.
Argitaratua izan da Nat Rev Gastroenterol Hepatol (2019)

Genomic instability in pancreatic adenocarcinoma: a new step towards precision medicine and novel therapeutic approaches

nork Sahin, Ibrahim H., Lowery, Maeve A., Stadler, Zsofia K., Salo-Mullen, Erin, Iacobuzio-Donahue, Christine A., Kelsen, David P., O’Reilly, Eileen M.
Argitaratua izan da Expert Rev Gastroenterol Hepatol (2016)

Faster FOLFOX: Oxaliplatin Can Be Safely Infused at a Rate of 1 mg/m(2)/min

nork Cercek, Andrea, Park, Vivian, Yaeger, Rona, Reidy-Lagunes, Diane, Kemeny, Nancy E., Stadler, Zsofia K., Segal, Neil H., Varghese, Anna, Saltz, Leonard B.
Argitaratua izan da J Oncol Pract (2016)

Acquired resistance to immunotherapy in MMR-D pancreatic cancer

nork Hu, Zishuo Ian, Hellmann, Matthew D., Wolchok, Jedd D., Vyas, Monika, Shia, Jinru, Stadler, Zsofia K., Diaz, Luis A., O’Reilly, Eileen M.
Argitaratua izan da J Immunother Cancer (2018)

Correction to: Resolving pathogenicity classification for the CDH1 c.[715G>A] (p.Gly239Arg) variant

nork Yelskaya, Zarina, Arnold, Angela G., Marcell, Vanessa J., Tang, Laura H., Salo-Mullen, Erin E., Strong, Vivian E., Stadler, Zsofia K., Zhang, Liying
Argitaratua izan da Eur J Hum Genet (2021)

Resolving pathogenicity classification for the CDH1 c.[715G>A] (p.Gly239Arg) Variant

nork Yelskaya, Zarina, Arnold, Angela G., Marcell, Vanessa J., Tang, Laura H., Salo-Mullen, Erin E., Strong, Vivian E., Stadler, Zsofia K., Zhang, Liying
Argitaratua izan da Eur J Hum Genet (2021)

Immunohistochemical null-phenotype for mismatch repair proteins in colonic carcinoma associated with concurrent MLH1 hypermethylation and somatic MSH2 mutations

nork Wang, Tao, Stadler, Zsofia K., Zhang, Liying, Weiser, Martin R., Basturk, Olca, Hechtman, Jaclyn F., Vakiani, Efsevia, Saltz, Lenard B., Klimstra, David S., Shia, Jinru
Argitaratua izan da Fam Cancer (2018)

Retained Mismatch Repair Protein Expression Occurs in Approximately 6% of Microsatellite Instability-High Cancers and is Associated with Missense Mutations in Mismatch Repair Genes...

nork Hechtman, Jaclyn F., Rana, Satshil, Middha, Sumit, Stadler, Zsofia K., Latham, Alicia, Benayed, Ryma, Soslow, Robert, Ladanyi, Marc, Yaeger, Rona, Zehir, Ahmet, Shia, Jinru
Argitaratua izan da Mod Pathol (2019)

Genome-Wide Association Studies of Cancer

nork Stadler, Zsofia K., Thom, Peter, Robson, Mark E., Weitzel, Jeffrey N., Kauff, Noah D., Hurley, Karen E., Devlin, Vincent, Gold, Bert, Klein, Robert J., Offit, Kenneth
Argitaratua 2010

CDH1 Missense Variant c.1679C>G (p.T560R) Completely Disrupts Normal Splicing through Creation of a Novel 5’ Splice Site

nork Yelskaya, Zarina, Bacares, Ruben, Salo-Mullen, Erin, Somar, Joshua, Lehrich, Deborah A., Fasaye, Grace-Ann, Coit, Daniel G., Tang, Laura H., Stadler, Zsofia K., Zhang, Liying
Argitaratua izan da PLoS One (2016)

Somatic HNF1A Mutations in the Malignant Transformation of Hepatocellular Adenomas: A Retrospective Analysis of Data from MSK-IMPACT and TCGA

nork Hechtman, Jaclyn F, Alfa, Ghassan K. Abou, Stadler, Zsofia K., Mandelker, Diana L, Roehrl, Michael H.A., Zehir, Ahmet, Vakiani, Efsevia, Middha, Sumit, Klimstra, David S, Shia, Jinru
Argitaratua izan da Hum Pathol (2018)

Outcome of Pancreatic Cancer Surveillance Among High-Risk Individuals Tested for Germline Mutations in BRCA1 and BRCA2

nork Saldia, Amethyst, Olson, Sara H., Nunes, Pamela, Liang, Xiaolin, Samson, Marguerite L., Salo-Mullen, Erin, Marcell, Vanessa, Stadler, Zsofia K., Allen, Peter J., Offit, Kenneth, Kurtz, Robert C.
Argitaratua izan da Cancer Prev Res (Phila) (2019)

Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing

nork Balmaña, Judith, Digiovanni, Laura, Gaddam, Pragna, Walsh, Michael F., Joseph, Vijai, Stadler, Zsofia K., Nathanson, Katherine L., Garber, Judy E., Couch, Fergus J., Offit, Kenneth, Robson, Mark E., Domchek, Susan M.
Argitaratua izan da J Clin Oncol (2016)

Characterization of a novel germline PALB2 duplication in a hereditary breast and ovarian cancer family

nork Yang, Ciyu, Arnold, Angela G., Trottier, Magan, Sonoda, Yukio, Abu-Rustum, Nadeem R., Zivanovic, Oliver, Robson, Mark E., Stadler, Zsofia K., Walsh, Michael F., Hyman, David M., Offit, Kenneth, Zhang, Liying
Argitaratua izan da Breast Cancer Res Treat (2016)

Risk of Metachronous Colorectal Neoplasm After a Segmental Colectomy in Lynch Syndrome Patients According to Mismatch Repair Gene Status

nork Quezada-Diaz, Felipe F, Hameed, Irbaz, von Mueffling, Alexa, Salo-Mullen, Erin E, Catalano, John D, Smith, J Joshua, Weiser, Martin R, Garcia-Aguilar, Julio, Stadler, Zsofia K, Guillem, Jose G
Argitaratua izan da J Am Coll Surg (2020)

Tolerability of Breast Radiotherapy Among Carriers of ATM Germline Variants

nork Modlin, Leslie A., Flynn, Jessica, Zhang, Zhigang, Cahlon, Oren, Mueller, Boris, Khan, Atif J., Gillespie, Erin F., McCormick, Beryl, Stadler, Zsofia K., Robson, Mark E., Powell, Simon N., Braunstein, Lior Z.
Argitaratua izan da JCO Precis Oncol (2021)

Contiguous Gene Deletion of Chromosome 2p16.3-p21 as a Cause of Lynch Syndrome

nork Salo-Mullen, Erin E., Lynn, Patricio B., Wang, Lu, Walsh, Michael, Gopalan, Anuradha, Shia, Jinru, Tran, Christina, Man, Fung Ying, McBride, Sean, Schattner, Mark, Zhang, Liying, Weiser, Martin R., Stadler, Zsofia K.
Argitaratua izan da Fam Cancer (2018)