Phase 1 trial evaluating cisplatin, gemcitabine, and veliparib in 2 patient cohorts: Germline BRCA mutation carriers and wild‐type BRCA pancreatic ductal adenocarcinoma von O'Reilly, Eileen M., Lee, Jonathan W., Lowery, Maeve A., Capanu, Marinela, Stadler, Zsofia K., Moore, Malcolm J., Dhani, Neesha, Kindler, Hedy L., Estrella, Hayley, Maynard, Hannah, Golan, Talia, Segal, Amiel, Salo‐Mullen, Erin E., Yu, Kenneth H., Epstein, Andrew S., Segal, Michal, Brenner, Robin, Do, Richard K., Chen, Alice P., Tang, Laura H., Kelsen, David P.

Volltext

Identification of germline genetic mutations in patients with pancreatic cancer von Salo‐Mullen, Erin E., O'Reilly, Eileen M., Kelsen, David P., Ashraf, Asad M., Lowery, Maeve A., Yu, Kenneth H., Reidy, Diane L., Epstein, Andrew S., Lincoln, Anne, Saldia, Amethyst, Jacobs, Lauren M., Rau‐Murthy, Rohini, Zhang, Liying, Kurtz, Robert C., Saltz, Leonard, Offit, Kenneth, Robson, Mark E., Stadler, Zsofia K.

Volltext

Disparities in cancer genetics care by race/ethnicity among pan‐cancer patients with pathogenic germline variants von Liu, Ying L., Maio, Anna, Kemel, Yelena, Salo‐Mullen, Erin E., Sheehan, Margaret, Tejada, Prince Ray, Trottier, Magan, Arnold, Angela G., Fleischut, Megan Harlan, Latham, Alicia, Carlo, Maria I., Murciano‐Goroff, Yonina R., Walsh, Michael F., Mandelker, Diana, Mehta, Nikita, Bandlamudi, Chaitanya, Arora, Kanika, Zehir, Ahmet, Berger, Michael F., Solit, David B., Aghajanian, Carol, Diaz, Luis A., Robson, Mark E., Brown, Carol L., Offit, Kenneth, Hamilton, Jada G., Stadler, Zsofia K.

Volltext

Pancreas cancer and BRCA: A critical subset of patients with improving therapeutic outcomes von Momtaz, Parisa, O’Connor, Catherine A., Chou, Joanne F., Capanu, Marinela, Park, Wungki, Bandlamudi, Chaitanya, Berger, Michael F., Kelsen, David P., Suehnholz, Sarah P., Chakravarty, Debyani, Yu, Kenneth H., Varghese, Anna M., Zervoudakis, Alice, Li, Jia, Ku, Geoffrey Y., Park, Jennifer S., Shcherba, Marina, Harding, James J., Goldberg, Zoe, Abou‐Alfa, Ghassan K., Salo‐Mullen, Erin E., Stadler, Zsofia K., Iacobuzio‐Donahue, Christine A., O’Reilly, Eileen M.

Volltext

Insertion of an SVA element in MSH2 as a novel cause of Lynch syndrome von Yang, Ciyu, Li, Yirong, Trottier, Magan, Farrell, Michael P., Rai, Vikas K., Salo‐Mullen, Erin, Gallagher, David J., Stadler, Zsofia K., van der Klift, Heleen M., Zhang, Liying

Volltext

Attitudes toward preimplantation genetic testing and quality of life among individuals with hereditary diffuse gastric cancer syndrome von Shah, Ibrahim H, Salo-Mullen, Erin E, Amoroso, Kimberly A, Kelsen, David, Stadler, Zsofia K, Hamilton, Jada G

Volltext

Reliable Detection of Mismatch Repair Deficiency in Colorectal Cancers Using Mutational Load in Next-Generation Sequencing Panels von Stadler, Zsofia K, Battaglin, Francesca, Middha, Sumit, Hechtman, Jaclyn F, Tran, Christina, Cercek, Andrea, Yaeger, Rona, Segal, Neil H, Varghese, Anna M, Reidy-Lagunes, Diane L, Kemeny, Nancy E, Salo-Mullen, Erin E, Ashraf, Asad, Weiser, Martin R, Garcia-Aguilar, Julio, Robson, Mark E, Offit, Kenneth, Arcila, Maria E, Berger, Michael F, Shia, Jinru, Solit, David B, Saltz, Leonard B

Volltext

Phase II trial of veliparib in patients with previously treated BRCA-mutated pancreas ductal adenocarcinoma von Lowery, Maeve A., Kelsen, David P., Capanu, Marinela, Smith, Sloane C., Lee, Jonathan W., Stadler, Zsofia K., Moore, Malcolm J., Kindler, Hedy L., Golan, Talia, Segal, Amiel, Maynard, Hannah, Hollywood, Ellen, Moynahan, MaryEllen, Salo-Mullen, Erin E., Do, Richard Kinh Gian, Chen, Alice P., Yu, Kenneth H., Tang, Laura H., O'Reilly, Eileen M.

Volltext

Indications for Total Gastrectomy in CDH1 Mutation Carriers and Outcomes of Risk-Reducing Minimally Invasive and Open Gastrectomies von Vos, Elvira L, Salo-Mullen, Erin E, Tang, Laura H, Schattner, Mark, Yoon, Sam S, Gerdes, Hans, Markowitz, Arnold J, Mandelker, Diana, Janjigian, Yelena, Offitt, Kenneth, Coit, Daniel G, Stadler, Zsofia K, Strong, Vivian E

Volltext

Uptake and acceptability of a mainstreaming model of hereditary cancer multigene panel testing among patients with ovarian, pancreatic, and prostate cancer von Hamilton, Jada G., Symecko, Heather, Spielman, Kelsey, Breen, Kelsey, Mueller, Rebecca, Catchings, Amanda, Trottier, Magan, Salo-Mullen, Erin E., Shah, Ibrahim, Arutyunova, Anna, Batson, Melissa, Gebert, Rebecca, Pundock, Stacy, Schofield, Elizabeth, Offit, Kenneth, Stadler, Zsofia K., Cadoo, Karen, Carlo, Maria I., Narayan, Vivek, Reiss, Kim A., Robson, Mark E., Domchek, Susan M.

Volltext

Ageing and Technology: A Review of the Research Literature von Blaschke, Christina M., Freddolino, Paul P., Mullen, Erin E.

Volltext

Prospective pan-cancer germline testing using MSK-IMPACT informs clinical translation in 751 patients with pediatric solid tumors von Fiala, Elise M., Jayakumaran, Gowtham, Mauguen, Audrey, Kennedy, Jennifer A., Bouvier, Nancy, Kemel, Yelena, Fleischut, Megan Harlan, Maio, Anna, Salo-Mullen, Erin E., Sheehan, Margaret, Arnold, Angela G., Latham, Alicia, Carlo, Maria I., Cadoo, Karen, Murkherjee, Semanti, Slotkin, Emily K., Trippett, Tanya, Glade Bender, Julia, Meyers, Paul A., Wexler, Leonard, Dela Cruz, Filemon S., Cheung, Nai-Kong, Basu, Ellen, Kentsis, Alex, Ortiz, Michael, Francis, Jasmine H., Dunkel, Ira J., Khakoo, Yasmin, Gilheeney, Stephen, Farouk Sait, Sameer, Forlenza, Christopher J., Sulis, Maria, Karajannis, Matthias, Modak, Shakeel, Gerstle, Justin T., Heaton, Todd E., Roberts, Stephen, Yang, Ciyu, Jairam, Sowmya, Vijai, Joseph, Topka, Sabine, Friedman, Danielle N., Stadler, Zsofia K., Robson, Mark, Berger, Michael F., Schultz, Nikolaus, Ladanyi, Marc, O'Reilly, Richard J., Abramson, David H., Ceyhan-Birsoy, Ozge, Zhang, Liying, Mandelker, Diana, Shukla, Neerav N., Kung, Andrew L., Offit, Kenneth, Zehir, Ahmet, Walsh, Michael F.

Volltext

Resolving pathogenicity classification for the CDH1 c.[715GA] (p.Gly239Arg) Variant von Yelskaya, Zarina, Arnold, Angela G., Marcell, Vanessa J., Tang, Laura H., Salo-Mullen, Erin E., Strong, Vivian, Stadler, Zsofia K., Zhang, Liying

Volltext

Correction to: Resolving pathogenicity classification for the CDH1 c.[715G>A] (p.Gly239Arg) variant von Yelskaya, Zarina, Arnold, Angela G, Marcell, Vanessa J, Tang, Laura H, Salo-Mullen, Erin E, Strong, Vivian E, Stadler, Zsofia K, Zhang, Liying

Volltext

Psychosocial factors associated with the uptake of contralateral prophylactic mastectomy among BRCA1/2 mutation noncarriers with newly diagnosed breast cancer von Hamilton, Jada G., Genoff, Margaux C., Salerno, Melissa, Amoroso, Kimberly, Boyar, Sherry R., Sheehan, Margaret, Fleischut, Megan Harlan, Siegel, Beth, Arnold, Angela G., Salo-Mullen, Erin E., Hay, Jennifer L., Offit, Kenneth, Robson, Mark E.

Volltext

Factors Influencing Patient Preferences for Telehealth Cancer Genetic Counseling During the COVID-19 Pandemic von Breen, Kelsey E, Tuman, Malwina, Bertelsen, Corinna E, Sheehan, Margaret, Wylie, David, Fleischut, Megan Harlan, Offit, Kenneth, Stadler, Zsofia K, Salo-Mullen, Erin E, Hamilton, Jada G

Volltext

Targeted therapy based on germline analysis of tumor-normal sequencing (MSK-IMPACT) in a pan-cancer population von Stadler, Zsofia Kinga, Maio, Anna, Kemel, Yelena, Sheehan, Margaret, Salo-Mullen, Erin E., Cadoo, Karen Anne, Carlo, Maria Isabel, Latham, Alicia, Walsh, Michael Francis, Drilon, Alexander E., Berger, Michael F., Solit, David B., Birsoy, Ozge, Mandelker, Diana, Diaz, Luis A., Offit, Kenneth, Robson, Mark E.

Volltext

Contiguous gene deletion of chromosome 2p16.3-p21 as a cause of Lynch syndrome von 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.

Volltext

The Prevalence of Thyroid Cancer and Benign Thyroid Disease in Patients With Familial Adenomatous Polyposis May Be Higher Than Previously Recognized von Steinhagen, Emily, Guillem, José G, Chang, Gerard, Salo-Mullen, Erin E, Shia, Jinru, Fish, Stephanie, Stadler, Zsofia K, Markowitz, Arnold J

Volltext

Mosaic partial deletion of the PTEN gene in a patient with Cowden syndrome von Salo-Mullen, Erin E., Shia, Jinru, Brownell, Isaac, Allen, Peter, Girotra, Monica, Robson, Mark E., Offit, Kenneth, Guillem, Jose G., Markowitz, Arnold J., Stadler, Zsofia K.

Volltext