Personalized medicine: new genomics, old lessons

por Offit, Kenneth
Publicado 2011

Heterozygous Mutations in DNA Repair Genes and Hereditary Breast Cancer: A Question of Power

por Ellis, Nathan A., Offit, Kenneth
Publicado 2012

Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements

por Hayes, James E., Trynka, Gosia, Vijai, Joseph, Offit, Kenneth, Raychaudhuri, Soumya, Klein, Robert J.
Publicado 2015

A case for expert curation: an overview of cancer curation in the Clinical Genome Resource (ClinGen)

por Ritter, Deborah I., Rao, Shruti, Kulkarni, Shashikant, Madhavan, Subha, Offit, Kenneth, Plon, Sharon E.
Publicado 2019

Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk

por Willis, Jason A., Mukherjee, Semanti, Orlow, Irene, Viale, Agnes, Offit, Kenneth, Kurtz, Robert C., Olson, Sara H., Klein, Robert J.
Publicado 2014

No major association between TGFBR1*6A and prostate cancer

por Kaklamani, Virginia, Baddi, Lisa, Rosman, Diana, Liu, Junjian, Ellis, Nathan, Oddoux, Carole, Ostrer, Harry, Chen, Yu, Ahsan, Habibul, Offit, Kenneth, Pasche, Boris
Publicado 2004

Towards Automation of Germline Variant Curation in Clinical Cancer Genetics

por Ravichandran, Vignesh, Shameer, Zarina, Kemel, Yelena, Walsh, Michael, Cadoo, Karen, Lipkin, Steven, Mandelker, Diana, Zhang, Liying, Stadler, Zsofia, Robson, Mark, Offit, Kenneth, Joseph, Vijai
Publicado 2019

Development of a novel measure of advanced cancer patients’ perceived utility of secondary germline findings from tumor genomic profiling

por Hamilton, Jada G., Shah, Ibrahim H., Salafia, Caroline, Schofield, Elizabeth, Garzon, Margaux Genoff, Cadet, Kechna, Stadler, Zsofia K., Hay, Jennifer L., Offit, Kenneth, Robson, Mark E.
Publicado 2023

Germline BRCA2 mutations detected in pediatric sequencing studies impact parents’ evaluation and care

por Walsh, Michael F., Kennedy, Jennifer, Harlan, Megan, Kentsis, Alex, Shukla, Neerav, Musinsky, Jacob, Roberts, Stephen, Kung, Andrew L., Robson, Mark, Kushner, Brian H., Meyers, Paul, Offit, Kenneth
Publicado 2017

Frequency of CHEK2*1100delC in New York breast cancer cases and controls

por Offit, Kenneth, Pierce, Heather, Kirchhoff, Tomas, Kolachana, Prema, Rapaport, Beth, Gregersen, Peter, Johnson, Steven, Yossepowitch, Orit, Huang, Helen, Satagopan, Jaya, Robson, Mark, Scheuer, Lauren, Nafa, Khedoudja, Ellis, Nathan
Publicado 2003

The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-...

por Pereira, Lutécia H Mateus, Pineda, Marbin A, Rowe, William H, Fonseca, Libia R, Greene, Mark H, Offit, Kenneth, Ellis, Nathan A, Zhang, Jinghui, Collins, Andrew, Struewing, Jeffery P
Publicado 2007

A combined analysis of outcome following breast cancer: differences in survival based on BRCA1/BRCA2 mutation status and administration of adjuvant treatment

por Robson, Mark E, Chappuis, Pierre O, Satagopan, Jaya, Wong, Nora, Boyd, Jeff, Goffin, John R, Hudis, Clifford, Roberge, David, Norton, Larry, Bégin, Louis R, Offit, Kenneth, Foulkes, William D
Publicado 2004

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

por 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.
Publicado 2016

Genetic Analysis of the Early Natural History of Epithelial Ovarian Carcinoma

por Pothuri, Bhavana, Leitao, Mario M., Levine, Douglas A., Viale, Agnès, Olshen, Adam B., Arroyo, Crispinita, Bogomolniy, Faina, Olvera, Narciso, Lin, Oscar, Soslow, Robert A., Robson, Mark E., Offit, Kenneth, Barakat, Richard R., Boyd, Jeff
Publicado 2010

Assessment of SLX4 Mutations in Hereditary Breast Cancers

por Shah, Sohela, Kim, Yonghwan, Ostrovnaya, Irina, Murali, Rajmohan, Schrader, Kasmintan A., Lach, Francis P., Sarrel, Kara, Rau-Murthy, Rohini, Hansen, Nichole, Zhang, Liyng, Kirchhoff, Tomas, Stadler, Zsofia, Robson, Mark, Vijai, Joseph, Offit, Kenneth, Smogorzewska, Agata
Publicado 2013

Pathogenic Loss-of-Function Germline TERT Mutations in Patients With Solid Tumors

por Walsh, Michael F., Sacca, Rosalba, Wildman, Temima, Amoroso, Kimberly, Kennedy, Jennifer, Zhang, Liying, Birsoy, Ozge, Mandelker, Diana, Steinsnyder, Zoe, Latham, Alicia, Carlo, Maria I., Cadoo, Karen, Kemel, Yelena, Robson, Mark, Stadler, Zsofia K., Offit, Kenneth
Publicado 2019

Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing

por Cheng, Donavan T., Prasad, Meera, Chekaluk, Yvonne, Benayed, Ryma, Sadowska, Justyna, Zehir, Ahmet, Syed, Aijazuddin, Wang, Yan Elsa, Somar, Joshua, Li, Yirong, Yelskaya, Zarina, Wong, Donna, Robson, Mark E., Offit, Kenneth, Berger, Michael F., Nafa, Khedoudja, Ladanyi, Marc, Zhang, Liying
Publicado 2017

Cascading After Peridiagnostic Cancer Genetic Testing: An Alternative to Population-Based Screening

por Offit, Kenneth, Tkachuk, Kaitlyn A., Stadler, Zsofia K., Walsh, Michael F., Diaz-Zabala, Hector, Levin, Jeffrey D., Steinsnyder, Zoe, Ravichandran, Vignesh, Sharaf, Ravi N., Frey, Melissa K., Lipkin, Steven M., Robson, Mark E., Hamilton, Jada G., Vijai, Joseph, Mukherjee, Semanti
Publicado 2020

Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genes

por Waller, Rosalie Griffin, Klein, Robert J, Vijai, Joseph, McKay, James D, Clay-Gilmour, Alyssa, Wei, Xiaomu, Madsen, Michael J, Sborov, Douglas W, Curtin, Karen, Slager, Susan L, Offit, Kenneth, Vachon, Celine M, Lipkin, Steven M, Dumontet, Charles, Camp, Nicola J
Publicado 2021

Clonal Hematopoiesis and COVID-19 Severity in Cancer Patients

por Bolton, Kelly L., Foote, Michael, Jee, Justin, Safonov, Anton, Ptashkin, Ryan, Devlin, Sean, Gedvilaite, Erika, Gao, Teng, Papaemmanuil, Elli, Pessin, Melissa S., Kamboj, Mini, Vijai, Joseph, Offit, Kenneth, Awadalla, Phillip, Nataranjan, Pradeep, Berger, Michael F., Norton, Larry, Levine, Ross L., Zehir, Ahmet
Publicado 2020