Personalized medicine: new genomics, old lessons

per Offit, Kenneth
Publicat 2011

The Future of Clinical Cancer Genomics

per Offit, Kenneth
Publicat a Semin Oncol (2016)

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

per Ellis, Nathan A., Offit, Kenneth
Publicat 2012

Ethical and Legal Implications of Cancer Genetic Testing: Do Physicians Have a Duty to Warn Patients' Relatives About Possible Genetic Risks?

per Storm, Courtney, Agarwal, Rinki, Offit, Kenneth
Publicat 2008

Association of a HOXB13 Variant with Breast Cancer

per Alanee, Shaheen, Couch, Fergus, Offit, Kenneth
Publicat 2012

Revealing the Incidentalome When Targeting the Tumor Genome

per Bombard, Yvonne, Robson, Mark, Offit, Kenneth
Publicat 2013

Genitourinary Cancers Other than Prostate Cancer in a BRCA-tested Cohort from a Single Institution

per Alanee, Shaheen, Schrader, Kasmintan, Offit, Kenneth
Publicat a Eur Urol (2015)

Two Decades After BRCA: Setting Paradigms in Personalized Cancer Care and Prevention

per Couch, Fergus J., Nathanson, Katherine L., Offit, Kenneth
Publicat 2014

A Rapid and Reliable Test for BRCA1 and BRCA2 Founder Mutation Analysis in Paraffin Tissue Using Pyrosequencing

per Zhang, Liying, Kirchhoff, Tomas, Yee, Cindy J., Offit, Kenneth
Publicat 2009

Genomic Biomarkers for Breast Cancer Risk

per Walsh, Michael F., Nathanson, Katherine L., Couch, Fergus J., Offit, Kenneth
Publicat a Adv Exp Med Biol (2016)

Cancer Genomics and Inherited Risk

per Stadler, Zsofia K., Schrader, Kasmintan A., Vijai, Joseph, Robson, Mark E., Offit, Kenneth
Publicat a J Clin Oncol (2014)

Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements

per Hayes, James E., Trynka, Gosia, Vijai, Joseph, Offit, Kenneth, Raychaudhuri, Soumya, Klein, Robert J.
Publicat a PLoS One (2015)

Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrier

per Alanee, Shaheen, Shah, Sohela, Murali, Rajmohan, Rau-Murthy, Rohini, Schrader, Kasmintan A., Offit, Kenneth
Publicat a Fam Cancer (2013)

Gene Patents and Personalized Cancer Care: Impact of the Myriad Case on Clinical Oncology

per Offit, Kenneth, Bradbury, Angela, Storm, Courtney, Merz, Jon F., Noonan, Kevin E., Spence, Rebecca
Publicat a J Clin Oncol (2013)

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

per Ritter, Deborah I., Rao, Shruti, Kulkarni, Shashikant, Madhavan, Subha, Offit, Kenneth, Plon, Sharon E.
Publicat a Cold Spring Harb Mol Case Stud (2019)

Genetics, Genomics and Cancer Risk Assessment: State of the art and future directions in the era of personalized medicine

per Weitzel, Jeffrey N., Blazer, Kathleen R., MacDonald, Deborah J., Culver, Julie O., Offit, Kenneth
Publicat 2011

Variants at IRX4 as prostate cancer expression quantitative trait loci

per Xu, Xing, Hussain, Wasay M, Vijai, Joseph, Offit, Kenneth, Rubin, Mark A, Demichelis, Francesca, Klein, Robert J
Publicat 2014

Polymorphisms of ADIPOQ and ADIPOR1 and prostate cancer risk

per Kaklamani, Virginia, Yi, Nengjun, Zhang, Kui, Sadim, Maureen, Offit, Kenneth, Oddoux, Carole, Ostrer, Harry, Mantzoros, Christos, Pasche, Boris
Publicat 2011

Variants of the Adiponectin and Adiponectin Receptor 1 Genes and Breast Cancer Risk

per Kaklamani, Virginia G., Sadim, Maureen, Hsi, Alex, Offit, Kenneth, Oddoux, Carole, Ostrer, Harry, Ahsan, Habibul, Pasche, Boris, Mantzoros, Christos
Publicat 2008

Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancer

per Alanee, Shaheen, Shah, Sohela, Vijai, Joseph, Schrader, Kasmintan, Rau-Murthy, Rohini, Sarrel, Kara, Manschreck, Christopher, Eastham, James, Offit, Kenneth
Publicat a Fam Cancer (2013)