Výsledky vyhledávání - Joseph Vijai
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Cancer Genomics and Inherited Risk Autor Zsofia K. Stadler, Kasmintan A. Schrader, Joseph Vijai, Mark E. Robson, Kenneth Offit
Vydáno 2014Artigo -
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Genetic Association Analysis of ATP Binding Cassette Protein Family Reveals a Novel Association of ABCB1 Genetic Variants with Epilepsy Risk, but Not with Drug-Resistance Autor Balan, Shabeesh, Bharathan, Sumitha Prameela, Vellichiramal, Neetha Nanoth, Sathyan, Sanish, Joseph, Vijai, Radhakrishnan, Kurupath, Banerjee, Moinak
Vydáno 2014Text -
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SNPs at SMG7 associated with time from biochemical recurrence to prostate cancer death Autor Song, Xiaoyu, Ru, Meng, Steinsnyder, Zoe, Tkachuk, Kaitlyn, Kopp, Ryan P., Sullivan, John, Gümüş, Zeynep H., Offit, Kenneth, Joseph, Vijai, Klein, Robert J.
Vydáno 2022Text -
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Towards Automation of Germline Variant Curation in Clinical Cancer Genetics Autor Ravichandran, Vignesh, Shameer, Zarina, Kemel, Yelena, Walsh, Michael, Cadoo, Karen, Lipkin, Steven, Mandelker, Diana, Zhang, Liying, Stadler, Zsofia, Robson, Mark, Offit, Kenneth, Joseph, Vijai
Vydáno 2019Text -
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Toward automation of germline variant curation in clinical cancer genetics Autor Vignesh Ravichandran, Zarina Shameer, Yelena Kemel, Michael F. Walsh, Karen A. Cadoo, Steven M. Lipkin, Diana Mandelker, Liying Zhang, Zsofia K. Stadler, Mark E. Robson, Kenneth Offit, Joseph Vijai
Vydáno 2019Artigo -
7
Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing Autor 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.
Vydáno 2016Text -
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Prevalence of <i>BRCA1</i> and <i>BRCA2</i> mutations in Ashkenazi Jewish families with breast and pancreatic cancer Autor Zsofia K. Stadler, Erin Salo‐Mullen, Sujata M. Patil, M. Catherine Pietanza, Joseph Vijai, Emmanouil Saloustros, Nichole Hansen, Noah D. Kauff, Robert C. Kurtz, David P. Kelsen, Kenneth Offit, Mark E. Robson
Vydáno 2011Artigo -
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Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing Autor Judith Balmañà, Laura DiGiovanni, Pragna Gaddam, Michael F. Walsh, Joseph Vijai, Zsofia K. Stadler, Katherine L. Nathanson, Judy E. Garber, Fergus J. Couch, Kenneth Offit, Mark E. Robson, Susan M. Domchek
Vydáno 2016Artigo -
10
Utilization of clinical genetic counseling among childhood and young adult cancer survivors in a registry trial Autor Anderson, Nassim, Delavar, Arash, Friedman, Danielle Novetsky, Joseph, Vijai, Mubdi, Nidha, Oeffinger, Kevin C., Sklar, Charles A., Offit, Kenneth, Matasar, Matthew, Raghunathan, Nirupa, Antal, Zoltan, Straus, David, Walsh, Michael, Latham, Alicia, Tonorezos, Emily S.
Vydáno 2020Text -
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Cascading After Peridiagnostic Cancer Genetic Testing: An Alternative to Population-Based Screening Autor Kenneth Offit, Kaitlyn Tkachuk, Zsofia K. Stadler, Michael F. Walsh, Héctor Díaz-Zabala, Jeffrey Levin, Zoe Steinsnyder, Vignesh Ravichandran, Ravi Sharaf, Melissa K. Frey, Steven M. Lipkin, Mark E. Robson, Jada G. Hamilton, Joseph Vijai, Semanti Mukherjee
Vydáno 2020Artigo -
12
Susceptibility Loci Associated with Prostate Cancer Progression and Mortality Autor David Gallagher, Joseph Vijai, Angel M. Cronin, Jasmine Bhatia, Andrew J. Vickers, Mia M. Gaudet, Samson W. Fine, Victor E. Reuter, Howard I. Scher, Christer Halldén, Ana Dutra-Clarke, Robert J. Klein, Peter T. Scardino, James A. Eastham, Hans Lilja, Tomas Kirchhoff, Kenneth Offit
Vydáno 2010Artigo -
13
Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA Autor Schrader, Kasmintan A., Cheng, Donavan T., Joseph, Vijai, Prasad, Meera, Walsh, Michael, Zehir, Ahmet, Ni, Ai, Thomas, Tinu, Benayed, Ryma, Ashraf, Asad, Lincoln, Annie, Arcila, Maria, Stadler, Zsofia, Solit, David, Hyman, David M., Zhang, Liying, Klimstra, David, Ladanyi, Marc, Offit, Kenneth, Berger, Michael, Robson, Mark
Vydáno 2016Text -
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Germline deletion of ETV6 in familial acute lymphoblastic leukemia Autor Rampersaud, Evadnie, Ziegler, David S., Iacobucci, Ilaria, Payne-Turner, Debbie, Churchman, Michelle L., Schrader, Kasmintan A., Joseph, Vijai, Offit, Kenneth, Tucker, Katherine, Sutton, Rosemary, Warby, Meera, Chenevix-Trench, Georgia, Huntsman, David G., Tsoli, Maria, Mead, R. Scott, Qu, Chunxu, Leventaki, Vasiliki, Wu, Gang, Mullighan, Charles G.
Vydáno 2019Text -
15
Case–control analysis identifies shared properties of rare germline variation in cancer predisposing genes Autor Artomov, Mykyta, Joseph, Vijai, Tiao, Grace, Thomas, Tinu, Schrader, Kasmintan, Klein, Robert J., Kiezun, Adam, Gupta, Namrata, Margolin, Lauren, Stratigos, Alexander J., Kim, Ivana, Shannon, Kristen, Ellisen, Leif W., Haber, Daniel, Getz, Gad, Tsao, Hensin, Lipkin, Steven M., Altshuler, David, Offit, Kenneth, Daly, Mark J.
Vydáno 2019Text -
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High-depth whole genome sequencing of an Ashekenazi Jewish reference panel: Enhancing sensitivity, accuracy, and imputation Autor Lencz, Todd, Yu, Jin, Palmer, Cameron, Carmi, Shai, Ben-Avraham, Danny, Barzilai, Nir, Bressman, Susan, Darvasi, Ariel, Cho, Judy H., Clark, Lorraine N., Gümüş, Zeynep H., Joseph, Vijai, Klein, Robert, Lipkin, Steven, Offit, Kenneth, Ostrer, Harry, Ozelius, Laurie J., Peter, Inga, Atzmon, Gil, Pe’er, Itsik
Vydáno 2018Text -
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Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA Autor Kasmintan A. Schrader, Donavan T. Cheng, Joseph Vijai, Meera Prasad, Michael F. Walsh, Ahmet Zehir, Ai Ni, Tinu Thomas, Ryma Benayed, Asad Ashraf, Anne Lincoln, Maria E. Arcila, Zsofia K. Stadler, David B. Solit, David M. Hyman, Liying Zhang, David S. Klimstra, Marc Ladanyi, Kenneth Offit, Michael F. Berger, Mark E. Robson
Vydáno 2015Artigo -
18
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer Autor Kara N. Maxwell, Steven N. Hart, Joseph Vijai, Kasmintan A. Schrader, Thomas P. Slavin, Tinu Thomas, Bradley Wubbenhorst, Vignesh Ravichandran, Raymond M. Moore, Chunling Hu, Lucia Guidugli, Brandon M. Wenz, Susan M. Domchek, Mark E. Robson, Csilla I. Szabo, Susan L. Neuhausen, Jeffrey N. Weitzel, Kenneth Offit, Fergus J. Couch, Katherine L. Nathanson
Vydáno 2016Artigo -
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Fumarate hydratase FH c.1431_1433dupAAA (p.Lys477dup) variant is not associated with cancer including renal cell carcinoma Autor Zhang, Liying, Walsh, Michael F., Jairam, Sowmya, Mandelker, Diana, Zhong, Yi, Kemel, Yelena, Chen, Ying-Bei, Musheyev, David, Zehir, Ahmet, Jayakumaran, Gowtham, Brzostowski, Edyta, Birsoy, Ozge, Yang, Ciyu, Li, Yirong, Somar, Joshua, DeLair, Deborah, Pradhan, Nisha, Berger, Michael F., Cadoo, Karen, Carlo, Maria I., Robson, Mark E., Stadler, Zsofia K., Iacobuzio-Donahue, Christine A., Joseph, Vijai, Offit, Kenneth
Vydáno 2019Text -
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Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies Autor Joseph Vijai, Tomas Kirchhoff, Kasmintan A. Schrader, Jennifer R. Brown, Ana Dutra-Clarke, Christopher Manschreck, Nichole Hansen, Rohini Rau‐Murthy, Kara Sarrel, Jennifer A. Przybylo, Sohela Shah, Srujana Cheguri, Zsofia K. Stadler, Liying Zhang, Ora Paltiel, Dina Ben‐Yehuda, Agnès Viale, Carol S. Portlock, David J. Straus, Steven M. Lipkin, Mortimer J. Lacher, Mark E. Robson, Robert J. Klein, Andrew D. Zelenetz, Kenneth Offit
Vydáno 2013Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Cancer
Medicine
Internal medicine
Mutation
Oncology
Germline mutation
Germline
Genotype
Single-nucleotide polymorphism
Breast cancer
Cancer research
Computational biology
Genome-wide association study
Allele
Bioinformatics
Genetic testing
Immunology
Prostate cancer
CHEK2
Disease
Environmental health
Exome sequencing
Genetic association
Genome
Locus (genetics)
Lymphoma
Odds ratio