Recommendations for Clinical CYP2C19 Genotyping Allele Selection: A Report of the Association for Molecular Pathology
Pratt, Victoria M, Del Tredici, Andria L, Hachad, Houda, Ji, Yuan, Kalman, Lisa V, Scott, Stuart A, Weck, Karen E
Published in The Journal of molecular diagnostics : JMD (01.05.2018)
Published in The Journal of molecular diagnostics : JMD (01.05.2018)
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College of American Pathologists' laboratory standards for next-generation sequencing clinical tests
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Published in Archives of pathology & laboratory medicine (1976) (01.04.2015)
Published in Archives of pathology & laboratory medicine (1976) (01.04.2015)
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Recommendations for Clinical CYP2D6 Genotyping Allele Selection: A Joint Consensus Recommendation of the Association for Molecular Pathology, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, and the European Society for Pharmacogenomics and Personalized Therapy
Pratt, Victoria M, Cavallari, Larisa H, Del Tredici, Andria L, Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V, Ly, Reynold C, Moyer, Ann M, Scott, Stuart A, van Schaik, R H N, Whirl-Carrillo, Michelle, Weck, Karen E
Published in The Journal of molecular diagnostics : JMD (01.09.2021)
Published in The Journal of molecular diagnostics : JMD (01.09.2021)
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Recommendations for Clinical CYP2C9 Genotyping Allele Selection: A Joint Recommendation of the Association for Molecular Pathology and College of American Pathologists
Pratt, Victoria M, Cavallari, Larisa H, Del Tredici, Andria L, Hachad, Houda, Ji, Yuan, Moyer, Ann M, Scott, Stuart A, Whirl-Carrillo, Michelle, Weck, Karen E
Published in The Journal of molecular diagnostics : JMD (01.09.2019)
Published in The Journal of molecular diagnostics : JMD (01.09.2019)
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Frequency and clinical outcomes of CYP2C19 genotype-guided escalation and de-escalation of antiplatelet therapy in a real-world clinical setting
Martin, Jesse, Williams, Alexis K, Klein, Melissa D, Sriramoju, Vindhya B, Madan, Shivanshu, Rossi, Joseph S, Clarke, Megan, Cicci, Jonathan D, Cavallari, Larisa H, Weck, Karen E, Stouffer, George A, Lee, Craig R
Published in Genetics in medicine (01.01.2020)
Published in Genetics in medicine (01.01.2020)
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An approach to integrating exome sequencing for fetal structural anomalies into clinical practice
Vora, Neeta L, Gilmore, Kelly, Brandt, Alicia, Gustafson, Chelsea, Strande, Natasha, Ramkissoon, Lori, Hardisty, Emily, Foreman, Ann Katherine M, Wilhelmsen, Kirk, Owen, Phillips, Weck, Karen E, Berg, Jonathan S, Powell, Cynthia M, Powell, Bradford C
Published in Genetics in medicine (01.05.2020)
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Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease
Hegde, Madhuri, Santani, Avni, Mao, Rong, Ferreira-Gonzalez, Andrea, Weck, Karen E, Voelkerding, Karl V
Published in Archives of pathology & laboratory medicine (1976) (01.06.2017)
Published in Archives of pathology & laboratory medicine (1976) (01.06.2017)
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CYP3A4 and CYP3A5 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase
Pratt, Victoria M, Cavallari, Larisa H, Fulmer, Makenzie L, Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V, Ly, Reynold C, Moyer, Ann M, Scott, Stuart A, van Schaik, Ron H N, Whirl-Carrillo, Michelle, Weck, Karen E
Published in The Journal of molecular diagnostics : JMD (01.09.2023)
Published in The Journal of molecular diagnostics : JMD (01.09.2023)
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PIK3CA Mutation in HPV-Associated OPSCC Patients Receiving Deintensified Chemoradiation
Beaty, Brian T, Moon, Dominic H, Shen, Colette J, Amdur, Robert J, Weiss, Jared, Grilley-Olson, Juneko, Patel, Shetal, Zanation, Adam, Hackman, Trevor G, Thorp, Brian, Blumberg, Jeffrey M, Patel, Samip N, Weissler, Mark C, Yarbrough, Wendell G, Sheets, Nathan C, Parker, Joel S, Neil Hayes, D, Weck, Karen E, Ramkissoon, Lori A, Mendenhall, William M, Dagan, Roi, Tan, Xianming, Gupta, Gaorav P, Chera, Bhishamjit S
Published in JNCI : Journal of the National Cancer Institute (01.08.2020)
Published in JNCI : Journal of the National Cancer Institute (01.08.2020)
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A phase II trial of UGT1A1 genotype-guided FOLFIRI plus bevacizumab as first-line therapy for advanced, unresectable colorectal cancer
Sanoff, Hanna K, Deal, Allison M, Patel, Jai, Sorah, Jonathan D, Gaddy, Jacquelyne, O’Neil, Bert, Turk, Anita, Irvin, William, Boles, Jeremiah, Lee, Michael S, McRee, Autumn, Wardell, Alexis C, Weck, Karen E, Basch, Ethan, Wood, William A, Innocenti, Federico
Published in The oncologist (Dayton, Ohio) (06.09.2024)
Published in The oncologist (Dayton, Ohio) (06.09.2024)
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Recommendations for Clinical Warfarin Genotyping Allele Selection: A Report of the Association for Molecular Pathology and the College of American Pathologists
Pratt, Victoria M, Cavallari, Larisa H, Del Tredici, Andria L, Hachad, Houda, Ji, Yuan, Kalman, Lisa V, Ly, Reynold C, Moyer, Ann M, Scott, Stuart A, Whirl-Carrillo, Michelle, Weck, Karen E
Published in The Journal of molecular diagnostics : JMD (01.07.2020)
Published in The Journal of molecular diagnostics : JMD (01.07.2020)
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Genotype-Guided Tamoxifen Dosing Increases Active Metabolite Exposure in Women With Reduced CYP2D6 Metabolism: A Multicenter Study
IRVIN, William J, WALKO, Christine M, RAAB, Rachel E, CORSO, Steven W, PEPPERCORN, Jeffrey M, ANDERSON, Steven M, FRIEDMAN, Kenneth J, OGBURN, Evan T, DESTA, Zeruesenay, FLOCKHART, David A, MCLEOD, Howard L, EVANS, James P, WECK, Karen E, CAREY, Lisa A, IBRAHIM, Joseph G, CHIU, WingK, DEES, E. Claire, MOORE, Susan G, OLAJIDE, Oludamilola A, GRAHAM, Mark L, CANALE, Sean T
Published in Journal of clinical oncology (20.08.2011)
Published in Journal of clinical oncology (20.08.2011)
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Clinical Outcomes and Sustainability of Using CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention
Lee, Craig R, Sriramoju, Vindhya B, Cervantes, Alexandra, Howell, Lucius A, Varunok, Nicholas, Madan, Shivanshu, Hamrick, Kasey, Polasek, Melissa J, Lee, John Andrew, Clarke, Megan, Cicci, Jonathan D, Weck, Karen E, Stouffer, George A
Published in Circulation. Cardiovascular genetics (01.04.2018)
Published in Circulation. Cardiovascular genetics (01.04.2018)
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TPMT and NUDT15 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase
Pratt, Victoria M., Cavallari, Larisa H., Fulmer, Makenzie L., Gaedigk, Andrea, Hachad, Houda, Ji, Yuan, Kalman, Lisa V., Ly, Reynold C., Moyer, Ann M., Scott, Stuart A., van Schaik, R.H.N., Whirl-Carrillo, Michelle, Weck, Karen E.
Published in The Journal of molecular diagnostics : JMD (01.10.2022)
Published in The Journal of molecular diagnostics : JMD (01.10.2022)
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Association of deep phenotyping with diagnostic yield of prenatal exome sequencing for fetal brain abnormalities
Drexler, Kathleen A., Talati, Asha N., Gilmore, Kelly L., Veazey, Rachel V., Powell, Bradford C., Weck, Karen E., Davis, Erica E., Vora, Neeta L.
Published in Genetics in medicine (01.10.2023)
Published in Genetics in medicine (01.10.2023)
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Public Interest in Population Genetic Screening for Cancer Risk
Roberts, Megan C., Foss, Kimberly S., Henderson, Gail E., Powell, Sabrina N., Saylor, Katherine W., Weck, Karen E., Milko, Laura V.
Published in Frontiers in genetics (22.07.2022)
Published in Frontiers in genetics (22.07.2022)
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