Use of a multi-gene pharmacogenetic panel reduces adverse drug effects

por Cavallari, Larisa H., Johnson, Julie A.
Publicado 2023

Role of cytochrome P450 genotype in the steps toward personalized drug therapy

por Cavallari, Larisa H, Jeong, Hyunyoung, Bress, Adam
Publicado 2011

2100 TL1 team approach to social and genetic determinants of nocturnal blood pressure

por Dumeny, Leanne, Chu Hsiao, Cavallari, Larisa H., Mulligan, Connie J., McCormack, Wayne T.
Publicado 2018

Assessing the Clinical Treatment Dynamics of Antiplatelet Therapy Following Acute Coronary Syndrome and Percutaneous Coronary Intervention in the US

por Wang, Yehua, Cavallari, Larisa H., Brown, Joshua D., Thomas, Cameron D., Winterstein, Almut G.
Publicado 2023

Evaluation of race and ethnicity disparities in outcome studies of CYP2C19 genotype-guided antiplatelet therapy

por Nguyen, Anh B., Cavallari, Larisa H., Rossi, Joseph S., Stouffer, George A., Lee, Craig R.
Publicado 2022

Reimbursement of pharmacogenetic tests at a tertiary academic medical center in the United States

por Lemke, Lauren K., Alam, Benish, Williams, Roy, Starostik, Petr, Cavallari, Larisa H., Cicali, Emily J., Wiisanen, Kristin
Publicado 2023

Cox-sMBPLS: An Algorithm for Disease Survival Prediction and Multi-Omics Module Discovery Incorporating Cis-Regulatory Quantitative Effects

por Vahabi, Nasim, McDonough, Caitrin W., Desai, Ankit A., Cavallari, Larisa H., Duarte, Julio D., Michailidis, George
Publicado 2021

Lessons from clinical implementation of a preemptive pharmacogenetic panel as part of a testing pilot program with an employer-sponsored medical plan

por Norris, Madeline, Dalton, Rachel, Alam, Benish, Eddy, Elizabeth, Nguyen, Khoa A., Cavallari, Larisa H., Sumfest, Jill, Wiisanen, Kristin, Cicali, Emily J.
Publicado 2023

Association of the HLA-B alleles with carbamazepine-induced Stevens–Johnson syndrome/toxic epidermal necrolysis in the Javanese and Sundanese population of Indonesia: the important...

por Yuliwulandari, Rika, Kristin, Erna, Prayuni, Kinasih, Sachrowardi, Qomariyah, Suyatna, Franciscus D, Menaldi, Sri Linuwih, Wichukchinda, Nuanjun, Mahasirimongkol, Surakameth, Cavallari, Larisa H
Publicado 2017

Utilizing a Human–Computer Interaction Approach to Evaluate the Design of Current Pharmacogenomics Clinical Decision Support

por Elchynski, Amanda L., Desai, Nina, D’Silva, Danielle, Hall, Bradley, Marks, Yael, Wiisanen, Kristin, Cicali, Emily J., Cavallari, Larisa H., Nguyen, Khoa A.
Publicado 2021

Genetic Polymorphisms in ADRB2 and ADRB1 Are Associated with Differential Survival in Heart Failure Patients Taking β-Blockers

por Guerra, Leonardo A., Lteif, Christelle, Arwood, Meghan J., McDonough, Caitrin W., Dumeny, Leanne, Desai, Ankit A., Cavallari, Larisa H., Duarte, Julio D.
Publicado 2022

Genetic and Non-Genetic Factors Impact on INR Normalization in Preprocedural Warfarin Management

por Eljilany, Islam, Elarref, Mohamed, Shallik, Nabil, Elzouki, Abdel-Naser, Bader, Loulia, El-Bardissy, Ahmed, Abdelsamad, Osama, Al-Badriyeh, Daoud, Cavallari, Larisa H, Elewa, Hazem
Publicado 2021

2235: Equipping health professional students to apply pharmacogenomic data to clinical decision making in real-world scenarios: Comparison of an active engagement Versus didactic t...

por Arwood, Meghan J., Rowe McDonough, Caitrin, Cavallari, Larisa H., Elsey, Amanda R., Frye, Reginald F., Gong, Yan, Johnson, Julie A., Weitzel, Kristin W., Langaee, Taimour
Publicado 2018

Characterizing OPRM1 DNA methylation in prescription opioid users with chronic musculoskeletal pain

por Sheikh, Sophia, Smotherman, Carmen, Patel, Monika, Langaee, Taimour, Wang, Danxin, Swaray, Edward, Velasquez, Esteban, Schmidt, Siegfried O.F., Hendry, Phyllis, Cavallari, Larisa H., Fillingim, Roger B.
Publicado 2022

Clinical Utility of Pharmacogene Panel‐Based Testing in Patients Undergoing Percutaneous Coronary Intervention

por El Rouby, Nihal, Alrwisan, Adel, Langaee, Taimour, Lipori, Gloria, Angiolillo, Dominick J, Franchi, Francesco, Riva, Alberto, Elsey, Amanda, Johnson, Julie A., Cavallari, Larisa H., Winterstein, Almut G.
Publicado 2020

Implications of Polymorphisms in the BCKDK and GATA‐4 Gene Regions on Stable Warfarin Dose in African Americans

por Bargal, Salma A., Kight, Jennifer N., Augusto de Oliveira, Felipe, Shahin, Mohamed H., Langaee, Taimour, Gong, Yan, Hamadeh, Issam S., Cooper-DeHoff, Rhonda M., Cavallari, Larisa H.
Publicado 2020

A pilot study to identify pharmacogenomic and clinical risk factors associated with opioid related falls and adverse effects in older adults

por Sheikh, Sophia, Fernandez, Rosemarie, Smotherman, Carmen, Brailsford, Jennifer, Langaee, Taimour, Velasquez, Esteban, Henson, Morgan, Munson, Taylor, Bertrand, Andrew, Hendry, Phyllis, Anton, Stephen, Fillingim, Roger B., Cavallari, Larisa H.
Publicado 2023

Endothelial nitric oxide synthase genotype is associated with pulmonary hypertension severity in left heart failure patients

por Duarte, Julio D., Kansal, Mayank, Desai, Ankit A., Riden, Katherine, Arwood, Meghan J., Yacob, Alex A., Stamos, Thomas D., Cavallari, Larisa H., Zamanian, Roham T., Shah, Sanjiv J., Machado, Roberto F.
Publicado 2018

Effect of Genetic and Nongenetic Factors on the Clinical Response to Mineralocorticoid Receptor Antagonist Therapy in Egyptians with Heart Failure

por Sarhan, Neven M., Shahin, Mohamed H., El Rouby, Nihal M., El‐Wakeel, Lamia M., Solayman, Mohamed H., Langaee, Taimour, Khorshid, Hazem, Schaalan, Mona F., Sabri, Nagwa A., Cavallari, Larisa H.
Publicado 2019

Clinical implementation of rapid CYP2C19 genotyping to guide antiplatelet therapy after percutaneous coronary intervention

por Cavallari, Larisa H., Franchi, Francesco, Rollini, Fabiana, Been, Latonya, Rivas, Andrea, Agarwal, Malhar, Smith, D. Max, Newsom, Kimberly, Gong, Yan, Elsey, Amanda R., Starostik, Petr, Johnson, Julie A., Angiolillo, Dominick J.
Publicado 2018