Pharmacogenomic Determinants of Interindividual Drug Response Variability: From Discovery to Implementation

por Scott, Stuart A., Swen, Jesse J.
Publicado 2021

Digital Health Applications for Pharmacogenetic Clinical Trials

por Naik, Hetanshi, Palaniappan, Latha, Ashley, Euan A., Scott, Stuart A.
Publicado 2020

Pharmacokinetics of dasatinib for Philadelphia-positive acute lymphocytic leukemia with acquired T315I mutation

por Takahashi, Naoto, Miura, Masatomo, Scott, Stuart A, Niioka, Takenori, Sawada, Kenichi
Publicado 2012

Adapting Data Processing To Compare Model and Experiment Accurately: A Discrete Element Model and Magnetic Resonance Measurements of a 3D Cylindrical Fluidized Bed

por Boyce, Christopher M., Holland, Daniel J., Scott, Stuart A., Dennis, John S.
Publicado 2013

Familial inheritance of the 3q29 microdeletion syndrome: case report and review

por Khan, Wahab A., Cohen, Ninette, Scott, Stuart A., Pereira, Elaine M.
Publicado 2019

Multi-ethnic Cytochrome-P450 Copy Number Profiling: Novel Pharmacogenetic Alleles and Mechanism of Copy Number Variation Formation

por Martis, Suparna, Mei, Hui, Vijzelaar, Raymon, Edelmann, Lisa, Desnick, Robert J., Scott, Stuart A.
Publicado 2012

Implementation and utilization of genetic testing in personalized medicine

por Abul-Husn, Noura S, Owusu Obeng, Aniwaa, Sanderson, Saskia C, Gottesman, Omri, Scott, Stuart A
Publicado 2014

Phased Haplotype Resolution of the SLC6A4 Promoter Using Long-Read Single Molecule Real-Time (SMRT) Sequencing

por Botton, Mariana R., Yang, Yao, Scott, Erick R., Desnick, Robert J., Scott, Stuart A.
Publicado 2020

Multi-ethnic Distribution of Clinically Relevant CYP2C Genotypes and Haplotypes

por Martis, Suparna, Peter, Inga, Hulot, Jean-Sébastien, Kornreich, Ruth, Desnick, Robert J., Scott, Stuart A.
Publicado 2012

Paroxysmal Kinesigenic Dyskinesia Caused by 16p11.2 Microdeletion

por Termsarasab, Pichet, Yang, Amy C., Reiner, Jennifer, Mei, Hui, Scott, Stuart A., Frucht, Steven J.
Publicado 2014

A de novo 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype

por Weisfeld-Adams, James D, Tkachuk, Amanda K, Maclean, Kenneth N, Meeks, Naomi L, Scott, Stuart A
Publicado 2016

A de novo 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype

por Weisfeld-Adams, James D, Tkachuk, Amanda K, Maclean, Kenneth N, Meeks, Naomi L, Scott, Stuart A
Publicado 2017

Enhanced Visible Light-Driven Photocatalytic Water-Splitting Reaction of Titanate Nanotubes Sensitised with Ru(II) Bipyridyl Complex

por Malizia, Mauro, Scott, Stuart A., Torrente-Murciano, Laura, Boies, Adam M., Aljohani, Talal A., Baldovi, Herme G.
Publicado 2023

Prenatal cytogenomic identification and molecular refinement of compound heterozygous STRC deletion breakpoints

por Shi, Lisong, Bai, Yan, Kharbutli, Yara, Oza, Andrea M., Amr, Sami S., Edelmann, Lisa, Mehta, Lakshmi, Scott, Stuart A.
Publicado 2019

An efficient genotyper and star-allele caller for pharmacogenomics

por Hari, Ananth, Zhou, Qinghui, Gonzaludo, Nina, Harting, John, Scott, Stuart A., Qin, Xiang, Scherer, Steve, Sahinalp, S. Cenk, Numanagić, Ibrahim
Publicado 2023

Re-envisioning community genetics: community empowerment in preventive genomics

por Wand, Hannah, Martschenko, Daphne O., Smitherman, Annamaria, Michelson, Sheryl, Pun, Ting, Witte, John S., Scott, Stuart A., Cho, Mildred K., Ashley, Euan A.
Publicado 2023

Quantitative and multiplexed DNA methylation analysis using long-read single-molecule real-time bisulfite sequencing (SMRT-BS)

por Yang, Yao, Sebra, Robert, Pullman, Benjamin S, Qiao, Wanqiong, Peter, Inga, Desnick, Robert J, Geyer, C Ronald, DeCoteau, John F, Scott, Stuart A
Publicado 2015

2042 CYP2C19*2 and PON1 Q192R polymorphisms are associated with platelet reactivity to clopidogrel in Puerto Rican Hispanics with cardiovascular disease

por Suarez, Dagmar F. H., Botton, Mariana R., Scott, Stuart A., Tomey, Matthew I., Melin, Kyle, Lopez-Candales, Angel, Renta, Jessicca Y., Duconge, Jorge
Publicado 2018

Physician Attitudes toward Adopting Genome-Guided Prescribing through Clinical Decision Support

por Overby, Casey Lynnette, Erwin, Angelika Ludtke, Abul-Husn, Noura S., Ellis, Stephen B., Scott, Stuart A., Obeng, Aniwaa Owusu, Kannry, Joseph L., Hripcsak, George, Bottinger, Erwin P., Gottesman, Omri
Publicado 2014

Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study

por Claudio-Campos, Karla, Labastida, Aurora, Ramos, Alga, Gaedigk, Andrea, Renta-Torres, Jessicca, Padilla, Dariana, Rivera-Miranda, Giselle, Scott, Stuart A., Ruaño, Gualberto, Cadilla, Carmen L., Duconge-Soler, Jorge
Publicado 2017