928. Clinical Characteristics and Microbiology Testing Patterns Among Transplant Recipients Admitted to Acute Care Hospitals for Suspected Infection

por Hill, T Matthew, Scott, Erick R, Bercovici, Sivan
Publicado 2021

An Examination of the Relationship between Lipid Levels and Associated Genetic Markers across Racial/Ethnic Populations in the Multi-Ethnic Study of Atherosclerosis

por Johnson, Lucia, Zhu, Jonathan, Scott, Erick R., Wineinger, Nathan E.
Publicado 2015

Estimating the causal effects of multiple intermittent treatments with application to COVID-19

por Hu, Liangyuan, Ji, Jiayi, Joshi, Himanshu, Scott, Erick R., Li, Fan
Publicado 2023

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

Sensitive, multiplex and direct quantification of RNA sequences using a modified RASL assay

por Larman, H. Benjamin, Scott, Erick R., Wogan, Megan, Oliveira, Glenn, Torkamani, Ali, Schultz, Peter G.
Publicado 2014

Evidence for Alteration of Gene Regulatory Networks through MicroRNAs of the HIV-Infected Brain: Novel Analysis of Retrospective Cases

por Tatro, Erick T., Scott, Erick R., Nguyen, Timothy B., Salaria, Shahid, Banerjee, Sugato, Moore, David J., Masliah, Eliezer, Achim, Cristian L., Everall, Ian P.
Publicado 2010

The asthma mobile health study, smartphone data collected using ResearchKit

por Chan, Yu-Feng Yvonne, Bot, Brian M., Zweig, Micol, Tignor, Nicole, Ma, Weiping, Suver, Christine, Cedeno, Rafhael, Scott, Erick R., Gregory Hershman, Steven, Schadt, Eric E., Wang, Pei
Publicado 2018

Multiplexed analysis of fixed tissue RNA using Ligation in situ Hybridization

por Credle, Joel J., Itoh, Christopher Y., Yuan, Tiezheng, Sharma, Rajni, Scott, Erick R., Workman, Rachael E., Fan, Yunfan, Housseau, Franck, Llosa, Nicolas J., Bell, W. Robert., Miller, Heather, Zhang, Sean X., Timp, Winston, Larman, H. Benjamin
Publicado 2017

Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data

por Middleton, Anna, Milne, Richard, Howard, Heidi, Niemiec, Emilia, Robarts, Lauren, Critchley, Christine, Nicol, Dianne, Prainsack, Barbara, Atutornu, Jerome, Vears, Danya F., Smith, James, Steed, Claire, Bevan, Paul, Scott, Erick R., Bobe, Jason, Goodhand, Peter, Kleiderman, Erika, Thorogood, Adrian, Morley, Katherine I.
Publicado 2019

Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi‐Ethnic Allele and Copy Number Variant Detection

por Scott, Stuart A., Scott, Erick R., Seki, Yoshinori, Chen, Annette J., Wallsten, Richard, Owusu Obeng, Aniwaa, Botton, Mariana R., Cody, Neal, Shi, Huanzhi, Zhao, Geping, Brake, Paul, Nicoletti, Paola, Yang, Yao, Delio, Maria, Shi, Lisong, Kornreich, Ruth, Schadt, Eric E., Edelmann, Lisa
Publicado 2020

A Genome Sequencing Program for Novel Undiagnosed Diseases

por Bloss, Cinnamon S., Scott-Van Zeeland, Ashley A., Topol, Sarah E., Darst, Burcu F., Boeldt, Debra L., Erikson, Galina A., Bethel, Kelly J., Bjork, Robert L., Friedman, Jennifer R., Hwynn, Nelson, Patay, Bradley A., Pockros, Paul J., Scott, Erick R., Simon, Ronald A., Williams, Gary W., Schork, Nicholas J., Topol, Eric J., Torkamani, Ali
Publicado 2015