Erick R. Scott

发表

RASLseqTools: open-source methods for designing and analyzing RNA-mediated oligonucleotide Annealing, Selection, and, Ligation sequencing (RASL-seq) experiments

Andrew I. Su, Peter G. Schultz, Max Nanis, 2016, bioRxiv.

Methods for Clustering Time Series Data Acquired from Mobile Health Apps

Pei Wang, Nicholas Genes, Yu-Feng Yvonne Chan, 2017, PSB.

A Look to the Future

Erick R. Scott, Richard L. Wallsten, Richard L. Wallsten, 2019, Pharmacogenomics.

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

Erick R. Scott, Michelle K. Lupton, D. Hernandez, 2013, Nature.

APPLaUD: access for patients and participants to individual level uninterpreted genomic data

Manuel Corpas, Laura Lyman Rodriguez, Jason Bobe, 2018, Human Genomics.

Sequencing the CYP2D6 gene: from variant allele discovery to clinical pharmacogenetic testing.

Erick R. Scott, M. R. Botton, S. Scott, 2017, Pharmacogenomics.

Whole-Genome Sequencing of a Healthy Aging Cohort

Ali Torkamani, Eric J. Topol, Erick R. Scott, 2016, Cell.

Institutional profile: translational pharmacogenomics at the Icahn School of Medicine at Mount Sinai.

Xiang Zhou, Joel Dudley, Judy H Cho, 2017, Pharmacogenomics.

VarCover: Allele Min-Set Cover Software.

Erick R. Scott, V. Bansal, S. Scott, 2019, The Journal of molecular diagnostics : JMD.

A Genome Sequencing Program for Novel Undiagnosed Diseases

Erick R Scott, Ali Torkamani, Eric J Topol, 2015, Genetics in Medicine.

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

Erick R. Scott, E. Masliah, C. Achim, 2010, PloS one.

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

Erick R. Scott, P. Schultz, A. Torkamani, 2014, Nucleic acids research.

Title Evidence for alteration of gene regulatory networks through microRNAs of the HIV-infected brain : Novel analysis of retrospective cases Permalink

Erick R. Scott, E. Masliah, C. Achim, 2010 .

Genomic newborn screening: public health policy considerations and recommendations

Erick R. Scott, S. Kingsmore, B. Knoppers, 2017, BMC Medical Genomics.

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

Erick R. Scott, Jason R. Bobe, Richard Milne, 2019, European Journal of Human Genetics.

APPLaUD: access for patients and participants to individual level uninterpreted genomic data

Erick R. Scott, Jason R. Bobe, A. Middleton, 2018, Human Genomics.

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

Erick R. Scott, N. Wineinger, Jonathan Zhu, 2015, PloS one.

VarCover

Erick R. Scott, Carl Meacham, Vikas Bansal, 2020, The Journal of Molecular Diagnostics.

Multiplexed analysis of fixed tissue RNA using Ligation in situ Hybridization

Erick R. Scott, W. Timp, J. Credle, 2017, Nucleic acids research.

Pharmacogenomic education among genetic counseling training programs in North America

Erick R. Scott, S. Scott, H. Naik, 2021, Journal of genetic counseling.

Genomic newborn screening: public health policy considerations and recommendations

Erick R. Scott, S. Kingsmore, B. Knoppers, 2017, BMC Medical Genomics.

'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods.

Erick R. Scott, Jason R. Bobe, A. Middleton, 2018, Personalized medicine.

Estimating Local Costs Associated With Clostridium difficile Infection Using Machine Learning and Electronic Medical Records

Erick R. Scott, A. Kasarskis, T. Pak, 2017, Infection Control & Hospital Epidemiology.

The Asthma Mobile Health Study, a large-scale clinical observational study using ResearchKit

Marcus A. Badgeley, Joel T Dudley, Pei Wang, 2017, Nature Biotechnology.

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

Erick R. Scott, M. R. Botton, R. Desnick, 2020, Genes.

The asthma mobile health study, smartphone data collected using ResearchKit

Pei Wang, Yu-Feng Yvonne Chan, Nicole Tignor, 2018, Scientific Data.

Long‐read HiFi sequencing of NUDT15: Phased full‐gene haplotyping and pharmacogenomic allele discovery

Erick R. Scott, J. Korlach, E. Schadt, 2022, Human mutation.

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

Erick R. Scott, E. Schadt, M. R. Botton, 2020, Clinical and translational science.

The Asthma Mobile Health Study, a large-scale clinical observational study using ResearchKit

Marcus A. Badgeley, Erick R. Scott, Rosalind J Wright, 2017, Nature Biotechnology.

Joint marginal structural models to estimate the causal effects of multiple longitudinal treatments in continuous time with application to COVID-19

Erick R. Scott, Fan Li, Liangyuan Hu, 2021 .

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

Erick R. Scott, Michelle K. Lupton, D. Hernandez, 2013, Nature.

Sequencing the CYP2D6 gene: from variant allele discovery to clinical pharmacogenetic testing.

Erick R. Scott, M. R. Botton, Yao Yang, 2017, Pharmacogenomics.