Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Erick R. Scott"'
Autor:
Stuart A. Scott, Erick R. Scott, Yoshinori Seki, Annette J. Chen, Richard Wallsten, Aniwaa Owusu Obeng, Mariana R. Botton, Neal Cody, Huanzhi Shi, Geping Zhao, Paul Brake, Paola Nicoletti, Yao Yang, Maria Delio, Lisong Shi, Ruth Kornreich, Eric E. Schadt, Lisa Edelmann
Publikováno v:
Clinical and Translational Science, Vol 14, Iss 1, Pp 204-213 (2021)
To develop a novel pharmacogenetic genotyping panel, a multidisciplinary team evaluated available evidence and selected 29 genes implicated in interindividual drug response variability, including 130 sequence variants and additional copy number varia
Externí odkaz:
https://doaj.org/article/7f804a0ee92b4221ad0fabbe49325591
Autor:
Erick R. Scott, Yao Yang, Mariana R. Botton, Yoshinori Seki, Keito Hoshitsuki, John Harting, Primo Baybayan, Neal Cody, Paola Nicoletti, Takaya Moriyama, Shreyasee Chakraborty, Jun J. Yang, Lisa Edelmann, Eric E. Schadt, Jonas Korlach, Stuart A. Scott
Publikováno v:
Human Mutation. 43:1557-1566
To determine the phase of NUDT15 sequence variants for more comprehensive star (*) allele diplotyping, we developed a novel long-read single-molecule real-time HiFi amplicon sequencing method. A 10.5 kb NUDT15 amplicon assay was validated using refer
Autor:
Ruth Kornreich, Lisong Shi, Mariana R. Botton, Yoshinori Seki, Neal Cody, Paola Nicoletti, Huanzhi Shi, Maria Delio, Erick R. Scott, Richard Wallsten, Aniwaa Owusu Obeng, Stuart A. Scott, Lisa Edelmann, Geping Zhao, Annette J. Chen, Eric E. Schadt, Yao Yang, Paul Brake
Publikováno v:
Clinical and Translational Science
Clinical and Translational Science, Vol 14, Iss 1, Pp 204-213 (2021)
Clinical and Translational Science, Vol 14, Iss 1, Pp 204-213 (2021)
To develop a novel pharmacogenetic genotyping panel, a multidisciplinary team evaluated available evidence and selected 29 genes implicated in interindividual drug response variability, including 130 sequence variants and additional copy number varia
Publikováno v:
The Journal of Molecular Diagnostics. 22:123-131
To facilitate reference-material selection for clinical genetic testing laboratories, we developed VarCover, open-source software hosted on GitHub, which accepts a file of variants and returns an approximately minimum set (min-set) of samples coverin
Autor:
Emily M Eichenberger, Nicholas Degner, Erick R Scott, Felicia Ruffin, John Franzone, Batu Sharma-Kuinkel, Pratik Shah, David Hong, Sudeb C Dalai, Lily Blair, Desiree Hollemon, Eliza Chang, Carine Ho, Lisa Wanda, Christiaan R de Vries, Vance G Fowler, Asim A Ahmed
Publikováno v:
Clin Infect Dis
Background The diagnosis of infective endocarditis (IE) can be difficult, particularly if blood cultures fail to yield a pathogen. This study evaluates the potential utility of microbial cell-free DNA (mcfDNA) as a tool to identify the microbial etio
Autor:
Asim A. Ahmed, Felicia Ruffin, Erick R Scott, Batu K. Sharma-Kuinkel, Desiree H Hollemon, Hon Seng, Nicholas R. Degner, Lily Blair, Lisa Wanda, Lawrence P. Park, Carine Ho, Emily M. Eichenberger, Pratik Shah, Vance G. Fowler, David S. Hong, Timothy A. Blauwkamp, Christiaan R de Vries
Publikováno v:
Clin Infect Dis
Background Microbial cell-free DNA (mcfDNA) sequencing of plasma can identify the presence of a pathogen in a host. In this study, we evaluated the duration of pathogen detection by mcfDNA sequencing vs conventional blood culture in patients with bac
Autor:
Stuart A. Scott, Elizabeth Loudon, Erick R. Scott, Randi E. Zinberg, Robert Rigobello, Hetanshi Naik
Publikováno v:
Journal of genetic counselingREFERENCES. 30(5)
The increasing number of genetic counselors participating directly in clinical pharmacogenomic post-test counseling prompted our evaluation of pharmacogenomic education across genetic counseling training programs in North America. Thirty-one program
Autor:
Peter Goodhand, Claire Steed, Jason Bobe, Katherine I. Morley, Richard Milne, Christine Critchley, Danya F. Vears, Erick R. Scott, Jerome Atutornu, Adrian Thorogood, Anna Middleton, Paul Bevan, Emilia Niemiec, Erika Kleiderman, Barbara Prainsack, Heidi Carmen Howard, Laurens Robarts, James Smith, Dianne Nicol
Publikováno v:
European Journal of Human Genetics
Funder: State Government of Victoria (Victorian Government); doi: https://doi.org/10.13039/501100004752
Funder: Victorian State Government
Public acceptance is critical for sharing of genomic data at scale. This paper examines how acceptanc
Funder: Victorian State Government
Public acceptance is critical for sharing of genomic data at scale. This paper examines how acceptanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::883c0d495f14640aa9176e4d12551cfe
Publikováno v:
Genes, Vol 11, Iss 1333, p 1333 (2020)
Genes
Volume 11
Issue 11
Genes
Volume 11
Issue 11
The SLC6A4 gene has been implicated in psychiatric disorder susceptibility and antidepressant response variability. The SLC6A4 promoter is defined by a variable number of homologous 20&ndash
24 bp repeats (5-HTTLPR), and long (L) and short (S) a
24 bp repeats (5-HTTLPR), and long (L) and short (S) a
Publikováno v:
Genes
The SLC6A4 gene has been implicated in psychiatric disorder susceptibility and antidepressant response variability. The SLC6A4 promoter is defined by a variable number of homologous 20–24 bp repeats (5-HTTLPR), and long (L) and short (S) alleles ar