Publications by authors named "Neil A Miller"

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Modeling.
Neil A Miller

J Aerosol Med Pulm Drug Deliv· February 2024

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CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project.
Andrea Gaedigk, Erin C Boone, Steven E Scherer, Seung-Been Lee, Ibrahim Numanagić, Neil A Miller

J Mol Diagn· April 2022

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Physiologically Based Pharmacokinetic Modelling of Inhaled Nemiralisib: Mechanistic Components for Pulmonary Absorption, Systemic Distribution, and Oral Absorption.
Neil A Miller, Rebecca H Graves, Chris D Edwards, Augustin Amour, Ed Taylor

Clin Pharmacokinet· February 2022

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Pharmacogene Variation Consortium: A Global Resource and Repository for Pharmacogene Variation.
Andrea Gaedigk, Scott T Casey, Michelle Whirl-Carrillo, Neil A Miller, Teri E Klein

Clin Pharmacol Ther· September 2021

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PharmVar GeneFocus: CYP2B6.
Zeruesenay Desta, Ahmed El-Boraie, Li Gong, Andrew A Somogyi, Volker M Lauschke, Neil A Miller

Clin Pharmacol Ther· July 2021

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ITGB2 (Integrin β2) Immunomodulatory Gene Variants in Premature Infants With Necrotizing Enterocolitis.
Lovya George, Heather Menden, Sheng Xia, Wei Yu, Anne Holmes, Neil A Miller

J Pediatr Gastroenterol Nutr· February 2021

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Long-Distance Phasing of a Tentative "Enhancer" Single-Nucleotide Polymorphism With Star Allele Definitions.
Erin C Boone, Wendy Y Wang, Roger Gaedigk, Mariana Cherner, Anick Bérard, Neil A Miller

Front Pharmacol· May 2020

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PharmVar and the Landscape of Pharmacogenetic Resources.
Andrea Gaedigk, Michelle Whirl-Carrillo, Victoria M Pratt, Neil A Miller, Teri E Klein

Clin Pharmacol Ther· January 2020

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Physiologically Based Pharmacokinetic Modelling for First-In-Human Predictions: An Updated Model Building Strategy Illustrated with Challenging Industry Case Studies.
Neil A Miller, Micaela B Reddy, Aki T Heikkinen, Viera Lukacova, Neil Parrott

Clin Pharmacokinet· June 2019

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Pharmacogene Variation Consortium Gene Introduction: NUDT15.
Jun J Yang, Michelle Whirl-Carrillo, Stuart A Scott, Amy J Turner, Matthias Schwab, Neil A Miller

Clin Pharmacol Ther· May 2019

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The Evolution of PharmVar.
Andrea Gaedigk, Katrin Sangkuhl, Michelle Whirl-Carrillo, Greyson P Twist, Teri E Klein, Neil A Miller

Clin Pharmacol Ther· January 2019

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Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Johanna M Huusko, Minna K Karjalainen, Britney E Graham, Ge Zhang, Emily G Farrow, Neil A Miller

PLoS Genet· September 2018

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Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Johanna M Huusko, Minna K Karjalainen, Britney E Graham, Ge Zhang, Emily G Farrow, Neil A Miller

PLoS Genet· July 2018

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The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP) Allele Nomenclature Database.
Andrea Gaedigk, Magnus Ingelman-Sundberg, Neil A Miller, J Steven Leeder, Michelle Whirl-Carrillo

Clin Pharmacol Ther· March 2018

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The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.
Josh E Petrikin, Julie A Cakici, Michelle M Clark, Laurel K Willig, Nathaly M Sweeney, Neil A Miller

NPJ Genom Med· February 2018

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In vivo characterization of CYP2D6*12, *29 and *84 using dextromethorphan as a probe drug: a case report.
Andrea Gaedigk, Greyson P Twist, Emily G Farrow, Jennifer A Lowry, Sarah E Soden, Neil A Miller

Pharmacogenomics· April 2017

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Erratum: Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, , from whole-genome sequences.
Greyson P Twist, Andrea Gaedigk, Neil A Miller, Emily G Farrow, Laurel K Willig

NPJ Genom Med· January 2017

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Clinical detection of deletion structural variants in whole-genome sequences.
Aaron C Noll, Neil A Miller, Laurie D Smith, Byunggil Yoo, Stephanie Fiedler

NPJ Genom Med· August 2016

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Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, , from whole-genome sequences.
Greyson P Twist, Andrea Gaedigk, Neil A Miller, Emily G Farrow, Laurel K Willig

NPJ Genom Med· January 2016

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MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates.
Anne Guimier, George C Gabriel, Fanny Bajolle, Michael Tsang, Hui Liu, Neil A Miller

Nat Genet· November 2015

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Renal systems biology of patients with systemic inflammatory response syndrome.
Ephraim L Tsalik, Laurel K Willig, Brandon J Rice, Jennifer C van Velkinburgh, Robert P Mohney, Neil A Miller

Kidney Int· October 2015

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A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases.
Neil A Miller, Emily G Farrow, Margaret Gibson, Laurel K Willig, Greyson Twist

Genome Med· September 2015

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Alström Syndrome: Mutation Spectrum of ALMS1.
Jan D Marshall, Jean Muller, Gayle B Collin, Gabriella Milan, Stephen F Kingsmore, Neil A Miller

Hum Mutat· July 2015

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Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
Laurel K Willig, Josh E Petrikin, Laurie D Smith, Carol J Saunders, Isabelle Thiffault, Neil A Miller

Lancet Respir Med· May 2015

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An integrated transcriptome and expressed variant analysis of sepsis survival and death.
Ephraim L Tsalik, Raymond J Langley, Darrell L Dinwiddie, Neil A Miller, Byunggil Yoo

Genome Med· December 2014

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