Publications by authors named "Meredith Wright"

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Closing the Practice Gap in Secondary Prevention After Acute Coronary Syndromes: a Provincial Implementation Pathway.
Palki Bhatt, Meredith K Wright, Carolyn Gall-Casey, Claudia Bucci, Noah Ivers

Can J Cardiol· December 2025

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Clinical utility and cost-effectiveness of BeginNGS newborn screening by genome sequencing and standard newborn screening for severe childhood genetic diseases: an adaptive, international and comparative clinical trial.
Rebecca Reimers, Miranda Bailey, Chester Brown, Kee Chan, Tom Defay, Meredith Wright

BMJ Open· November 2025

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Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection.
Stephen F Kingsmore, Meredith Wright, Laurie D Smith, Yupu Liang, William R Mowrey

Am J Hum Genet· December 2024

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Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial.
Stephen F Kingsmore, Meredith Wright, Lauren Olsen, Brandan Schultz, Liana Protopsaltis

Am J Hum Genet· December 2024

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Myocarditis and Pericarditis After mRNA COVID-19 Vaccination: 2024 Status and Management Update.
Michael A McDonald, Tahir S Kafil, Michael Khoury, Adriana C Luk, Meredith K Wright

Can J Cardiol· September 2024

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Spliceosome malfunction causes neurodevelopmental disorders with overlapping features.
Dong Li, Qin Wang, Allan Bayat, Mark R Battig, Yijing Zhou, Meredith Wright

J Clin Invest· January 2024

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Report of two cases of Schaaf-Yang syndrome: Same genotype and different phenotype.
Ana Maria Rodriguez, Katherine Schain, Parul Jayakar, Meredith S Wright, Shimul Chowdhury

Clin Case Rep· August 2023

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Response to Grosse et al.
Stephen F Kingsmore, Laurie D Smith, Chris M Kunard, Matthew Bainbridge, Sergey Batalov, Meredith Wright

Am J Hum Genet· June 2023

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Fc-competent multispecific PDL-1/TIGIT/LAG-3 antibodies potentiate superior anti-tumor T cell response.
Riyao Yang, Su Huang, Cai Huang, Nathan S Fay, Yanan Wang, Kimberly Wright, Meredith Wright

Sci Rep· June 2023

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Rapid Whole Genome Sequencing for Diagnosis of Single Locus Genetic Diseases in Critically Ill Children.
Mallory J Owen, Sergey Batalov, Katarzyna A Ellsworth, Meredith Wright, Sylvia Breeding

Methods Mol Biol· April 2023

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Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing.
Mallory J Owen, Meredith S Wright, Sergey Batalov, Yonghyun Kwon, Yan Ding

JAMA Netw Open· February 2023

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Autosomal recessive LRP1-related syndrome featuring cardiopulmonary dysfunction, bone dysmorphology, and corneal clouding.
Paul R Mark, Stephen A Murray, Tao Yang, Alexandra Eby, Angela Lai, Meredith S Wright

Cold Spring Harb Mol Case Stud· October 2022

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A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases.
Stephen F Kingsmore, Laurie D Smith, Chris M Kunard, Matthew Bainbridge, Sergey Batalov, Meredith Wright

Am J Hum Genet· September 2022

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An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases.
Mallory J Owen, Sebastien Lefebvre, Christian Hansen, Chris M Kunard, David P Dimmock, Meredith S Wright

Nat Commun· July 2022

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A novel IgG Fc by computer-aided design enhances heavy-chain heterodimerization in bi- or trispecific antibodies.
Bo Wang, Jun Lin, Matthew R Hoag, Meredith Wright, Mingjun Ma

Antib Ther· July 2022

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First-in-class trispecific VHH-Fc based antibody with potent prophylactic and therapeutic efficacy against SARS-CoV-2 and variants.
Allison Titong, Sachith Gallolu Kankanamalage, Jianbo Dong, Betty Huang, Nicholas Spadoni, Meredith Wright

Sci Rep· March 2022

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Abnormal SCID Newborn Screening and Spontaneous Recovery Associated with a Novel Haploinsufficiency IKZF1 Mutation.
Hye Sun Kuehn, Nicholas J Gloude, David Dimmock, Mari Tokita, Meredith Wright

J Clin Immunol· August 2021

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Uncertain, Not Unimportant: Callosal Dysgenesis and Variants of Uncertain Significance in .
Therese S Woodring, Mohammed H Mirza, Valeria Benavides, Katarzyna A Ellsworth, Meredith S Wright

Pediatrics· July 2021

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Rapid Sequencing-Based Diagnosis of Thiamine Metabolism Dysfunction Syndrome.
Mallory J Owen, Anna-Kaisa Niemi, David P Dimmock, Mark Speziale, Mark Nespeca, Meredith S Wright

N Engl J Med· June 2021

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Characterization of Pneumococcal Colonization Dynamics and Antimicrobial Resistance Using Shotgun Metagenomic Sequencing in Intensively Sampled South African Infants.
Rendani I Manenzhe, Felix S Dube, Meredith Wright, Katie Lennard, Stephanie Mounaud

Front Public Health· May 2021

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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Madelyn A Gillentine, Tianyun Wang, Kendra Hoekzema, Jill Rosenfeld, Pengfei Liu, Meredith S Wright

Genome Med· April 2021

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Capsule carbohydrate structure determines virulence in Acinetobacter baumannii.
Yuli Talyansky, Travis B Nielsen, Jun Yan, Ulrike Carlino-Macdonald, Gisela Di Venanzio, Meredith S Wright

PLoS Pathog· February 2021

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Author Correction: Development of humanized tri-specific nanobodies with potent neutralization for SARS-CoV-2.
Jianbo Dong, Betty Huang, Bo Wang, Allison Titong, Sachith Gallolu Kankanamalage, Meredith Wright

Sci Rep· February 2021

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A Case of UDP-Galactose 4'-Epimerase Deficiency Associated with Dyshematopoiesis and Atrioventricular Valve Malformations: An Exceptional Clinical Phenotype Explained by Altered N-Glycosylation with Relative Preservation of the Leloir Pathway.
Christopher A Febres-Aldana, Liset Pelaez, Meredith S Wright, Ossama M Maher, Anthony J Febres-Aldana

Mol Syndromol· December 2020

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Development of humanized tri-specific nanobodies with potent neutralization for SARS-CoV-2.
Jianbo Dong, Betty Huang, Bo Wang, Allison Titong, Sachith Gallolu Kankanamalage, Meredith Wright

Sci Rep· October 2020

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