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Author Details

Tracy L McGregor
Alnylam Pharmaceuticals
2009
35
19
PMIDPaper TitleJournal TitlePublished Year
37458799Natural history of urine and plasma oxalate in children with primary hyperoxaluria type 1.Pediatr Nephrol2024
35913563Efficacy and safety of lumasiran for infants and young children with primary hyperoxaluria type 1: 12-month analysis of the phase 3 ILLUMINATE-B trial.Pediatr Nephrol2023
35843439Lumasiran for Advanced Primary Hyperoxaluria Type 1: Phase 3 ILLUMINATE-C Trial.Am J Kidney Dis2023
34906487Phase 3 trial of lumasiran for primary hyperoxaluria type 1: A new RNAi therapeutic in infants and young children.Genet Med2022
33372121Management Principles for Acute Illness in Patients With Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency.Pediatrics2021
33789010Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1.N Engl J Med2021
35257062Randomized Clinical Trial on the Long-Term Efficacy and Safety of Lumasiran in Patients With Primary Hyperoxaluria Type 1.Kidney Int Rep2021
33985991Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1: A Placebo-Controlled Randomized Clinical Trial.Clin J Am Soc Nephrol2021
31454829Acute kidney injury risk-based screening in pediatric inpatients: a pragmatic randomized trial.Pediatr Res2020
32207686Characterising a healthy adult with a rare HAO1 knockout to support a therapeutic strategy for primary hyperoxaluria.Elife2020
32165440End Points for Clinical Trials in Primary Hyperoxaluria.Clin J Am Soc Nephrol2020
29341265Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias.Exp Dermatol2018
29388319Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant.Am J Med Genet A2018
29590070Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.Science2018
27295947Molecular analysis of idiopathic subglottic stenosis for Mycobacterium species.Laryngoscope2017
28486440Electronic health record-based predictive models for acute kidney injury screening in pediatric inpatients.Pediatr Res2017
27296163Idiopathic subglottic stenosis is associated with activation of the inflammatory IL-17A/IL-23 axis.Laryngoscope2016
26319754Acute Kidney Injury Incidence in Noncritically Ill Hospitalized Children, Adolescents, and Young Adults: A Retrospective Observational Study.Am J Kidney Dis2016
26261062Attitudes of clinicians following large-scale pharmacogenomics implementation.Pharmacogenomics J2016
27654872PharmGKB summary: very important pharmacogene information for MT-RNR1.Pharmacogenet Genomics2016
26030142Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.PLoS One2015
26343839Efficacy and safety of cyclic pyranopterin monophosphate substitution in severe molybdenum cofactor deficiency type A: a prospective cohort study.Lancet2015
23889335Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes.Clin Genet2014
23281421Inclusion of pediatric samples in an opt-out biorepository linking DNA to de-identified medical records: pediatric BioVU.Clin Pharmacol Ther2013
24363766Pharmacogenetics in clinical pediatrics: challenges and strategies.Per Med2013
23962833Opioid use after cardiac surgery in children with Down syndrome.Pediatr Crit Care Med2013
23196672Mapping the incidentalome: estimating incidental findings generated through clinical pharmacogenomics testing.Genet Med2013
21948486Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.Hum Mutat2012
22150416Two novel large ANKH deletion mutations in sporadic cases with craniometaphyseal dysplasia.Clin Genet2012
21740577Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype.BMC Med Genet2011
21533219An evolutionary genomic approach to identify genes involved in human birth timing.PLoS Genet2011
20422016Consanguinity mapping of congenital heart disease in a South Indian population.PLoS One2010
21347066Specialized Pediatric Growth Charts For Electronic Health Record Systems: the example of Down syndrome.AMIA Annu Symp Proc2010
21184677Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth.BMC Med Genomics2010
19938076Evidence suggesting digenic inheritance of Waardenburg syndrome type II with ocular albinism.Am J Med Genet A2009
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Mayo Clinic
Co-authored papers 7
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Co-authored papers 5
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Vanderbilt University
Co-authored papers 4
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Vanderbilt University
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Leena Peltonen
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Thomas M Morgan
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Murray H Brilliant
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E Clayton
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 2
Digna R Velez Edwards
Vanderbilt University Medical Center
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Martha F Wright
Vanderbilt University Medical Center
Co-authored papers 1
Lisa Bastarache
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Co-authored papers 1
Christian M Shaffer
Vanderbilt University
Co-authored papers 1
John A Phillips
Vanderbilt University Medical Center
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David Sexton
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Release 1.2