Charlotte A. Hobbs

Affiliations: 
Interdisciplinary Biomedical Sciences University of Arkansas for Medical Sciences, United States 
Area:
Genetics, Epidemiology
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"Charlotte Hobbs"
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Publications

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Huang M, Lyu C, Liu N, et al. (2023) A gene-based association test of interactions for maternal-fetal genotypes identifies genes associated with nonsyndromic congenital heart defects. Genetic Epidemiology
Webber DM, Li M, MacLeod SL, et al. (2023) Gene-Folic Acid Interactions and Risk of Conotruncal Heart Defects: Results from the National Birth Defects Prevention Study. Genes. 14
Owen MJ, Lefebvre S, Hansen C, et al. (2022) An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases. Nature Communications. 13: 4057
Sanford Kobayashi E, Waldman B, Engorn BM, et al. (2022) Cost Efficacy of Rapid Whole Genome Sequencing in the Pediatric Intensive Care Unit. Frontiers in Pediatrics. 9: 809536
Palmquist R, Jenkins SM, Bentley D, et al. (2022) Evaluating use of changing technologies for rapid next-generation sequencing in pediatrics. Pediatric Research
Dimmock D, Caylor S, Waldman B, et al. (2021) Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children's hospitals demonstrates improved clinical outcomes and reduced costs of care. American Journal of Human Genetics
Owen MJ, Niemi AK, Dimmock DP, et al. (2021) Rapid Sequencing-Based Diagnosis of Thiamine Metabolism Dysfunction Syndrome. The New England Journal of Medicine. 384: 2159-2161
Sweeney NM, Nahas SA, Chowdhury S, et al. (2021) Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. Npj Genomic Medicine. 6: 38
Sweeney NM, Nahas SA, Chowdhury S, et al. (2021) Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. Npj Genomic Medicine. 6: 39
Sweeney NM, Nahas SA, Chowdhury S, et al. (2021) Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. Npj Genomic Medicine. 6: 29
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