Vicky L Funanage, PhD

Key Considerations for Selecting a Genomic Decision Support Platform for Implementing Pharmacogenomics; Clinical Pharmacology and Therapeutics; (2021).

Utilizing partnership flexibility and strengths: Key elements for driving 3d printed face-shield production during the covid-19 pandemic; Delaware Journal of Public Health; (2020).

Knowledge and attitudes on pharmacogenetics among pediatricians; Journal of Human Genetics; (2020).

The importance of research in addressing the covid-19 pandemic: Focus on the use of serology testing; Delaware Journal of Public Health; (2020).

Smn1 and smn2 copy numbers in cell lines derived from patients with spinal muscular atrophy as measured by array digital pcr; Molecular Genetics and Genomic Medicine; (2015).

A mutation in TRPV4 results in altered chondrocyte calcium signaling in severe metatropic dysplasia; American Journal of Medical Genetics, Part A; (2015).

A homozygous double mutation in SMN1: A complicated genetic diagnosis of SMA; Molecular Genetics and Genomic Medicine; (2013).

Changes in circulating satiety hormones in obese children: A randomized controlled physical activity-based intervention study; Obesity; (2010).

Erratum: Robust quantification of the SMN gene copy number by real-time TaqMan PCR (Neurogenetics (2007) 8 (271-278) DOI: 10.1007/s10048-007-0093-1); Neurogenetics; (2009).

Increased susceptibility of spinal muscular atrophy fibroblasts to camptothecin is p53-independent; BMC Cell Biology; (2009).

Recombinant human Clara cell secretory protein treatment increases lung mRNA expression of surfactant proteins and vascular endothelial growth factor in a premature lamb model of respiratory distress syndrome; American Journal of Perinatology; (2008).

Reduction of elevated serum retinol binding protein in obese children by lifestyle intervention: Association with subclinical inflammation; Journal of Clinical Endocrinology and Metabolism; (2007).

Robust quantification of the SMN gene copy number by real-time TaqMan PCR; Neurogenetics; (2007).

Multiple transmissions of Barth syndrome through an oocyte donor with a de novo TAZ mutation; Fertility and Sterility; (2007).

3-Methylglutaconic aciduria disorders: The clinical spectrum increases; Journal of Pediatric Hematology/Oncology; (2006).

Leptin enhances lung maturity in the fetal rat; Pediatric Research; (2006).

Increased susceptibility of spinal muscular atrophy fibroblasts to camptothecin-induced cell death; Molecular Genetics and Metabolism; (2005).

Reversal of obesity-related hypoadiponectinemia by lifestyle intervention: A controlled, randomized study in obese adolescents; Journal of Clinical Endocrinology and Metabolism; (2005).

Leptin is not present in infant formulas; Journal of Endocrinological Investigation; (2003).

Leptin and estradiol as related to change in pubertal status and body weight; Medical Science Monitor; (2002).

Hyperoxia and nitric oxide reduce surfactant components (DSPC and surfactant proteins) and increase apoptosis in adult and fetal rat type II pneumocytes; Lung; (2002).

Leptin: A new growth factor for the small intestine; Journal of Pediatric Surgery; (2002).

Immaturity or starvation? Longitudinal study of leptin levels in premature infants; Biology of the Neonate; (2001).

Leptin levels in preterm human breast milk and infant formula.; Pediatrics; (2001).

A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection of PLP1 gene duplication in Pelizaeus-Merzbacher disease.; Human mutation; (2001).

Effect of triplet repeat expansion on chromatin structure and expression of dmpk and neighboring genes, six5 and dmwd, in myotonic dystrophy; Molecular Genetics and Metabolism; (2001).

Mutations in noncoding regions of the proteolipid protein gene in Pelizaeus-Merzbacher disease; Neurology; (2000).

Developmental expression of creatine kinase isoenzymes in chicken growth cartilage; Journal of Bone and Mineral Research; (1999).

Glucocorticoids decrease interleukin-6 levels and induce mineralization of cultured osteogenic cells from children with fibrous dysplasia; Journal of Bone and Mineral Research; (1999).

Molecular diagnosis of thiopurine s-methyltransferase deficiency as a guide to 6-mercaptopurine therapy in childhood ibd; Journal of Pediatric Gastroenterology and Nutrition; (1998).

Leptin expression in human mammary epithelial cells and breast milk; Journal of Clinical Endocrinology and Metabolism; (1998).

Mutation characterization and genotype, phenotype correlation in Barth syndrome; American Journal of Human Genetics; (1997).

Placental leptin: an important new growth factor in intrauterine and neonatal development?; Pediatrics; (1997).

Thiopurine s-methyltransferase genotyping for children and adolescents with inflammatory bowel disease: 39; Journal of Pediatric Gastroenterology and Nutrition; (1997).

Identification and functional characterization of human intestinal creatine transport activity; Journal of Pediatric Gastroenterology and Nutrition; (1996).

Identification of a testis-expressed creatine transporter gene at 16p11.2 and confirmation of the X-linked locus to Xq28; Genomics; (1996).

Regional chromosomal assignments for four members of the mads domain transcription enhancer factor 2 (MEF2) gene family to human chromosomes 15q26, 19p12, 5q14, and 1q12-q23; Genomics; (1995).

Overexpression of DM20 messenger RNA in two brothers with pelizaeus-merzbacher disease; Annals of Neurology; (1995).

Effect of myotonic dystrophy trinucleotide repeat expansion on dmpk transcription and processing; Genomics; (1995).

Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy; Genomics; (1993).

Creatine kinase activity is required for mineral deposition and matrix synthesis in endochondral growth cartilage; Bone and Mineral; (1992).

Entactin promotes adhesion and long-term maintenance of cultured regenerated skeletal myotubes; Journal of Cellular Physiology; (1992).

Developmental regulation of creatine kinase activity in cells of the epiphyseal growth cartilage; Journal of Bone and Mineral Research; (1992).

A genetic linkage map of human chromosome 5 with 60 RFLP loci; Genomics; (1991).

Hemin enhances differentiation and maturation of cultured regenerated skeletal myotubes; Journal of Cellular Physiology; (1989).

Hemin increases aerobic capacity of cultured regenerating skeletal myotubes; American Journal of Physiology - Cell Physiology; (1988).

Effect of gamma rays at the dihydrofolate reductase locus: Deletions and inversions; Somatic Cell and Molecular Genetics; (1986).

Localization of Chinese hamster dihydrofolate reductase gene to band p23 of chromosome 2; Somatic Cell and Molecular Genetics; (1986).

Coregulation of dihydrofolate reductase and thymidylate synthase B in Bacillus subtilis; BBA - Gene Structure and Expression; (1985).

Assignment of the human dihydrofolate reductase gene to the q11----q22 region of chromosome 5; Molecular and Cellular Biology; (1984).

Cloning and mapping of the dihydrofolate reductase gene of Bacillus subtilis; Gene; (1984).

Isolation and characterization of 5,6-dichloro-1-β-D-ribofuranosylbenzimidazole-resistant mutants of the Chinese hamster ovary cell line; Molecular and Cellular Biology; (1982).

Salmonella typhimurium LT-2 mutants with altered glutamine synthetase levels and amino acid uptake activities; Journal of Bacteriology; (1978).

Characterization of Salmonella typhimurium mutants with altered glutamine synthetase activity; Genetics; (1977).