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Rani H. Singh

Affiliations: 
Biological and Biomedical Sciences Emory University, Atlanta, GA 
Area:
Nutrition, Neuroscience Biology
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"Rani Singh"
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Parents

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Children

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Sarah H. Yi grad student 2010 Emory
Teresa D. Douglas grad student 2012 Emory
Meghan E. Quirk grad student 2012 Emory

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Publications

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Douglas TD, Newby LK, Eckstrand J, et al. (2020) Lipid changes in the metabolome of a single case study with maple syrup urine disease (MSUD) after five days of improved diet adherence of controlled branched-chain amino acids (BCAA). Molecular Genetics and Metabolism Reports. 25: 100651
Schultz MJ, Netzel BC, Singh RH, et al. (2020) Laboratory monitoring of patients with hereditary tyrosinemia type I. Molecular Genetics and Metabolism
Douglas TD, Nucci AM, Berry AM, et al. (2019) Large neutral amino acid status in association with P:T ratio and diet in adult and pediatric patients with phenylketonuria. Jimd Reports. 50: 50-59
Douglas T, Singh R. (2019) Elevated Urine Creatinine in Relation to Protein Intake in Adolescent and Adult Females with Phenylketonuria (PKU) with Comparison to NHANES (P08-060-19) Current Developments in Nutrition. 3
Brantley KD, Douglas TD, Singh RH. (2018) One-year follow-up of B vitamin and Iron status in patients with phenylketonuria provided tetrahydrobiopterin (BH4). Orphanet Journal of Rare Diseases. 13: 192
Li H, Zhao L, Singh R, et al. (2018) The first pediatric case of glucagon receptor defect due to biallelic mutations in is identified by newborn screening of elevated arginine. Molecular Genetics and Metabolism Reports. 17: 46-52
MacDonald A, Singh RH, Rocha JC, et al. (2018) Optimising amino acid absorption: essential to improve nitrogen balance and metabolic control in phenylketonuria. Nutrition Research Reviews. 1-9
Kenneson A, Osara Y, Pringle T, et al. (2018) Natural history of children and adults with maple syrup urine disease in the NBS-MSUD Connect registry. Molecular Genetics and Metabolism Reports. 15: 22-27
Montoya Parra GA, Singh RH, Cetinyurek-Yavuz A, et al. (2018) Status of nutrients important in brain function in phenylketonuria: a systematic review and meta-analysis. Orphanet Journal of Rare Diseases. 13: 101
Jani R, Coakley K, Douglas T, et al. (2017) Protein intake and physical activity are associated with body composition in individuals with phenylalanine hydroxylase deficiency. Molecular Genetics and Metabolism
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