Rani H. Singh - Concepedia

Author

Rani H. Singh

Also Known As

Maryam Rakhshandehroo, R Singh, R. H. Singh, R. Singh, R.H. Singh, RANI H SINGH, Rani H Singh, Rani H. Singh, Rani Singh, Rohr, Fran

138

Publications

4.1K

Citations

H-Index

109

Concepts

All Affiliations

Emory University Boston Children's Hospital University of Utah Lurie Children's Hospital University of Miami

About

Rani H. Singh is an author at Emory University specializing in medicine, nutrition, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	27	1.3K
2	Health Sciences	8	8	267
3	Education	1	1	29
4	Language Studies	1	1	34
5	Nursing	1	1	16

Rani H. Singh

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Phenylketonuria Scientific Review Conference: State of the science and future research needs Kathryn Camp, Melissa A. Parisi, Phyllis B. Acosta, Molecular Genetics and Metabolism Translational MedicineChronic Kidney DiseaseRenal PathologyPathologyTranslational Research	2014	263
A prevalent mutation for galactosemia among black Americans Kent Lai, Sharon D. Langley, Rani H. Singh, The Journal of Pediatrics Human VariationPrevalent MutationGeneticsDiabetesGenetic Epidemiology	1996	117
Risk factors for premature ovarian failure in females with galactosemia Nicole Guerrero, Rani H. Singh, Amita K. Manatunga, The Journal of Pediatrics InfertilityFertilityFemale InfertilityReproductive HealthGynecology	2000	115
Nutrient intakes and physical growth of children with phenylketonuria undergoing nutrition therapy Phyllis B. Acosta, Steven Yannicelli, Rani H. Singh, Journal of the American Dietetic Association MalnutritionNutritionNutritional InterventionsNutrition DevelopmentClinical Nutrition	2003	95
Verbal Dyspraxia and Galactosemia Amy Webb, Rani H. Singh, Mary Jane Kennedy, Pediatric Research Electrolyte DisorderApraxia Of SpeechNeuropsychologyPhysiologyVerbal Dyspraxia	2003	67
Cystathionine?-synthase deficiency in Georgia (USA): Correlation of clinical and biochemical phenotype with genotype Warren D. Kruger, Lu Wang, Kwang-Hwan Jhee, Human Mutation	2003	65
Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency Fernando Scaglia, Yuhuan Wang, Rani H. Singh, Genetics in Medicine UrologyBiochemistryPrimary Carnitine DeficiencyPhysiologyMetabolism	1998	60
Barriers to successful dietary control among pregnant women with phenylketonuria Amanda Savage Brown, Paul M. Fernhoff, Susan E. Waisbren, Genetics in Medicine NutritionPublic Health NutritionGynecologyWomen's HealthMaternal Health	2002	59
Management of Fatty Acid Oxidation Disorders JAVA O SOLIS, Rani H. Singh Journal of the American Dietetic Association Metabolic SyndromeMetabolic DisorderOmega-3 Fatty AcidMedicinePhysiology	2002	57
Acute liver failure in neonates with undiagnosed hereditary fructose intolerance due to exposure from widely available infant formulas Hong Li, Heather M. Byers, Alicia Diaz‐Kuan, Molecular Genetics and Metabolism NeonatologyHepatologyLiver PhysiologyInfant NutritionPediatrics	2018	57

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