Rani H. Singh

4.2k total citations
109 papers, 2.7k citations indexed

About

Rani H. Singh is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Rani H. Singh has authored 109 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 88 papers in Clinical Biochemistry, 51 papers in Physiology and 36 papers in Molecular Biology. Recurrent topics in Rani H. Singh's work include Metabolism and Genetic Disorders (88 papers), Diet and metabolism studies (49 papers) and Folate and B Vitamins Research (24 papers). Rani H. Singh is often cited by papers focused on Metabolism and Genetic Disorders (88 papers), Diet and metabolism studies (49 papers) and Folate and B Vitamins Research (24 papers). Rani H. Singh collaborates with scholars based in United States, Netherlands and United Kingdom. Rani H. Singh's co-authors include Louis J. Elsas, Patricia L. Splett, Teresa D. Douglas, Kathryn E. Coakley, Dianne M. Frazier, Beth Ogata, Fran Rohr, Shideh Mofidi, Aileen Kenneson and Wendy E. Smith and has published in prestigious journals such as American Journal of Clinical Nutrition, The FASEB Journal and Cochrane Database of Systematic Reviews.

In The Last Decade

Rani H. Singh

106 papers receiving 2.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Rani H. Singh United States	31	2.1k	1.1k	975	572	502	109	2.7k
Kevin Carpenter Australia	24	1.5k 0.7×	1.4k 1.3×	617 0.6×	611 1.1×	424 0.8×	63	2.5k
Luis Aldámiz‐Echevarría Spain	24	633 0.3×	509 0.5×	560 0.6×	202 0.4×	235 0.5×	87	1.5k
Teruo Kitagawa Japan	25	507 0.2×	715 0.7×	1.1k 1.1×	314 0.5×	289 0.6×	108	2.6k
M. Rebecca Heiner‐Fokkema Netherlands	18	540 0.3×	441 0.4×	382 0.4×	99 0.2×	197 0.4×	85	1.2k
V. G. Oberholzer United Kingdom	19	699 0.3×	595 0.6×	219 0.2×	241 0.4×	198 0.4×	56	1.4k
Daniel Rudman United States	24	360 0.2×	323 0.3×	393 0.4×	139 0.2×	282 0.6×	34	1.9k
Fernando Andrade Spain	20	316 0.2×	330 0.3×	411 0.4×	97 0.2×	108 0.2×	58	1.1k
Wolfgang Erwa Austria	21	297 0.1×	401 0.4×	202 0.2×	166 0.3×	175 0.3×	37	1.1k
Karolina M. Stępień United Kingdom	20	176 0.1×	408 0.4×	463 0.5×	148 0.3×	182 0.4×	107	1.4k
Svante Norgren Sweden	28	56 0.0×	848 0.8×	443 0.5×	192 0.3×	247 0.5×	70	2.1k

Countries citing papers authored by Rani H. Singh

Since Specialization

Citations

This map shows the geographic impact of Rani H. Singh's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Rani H. Singh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rani H. Singh more than expected).

Fields of papers citing papers by Rani H. Singh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rani H. Singh. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Rani H. Singh. The network helps show where Rani H. Singh may publish in the future.

Co-authorship network of co-authors of Rani H. Singh

This figure shows the co-authorship network connecting the top 25 collaborators of Rani H. Singh. A scholar is included among the top collaborators of Rani H. Singh based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Rani H. Singh. Rani H. Singh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Jurecki, Elaina, Keiko Ueda, Dianne M. Frazier, et al.. (2019). Nutrition management guideline for propionic acidemia: An evidence- and consensus-based approach. Molecular Genetics and Metabolism. 126(4). 341–354. 40 indexed citations

Burlina, Alberto, Sebastian Tims, Francjan van Spronsen, et al.. (2018). The potential role of gut microbiota and its modulators in the management of propionic and methylmalonic acidemia. Expert Opinion on Orphan Drugs. 6(11). 683–692. 5 indexed citations

Singh, Rani H., et al.. (2018). Status of nutrients important in brain function in phenylketonuria: a systematic review and meta-analysis. Orphanet Journal of Rare Diseases. 13(1). 101–101. 23 indexed citations

Zhao, Lihua, Rani H. Singh, Doris Fadoju, et al.. (2018). The first pediatric case of glucagon receptor defect due to biallelic mutations in GCGR is identified by newborn screening of elevated arginine. Molecular Genetics and Metabolism Reports. 17. 46–52. 18 indexed citations

Li, Hong, Heather M. Byers, Miriam B. Vos, et al.. (2018). Acute liver failure in neonates with undiagnosed hereditary fructose intolerance due to exposure from widely available infant formulas. Molecular Genetics and Metabolism. 123(4). 428–432. 29 indexed citations

Coakley, Kathryn E., Eric I. Felner, Vin Tangpricha, Peter W.F. Wilson, & Rani H. Singh. (2017). Impact of Dietary Intake on Bone Turnover in Patients with Phenylalanine Hydroxylase Deficiency. JIMD Reports. 36. 67–77. 3 indexed citations

Coakley, Kathryn E., et al.. (2017). Development of newborn screening connect (NBS connect): a self-reported patient registry and its role in improvement of care for patients with inherited metabolic disorders. Orphanet Journal of Rare Diseases. 12(1). 132–132. 9 indexed citations

Frazier, Dianne M., Caroline Homer, Barbara Marriage, et al.. (2014). Nutrition management guideline for maple syrup urine disease: An evidence- and consensus-based approach. Molecular Genetics and Metabolism. 112(3). 210–217. 129 indexed citations

Singh, Rani H., Fran Rohr, Dianne M. Frazier, et al.. (2014). Recommendations for the nutrition management of phenylalanine hydroxylase deficiency. Genetics in Medicine. 16(2). 121–131. 140 indexed citations

10.

Yi, Sarah H., Julie A. Kable, Marian L. Evatt, & Rani H. Singh. (2011). A randomized, placebo-controlled, double-blind trial of supplemental docosahexaenoic acid on cognitive processing speed and executive function in females of reproductive age with phenylketonuria: A pilot study. Prostaglandins Leukotrienes and Essential Fatty Acids. 85(6). 317–327. 7 indexed citations

11.

Hinman, Alan R., Marie Y. Mann, & Rani H. Singh. (2009). Newborn dried bloodspot screening: mapping the clinical and public health components and activities. Genetics in Medicine. 11(6). 418–424. 17 indexed citations

12.

Braun, Kim Van Naarden, et al.. (2009). Prevalence of Developmental Disabilities and Receipt of Special Education Services among Children with an Inborn Error of Metabolism. The Journal of Pediatrics. 156(3). 420–426. 8 indexed citations

13.

Gregory, Cria O., Chunli Yu, & Rani H. Singh. (2007). Blood phenylalanine monitoring for dietary compliance among patients with phenylketonuria: comparison of methods. Genetics in Medicine. 9(11). 761–765. 43 indexed citations

14.

Smith, Wendy E., Priya S. Kishnani, Brendan Lee, et al.. (2005). Urea Cycle Disorders: Clinical Presentation Outside the Newborn Period. Critical Care Clinics. 21(4). S9–S17. 66 indexed citations

15.

Acosta, Phyllis B., Steven Yannicelli, Rani H. Singh, et al.. (2004). Iron status of children with phenylketonuria undergoing nutrition therapy assessed by transferrin receptors. Genetics in Medicine. 6(2). 96–101. 29 indexed citations

16.

Kruger, Warren D., Lu Wang, Kwang-Hwan Jhee, Rani H. Singh, & Louis J. Elsas. (2003). Cystathionine?-synthase deficiency in Georgia (USA): Correlation of clinical and biochemical phenotype with genotype. Human Mutation. 22(6). 434–441. 49 indexed citations

17.

Fernhoff, Paul M., Susan E. Waisbren, Dianne M. Frazier, et al.. (2002). Barriers to successful dietary control among pregnant women with phenylketonuria. Genetics in Medicine. 4(2). 84–89. 41 indexed citations

18.

Berry, Gerard T., Rani H. Singh, Alice Mazur, et al.. (2000). Galactose Breath Testing Distinguishes Variant and Severe Galactose-1-Phosphate Uridyltransferase Genotypes. Pediatric Research. 48(3). 323–328. 36 indexed citations

19.

Scaglia, Fernando, Yuhuan Wang, Rani H. Singh, et al.. (1998). Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency. Genetics in Medicine. 1(1). 34–39. 54 indexed citations

20.

Berry, Gerard T., Itzhak Nissim, A. Mazur, et al.. (1995). In Vivo Oxidation of [13C]Galactose in Patients with Galactose-1-Phosphate Uridyltransferase Deficiency. Biochemical and Molecular Medicine. 56(2). 158–165. 26 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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