Surekha Pendyal

593 total citations
21 papers, 366 citations indexed

About

Surekha Pendyal is a scholar working on Rheumatology, Physiology and Genetics. According to data from OpenAlex, Surekha Pendyal has authored 21 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Rheumatology, 9 papers in Physiology and 7 papers in Genetics. Recurrent topics in Surekha Pendyal's work include Glycogen Storage Diseases and Myoclonus (15 papers), Lysosomal Storage Disorders Research (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Surekha Pendyal is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (15 papers), Lysosomal Storage Disorders Research (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Surekha Pendyal collaborates with scholars based in United States, Netherlands and Italy. Surekha Pendyal's co-authors include Priya S. Kishnani, Stephanie Austin, Deeksha Bali, Rani H. Singh, Patricia L. Splett, Adrya Stembridge, Jennifer Goldstein, Areeg El‐Gharbawy, Teresa D. Douglas and Amy Cunningham and has published in prestigious journals such as SHILAP Revista de lepidopterología, Nutrients and Genetics in Medicine.

In The Last Decade

Surekha Pendyal

18 papers receiving 359 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Surekha Pendyal United States	9	214	158	128	121	89	21	366
Joanna Taybert Poland	8	111 0.5×	76 0.5×	56 0.4×	72 0.6×	118 1.3×	17	274
Sommer Gaughan United States	4	69 0.3×	124 0.8×	42 0.3×	63 0.5×	91 1.0×	10	239
P. J. Lee United Kingdom	13	156 0.7×	170 1.1×	186 1.5×	40 0.3×	109 1.2×	20	366
Uta Meyer Germany	7	94 0.4×	162 1.0×	82 0.6×	50 0.4×	67 0.8×	11	239
Mike Champion United Kingdom	6	80 0.4×	198 1.3×	58 0.5×	55 0.5×	191 2.1×	6	357
Fernanda Sperb‐Ludwig Brazil	11	52 0.2×	61 0.4×	100 0.8×	33 0.3×	97 1.1×	38	288
A Burlina Italy	7	92 0.4×	263 1.7×	79 0.6×	35 0.3×	212 2.4×	17	374
Vladimı́r Bzdúch Slovakia	8	42 0.2×	65 0.4×	83 0.6×	39 0.3×	103 1.2×	28	259
Chuan‐Hong Kao Taiwan	7	102 0.5×	141 0.9×	204 1.6×	39 0.3×	158 1.8×	10	411
Liliane Loridan United States	11	90 0.4×	92 0.6×	195 1.5×	119 1.0×	170 1.9×	16	442

Countries citing papers authored by Surekha Pendyal

Since Specialization

Citations

This map shows the geographic impact of Surekha Pendyal'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 Surekha Pendyal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Surekha Pendyal more than expected).

Fields of papers citing papers by Surekha Pendyal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Surekha Pendyal. 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 Surekha Pendyal. The network helps show where Surekha Pendyal may publish in the future.

Co-authorship network of co-authors of Surekha Pendyal

This figure shows the co-authorship network connecting the top 25 collaborators of Surekha Pendyal. A scholar is included among the top collaborators of Surekha Pendyal 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 Surekha Pendyal. Surekha Pendyal 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

Pendyal, Surekha, et al.. (2025). An Assessment of Dietary Intake, Feeding Practices, Growth, and Swallowing Function in Young Children with Late-Onset Pompe Disease: A Framework for Developing Nutrition Guidelines. Nutrients. 17(11). 1909–1909.

Boyer, Monica, et al.. (2024). Nutrition Management in Children Less than 5 Years of Age with Glycogen Storage Disease Type I: Survey Results. Nutrients. 16(19). 3244–3244.

Grünert, Sarah C., Terry G. J. Derks, Helen Mundy, et al.. (2024). Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop. Molecular Genetics and Metabolism. 141(3). 108144–108144. 8 indexed citations

Boyer, M., et al.. (2024). O.1 A survey: nutrition management of children less than five years of age with glycogen storage disease type I. Molecular Genetics and Metabolism. 141. 108364–108364. 1 indexed citations

Soler‐Alfonso, Claudia, Ariana L. Smith, Deeksha Bali, et al.. (2023). Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource. Molecular Genetics and Metabolism. 138(3). 107525–107525. 21 indexed citations

Pendyal, Surekha, et al.. (2023). Development of hepatocellular adenomas in a patient with glycogen storage disease Ia treated with growth hormone therapy. JIMD Reports. 64(5). 303–311. 2 indexed citations

Koch, Rebecca E., Claudia Soler‐Alfonso, Bridget Kiely, et al.. (2023). O18: A path forward for patients with glycogen branching enzyme deficiency: Consensus on diagnosing and managing glycogen storage disease type IV*. SHILAP Revista de lepidopterología. 1(1). 100114–100114. 1 indexed citations

Pendyal, Surekha, et al.. (2022). Very early-onset inflammatory bowel disease: Novel description in glycogen storage disease type Ia. Molecular Genetics and Metabolism Reports. 31. 100848–100848. 2 indexed citations

Ryan, Katherine, et al.. (2022). Clinical insights from Wolman disease: Evaluating infantile hepatosplenomegaly. American Journal of Medical Genetics Part A. 188(11). 3364–3368. 1 indexed citations

10.

Young, Sarah P., Bruce A. Smith, Laura E. Case, et al.. (2022). A RETROSPECTIVE LONGITUDINAL STUDY AND COMPREHENSIVE REVIEW OF ADULT PATIENTS WITH GLYCOGEN STORAGE DISEASE TYPE III. Molecular Genetics and Metabolism. 135(4). 275–276. 1 indexed citations

11.

Young, Sarah P., Brian P. Smith, Laura E. Case, et al.. (2021). A retrospective longitudinal study and comprehensive review of adult patients with glycogen storage disease type III. Molecular Genetics and Metabolism Reports. 29. 100821–100821. 12 indexed citations

12.

Calcar, Sandra C. Van, et al.. (2020). Nutrition management guideline for very-long chain acyl-CoA dehydrogenase deficiency (VLCAD): An evidence- and consensus-based approach. Molecular Genetics and Metabolism. 131(1-2). 23–37. 45 indexed citations

13.

Rossi, Alessandro, Foekje de Boer, C Montanari, et al.. (2020). Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations. Journal of Inherited Metabolic Disease. 43(4). 770–777. 21 indexed citations

14.

Young, Sarah P., Stephanie Austin, Deeksha Bali, et al.. (2019). Liver fibrosis during clinical ascertainment of glycogen storage disease type III: a need for improved and systematic monitoring. Genetics in Medicine. 21(12). 2686–2694. 29 indexed citations

15.

Kishnani, Priya S., Jennifer Goldstein, Stephanie Austin, et al.. (2019). Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 21(4). 772–789. 86 indexed citations

16.

Bali, Deeksha, Jennifer Goldstein, Stephanie Austin, et al.. (2017). Clinical and Molecular Variability in Patients with PHKA2 Variants and Liver Phosphorylase b Kinase Deficiency. JIMD Reports. 37. 63–72. 15 indexed citations

17.

Pendyal, Surekha, et al.. (2017). Early Diagnosed and Treated Glutaric Acidemia Type 1 Female Presenting with Subependymal Nodules in Adulthood. JIMD Reports. 40. 85–90. 3 indexed citations

18.

Singh, Rani H., Amy Cunningham, Shideh Mofidi, et al.. (2016). Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach. Molecular Genetics and Metabolism. 118(2). 72–83. 88 indexed citations

19.

Willis, Monte S., Alice Basinger, Zheng Fan, et al.. (2006). Hepatosplenomegaly in an 8-Month-Old Child. Laboratory Medicine. 37(11). 665–695. 1 indexed citations

20.

Frazier, Dianne M. & Surekha Pendyal. (1999). The Effect of the Cost and Perceived Cost of Special Low Protein Foods on their Utilization and Dietary Compliance in Phenylketonuria. Journal of the American Dietetic Association. 99(9). A106–A106. 1 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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