Shree Pandya

9.1k total citations · 3 hit papers
59 papers, 5.4k citations indexed

About

Shree Pandya is a scholar working on Molecular Biology, Biomedical Engineering and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Shree Pandya has authored 59 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 15 papers in Biomedical Engineering and 14 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Shree Pandya's work include Muscle Physiology and Disorders (49 papers), Genetic Neurodegenerative Diseases (13 papers) and Neurogenetic and Muscular Disorders Research (12 papers). Shree Pandya is often cited by papers focused on Muscle Physiology and Disorders (49 papers), Genetic Neurodegenerative Diseases (13 papers) and Neurogenetic and Muscular Disorders Research (12 papers). Shree Pandya collaborates with scholars based in United States, United Kingdom and Canada. Shree Pandya's co-authors include David J. Birnkrant, Laura E. Case, Jean Tomezsko, K. Bushby, Paula R. Clemens, Richard S. Finkel, Kathi Kinnett, Frederic Shapiro, Carolyn M. Constantin and Craig M. McDonald and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and PEDIATRICS.

In The Last Decade

Shree Pandya

59 papers receiving 5.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management

2009 1.4k citations K. Bushby, Richard S. Finkel et al. The Lancet Neurology profile →
Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care

2009 785 citations K. Bushby, Richard S. Finkel et al. The Lancet Neurology profile →
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management

2018 781 citations David J. Birnkrant, K. Bushby et al. The Lancet Neurology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Shree Pandya United States	27	4.2k	1.2k	1.0k	953	860	59	5.4k
K. Bushby United Kingdom	19	3.6k 0.9×	1.1k 0.9×	955 0.9×	736 0.8×	733 0.9×	38	4.7k
David J. Birnkrant United States	22	3.8k 0.9×	1.3k 1.1×	1.0k 1.0×	955 1.0×	412 0.5×	61	5.4k
Julaine Florence United States	36	2.9k 0.7×	1.4k 1.1×	562 0.5×	812 0.9×	631 0.7×	66	5.0k
Richard T. Abresch United States	40	2.8k 0.7×	986 0.8×	573 0.6×	955 1.0×	886 1.0×	98	5.1k
Michelle Eagle United Kingdom	31	2.8k 0.7×	896 0.7×	856 0.8×	669 0.7×	602 0.7×	64	3.9k
Linda Cripe United States	30	4.3k 1.0×	977 0.8×	2.4k 2.3×	783 0.8×	439 0.5×	87	6.0k
Laura E. Case United States	28	3.4k 0.8×	1.1k 0.9×	834 0.8×	721 0.8×	384 0.4×	86	6.0k
Francesco Muntoni United Kingdom	50	5.1k 1.2×	1.6k 1.3×	1.7k 1.6×	540 0.6×	1.6k 1.9×	250	7.5k
Wendy King United States	27	2.5k 0.6×	828 0.7×	529 0.5×	539 0.6×	602 0.7×	45	3.8k
Jean Tomezsko United States	10	2.4k 0.6×	697 0.6×	612 0.6×	560 0.6×	288 0.3×	11	3.4k

Countries citing papers authored by Shree Pandya

Since Specialization

Citations

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

Fields of papers citing papers by Shree Pandya

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shree Pandya

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

Paramsothy, Pangaja, Kristin M. Conway, Nicholas E. Johnson, et al.. (2022). Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research Network. Neuromuscular Disorders. 32(6). 468–476. 8 indexed citations

James, Katherine A., Jane Gralla, Angela S. Czaja, et al.. (2020). Left ventricular dysfunction in Duchenne muscular dystrophy. Cardiology in the Young. 30(2). 171–176. 12 indexed citations

Conway, Kristin M., Paul A. Romitti, Molly M. Lamb, et al.. (2018). A Review of MD STARnet’s Research Contributions to Pediatric-Onset Dystrophinopathy in the United States; 2002-2017. Journal of Child Neurology. 34(1). 44–53. 6 indexed citations

Weber, David R., Shiny Thomas, Stephen W. Erickson, et al.. (2018). Bone Health and Endocrine Care of Boys with Duchenne Muscular Dystrophy: Data from the MD STARnet. Journal of Neuromuscular Diseases. 5(4). 497–507. 9 indexed citations

Birnkrant, David J., K. Bushby, Carla Bann, et al.. (2018). Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. The Lancet Neurology. 17(3). 251–267. 781 indexed citations breakdown →

Conway, Kristin M., Christina Trout, Christina Westfield, Deborah Fox, & Shree Pandya. (2018). A Pilot Survey Study of Adherence to Care Considerations for Duchenne Muscular Dystrophy. PLoS Currents. 10. 8 indexed citations

Paramsothy, Pangaja, Molly M. Lamb, Kathi Kinnett, et al.. (2018). Health Care Transition Experiences of Males with Childhood-onset Duchenne and Becker Muscular Dystrophy: Findings from the Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet) Health Care Transitions and Other Life Experiences Survey. PLoS Currents. 10. 8 indexed citations

Montes, Jacqueline, Allan M. Glanzman, Elena Mazzone, et al.. (2015). Spinal muscular atrophy functional composite score: A functional measure in spinal muscular atrophy. Muscle & Nerve. 52(6). 942–947. 18 indexed citations

Pandya, Shree, et al.. (2014). Sociodemographic and Health Related Profile of Adults with Duchenne/Becker Muscular Dystrophy (DBMD): Data from the Muscular Dystrophy Surveillance, Tracking and Research Network (MD STARnet) (P5.090). Neurology. 82(10_supplement). 1 indexed citations

10.

Barber, Brent J., Jennifer Andrews, Zhenqiang Lu, et al.. (2013). Oral Corticosteroids and Onset of Cardiomyopathy in Duchenne Muscular Dystrophy. The Journal of Pediatrics. 163(4). 1080–1084.e1. 101 indexed citations

11.

Rose, Michael R., Reza Sadjadi, John Weinman, et al.. (2012). Role of disease severity, illness perceptions, and mood on quality of life in muscle disease. Muscle & Nerve. 46(3). 351–359. 57 indexed citations

12.

Nabukera, Sarah K., Paul A. Romitti, Kimberley A. Campbell, et al.. (2011). Use of Complementary and Alternative Medicine by Males With Duchenne or Becker Muscular Dystrophy. Journal of Child Neurology. 27(6). 734–740. 21 indexed citations

13.

Meaney, F. John, Jennifer Andrews, Emma Ciafaloni, et al.. (2011). Disparities in the diagnostic process of Duchenne and Becker muscular dystrophy. Genetics in Medicine. 13(11). 942–947. 31 indexed citations

14.

Andrews, Jennifer, Shree Pandya, Christina Trout, et al.. (2011). Palliative care services in families of males with duchenne muscular dystrophy. Muscle & Nerve. 44(1). 93–101. 33 indexed citations

15.

Sadjadi, Reza, Alison Carr, Jessica Walburn, et al.. (2011). Validation of the individualised neuromuscular quality of life for the USA with comparison of the impact of muscle disease on those living in USA versus UK. Health and Quality of Life Outcomes. 9(1). 114–114. 19 indexed citations

16.

Bushby, K., Richard S. Finkel, David J. Birnkrant, et al.. (2009). Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management. The Lancet Neurology. 9(1). 77–93. 1378 indexed citations breakdown →

17.

Logigian, Eric L., Emma Ciafaloni, Nuran Dilek, et al.. (2007). Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy. Muscle & Nerve. 35(4). 479–485. 57 indexed citations

18.

Moxley, Richard T., Eric L. Logigian, William B. Martens, et al.. (2007). Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1). Muscle & Nerve. 36(3). 320–328. 41 indexed citations

19.

Miller, Lisa A., Paul A. Romitti, Christopher Cunniff, et al.. (2006). The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): Surveillance methodology. Birth Defects Research Part A Clinical and Molecular Teratology. 76(11). 793–797. 93 indexed citations

20.

Florence, Julaine, Shree Pandya, Wendy King, et al.. (1992). Intrarater Reliability of Manual Muscle Test (Medical Research Council Scale) Grades in Duchenne's Muscular Dystrophy. Physical Therapy. 72(2). 115–122. 265 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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