T. Burrow

1.3k total citations
46 papers, 497 citations indexed

About

T. Burrow is a scholar working on Language and Linguistics, Physiology and Archeology. According to data from OpenAlex, T. Burrow has authored 46 papers receiving a total of 497 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Language and Linguistics, 12 papers in Physiology and 11 papers in Archeology. Recurrent topics in T. Burrow's work include Linguistics and language evolution (17 papers), Lysosomal Storage Disorders Research (12 papers) and Ancient Near East History (11 papers). T. Burrow is often cited by papers focused on Linguistics and language evolution (17 papers), Lysosomal Storage Disorders Research (12 papers) and Ancient Near East History (11 papers). T. Burrow collaborates with scholars based in United States, United Kingdom and Australia. T. Burrow's co-authors include Robert J. Hopkin, M. B. Emeneau, Gregory A. Grabowski, Nancy D. Leslie, Carlos E. Prada, Laurie Bailey, Lisa J. Martin, Robin T. Cotton, Howard M. Saal and Alessandro de Alarcón and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and The Journal of Pediatrics.

In The Last Decade

T. Burrow

31 papers receiving 434 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
T. Burrow United States 15 212 124 109 82 81 46 497
Emily C. Lisi United States 13 123 0.6× 142 1.1× 64 0.6× 59 0.7× 26 0.3× 22 411
Suresh Vijayaraghavan United Kingdom 7 756 3.6× 98 0.8× 264 2.4× 59 0.7× 125 1.5× 11 862
Avinoam Adam Israel 13 120 0.6× 148 1.2× 25 0.2× 115 1.4× 33 0.4× 21 539
Thomas Andrew Burrow United States 11 442 2.1× 226 1.8× 44 0.4× 31 0.4× 239 3.0× 24 757
Akella Radha Rama Devi India 15 42 0.2× 176 1.4× 136 1.2× 74 0.9× 18 0.2× 30 621
Hyon J. Kim South Korea 14 60 0.3× 191 1.5× 57 0.5× 12 0.1× 49 0.6× 28 532
Lúcia Lacerda Portugal 16 745 3.5× 286 2.3× 149 1.4× 23 0.3× 294 3.6× 39 936
Renske Olmer Netherlands 7 210 1.0× 396 3.2× 53 0.5× 30 0.4× 68 0.8× 8 855
Sara Cathey United States 13 243 1.1× 130 1.0× 26 0.2× 17 0.2× 123 1.5× 24 427
Barbara Nagel United States 12 76 0.4× 239 1.9× 36 0.3× 12 0.1× 49 0.6× 15 516

Countries citing papers authored by T. Burrow

Since Specialization
Citations

This map shows the geographic impact of T. Burrow'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 T. Burrow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Burrow more than expected).

Fields of papers citing papers by T. Burrow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Burrow

This figure shows the co-authorship network connecting the top 25 collaborators of T. Burrow. A scholar is included among the top collaborators of T. Burrow 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 T. Burrow. T. Burrow is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
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
2.
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
3.
Weinreb, Neal J., Özlem Göker-Alpan, Priya S. Kishnani, et al.. (2022). The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?. Molecular Genetics and Metabolism. 136(1). 4–21. 33 indexed citations
4.
Burrow, T., et al.. (2021). Evaluating psychosocial stressors in families of children with inborn errors of metabolism. Molecular Genetics and Metabolism Reports. 27. 100740–100740. 1 indexed citations
5.
Mistry, Pramod K., Manisha Balwani, Deborah Barbouth, et al.. (2020). Gaucher disease and SARS-CoV-2 infection: Emerging management challenges. Molecular Genetics and Metabolism. 130(3). 164–169. 23 indexed citations
6.
Serai, Suraj D., et al.. (2018). Correlating liver stiffness with disease severity scoring system (DS3) values in Gaucher disease type 1 (GD1) patients. Molecular Genetics and Metabolism. 123(3). 357–363. 16 indexed citations
7.
Lesmana, Harry, Seyed Ali Hosseini, T. Burrow, et al.. (2018). CNTNAP1-Related Congenital Hypomyelinating Neuropathy. Pediatric Neurology. 93. 43–49. 14 indexed citations
8.
Coman, David, Lisenka E.L.M. Vissers, Lisa G. Riley, et al.. (2018). Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis. The American Journal of Human Genetics. 103(1). 125–130. 23 indexed citations
9.
Elstein, Deborah, T. Burrow, Joel Charrow, et al.. (2016). Home infusion of intravenous velaglucerase alfa: Experience from pooled clinical studies in 104 patients with type 1 Gaucher disease. Molecular Genetics and Metabolism. 120(1-2). 111–115. 9 indexed citations
10.
Cox, Timothy M., T. Burrow, Pilar Giraldo, et al.. (2016). Stability is maintained in adults with Gaucher disease type 1 switched from velaglucerase alfa to eliglustat or imiglucerase: A sub-analysis of the eliglustat ENCORE trial. Molecular Genetics and Metabolism Reports. 9. 25–28. 13 indexed citations
11.
Hallinan, Barbara, et al.. (2015). A Novel Catastrophic Presentation of X-Linked Adrenoleukodystrophy. JIMD Reports. 24. 97–102. 9 indexed citations
12.
Prada, Carlos E., Ajay Kaul, Robert J. Hopkin, et al.. (2012). Recurrent pancreatitis in ornithine transcarbamylase deficiency. Molecular Genetics and Metabolism. 106(4). 482–484. 3 indexed citations
13.
Burrow, T., et al.. (2010). Acute Progression of Neuromuscular Findings in Infantile Pompe Disease. Pediatric Neurology. 42(6). 455–458. 39 indexed citations
14.
Burrow, T., Howard M. Saal, Alessandro de Alarcón, et al.. (2009). Characterization of Congenital Anomalies in Individuals With Choanal Atresia. Archives of Otolaryngology - Head and Neck Surgery. 135(6). 543–543. 62 indexed citations
15.
Burrow, T., Mitchell B. Cohen, Ronald E. Bokulic, et al.. (2007). Gaucher Disease: Progressive Mesenteric and Mediastinal Lymphadenopathy Despite Enzyme Therapy. The Journal of Pediatrics. 150(2). 202–206. 24 indexed citations
16.
Burrow, T. & M. B. Emeneau. (1972). Dravidian Etymological Notes: Supplement to DED, DEDS, and DBIA, Pt. I. Journal of the American Oriental Society. 92(3). 397–397. 3 indexed citations
17.
Bright, William, T. Burrow, & M. B. Emeneau. (1969). A Dravidian Etymological Dictionary: Supplement. Language. 45(3). 680–680. 16 indexed citations
18.
19.
Burrow, T., et al.. (1963). A Dravidian Etymological Dictionary. Language. 39(3). 556–556. 13 indexed citations
20.
Burrow, T.. (1959). On the Phonological History of Sanskrit kṣám- 'Earth,' rkṣa- 'Bear' and likṣa 'Nit'. Journal of the American Oriental Society. 79(2). 85–85. 2 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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