T D Palella

959 total citations
23 papers, 751 citations indexed

About

T D Palella is a scholar working on Molecular Biology, Epidemiology and Infectious Diseases. According to data from OpenAlex, T D Palella has authored 23 papers receiving a total of 751 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 13 papers in Epidemiology and 10 papers in Infectious Diseases. Recurrent topics in T D Palella's work include Biochemical and Molecular Research (19 papers), Cytomegalovirus and herpesvirus research (11 papers) and HIV/AIDS drug development and treatment (10 papers). T D Palella is often cited by papers focused on Biochemical and Molecular Research (19 papers), Cytomegalovirus and herpesvirus research (11 papers) and HIV/AIDS drug development and treatment (10 papers). T D Palella collaborates with scholars based in United States and Japan. T D Palella's co-authors include William N. Kelley, Beverly L. Davidson, Susan A. Tarlé, Irving H. Fox, Yuji Hidaka, James M. Wilson, Timothy E. O’Toole, C. Thomas Caskey, Naoyuki Kamatani and Shin Fujimori and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Molecular and Cellular Biology.

In The Last Decade

T D Palella

22 papers receiving 726 citations

Peers

T D Palella

EPIDE

GENET

PPCH

C. H. M. M. de Bruyn Netherlands

Wolf Gutensohn Germany

Thaneas Prabakaran Denmark

Koji Orii Japan

Jiing-Kuan Yee United States

P. Hösli France

Lisya Gerez Netherlands

Keishin Sugawara Japan

B. W. Lacey United Kingdom

Viviana Marin‐Esteban France

C. H. M. M. de Bruyn Netherlands

T D Palella

533 ×0.9

292 ×1.0

EPIDE

171 ×0.8

34 ×0.3

GENET

68 ×0.8

PPCH

Citations per year, relative to T D Palella T D Palella (= 1×) peers C. H. M. M. de Bruyn

Countries citing papers authored by T D Palella

Since Specialization

Citations

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

Fields of papers citing papers by T D Palella

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T D Palella

This figure shows the co-authorship network connecting the top 25 collaborators of T D Palella. A scholar is included among the top collaborators of T D Palella 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 D Palella. T D Palella 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

Becker, Michael A., et al.. (1995). Point Mutations in PRPS1, the Gene Encoding the PRPP Synthetase (PRS) 1 Isoform, Underlie X-Linked PRS Superactivity Associated with Purine Nucleotide Inhibitor-Resistance. Advances in experimental medicine and biology. 370. 707–710. 5 indexed citations

Roessler, Blake J., Patrick Smith, Steven A. Heidler, et al.. (1993). Human X-linked phosphoribosylpyrophosphate synthetase superactivity is associated with distinct point mutations in the PRPS1 gene.. Journal of Biological Chemistry. 268(35). 26476–26481. 45 indexed citations

Becker, Michael A., Steven A. Heidler, Robert L. Switzer, et al.. (1991). Human Phosphoribosylpyrophosphate Synthetase (PRS) 2: An Independent Active, X Chromosone-Linked PRS Isoform. Advances in experimental medicine and biology. 309B. 129–132. 8 indexed citations

Davidson, Beverly L., Susan A. Tarlé, Dorothy A. Gibbs, et al.. (1991). Identification of 17 independent mutations responsible for human hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency.. PubMed. 48(5). 951–8. 61 indexed citations

Kamatani, Naoyuki, et al.. (1990). Crossovers within a short DNA sequence indicate a long evolutionary history of the APRT*J mutation. Human Genetics. 85(6). 600–4. 17 indexed citations

Palella, T D, et al.. (1990). Mutations induced at the hypoxanthine-guanine phosphoribosyltransferase locus of human T-lymphoblasts by perturbations of purine deoxyribonucleoside triphosphate pools.. PubMed. 50(15). 4566–71. 35 indexed citations

Fujimori, Shin, Beverly L. Davidson, William N. Kelley, & T D Palella. (1989). Identification of a single nucleotide change in the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTYale) responsible for Lesch-Nyhan syndrome.. Journal of Clinical Investigation. 83(1). 11–13. 24 indexed citations

Palella, T D, et al.. (1989). Transfer of Human HPRT Gene Sequence into Neuronal Cells by a Herpes Simplex Virus Derived Vector. Advances in experimental medicine and biology. 253A. 549–554. 5 indexed citations

Davidson, Beverly L., Susan A. Tarlé, T D Palella, & William N. Kelley. (1989). Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in ten subjects determined by direct sequencing of amplified transcripts.. Journal of Clinical Investigation. 84(1). 342–346. 78 indexed citations

10.

Davidson, Beverly L., Mohammad Pashmforoush, William N. Kelley, & T D Palella. (1989). Human Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency. Journal of Biological Chemistry. 264(1). 520–525. 31 indexed citations

11.

Kamatani, Naoyuki, et al.. (1989). Detection of an amino acid substitution in the mutant enzyme for a special type of adenine phosphoribosyltransferase (APRT) deficiency by sequence-specific protein cleavage.. PubMed. 45(2). 325–31. 13 indexed citations

12.

Hidaka, Yuji, Susan A. Tarlé, Shin Fujimori, et al.. (1988). Human adenine phosphoribosyltransferase deficiency. Demonstration of a single mutant allele common to the Japanese.. Journal of Clinical Investigation. 81(3). 945–950. 48 indexed citations

13.

Davidson, Beverly L., et al.. (1988). Hypoxanthine-guanine phosphoribosyltransferase. Genetic evidence for identical mutations in two partially deficient subjects.. Journal of Clinical Investigation. 82(6). 2164–2167. 20 indexed citations

14.

Hidaka, Yuji, T D Palella, Timothy E. O’Toole, Susan A. Tarlé, & William N. Kelley. (1987). Human adenine phosphoribosyltransferase. Identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzyme.. Journal of Clinical Investigation. 80(5). 1409–1415. 80 indexed citations

15.

Pierson, C., et al.. (1986). Protothecal Olecranon Bursitis: Treatment with Intrabursal Amphotericin B. Clinical Infectious Diseases. 8(6). 952–954. 21 indexed citations

16.

Wilson, James M., J. Timothy Stout, T D Palella, et al.. (1986). A molecular survey of hypoxanthine-guanine phosphoribosyltransferase deficiency in man.. Journal of Clinical Investigation. 77(1). 188–195. 84 indexed citations

17.

Wojtys, Edward M., et al.. (1986). Discordance for ankylosing spondylitis in a B27 negative monozygotic twin.. PubMed. 13(1). 205–7. 1 indexed citations

18.

Palella, T D & William N. Kelley. (1984). An approach to hyperuricemia and gout.. PubMed. 39(11). 89–92, 95. 4 indexed citations

19.

Palella, T D, et al.. (1980). Human placental adenosine kinase. Kinetic mechanism and inhibition.. Journal of Biological Chemistry. 255(11). 5264–5269. 92 indexed citations

20.

Rich, Kenneth, et al.. (1978). 731 PURINE NUCLEOSIDE PHOSPHORYLASE (PNP) DEFICIENCY WITH CELLULAR IMMUNE DEFICIENCY. Pediatric Research. 12. 485–485. 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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