T. L. Oei

550 total citations
40 papers, 436 citations indexed

About

T. L. Oei is a scholar working on Molecular Biology, Epidemiology and Physiology. According to data from OpenAlex, T. L. Oei has authored 40 papers receiving a total of 436 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 16 papers in Epidemiology and 7 papers in Physiology. Recurrent topics in T. L. Oei's work include Biochemical and Molecular Research (27 papers), Cytomegalovirus and herpesvirus research (15 papers) and Adenosine and Purinergic Signaling (7 papers). T. L. Oei is often cited by papers focused on Biochemical and Molecular Research (27 papers), Cytomegalovirus and herpesvirus research (15 papers) and Adenosine and Purinergic Signaling (7 papers). T. L. Oei collaborates with scholars based in Netherlands, France and United States. T. L. Oei's co-authors include C. H. M. M. de Bruyn, P. Hösli, S. Van Creveld, W.C. Hülsmann, Ron A. Wevers, E.M.G. Joosten, R. A. Binkhorst, Coen A. M. van Bennekom, B. G. A. ter Haar and Hans‐Hilger Ropers and has published in prestigious journals such as The Lancet, Analytical Biochemistry and Biochemical and Biophysical Research Communications.

In The Last Decade

T. L. Oei

40 papers receiving 406 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
T. L. Oei Netherlands	12	279	146	68	55	52	40	436
Dorothy A. Gibbs United Kingdom	14	356 1.3×	132 0.9×	70 1.0×	67 1.2×	59 1.1×	30	584
M. J. Danon United States	11	438 1.6×	102 0.7×	35 0.5×	184 3.3×	169 3.3×	21	765
Dag Malm Norway	13	213 0.8×	167 1.1×	31 0.5×	36 0.7×	26 0.5×	28	766
J. Gehler Germany	12	176 0.6×	52 0.4×	21 0.3×	61 1.1×	26 0.5×	30	446
G Bargsten Germany	11	207 0.7×	45 0.3×	13 0.2×	8 0.1×	9 0.2×	19	454
Tatsuhiro Yamanaka Japan	10	334 1.2×	100 0.7×	25 0.4×	32 0.6×	23 0.4×	19	632
Yongdong Zhou United States	12	278 1.0×	95 0.7×	36 0.5×	17 0.3×	13 0.3×	19	518
Leina B. Saito Canada	8	387 1.4×	72 0.5×	68 1.0×	22 0.4×	8 0.2×	9	585
Urszula Lechowicz Poland	11	177 0.6×	41 0.3×	24 0.4×	10 0.2×	29 0.6×	33	369
Angela Robbiano Italy	9	265 0.9×	51 0.3×	49 0.7×	37 0.7×	60 1.2×	10	629

Countries citing papers authored by T. L. Oei

Since Specialization

Citations

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

Fields of papers citing papers by T. L. Oei

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. L. Oei

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

Brunner, Han G., et al.. (1988). The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK. Human Genetics. 80(4). 337–340. 50 indexed citations

Wevers, Ron A., et al.. (1988). Myoadenylate deaminase deficiency: A clinical, genetic, and biochemical study in nine families. Muscle & Nerve. 11(4). 312–317. 23 indexed citations

Binkhorst, R. A., et al.. (1987). AMP deaminase deficiency: Study of the human skeletal muscle purine metabolism during ischaemic isometric exercise. Clinical Science. 72(4). 475–482. 22 indexed citations

Daanen, H.A.M., et al.. (1985). The relation between blood lactate and ammonia in ischemic handgrip exercise. Muscle & Nerve. 8(6). 523–527. 27 indexed citations

Joosten, E.M.G., Coen A. M. van Bennekom, Frank Oerlemans, et al.. (1984). Myoadenylate Deaminase Deficiency: An Enzyme Defect in Search of a Disease. Advances in experimental medicine and biology. 165 Pt A. 85–89. 6 indexed citations

Wevers, Ron A., et al.. (1984). Clinical chemistry and the diagnosis of muscular disease; the ischemic forearm excercise test. Clinical Neurology and Neurosurgery. 86(3). 225–225. 1 indexed citations

Bruyn, C. H. M. M. de, et al.. (1978). Characterisation of Purine Nucleoside Phosphorylase from Fibroblasts Using Ultra-Microchemical Methods. Human Heredity. 28(2). 151–160. 9 indexed citations

Bruyn, C. H. M. M. de, et al.. (1978). A new ultramicrochemical assay for purine nucleoside phosphorylase. Analytical Biochemistry. 84(1). 147–153. 11 indexed citations

Bruyn, C. H. M. M. de, et al.. (1978). Fluctuating adenosine deaminase activities in cultured fibroblasts. Biochemical Medicine. 20(1). 54–62. 7 indexed citations

10.

Bruyn, C. H. M. M. de, et al.. (1977). Ultramicrochemical Studies on Enzyme Kinetics. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 76A. 597–604. 5 indexed citations

11.

Bruyn, C. H. M. M. de, et al.. (1977). Enzymes of galactose metabolism in human hair roots. British Journal of Dermatology. 97(5). 487–495. 5 indexed citations

12.

Bruyn, C. H. M. M. de & T. L. Oei. (1977). Purine Phosphoribosyl Transferases in Human Erythrocyte Ghosts. PubMed. 76A. 139–152. 3 indexed citations

13.

Bruyn, C. H. M. M. de & T. L. Oei. (1977). Incorporation of Purine Bases by Intact Red Blood Cells. Advances in experimental medicine and biology. 76B. 139–150. 11 indexed citations

14.

Oei, T. L., et al.. (1976). Metabolic cooperation studied by a quantitative enzyme assay of single cells. Biochemical and Biophysical Research Communications. 71(2). 574–578. 6 indexed citations

15.

Bruyn, C. H. M. M. de & T. L. Oei. (1974). Purine Metabolism in Intact Erythrocytes from Controls and HG-PRT Deficient Individuals. Advances in experimental medicine and biology. 41. 223–227. 11 indexed citations

16.

Bruyn, C. H. M. M. de & T. L. Oei. (1974). Purine Phosphoribosyl Transferases in Human Hair Roots. Dermatology. 149(2). 101–109. 1 indexed citations

17.

Geerdink, R. A., Wytske de Vries, J. Willemse, T. L. Oei, & C. H. M. M. de Bruyn. (1973). An atypical case of hypoxanthine‐guanine phosphoribosyltransferase deficiency (Lesch‐Nyhan syndrome). Clinical Genetics. 4(4). 348–352. 14 indexed citations

18.

Oei, T. L.. (1962). Hexose monophosphate, pyruvate and lactate In the peripheral blood in glycogen-storage disease Type I. Clinica Chimica Acta. 7(2). 193–198. 13 indexed citations

19.

Oei, T. L.. (1961). A GENETIC INVESTIGATION ARISING FROM TWO CASES OF FAVISM. Human Heredity. 11(3). 205–216. 1 indexed citations

20.

Hülsmann, W.C., T. L. Oei, & S. Van Creveld. (1961). PHOSPHORYLASE ACTIVITY IN LEUCOCYTES FROM PATIENTS WITH GLYCOGEN-STORAGE DISEASE. The Lancet. 278(7202). 581–583. 47 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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