R.S. Kandt

861 total citations
12 papers, 571 citations indexed

About

R.S. Kandt is a scholar working on Physiology, Molecular Biology and Oncology. According to data from OpenAlex, R.S. Kandt has authored 12 papers receiving a total of 571 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Physiology, 4 papers in Molecular Biology and 4 papers in Oncology. Recurrent topics in R.S. Kandt's work include Tuberous Sclerosis Complex Research (6 papers), Polyomavirus and related diseases (4 papers) and RNA modifications and cancer (2 papers). R.S. Kandt is often cited by papers focused on Tuberous Sclerosis Complex Research (6 papers), Polyomavirus and related diseases (4 papers) and RNA modifications and cancer (2 papers). R.S. Kandt collaborates with scholars based in United States and New Zealand. R.S. Kandt's co-authors include Allen D. Roses, R. J. M. Gardner, Jonathan L. Haines, M. Smith, Pamela Flodman, Marcy C. Speer, M. Priscilla Short, S. A. Wall, Ann Jewell and J L Weber and has published in prestigious journals such as The Lancet, Nature Genetics and Neurology.

In The Last Decade

R.S. Kandt

10 papers receiving 548 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R.S. Kandt United States	10	289	195	107	95	84	12	571
Julita Borkowska Poland	15	558 1.9×	293 1.5×	160 1.5×	56 0.6×	193 2.3×	36	845
Ksenia Orlova United States	10	342 1.2×	410 2.1×	212 2.0×	29 0.3×	94 1.1×	21	777
L Iselius Sweden	7	130 0.4×	189 1.0×	83 0.8×	84 0.9×	96 1.1×	11	711
Rick van Minkelen Netherlands	20	222 0.8×	292 1.5×	150 1.4×	472 5.0×	45 0.5×	36	878
Tadeusz Mazurczak Poland	17	106 0.4×	299 1.5×	444 4.1×	29 0.3×	70 0.8×	57	763
Irene Szijan Argentina	15	69 0.2×	410 2.1×	111 1.0×	65 0.7×	112 1.3×	59	749
Graeme R. Clark United Kingdom	12	112 0.4×	367 1.9×	181 1.7×	233 2.5×	72 0.9×	19	815
Georg Dorfmüller France	11	139 0.5×	180 0.9×	209 2.0×	69 0.7×	40 0.5×	16	563
Zuo Luan China	15	103 0.4×	192 1.0×	33 0.3×	38 0.4×	30 0.4×	55	598
Wolf-Rüdiger Schäbitz Germany	4	69 0.2×	186 1.0×	29 0.3×	131 1.4×	40 0.5×	5	717

Countries citing papers authored by R.S. Kandt

Since Specialization

Citations

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

Fields of papers citing papers by R.S. Kandt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R.S. Kandt. 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 R.S. Kandt. The network helps show where R.S. Kandt may publish in the future.

Co-authorship network of co-authors of R.S. Kandt

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

All Works

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12 of 12 papers shown

1.

Gilbert, John R., Arun Kumar, Chantelle M. Wolpert, et al.. (1998). Mutation and polymorphism analysis in the tuberous sclerosis 2 ( TSC2 ) gene. Neurogenetics. 1(4). 267–272. 13 indexed citations

2.

Kumar, Arun, et al.. (1997). A novel splice site mutation (156 + 1G→A) in theTSC2 gene. Human Mutation. 9(1). 64–65. 9 indexed citations

3.

Kumar, Arun, et al.. (1995). Mutation analysis of the TSC2 gene in an African-American family. Human Molecular Genetics. 4(12). 2295–2298. 25 indexed citations

4.

Kumar, Anoop, et al.. (1995). A de novo frame-shift mutation in the tuberin gene. Human Molecular Genetics. 4(8). 1471–1472. 30 indexed citations

5.

Kandt, R.S., Jonathan L. Haines, M. Smith, et al.. (1992). Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease. Nature Genetics. 2(1). 37–41. 248 indexed citations

6.

Kandt, R.S., Jeffery M. Vance, Wu-Yen Hung, et al.. (1991). Linkage Studies in Tuberous Sclerosis. Annals of the New York Academy of Sciences. 615(1). 284–297. 17 indexed citations

7.

Kandt, R.S., Jeffery M. Vance, Wu-Yen Hung, et al.. (1989). Absence of linkage of ABO blood group locus to familial tuberous sclerosis. Experimental Neurology. 104(3). 223–228. 19 indexed citations

8.

Siddique, Teepu, Margaret A. Pericak‐Vance, Larry H. Yamaoka, et al.. (1988). Update on the molecular genetics of Duchenne muscular dystrophy.. PubMed. 24 Suppl 1. 9–14.

9.

Bartlett, Richard J., Margaret A. Pericak‐Vance, Jin‐Young Koh, et al.. (1988). Duchenne muscular dystrophy. Neurology. 38(1). 1–1. 170 indexed citations

10.

Koh, James, M. A. Pericak‐Vance, Larry H. Yamaoka, et al.. (1987). INHERITED DELETION AT DUCHENNE DYSTROPHY LOCUS IN NORMAL MALE. The Lancet. 330(8568). 1154–1155. 15 indexed citations

11.

Latack, J T, et al.. (1984). Postoperative regression of opticochiasmatic astrocytoma. Neurosurgery. 15(3). 421–423.

12.

Kandt, R.S., et al.. (1983). Recovery From Probable Central Pontine Myelinolysis Associated With Addison's Disease. Archives of Neurology. 40(2). 118–119. 25 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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