G Bruns

1.3k total citations
27 papers, 1.1k citations indexed

About

G Bruns is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, G Bruns has authored 27 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Neurology. Recurrent topics in G Bruns's work include RNA modifications and cancer (4 papers), RNA and protein synthesis mechanisms (4 papers) and RNA Research and Splicing (4 papers). G Bruns is often cited by papers focused on RNA modifications and cancer (4 papers), RNA and protein synthesis mechanisms (4 papers) and RNA Research and Splicing (4 papers). G Bruns collaborates with scholars based in United States, Japan and United Kingdom. G Bruns's co-authors include Irving M. London, S.A. Latt, N Kanda, Rhona Schreck, Yosef Shiloh, Nicholas C. Dracopoli, Doris Karibian, Tim Donlon, David Baltimore and Frederick W. Alt and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Neuron.

In The Last Decade

G Bruns

27 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G Bruns United States	17	743	220	186	139	103	27	1.1k
Antony E. Shrimpton United States	21	842 1.1×	531 2.4×	334 1.8×	84 0.6×	230 2.2×	51	2.0k
Thomas F. Wienker Germany	20	658 0.9×	382 1.7×	105 0.6×	58 0.4×	139 1.3×	59	1.3k
J D Gearhart United States	25	1.1k 1.5×	586 2.7×	160 0.9×	96 0.7×	354 3.4×	35	2.0k
Connie E. Gee United States	9	865 1.2×	280 1.3×	121 0.7×	470 3.4×	77 0.7×	11	1.4k
H Kikuchi Japan	18	527 0.7×	177 0.8×	74 0.4×	96 0.7×	47 0.5×	41	1.2k
H F Willard United States	22	1.2k 1.6×	804 3.7×	112 0.6×	60 0.4×	130 1.3×	28	1.8k
Michał Milewski Poland	12	605 0.8×	108 0.5×	253 1.4×	79 0.6×	93 0.9×	34	1.1k
Keiko Nakanishi Japan	17	583 0.8×	92 0.4×	82 0.4×	87 0.6×	56 0.5×	30	989
Carole Doré Canada	14	792 1.1×	165 0.8×	118 0.6×	51 0.4×	152 1.5×	23	1.3k
Ning‐Ai Liu United States	19	588 0.8×	147 0.7×	417 2.2×	53 0.4×	61 0.6×	29	1.2k

Countries citing papers authored by G Bruns

Since Specialization

Citations

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

Fields of papers citing papers by G Bruns

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G Bruns

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

Klamt, Barbara, Denis Le Paslier, Ilya Chumakov, et al.. (1995). An Integrated YAC Clone Contig for the WAGR Region on Human Chromosome 11p13–p14.1. Genomics. 30(1). 37–45. 5 indexed citations

Gessler, Manfred, Anna‐Katharina König, Karen C. Arden, et al.. (1994). Infrequent mutation of theWT1 gene in 77 Wilms' tumors. Human Mutation. 3(3). 212–222. 86 indexed citations

Dracopoli, Nicholas C. & G Bruns. (1994). Report of the First International Workshop on Human Chromosome 1 Mapping 1994. Cytogenetic and Genome Research. 67(3). 143–174. 35 indexed citations

Miwa, T., Kiyoshi Kurokawa, Shinji Kamada, et al.. (1991). Structure, chromosome location, and expression of the human smooth muscle (enteric type) gamma-actin gene: evolution of six human actin genes.. Molecular and Cellular Biology. 11(6). 3296–3306. 96 indexed citations

Miwa, Takeshi, Kiyoshi Kurokawa, Shinji Kamada, et al.. (1991). Structure, Chromosome Location, and Expression of the Human Smooth Muscle (Enteric Type) γ-Actin Gene: Evolution of Six Human Actin Genes. Molecular and Cellular Biology. 11(6). 3296–3306. 19 indexed citations

Ueyama, Hisao, G Bruns, & Naotoshi Kanda. (1990). Assignment of the vascular smooth muscle actin geneACTSA to human chromosome 10. The Japanese Journal of Human Genetics. 35(2). 145–150. 14 indexed citations

Sims, Katherine B., Albert de la Chapelle, Reijo Norio, et al.. (1989). Monoamine oxidase deficiency in males with an X chromosome deletion. Neuron. 2(1). 1069–1076. 90 indexed citations

Kwan, Sau‐Ping, L. A. Sandkuyl, Michael Blaese, et al.. (1988). Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers. Genomics. 3(1). 39–43. 45 indexed citations

Ozelius, Laurie J., Yun‐Pung P. Hsu, G Bruns, et al.. (1988). Human monoamine oxidase gene (MAOA): Chromosome position (Xp21-p11) and DNA polymorphism. Genomics. 3(1). 53–58. 85 indexed citations

10.

Matsuoka, Rumiko, Misa Kimura, Naotoshi Kanda, et al.. (1988). Molecular cloning and chromosomal localization of a gene coding for human cardiac myosin heavy‐chain. American Journal of Medical Genetics. 29(2). 369–376. 19 indexed citations

11.

Müller, U., Timothy A. Donlon, Peter C. Harris, et al.. (1987). Highly polymorphic DNA sequences in the distal region of the long arm of human chromosome 18. Cytogenetic and Genome Research. 45(1). 16–20. 16 indexed citations

12.

Shiloh, Yosef, Tim Donlon, G Bruns, Martin L. Breitman, & Lap‐Chee Tsui. (1986). Assignment of the human ?-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33?36. Human Genetics. 73(1). 17–19. 48 indexed citations

13.

Latt, S.A., Yosef Shiloh, G M Brodeur, et al.. (1986). Novel DNA rearrangement phenomena associated with DNA amplification in human neuroblastomas and neuroblastoma cell lines.. PubMed. 209A. 601–12. 2 indexed citations

14.

Bruns, G, Paula Kavathas, Yosef Shiloh, et al.. (1985). The human T cell antigen Leu-2 (T8) is encoded on chromosome 2. Human Genetics. 70(4). 311–314. 9 indexed citations

15.

Latt, S.A., David M. Kurnit, G Bruns, et al.. (1984). Molecular genetic approaches to human diseases involving mental retardation.. PubMed. 88(5). 561–71. 2 indexed citations

16.

Kanda, N, Rhona Schreck, Frederick W. Alt, et al.. (1983). Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomes.. Proceedings of the National Academy of Sciences. 80(13). 4069–4073. 104 indexed citations

17.

Kunkel, Louis M., Umadevi Tantravahi, David M. Kurnit, et al.. (1983). Identification and isolation of transcribed human X chromosome DNA sequences. Nucleic Acids Research. 11(22). 7961–7979. 40 indexed citations

18.

Benn, Peter, et al.. (1977). Assignment of the genes for human β-glucuronidase and mitochondrial malate dehydrogenase to the region pter→q22 of chromosome 7. Cytogenetic and Genome Research. 19(5). 273–280. 5 indexed citations

19.

Bruns, G, Siegmund Fischer, & Bertram A. Lowy. (1965). A study of the synthesis and interrelationships of ribonucleic acids in duck erythrocytes. Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis. 95(2). 280–290. 16 indexed citations

20.

London, Irving M., G Bruns, & Doris Karibian. (1964). THE REGULATION OF HEMOGLOBIN SYNTHESIS AND THE PATHOGENESIS OF SOME HYPOCHROMIC ANEMIAS. Medicine. 43(6). 789–802. 54 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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