G.A.P. Bruns

12.3k total citations · 3 hit papers
108 papers, 9.7k citations indexed

About

G.A.P. Bruns is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, G.A.P. Bruns has authored 108 papers receiving a total of 9.7k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Molecular Biology, 29 papers in Genetics and 10 papers in Oncology. Recurrent topics in G.A.P. Bruns's work include Renal and related cancers (14 papers), RNA modifications and cancer (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). G.A.P. Bruns is often cited by papers focused on Renal and related cancers (14 papers), RNA modifications and cancer (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). G.A.P. Bruns collaborates with scholars based in United States, United Kingdom and Canada. G.A.P. Bruns's co-authors include Stuart H. Orkin, Rachael L. Neve, Manfred Gessler, Webster K. Cavenee, Annemarie Poustka, David M. Kurnit, James F. Gusella, Samuel A. Latt, Margaret L. Van Keuren and Paul C. Watkins and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

G.A.P. Bruns

108 papers receiving 9.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Amyloid β Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage Near the Alzheimer Locus

1987 1.3k citations Rudolph E. Tanzi, James F. Gusella et al. Science profile →
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

1990 1.1k citations Manfred Gessler, Webster K. Cavenee et al. profile →
Transposition and amplification of oncogene-related sequences in human neuroblastomas

1983 607 citations G.A.P. Bruns et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G.A.P. Bruns United States	50	6.0k	1.9k	1.7k	1.4k	812	108	9.7k
Roger L. Eddy United States	53	5.7k 0.9×	1.5k 0.8×	1.0k 0.6×	1.6k 1.2×	695 0.9×	129	9.9k
T.B. Shows United States	45	4.8k 0.8×	1.6k 0.8×	1.0k 0.6×	836 0.6×	362 0.4×	145	7.4k
R. Blake Pepinsky United States	56	6.7k 1.1×	1.6k 0.8×	1.0k 0.6×	1.5k 1.1×	380 0.5×	138	11.9k
Susan L. Naylor United States	49	6.9k 1.1×	2.2k 1.2×	1.2k 0.7×	856 0.6×	375 0.5×	148	10.7k
Yoram Groner Israel	58	6.6k 1.1×	1.2k 0.6×	834 0.5×	2.4k 1.8×	1.3k 1.5×	172	11.2k
Nigel K. Spurr United Kingdom	53	5.6k 0.9×	1.9k 1.0×	557 0.3×	878 0.6×	1.2k 1.4×	179	9.8k
L T Williams United States	49	7.2k 1.2×	962 0.5×	863 0.5×	985 0.7×	368 0.5×	65	10.2k
David R. Beier United States	58	7.1k 1.2×	3.4k 1.8×	2.5k 1.5×	2.1k 1.6×	1.0k 1.3×	175	13.7k
N.A. Jenkins United States	44	4.9k 0.8×	1.3k 0.7×	629 0.4×	2.5k 1.8×	511 0.6×	115	9.5k
Alan Buckler United States	36	6.9k 1.1×	1.9k 1.0×	609 0.4×	1.1k 0.8×	392 0.5×	66	10.1k

Countries citing papers authored by G.A.P. Bruns

Since Specialization

Citations

This map shows the geographic impact of G.A.P. 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.A.P. 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.A.P. Bruns more than expected).

Fields of papers citing papers by G.A.P. Bruns

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G.A.P. Bruns

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Schwartz, Faina, R.E. Eisenman, Joan H.M. Knoll, Manfred Gessler, & G.A.P. Bruns. (1995). cDNA Sequence, Genomic Organization, and Evolutionary Conservation of a Novel Gene from the WAGR Region. Genomics. 29(2). 526–532. 17 indexed citations

Krainc, Dimitri, Melanie Haas, David C. Ward, et al.. (1995). Assignment of Human Myocyte-Specific Enhancer Binding Factor 2C (hMEF2C) to Human Chromosome 5q14 and Evidence That MEF2C Is Evolutionarily Conserved. Genomics. 29(3). 809–811. 1 indexed citations

Guay‐Woodford, Lisa M., G.A.P. Bruns, & Peter D’Eustachio. (1994). Identification of a simple sequence polymorphism within the mouse locus D12Nyu2. Mammalian Genome. 5(4). 251–252. 1 indexed citations

Henry, Isabelle, J.M.N. Hoovers, F. Barichard, et al.. (1993). Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family. Genes Chromosomes and Cancer. 7(1). 57–62. 10 indexed citations

Dorfman, David M., David B. Wilson, G.A.P. Bruns, & Stuart H. Orkin. (1992). Human transcription factor GATA-2. Evidence for regulation of preproendothelin-1 gene expression in endothelial cells.. Journal of Biological Chemistry. 267(2). 1279–1285. 263 indexed citations

Dinauer, Mary C., Eric A. Pierce, G.A.P. Bruns, J T Curnutte, & Stuart H. Orkin. (1990). Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.. Journal of Clinical Investigation. 86(5). 1729–1737. 254 indexed citations

Fontaine, Bertrand, Tejvir S. Khurana, Eric P. Hoffman, et al.. (1990). Hyperkalemic Periodic Paralysis and the Adult Muscle Sodium Channel α-Subunit Gene. Science. 250(4983). 1000–1002. 238 indexed citations

Sastry, K, Geneviève Herman, L. E. Day, et al.. (1989). The human mannose-binding protein gene. Exon structure reveals its evolutionary relationship to a human pulmonary surfactant gene and localization to chromosome 10.. The Journal of Experimental Medicine. 170(4). 1175–1189. 214 indexed citations

Gessler, Manfred & G.A.P. Bruns. (1989). A physical map around the WAGR complex on the short arm of chromosome 11. Genomics. 5(1). 43–55. 47 indexed citations

10.

Arbiser, Jack L., et al.. (1988). Human corticotropin releasing hormone gene is located on the long arm of chromosome 8. Cytogenetic and Genome Research. 47(3). 113–116. 53 indexed citations

11.

Tanzi, Rudolph E., James F. Gusella, Paul C. Watkins, et al.. (1987). Amyloid β Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage Near the Alzheimer Locus. Science. 235(4791). 880–884. 1257 indexed citations breakdown →

12.

Gold, Daniel P., Jacques J. M. van Dongen, Cynthia C. Morton, et al.. (1987). The gene encoding the epsilon subunit of the T3/T-cell receptor complex maps to chromosome 11 in humans and to chromosome 9 in mice.. Proceedings of the National Academy of Sciences. 84(6). 1664–1668. 53 indexed citations

13.

Goldberger, Gabriel, G.A.P. Bruns, M Rits, Michael D. Edge, & D J Kwiatkowski. (1987). Human complement factor I: analysis of cDNA-derived primary structure and assignment of its gene to chromosome 4.. Journal of Biological Chemistry. 262(21). 10065–10071. 97 indexed citations

14.

Ma, N.S.F., Daniela S. Gerhard, David E. Housman, Stuart H. Orkin, & G.A.P. Bruns. (1986). Owl monkey gene mapping: the assignment of gene loci for catalase, β-globin gene cluster, HRAS1, insulin, and parathyroid hormone. Cytogenetic and Genome Research. 43(1-2). 57–68. 7 indexed citations

15.

Litt, M., G.A.P. Bruns, Robert R. Sheehy, & R.E. Magenis. (1986). A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37.. PubMed. 38(3). 288–96. 9 indexed citations

16.

Davis, Alvin E., Alexander S. Whitehead, R. A. Harrison, et al.. (1986). Human inhibitor of the first component of complement, C1: characterization of cDNA clones and localization of the gene to chromosome 11.. Proceedings of the National Academy of Sciences. 83(10). 3161–3165. 87 indexed citations

17.

Elsen, Peter J. van den, G.A.P. Bruns, Daniela S. Gerhard, et al.. (1985). Assignment of the gene coding for the T3-delta subunit of the T3-T-cell receptor complex to the long arm of human chromosome 11 and to mouse chromosome 9.. Proceedings of the National Academy of Sciences. 82(9). 2920–2924. 56 indexed citations

18.

Kurnit, David M., et al.. (1984). Recent evolution of DNA sequence homology in the pericentromeric regions of human acrocentric chromosomes. Cytogenetic and Genome Research. 38(2). 99–105. 25 indexed citations

19.

Dryja, Thaddeus P., Webster K. Cavenee, R. White, et al.. (1984). Homozygosity of Chromosome 13 in Retinoblastoma. New England Journal of Medicine. 310(9). 550–553. 207 indexed citations

20.

Caccia, Nicolette, Mitchell Kronenberg, Debra Saxe, et al.. (1984). The T cell receptor β chain genes are located on chromosome 6 in mice and chromosome 7 in humans. Cell. 37(3). 1091–1099. 177 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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