G.A.P. Bruns

12.3k citations

108 papers · 9.7k indexed · 3 hit papers · h-index 50

Molecular Biology top 0.5%
- Renal and related cancers 14
- RNA modifications and cancer 8
- Biochemical and Molecular Research 7
- CRISPR and Genetic Engineering 7
- Ubiquitin and proteasome pathways 7
- Genomics and Chromatin Dynamics 7
- Retinal Development and Disorders 7
Hematology top 1%
Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders 8
Physiology top 1%
Immunology top 2%

Co-authors: Stuart H. Orkin Rachael L. Neve Manfred Gessler Webster K. Cavenee Annemarie Poustka David M. Kurnit James F. Gusella Samuel A. Latt
Cited by: Molecular Biology Hematology Genetics
Journals: Cytogenetic and Genome Research (14 papers)Human Genetics (10 papers)Journal of Biological Chemistry (9 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

G.A.P. Bruns

108 papers receiving 9.3k citations

Hit Papers

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Peers

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

The 25 scholars most cited alongside G.A.P. Bruns, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with G.A.P. Bruns Line = papers co-authored together G.A.P. Bruns links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	cDNA Sequence, Genomic Organization, and Evolutionary Conservation of a Novel Gene from the WAGR Region Genomics ·Faina Schwartz,R.E. Eisenman,Joan H.M. Knoll,Manfred Gessler,G.A.P. Bruns	1995	17
2	Assignment of Human Myocyte-Specific Enhancer Binding Factor 2C (hMEF2C) to Human Chromosome 5q14 and Evidence That MEF2C Is Evolutionarily Conserved Genomics ·Dimitri Krainc,Melanie Haas,David C. Ward,Stuart A. Lipton,G.A.P. Bruns,Dana Leifer	1995	1
3	Identification of a simple sequence polymorphism within the mouse locus D12Nyu2 Mammalian Genome ·Lisa M. Guay‐Woodford,G.A.P. Bruns,Peter D’Eustachio	1994	1
4	A WAGR region gene between PAX-6 and FSHB expressed in fetal brain Human Genetics ·Faina Schwartz,Rachael L. Neve,Robert N. Eisenman,Manfred Gessler,G.A.P. Bruns	1994	21
5	(CA) repeat polymorphism in the chromosome 18 encoded dystrophin-like protein Human Molecular Genetics ·Xu-Qing Tang,Elizabeth C. Engle,Richard Rodney Bennett,Gary A. Silverman,Uzma Nazir,G.A.P. Bruns,Louis M. Kunkel	1994	14
6	Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family Genes Chromosomes and Cancer ·Isabelle Henry,J.M.N. Hoovers,F. Barichard,Yusuf U. A,Anne Puech,Fabienne Prieur,Manfred Gessler,G.A.P. Bruns,Marcel M. A. M. Mannens,Claudine Junien	1993	10
7	The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3 Human Molecular Genetics ·Katherine B. Sims,R V Lebo,Gail V. Benson,Christo Shalish,Deborah E. Schuback,Francisco Jos Navarro-Trivi o,G.A.P. Bruns,Ian Craig,Mitchell S. Golbus,Xandra O. Breakefield	1992	33
8	On the structure and chromosome location of the 72- and 92-kDa human type IV collagenase genes Genomics ·Ivan E. Collier,G.A.P. Bruns,Gregory I. Goldberg,Daniela S. Gerhard	1991	56
9	Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase Experimental Eye Research ·裕美行田,G.A.P. Bruns,Eliot L. Berson,Thaddeus P. Dryja	1991	18
10	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 ·Mary C. Dinauer,Eric A. Pierce,G.A.P. Bruns,J T Curnutte,Stuart H. Orkin	1990	254
11	DXS26 (HU16) is located in Xq21.1 Human Genetics ·Eeva‐Marja Sankila,G.A.P. Bruns,Marianne Schwartz,Eeva Nikoskelainen,E. Niebuhr,Shirley V. Hodgson,Alan F. Wright,Albert de la Chapelle	1990	9
12	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 ·K Sastry,Geneviève Herman,L. E. Day,Shaobo Pan,G.A.P. Bruns,Cynthia C. Morton,R. Alan B. Ezekowitz	1989	214
13	A physical map around the WAGR complex on the short arm of chromosome 11 Genomics ·Manfred Gessler,G.A.P. Bruns	1989	47
14	Human corticotropin releasing hormone gene is located on the long arm of chromosome 8 Cytogenetic and Genome Research ·Jack L. Arbiser,朝何汝,G.A.P. Bruns,Joseph A. Majzoub	1988	53
15	Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p Human Genetics ·Peter C. Harris,Marc Lalande,Helene Stroh,G.A.P. Bruns,Alan Flint,Samuel A. Latt	1987	27
16	Owl monkey gene mapping: the assignment of gene loci for catalase, β-globin gene cluster, HRAS1, insulin, and parathyroid hormone Cytogenetic and Genome Research ·N.S.F. Ma,Daniela S. Gerhard,David E. Housman,Stuart H. Orkin,G.A.P. Bruns	1986	7
17	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 ·Peter J. van den Elsen,G.A.P. Bruns,Daniela S. Gerhard,Dimitrina D. Pravtcheva,C. Jones,David E. Housman,AlessandroCapucci,Stuart H. Orkin,Cox Terhorst	1985	56
18	T cell receptor alpha chain genes are located on chromosome 14 at 14q11-14q12 in humans. The Journal of Experimental Medicine ·A. Veretennikov,G.A.P. Bruns,Ilan R. Kirsch,Gregory Hollis,Virginia Bertness,Tak W. Mak	1985	57
19	Recent evolution of DNA sequence homology in the pericentromeric regions of human acrocentric chromosomes Cytogenetic and Genome Research ·David M. Kurnit,Rachael L. Neve,朝何汝,G.A.P. Bruns,隆行芦辺,David R. Cox,H.P. Klinger	1984	25
20	The erythroid cells and haemoglobins of the chick embryo Philosophical transactions of the Royal Society of London. Series B, Biological sciences ·G.A.P. Bruns,Vernon M. Ingram	1973	182

About G.A.P. Bruns

G.A.P. Bruns is a scholar working on Molecular Biology, Genetics and Ophthalmology, having authored 108 papers that have together received 9.7k indexed citations. Recurring topics across this work include Renal and related cancers (14 papers), RNA modifications and cancer (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Biochemical and Molecular Research (7 papers), CRISPR and Genetic Engineering (7 papers), Ubiquitin and proteasome pathways (7 papers), Genomics and Chromatin Dynamics (7 papers) and Retinal Development and Disorders (7 papers). The work is most often cited by research in Molecular Biology (6.0k citations), Hematology (812 citations) and Genetics (1.9k citations). G.A.P. Bruns has collaborated with scholars based in United States, United Kingdom and Canada. Frequent 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. Their work appears in journals such as Cytogenetic and Genome Research, Human Genetics, Journal of Biological Chemistry, Proceedings of the National Academy of Sciences and Genomics.

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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