G. Bruun‐Petersen

1.1k total citations
25 papers, 477 citations indexed

About

G. Bruun‐Petersen is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, G. Bruun‐Petersen has authored 25 papers receiving a total of 477 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Pediatrics, Perinatology and Child Health and 5 papers in Molecular Biology. Recurrent topics in G. Bruun‐Petersen's work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). G. Bruun‐Petersen is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). G. Bruun‐Petersen collaborates with scholars based in Denmark, United Kingdom and Poland. G. Bruun‐Petersen's co-authors include D. G. Crüger, L.U. Lamm, Jan Hansen, Inge Agerholm, Jens Fedder, Steen Kølvraa, John R. Østergaard, Tom Kristensen, F Hald and Bente Skovsby Toft and has published in prestigious journals such as Human Molecular Genetics, European Respiratory Journal and Human Reproduction.

In The Last Decade

G. Bruun‐Petersen

23 papers receiving 433 citations

Peers

G. Bruun‐Petersen

GENET

PPCH

PHEOH

Elsa Reich United States

J G Lesko United States

Daniela Bettio Italy

Paolo Guanciali‐Franchi Italy

Jürgen Föll Germany

B. Rafael Elejalde United States

Ernest Lieber United States

Jos Dreesen Netherlands

Marie‐France Portnoï France

Paolo Guanciali Franchi Italy

Elsa Reich United States

G. Bruun‐Petersen

328 ×1.4

GENET

301 ×1.9

95 ×0.7

PPCH

51 ×0.6

PHEOH

65 ×0.8

Citations per year, relative to G. Bruun‐Petersen G. Bruun‐Petersen (= 1×) peers Elsa Reich

Countries citing papers authored by G. Bruun‐Petersen

Since Specialization

Citations

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

Fields of papers citing papers by G. Bruun‐Petersen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Bruun‐Petersen

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

Li, Jian, Kai Wang, Jan Lindebjerg, et al.. (2011). Identification of chromosome aberrations in sporadic microsatellite stable and unstable colorectal cancers using array comparative genomic hybridization. Cancer Genetics. 204(2). 84–95. 16 indexed citations

Ryman, Nils, G. Beckman, G. Bruun‐Petersen, & Christina Reuterwall. (2009). Variability of red cell enzymes and genetic implications of management policies in Scandinavian moose (Alces alces). Hereditas. 85(2). 157–162. 10 indexed citations

Østergaard, John R., G. Bruun‐Petersen, & Bent Ø. Kristensen. (2009). The C3-F gene in patients with intracranial saccular aneurysms. Acta Neurologica Scandinavica. 74(5). 356–359. 2 indexed citations

Agerholm, Inge, et al.. (2008). Resumption of mitosis in frozen–thawed embryos is not related to the chromosomal constitution. Fertility and Sterility. 90(5). 1649–1655. 7 indexed citations

Agerholm, Inge, Christina Hnida, D. G. Crüger, et al.. (2008). Nuclei size in relation to nuclear status and aneuploidy rate for 13 chromosomes in donated four cells embryos. Journal of Assisted Reproduction and Genetics. 25(2-3). 95–102. 24 indexed citations

Bugge, Merete, Andrew Collins, Jens Michael Hertz, et al.. (2007). Non-disjunction of chromosome 13. Human Molecular Genetics. 16(16). 2004–2010. 43 indexed citations

Bache, Iben, Mads F. Hjorth, Merete Bugge, et al.. (2006). Systematic re-examination of carriers of balanced reciprocal translocations: a strategy to search for candidate regions for common and complex diseases. European Journal of Human Genetics. 14(4). 410–417. 19 indexed citations

Jensen, Lars Henrik, et al.. (2006). Laser microdissection and microsatellite analysis of colorectal adenocarcinomas.. PubMed. 26(3A). 2069–74. 11 indexed citations

Crüger, D. G., et al.. (2003). Genetic analysis of males from intracytoplasmic sperm injection couples. Clinical Genetics. 64(3). 198–203. 36 indexed citations

10.

Crüger, D. G., et al.. (2002). Fertility and pregnancy outcome in Danish women with Turner syndrome. Clinical Genetics. 61(1). 35–39. 96 indexed citations

11.

Crüger, D. G., Bente Skovsby Toft, Inge Agerholm, et al.. (2001). Birth of a healthy girl after ICSI with ejaculated spermatozoa from a man with non-mosaic Klinefelter's syndrome: Case report. Human Reproduction. 16(9). 1909–1911. 36 indexed citations

12.

Crüger, D. G., G. Bruun‐Petersen, & Steen Kølvraa. (1997). Quantitative evaluation of fluorescencein situ hybridization (FISH) signals in uncultured coelomic cells. Prenatal Diagnosis. 17(7). 635–642. 6 indexed citations

13.

Crüger, D. G., G. Bruun‐Petersen, & Steen Kølvraa. (1996). EARLY PRENATAL DIAGNOSIS: STANDARD CYTOGENETIC ANALYSIS OF COELOMIC CELLS OBTAINED BY COELOCENTESIS. Prenatal Diagnosis. 16(10). 945–949. 11 indexed citations

14.

Petersen, Michael B., et al.. (1994). Pseudodicentric chromosome 18 diagnosed by chromosome painting and primed in situ labelling (PRINS).. Journal of Medical Genetics. 31(2). 99–102. 11 indexed citations

15.

Bruun‐Petersen, G., et al.. (1992). Alpha 1-antitrypsin alleles in patients with pulmonary emphysema, detected by DNA amplification (PCR) and oligonucleotide probes. European Respiratory Journal. 5(5). 531–537. 8 indexed citations

16.

Birkebæk, Niels, et al.. (1992). Normal karyotype in cultured chorionic villus cells, but mosaicism in amniotic and fetal cells. Prenatal Diagnosis. 12(11). 951–953.

17.

Østergaard, John R., G. Bruun‐Petersen, & L.U. Lamm. (1986). HLA antigens and complement types in patients with intracranial saccular aneurysms. Tissue Antigens. 28(3). 176–181. 27 indexed citations

18.

Pedersen, E. B., L.U. Lamm, M. Madsen, et al.. (1985). Familial Cranial Diabetes Insipidus: A Report of Five Families. Genetic, Diagnostic and Therapeutic Aspects. QJM. 57(224). 883–96. 13 indexed citations

19.

Rittner, Ch., Patricia Tippett, Carolyn M. Giles, et al.. (1984). An International Reference Typing for Ch and Rg Determinants on Rare Human C4 Allotypes¹. Vox Sanguinis. 46(4). 224–234. 13 indexed citations

20.

Friedrich, Ursula, et al.. (1982). Chromosomal Studies of Children with Developmental Language Retardation. Developmental Medicine & Child Neurology. 24(6). 645–652. 17 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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