Merete Bugge

1.8k total citations · 1 hit paper
15 papers, 1.2k citations indexed

About

Merete Bugge is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Merete Bugge has authored 15 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Merete Bugge's work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Merete Bugge is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Merete Bugge collaborates with scholars based in Denmark, Germany and Greece. Merete Bugge's co-authors include Niels Tommerup, Déborah Bourc’his, E. Viégas-Pèquignot, Chih-Lin Hsieh, Maj Hultén, Xiaoyan Qu, Guoliang Xu, James J. Russo, Timothy H. Bestor and E. Niebuhr and has published in prestigious journals such as Nature, Human Mutation and Human Genetics.

In The Last Decade

Merete Bugge

15 papers receiving 1.1k 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.

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

1999 884 citations Guoliang Xu, Timothy H. Bestor et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Merete Bugge Denmark	10	935	584	146	107	71	15	1.2k
Jacques C. Giltay Netherlands	23	665 0.7×	760 1.3×	306 2.1×	130 1.2×	38 0.5×	65	1.3k
Vanna Pecile Italy	17	443 0.5×	499 0.9×	175 1.2×	112 1.0×	50 0.7×	54	825
Sung‐Hae Kang United States	20	737 0.8×	925 1.6×	348 2.4×	180 1.7×	81 1.1×	30	1.4k
Kosuke Izumi United States	19	606 0.6×	635 1.1×	185 1.3×	126 1.2×	58 0.8×	77	1.1k
Shila Mekhoubad United States	5	1.2k 1.3×	356 0.6×	147 1.0×	71 0.7×	80 1.1×	5	1.3k
Alina T. Midro Poland	16	436 0.5×	575 1.0×	244 1.7×	192 1.8×	114 1.6×	74	943
Andreas Dufke Germany	22	695 0.7×	865 1.5×	351 2.4×	310 2.9×	50 0.7×	60	1.4k
Ghazala Mirza United Kingdom	18	552 0.6×	714 1.2×	120 0.8×	116 1.1×	182 2.6×	20	1.1k
E. Boyd United Kingdom	22	623 0.7×	804 1.4×	233 1.6×	304 2.8×	65 0.9×	55	1.3k
Marie‐France Portnoï France	19	446 0.5×	574 1.0×	166 1.1×	119 1.1×	22 0.3×	29	908

Countries citing papers authored by Merete Bugge

Since Specialization

Citations

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

Fields of papers citing papers by Merete Bugge

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Merete Bugge

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

All Works

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15 of 15 papers shown

Gilling, Mette, Allan Lind-Thomsen, Yuan Mang, et al.. (2011). Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation. European Journal of Medical Genetics. 54(4). e383–e388. 7 indexed citations

Jakobsen, Linda P., Merete Bugge, Reinhard Ullmann, et al.. (2011). 500K SNP array analyses in blood and saliva showed no differences in a pair of monozygotic twins discordant for cleft lip. American Journal of Medical Genetics Part A. 155(3). 652–655. 7 indexed citations

Kalscheuer, Vera M., David Fitzpatrick, Niels Tommerup, et al.. (2007). Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation. Human Genetics. 121(3-4). 501–509. 88 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

Jakobsen, Linda P., Mary A. Knudsen, James Lespinasse, et al.. (2005). The Genetic Basis of the Pierre Robin Sequence. The Cleft Palate-Craniofacial Journal. 5 indexed citations

Bugge, Merete, C.D. DeLozier-Blanchet, Mads Bak, et al.. (2004). Trisomy 13 due to rea(13q;13q) is caused by i(13) and not rob(13;13)(q10;q10) in the majority of cases. American Journal of Medical Genetics Part A. 132A(3). 310–313. 21 indexed citations

Bugge, Merete, et al.. (2004). DNA studies of mono‐ and pseudodicentric isochromosomes 18q. American Journal of Medical Genetics Part A. 127A(3). 230–233. 5 indexed citations

Kjaer, Klaus, et al.. (2002). HOXD13 polyalanine tract expansion in classical synpolydactyly type Vordingborg. American Journal of Medical Genetics. 110(2). 116–121. 22 indexed citations

Kirchhoff, Maria, Hanne Rose, Jan Maahr, et al.. (2000). High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes. European Journal of Human Genetics. 8(9). 661–668. 38 indexed citations

10.

Silahtaroglu, Asli, Frans A. Hol, Martin Erdel, et al.. (1999). Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome. European Journal of Human Genetics. 7(1). 68–76. 16 indexed citations

11.

Xu, Guoliang, Timothy H. Bestor, Déborah Bourc’his, et al.. (1999). Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. Nature. 402(6758). 187–191. 884 indexed citations breakdown →

12.

Bartsch, Oliver, Georg Klaus Hinkel, Merete Bugge, et al.. (1997). A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region. Human Genetics. 100(5-6). 669–675. 19 indexed citations

13.

Gravholt, Claus Højbjerg, et al.. (1997). A patient with Edwards syndrome caused by a rare pseudodicentric chromosome 18 of paternal origin. Clinical Genetics. 52(1). 56–60. 8 indexed citations

14.

Bugge, Merete, Elisabeth Blennow, Michael B. Petersen, et al.. (1996). Tetrasomy 18p de novo: Parental Origin and Different Mechanisms of Formation. European Journal of Human Genetics. 4(3). 160–167. 33 indexed citations

15.

Tromp, Gerard, et al.. (1996). Direct sequencing of PCR products derived from cDNAs for the proα1 and proα2 chains of type I procollagen as a screening method to detect mutations in patients with osteogenesis imperfecta. Human Mutation. 7(2). 89–99. 10 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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