Lukrecija Brečević

1.1k total citations
31 papers, 749 citations indexed

About

Lukrecija Brečević is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Lukrecija Brečević has authored 31 papers receiving a total of 749 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 14 papers in Molecular Biology and 11 papers in Plant Science. Recurrent topics in Lukrecija Brečević's work include Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (11 papers) and Prenatal Screening and Diagnostics (9 papers). Lukrecija Brečević is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (11 papers) and Prenatal Screening and Diagnostics (9 papers). Lukrecija Brečević collaborates with scholars based in Switzerland, Germany and Croatia. Lukrecija Brečević's co-authors include Albert Schinzel, Franz Binkert, Dieter Kotzot, Wendy P. Robinson, Damina Balmer, Fabrizio Dutly, Fosco Bernasconi, Claudio Castellan, Mariluce Riegel and A. Schinzel and has published in prestigious journals such as SHILAP Revista de lepidopterología, European Journal of Biochemistry and Experimental Cell Research.

In The Last Decade

Lukrecija Brečević

30 papers receiving 712 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lukrecija Brečević Switzerland 17 479 361 174 161 64 31 749
Anita S. Kulharya United States 14 452 0.9× 509 1.4× 147 0.8× 106 0.7× 59 0.9× 31 843
Benno Röthlisberger Switzerland 17 462 1.0× 313 0.9× 163 0.9× 92 0.6× 24 0.4× 34 729
Andreas Dufke Germany 22 865 1.8× 695 1.9× 351 2.0× 310 1.9× 37 0.6× 60 1.4k
Merete Bugge Denmark 10 584 1.2× 935 2.6× 146 0.8× 107 0.7× 42 0.7× 15 1.2k
Karen J. Harrison Canada 10 252 0.5× 248 0.7× 88 0.5× 71 0.4× 77 1.2× 17 461
Martine Doco‐Fenzy France 15 302 0.6× 349 1.0× 80 0.5× 70 0.4× 35 0.5× 29 690
Marsha Speevak Canada 17 420 0.9× 302 0.8× 141 0.8× 96 0.6× 29 0.5× 37 636
Kosuke Izumi United States 19 635 1.3× 606 1.7× 185 1.1× 126 0.8× 145 2.3× 77 1.1k
Iosif W. Lurie United States 23 1.1k 2.2× 730 2.0× 590 3.4× 203 1.3× 64 1.0× 72 1.6k
Sandra Chantot‐Bastaraud France 24 939 2.0× 759 2.1× 404 2.3× 152 0.9× 22 0.3× 67 1.4k

Countries citing papers authored by Lukrecija Brečević

Since Specialization
Citations

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

Fields of papers citing papers by Lukrecija Brečević

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lukrecija Brečević

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

All Works

20 of 20 papers shown
1.
Radoš, Milan, Željka Krsnik, Kristina Gotovac, et al.. (2016). Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex. Molecular Cytogenetics. 9(1). 19–19. 10 indexed citations
2.
Guilherme, Roberta Santos, Elisabeth Klein, Ahmed B. Hamid, et al.. (2013). Human Ring Chromosomes – New Insights for their Clinical Significance. SHILAP Revista de lepidopterología. 16(1). 13–19. 16 indexed citations
3.
Kosztolányi, György, et al.. (2010). Mosaic supernumerary ring chromosome 1 in a three-generational family: 10-year follow-up report. European Journal of Medical Genetics. 54(2). 152–156. 16 indexed citations
4.
Liehr, Thomas, Т. В. Карамышева, Lukrecija Brečević, et al.. (2010). Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes. Current Genomics. 11(6). 432–439. 39 indexed citations
5.
Wagner, Jasenka, Feodora Stipoljev, Ivana Škrlec, et al.. (2009). Partial monosomy 4q and partial trisomy 13q: phenotype and molecular mapping of the breakpoints. Chromosome Research. 1 indexed citations
6.
Brečević, Lukrecija, S. Michel, Heike Starke, et al.. (2006). Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines. Cytogenetic and Genome Research. 114(3-4). 319–324. 11 indexed citations
7.
Bosnar, Maja Herak, Jean de Gunzburg, Ružica Bago, et al.. (2004). Subcellular localization of A and B Nm23/NDPK subunits. Experimental Cell Research. 298(1). 275–284. 40 indexed citations
8.
Gebhart, E., et al.. (2000). Delimiting the use of comparative genomic hybridization in human myeloid neoplastic disorders.. International Journal of Oncology. 16(6). 1099–105. 13 indexed citations
9.
Frascella, E., Elisabetta Lenzini, Beat W. Schäfer, et al.. (2000). Concomitant Amplif ication and Expression of PAX7-FKHR and MYCN in a Human Rhabdomyosarcoma Cell Line Carrying a Cryptic t(1;13)(p36;q14). Cancer Genetics and Cytogenetics. 121(2). 139–145. 19 indexed citations
10.
Utkus, Algirdas, Vaidutis Kučinskas, Benno Röthlisberger, et al.. (1999). Duplication of segment 1p21 following paternal insertional translocation, ins(6;1)(q25;p13.3p22.1). Journal of Medical Genetics. 36(1). 73–76. 8 indexed citations
11.
Röthlisberger, Benno, Dieter Kotzot, Lukrecija Brečević, et al.. (1999). Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes. European Journal of Human Genetics. 7(8). 873–883. 45 indexed citations
12.
Riegel, Mariluce, Claudio Castellan, Damina Balmer, Lukrecija Brečević, & A. Schinzel. (1999). Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes. American Journal of Medical Genetics. 82(3). 249–253. 48 indexed citations
13.
Chrzańowska, Krystyńa, et al.. (1998). Kabuki (Niikawa‐Kuroki) syndrome associated with immunodeficiency. Clinical Genetics. 53(4). 308–312. 35 indexed citations
14.
Fokstuen, Siv, U Arbenz, Sevilhan Artan, et al.. (1998). 22q11.2 deletions in a series of patients with non‐selective congenital heart defects: incidence, type of defects and parental origin. Clinical Genetics. 53(1). 63–69. 9 indexed citations
15.
Schinzel, Albert, Christian Braegger, Lukrecija Brečević, Fabrizio Dutly, & Franz Binkert. (1997). Interstitial deletion, del(4)(q12q21.1), owing to de novo unbalanced translocation in a 2 year old girl: further evidence that the piebald trait maps to proximal 4q12.. Journal of Medical Genetics. 34(8). 692–695. 8 indexed citations
16.
Schrimpf, Sabine, Lukrecija Brečević, Serguei Kozlov, et al.. (1997). Human Neuroserpin (PI12): cDNA Cloning and Chromosomal Localization to 3q26. Genomics. 40(1). 55–62. 54 indexed citations
17.
Kotzot, Dieter, Lukrecija Brečević, Iosif W. Lurie, et al.. (1996). Isochromosome 18p Results from Maternal Meiosis II Nondisjunction. European Journal of Human Genetics. 4(3). 168–174. 47 indexed citations
18.
Brečević, Lukrecija, et al.. (1996). Chromosomal Localization, Genomic Structure and Characterization of the Human Gene and a Retropseudogene for 6‐Pyruvoyltetrahydropterin Synthase. European Journal of Biochemistry. 240(2). 477–484. 24 indexed citations
19.
Kotzot, Dieter, Fosco Bernasconi, Lukrecija Brečević, et al.. (1995). Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus. European Journal of Pediatrics. 154(6). 477–482. 35 indexed citations
20.
Brečević, Lukrecija, et al.. (1981). Interstitial deletion 4q and Rieger syndrome. Clinical Genetics. 20(5). 323–327. 35 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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