Author

Lukrecija Brečević

Observed names: Brecevic Lukrecija, Brecevic, Lukrecija, L Brecevic, L Brecević, L Brečević, L. Brecevic, LUKRECIJA BRECEVIC, Lukrecija Brecevic

Institutions: University of Zagreb, Hrvatski institut za istraživanje mozga

Observed institutions: University Hospital Centre Zagreb, National Academy of Sciences of Belarus, University of Rijeka, Vilnius University, University of Zagreb, Friedrich-Alexander-Universität Erlangen-Nürnberg, University of Zurich, Research Centre for Medical Genetics, Hrvatski institut za istraživanje mozga, Istanbul University, Friedrich Schiller University Jena

OpenAlex ID: A5112213074

Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes

1999 · Benno Röthlisberger, Dieter Kotzot, et al. · European Journal of Human Genetics · 104

Intrachromosomal triplication of 15q11-q13.

1994 · A A Schinzel, L Brecevic, et al. · Journal of Medical Genetics · 100

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22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin

1998 · S Fokstuen, U Arbenz, et al. · Clinical Genetics · 78

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Mosaic supernumerary ring chromosome 1 in a three-generational family: 10-year follow-up report

2010 · G. Kosztolányi, L. Brecevic, et al. · European Journal of Medical Genetics · 73

Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes

1999 · Mariluce Riegel, Claudio Castellan, et al. · American Journal of Medical Genetics · 69

Isochromosome 18p Results from Maternal Meiosis II Nondisjunction

1996 · Dieter Kotzot, Gertrud Bundscherer, et al. · European Journal of Human Genetics · 62

Human Neuroserpin (PI12): cDNA Cloning and Chromosomal Localization to 3q26

1997 · Sabine P. Schrimpf, Andreas J. Bleiker, et al. · Genomics · 57

Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus

1995 · D. Kotzot, F. Bernasconi, et al. · European Journal of Pediatrics · 54

Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

2010 · Thomas Liehr, Tatyana Karamysheva, et al. · Current Genomics · 51

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Subcellular localization of A and B Nm23/NDPK subunits

2004 · Maja Herak Bosnar, Jean de Gunzburg, et al. · Experimental Cell Research · 48

Kabuki (Niikawa‐Kuroki) syndrome associated with immunodeficiency

1998 · Krystyna H Chrzanowska, M. Krajewska‐Walasek, et al. · Clinical Genetics · 47

Trisomy First, Translocation Second, Uniparental Disomy and Partial Trisomy Third: A New Mechanism for Complex Chromosomal Aneuploidy

1997 · Albert Schinzel, Dieter Kotzot, et al. · European Journal of Human Genetics · 44

Interstitial deletion 4q and Rieger syndrome

1981 · Ivo Ligutić, Lukrecija Brečević, et al. · Clinical Genetics · 42

Chromosomal Localization, Genomic Structure and Characterization of the Human Gene and a Retropseudogene for 6‐Pyruvoyltetrahydropterin Synthase

1996 · Claudia Kluge, Lukrecija Brecevic, et al. · European Journal of Biochemistry · 30

Concomitant Amplif ication and Expression of PAX7-FKHR and MYCN in a Human Rhabdomyosarcoma Cell Line Carrying a Cryptic t(1;13)(p36;q14)

2000 · Emanuela Frascella, Elisabetta Lenzini, et al. · Cancer Genetics and Cytogenetics · 23

Multiple congenital anomalies including the Rieger eye malformation in a boy with interstitial deletion of (4) (q25-->q27) secondary to a balanced insertion in his normal father: evidence for haplotype insufficiency causing the Rieger malformation.

1997 · A Schinzel, L Brecevic, et al. · Journal of Medical Genetics · 22

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Human Ring Chromosomes – New Insights for their Clinical Significance

2013 · R.S. Guilherme, E Klein, et al. · Balkan Journal of Medical Genetics · 20

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Comparative genomic hybridization-aided unraveling of complex karyotypes in human hematopoietic neoplasias

2001 · Irmgard Verdorfer, Lukrecija Brecevic, et al. · Cancer Genetics and Cytogenetics · 15

Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines

2006 · L. Brecevic, S. Michel, et al. · Cytogenetic and Genome Research · 14

Delimiting the use of comparative genomic hybridization in human myeloid neoplastic disorders.

2000 · E Gebhart, I Verdorfer, et al. · International Journal of Oncology · 14

Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex

2016 · Martina Rincic, Milan Rados, et al. · Molecular Cytogenetics · 12

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Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma

2015 · Lukrecija Brečević, Martina Rinčić, et al. · Translational Neuroscience · 11

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Duplication of segment 1p21 following paternal insertional translocation, ins(6;1)(q25;p13.3p22.1)

1999 · Algirdas Utkus, Irina Sorokina, et al. · Journal of Medical Genetics · 11

Tandem triplication of chromosome 13q14 with inverted interstitial segment in a 4 year old girl

2000 · LUKRECIJA BRECEVIC, SEHER BASARAN, et al. · Journal of Medical Genetics · 9

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.

1997 · A Schinzel, C P Braegger, et al. · Journal of Medical Genetics · 9

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Works count: 47

Citation count: 1,042

H-index: 17

I10-index: 23