| # | Title | Journal | Year | Citations |
|---|
| 1 | Specific miRNA signatures are associated with metastasis and poor prognosis in clear cell renal cell carcinoma | World Journal of Urology | 2011 | 177 |
| 2 | Cytogenetic contribution to uniparental disomy (UPD) | Molecular Cytogenetics | 2010 | 116 |
| 3 | Transforming Growth Factor-Beta Receptor Type II Mutation in a Patient With Bicuspid Aortic Valve Disease and Intraoperative Aortic Dissection | Annals of Thoracic Surgery | 2011 | 62 |
| 4 | Handling small supernumerary marker chromosomes in prenatal diagnostics | Expert Review of Molecular Diagnostics | 2009 | 49 |
| 5 | Early Embryonic Chromosome Instability Results in Stable Mosaic Pattern in Human Tissues | PLoS ONE | 2010 | 46 |
| 6 | Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes | Current Genomics | 2010 | 44 |
| 7 | The Human Genome Puzzle — the Role of Copy Number Variation in Somatic Mosaicism | Current Genomics | 2010 | 43 |
| 8 | A Specific Gene Expression Signature Characterizes Metastatic Potential in Clear Cell Renal Cell Carcinoma | Journal of Urology | 2011 | 36 |
| 9 | Small supernumerary marker chromosomes and their correlation with specific syndromes | Advanced Biomedical Research | 2015 | 34 |
| 10 | Annexin A5 is involved in migration and invasion of oral carcinoma | Cell Cycle | 2009 | 31 |
| 11 | X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation | Molecular Cytogenetics | 2010 | 24 |
| 12 | First Case of a Neocentromere Formation in an Otherwise Normal Chromosome 7 | Cytogenetic and Genome Research | 2010 | 24 |
| 13 | Centromere activity in dicentric small supernumerary marker chromosomes | Chromosome Research | 2010 | 20 |
| 14 | The use of array-CGH in a cohort of Greek children with developmental delay | Molecular Cytogenetics | 2010 | 20 |
| 15 | Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics | International Journal of Molecular Medicine | 2009 | 19 |
| 16 | New insights into the karyotypic evolution in muroid rodents revealed by multicolor banding applying murine probes | Chromosome Research | 2010 | 19 |
| 17 | Small Supernumerary Marker Chromosomes (sSMCs): A Spotlight on Some Nomenclature Problems | Journal of Histochemistry and Cytochemistry | 2009 | 18 |
| 18 | CD8 Locus Nuclear Dynamics during Thymocyte Development | Journal of Immunology | 2010 | 18 |
| 19 | Inhibition of MAPK-signaling pathway promotes the interaction of the corepressor SMRT with the human androgen receptor and mediates repression of prostate cancer cell growth in the presence of antiandrogens | Journal of Molecular Endocrinology | 2009 | 17 |
| 20 | An unbalanced translocation resulting in a duplication of Xq28 causes a Rett syndrome‐like phenotype in a female patient | Clinical Genetics | 2010 | 17 |
| 21 | Characterization of sSMC by FISH and molecular techniques | European Journal of Medical Genetics | 2011 | 16 |
| 22 | A First Generation Comparative Chromosome Map between Guinea Pig (Cavia porcellus) and Humans | PLoS ONE | 2015 | 14 |
| 23 | A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report | Molecular Cytogenetics | 2009 | 13 |
| 24 | Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances | Journal of Applied Genetics | 2011 | 13 |
| 25 | Molecular Cytogenetic Characterization of the Human Cerebral Microvessel Endothelial Cell Line hCMEC/D3 | Cytogenetic and Genome Research | 2009 | 12 |
| 26 | A Neocentric Isochromosome Yp Present as Additional Small Supernumerary Marker Chromosome – Evidence against U-Type Exchange Mechanism? | Cytogenetic and Genome Research | 2009 | 11 |
| 27 | Regulation of the anaphase-promoting complex by the COP9 signalosome | Cell Cycle | 2009 | 11 |
| 28 | Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy | American Journal of Medical Genetics, Part A | 2009 | 11 |
| 29 | New aspects on chromosomal instability: chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sites | International Journal of Oncology | 2010 | 11 |
| 30 | Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report | Molecular Cytogenetics | 2009 | 10 |
| 31 | Automated detection of residual cells after sex-mismatched stem-cell transplantation – evidence for presence of disease-marker negative residual cells | Molecular Cytogenetics | 2009 | 8 |
| 32 | Duplication 4q associated with chronic cholestatic changes in liver biopsy | European Journal of Medical Genetics | 2010 | 8 |
| 33 | Deletion 2q31.2‐q31.3 in a 4‐year‐old girl with microcephaly and severe mental retardation | American Journal of Medical Genetics, Part A | 2011 | 8 |
| 34 | New aspects on chromosomal instability: Chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sites | International Journal of Oncology | 2009 | 7 |
| 35 | Presence of harmless small supernumerary marker chromosomes hampers molecular genetic diagnosis: a case report | Molecular Medicine Reports | 2010 | 7 |
| 36 | Transforming Growth Factor Beta-2 Mutations in Barlow’s Disease and Aortic Dilatation | Annals of Thoracic Surgery | 2017 | 7 |
| 37 | Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 → qter) detected in an autistic boy | Molecular Cytogenetics | 2009 | 6 |
| 38 | A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3 | Molecular Cytogenetics | 2010 | 6 |
| 39 | Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization | Molecular Medicine Reports | 2010 | 6 |
| 40 | Insertion of the 3′ ABL region into the long arm of chromosome 1 in a Philadelphia chromosome-negative chronic myeloid leukemia case | Oncology Letters | 2010 | 5 |
| 41 | Small Supernumerary Marker Chromosomes 1 With a Normal Phenotype | Journal of the Chinese Medical Association | 2010 | 5 |
| 42 | Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature | Experimental and Therapeutic Medicine | 2014 | 5 |
| 43 | Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia | Cancer Genetics and Cytogenetics | 2010 | 4 |
| 44 | Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation? | Molecular Cytogenetics | 2010 | 4 |
| 45 | A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5 | Blood Cells, Molecules, and Diseases | 2010 | 4 |
| 46 | Complex karyotype defined by molecular cytogenetic FISH and M-FISH in an infant with acute megakaryoblastic leukemia and neurofibromatosis | Cancer Genetics and Cytogenetics | 2010 | 3 |
| 47 | Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature | Birth Defects Research Part A: Clinical and Molecular Teratology | 2014 | 3 |
| 48 | Double-Hit Mutations in Bicuspid Aortic Valve and Blunt Traumatic Acute Aortic Dissection | Annals of Thoracic Surgery | 2021 | 3 |
| 49 | Unusual childhood biphenotypic acute leukemia with a yet unreported t(3;13)(p25.1;q13) | Leukemia Research | 2010 | 2 |
| 50 | Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case report | Journal of Medical Case Reports | 2010 | 2 |
