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Peer Reviewed Papers, Books, Chapters

Year Title Citation Authors Review type Summary Keywords File filename File mime type
1. 2011 Opening the archives for state of the art tumour genetic research: sample processing for array-CGH using decalcified, formalin-fixed, paraffin-embedded tissue-derived DNA samples. BMC Res Notes. 2011 Jan 4;4:1.
2. 2011 Analysis of stromal cells in osteofibrous dysplasia and adamantinoma of long bones. Mod Pathol. 2011 Oct 7. doi: 10.1038/modpathol.2011.141. [Epub ahead of print]
3. 2011 Chromosome segregation errors as a cause of DNA damage and structural chromosome aberrations. Science. 2011 Sep 30;333(6051):1895-8.
4. 2011 Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization. Am J Med Genet A. 2011 Sep 21. doi: 10.1002/ajmg.a.34168. [Epub ahead of print]
5. 2011 Oncogenic functions of hMDMX in in vitro transformation of primary human fibroblasts and embryonic retinoblasts. Mol Cancer. 2011 Sep 12;10:111.
6. 2011 Maffucci syndrome: a genome-wide analysis using high resolution single nucleotide polymorphism and expression arrays on four cases. Genes Chromosomes Cancer. 2011 Sep;50(9):673-9. doi: 10.1002/gcc.20889. Epub 2011 May 16.
7. 2011 1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma. Oncogene. 2011 Aug 8. doi: 10.1038/onc.2011.317. [Epub ahead of print]
8. 2011 Familial adenomatous polyposis-associated desmoids display significantly more genetic changes than sporadic desmoids. PLoS One. 2011;6(9):e24354. Epub 2011 Sep 9.
9. 2011 Secondary peripheral chondrosarcoma evolving from osteochondroma as a result of outgrowth of cells with functional EXT. Oncogene. 2011 Aug 1. doi: 10.1038/onc.2011.311. [Epub ahead of print]
10. 2011 Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 multiple osteochondromas families. BMC Med Genet. 2011 Jun 26;12:85.
11. 2011 A short-term in vivo model for giant cell tumor of bone. BMC Cancer. 2011 Jun 13;11:241. doi: 10.1186/1471-2407-11-241.
12. 2011 Loss of p53 partially rescues embryonic development of Palb2 knockout mice but does not foster haploinsufficiency of Palb2 in tumour suppression. J Pathol. 2011 May;224(1):10-21. doi: 10.1002/path.2861. Epub 2011 Mar 14.
13. 2011 Chemotherapy-resistant osteosarcoma is highly susceptible to IL-15-activated allogeneic and autologous NK cells. Cancer Immunol Immunother. 2011 Apr;60(4):575-86. Epub 2011 Jan 15.
14. 2011 Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients. Hum Mutat. 2011 Feb;32(2):E2036-49. doi: 10.1002/humu.21423. Epub 2010 Dec 7.
15. 2011 Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study. J Pathol. 2011 Feb;223(3):327-35. doi: 10.1002/path.2816. Epub 2010 Nov 24.
16. 2011 Genome-wide analysis of Ollier disease: Is it all in the genes? Orphanet J Rare Dis. 2011 Jan 14;6:2.
17. 2010 Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients. Hum Mutat. 2010 Dec 7. [Epub ahead of print]
18. 2010 Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy. Epilepsia. 2010 Dec;51(12):2457-60. doi: 10.1111/j.1528-1167.2010.02742.x. Epub 2010 Sep 30.
19. 2010 Small deletions but not methylation underlie CDKN2A/p16 loss of expression in conventional osteosarcoma. Genes Chromosomes Cancer. 2010 Dec;49(12):1095-103.
20. 2010 Array-based comparative genomic hybridisation analysis reveals recurrent chromosomal alterations in primary diffuse large B cell lymphoma of bone. J Clin Pathol. 2010 Dec;63(12):1095-100. Epub 2010 Oct 20.
21. 2010 No haploinsufficiency but loss of heterozygosity for EXT in multiple osteochondromas. Am J Pathol. 2010 Oct;177(4):1946-57. Epub 2010 Sep 2.
22. 2010 Kinome profiling of myxoid liposarcoma reveals NF-kappaB-pathway kinase activity and casein kinase II inhibition as a potential treatment option. Mol Cancer. 2010 Sep 23;9:257.
23. 2010 Heterogeneous and complex rearrangements of chromosome arm 6q in chondromyxoid fibroma: delineation of breakpoints and analysis of candidate target genes. Am J Pathol. 2010 Sep;177(3):1365-76. Epub 2010 Aug 9.
24. 2010 Evaluation of high-resolution microarray platforms for genomic profiling of bone tumours. BMC Res Notes. 2010 Aug 8;3:223.
25. 2010 Centriole movements in mammalian epithelial cells during cytokinesis. BMC Cell Biol. 2010 May 21;11:34.
26. 2010 Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome. Clin Genet. 2010 Apr;77(4):404-7. Epub 2010 Jan 20. No abstract available.
27. 2010 Cutaneous anaplastic large cell lymphoma and peripheral T-cell lymphoma NOS show distinct chromosomal alterations and differential expression of chemokine receptors and apoptosis regulators. J Invest Dermatol. 2010 Feb;130(2):563-75. Epub 2009 Aug 27.
28. 2009 No genomic aberrations in Langerhans cell histiocytosis as assessed by diverse molecular technologies. Genes Chromosomes Cancer. 2009 Mar;48(3):239-49.
29. 2009 Presence of a high amount of stroma and downregulation of SMAD4 predict for worse survival for stage I-II colon cancer patients. Cell Oncol. 2009;31(3):169-78.
30. 2009 A balanced t(5;17) (p15;q22-23) in chondroblastoma: frequency of the re-arrangement and analysis of the candidate genes. BMC Cancer. 2009 Nov 10;9:393.
31. 2009 Osteosarcoma originates from mesenchymal stem cells in consequence of aneuploidization and genomic loss of Cdkn2. J Pathol. 2009 Nov;219(3):294-305.
32. 2009 Multiple genomic aberrations in a patient with mental retardation and hypogonadism: 45,X/46,X,psu dic(Y) karyotype, thyroid hormone receptor beta (THRB) mutation and heterozygosity for Wilson disease. Am J Med Genet A. 2009 Oct;149A(10):2231-5.
33. 2009 Human cardiomyocyte progenitor cell transplantation preserves long-term function of the infarcted mouse myocardium. Cardiovasc Res. 2009 Aug 1;83(3):527-35. Epub 2009 May 9.
34. 2009 LSAMP, a novel candidate tumor suppressor gene in human osteosarcomas, identified by array comparative genomic hybridization. Genes Chromosomes Cancer. 2009 Aug;48(8):679-93.
35. 2009 Cellular/intramuscular myxoma and grade I myxofibrosarcoma are characterized by distinct genetic alterations and specific composition of their extracellular matrix. J Cell Mol Med. 2009 Jul;13(7):1291-301. Epub 2009 Mar 13.
36. 2009 Genomic instability in giant cell tumor of bone. A study of 52 cases using DNA ploidy, relocalization FISH, and array-CGH analysis. Genes Chromosomes Cancer. 2009 Jun;48(6):468-79.
37. 2009 A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents. J Med Genet. 2009 Jun;46(6):412-7. Epub 2009 Feb 25.
38. 2009 The NFATc2 gene is involved in a novel cloned translocation in a Ewing sarcoma variant that couples its function in immunology to oncology. Clin Cancer Res. 2009 Apr 1;15(7):2259-68. Epub 2009 Mar 24.
39. 2009 Oncogenomic analysis of mycosis fungoides reveals major differences with Sezary syndrome. Blood. 2009 Jan 1;113(1):127-36. Epub 2008 Oct 1.
40. 2009 BRCA2 heterozygosity delays cytokinesis in primary human fibroblasts. Cell Oncol. 2009;31(3):191-201.
41. 2009 Aberrant heparan sulfate proteoglycan localization, despite normal exostosin, in central chondrosarcoma. Am J Pathol. 2009 Mar;174(3):979-88. Epub 2009 Jan 29.
42. 2009 Long-term culture of primary human lymphoblastic leukemia cells in the absence of serum or hematopoietic growth factors. Exp Hematol. 2009 Mar;37(3):376-85. Epub 2009 Jan 9.
43. 2008 Genomic imbalances associated with mullerian aplasia. J Med Genet. 2008 Apr;45(4):228-32. Epub 2007 Nov 26.
44. 2008 Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting. Cytogenet Genome Res. 2008;123(1-4):65-78. Epub 2009 Mar 11.
45. 2008 Genomic alterations and gene expression in primary diffuse large B-cell lymphomas of immune-privileged sites: the importance of apoptosis and immunomodulatory pathways. J Pathol. 2008 Oct;216(2):209-17.
46. 2008 Establishment and cytogenetic characterization of a human acute lymphoblastic leukemia cell line (ALL-VG) with ETV6/ABL1 rearrangement. Cancer Genet Cytogenet. 2008 Aug;185(1):37-42.
47. 2008 Novel and highly recurrent chromosomal alterations in Sézary syndrome. Cancer Res. 2008 Apr 15;68(8):2689-98.
48. 2008 Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation. Br J Cancer. 2008 Jan 29;98(2):434-42. Epub 2007 Dec 11.
49. 2007 Interstitial deletion of 6q without phenotypic effect. Am J Med Genet A. 2007 Jun 15;143A(12):1354-7.
50. 2007 EWSR1-CREB1 and EWSR1-ATF1 fusion genes in angiomatoid fibrous histiocytoma. Clin Cancer Res. 2007 Dec 15;13(24):7322-8.
51. 2007 Guidelines for molecular karyotyping in constitutional genetic diagnosis. Eur J Hum Genet. 2007 Nov;15(11):1105-14. Epub 2007 Jul 18. Review.
52. 2007 CT-guided, COBRA-FISH-assisted diagnosis of well-differentiated liposarcoma (inflammatory subtype) of the retroperitoneum. Histopathology. 2007 Sep;51(3):422-6. No abstract available.
53. 2007 Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome. Am J Med Genet A. 2007 Aug 1;143A(15):1790-5. No abstract available.
54. 2007 Optimized amplification and fluorescent labeling of small cell samples for genomic array-CGH. Cytometry A. 2007 Aug;71(8):585-91.
55. 2007 Does parosteal liposarcoma differ from other atypical lipomatous tumors/well-differentiated liposarcomas? A molecular cytogenetic study using combined multicolor COBRA-FISH karyotyping and array-based comparative genomic hybridization. Cancer Genet Cytogenet. 2007 Jul 15;176(2):115-20.
56. 2007 Single nucleotide polymorphism array analysis of chromosomal instability patterns discriminates rectal adenomas from carcinomas. J Pathol. 2007 Jul;212(3):269-77.
57. 2007 Physical status of multiple human papillomavirus genotypes in flow-sorted cervical cancer cells. Cancer Genet Cytogenet. 2007 Jun;175(2):132-7.
58. 2007 Differences in telomerase expression by the CD1a+ cells in Langerhans cell histiocytosis reflect the diverse clinical presentation of the disease. J Pathol. 2007 Jun;212(2):188-97.
59. 2007 Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion. Eur J Hum Genet. 2007 May;15(5):548-55. Epub 2007 Mar 7.
60. 2007 Diagnosis of genetic abnormalities in developmentally delayed patients: a new strategy combining MLPA and array-CGH. Am J Med Genet A. 2007 Mar 15;143(6):610-4. No abstract available.
61. 2007 The role of EXT1 in nonhereditary osteochondroma: identification of homozygous deletions. J Natl Cancer Inst. 2007 Mar 7;99(5):396-406.
62. 2007 High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays. Genome Res. 2007 Mar;17(3):368-76. Epub 2007 Jan 31.
63. 2007 Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer. BMC Genomics. 2007 Feb 20;8:53.
64. 2007 Gene-expression profiling and array-based CGH classify CD4+CD56+ hematodermic neoplasm and cutaneous myelomonocytic leukemia as distinct disease entities. Blood. 2007 Feb 15;109(4):1720-7. Epub 2006 Oct 26.
65. 2007 Sarcoma derived from cultured mesenchymal stem cells. Stem Cells. 2007 Feb;25(2):371-9. Epub 2006 Oct 12.
66. 2007 Detection and molecular cytogenetic characterization of a novel ring chromosome in a histological variant of Ewing sarcoma. Cancer Genet Cytogenet. 2007 Jan 1;172(1):12-22.
67. 2007 The carcinoma-stromal ratio of colon carcinoma is an independent factor for survival compared to lymph node status and tumor stage. Cell Oncol. 2007;29(5):387-98.
68. 2006 Chromosomal and microsatellite instability of adenocarcinomas and dysplastic lesions (DALM) in ulcerative colitis. Diagn Mol Pathol. 2006 Dec;15(4):216-22.
69. 2006 Clonal T- and natural killer-cell large granular lymphocyte proliferations in a single patient established by array-based comparative genomic hybridization analysis. Leukemia. 2006 Dec;20(12):2212-4. Epub 2006 Oct 26. No abstract available.
70. 2006 Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase. Am J Hum Genet. 2006 Sep;79(3):562-6. Epub 2006 Jul 19. Erratum in: Am J Hum Genet. 2006 Nov;79(5):985.
71. 2006 A complex rearrangement on chromosome 22 affecting both homologues; haplo-insufficiency of the Cat eye syndrome region may have no clinical relevance. Hum Genet. 2006 Aug;120(1):77-84. Epub 2006 May 18.
72. 2006 Array-comparative genomic hybridization of central chondrosarcoma: identification of ribosomal protein S6 and cyclin-dependent kinase 4 as candidate target genes for genomic aberrations. Cancer. 2006 Jul 15;107(2):380-8.
73. 2006 Report of a del22q11 in a patient with Mayer-Rokitansky-Küster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women. Am J Med Genet A. 2006 Jun 15;140(12):1339-42. No abstract available.
74. 2006 Genomic analysis of early adenocarcinoma of the esophagus or gastroesophageal junction: tumor progression is associated with alteration of 1q and 8p sequences. Genes Chromosomes Cancer. 2006 May;45(5):516-25.
75. 2006 Molecular cytogenetic characterization of four previously established and two newly established Ewing sarcoma cell lines. Cancer Genet Cytogenet. 2006 Apr 15;166(2):173-9.
76. 2006 Genomic array and expression analysis of frequent high-level amplifications in adenocarcinomas of the gastro-esophageal junction. Cancer Genet Cytogenet. 2006 Apr 15;166(2):157-62.
77. 2006 Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and review. Am J Med Genet A. 2006 Mar 15;140(6):611-7. Review.
78. 2006 Array-based genomic analysis of screen-detected Gleason score 6 and 7 prostatic adenocarcinomas. Anticancer Res. 2006 Mar-Apr;26(2A):1193-200.
79. 2006 Local recurrence of myxofibrosarcoma is associated with increase in tumour grade and cytogenetic aberrations, suggesting a multistep tumour progression model. Mod Pathol. 2006 Mar;19(3):407-16.
80. 2006 Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams-Beuren duplications. Eur J Hum Genet. 2006 Feb;14(2):180-9.
81. 2006 Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents. J Med Genet. 2006 Feb;43(2):180-6. Epub 2005 Jun 24.
82. 2006 Array-based comparative genomic hybridization analysis reveals recurrent chromosomal alterations and prognostic parameters in primary cutaneous large B-cell lymphoma. J Clin Oncol. 2006 Jan 10;24(2):296-305. Epub 2005 Dec 5.
83. 2006 Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations. Cytogenet Genome Res. 2006;115(3-4):254-61.
84. 2006 A 17q21.31 microdeletion encompassing the MAPT gene in a mentally impaired patient. Cytogenet Genome Res. 2006;114(1):89-92.
85. 2006 COBRA: combined binary ratio labeling of nucleic-acid probes for multi-color fluorescence in situ hybridization karyotyping. Nat Protoc. 2006;1(1):264-75.
86. 2005 Distinct nuclear gene expression profiles in cells with mtDNA depletion and homoplasmic A3243G mutation. Mutat Res. 2005 Oct 15;578(1-2):43-52.
87. 2005 Rapid detection of genomic imbalances using micro-arrays consisting of pooled BACs covering all human chromosome arms. Nucleic Acids Res. 2005 Oct 12;33(18):e159.
88. 2005 Array CGH detection of a cryptic deletion in a complex chromosome rearrangement. Hum Genet. 2005 Apr;116(5):390-4. Epub 2005 Feb 22.
89. 2005 GJB2 mutations in hearing impairment: identification of a broad clinical spectrum for improved genetic counseling. Laryngoscope. 2005 Mar;115(3):461-5.
90. 2005 Insights from genomic microarrays into structural chromosome rearrangements. Am J Med Genet A. 2005 Jan 1;132A(1):36-40.
91. 2005 Expression analysis of candidate breast tumour suppressor genes on chromosome 16q. Breast Cancer Res. 2005;7(6):R998-1004. Epub 2005 Oct 18.
92. 2004 Primary synovial sarcoma of the heart: a cytogenetic and molecular genetic analysis combining RT-PCR and COBRA-FISH of a case with a complex karyotype. Mod Pathol. 2004 Nov;17(11):1434-9.
93. 2004 Positioning of cervical carcinoma and Burkitt lymphoma translocation breakpoints with respect to the human papillomavirus integration cluster in FRA8C at 8q24.13. Cancer Genet Cytogenet. 2004 Oct 1;154(1):1-9.
94. 2004 Cathepsin K is the principal protease in giant cell tumor of bone. Am J Pathol. 2004 Aug;165(2):593-600.
95. 2004 Multicolor fluorescence in situ hybridization analysis of a synovial sarcoma of the larynx with a t(X;18)(p11.2;q11.2) and trisomies 2 and 8. Cancer Genet Cytogenet. 2004 Aug;153(1):48-52.
96. 2004 Disruption of Drosophila Rad50 causes pupal lethality, the accumulation of DNA double-strand breaks and the induction of apoptosis in third instar larvae. DNA Repair (Amst). 2004 Jun 3;3(6):603-15.
97. 2004 A novel t(6;14)(q25-q27;q32) in acute myelocytic leukemia involves the BCL11B gene. Cancer Genet Cytogenet. 2004 Feb;149(1):72-6.
98. 2002 Real-time monitoring of rolling-circle amplification using a modified molecular beacon design. Nucleic Acids Res. 2002 Jul 15;30(14):e66.
99. 2002 Connexin 26 mutations in cases of sensorineural deafness in eastern Austria. Eur J Hum Genet. 2002 Jul;10(7):427-32.
100. 2002 Simultaneous mapping of human papillomavirus integration sites and molecular karyotyping in short-term cultures of cervical carcinomas by using 49-color combined binary ratio labeling fluorescence in situ hybridization. Cancer Genet Cytogenet. 2002 Apr 15;134(2):145-50.
101. 2001 A novel strategy for human papillomavirus detection and genotyping with SybrGreen and molecular beacon polymerase chain reaction. Am J Pathol. 2001 Nov;159(5):1651-60.
102. 2001 A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the disease. Eur J Hum Genet. 2001 Mar;9(3):171-7.
103. 2001 Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by a multiplex molecular beacon based real-time fluorescence PCR. Nucleic Acids Res. 2001 Feb 1;29(3):E13.
104. 2000 [Incidence and distribution of t(12;21) in prognostic groups of pediatric acute lymphoblastic leukemia]. Orv Hetil. 2000 Jul 2;141(27):1495-500. Hungarian.
105. 2000 Simultaneous molecular karyotyping and mapping of viral DNA integration sites by 25-color COBRA-FISH. Genes Chromosomes Cancer. 2000 May;28(1):92-7.
106. 2000 Silent Philadelphia chromosome: a distinct developmental stage in a philadelphia chromosome-positive chronic myeloproliferation? Cancer Genet Cytogenet. 2000 Apr 1;118(1):14-9.
107. 1999 Recurrent integration of human papillomaviruses 16, 45, and 67 near translocation breakpoints in new cervical cancer cell lines. Cancer Res. 1999 Nov 1;59(21):5615-24.
108. 1998 Combined metaphase, interphase cytogenetic, and flow cytometric analysis of DNA content of pediatric acute lymphoblastic leukemia. Cytometry. 1998 Apr 15;34(2):87-94.
109. 1997 [Application of interphase cytogenetics for the determination of changes in the DNA content in acute childhood lymphoid leukemia]. Orv Hetil. 1997 Dec 7;138(49):3111-9. Hungarian.
110. 1997 Multiple tumor case: report and analysis of an autopsy case. Tumori. 1997 May-Jun;83(3):715-7.


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