Sakari Knuutila
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Computer Science
Sakari Knuutila's Degrees
- PhD Computer Science University of Helsinki
- Masters Computer Science University of Helsinki
- Bachelors Computer Science University of Helsinki
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(Suggest an Edit or Addition)Sakari Knuutila's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Prognostic subgroups in B-cell chronic lymphocytic leukemia defined by specific chromosomal abnormalities. (1990) (638)
- DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies. (1998) (607)
- Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis (1997) (522)
- DNA copy number losses in human neoplasms. (1999) (412)
- A novel endothelial cell surface receptor tyrosine kinase with extracellular epidermal growth factor homology domains (1992) (367)
- CDKN2A, NF2, and JUN are dysregulated among other genes by miRNAs in malignant mesothelioma—A miRNA microarray analysis (2009) (276)
- Rearrangement of ALL1 (MLL) in acute myeloid leukemia with normal cytogenetics. (1998) (243)
- DNA sequence copy number changes in gastrointestinal stromal tumors: tumor progression and prognostic significance. (2000) (234)
- Identification of a gene at 11q23 encoding a guanine nucleotide exchange factor: evidence for its fusion with MLL in acute myeloid leukemia. (2000) (229)
- BCL2 overexpression associated with chromosomal amplification in diffuse large B-cell lymphoma. (1997) (222)
- RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability. (2005) (216)
- Partial tandem duplication of ALL1 as a recurrent molecular defect in acute myeloid leukemia with trisomy 11. (1996) (210)
- Concomitant loss of chromosome 3 and whole arm losses and gains of chromosome 1, 6, or 8 in metastasizing primary uveal melanoma. (2001) (202)
- Increased expression of high mobility group A proteins in lung cancer (2006) (196)
- Identification of differentially expressed genes in pulmonary adenocarcinoma by using cDNA array (2002) (184)
- Uniparental disomy in cancer. (2009) (183)
- Gains and losses of DNA sequences in osteosarcomas by comparative genomic hybridization. (1995) (171)
- Targets of gene amplification and overexpression at 17q in gastric cancer. (2002) (171)
- Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer families. (2002) (169)
- DNA copy number changes in diffuse large B-cell lymphoma--comparative genomic hybridization study. (1996) (164)
- Hepatocyte growth factor receptor, matrix metalloproteinase-11, tissue inhibitor of metalloproteinase-1, and fibronectin are up-regulated in papillary thyroid carcinoma: a cDNA and tissue microarray study. (2003) (161)
- DNA sequence copy number increase at 8q: A potential new prognostic marker in high‐grade osteosarcoma (1999) (156)
- BAALC, the human member of a novel mammalian neuroectoderm gene lineage, is implicated in hematopoiesis and acute leukemia (2001) (156)
- Persistence of the AML1/ETO fusion transcript in patients treated with allogeneic bone marrow transplantation for t(8;21) leukemia. (1996) (153)
- Differentially expressed genes in nonsmall cell lung cancer: expression profiling of cancer-related genes in squamous cell lung cancer. (2004) (150)
- Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study. (1991) (144)
- Comparison of Targeted Next‐Generation Sequencing (NGS) and Real‐Time PCR in the Detection of EGFR, KRAS, and BRAF Mutations on Formalin‐Fixed, Paraffin‐Embedded Tumor Material of Non‐Small Cell Lung Carcinoma—Superiority of NGS (2013) (143)
- DNA gains in 3q occur frequently in squamous cell carcinoma of the lung, but not in adenocarcinoma (1998) (141)
- Gene Expression Profiling of Ameloblastoma and Human Tooth Germ by Means of a cDNA Microarray (2002) (140)
- Gain of 3q and deletion of 11q22 are frequent aberrations in mantle cell lymphoma (1998) (139)
- miR‐34a predicts survival of Ewing's sarcoma patients and directly influences cell chemo‐sensitivity and malignancy (2012) (137)
- Integrative analysis of microRNA, mRNA and aCGH data reveals asbestos‐ and histology‐related changes in lung cancer (2011) (133)
- Gene amplifications in osteosarcoma—CGH microarray analysis (2005) (130)
- DNA copy number losses in chromosome 14: an early change in gastrointestinal stromal tumors. (1996) (129)
- Undifferentiated Intimal Sarcoma of Large Systemic Blood Vessels: Report of 14 Cases With Immunohistochemical Profile and Review of the Literature (2005) (128)
- Online access to CGH data of DNA sequence copy number changes. (2000) (127)
- Impairment of the Ubiquitin-Proteasome Pathway Is a Downstream Endoplasmic Reticulum Stress Response Induced by Extracellular Human Islet Amyloid Polypeptide and Contributes to Pancreatic β-Cell Apoptosis (2007) (125)
- DNA copy number amplification profiling of human neoplasms (2006) (124)
- Overcoming resistance to conventional drugs in Ewing sarcoma and identification of molecular predictors of outcome. (2009) (124)
- Molecular targets for tumour progression in gastrointestinal stromal tumours (2004) (121)
- DNA copy number changes in thyroid carcinoma. (1999) (118)
- Optimization of comparative genomic hybridization using fluorochrome conjugated to dCTP and dUTP nucleotides. (1997) (117)
- Recurrent gains of 1q, 8 and 12 in the Ewing family of tumours by comparative genomic hybridization. (1997) (115)
- Molecular mechanisms of CD99-induced caspase-independent cell death and cell–cell adhesion in Ewing's sarcoma cells: actin and zyxin as key intracellular mediators (2004) (112)
- AML1 gene amplification: a novel finding in childhood acute lymphoblastic leukemia. (2000) (110)
- DNA copy number changes in development and progression in leiomyosarcomas of soft tissues. (1998) (109)
- Genomic profiles and CRTC1–MAML2 fusion distinguish different subtypes of mucoepidermoid carcinoma (2013) (109)
- Abnormal expression of apoptosis‐related genes in haematological malignancies: overexpression of MYC is poor prognostic sign in mantle cell lymphoma (2003) (108)
- Cytogenetic Findings and Survival in B-cell Chronic Lymphocytic Leukemia. Second IWCCLL Compilation of Data on 662 Patients. (1991) (107)
- Trisomy 12 in B cells of patients with B-cell chronic lymphocytic leukemia. (1986) (106)
- 17q12‐21 amplicon, a novel recurrent genetic change in intestinal type of gastric carcinoma: A comparative genomic hybridization study (1997) (105)
- Gastric cancers overexpress DARPP-32 and a novel isoform, t-DARPP. (2002) (103)
- Prognostic impact of chromosomal aberrations in Ewing tumours (2002) (101)
- Different patterns of DNA copy number changes in gastrointestinal stromal tumors, leiomyomas, and schwannomas. (1998) (101)
- Cytogenetic and molecular genetic changes in malignant mesothelioma. (2006) (101)
- MSX1 Gene is Deleted in Wolf-Hirschhorn Syndrome Patients with Oligodontia (2003) (100)
- Pallister‐Killian syndrome: cytogenetic and molecular studies (1987) (100)
- MicroRNA profiling differentiates colorectal cancer according to KRAS status (2012) (100)
- Culture of bone marrow reveals more cells with chromosomal abnormalities than the direct method in patients with hematologic disorders. (1981) (100)
- Comparison of DNA copy number changes in malignant mesothelioma, adenocarcinoma and large-cell anaplastic carcinoma of the lung. (1998) (98)
- 1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma (2012) (97)
- Chromosomal abnormalities and their correlations with asbestos exposure and survival in patients with mesothelioma. (1989) (96)
- Ring chromosomes in parosteal osteosarcoma contain sequences from 12q13–15: A combined cytogenetic and comparative genomic hybridization study (1996) (96)
- Chromosomal alterations in human pancreatic endocrine tumors (2000) (96)
- Comparative genomic hybridization of malignant fibrous histiocytoma reveals a novel prognostic marker. (1997) (95)
- Cytogenetic study of 249 consecutive patients examined for a bone tumor. (1993) (94)
- Impact of TP53 mutation and 17p deletion in mantle cell lymphoma (2011) (93)
- Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations (2005) (92)
- Recurrent DNA copy number changes in 1q, 4q, 6q, 9p, 13q, 14q and 22q detected by comparative genomic hybridization in malignant mesothelioma. (1997) (92)
- Expression profiling of gastric adenocarcinoma using cDNA array (2001) (92)
- ACUTE MYELOGENOUS LEUKAEMIA WITH C-MYC AMPLIFICATION AND DOUBLE MINUTE CHROMOSOMES (1985) (92)
- High‐resolution deletion mapping of chromosome 14 in stromal tumors of the gastrointestinal tract suggests two distinct tumor suppressor loci (2000) (92)
- Gains, losses, and amplifications of DNA sequences evaluated by comparative genomic hybridization in chondrosarcomas. (1997) (91)
- Epigenetic signatures of familial cancer are characteristic of tumor type and family category. (2008) (91)
- Comparative genomic hybridization reveals complex genetic changes in primary breast cancer tumors and their cell lines. (2000) (90)
- CDK4 is a probable target gene in a novel amplicon at 12q13.3–q14.1 in lung cancer (2005) (90)
- Gains and losses of DNA sequences in liposarcomas evaluated by comparative genomic hybridization (1996) (89)
- Acute lymphoblastic leukemia in adolescents and young adults in Finland (2008) (89)
- Overexpression of translocation-associated fusion genes of FGFRI, MYC, NPMI, and DEK, but absence of the translocations in acute myeloid leukemia. A microarray analysis. (2002) (89)
- Hsa-miR-31-3p Expression Is Linked to Progression-free Survival in Patients with KRAS Wild-type Metastatic Colorectal Cancer Treated with Anti-EGFR Therapy (2014) (88)
- Consistent genetic alterations in xenografts of proximal stomach and gastro-esophageal junction adenocarcinomas. (1998) (88)
- Tumor size-related DNA copy number changes occur in solitary fibrous tumors but not in hemangiopericytomas. (1997) (88)
- Distinct gene expression profiling in chronic lymphocytic leukemia with 11q23 deletion (2001) (86)
- Genetic differences between adenocarcinomas arising in Barrett's esophagus and gastric mucosa. (2001) (85)
- Erythroid and granulocyte-macrophage colony formation in myelodysplastic syndromes. (2009) (84)
- Comparison of fluorescein isothiocyanate- and Texas red-conjugated nucleotides for direct labeling in comparative genomic hybridization. (1998) (84)
- Clinical correlations of genetic changes by comparative genomic hybridization in Ewing sarcoma and related tumors. (1999) (83)
- Deletion of 11q23 and cyclin D1 overexpression are frequent aberrations in parathyroid adenomas. (2001) (83)
- Gene expression profiles in asbestos-exposed epithelial and mesothelial lung cell lines (2007) (82)
- High Expression of Complement Component 5 (C5) at Tumor Site Associates with Superior Survival in Ewing's Sarcoma Family of Tumour Patients (2011) (81)
- Distinct differentiation characteristics of individual human embryonic stem cell lines (2006) (80)
- Evidence for divergence of DNA copy number changes in serous, mucinous and endometrioid ovarian carcinomas. (1997) (80)
- Proposals for standardized protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes (2007) (78)
- MicroRNA profiling predicts survival in anti-EGFR treated chemorefractory metastatic colorectal cancer patients with wild-type KRAS and BRAF. (2012) (78)
- A method for simultaneous study of the karyotype, morphology, and immunologic phenotype of mitotic cells in hematologic malignancies. (1984) (77)
- Comparative genomic hybridization of low-grade central osteosarcoma. (1998) (74)
- Nonrandom chromosomal abnormalities in malignant pleural mesothelioma. (1988) (74)
- High incidence of PTLD after non-T-cell-depleted allogeneic haematopoietic stem cell transplantation as a consequence of intensive immunosuppressive treatment (2003) (74)
- Overrepresentation of 1q21-23 and 12q13-21 in lipoma-like liposarcomas but not in benign lipomas: a comparative genomic hybridization study. (1997) (74)
- Distinct chromosomal imbalances in uterine serous and endometrioid carcinomas. (1998) (72)
- Genomic Profiling of Chondrosarcoma: Chromosomal Patterns in Central and Peripheral Tumors (2009) (71)
- Array comparative genomic hybridization analysis of chromosomal imbalances and their target genes in gastrointestinal stromal tumors (2007) (71)
- Combined use of expression and CGH arrays pinpoints novel candidate genes in Ewing sarcoma family of tumors (2009) (71)
- Integrated gene copy number and expression microarray analysis of gastric cancer highlights potential target genes (2008) (70)
- Genetic changes in inherited and sporadic ovarian carcinomas by comparative genomic hybridization: extensive similarity except for a difference at chromosome 2q24-q32. (1998) (70)
- Gene expression analysis of 1,25(OH)2D3‐dependent differentiation of HL‐60 cells: a cDNA array study (2002) (69)
- Darpp-32: a novel antiapoptotic gene in upper gastrointestinal carcinomas. (2005) (69)
- Genome-wide differences between microsatellite stable and unstable colorectal tumors. (2006) (69)
- Novel findings in gene expression detected in human osteosarcoma by cDNA microarray. (2000) (67)
- CDKN2A deletions in acute lymphoblastic leukemia of adolescents and young adults: an array CGH study. (2008) (67)
- Investigatory and analytical approaches to differential gene expression profiling in mantle cell lymphoma (2002) (67)
- Cytogenetic aberrations and their prognostic impact in chondrosarcoma (2002) (65)
- Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p. (2000) (65)
- Manifestation, mechanisms and mysteries of gene amplifications. (2006) (65)
- Aberrant Expression of HOXA9, DEK, CBL and CSF1R in Acute Myeloid Leukemia (2003) (65)
- Causes and Consequences of BCL2 Overexpression in Diffuse Large B-Cell Lymphoma (2001) (63)
- Comparative genomic hybridization analysis of chromosomal changes occurring during development of acquired resistance to cisplatin in human ovarian carcinoma cells (1997) (63)
- Gene expression profiling of malignant mesothelioma cell lines: cDNA array study (2001) (63)
- Restriction landmark genome scanning for aberrant methylation in primary refractory and relapsed acute myeloid leukemia; involvement of the WIT-1 gene (1999) (63)
- Dedifferentiation of a well-differentiated liposarcoma to a highly malignant metastatic osteosarcoma: amplification of 12q14 at all stages and gain of 1q22-q24 associated with metastases. (2001) (63)
- Amplification of 17p11.2∼p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma (2002) (62)
- Coamplified and overexpressed genes at ERBB2 locus in gastric cancer (2004) (62)
- Comparative genomic hybridization study on pooled DNAs from tumors of one clinical-pathological entity. (1998) (61)
- Comparison of benign and malignant follicular thyroid tumours by comparative genomic hybridization. (1998) (61)
- Cytogenetic and immunologic characterization of mitotic cells in chronic lymphocytic leukaemia (1987) (60)
- Unique display of a pathologic karyotype in Hodgkin's disease by Reed-Sternberg cells. (1988) (60)
- Frequent loss of the 11q14‐24 region in chronic lymphocytic leukemia: A study by comparative genomic hybridization (1997) (60)
- Immunophenotyping of aneuploid cells. (1989) (60)
- Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia. (2003) (60)
- Increased frequency of micronuclei in B and T8 lymphocytes from smokers. (1991) (60)
- DNA copy number changes and evaluation of MYC, IGF1R, and FES amplification in xenografts of pancreatic adenocarcinoma. (2000) (59)
- Cell lineage involvement of recurrent chromosomal abnormalities in hematologic neoplasms (1994) (59)
- Identification of specific gene copy number changes in asbestos-related lung cancer. (2006) (58)
- Gene copy number analysis in malignant pleural mesothelioma using oligonucleotide array CGH (2007) (58)
- Caveolins as tumour markers in lung cancer detected by combined use of cDNA and tissue microarrays (2004) (58)
- Specificity, selection and significance of gene amplifications in cancer. (2007) (57)
- Fetal granulocytes in maternal venous blood detected by in situ hybridization (1992) (56)
- Downregulation of Plasma MiR-142-3p and MiR-26a-5p in Patients With Colorectal Carcinoma (2015) (55)
- High-resolution oligonucleotide array-CGH pinpoints genes involved in cryptic losses in chronic lymphocytic leukemia (2007) (55)
- Positional cloning identifies a novel cyclophilin as a candidate amplified oncogene in 1q21 (2002) (55)
- Concomitant DNA copy number amplification at 17q and 22q in dermatofibrosarcoma protuberans (2001) (52)
- Stool Microbiota Composition Differs in Patients with Stomach, Colon, and Rectal Neoplasms (2018) (52)
- Oligonucleotide array-CGH reveals cryptic gene copy number alterations in karyotypically normal acute myeloid leukemia (2007) (52)
- Gene copy number profiling of soft-tissue leiomyosarcomas by array-comparative genomic hybridization. (2006) (52)
- Abnormalities of chromosome 13 in myelofibrosis. (2009) (52)
- Molecular characterization of deletion at 11q22.1‐23.3 in mantle cell lymphoma (1999) (51)
- Detection of residual host cells after bone marrow transplantation using non-isotopic in situ hybridization and karyotype analysis. (1993) (51)
- RELP, a novel human REG-like protein with up-regulated expression in inflammatory and metaplastic gastrointestinal mucosa. (2003) (51)
- Evaluation of STOX1 as a preeclampsia candidate gene in a population-wide sample (2007) (51)
- Cell proliferation and chromosomal changes in human ameloblastoma. (2002) (51)
- A broad amplification pattern at 3q in squamous cell lung cancer--a fluorescence in situ hybridization study. (2000) (50)
- Changes in apoptosis-related pathways in acute myelocytic leukemia. (2003) (50)
- Targeted Resequencing Reveals ALK Fusions in Non-Small Cell Lung Carcinomas Detected by FISH, Immunohistochemistry, and Real-Time RT-PCR: A Comparison of Four Methods (2013) (49)
- ALK/EML4 Fusion Gene May Be Found in Pure Squamous Carcinoma of the Lung (2014) (49)
- Gains and losses of DNA sequences in malignant mesothelioma by comparative genomic hybridization. (1996) (49)
- DNA copy number changes in Schistosoma-associated and non-Schistosoma-associated bladder cancer. (2000) (49)
- BCL 2 Overexpression Associated With Chromosomal Amplification in Diffuse Large B-Cell Lymphoma (1997) (48)
- Age-associated micronuclei containing centromeres and the X chromosome in lymphocytes of women (1995) (48)
- Genetic imbalances in 67 synovial sarcomas evaluated by comparative genomic hybridization (1998) (47)
- Array comparative genomic hybridization analysis of olfactory neuroblastoma (2008) (47)
- L1CAM, INP10, P-cadherin, tPA and ITGB4 over-expression in malignant pleural mesotheliomas revealed by combined use of cDNA and tissue microarray. (2004) (47)
- Loss in 3p and 4p and Gain of 3q Are Concomitant Aberrations in Squamous Cell Carcinoma of the Vulva (2001) (46)
- Unique microRNA profile in Dupuytren's contracture supports deregulation of β-catenin pathway (2010) (46)
- Clinical importance of genomic imbalances in synovial sarcoma evaluated by comparative genomic hybridization. (1999) (46)
- Novel DNA copy number losses in chromosome 12q12--q13 in adenoid cystic carcinoma. (2001) (46)
- 11q Deletions in Hematological Malignancies (2001) (45)
- t(1;3)(p36;q21) in acute nonlymphocytic leukemia: a new cytogenetic- clinicopathologic association (1985) (45)
- Lymphoproliferative disease after allogeneic stem cell transplantation--pre-emptive diagnosis by quantification of Epstein-Barr virus DNA in serum. (2003) (44)
- DNA copy number profiling in esophageal Barrett adenocarcinoma: comparison with gastric adenocarcinoma and esophageal squamous cell carcinoma. (2001) (44)
- Malignant fibrous histiocytoma of bone: analysis of genomic imbalances by comparative genomic hybridisation and C-MYC expression by immunohistochemistry. (2006) (44)
- Gene expression and copy number profiling suggests the importance of allelic imbalance in 19p in asbestos-associated lung cancer (2007) (44)
- Microdeletions in 9p21.3 induce false negative results in CDKN2A FISH analysis of Ewing sarcoma (2007) (44)
- Follicular Lymphoma Cell Lines, an In Vitro Model for Antigenic Selection and Cytokine‐Mediated Growth Regulation of Germinal Centre B Cells (2003) (44)
- Different gene expression in immunoglobulin-mutated and immunoglobulin-unmutated forms of chronic lymphocytic leukemia. (2004) (44)
- Amplified, lost, and fused genes in 11q23–25 amplicon in acute myeloid leukemia, an array‐CGH study (2006) (43)
- Sister chromatid exchanges in human bone marrow cells. I. Control subjects and patients with leukaemia. (2009) (43)
- Amplification of 17p11.2 approximately p12, including PMP22, TOP3A, and MAPK7, in high-grade osteosarcoma. (2002) (43)
- Genomic alterations in fallopian tube carcinoma: comparison to serous uterine and ovarian carcinomas reveals similarity suggesting likeness in molecular pathogenesis. (1998) (42)
- Age-associated micronuclei containing centromeres and the X chromosome in lymphocytes of women. (1996) (42)
- Expression of myeloid-specific genes in childhood acute lymphoblastic leukemia – a cDNA array study (2002) (42)
- Genetic profile, PTEN mutation and therapeutic role of PTEN in glioblastomas. (2002) (42)
- Array CGH in molecular diagnosis of mental retardation—A study of 150 Finnish patients (2010) (42)
- Among numerous DNA copy number changes, losses of chromosome 13 are highly recurrent in plasmacytoma (1999) (41)
- Recurrent DNA copy number changes revealed by comparative genomic hybridization in primary Merkel cell carcinomas (2004) (41)
- A cytogenetic study of malignant fibrous histiocytoma. (1995) (41)
- Analysis of genotype and phenotype on the same interphase or mitotic cell. A manual of MAC (morphology antibody chromosomes) methodology. (1994) (40)
- DNA copy number aberrations in intestinal-type gastric cancer revealed by array-based comparative genomic hybridization. (2006) (40)
- Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3. (1996) (40)
- Amplification of ornithine decarboxylase gene in response to polyamine deprivation in Chinese hamster ovary cells. (1985) (39)
- Deletions at 11q23 in different lymphoma subtypes. (2000) (39)
- Simultaneous Underexpression of let-7a-5p and let-7f-5p microRNAs in Plasma and Stool Samples from Early Stage Colorectal Carcinoma (2015) (39)
- Characterization of gene expression in major types of salivary gland carcinomas with epithelial differentiation. (2005) (39)
- Classification of human cancers based on DNA copy number amplification modeling (2008) (38)
- BCL2 overexpression in diffuse large B-cell lymphoma. (1999) (38)
- Molecular Dissection of 17q12 Amplicon in Upper Gastrointestinal Adenocarcinomas (2006) (38)
- Polyamine deprivation causes major chromosome aberrations in a polyamine-dependent Chinese hamster ovary cell line. (1982) (38)
- Molecular cytogenetic characterization of desmoid tumors. (2003) (38)
- Maternal origin of nucleated erythrocytes in peripheral venous blood of pregnant women (1995) (38)
- Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumor (2004) (37)
- Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysis (1999) (37)
- DNA copy number changes in familial malignant mesothelioma. (2001) (36)
- Concomitant gastrin and ERBB2 gene amplifications at 17q12–q21 in the intestinal type of gastric cancer (1999) (36)
- Genetic Changes in Sporadic Keratocystic Odontogenic Tumors (Odontogenic Keratocysts) (2007) (36)
- Further evidence for a relationship between the 5p15 chromosome region and the oculoauriculovertebral anomaly (2008) (36)
- Clinical significance of genetic imbalances revealed by comparative genomic hybridization in chondrosarcomas. (1999) (36)
- True 3q Chromosomal Amplification in Squamous Cell Lung Carcinoma by FISH and aCGH Molecular Analysis: Impact on Targeted Drugs (2012) (35)
- Presence of high-level DNA copy number gains in gastric carcinoma and severely dysplastic adenomas but not in moderately dysplastic adenomas. (1998) (35)
- Comparative genomic hybridization in childhood acute lymphoblastic leukemia (1998) (35)
- Driver Gene and Novel Mutations in Asbestos-Exposed Lung Adenocarcinoma and Malignant Mesothelioma Detected by Exome Sequencing (2016) (35)
- Differentiating soft tissue leiomyosarcoma and undifferentiated pleomorphic sarcoma: A miRNA analysis (2014) (35)
- Chromosomal breakpoints and changes in DNA copy number in refractory acute myeloid leukemia (1997) (35)
- Higher frequency of 51--clone in bone marrow mitoses after culture than by a direct method. (2009) (34)
- Minimal residual disease after allogeneic bone marrow transplantation for chronic myeloid leukaemia: a metaphase‐FISH study (1996) (34)
- An integrated analysis of miRNA and gene copy numbers in xenografts of Ewing's sarcoma (2012) (34)
- MicroRNA Expression Profiles in Kaposi’s Sarcoma (2013) (34)
- Potential role of a navigator gene NAV3 in colorectal cancer (2011) (34)
- Recurrent DNA copy number losses associated with metastasis of larynx carcinoma (1999) (33)
- Focal 9p instability in hematologic neoplasias revealed by comparative genomic hybridization and single‐nucleotide polymorphism microarray analyses (2009) (33)
- CanGEM: mining gene copy number changes in cancer (2007) (33)
- DNA copy number changes in gastrointestinal stromal tumors--a distinct genetic entity. (1998) (33)
- Expression of L-myc and N-myc proto-oncogenes in human leukemias and leukemia cell lines. (1991) (32)
- Methotrexate-induced increase in gap formation in human chromosome band 3p14. (2008) (32)
- In situ hybridization using a Y-specific probe--a sensitive method for distinguishing residual male recipient cells from female donor cells in bone marrow transplantation. (1989) (32)
- RB1 gene in Merkel cell carcinoma: hypermethylation in all tumors and concurrent heterozygous deletions in the polyomavirus‐negative subgroup (2014) (32)
- Aberrations of chromosome 19 in asbestos-associated lung cancer and in asbestos-induced micronuclei of bronchial epithelial cells in vitro. (2008) (32)
- Array comparative genomic hybridization identifies a distinct DNA copy number profile in renal cell cancer associated with hereditary leiomyomatosis and renal cell cancer (2009) (32)
- Micronucleus formation in different lymphocyte subpopulations in peplomycin-treated and control cultures. (1989) (31)
- Treatment of adrenoleukodystrophy with bone marrow transplantation (1997) (31)
- Gain of chromosome 3 and loss of 13q are frequent alterations in pituitary adenomas. (2001) (31)
- Discontinuous deletions at 11q23 in B cell chronic lymphocytic leukemia (1999) (31)
- Down-regulation of miR-181c in imatinib-resistant chronic myeloid leukemia (2013) (31)
- Megakaryocyte colony formation by bone marrow progenitors in myelodysplasia syndromes (1986) (31)
- Heme arginate treatment for myelodysplastic syndromes. (1988) (31)
- Chromosomal in situ suppression hybridization of immunologically classified mitotic cells in hematologic malignancies (1992) (31)
- FGF4 and INT2 Oncogenes Are Amplified and Expressed in Kaposi's Sarcoma (2000) (31)
- Bone-marrow chromosomes in healthy subjects. (2009) (30)
- Evidence of somatic mutations in osteoarthritis (1996) (30)
- Clustering of molecular alterations in gastroesophageal carcinomas. (2004) (30)
- DNA copy number changes in young gastric cancer patients with special reference to chromosome 19 (2003) (30)
- Cell lineage involvement in four patients with myelodysplastic syndrome and t(1;7) or trisomy 8 studied by simultaneous immunophenotyping and fluorescence in situ hybridization. (1993) (30)
- Relative proportions of mitotic T and B cells in PHA-stimulated lymphocyte cultures. (1987) (30)
- A cluster of familial malignant mesothelioma with del(9p) as the sole chromosomal anomaly. (2002) (30)
- Chromosome abnormalities in 16 Finnish patients with Burkitt's lymphoma or L3 acute lymphocytic leukemia. (1984) (30)
- Decreased expression of fecal miR-4478 and miR-1295b-3p in early-stage colorectal cancer. (2015) (30)
- Spindle cell tumours of the pleura: a clinical, histological and comparative genomic hybridization analysis of 14 cases (2006) (29)
- Metaphase fluorescence in situ hybridization (FISH) in the follow‐up of 60 patients with haemkopietic malignancies (1994) (29)
- Increased sister chromatid exchange in megaloblastic anaemia-studies on bone marrow cells and lymphocytes. (2009) (29)
- Does comparative genomic hybridization reveal distinct differences in DNA copy number sequence patterns between leiomyosarcoma and malignant fibrous histiocytoma? (2008) (29)
- Comparison of genetic changes in primary sarcomas and their pulmonary metastases (1999) (29)
- MicroRNA expression profiles in metastatic and non-metastatic giant cell tumor of bone. (2013) (29)
- Establishment and characterization of a rat glomerular endothelial cell line. (1993) (29)
- Renal cell carcinoma with smooth muscle stroma lacks chromosome 3p and VHL alterations (2014) (29)
- Chromosome banding techniques for morphologically classified cells. (1985) (28)
- Chromosome instability is associated with hypodiploid clones in myelodysplastic syndromes. (2008) (28)
- t(1;3)(p36;q21) in acute nonlymphocytic leukemia: a new cytogenetic-clinicopathologic association. (1985) (28)
- Cytogenetic study of 105 children with acute lymphoblastic leukemia (1988) (28)
- Cross-linking of surface IgG induces apoptosis in a bcl-2 expressing human follicular lymphoma line of mature B cell phenotype. (1994) (28)
- Driver Gene Mutations of Non-Small-Cell Lung Cancer are Rare in Primary Carcinoids of the Lung: NGS Study by Ion Torrent (2015) (28)
- Malignant mesothelioma: clinical characteristics, asbestos mineralogy and chromosomal abnormalities of 41 patients. (1992) (28)
- Gene expression profile by blocking the SYT-SSX fusion gene in synovial sarcoma cells. Identification of XRCC4 as a putative SYT-SSX target gene (2003) (28)
- DNA copy number changes in alveolar soft part sarcoma: a comparative genomic hybridization study. (1998) (28)
- Constitutional translocation t(3;6)(p14;p11) in a family with hematologic malignancies. (1987) (27)
- Array comparative genomic hybridization reveals frequent alterations of G1/S checkpoint genes in undifferentiated pleomorphic sarcoma of bone (2011) (27)
- Detection of minimal residual disease using fluorescence DNA in situ hybridization: a follow-up study in leukemia and lymphoma patients. (1994) (27)
- Power of the MAC (Morphology‐Antibody‐Chromosomes) method in distinguishing reactive and clonal cells: Report of a patient with acute lymphatic leukemia, eosinophilia, and t(5;14) (1993) (27)
- Dependency detection with similarity constraints (2009) (27)
- Dedifferentiated chondrosarcoma with t(9;22)(q34;q 11‐12) (1994) (27)
- Interphase cytogenetics on paraffin sections of malignant pleural mesothelioma. A comparison to conventional karyotyping and flow cytometric studies. (1992) (27)
- Ultrastructural and chromosomal studies on manganese superoxide dismutase in malignant mesothelioma. (2004) (26)
- Digital Multiplex Ligation-Dependent Probe Amplification for Detection of Key Copy Number Alterations in T- and B-Cell Lymphoblastic Leukemia. (2017) (26)
- Epidermal Growth Factor Receptor Mutations in 510 Finnish Non–Small-Cell Lung Cancer Patients (2014) (26)
- Gain in 1q is a Common Abnormality in Phyllodes Tumours of the Breast (2003) (26)
- Two cases of an abnormal short arm of chromosome 8 (8p+) associated with mental retardation (1978) (26)
- BRAF V600E mutation does not predict recurrence after long‐term follow‐up in TNM stage I or II papillary thyroid carcinoma patients (2012) (26)
- Hotspot mutations in polyomavirus positive and negative Merkel cell carcinomas. (2016) (26)
- MicroRNA Profiling in Chemoresistant and Chemosensitive Acute Myeloid Leukemia (2013) (26)
- Chromosome abnormalities in peripheral T‐cell lymphoma (1987) (26)
- Complexity of 12q13–22 amplicon in liposarcoma: Microsatellite repeat analysis (1997) (26)
- Flow cytometric analysis of the cell cycle in polyamine-depleted cells. (1994) (25)
- LINEAGE SPECIFICITY IN HAEMATOLOGICAL NEOPLASMS (1997) (25)
- Complexity of 12q13-22 amplicon in liposarcoma: microsatellite repeat analysis. (1997) (25)
- Optimized mitogen stimulation induces proliferation of neoplastic B cells in chronic lymphocytic leukemia: significance for cytogenetic analysis (1998) (25)
- A recurrent chondromyxoid fibroma with chromosome aberrations ins(5;2)(q13;p21p25) and 2p deletion: a case report. (1993) (25)
- Trisomy 12 in B-cell chronic lymphocytic leukemia: correlation with advanced disease, atypical morphology, high levels of sCD25, and with refractoriness to treatment. (1995) (25)
- 19p13.3 Aberrations Are Associated with Dysmorphic Features and Deviant Psychomotor Development (2010) (25)
- Immunophenotype and sister chromatid differentiation: a combined methodology for analyzing cell proliferation in unfractionated lymphocyte cultures. (1990) (25)
- Hot spot mutations in Finnish non-small cell lung cancers. (2016) (24)
- Glycodelin reduces carcinoma-associated gene expression in endometrial adenocarcinoma cells. (2005) (24)
- Two novel human B‐cell lymphoma lines of lymphatic follicle origin: Cytogenetic, molecular genetic and histopathological characterisation (1994) (24)
- Comparative genomic hybridization reveals differences in DNA copy number changes between sporadic gastric carcinomas and gastric carcinomas from patients with hereditary nonpolyposis colorectal cancer. (1998) (24)
- Genetic analysis of fibrosarcoma of bone, a rare tumour entity closely related to osteosarcoma and malignant fibrous histiocytoma of bone. (2004) (24)
- Recurrent and multiple bladder tumors show conserved expression profiles (2008) (23)
- Clonal karyotype abnormalities in erythroid and granulocyte-monocyte precursors in polycythaemia vera and myelofibrosis. (2009) (23)
- Chromosome 1q+ in erythroid and granulocyte-monocyte precursors in a patient with essential thrombocythemia. (1983) (23)
- Validation of 34betaE12 immunoexpression in clear cell papillary renal cell carcinoma as a sensitive biomarker. (2017) (22)
- Polyamine starvation causes parallel increase in nuclear and chromosomal aberrations in a polyamine-dependent strain of CHO. (1983) (22)
- PPP2R1B Gene in Chronic Lymphocytic Leukemias and Mantle Cell Lymphomas (2001) (22)
- miRNA-34a underexpressed in Merkel cell polyomavirus-negative Merkel cell carcinoma (2015) (22)
- Copy number gains on 5p15, 6p11-q11, 7p12, and 8q24 are rare in sputum cells of individuals at high risk of lung cancer. (2006) (22)
- Comparison of DNA and karyotype ploidy in malignant mesothelioma. (1992) (22)
- Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm (1997) (22)
- Abnormalities of chromosomes 7 and 22 in human malignant pleural mesothelioma: Correlation between southern blot and cytogenetic analyses (1992) (21)
- Cytogenetics and molecular pathology in cancer diagnostics (2004) (21)
- miRNA expression profiles in myelodysplastic syndromes reveal Epstein–Barr virus miR-BART13 dysregulation (2011) (21)
- Prognostic classification of patients with acute lymphoblastic leukemia by using gene copy number profiles identified from array-based comparative genomic hybridization data. (2010) (21)
- MicroRNA microarrays on archive bone marrow core biopsies of leukemias--method validation. (2011) (21)
- Chromosomal effects of sodium selenite in vivo II. Aberrations in mouse bone marrow and primary spermatocytes. (2009) (21)
- Comparison of bone marrow high mitotic index metaphase fluorescence in situ hybridization to peripheral blood and bone marrow real time quantitative polymerase chain reaction on the International Scale for detecting residual disease in chronic myeloid leukemia (2008) (21)
- Genetic alterations in periprosthetic soft-tissue masses from patients with metal-on-metal hip replacement. (2015) (21)
- Maternal origin of transferrin receptor positive cells in venous blood of pregnant women (1996) (21)
- Suppression of immune system genes by methylprednisolone in exacerbations of multiple sclerosis (2004) (21)
- Aberrant expression of ALK and EZH2 in Merkel cell carcinoma (2017) (21)
- Genomic imbalances in Schistosoma-associated and non-Schistosoma-associated bladder carcinoma. An array comparative genomic hybridization analysis. (2007) (20)
- Do DNA copy number changes differentiate uterine from non-uterine leiomyosarcomas and predict metastasis? (2006) (20)
- Comparative genomic hybridization and conventional cytogenetic analyses in childhood acute myeloid leukemia. (1999) (20)
- Exhaled breath condensate as a source of biomarkers for lung carcinomas. A focus on genetic and epigenetic markers—A mini‐review (2016) (20)
- Presence of cancer-associated mutations in exhaled breath condensates of healthy individuals by next generation sequencing (2017) (20)
- Duchenne‐like muscular dystrophy in two sisters with normal karyotypes: evidence for autosomal recessive inheritance (1985) (20)
- Prognostic value of metaphase-fluorescence in situ hybridization in follow-up of patients with acute myeloid leukemia in remission. (1997) (20)
- A human follicular lymphoma B cell line hypermutates its functional immunoglobulin genes in vitro (1995) (20)
- DNA Copy Number Changes in Epithelioid Sarcoma and Its Variants: A Comparative Genomic Hybridization Study (2000) (20)
- More extensive genetic alterations in unmutated than in hypermutated cases of chronic lymphocytic leukemia (2003) (20)
- DNA copy number changes in childhood acute lymphoblastic leukemia. (1998) (20)
- Role of free radicals in genetic damage (mutation). (1984) (20)
- Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial cases (2003) (20)
- A method for analysis of cell morphology, banded karyotype, and immunoperoxidase identification of lymphocyte subset on the same cell. (1986) (20)
- Truncation of MBD4 predisposes to reciprocal chromosomal translocations and alters the response to therapeutic agents in colon cancer cells. (2008) (19)
- Gene copy number changes in dermatofibrosarcoma protuberans – a fine-resolution study using array comparative genomic hybridization (2006) (19)
- Single nucleotide polymorphism microarray analysis of karyotypically normal acute myeloid leukemia reveals frequent copy number neutral loss of heterozygosity (2008) (19)
- Clonal CD5-positive B lymphocytes in myelodysplastic syndrome with systemic vasculitis and trisomy 8 (1997) (19)
- Complex chromosomal aberrations in chronic lymphocytic leukemia are associated with cellular drug and irradiation resistance (2000) (19)
- No gene copy number changes in Dupuytren's contracture by array comparative genomic hybridization. (2008) (19)
- A novel method for gene expression mapping of metastatic competence in human bladder cancer. (2006) (19)
- Targeted resequencing of 9p in acute lymphoblastic leukemia yields concordant results with array CGH and reveals novel genomic alterations. (2013) (19)
- Chromosome band 1q21 is recurrently gained in desmoid tumors (1998) (19)
- Mitotic cells in different lymphocyte subsets in unfractionated cultures stimulated by phytohaemagglutinin or pokeweed mitogen. (2008) (19)
- Pathways affected by asbestos exposure in normal and tumour tissue of lung cancer patients (2008) (18)
- Recurrent DNA sequence copy losses on chromosomal arm 6q in capillary hemangioblastoma. (2002) (18)
- Integrated Analysis of Gene Copy Number, Copy Neutral LOH, and microRNA Profiles in Adult Acute Lymphoblastic Leukemia (2012) (18)
- Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion (2014) (18)
- The Role of Chromosomal Instability and Epigenetics in Colorectal Cancers Lacking β-Catenin/TCF Regulated Transcription (2016) (18)
- Can bladder adenocarcinomas be distinguished from schistosomiasis-associated bladder cancers by using array comparative genomic hybridization analysis? (2007) (18)
- Chromosomal abnormalities in acute promyelocytic leukaemia. (2009) (18)
- Gut Microbiota and Host Gene Mutations in Colorectal Cancer Patients and Controls of Iranian and Finnish Origin (2020) (18)
- Characterization of the 17p amplicon in human sarcomas: microsatellite marker analysis. (1997) (18)
- A microduplication on chromosome 17p13.1p13.3 including the PAFAH1B1 (LIS1) gene (2011) (18)
- Frequent deletion of CDKN2A and recurrent coamplification of KIT, PDGFRA, and KDR in fibrosarcoma of bone—An array comparative genomic hybridization study (2010) (17)
- Restoring mismatch repair does not stop the formation of reciprocal translocations in the colon cancer cell line HCA7 but further destabilizes chromosome number (2005) (17)
- No elevated sister chromatid exchange in Alzheimer's disease (1979) (17)
- Follow-up of residual disease using metaphase-FISH in patients with acute lymphoblastic leukemia in remission (1997) (17)
- Characterizing genetically stable and unstable gastric cancers by microsatellites and array comparative genomic hybridization. (2006) (17)
- Molecular Alterations at 9q33.1 and Polyploidy in Asbestos-Related Lung Cancer (2009) (17)
- Lymphotoxin beta expression is high in chronic lymphocytic leukemia but low in small lymphocytic lymphoma: a quantitative real-time reverse transcriptase polymerase chain reaction analysis. (2003) (17)
- Wide spetcrum mutational analysis of metastatic renal cell cancer: a retrospective next generation sequencing approach (2016) (17)
- Chromosomal effects of sodium selenite in vivo. I. Aberrations and sister chromatid exchanges in human lymphocytes. (2009) (17)
- The hypermethylation of the O6‐methylguanine‐DNA methyltransferase gene promoter in gliomas—correlation with array comparative genome hybridization results and IDH1 mutation (2012) (16)
- A chromosome survey of 1062 mentally retarded patients. Evaluation of a long-term study at the Rinnekoti institution, Finland. (2009) (16)
- DNA copy number losses are more frequent in primary larynx tumors with lymph node metastases than in tumors without metastases. (1999) (16)
- The proportion of mitoses in different cell lineages changes during short-term culture of normal human bone marrow. (1986) (16)
- Mapping of amplified c-myb oncogene, sister chromatid exchanges, and karyotypic analysis of the COLO 205 colon carcinoma cell line. (1985) (16)
- Appearance of bone marrow lymphocytosis predicts an optimal response to imatinib therapy in patients with chronic myeloid leukemia (2007) (16)
- The diagnostic use of cytogenetic and molecular genetic techniques in the assessment of small round cell tumours (2002) (16)
- Mutated Ephrin Receptor Genes in Non‐Small Cell Lung Carcinoma and Their Occurrence with Driver Mutations—Targeted Resequencing Study on Formalin‐Fixed, Paraffin‐Embedded Tumor Material of 81 Patients (2013) (15)
- No evidence of microsatellite instability in bone tumours. (1996) (15)
- Data-driven information retrieval in heterogeneous collections of transcriptomics data links SIM2s to malignant pleural mesothelioma (2011) (15)
- Chromosome number correlates with survival in patients with malignant pleural mesothelioma. (1992) (15)
- 3 Determination of cell morphology, immunologic phenotype and numerical chromosomal abnormalities on the same mitotic or interphase cancer cell (1989) (15)
- Gut microbiota of patients with different subtypes of gastric cancer and gastrointestinal stromal tumors (2021) (15)
- Copy number alterations and neoplasia‐specific mutations in MELK, PDCD1LG2, TLN1, and PAX5 at 9p in different neoplasias (2014) (15)
- Analysis of phenotype and genotype of individual cells in neoplasms. (1993) (15)
- DNA copy number amplifications in sarcomas with homogeneously staining regions and double minutes. (2001) (15)
- Induction of major chromosome aberrations in Chinese hamster ovary cells by alpha-difluoromethylornithine. (1984) (15)
- Colony formation by megakaryocyte progenitors in myelodysplatic syndromes (1989) (15)
- Establishment and characterisation of human papillomavirus type 16 DNA immortalised human tonsillar epithelial cell lines. (2003) (15)
- Favorable outcome in 20‐year follow‐up of children with very‐low‐risk ALL and minimal standard therapy, with special reference to TEL–AML1 fusion (2004) (14)
- Hotspot Mutations Detectable by Next-generation Sequencing in Exhaled Breath Condensates from Patients with Lung Cancer (2018) (14)
- BCR-ABL isoforms associated with intrinsic or acquired resistance to imatinib: more heterogeneous than just ABL kinase domain point mutations? (2012) (14)
- ALK fusion and its association with other driver gene mutations in Finnish non‐small cell lung cancer patients (2014) (14)
- Acute lymphoblastic leukemias with normal karyotypes are not without genomic aberrations. (2009) (14)
- Cytogenetic study of extraskeletal mesenchymal chondrosarcoma. A case report. (1996) (14)
- Simultaneous Paired Analysis of Numerical Chromosomal Aberrations and DNA Content in Osteosarcoma (2001) (14)
- An increased frequency of chromosomal changes and SCE's in cultured blood lymphocytes of 12 subjects vaccinated against smallpox (1978) (14)
- Helicobacter pylori infection activates FOS and stress‐response genes and alters expression of genes in gastric cancer–specific loci (2004) (14)
- Chromosome studies in acute lymphoblastic leukaemia (ALL). (2009) (14)
- t(11;19)(q23;p11) in a child with acute T-cell leukemia. (1985) (14)
- DNA methylation changes and somatic mutations as tumorigenic events in Lynch syndrome-associated adenomas retaining mismatch repair protein expression (2018) (14)
- Oligonucleotide array comparative genomic hybridization refines the structure of 8p23.1, 17q12 and 20q13.2 amplifications in gastric carcinomas (2007) (14)
- Monocytic involvement by monosomy 7 preceded acute myelomonocytic leukemia in a patient with myelodysplastic syndrome. (1988) (14)
- Alterations in the suppressor gene PPP2R1B in parathyroid hyperplasias and adenomas. (2002) (14)
- CB1093, a novel vitamin D analog; effects on differentiation and clonal growth on HL-60 and de novo leukemia cells. (1997) (14)
- Loss at 12p detected by comparative genomic hybridization (CGH): association with TEL-AML1 fusion and favorable prognostic features in childhood acute lymphoblastic leukemia (ALL). A multi-institutional study. (2001) (14)
- Bone marrow cytogenetics: the lineage of dividing cells changes during the first few hours in culture. (1987) (14)
- Expression Analysis of Previously Verified Fecal and Plasma Dow-regulated MicroRNAs (miR-4478, 1295-3p, 142-3p and 26a-5p), in FFPE Tissue Samples of CRC Patients. (2017) (14)
- Translocation (2;11) (p21;q23) in acute non-lymphocytic leukaemia: a non-random association. (2009) (13)
- Comparison of cytogenetics, interphase cytogenetics, and DNA flow cytometry in bone tumors. (1996) (13)
- Genetic changes including gene copy number alterations and their relation to prognosis in childhood acute myeloid leukemia (2010) (13)
- A duplication within the critical fertility region of X chromosome in a mentally retarded woman with normal menarche. (2008) (13)
- Microsatellite markers as tools for characterization of DNA amplifications evaluated by comparative genomic hybridization. (1997) (13)
- Primary Soft Tissue Sarcoma and Its Local Recurrence: Genetic Changes Studied by Comparative Genomic Hybridization (2001) (13)
- Cloning and characterization of the human t(3;6)(p14;p11) translocation breakpoint associated with hematologic malignancies. (1993) (13)
- Expression of GATA-6 transcription factor in pleural malignant mesothelioma and metastatic pulmonary adenocarcinoma (2008) (13)
- Fluorescent in situ hybridization on archival G-banded slides. (1996) (13)
- Demethylation of two specific DNA sequences in expressed human immunoglobulin light kappa constant genes (1988) (13)
- Differential roles of EPS8 in carcinogenesis: loss of protein expression in a subset of colorectal carcinoma and adenoma. (2012) (12)
- Acute erythroleukaemia with L3 morphology and the 14q+ chromosome. (2009) (12)
- Characterization of the 17p amplicon in human sarcomas: Microsatellite marker analysis (1999) (12)
- Malignant fibrous histiocytoma arising in a previous site of fracture and osteomyelitis. (1993) (12)
- Can Nucleated Erythrocytes Found in Maternal Venous Blood Be Used in the Noninvasive Prenatal Diagnosis of Fetal Chromosome Abnormalities? (1995) (12)
- Low number of DNA copy number changes in small lymphocytic lymphoma. (1998) (12)
- Driver Gene Mutations in Stools of Colorectal Carcinoma Patients Detected by Targeted Next-Generation Sequencing. (2016) (11)
- 35th Annual meeting of the European Association for the Study of Diabetes. Brussels, Belgium, 28 September-2 October, 1999. Abstracts. (1999) (11)
- Genetic susceptibility and familial malignant mesothelioma (2001) (11)
- Immunoglobulin kappa and lambda light chain dual genotype rearrangement in a patient with kappa-secreting B-CLL. (1988) (11)
- Narcolepsy patients' blood‐based miRNA expression profiling: miRNA expression differences with Pandemrix vaccination (2017) (11)
- DNA Copy Number Changes in Lung Adenocarcinoma in Younger Patients (2002) (11)
- MAC (Morphology, Antibody, Chromosomes) Method for Study of Cell Proliferation in Unfractionated Human Hematopoietic Cell Cultures (1992) (11)
- ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population. (2009) (11)
- Extracellular matrix-induced changes in expression of cell cycle-related proteins and proteasome components in endometrial adenocarcinoma cells. (2006) (10)
- Different responses of colorectal cancer cells to alternative sequences of cetuximab and oxaliplatin (2018) (10)
- Lymphatic leukaemia cell line 3447 from the dog--a karyotypic analysis. (2008) (10)
- Molecular cytogenetic study of patients with Pallister-Killian syndrome (1993) (10)
- Nucleated erythrocytes in enriched and unenriched peripheral venous blood samples from pregnant and nonpregnant women. (1994) (10)
- Chromosome pulverization in blood diseases. (2009) (10)
- Comparison of DNA and karyotype aneuploidy in malignant lymphomas. (1990) (10)
- Burkitt lymphoma and Ewing sarcoma in a child with Williams syndrome (2014) (10)
- A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat. (1995) (10)
- 9q22 Deletion - First Familial Case (2011) (9)
- Amplification at 9p in Cervical Carcinoma by Comparative Genomic Hybridization (2001) (9)
- 8;21 and 15;17 translocations: abnormalities in a single cell lineage in acute myeloid leukemia. (1994) (9)
- Loss of TP53 in sarcomas with 17p12~p11 gain. A fine-resolution oligonucleotide array comparative genomic hybridization study (2007) (9)
- Myeloid lineage involvement in acute lymphoblastic leukemia: a morphology antibody chromosomes (MAC) study. (1995) (9)
- Comparative genomic hybridization reveals changes in DNA-copy number in poor-risk neuroblastoma. (2001) (9)
- Oligoarray comparative genomic hybridization in polycythemia vera and essential thrombocythemia (2008) (9)
- Chromosomal abnormality limited to T4 lymphocytes in a patient with T‐cell chronic lymphocytic leukaemia (1990) (9)
- Gene mutations in stool from gastric and colorectal neoplasia patients by next-generation sequencing (2017) (9)
- Genetic characterization of bone and soft tissue tumors (2004) (9)
- Microbiota Alterations and Their Association with Oncogenomic Changes in Pancreatic Cancer Patients (2021) (9)
- Somatic Hypermutations in the Immunoglobulin Genes of Two New Human Lymphoma Lines of Lymphatic Follicle Origin (1994) (9)
- A new heritable fragile site on human chromosome 3. (2008) (9)
- JAK2V617F mutation and spontaneous megakaryocytic or erythroid colony formation in patients with essential thrombocythaemia (ET) or polycythaemia vera (PV). (2009) (9)
- Gene expression profiles in human mesothelioma cell lines in response to interferon-γ treatment (2004) (9)
- DNA copy number losses at 1p32-pter in monozygotic twins concordant for breast cancer. (1999) (9)
- Low Expression of miR-18a as a Characteristic of Pediatric Acute Lymphoblastic Leukemia (2017) (8)
- Monosomy of chromosome 17 in breast cancer during interpretation of HER2 gene amplification. (2015) (8)
- The human S-adenosylmethionine decarboxylase gene: nucleotide sequence of a pseudogene and chromosomal localization of the active gene (AMD1) and the pseudogene (AMD2). (1995) (8)
- t(2;5) (p23;q35)-A Specific Chromosome Abnormality in Large Cell Anaplastic (Ki-1) Lymphoma. (1990) (8)
- No DNA copy number changes in osteochondromas: a comparative genomic hybridization study. (1997) (8)
- Chromosomal effects of sodium selenite in vivo. III. Aberrations and sister chromatid exchanges in Chinese hamster bone marrow. (1980) (8)
- Identification of human specific gene duplications relative to other primates by array CGH and quantitative PCR. (2010) (8)
- MicroRNA profiling in pediatric acute lymphoblastic leukemia: novel prognostic tools (2012) (8)
- Peripheral blood cells in the study of chromosome aberrations of patients with chronic myeloid leukaemia or myelofibrosis. (1983) (8)
- Loss of TP53 in sarcomas with 17p12 to approximately p11 gain. A fine-resolution oligonucleotide array comparative genomic hybridization study. (2007) (8)
- Decreased sister chromatid exchange in Down's syndrome after measles vaccination. (2009) (8)
- A method combining morphological, immunocytochemical and chromosomal examinations of the same cell in the study of lymphoproliferative diseases (1988) (8)
- DNA-fingerprint changes compared to karyotypes in acute leukemia. (1990) (8)
- RAF-1 over-expression does condition survival of patients affected by aggressive mantle cell lymphoma. (2007) (7)
- Involvement of natural killer cells in chronic myeloid leukemia. (1995) (7)
- Familial 6p22.2 duplication associates with mild developmental delay and increased SSADH activity (2011) (7)
- MAC technique (morphology antibody chromosomes) in phenotypic identification of proliferating NK and T cells in interleukin-2-stimulated lymphocyte cultures. (1989) (7)
- Ploidy in bone marrow cells from healthy donors: a MAC (morphology antibody chromosomes) study (1994) (7)
- High-resolution oligonucleotide array comparative genomic hybridization study and methylation status of the RPS14 gene in de novo myelodysplastic syndromes. (2010) (7)
- A novel splice site mutation of the EXT2 gene in a Finnish hereditary multiple exostoses family. Mutations in brief no. 197. Online. (1998) (7)
- Reprofiling Metastatic Samples for Chromosome 9p and 14q Aberrations as a Strategy to Overcome Tumor Heterogeneity in Clear-cell Renal Cell Carcinoma (2017) (7)
- Lineage involvement and karyotype in a patient with myelodysplasia and blood basophilia (1994) (7)
- Correlation between bone marrow karyotype and the occurrence of erythroblast micronuclei and nuclear budding in patients with myelodysplastic syndromes (1987) (6)
- In vivo method for sister chromatid exchanges in Chinese hamster foetal and bone marrow cells. (2009) (6)
- Gene expression profiles in human mesothelioma cell lines in response to interferon-gamma treatment. (2004) (6)
- Sister chromatid differentiation and chromosomal in situ suppression hybridization: a combined methodology for analyzing cell proliferation and SCEs in individual chromosomes. (1992) (6)
- Long-term use of phenytoin: effects on bone-marrow chromosomes in man. (1977) (6)
- The inheritance of fragile sites: apparent absence of fra(2)(q13) in the parents of three unrelated probands. (1987) (6)
- Clinical and practical value of metaphase fluorescent in situ hybridization in follow-up after allogeneic stem cell transplantation in chronic myeloid leukemia. (2004) (6)
- New Insights into the Cellular Pathways Affected in Primary Uterine Leiomyosarcoma. (2006) (6)
- A cloned human germ cell tumor‐derived cell line differentiating in culture (1998) (6)
- Concordant Results of Epidermal Growth Factor Receptor Mutation Detection by Real-Time Polymerase Chain Reaction and Ion Torrent Technology in Non-Small Cell Lung Cancer (2016) (6)
- Heteromorphic X Chromosomes in 46,XX males? (1979) (6)
- Characterization of neoplastic and reactive cells in T‐cell lymphomas with cytogenetic, surface marker, and DNA methods (1989) (6)
- Report of interstitial 22q13.1q13.2 microduplication in two siblings with distinctive dysmorphic features, heart defect and mental retardation. (2013) (6)
- Major and minor breakpoint sites of chromosomal translocation t(14;18) in subtypes of non-Hodgkin's lymphomas. (1994) (6)
- Trisomy 7 in non-neoplastic tubular epithelial cells of the kidney (1995) (6)
- Etiology of specific molecular alterations in human malignancies (2007) (6)
- Y chromosome instability in lymphoproliferative disorders. (2003) (5)
- CGHpower: exploring sample size calculations for chromosomal copy number experiments (2010) (5)
- High dietary selenium increases radiation-induced micronucleus formation in mouse bone marrow. (2008) (5)
- Philadelphia chromosome as the sole abnormality and p210 bcr-abl chimeric protein expression in an Epstein-Barr virus-transformed B cell line from a patient with chronic myeloid leukemia. (1993) (5)
- Long-term of phenytoin: Effects on whole blood and red cell folate and haematological parameters. (2009) (5)
- Chromosomal effects of sodium selenite in vivo (2009) (5)
- Requirement of CD4+ Lymphocytes in IL‐2‐Stimulated NK Cell Proliferation (1995) (5)
- Chromosomal abnormalities in human malignant mesothelioma (1994) (5)
- Lymphoid involvement in a patient with acute myeloid leukemia: A direct phenotypic and genotypic study of single cells (1996) (5)
- Spa-RQ: an Image Analysis Tool to Visualise and Quantify Spatial Phenotypes Applied to Non-Small Cell Lung Cancer (2019) (5)
- Effect of a low-molecular-weight B cell growth factor on the proliferation of normal and neoplastic lymphocytes in lymphomas. (1990) (5)
- ALK gene copy number in lung cancer: Unspecific polyploidy versus specific amplification visible as double minutes. (2017) (5)
- Cryopreserved chronic lymphocytic leukemia cells analyzed by multicolor fluorescence in situ hybridization after optimized mitogen stimulation (2002) (5)
- Critical chromosome rearrangement in acute promyelocytic leukemia. (1984) (5)
- Variation in sister chromatid exchange frequencies and cell-cycle kinetics between human whole blood and plasma leukocyte cultures (1996) (5)
- Allogeneic stem cell transplantation reverses the poor prognosis of CML patients with deletions in derivative chromosome 9 (2005) (5)
- Erratum: Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion (2017) (4)
- Chromosome study of 249 patients examined for a bone tumor. (1993) (4)
- Oncogenomic Changes in Pancreatic Cancer and Their Detection in Stool (2022) (4)
- Prenatal sex determination by in situ hybridization on fetal nucleated cells in maternal whole venous blood (1994) (4)
- Chromosomal abnormalities in bone-marrow cells and in cultured lymphocytes in a variety of human viral infections. (1977) (4)
- Pig plasma modulates cell cycle kinetics but not the baseline frequency of sister-chromatid exchanges in human lymphocytes. (1993) (4)
- Polyploid mitoses in human bone-marrow cells. (2009) (4)
- Gains and losses of DNA sequences in osteosarcomas by comparative genome hybridization (1995) (4)
- The pattern of methylation in rearranged and germ-line human immunoglobulin constant mu genes. (1987) (4)
- Homozygous deletions of cadherin genes in chondrosarcoma-an array comparative genomic hybridization study. (2012) (4)
- A mentally and physically retarded girl with a familial balanced reciprocal translocation t(7;13). (2009) (4)
- Immunophenotyping and molecular cytogenetics. (1992) (3)
- Simultaneous detection of high-resolution R-banding and fluorescence in situ hybridization signals after fluorouracil-induced cellular synchronization. (2004) (3)
- Effect of difluoromethylornithine on chromosomes in living organisms and in tissue culture cells. (2008) (3)
- Cytogenetic chromosomal preparations using 2-methoxyestradiol. (1998) (3)
- Simultaneous Underexpression of let-7 a-5 p and let-7 f-5 p microRNAs in Plasma and Stool Samples from Early Stage Colorectal Carcinoma : Supplementary Issue : Biomarkers for Colon (3)
- Malignant Mesothelioma: Molecular Markers (2020) (3)
- Malignant Mesothelioma: Mechanism of Carcinogenesis (2020) (3)
- Molecular karyotyping in sarcoma diagnostics and research. (2006) (3)
- Notable chromosomal anomalies in a woman receiving drugs during the period of viremia after rubella vaccination. (2009) (3)
- Absence of trisomy 7 in nonneoplastic human ascitic and pleural fluid cells. An interphase cytogenetic study. (1994) (3)
- Follow-up of Minimal Residual Disease in Pediatric Acute Myeloblastic Leukemia Using Metaphase-FISH (2002) (2)
- Combination of In Situ Hybridization Cytogenetics and Immunologic Cell Identification in Diagnosing Minimal Residual Disease (1992) (2)
- [MicroRNAs and cancer]. (2013) (2)
- Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes (2016) (2)
- DNA sequence copy number changes in lipomatous tumors (1997) (2)
- 60 Asbestos-associatedmalignancies in the lung and pleura show distinct genetic aberrations (2006) (2)
- Comparative genomic hybridization technique. (2001) (2)
- ISH and PCR Study with Y‐Specific Probe/Primers a (1994) (2)
- Exhaled breath condensates as a method for detection of mutations in lung cancer patients by next generation sequencing (2017) (2)
- Trisomy 12 in hematologic disorders [letter] (1980) (2)
- Radiation therapy for breast cancer and clonal chromosome translocations: a fluorescence in situ hybridization study. (1998) (2)
- The fluorescence pattern of a human Yq Plus chromosome. (1972) (2)
- Chromosome 7 in glioblastoma tissue. Parenchymal vs. endothelial cells. (1995) (2)
- Trisomy 12 in hematologic disorders. (1980) (2)
- Chromosomal abnormalities in malignant pleural mesothelioma (1987) (1)
- JAK2 Gene Is Mutated in Patients with Myeloproliferative Disorders and Spontaneous Erythroid Colony Formation but Not in Patients with Spontaneous Megakaryocyte Growth Only. (2006) (1)
- Mesothelioma and lung carcinomas (1997) (1)
- Tumors of the lung (2015) (1)
- No DNA sequence copy number changes in essential thrombocythemia. (2001) (1)
- Morphology Antibody Chromosome Technique for Determining Phenotype and Genotype of the Same Cell (2005) (1)
- Simultaneous detection of immunophenotype and genome by the MAC method. (1993) (1)
- Combined RT‐PCR and Metaphase‐FISH Posttransplant Studies in Pediatric Patients with Chronic Myeloid Leukemia (1998) (1)
- Karyotype and BCR studies after bone marrow transplantation for chronic myeloid leukaemia. (1991) (1)
- Low Epression of MiR-18a Distinguishes Pediatric and Adult Acute Lymphoblastic Leukemia from Each Other (2015) (1)
- Molecular cytogenetic applications in leukemias. (1993) (1)
- IL-4 and 12 kD B cell growth factor promote IL-2-induced NK cell proliferation (1991) (1)
- An integrated analysis of miRNA and gene copy numbers in xenografts of Ewing's sarcoma (2012) (1)
- Mutations by Next Generation Sequencing in Stool DNA from Colorectal Carcinoma Patients - A Literature Review and our Experience with this Methodology (2016) (1)
- Down-regulation of miR-181c in imatinib-resistant chronic myeloid leukemia (2013) (1)
- MMC-E cells--origin and changes in karyotype accompanying malignant transformation. (1985) (1)
- Occurrence of Nucleated Erythrocytes in Peripheral Blood of Pregnant Women (1994) (1)
- Journal size increases to four volumes per year Editorial Board additions (1995) (1)
- Minimal residual disease by metaphase FISH in children with ALL: clonal cells during or after chemotherapy may not predict relapse. (2002) (1)
- Inducible fragile site on chromosome 3 (2004) (1)
- Gene expression profiling of mantle cell lymphoma and its blastoid variant (2001) (1)
- Superior Survival of Ewing Sarcoma Family of Tumor Patients Associates With High Expression of C5 at Tumor Site (2009) (0)
- Duchenne like muscular dystrophy in two sisters: evidence for autosomal recessive inheritance (1984) (0)
- 672: ALK fusion in a cohort of 469 Finnish patients with non-small cell lung cancer (2014) (0)
- Psoriasis Cured in Biological Dietary Therapy with a Lymphopoietic Ti-lipid Spinal Cord Factor Simulating Anti-angiogenesis, also Analyzed with MicroRNA Profiling (2013) (0)
- Abstract 5196: Different miRNAs expression in leiomyosarcoma and undifferentiated pleomorphic sarcoma (2014) (0)
- Phenotype of Mitotic Cells in Hematologic Malignancies (2011) (0)
- DNA copy number changes in chondrosarcomas. Comparative genomic hybridization study (1996) (0)
- Subject Index, Vol. 90, 1993 (1993) (0)
- Cytogenetic and Molecular Genetic Alterations in Bone Tumors (2010) (0)
- O17: Characterization of primary gastric tumors with CGH and expression microarray analyses (2005) (0)
- Morphology Antibody Chromosome Technique for Determining Phenotype and Genotype of the Same Cell (1996) (0)
- Subject Index, Vol. 73, 1996 (1996) (0)
- Digital MLPA(TM) for copy number detection in childhood acute lymphoblasic leukemia : a novel multiplex NGS-based assay (2016) (0)
- allogeneic bone marrow transplantation for t(8;21) leukemia Persistence of the AML1/ETO fusion transcript in patients treated with (2011) (0)
- Different responses of colorectal cancer cells to alternative sequences of cetuximab and oxaliplatin (2018) (0)
- Predictive Biomarkers and Personalized Medicine Hsa-miR-31-3 p Expression Is Linked to Progression-free Survival in Patients with KRAS Wild-type Metastatic Colorectal Cancer Treated with Anti-EGFR Therapy (2014) (0)
- Contents Vol. 115, 2006 (2006) (0)
- [Not Available]. (2006) (0)
- A Novel Multiplex NGS-Based Digital MLPA Assay for Copy Number Detection of 700 Target Sequences in Childhood Acute Lymphoblastic Leukemia (2016) (0)
- Gene expression profiling of malignant mesothelioma cell lines treated with IFN-gamma (2001) (0)
- 102 DNA copy number profiling in malignant pleural mesothelioma by array CGH (2006) (0)
- Meta- and synchronous urothelial carcinomas with divergent genomic profiles show highly similar gene-expression profiles (2006) (0)
- Comparative genomic hybridization in phyllodes tumors of the breast (2001) (0)
- Novel amplification and deletions in osteosarcomas detected by comparative genomic hybridization (1994) (0)
- Editorial Expression of Concern: Gene expression profile by blocking the SYT-SSX fusion gene in synovial sarcoma cells. Identification of XRCC4 as a putative SYT-SSX target gene (2022) (0)
- Chapter 28 – Cytogenetic and molecular genetic alterations in bone tumors (2015) (0)
- P-253 Copy number changes on CEP6, 5p15, 8q24 and 7p12 in sputum samples of asbestos exposed individuals (2005) (0)
- Aberrant expression of ALK and EZH2 in Merkel cell carcinoma (2017) (0)
- Genetic analysis using microarrays. (2001) (0)
- Genetic Changes in Tumours by Microarray Analysis (2002) (0)
- Promoter analysis of co-expressing genes after exposure to asbestos: P2-023 (2007) (0)
- MAC (morphology-antibody-chromosome) method in cytogenetic study of lymphomas (1987) (0)
- Morphology Antibody Chromosome Technique for Determining Phenotype and Genetic Status of the Same Cell (1996) (0)
- Two chromosome fragments in a child with Down's syndrome and transient chromosome aberrations in the mother. (1983) (0)
- [Identification of fetal chromosome abnormalities and gene defects from maternal blood]. (1993) (0)
- MAC (morphology antibody chromosomes) technique for in situ chromosome preparations (1991) (0)
- Direct Demonstration of Lineage Specificity in Hematologic Neoplasms (1997) (0)
- Myllykangas et al. Helicobacter pylori Infection Activates FOS and Stress‐Response Genes and Alters Expression of Genes in Gastric Cancer–Specific Loci. Genes Chromosomes Cancer 2004; 40:334–341 (2004) (0)
- Microarray screening and microsatellite analysis suggest the significance of allelic imbalance of 19p-region in asbestos-associated lung cancer (2007) (0)
- Digital Multiplex Ligation-Dependent Probe Ampli fi cation for Detection of Key Copy Number (2017) (0)
- Contents Vol. 136, 2012 (2012) (0)
- Contents Vol. 141, 2013 (2013) (0)
- Dr. John L. Hamerton steps-down from the Associate Editorship (1995) (0)
- The fluorescence pattern of a human Yq+ chromosome (2009) (0)
- Pathway analysis suggests novel biological processes, molecular functions and cellular components for asbestos-related lung carcinogenesis (2007) (0)
- A leukemia-enriched cDNA microarray platform identifies new transcripts with relevance to the biology of leukemias. (2005) (0)
- Supplementary material 1 (2015) (0)
- Role of clozapine in the occurrence of chromosomal abnormalities in human bone-marrow cells in vivo and in cultured lymphocytes in vitro (1977) (0)
- 376 POSTER NAV3–anovel cancer biomarker (2008) (0)
- Asbestos- and histology-related microRNAs in lung cancer (2011) (0)
- 86 Cytogenetic studies on human breast carcinomas (1989) (0)
- Novel DNA Copy Number Changes in Hematological Malignancies: A cDNA-Based CGH Microarray Screening of CML, AML and CLL Cases without Chromosomal Imbalances in G-Banding. (2004) (0)
- Analysis of Previously Verified Fecal and Plasma Dow-regulated MicroRNAs in FFPE Tissue Samples of CRC Patients (2017) (0)
- The 17q in upper GI malignancies (2003) (0)
- Erratum to: high-resolution SNP array analysis of patients with developmental disorder and normal array CGH result (2014) (0)
- Front & Back Matter (2012) (0)
- Stem Cell Transplantation Clinical and practical value of metaphase fluorescence in situ hybridization in follow-up after allogeneic stem cell transplantation in chronic myeloid leukemia (2004) (0)
- P150 Expression of ZAP-70, RAF-1 and C-MYC in B-cell lymphomas and chronic leukaemia. Overexpression of ZAP70 predicts poor survival in mantle cell lymphoma (2007) (0)
- [DNA analysis of the Philadelphia chromosome: a useful application of molecular biology]. (1986) (0)
- Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by CISS hybridization in a case of RARS complicating the course of PNH (1991) (0)
- Altered expression of myeloperoxidase precursor, myeloid cell nuclear differentiation antigen, Fms-related tyrosine kinase 3 ligand, and antigen CD11A genes in leukocytes of clozapine-treated schizophrenic patients. (2006) (0)
- Comparative genomic hybridization and its application to malignant pleural mesothelioma (1996) (0)
- Contents, Vol. 90, 1993 (1993) (0)
- A NUMBER OF recurring chromosome translocations (2011) (0)
- [Clinical molecular cytogenetics]. (1993) (0)
- Acute Lymphoblastic Leukemia with “Normal” Karyotype is not without Genomic Aberrations. (2008) (0)
- Subject Index Vol. 92, 2001 (2001) (0)
- Detection of cancer associated mutations in exhaled breath condensates of healthy subjects by next generation sequencing. (2017) (0)
- 132 Malignant pleural mesothelioma: Chromosome and DNA analysis (1989) (0)
- The Lymphatic leukaemia cell line 3447 of dog-1-a karyotypic analysis (1987) (0)
- PD-024 Expression of High Mobility Group A proteins in lung cancer correlates with survival (2005) (0)
- [The use of polymerase chain reaction in the diagnosis of non-Hodgkin's lymphoma]. (1990) (0)
- [Diagnosis of soft tissue tumors--multidisciplinary collaboration]. (2015) (0)
- Lead article Changes in apoptosis-related pathways in acute myelocytic leukemia (2003) (0)
- Defect in Acute Myeloid Leukemia with Trisomy 11 as a Recurrent Molecular ALL 1 Partial Tandem Duplication of Updated (2006) (0)
- 551 DNA copy number changes in non-small cell lung cancer (NSCLC) (1997) (0)
- 2.O.03 PROGNOSIS AND THERAPEUTIC TARGETS IN THE EWING FAMILY OF TUMOURS – 6TH FRAMEWORK PROGRAMME (2010) (0)
- Contents Vol. 118, 2007 (2007) (0)
- Frequent DNA copy number changes in mantle cell lymphoma: Gain of 3q and loss of 11q22 (1997) (0)
- 820PLOSS OF CHROMOSOMES 9P AND 14Q: RE-PROFILING METASTATIC TISSUE FOR RE-TARGETING PATIENTS WITH METASTATIC RENAL CELL CARCINOMA. (2014) (0)
- DNA gains and losses in gastrointestinal tract stromal tumors, leiomyomas, and leiomyosarcomas using comparative genomic hybridization (1997) (0)
- Theinheritance offragile sites: apparentabsence offra(2)(q13) intheparentsofthreeunrelated probands (1987) (0)
- Acquired Extramedullary Resistance to Dasatinib Due to Selection of Philadelphia-Positive Lymphoblast Clone Harboring a T315I BCR-ABL Gene Mutation: Reversal by Dose Escalation and Hydroxyurea. (2005) (0)
- Radio(Chemo)therapy of Non-Small Cell Lung Cancer (2016) (0)
- cytogenetic study Trisomy 12 in chronic lymphocytic leukemia: an interphase (2011) (0)
- Amplification of 17q12–21 in sporadic gastric carcinomas but not in gastric carcinoma from patients with hereditary nonpolyposis colorectal cancer (1998) (0)
- Biomarker analysis in human neoplasias: superior next-generation sequencing on frozen bone marrow cells and on formalin-fixed, paraffin-embedded tumor tissues (2013) (0)
- TP53 and NRAS are the Most Frequently Mutated Genes in Stool DNA of CRC Patients from Central Part of Iran (2021) (0)
- Discontinuity of 12q13-22 amplicon in liposarcoma — microsatellite repeat analysis (1996) (0)
- Subject Index, Vol. 70, 1995 (1995) (0)
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What Schools Are Affiliated With Sakari Knuutila?
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