# | Title | Journal | Year | Citations |
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1 | Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases and remarkable consistency of t(11;22)(q24;q12) | Cancer Genetics and Cytogenetics | 1988 | 488 |
2 | Karyotypes in 90 human gliomas | Cancer Genetics and Cytogenetics | 1992 | 413 |
3 | Cytogenetic findings in 200 patients with multiple myeloma | Cancer Genetics and Cytogenetics | 1995 | 343 |
4 | Application of long-term collagenase disaggregation for the cytogenetic analysis of human solid tumors | Cancer Genetics and Cytogenetics | 1986 | 341 |
5 | Abnormal sexual differentiation and neoplasia | Cancer Genetics and Cytogenetics | 1987 | 332 |
6 | The 5q− anomaly | Cancer Genetics and Cytogenetics | 1985 | 327 |
7 | Molecular genotyping shows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer | Cancer Genetics and Cytogenetics | 1996 | 317 |
8 | A nonrandom chromosomal abnormality, del 3p(14–23), in human small cell lung cancer (SCLC) | Cancer Genetics and Cytogenetics | 1982 | 311 |
9 | Cytogenetic characterization of selected small round cell tumors of childhood | Cancer Genetics and Cytogenetics | 1986 | 298 |
10 | Chromosome study of Ewing's Sarcoma (ES) cell lines. Consistency of a reciprocal translocation t(11;22)(q24;q12) | Cancer Genetics and Cytogenetics | 1984 | 296 |
11 | Bloom's syndrome. XX. The first 100 cancers | Cancer Genetics and Cytogenetics | 1997 | 290 |
12 | Are chromosome aberrations in circulating lymphocytes predictive of future cancer onset in humans? Preliminary results of an Italian cohort study | Cancer Genetics and Cytogenetics | 1995 | 286 |
13 | Cytological and cytogenetical studies on human meningioma | Cancer Genetics and Cytogenetics | 1982 | 276 |
14 | Down's syndrome and leukemia: Epidemiology, genetics, cytogenetics and mechanisms of leukemogenesis | Cancer Genetics and Cytogenetics | 1987 | 256 |
15 | Leukemia and preleukemia in Fanconi anemia patients | Cancer Genetics and Cytogenetics | 1991 | 247 |
16 | A cytogenetic study of 53 human gliomas | Cancer Genetics and Cytogenetics | 1989 | 240 |
17 | Chromosome pattern, occupation, and clinical features in patients with acute nonlymphocytic leukemia | Cancer Genetics and Cytogenetics | 1981 | 239 |
18 | Cytogenetic studies of adipose tissue tumors. II. Recurrent reciprocal translocation t(12;16)(q13;p11) in myxoid liposarcomas | Cancer Genetics and Cytogenetics | 1986 | 235 |
19 | Consistent chromosomal translocation in alveolar rhabdomyosarcoma | Cancer Genetics and Cytogenetics | 1986 | 230 |
20 | Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: osteosarcoma and related tumors | Cancer Genetics and Cytogenetics | 2003 | 230 |
21 | Convention on nomenclature for DNA cytometry | Cancer Genetics and Cytogenetics | 1984 | 216 |
22 | Fluorodeoxyuridine synchronization of bone marrow cultures | Cancer Genetics and Cytogenetics | 1983 | 209 |
23 | Cytogenetics of human brain tumors | Cancer Genetics and Cytogenetics | 1990 | 208 |
24 | Characterization of chromosomal anomalies in human breast cancer | Cancer Genetics and Cytogenetics | 1990 | 206 |
25 | Cytogenetics of human malignant melanoma and premalignant lesions | Cancer Genetics and Cytogenetics | 1984 | 198 |
26 | Translocation involving chromosome 22 in Ewing's Sarcoma. A cytogenetic study of four fresh tumors | Cancer Genetics and Cytogenetics | 1984 | 197 |
27 | Chromosome 1 aberrations in cancer | Cancer Genetics and Cytogenetics | 1986 | 194 |
28 | Cytogenetic studies on African Burkitt's lymphoma cell lines: t(8;14), t(2;8) and t(8;22) translocations | Cancer Genetics and Cytogenetics | 1981 | 193 |
29 | An update of HNPCC (Lynch syndrome) | Cancer Genetics and Cytogenetics | 1997 | 190 |
30 | A direct bone marrow chromosome technique for acute lymphoblastic leukemia | Cancer Genetics and Cytogenetics | 1984 | 188 |
31 | Cytogenetic analysis of 109 pediatric central nervous system tumors | Cancer Genetics and Cytogenetics | 1993 | 188 |
32 | Structural chromosomal abnormalities in human medulloblastoma | Cancer Genetics and Cytogenetics | 1988 | 185 |
33 | Recurrent chromosomal defects are found in most patients with non-Hodgkin's-lymphoma | Cancer Genetics and Cytogenetics | 1984 | 184 |
34 | Genetic studies on hydatidiform moles. I. The origin of partial moles | Cancer Genetics and Cytogenetics | 1982 | 183 |
35 | The Journal “Impact Factor” | Cancer Genetics and Cytogenetics | 1998 | 183 |
36 | i(12p): Specific chromosomal marker in seminoma and malignant teratoma of the testis? | Cancer Genetics and Cytogenetics | 1983 | 179 |
37 | Double minutes in human tumor cells | Cancer Genetics and Cytogenetics | 1982 | 178 |
38 | Molecular biology and genetics of human neuroblastoma | Cancer Genetics and Cytogenetics | 1989 | 176 |
39 | Progressive telomere shortening and telomerase reactivation during hepatocellular carcinogenesis | Cancer Genetics and Cytogenetics | 1997 | 176 |
40 | Karyotypic evolution in human malignant melanoma | Cancer Genetics and Cytogenetics | 1986 | 174 |
41 | Abnormalities of chromosome 1p in human neuroblastoma tumors and cell lines | Cancer Genetics and Cytogenetics | 1982 | 173 |
42 | Cytogenetic study of B-cell lymphoma of mucosa-associated lymphoid tissue | Cancer Genetics and Cytogenetics | 1992 | 173 |
43 | Frequent Hypomethylation in Wilms Tumors of Pericentromeric DNA in Chromosomes 1 and 16 | Cancer Genetics and Cytogenetics | 1999 | 173 |
44 | Pathogenesis of adult testicular germ cell tumors | Cancer Genetics and Cytogenetics | 1990 | 169 |
45 | Bilateral retinoblastoma with ectopic intracranial retinoblastoma: Trilateral retinoblastoma | Cancer Genetics and Cytogenetics | 1982 | 168 |
46 | Cytogenetic and fluorescence in situ hybridization investigation of ring chromosomes characterizing a specific pathologic subgroup of adipose tissue tumors | Cancer Genetics and Cytogenetics | 1993 | 167 |
47 | Analysis of the p16INK4, p14ARF, p15, TP53, and MDM2 Genes and Their Prognostic Implications in Osteosarcoma and Ewing Sarcoma | Cancer Genetics and Cytogenetics | 2000 | 166 |
48 | Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors. Synovial sarcoma | Cancer Genetics and Cytogenetics | 2002 | 166 |
49 | Gain at chromosomal region 5p15.33, containing TERT, is the most frequent genetic event in early stages of non-small cell lung cancer | Cancer Genetics and Cytogenetics | 2008 | 162 |
50 | Is the chromosomal region 9q34 always involved in variants of the Ph1 translocation? | Cancer Genetics and Cytogenetics | 1984 | 160 |