Cees J. Cornelisse
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Philosophy Biology
Cees J. Cornelisse's Degrees
- PhD Genetics University of California, Berkeley
- Doctorate Medicine Stanford University
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(Suggest an Edit or Addition)Cees J. Cornelisse's Published Works
Number of citations in a given year to any of this author's works
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
- Identification of the breast cancer susceptibility gene BRCA2 (1995) (2451)
- Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. (2000) (1616)
- Identification of the breast cancer susceptibility gene BRCA2 (1996) (1451)
- A new method to detect apoptosis in paraffin sections: in situ end-labeling of fragmented DNA. (1993) (837)
- Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations. (1998) (700)
- Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype (2005) (667)
- Micrometastases and survival in stage II colorectal cancer. (1998) (617)
- Familial endometrial cancer in female carriers of MSH6 germline mutations (1999) (465)
- BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients (1997) (452)
- CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies. (2004) (442)
- Instability of short tandem repeats (microsatellites) in human cancers (1994) (440)
- Amplification of the neu (c-erbB-2) oncogene in human mammmary tumors is relatively frequent and is often accompanied by amplification of the linked c-erbA oncogene (1987) (348)
- Rapid detection of BRCA1 mutations by the protein truncation test (1995) (334)
- Simultaneous loss of E‐cadherin and catenins in invasive lobular breast cancer and lobular carcinoma in situ (1997) (304)
- Positional cloning of the Fanconi anaemia group A gene (1996) (296)
- Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes. (1988) (256)
- Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q. (1991) (234)
- DNA ploidy and survival in breast cancer patients. (1987) (228)
- Somatic genetic changes in human breast cancer. (1994) (225)
- At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma. (1989) (223)
- Cell-cycle-related staining patterns of anti-proliferating cell nuclear antigen monoclonal antibodies. Comparison with BrdUrd labeling and Ki-67 staining. (1991) (222)
- Amplification of genes within the chromosome 11q13 region is indicative of poor prognosis in patients with operable breast cancer. (1992) (213)
- A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter. (1992) (207)
- TP53 mutations and breast cancer prognosis: Particularly poor survival rates for cases with mutations in the zinc‐binding domains (1995) (206)
- Complete sequencing of TP53 predicts poor response to systemic therapy of advanced breast cancer. (2000) (202)
- Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients (2000) (196)
- Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter tts DNA-binding specificity. (2002) (186)
- Nuclear distribution of the Ki-67 antigen during the cell cycle: comparison with growth fraction in human breast cancer cells. (1989) (185)
- Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene (2001) (180)
- A common variant of the methylenetetrahydrofolate reductase gene (1p36) is associated with an increased risk of cancer. (2003) (171)
- Myocardial changes in pressure overload-induced left ventricular hypertrophy. A study on tissue composition, polyploidization and multinucleation. (1991) (168)
- Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21. (1986) (166)
- Tumor ploidy as a major prognostic factor in advanced ovarian cancer (1987) (166)
- Genetic susceptibility for breast cancer: how many more genes to be found? (2007) (160)
- Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization. (1990) (153)
- Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families (2004) (153)
- Does Intervention Improve the Natural Course of Glomus Tumors? (1992) (152)
- A genome wide linkage search for breast cancer susceptibility genes (2006) (146)
- Flow cytometric detection of aneuploidy in colorectal adenomas. (1985) (143)
- Comparative genomic hybridization profiles in human BRCA1 and BRCA2 breast tumors highlight differential sets of genomic aberrations. (2005) (142)
- Molecular genetic evidence for the conversion hypothesis of the origin of malignant mixed Müllerian tumours (1997) (136)
- The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families. (2003) (134)
- The relationship of DNA aneuploidy to molecular genetic alterations in colorectal carcinoma. (1992) (122)
- Establishment and characterization of 7 ovarian carcinoma cell lines and one granulosa tumor cell line: Growth features and cytogenetics (1993) (120)
- DNA Cytometry Consensus Conference. Consensus review of the clinical utility of DNA cytometry in carcinoma of the breast. (1993) (119)
- Breast cancer survival and tumor characteristics in premenopausal women carrying the CHEK2*1100delC germline mutation. (2006) (119)
- Ever since Knudson. (2001) (115)
- Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma. (1991) (112)
- Intronic variants in BRCA1 and BRCA2 that affect RNA splicing can be reliably selected by splice‐site prediction programs (2009) (110)
- Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13. (1995) (110)
- Loss of heterozygosity and DNA ploidy point to a diverging genetic mechanism in the origin of peripheral and central chondrosarcoma (1999) (108)
- Subdivision of S-phase by analysis of nuclear 5-bromodeoxyuridine staining patterns. (1989) (104)
- Somatic genetic changes on chromosome 18 in breast carcinomas: is the DCC gene involved? (1991) (102)
- Evidence for a gene on 17p13.3, distal to TP53, as a target for allele loss in breast tumors without p53 mutations. (1994) (102)
- Immunoglobulin containing cells in inflammatory bowel disease of the colon: a morphometric and immunohistochemical study. (1980) (101)
- HNPCC versus sporadic microsatellite-unstable colon cancers follow different routes toward loss of HLA class I expression (2007) (99)
- At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer. (1994) (94)
- Differential gene expression in ovarian tumors reveals Dusp 4 and Serpina 5 as key regulators for benign behavior of serous borderline tumors. (2005) (93)
- Flow cytometric analysis of DNA stemline heterogeneity in primary and metastatic breast cancer. (1991) (88)
- Inactivation of SDH and FH cause loss of 5hmC and increased H3K9me3 in paraganglioma/pheochromocytoma and smooth muscle tumors (2015) (86)
- FBXO31 is the chromosome 16q24.3 senescence gene, a candidate breast tumor suppressor, and a component of an SCF complex. (2005) (83)
- Impact of Age at Primary Breast Cancer on Contralateral Breast Cancer Risk in BRCA1/2 Mutation Carriers. (2016) (82)
- Specificity of seven monoclonal antibodies against p53 evaluated with Western blotting, immunohistochemistry, confocal laser scanning microscopy, and flow cytometry. (1997) (81)
- Sequence heterogeneity within the human alphoid repetitive DNA family. (1986) (78)
- PCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue. (1993) (78)
- Localization and polymorphism of a chromosome 12-specific alpha satellite DNA sequence. (1990) (78)
- High frequency of BRCA1 5382insC mutation in Russian breast cancer patients. (2006) (78)
- Founder mutations in early-onset, familial and bilateral breast cancer patients from Russia (2007) (76)
- Presymptomatic testing for BRCA1 and BRCA2: how distressing are the pre-test weeks? Rotterdam/Leiden Genetics Working Group. (1999) (74)
- Karyotyping and DNA flow cytometry of mature residual teratoma after intensive chemotherapy of disseminated nonseminomatous germ cell tumor of the testis: a report of two cases. (1986) (73)
- Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions. (1993) (73)
- CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3. (2002) (73)
- Prognostic impact of BRCA1 pathogenic and BRCA1/BRCA2 unclassified variant mutations in patients with ovarian carcinoma (2005) (71)
- P53 gene mutations in osteosarcomas in the dog. (1997) (70)
- Use of morphometry and immunohistochemistry of small intestinal biopsy specimens in the diagnosis of food allergy. (1980) (68)
- Consensus review of the clinical utility of DNA cytometry in carcinoma of the breast (1993) (68)
- P53 mutations in mammary tumor cell lines and corresponding tumor tissues in the dog. (1996) (67)
- Further Localization of the Gene for Hereditary Paragangliomas and Evidence for Linkage in Unrelated Families (1994) (66)
- Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomes. (1990) (62)
- A targeted mouse Brca1 mutation removing the last BRCT repeat results in apoptosis and embryonic lethality at the headfold stage (2001) (62)
- NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia (2005) (61)
- Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL (1994) (60)
- Repositioning the hereditary paraganglioma critical region on chromosome band 11q23 (1999) (57)
- Recent developments in the molecular genetic understanding of breast cancer. (1994) (56)
- Flow cytometric analysis of DNA ploidy in canine mammary tumors. (1988) (54)
- Men at risk of being a mutation carrier for hereditary breast/ovarian cancer: an exploration of attitudes and psychological functioning during genetic testing (2001) (54)
- Molecular genetic analysis of flow-sorted ovarian tumour cells: improved detection of loss of heterozygosity. (1994) (52)
- Simultaneous measurement of two cellular antigens and DNA using fluorescein-isothiocyanate, R-phycoerythrin, and propidium iodide on a standard FACScan. (1994) (51)
- Statistical methods in interphase cytogenetics: an experimental approach. (1993) (51)
- The relevance of morphometry in the differential diagnosis of cutaneous T cell lymphomas (1981) (50)
- Feasibility of in situ hybridisation with chromosome specific DNA probes on paraffin wax embedded tissue. (1991) (48)
- DNA image cytometry on machine-selected breast cancer cells and a comparison between flow cytometry and scanning cytophotometry. (1985) (48)
- High levels of DNA index heterogeneity in advanced breast carcinomas. Evidence for DNA ploidy differences between lymphatic and hematogenous metastases (1993) (48)
- Molecular genetic evidence for monoclonal origin of bilateral ovarian serous borderline tumors. (2003) (47)
- Allelotype analysis of flow‐sorted breast cancer cells demonstrates genetically related diploid and aneuploid subpopulations in primary tumors and lymph node metastases (2000) (47)
- Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes. (1990) (47)
- A new type of two-color fluorescence staining for cytology specimens. (1976) (46)
- Sdhd and Sdhd/H19 Knockout Mice Do Not Develop Paraganglioma or Pheochromocytoma (2009) (46)
- Biochemical and quantitative histochemical study of reduced pyridine nucleotide dehydrogenation by human colonic carcinomas. (1983) (45)
- The canine p53 gene is subject to somatic mutations in thypoid carcinoma. (1994) (45)
- Fractional allelic imbalance in human breast cancer increases with tetraploidization and chromosome loss (1992) (45)
- Genetics of human breast cancer. (1990) (44)
- Serrated adenomas and mixed polyposis caused by a splice acceptor deletion in the mouse Smad4 gene (2003) (43)
- Morphometric quantification of myocyte dimensions validated in normal growing rat hearts and applied to hypertrophic human hearts. (1987) (43)
- Limited loss of nine tumor-associated surface antigenic determinants after tryptic cell dissociation. (1995) (42)
- DNA aneuploidy in colorectal adenomas. (1987) (42)
- Expression analysis of candidate breast tumour suppressor genes on chromosome 16q (2005) (42)
- The role of DNA damage and inhibition of poly(ADP-ribosyl)ation in loss of clonogenicity of murine L929 fibroblasts, caused by photodynamically induced oxidative stress. (1994) (41)
- Confinement of PGL, an Imprinted Gene Causing Hereditary Paragangliomas, to a 2-cM Interval on 11q22–q23 and Exclusion of DRD2 and NCAM as Candidate Genes (1996) (40)
- Frequency and degree of aneuploidy in benign and malignant thyroid neoplasms (1990) (40)
- Presymptomatic testing for BRCA1 andBRCA2: how distressing are the pre-test weeks? (1999) (40)
- CHEK2 1100delC mutation is frequent among Russian breast cancer patients (2006) (39)
- Paragangliomas of the head and neck region show complete loss of heterozygosity at 11q22-q23 in chief cells and the flow-sorted DNA aneuploid fraction. (1998) (38)
- Prevalence of BRCA1 in a hospital-based population of Dutch breast cancer patients (1999) (38)
- Morphological, cytochemical, functional, and proliferative characteristics of four murine macrophage-like cell lines. (1985) (38)
- Outgrowth of BT-474 human breast cancer cells in immune-deficient mice: a new in vivo model for hormone-dependent breast cancer. (1995) (37)
- Morphometric characterization of diffuse large-cell (histiocytic) lymphomas. (1982) (36)
- Gene-expression of metastasized versus non-metastasized primary head and neck squamous cell carcinomas: A pathway-based analysis (2008) (36)
- Characterization of Familial Non-BRCA1/2 Breast Tumors by Loss of Heterozygosity and Immunophenotyping (2006) (36)
- The amount of white pulp in the spleen; a morphometrical study done in methacrylate‐embedded splenectomy specimens (1983) (36)
- DNA flow cytometry and morphometry as prognostic indicators in advanced ovarian cancer: a step forward in predicting the clinical outcome. (1988) (36)
- Polyploidy of myocyte nuclei in pressure overloaded human hearts: a flow cytometric study in left and right ventricular myocardium. (1995) (35)
- DNA index reflects the biological behavior of ovarian carcinoma stage I-IIa. (1996) (34)
- DNA aberrations in the epithelial cell component of adamantinoma of long bones. (1995) (34)
- Loss of heterozygosity on 17p in human breast carcinomas: defining the smallest common region of deletion. (1990) (34)
- Prognostic factors in well‐differentiated early‐stage epithelial ovarian cancer (1993) (34)
- Genome-wide allelic state analysis on flow-sorted tumor fractions provides an accurate measure of chromosomal aberrations. (2008) (33)
- Mutations in exons 5–8 of the p53 gene, independent of their type and location, are associated with increased apoptosis and mitosis in invasive breast carcinoma (1999) (33)
- A NEW METHOD FOR THE INVESTIGATION OF THE KINETICS OF THE CAPTURE REACTION IN PHOSPHATASE CYTOCHEMISTRY II. THEORETICAL AND EXPERIMENTAL STUDY OF PHOSPHATE DIFFUSION FROM THIN POLYACRYLAMIDE FILMS (1973) (31)
- Tissue chimerism in human cryopreserved homograft valve explants demonstrated by in situ hybridization. (1998) (31)
- Ploidy of malignant mediastinal germ-cell tumors. (1990) (29)
- Four-color multiparameter DNA flow cytometric method to study phenotypic intratumor heterogeneity in cervical cancer. (2000) (29)
- Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases - preliminary report. (2005) (28)
- The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family (2010) (28)
- Defining regions of loss of heterozygosity of 16q in breast cancer cell lines. (2002) (28)
- Infiltrating leukocytes confound the detection of E-cadherin promoter methylation in tumors. (2004) (27)
- Evidence of clonal divergence in colorectal carcinoma (1997) (27)
- A prolactin-dependent, metastasising rat mammary carcinoma as a model for endocrine-related tumour dormancy. (1991) (27)
- Use of DNA image cytometry in addition to flow cytometry for the study of patients with advanced ovarian cancer. (1987) (27)
- Correspondence re: A. Müller et al., Exclusion of breast cancer as an integral tumor of hereditary nonpolyposis colorectal cancer. Cancer Res., 62: 1014-1019, 2002. (2003) (27)
- Analysis of tumor heterogeneity in a patient with synchronously occurring female genital tract malignancies by DNA flow cytometry, dna fingerprinting, and immunohistochemistry (1988) (26)
- Genes responsible for familial breast cancer. (1996) (26)
- A NEW METHOD FOR THE INVESTIGATION OF THE KINETICS OF THE CAPTURE REACTION IN PHOSPHATASE CYTOCHEMISTRY I. THEORETICAL ASPECTS OF THE LOCAL FORMATION OF CRYSTALLINE PRECIPITATES (1973) (26)
- High-resolution analysis of HLA class I alterations in colorectal cancer (2006) (26)
- Effectiveness of isolated liver perfusion with mitomycin C in the treatment of liver tumours of rat colorectal cancer. (1991) (25)
- Diagnostic morphometry of isolated lymph node cells from patients with mycosis fungoides and Sézary’s syndrome (1980) (25)
- DNA flow cytometry of canine mammary tumours: the relationship of DNA ploidy and S-phase fraction to clinical and histological features. (1995) (25)
- Nuclear DNA content and morphological characteristics in the prognosis of adrenocortical carcinoma. (1993) (25)
- DNA ploidy and cell kinetic characteristics in canine non-Hodgkin's lymphoma. (1993) (24)
- Surgically induced cytokinetic responses in experimental rat mammary tumor models (1991) (23)
- Texture analysis of cervical cell nuclei by segmentation of chromatin patterns. (1979) (23)
- Clinical and pathological features of BRCA1 associated carcinomas in a hospital-based sample of Dutch breast cancer patients (2001) (22)
- Increased HIF1α in SDH and FH deficient tumors does not cause microsatellite instability (2007) (22)
- Genome‐wide linkage scan in Dutch hereditary non‐BRCA1/2 breast cancer families identifies 9q21‐22 as a putative breast cancer susceptibility locus (2008) (22)
- Different calculation methods for flow cytometric S-phase fraction: prognostic implications in breast cancer? The Swedish Society of Cancer Study Group. (1998) (22)
- One-tube triple staining method for flow cytometric analysis of DNA ploidy and phenotypic heterogeneity of human solid tumors using single laser excitation. (1996) (22)
- ALLELE LOSSES IN BREAST CANCER (1989) (22)
- Polyploidy in the Freshwater Snail Lymnaea Stagnalis (Gastropoda, Pulmonata). a Cytophotometric Analysis of the Dna in Neurons and Some Other Cell Types (1976) (22)
- ATBF1 and NQO1 as candidate targets for allelic loss at chromosome arm 16q in breast cancer: Absence of somatic ATBF1 mutations and no role for the C609T NQO1 polymorphism (2008) (21)
- Assessing genetic markers of tumour progression in the context of intratumour heterogeneity. (1998) (21)
- Relationship between DNA ploidy, antigen expression and survival in renal cell carcinoma (1988) (21)
- Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas (2017) (21)
- DNA ploidy level as prognostic factor in low stage carcinoma of the uterine cervix. (1990) (20)
- Human papillomavirus type 16 in tumor tissue of low‐stage squamous carcinoma of the uterine cervix in relation to ploidy grade and prognosis (1993) (20)
- In situ hybridization: a new technique to determine the origin of fibroblasts in cryopreserved aortic homograft valve explants. (1995) (19)
- Real-time morphometric analysis of type I and type II fibers in cryostat sections of human muscle biopsies. (1980) (18)
- Image and flow cytometric analysis of DNA content in breast cancer. Relation to estrogen receptor content and lymph node involvement. (1984) (18)
- DNA flow cytometry of hereditary and sporadic paragangliomas (glomus tumours). (1991) (18)
- Rapid Identification of Mixed Up Bladder Biopsy Specimens Using Polymorphic Microsatellite Markers (1995) (18)
- Flow cytometric DNA ploidy analysis of feline mammary tumors. (1990) (18)
- Expression of epidermal growth factor receptor (EGFR) in non-affected and tumorous mammary tissue of female dogs (2004) (18)
- The Majority of 22 Dutch High-Risk Breast Cancer Families Are due to Either BRCA1 or BRCA2 (1996) (17)
- Quantitative electron microscopy in the early diagnosis of cutaneous T-cell lymphomas. A long-term follow-up study of 77 patients. (1986) (17)
- Complete Sequencing of TP 53 Predicts Poor Response to Systemic Therapy of Advanced Breast Cancer 1 (2000) (17)
- Malignant lymphoma of true histiocytic origin: Histiocytic Sarcoma (2004) (16)
- Similar gene expression profiles of sporadic, PGL2-, and SDHD-linked paragangliomas suggest a common pathway to tumorigenesis (2009) (16)
- Identification of an EWS-pseudogene using translocation detection by RT-PCR in Ewing's sarcoma. (1995) (16)
- Bias in detection of instability of the (C)8 mononucleotide repeat of MSH6 in tumours from HNPCC patients (2001) (16)
- Extending the p16-Leiden tumour spectrum by respiratory tract tumours (2004) (15)
- Paired distribution of molecular subtypes in bilateral breast carcinomas. (2011) (15)
- Exclusion of BBC1 and CMAR as candidate breast tumour-suppressor genes. (1997) (15)
- Basic fibroblast growth factor and fibroblastic growth factor receptor-1 may contribute to head and neck paraganglioma development by an autocrine or paracrine mechanism. (2007) (15)
- DNA ploidy of primary breast cancer and local recurrence after breast-conserving therapy. (1991) (15)
- Combined flow cytometry and image cytometry of the same cytological sample (1983) (14)
- Distinction between HLA class I-positive and -negative cervical tumor subpopulations by multiparameter DNA flow cytometry. (2000) (14)
- Increased HIF1 alpha in SDH and FH deficient tumors does not cause microsatellite instability. (2007) (14)
- A family history of breast cancer will not predict female early onset breast cancer in a population-based setting (2008) (13)
- Flow cytometry of human solid tumours: clinical and research applications (2002) (13)
- Genetic analysis of a breast–ovarian cancer family, with 7 cases of colorectal cancer linked to BRCA1, fails to support a role for BRCA1 in colorectal tumorigenesis (2000) (12)
- Improved single laser measurement of two cellular antigens and DNA-ploidy by the combined use of propidium iodide and TO-PRO-3 iodide. (1997) (12)
- The influence of the oncogenes NRAS and MYC on the radiation sensitivity of cells of a human melanoma cell line. (1996) (12)
- Prognostic value of nuclear DNA content in papillary and follicular thyroid cancer (1988) (12)
- Facts in cancer genetics. (1997) (12)
- Loss of heterozygosity, chromosome 7q, and breast cancer (1992) (12)
- Mapping of the breast basic conserved gene (D16S444E) to human chromosome band 16q24.3. (1995) (12)
- A NEW METHOD FOR THE INVESTIGATION OF THE CAPTURE REACTION IN PHOSPHATASE CYTOCHEMISTRY III. EFFECTS OF THE COMPOSITION OF THE INCUBATION MEDIUM ON THE TRAPPING OF PHOSPHATE IONS IN A MODEL SYSTEM (1974) (12)
- Aneuploidy and expression of gastric-associated mucus antigens M1 and CEA in colorectal adenomas. (1987) (11)
- Quantitative analysis of the nuclear area variation in benign and malignant breast cytology specimens. (1981) (11)
- Some shape parameters for cell recognition (1980) (11)
- Genomic structure of the human PLZF gene. (1999) (11)
- Software compensation improves the analysis of heterogeneous tumor samples stained for multiparameter DNA flow cytometry. (2002) (10)
- Characterization of a slow-growing, transplantable rat mammary tumor (MCR-83): a model for endocrine-related cell kinetic studies. (1987) (10)
- Association of aneuploidy in index adenomas with metachronous colorectal adenoma development and a comparison (1992) (10)
- Nonrandom distribution of oncogene amplifications in bilateral breast carcinomas: Possible role of host factors and survival bias (2007) (10)
- Myocardial (iso)enzyme activities, DNA concentration and nuclear polyploidy in hearts of patients operated upon for congenital heart disease, and in normal and hypertrophic adult human hearts at autopsy (1989) (10)
- Comparative genomic hybridization with lissamine- and fluorescein-labeled nucleotides. (1998) (10)
- International System for Cytogenetic Nomenclature (ISCN) — guidelines on cancer cytogenetics (1990) (9)
- Metastasis of breast carcinoma to a primary mucinous cystadenocarcinoma of the ovary. (1994) (9)
- Identification of host and donor cells in porcine homograft heart valve explants by fluorescence in situ hybridization (1997) (9)
- Searching for susceptibility alleles: Emphasis on bilateral breast cancer (2007) (9)
- A cytophotometric and autoradiographic study of DNA synthesis in macrophages and multinucleate foreign body giant cells. (1975) (9)
- A theoretical study of concentration of profiles of primary cytochemical-enzyme reaction products in membrane-bound cell organelles and its application to lysosomal acid phosphatase (1976) (9)
- G2M arrest, blocked apoptosis, and low growth fraction may explain indolent behavior of head and neck paragangliomas. (2003) (8)
- Carotid body tumors in humans caused by a mutation in the gene for succinate dehydrogenase D (SDHD). (2004) (8)
- Molecular identification of a partial hydatidiform mole. (1997) (8)
- Flow karyotyping of human melanoma cell lines. (1986) (8)
- Flow-cytometric DNA ploidy analysis in primary and metastatic canine thyroid carcinomas. (1991) (8)
- Corrigendum: BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients (1997) (8)
- Cytometric analysis of DNA content, nuclear size and chromatin texture in benign breast lesions (1980) (8)
- Methodological aspects of flow cytometric analysis of DNA polyploidy in human heart tissue (2004) (6)
- Relevance of Morphometry in the Diagnosis and Prognosis of Cutaneous T Cell Lymphomas (1982) (6)
- Mutant BRCA1 alleles transmission: Different approaches and different biases (2005) (6)
- Assessment of hypertrophy in myocardial biopsies taken during correction of congenital heart disease. (1988) (6)
- DNA Ploidy Status as a Prognostic Marker and Predictor of Lymph Node Metastasis in Laryngeal Carcinoma (2002) (5)
- “Flow Cytometric Analysis of Nuclear DNA Content in Solid Tumors” (1991) (5)
- Automated recognition of atypical nuclei in breast cancer cytology specimens by iterative image transformations (1985) (5)
- Nuclear DNA content of medullary thyroid carcinoma in a large family with the MEN-2A syndrome (1991) (5)
- An image segmentation approach to the analysis of nuclear texture of cervical cells. (1979) (5)
- CBFA 2 T 3 ( MTG 16 ) Is a Putative Breast Tumor Suppressor Gene from the Breast Cancer Loss of Heterozygosity Region at 16 q 24 . 31 (2002) (5)
- The difference in DNA ploidy pattern between some canine and human neoplasms appears to be genuine and a reflection of dissimilarities in DNA aneuploidy evolution. (1994) (4)
- Evidence for a Gene on l 7 pl 3 . 3 , Distal to TP 53 , as a Target for Allele Loss in Breast Tumors without p 53 Mutations ' (2006) (4)
- In situ hybridization for molecular cytogenetics (1992) (4)
- Frequent mutations in the 3′-untranslated region of IFNGR1 lack functional impairment in microsatellite-unstable colorectal tumours (2008) (4)
- [From gene to disease; from BRCA1 or BRCA2 to breast cancer]. (2000) (4)
- DNA ploidy analysis and cytologic examination of sorted cell populations from human breast tumors. (1983) (3)
- of Candidate Regions 712 Breast Tumors Reveals Factors that Influence Delineation Loss of Heterozygosity Mapping at Chromosome Arm 16 q in Updated (2001) (3)
- Polidy of subtypes of primary germ cell tumors of the stress of the testis: Pathogenetic and clinical relevance (1989) (3)
- A partial BRCA1 sequence homology mapping to 4q28 (2001) (3)
- Applications of Morphometry in Non-tumour Pathology (1983) (3)
- Selection of families for predictive testing for breast cancer (1994) (2)
- 58 Difference in ploidy in subtypes of testicular germ cell tumor (1987) (2)
- Automated chromatin analysis using the Leyden Television Analysis System (LEYTAS). (1979) (2)
- Alexander F. Zakharov (1986) (1)
- Acriflavine-Feulgen-Stilbene: a combined DNA-protein staining procedure. (1979) (1)
- 89 Loss of constitutional heterozygosity of chromosomes 11, 13 and 17 markers in primary human breast carcinoma (1989) (1)
- Allelotype of human breast carcinoma: Present status and deletion-mapping on chromosomes 3p, 6, and 18q. (1991) (1)
- Subject Index Vol. 53, 1990 (1990) (1)
- Assessment of Genetic Changes in Human Cancers Using Flow and Image Cytometry (1997) (1)
- Journal size increases to four volumes per year Editorial Board additions (1995) (1)
- Cutaneous T-Cell Lymphoma: Morphological and Immunological Aspects (1980) (1)
- Four-color multiparameter DNA flow cytometric method to study phenotypic intratumor heterogeneity in cervical cancerPart of this work was presented at the 11th Heidelberg Cytometry Symposium, Heidelberg, 22-24 October, 1998. (2000) (1)
- Effect of hormone depletion on cell survival in the EMR-86 rat mammary carcinoma. (1996) (1)
- Functional analysis of BRCA1 in breast cancer development (2001) (0)
- [Cloning of the first gene for breast/ovarian cancer (BRCA1), mapping of a second gene locus (BRCA2) and consequences for clinical practice]. (1995) (0)
- Allelotype of 18 paragangliomas: Infrequent LOH at all chromosome arms, including the region 11q containing the predisposing locus (1992) (0)
- 349 POSTER Concordance of expression subtypes in synchronous but not metachronous bilateral breast carcinomas (2007) (0)
- Quantitative Electron Microscopy in the Early Diagnosis of Cutaneous TCell Lymphomas (2007) (0)
- 90 Detection of chromosomal aberrations in interphase nuclei from human primary breast tumors using in situ hybridization with chromosome-specific repetitive DNA-probes (1989) (0)
- The Risk of Head and Neck Paragangliomas and Pheochromocytomas in SDHD Mutation Carriers (2009) (0)
- Dr. John L. Hamerton steps-down from the Associate Editorship (1995) (0)
- Contents, Vol. 53, 1990 (1990) (0)
- 73 Detection of numerical chromosome changes in interphase nuclei using chromosome specific repetitive probes (1987) (0)
- Discovering genetic profiles by array-CGH in familial breast tumors (2005) (0)
- O20: Discovering genetic profiles by array-CGH in familial breast tumors (2005) (0)
- Search for new breast cancer susceptibility genes (1999) (0)
- Hereditary paragangliomas caused by mutations in the SDHD gene (2001) (0)
- Flow Cytometric Analysis of DNA Ploidy in Canine Mammary Tumors1 (2006) (0)
- CLINICAL AND MOLECULAR CHARACTERISTICS OF OVARIAN CANCER BRCA1 AND BRCA2 MUTATION CARRIERS AND UNCLASSIFIED VARIANTS (2004) (0)
- Simultaneous flow cytometric detection of DNA and cellular protein molecules. (2001) (0)
- PCR in clinical pathology (1997) (0)
- [Oncogenes, tumor suppression genes and medical genetics of cancer]. (1992) (0)
- Eleventh International Chromosome Conference (2004) (0)
- Expression-based positional cloning of breast tumour suppressor genes on chromosome arm 16q (2000) (0)
- Abstract #4439: Differential allelic expression of BRCA1 and BRCA2 as a breast cancer susceptibility factor (2009) (0)
- A linkage search for new breast cancer predisposition genes (1999) (0)
- Candidate breast tumor suppressor genes on chromosomal band 16q243 (1997) (0)
- 544 POSTER Searching for susceptibility alleles: emphasis on bilateral breast cancer (2007) (0)
- Molecular and genetic tumour pathology of solid tumours (2001) (0)
- Mechanism of tumorigenesis of hereditary paragangliomas of the head and neck (2002) (0)
- In situ hybridization and its potential use for interphase cytogenetics: Mapping of a series of yeast artificial chromosomes carrying inserts from human chromosome 1p. (1991) (0)
- Refining risk assessment in BRCA1- and BRCA2-carriers: analysis of unclassified variants and a search for risk-modifying factors (2001) (0)
- Mutations in the p53 gene, both within and outside the zinc-binding domains, are associated with increased apoptosis and mitosis in invasive breast carcinomas (1998) (0)
- Cross-talk between E-cadherin and Ep-Cam in mammary gland development and carcinogenesis. (1999) (0)
- [The value of DNA flow cytometry in solid tumors]. (1989) (0)
- Subject Index Vol. 41, 1986 (2004) (0)
- Allelic imbalance in paragangliomas is specific for chromosome 11, the site of the predisposing gene (1994) (0)
- 4 Detection of chromosomal aberrations in tissue sections of solid tumors by in situ hybridization (1989) (0)
- Cell Origins and Fates Following Transplantation of Cryopreserved Allografts (2005) (0)
- Quantitative heritable variation in gene expression as a cause for breast cancer susceptibility (2006) (0)
- Molecular tumor pathology and tumor genetics (2003) (0)
- A metastasizing rat mammary tumor model (EMR-86) for studying hormone-dependent growth kinetics (1990) (0)
- Specificity Transcription Factor Selectively Alter Its DNA-binding Tumor-associated Zinc Finger Mutations in the CTCF Updated Version (2001) (0)
- Nuclear DNA content andmorphological characteristics intheprognosis ofadrenocortical carcinoma (1993) (0)
- An LOH map of chromosome 17 determined from 107 primary breast carcinomas indicates complex chromosome involvement (1992) (0)
- Evaluation of quantitative electron microscopic methods in the early diagnosis of cutaneous T-cell lymphomas (1986) (0)
- The comparison of the DNA ploidy distribution pattern in canine inflammatory lesions, benign tumors, sarcomas, and malignant thymomas (2010) (0)
- Embryonic lethality in the Brca1-1700T mouse model suggests inhibition of p53-dependent pathways (2000) (0)
- SHORT REPORT Increased HIF1a in SDH and FH deficient tumors does not cause microsatellite instability (2007) (0)
- 76 Comparison between ‘metaphase cytogenetics’ and ‘interphase cytogenetics’ of ovarian cancer cell lines (1989) (0)
- Detection of loss of heterozygosity in flow sorted ovarian tumor cells: Evidence for intra-tumor heterogeneity (1994) (0)
- Clinical pathological electron microscopyEarly morphometric diagnosis of cutaneo cutaneous T cell lymphomas (1979) (0)
- Identification of E-cadherin mediated expression patterns involved in the development of lobular breast cancer (2000) (0)
- Flow Cytometric Analysis of DNA Ploidy in Canine Mammary Tumors 1 (2006) (0)
- The blueprint of cancer cells (2003) (0)
- Molecular genetic analysis offlow-sorted ovarian tumourcells: improved detection ofloss ofheterozygosity (1994) (0)
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What Schools Are Affiliated With Cees J. Cornelisse?
Cees J. Cornelisse is affiliated with the following schools:
