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1980 …2019
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Research Output 1986 2019

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Article
1998
33 Citations (Scopus)

Familial chordoma with probable autosomal dominant inheritance.

Stepanek, J., Cataldo, S. A., Ebersold, M. J., Lindor, N. M., Jenkins, R. B., Unni, K., Weinshenker, B. G. & Rubenstein, R. L., 1998, In : American Journal of Medical Genetics. 75, 3, p. 335-336 2 p.

Research output: Contribution to journalArticle

Spinal Neoplasms
Nasopharyngeal Neoplasms
Chordoma
Adenoids
Dominant Genes
68 Citations (Scopus)
Prostatic Neoplasms
Fishes
Clone Cells
Breast Neoplasms
Hybrid Cells
64 Citations (Scopus)

FRA7G extends over a broad region: Coincidence of human endogenous retroviral sequences (HERV-H) and small polydispersed circular DNAs (spcDNA) and fragile sites

Huang, H., Qian, J., Proffit, J., Wilber, K., Jenkins, R. B. & Smith, D. I., May 7 1998, In : Oncogene. 16, 18, p. 2311-2319 9 p.

Research output: Contribution to journalArticle

Endogenous Retroviruses
Circular DNA
Clone Cells
Aphidicolin
Virus Integration
33 Citations (Scopus)

Frequent homozygous deletions in the FRA3B region in tumor cell lines still leave the FHIT exons intact

Wang, L., Darling, J., Zhang, J. S., Qian, C. P., Hartmann, L., Conover, C. A., Jenkins, R. B. & Smith, D. I., Feb 5 1998, In : Oncogene. 16, 5, p. 635-642 8 p.

Research output: Contribution to journalArticle

Tumor Cell Line
Exons
Cell Line
Virus Integration
Trinucleotide Repeats
67 Citations (Scopus)

Gene amplification as a prognostic factor in primary and secondary high- grade malignant gliomas

Galanis, E., Buckner, J. C., Kimmel, D., Jenkins, R. B., Alderete, B., O'Fallon, J., Wang, C. H., Scheithauer, B. W. & James, C. D., 1998, In : International Journal of Oncology. 13, 4, p. 717-724 8 p.

Research output: Contribution to journalArticle

Gene Amplification
Glioma
Oncogenes
Oligodendroglioma
myc Genes
72 Citations (Scopus)

Genomic organization and mutation analysis of p73 in oligodendrogliomas with chromosome 1 p-arm deletions

Mai, M., Huang, H., Reed, C., Qian, C., Smith, J. S., Alderete, B., Jenkins, R. B., Smith, D. I. & Liu, W., Aug 1 1998, In : Genomics. 51, 3, p. 359-363 5 p.

Research output: Contribution to journalArticle

Oligodendroglioma
Chromosomes, Human, Pair 1
Mutation
Introns
Neuroblastoma
124 Citations (Scopus)

Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors

Bahuau, M., Vidaud, D., Jenkins, R. B., Bièche, I., Kimmel, D. W., Assouline, B., Smith, J. S., Alderete, B., Cayuela, J. M., Harpey, J. P., Caille, B. & Vidaud, M., Jun 1 1998, In : Cancer Research. 58, 11, p. 2298-2303 6 p.

Research output: Contribution to journalArticle

Nervous System Neoplasms
Germ Cells
Melanoma
Tumor Suppressor Genes
Neoplasms
147 Citations (Scopus)

Independent origin of multiple foci of prostatic intraepithelial neoplasia: Comparison with matched foci of prostate carcinoma

Bostwick, D. G., Shan, A., Qian, J., Darson, M., Maihle, N. J., Jenkins, R. B. & Cheng, L., Nov 1 1998, In : Cancer. 83, 9, p. 1995-2002 8 p.

Research output: Contribution to journalArticle

Prostatic Intraepithelial Neoplasia
Allelic Imbalance
Prostate
Carcinoma
Microsatellite Repeats
33 Citations (Scopus)

Mutation analysis of the putative tumor suppressor PTEN/MMAC1 in human ovarian cancer

Yokomizo, A., Tindall, D. J., Hartmann, L., Jenkins, R. B., Smith, D. I. & Liu, W., Jul 1998, In : International Journal of Oncology. 13, 1, p. 101-105 5 p.

Research output: Contribution to journalArticle

Ovarian Neoplasms
Mutation
Neoplasms
Multiplex Polymerase Chain Reaction
DNA Sequence Analysis
75 Citations (Scopus)

Prognostic significance of allelic imbalance of chromosome arms 7q, 8p, 16q, and 18q in stage T3N0M0 prostate cancer

Jenkins, R. B., Takahashi, S., DeLacey, K., Bergstralh, E. & Lieber, M., Feb 1998, In : Genes Chromosomes and Cancer. 21, 2, p. 131-143 13 p.

Research output: Contribution to journalArticle

Allelic Imbalance
Prostatic Neoplasms
Chromosomes
Neoplasms
DNA
1997
107 Citations (Scopus)

Analysis of proliferation markers and p53 expression in gliomas of astrocytic origin: Relationships and prognostic value

Cunningham, J. M., Kimmel, D. W., Scheithauer, B. W., O'Fallon, J. R., Novotny, P. J. & Jenkins, R. B., Jan 1997, In : Journal of Neurosurgery. 86, 1, p. 121-130 10 p.

Research output: Contribution to journalArticle

Astrocytoma
Proliferating Cell Nuclear Antigen
Neoplasms
Aneuploidy
Glioma

Astrocytoma and Ki-67 (multiple letters)

Joseph, J. T., Cunningham, J. M., Kimmel, D. W., Scheithauer, B. W., O'Fallon, J. R., Novotny, P. J. & Jenkins, R. B., 1997, In : Journal of Neurosurgery. 87, 1, p. 133-134 2 p.

Research output: Contribution to journalArticle

Ki-67 Antigen
Astrocytoma
Tumor Biomarkers
Cell Division
39 Citations (Scopus)

Chromosomal anomalies in stage D1 prostate adenocarcinoma primary tumors and lymph node metastases detected by fluorescence in situ hybridization

Gburek, B. M., Kollmorgen, T. A., Qian, J., D'Souza-Gburek, S. M., Lieber, M. M. & Jenkins, R. B., Jan 1997, In : Journal of Urology. 157, 1, p. 223-227 5 p.

Research output: Contribution to journalArticle

Fluorescence In Situ Hybridization
Prostate
Adenocarcinoma
Lymph Nodes
Neoplasm Metastasis
19 Citations (Scopus)

Clinical correlations of immunophenotypic variations and the presence of trisomy 12 in B-cell chronic lymphocytic leukemia

Tefferi, A., Bartholmai, B. J., Witzig, T. E., Jenkins, R. B., Li, C. Y., Hanson, C. A., Mesa, R. A. & Phyliky, R. L., Jun 1997, In : Cancer Genetics and Cytogenetics. 95, 2, p. 173-177 5 p.

Research output: Contribution to journalArticle

Trisomy
B-Cell Chronic Lymphocytic Leukemia
B-Cell Antigen Receptors
Disease Progression
Prolymphocytic Leukemia
17 Citations (Scopus)

Current applications of molecular cytogenetic technologies

Mark, H. F. L., Jenkins, R. B. & Miller, W. A., 1997, In : Annals of Clinical and Laboratory Science. 27, 1, p. 47-56 10 p.

Research output: Contribution to journalArticle

Fluorescence In Situ Hybridization
Cytogenetics
Clinical laboratories
Technology
Aneuploidy
93 Citations (Scopus)
Prostatic Intraepithelial Neoplasia
myc Genes
Gene Amplification
Carcinoma in Situ
Fluorescence In Situ Hybridization
360 Citations (Scopus)

Detection of c-myc oncogene amplification and chromosomal anomalies in metastatic prostatic carcinoma by fluorescence in Situ hybridization

Jenkins, R. B., Qian, J., Lieber, M. M. & Bostwick, D. G., 1997, In : Cancer Research. 57, 3, p. 524-531 8 p.

Research output: Contribution to journalArticle

Prostatic Intraepithelial Neoplasia
myc Genes
Carcinoma in Situ
Fluorescence In Situ Hybridization
Chromosomes, Human, Pair 8
59 Citations (Scopus)

Detection of p16 gene deletions in gliomas: A comparison of fluorescence in situ hybridization (FISH) versus quantitative PCR

Perry, A., Nobori, T., Ru, N., Anderl, K., Borell, T. J., Mohapatra, G., Feuerstein, B. G., Jenkins, R. B. & Carson, D. A., Sep 1997, In : Journal of Neuropathology and Experimental Neurology. 56, 9, p. 999-1008 10 p.

Research output: Contribution to journalArticle

p16 Genes
Gene Deletion
Fluorescence In Situ Hybridization
Glioma
Polymerase Chain Reaction
102 Citations (Scopus)

Frequent loss of heterozygosity on chromosomes 3p and 17p without VHL or p53 mutations suggests involvement of unidentified tumor suppressor genes in follicular thyroid carcinoma

Grebe, S. K. G., McIver, B., Hay, I. D., Wu, P. S. C., Maciel, L. M. Z., Drabkin, H. A., Goellner, J. R., Grant, C. S., Jenkins, R. B. & Eberhardt, N. L., 1997, In : Journal of Clinical Endocrinology and Metabolism. 82, 11, p. 3684-3691 8 p.

Research output: Contribution to journalArticle

Follicular Adenocarcinoma
Loss of Heterozygosity
Chromosomes
Tumor Suppressor Genes
Tumors
14 Citations (Scopus)

Lack of germ-line mutations of CDK4, p16(INK4A), and p15(INK4B) in families with glioma

Gao, L., Liu, L., Van Meyel, D., Cairncross, G., Forsyth, P., Kimmel, D., Jenkins, R. B., Lassam, N. J. & Hogg, D., Jun 1997, In : Clinical Cancer Research. 3, 6, p. 977-981 5 p.

Research output: Contribution to journalArticle

Cyclin-Dependent Kinase Inhibitor p16
Germ-Line Mutation
Glioma
Neuroglia
Genes
170 Citations (Scopus)

PTEN/MMAC1 mutations and EGFR amplification in glioblastomas

Liu, W., James, C. D., Frederick, L., Alderete, B. E. & Jenkins, R. B., Dec 1 1997, In : Cancer Research. 57, 23, p. 5254-5257 4 p.

Research output: Contribution to journalArticle

Loss of Heterozygosity
Glioblastoma
Chromosomes, Human, Pair 10
Mutation
Alleles
77 Citations (Scopus)

Simultaneous chromosome 7 and 17 gain and sex chromosome loss provide evidence that renal metanephric adenoma is related to papillary renal cell carcinoma

Brown, J. A., Anderl, K. L., Borell, T. J., Qian, J., Bostwick, D. G. & Jenkins, R. B., Aug 1997, In : Journal of Urology. 158, 2, p. 370-374 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 17
Sex Chromosomes
Chromosomes, Human, Pair 7
Renal Cell Carcinoma
Adenoma
168 Citations (Scopus)

Soft-tissue perineurioma: Evidence for an abnormality of chromosome 22, criteria for diagnosis, and review of the literature

Giannini, C., Scheithauer, B. W., Jenkins, R. B., Erlandson, R. A., Perry, A., Borell, T. J., Hoda, R. S. & Woodruff, J. M., 1997, In : American Journal of Surgical Pathology. 21, 2, p. 164-173 10 p.

Research output: Contribution to journalArticle

Nerve Sheath Neoplasms
Chromosomes, Human, Pair 22
Neoplasms
Minor Lymphocyte Stimulatory Loci
Mucin-1
464 Citations (Scopus)

Sporadic medulloblastomas contain PTCH mutations

Raffel, C., Jenkins, R. B., Frederick, L., Hebrink, D., Alderete, B., Fults, D. W. & David James, C., 1997, In : Cancer Research. 57, 5, p. 842-845 4 p.

Research output: Contribution to journalArticle

Basal Cell Nevus Syndrome
Medulloblastoma
Loss of Heterozygosity
Mutation
Basal Cell Neoplasms
1996
34 Citations (Scopus)

Absence of mutations in DNA mismatch repair genes in sporadic endometrial tumors with microsatellite instability

Lim, P. C., Tester, D., Cliby, W. A., Ziesmer, S. C., Roche, P. C., Hartmann, L., Thibodeau, S. N., Podratz, K. C. & Jenkins, R. B., Nov 1996, In : Clinical Cancer Research. 2, 11, p. 1907-1911 5 p.

Research output: Contribution to journalArticle

Microsatellite Instability
DNA Mismatch Repair
Mutation
Endometrial Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms
163 Citations (Scopus)

Allelic imbalance and microsatellite instability in prostatic adenocarcinoma

Cunningham, J. M., Shan, A., Wick, M. J., McDonnell, S. K., Schaid, D. J., Tester, D. J., Qian, J., Takahashi, S., Jenkins, R. B., Bostwick, D. G. & Thibodeau, S. N., Oct 1 1996, In : Cancer Research. 56, 19, p. 4475-4482 8 p.

Research output: Contribution to journalArticle

Allelic Imbalance
Microsatellite Instability
Adenocarcinoma
Chromosomes, Human, Pair 16
Tumor Suppressor Genes
55 Citations (Scopus)

Aneusomies of chromosomes 8 and Y detected by fluorescence in situ hybridization are prognostic markers for pathological stage C (pT3N0M0) prostate carcinoma

Takahashi, S., Alcaraz, A., Brown, J. A., Borell, T. J., Herath, J. F., Bergstralh, E. J., Lieber, M. M. & Jenkins, R. B., Jan 1996, In : Clinical Cancer Research. 2, 1, p. 137-145 9 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 8
Fluorescence In Situ Hybridization
Prostate
Carcinoma
Y Chromosome
17 Citations (Scopus)

Application of fluorescent in situ hybridization with X and Y chromosome specific probes to buccal smear analysis

Schad, C. R., Kuffel, D. G., Wyatt, W. A., Zinsmeister, A. R., Jenkins, R. B., Dewald, G. W. & Jalal, S. M., Dec 11 1996, In : American Journal of Medical Genetics. 66, 2, p. 187-192 6 p.

Research output: Contribution to journalArticle

Sex Chromosomes
Cheek
Y Chromosome
X Chromosome
Fluorescence In Situ Hybridization
37 Citations (Scopus)

Chromosome-specific aneusomy in carcinoma of the breast

Persons, D. L., Robinson, R. A., Hsu, P. H., Seelig, S. A., Borell, T. J., Hartmann, L. C. & Jenkins, R. B., May 1996, In : Clinical Cancer Research. 2, 5, p. 883-888 6 p.

Research output: Contribution to journalArticle

Chromosomes
Chromosomes, Human, Pair 4
Breast Neoplasms
Lymph Nodes
Neoplasms
70 Citations (Scopus)

Comparison of fluorescence in situ hybridization analysis of isolated nuclei and routine histological sections from paraffin-embedded prostatic adenocarcinoma specimens

Qian, J., Bostwick, D. G., Takahashi, S., Borell, T. J., Brown, J. A., Lieber, M. M. & Jenkins, R. B., 1996, In : American Journal of Pathology. 149, 4, p. 1193-1199 7 p.

Research output: Contribution to journalArticle

Fluorescence In Situ Hybridization
Paraffin
Adenocarcinoma
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 7
65 Citations (Scopus)

Cytogenetic analysis of aggressive meningiomas: Possible diagnostic and prognostic implications

Perry, A., Jenkins, R. B., Dahl, R. J., Moertel, C. A. & Scheithauer, B. W., Jun 15 1996, In : Cancer. 77, 12, p. 2567-2573 7 p.

Research output: Contribution to journalArticle

Cytogenetic Analysis
Meningioma
Karyotype
Chromosomes, Human, Pair 1
Monosomy
76 Citations (Scopus)

Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex)

Stratakis, C. A., Jenkins, R. B., Pras, E., Mitsiadis, C. S., Raff, S. B., Stalboerger, P. G., Tsigos, C., Carney, J. A. & Chrousos, G. P., 1996, In : Journal of Clinical Endocrinology and Metabolism. 81, 10, p. 3607-3614 8 p.

Research output: Contribution to journalArticle

Carney Complex
Skin Pigmentation
Chromosomes
Myxoma
Cytogenetics

Erratum: Frequent loss of heterozygosity at 7q31.1 is associated with tumor aggressiveness and progression (Cancer Research (September 15, 1995) 55 (4114-4119))

Takahashi, S., Shan, A. L., Ritland, S. R., Delacey, K. A., Bostwick, D. G., Lieber, M. M., Thibodeau, S. N. & Jenkins, R. B., 1996, In : Cancer Research. 56, 10, p. 2461 1 p.

Research output: Contribution to journalArticle

Loss of Heterozygosity
Research
Neoplasms
53 Citations (Scopus)

Fluorescence in situ hybridization analysis of renal oncocytoma reveals frequent loss of chromosomes Y and 1

Brown, J. A., Takahashi, S., Alcaraz, A., Borell, T. J., Anderl, K. L., Qian, J., Persons, D. L., Bostwick, D. G., Lieber, M. M. & Jenkins, R. B., Jul 1996, In : Journal of Urology. 156, 1, p. 31-35 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 1
Fluorescence In Situ Hybridization
Chromosomes, Human, Pair 12
Paraffin
Neoplasms
24 Citations (Scopus)

Potential markers of aggressiveness in prostatic intraepithelial neoplasia detected by fluorescence in situ hybridization

Qian, J., Jenkins, R. B. & Bostwick, D. G., 1996, In : European Urology. 30, 2, p. 177-184 8 p.

Research output: Contribution to journalArticle

Prostatic Intraepithelial Neoplasia
Fluorescence In Situ Hybridization
Carcinoma
Chromosomes, Human, Pair 8
Prostate
113 Citations (Scopus)

The Glial and Mesenchymal Elements of Gliosarcomas Share Similar Genetic Alterations

Boerman, R. H., Anderl, K., Herath, J., Borell, T., Johnson, N., Schaeffer-Klein, J., Kirchhof, A., Raap, A. K., Scheithauer, B. W. & Jenkins, R. B., 1996, In : Journal of Neuropathology and Experimental Neurology. 55, 9, p. 973-981 9 p.

Research output: Contribution to journalArticle

Gliosarcoma
Neuroglia
Glioblastoma
Sarcoma
Allelic Imbalance
1995

[14] Analysis of p53 mutations in human gliomas by RNA single-strand conformational polymorphism

Cheng, T. M., Ganju, V., Ritland, S. R., Sarkar, G. & Jenkins, R. B., 1995, In : Methods in Neurosciences. 26, C, p. 210-224 15 p.

Research output: Contribution to journalArticle

Glioma
RNA
Mutation
Germ-Line Mutation
Neoplasms
38 Citations (Scopus)

Chromosomal anomalies in atypical adenomatous hyperplasia and carcinoma of the prostate using fluorescence in situ hybridization

Qian, J., Jenkins, R. B. & Bostwick, D. G., 1995, In : Urology. 46, 6, p. 837-842 6 p.

Research output: Contribution to journalArticle

Fluorescence In Situ Hybridization
Hyperplasia
Prostate
Carcinoma
Adenocarcinoma
199 Citations (Scopus)

Chromosomal anomalies in prostatic intraepithelial neoplasia and carcinoma detected by fluorescence in situ hybridization

Qian, J., Bostwick, D. G., Takahashi, S., Borell, T. J., Jenkins, R. B., Lieber, M. M. & Jenkins, R. B., 1995, In : Cancer Research. 55, 22, p. 5408-5414 7 p.

Research output: Contribution to journalArticle

Prostatic Intraepithelial Neoplasia
Carcinoma in Situ
Fluorescence In Situ Hybridization
Carcinoma
Chromosomes, Human, Pair 8
4 Citations (Scopus)

Cytogenetic analysis of prostate carcinoma by fluorescence in situ hybridization

Takahashi, S., Jenkins, R. B. & Lieber, M. M., Sep 1995, In : International Journal of Urology. 2, 4, p. 215-223 9 p.

Research output: Contribution to journalArticle

Cytogenetic Analysis
Carcinoma in Situ
Fluorescence In Situ Hybridization
Cytogenetics
Prostate
93 Citations (Scopus)

DNA Sequence Amplification in Human Prostate Cancer Identified by Chromosome Microdissection: Potential Prognostic Implications

Van Den Berg, C., Von Hoff, D., Sarosdy, M., Guan, X. Y., Bittner, M., Meltzer, P., Trent, J., Jenkins, R. B., Herath, J., Griffin, C., Epstein, J., Kallioniemi, O., Visakorpi, T., Von Hoff, D. & McGill, J., Jan 1 1995, In : Clinical Cancer Research. 1, 1, p. 11-18 8 p.

Research output: Contribution to journalArticle

Microdissection
Gene Amplification
Prostatic Neoplasms
Chromosomes
Fluorescence In Situ Hybridization
16 Citations (Scopus)

Fluorescence in situ hybridization for rapid differentiation of zygosity in transgenic mice

Nishino, H., Herath, J. F., Jenkins, R. B. & Sommer, S. S., 1995, In : BioTechniques. 19, 4, p. 587-592 6 p.

Research output: Contribution to journalArticle

Rhodamines
DNA Probes
Fibroblasts
Animals
Fluorescence
642 Citations (Scopus)

Frequency of homozygous deletion at p16/CDKN2 in primary human tumours

Cairns, P., Polascik, T. J., Eby, Y., Tokino, K., Califano, J., Merlo, A., Mao, L., Herath, J., Jenkins, R. B., Westra, W., Rutter, J. L., Buckler, A., Gabrielson, E., Tockman, M., Cho, K. R., Hedrick, L., Bova, G. S., Isaacs, W. & Sidransky, D., 1995, In : Nature Genetics. 11, 2, p. 210-212 3 p.

Research output: Contribution to journalArticle

Neoplasms
Suppressor Genes
Tumor Cell Line
Urinary Bladder Neoplasms
Microsatellite Repeats
127 Citations (Scopus)

Frequent loss of heterozygosity at 7q31.1 in primary prostate cancer is associated with tumor aggressiveness and progression

Takahashi, S., Shan, A. L., Ritland, S. R., Delacey, K. A., Bostwick, D. G., Lieber, M. M., Thibodeau, S. N. & Jenkins, R. B., 1995, In : Cancer Research. 55, 18, p. 4114-4119 6 p.

Research output: Contribution to journalArticle

Loss of Heterozygosity
Chromosomes, Human, Pair 7
Allelic Imbalance
Prostatic Neoplasms
Neoplasms
94 Citations (Scopus)

Germline p16INK4A mutation and protein dysfunction in a family with inherited melanoma

Liu, L., Lassam, N. J., Slingerland, J. M., Bailey, D., Cole, D., Jenkins, R. B. & Hogg, D., Jul 20 1995, In : Oncogene. 11, 2, p. 404-412 9 p.

Research output: Contribution to journalArticle

Cyclin-Dependent Kinase Inhibitor p16
p16 Genes
Germ-Line Mutation
Melanoma
Alleles
183 Citations (Scopus)

Intraneural perineurioma: A clonal neoplasm associated with abnormalities of chromosome 22

Emory, T. S., Scheithauer, B. W., Hirose, T., Wood, M., Onofrio, B. M. & Jenkins, R. B., 1995, In : American Journal of Clinical Pathology. 103, 6, p. 696-704 9 p.

Research output: Contribution to journalArticle

Nerve Sheath Neoplasms
Chromosomes, Human, Pair 22
S100 Proteins
Neoplasms
Chromosomes, Human, Pair 14
86 Citations (Scopus)

Region-specific loss of heterozygosity on chromosome 19 is related to the morphologic type of human glioma

Ritland, S. R., Ganju, V. & Jenkins, R. B., 1995, In : Genes Chromosomes and Cancer. 12, 4, p. 277-282 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 19
Loss of Heterozygosity
Astrocytoma
Glioma
Oligodendroglioma
12 Citations (Scopus)

Uniparental disomy in congenital disorders: A prospective study

Lindor, N. M., Karnes, P. S., Michels, V. V., Dewald, G. W., Goerss, J., Jalal, S., Jenkins, R. B., Vockley, G. & Thibodeau, S. N., 1995, In : American Journal of Medical Genetics. 58, 2, p. 143-146 4 p.

Research output: Contribution to journalArticle

Uniparental Disomy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Prospective Studies
Chromosomes
Intellectual Disability
25 Citations (Scopus)

Use of fluorescence in situ hybridization to detect loss of chromosome 10 in astrocytomas

Dalrymple, S. J., Herath, J. F., Ritland, S. R., Moertel, C. A. & Jenkins, R. B., 1995, In : Journal of Neurosurgery. 83, 2, p. 316-323 8 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 10
Astrocytoma
Fluorescence In Situ Hybridization
Loss of Heterozygosity
Molecular Biology
1994
49 Citations (Scopus)

Aggressive medulloblastoma with high-level N-myc amplification

Tomlinson, F. H., Jenkins, R. B., Scheithauer, B. W., Keelan, P. A., Ritland, S., Parisi, J. E., Cunningham, J. M. & Olsen, K. D., 1994, In : Mayo Clinic Proceedings. 69, 4, p. 359-365 7 p.

Research output: Contribution to journalArticle

Medulloblastoma
myc Genes
p53 Genes
Cytogenetics
Base Pairing