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1980 …2019
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Research Output 1986 2019

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42 Citations (Scopus)

ERBB2, TBX2, RPS6KB1, and MYC alterations in breast tissues of BRCA1 and BRCA2 mutation carriers

Adem, C., Soderberg, C. L., Hafner, K., Reynolds, C., Slezak, J. M., Sinclair, C. S., Sellers, T. A., Schaid, D. J., Couch, F. J., Hartmann, L. C. & Jenkins, R. B., Sep 2004, In : Genes Chromosomes and Cancer. 41, 1, p. 1-11 11 p.

Research output: Contribution to journalArticle

Breast
Mutation
Breast Neoplasms
Mastectomy
Neoplasms
7 Citations (Scopus)

ERBB2 and MYC alterations in BRCAI- and BRCA2-associated cancers [2] (multiple letters)

Palacios, J., Honrado, E., Cigudosa, J. C., Benítez, J., Jenkins, R. B., Adem, C., Couch, F. J. & Hartmann, L. C., Feb 2005, In : Genes Chromosomes and Cancer. 42, 2, p. 204-206 3 p.

Research output: Contribution to journalArticle

BRCA2 Gene
BRCA1 Gene
erbB-2 Genes
Carcinoma, Ductal, Breast
myc Genes
2 Citations (Scopus)

Erratum: Molecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: Guideline from the College of American Pathologists, International Association for the Study of Lung Cancer, and Association for Molecular Pathology (Journal of Thoracic Oncology (2013) 8 (823-859))

Lindeman, N. I., Cagle, P. T., Beasley, M. B., Chitale, D. A., Dacic, S., Giaccone, G., Jenkins, R. B., Kwiatkowski, D. J., Saldivar, J. S., Squire, J., Thunnissen, E. & Ladanyi, M., 2013, In : Journal of Thoracic Oncology. 8, 10, p. 1343 1 p.

Research output: Contribution to journalArticle

Molecular Pathology
Protein-Tyrosine Kinases
Lung Neoplasms
Thorax
Guidelines

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

Erratum: Survey of familial glioma and role of germline p16 INK4A/p14ARF and p53 mutation (Familial Cancer DOI: 10.1007/s10689-010-9346-5)

Robertson, L. B., Armstrong, G. N., Olver, B. D., Lloyd, A. L., Shete, S., Lau, C., Claus, E. B., Barnholtz-Sloan, J., Lai, R., Il'yasova, D., Schildkraut, J., Bernstein, J. L., Olson, S. H., Jenkins, R. B., Yang, P., Rynearson, A. L., Wrensch, M., McCoy, L., Wienkce, J. K., McCarthy, B. & 11 others, Davis, F., Vick, N. A., Johansen, C., Bødtcher, H., Sadetzki, S., Bruchim, R. B. S., Yechezkel, G. H., Andersson, U., Melin, B. S., Bondy, M. L. & Houlston, R. S., Sep 2010, In : Familial Cancer. 9, 3, p. 423-424 2 p.

Research output: Contribution to journalArticle

Tumor Suppressor Protein p14ARF
Cyclin-Dependent Kinase Inhibitor p16
Glioma
Mutation
Neoplasms
11 Citations (Scopus)

Evaluating the clinical impact of a genomic classifier in prostate cancer using individualized decision analysis

Lobo, J. M., Dicker, A. P., Buerki, C., Daviconi, E., Karnes, R. J., Jenkins, R. B., Patel, N., Den, R. B. & Showalter, T. N., Apr 2 2015, In : PLoS One. 10, 4, e0116866.

Research output: Contribution to journalArticle

Decision Support Techniques
Decision theory
prostatic neoplasms
Prostatic Neoplasms
Classifiers
5 Citations (Scopus)

Evaluation of a 24-gene signature for prognosis of metastatic events and prostate cancer-specific mortality

Pellegrini, K. L., Sanda, M. G., Patil, D., Long, Q., Santiago-Jiménez, M., Takhar, M., Erho, N., Yousefi, K., Davicioni, E., Klein, E. A., Jenkins, R. B., Karnes, R. J. & Moreno, C. S., 2017, (Accepted/In press) In : BJU International.

Research output: Contribution to journalArticle

Prostatic Neoplasms
Mortality
Genes
Prostatectomy
Neoplasm Metastasis
79 Citations (Scopus)

Evidence of functional RB protein in epithelial ovarian carcinomas despite loss of heterozygosity at the RB locus

Dodson, M. K., Cliby, W. A., Xu, H. J., DeLacey, K. A., Hu, S. X., Keeney, G., Li, J., Podratz, K. C., Jenkins, R. B. & Benedict, W. F., Feb 1 1994, In : Cancer Research. 54, 3, p. 610-613 4 p.

Research output: Contribution to journalArticle

Retinoblastoma Protein
Retinoblastoma
Loss of Heterozygosity
Carcinoma
Neoplasms
14 Citations (Scopus)

Experience with precision genomics and tumor board, indicates frequent target identification, but barriers to delivery

Bryce, A. H., Egan, J. B., Borad, M. J., Stewart, A. K., Nowakowski, G. S., Chanan Khan, A. A., Patnaik, M. M., Ansell, S. M., Banck, M. S., Robinson, S., Mansfield, A., Klee, E. W., Oliver, G. R., McCormick, J. B., Huneke, N. E., Tagtow, C. M., Jenkins, R. B., Rumilla, K. M., Kerr, S. E., Kocher, J-P. & 5 others, Beck, S. A., Fernandez-Zapico, M. E., Farrugia, G., Lazaridis, K. N. & Mc Williams, R. R., 2017, In : Oncotarget. 8, 16, p. 27145-27154 10 p.

Research output: Contribution to journalArticle

Genomics
Neoplasms
Precision Medicine
Standard of Care
Therapeutics
11 Citations (Scopus)

Expression profiling of formalin-fixed paraffin-embedded primary breast tumors using cancer-specific and whole genome gene panels on the DASL platform

Reinholz, M. M., Eckel-Passow, J. E., Anderson, S. K., Asmann, Y., Zschunke, M. A., Oberg, A. L., McCullough, A. E., Dueck, A., Chen, B., April, C. S., Wickham-Garcia, E., Jenkins, R. B., Cunningham, J. M., Jen, J., Perez, E. A., Fan, J. B. & Lingle, W. L., 2010, In : BMC Medical Genomics. 3, 60.

Research output: Contribution to journalArticle

Paraffin
Formaldehyde
Genome
Breast Neoplasms
Genes
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
120 Citations (Scopus)

Fluorescence in situ hybridization: A sensitive method for trisomy 8 detection in bone marrow specimens

Jenkins, R. B., Le Beau, M. M., Kraker, W. J., Borell, T. J., Stalboerger, P. G., Davis, E. M., Penland, L., Fernald, A., Espinosa, R., Schaid, D. J., Noel, P. & Dewald, G. W., 1992, In : Blood. 79, 12, p. 3307-3315 9 p.

Research output: Contribution to journalArticle

Fluorescence In Situ Hybridization
Bone
Metaphase
Bone Marrow
Fluorescence
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
37 Citations (Scopus)

Fluorescence in situ hybridization analysis of trisomy 12 in ovarian tumors

Persons, D. L., Hartmann, L. C., Herath, J. F., Keeney, G. & Jenkins, R. B., 1994, In : American Journal of Clinical Pathology. 102, 6, p. 775-779 5 p.

Research output: Contribution to journalArticle

Trisomy
Fluorescence In Situ Hybridization
Granulosa Cell Tumor
Neoplasms
Fibroma
11 Citations (Scopus)

Fluorescence in situ hybridization aneuploidy as a predictor of clinical disease recurrence and prostate-specific antigen level 3 years after radical prostatectomy

Brown, J. A., Slezak, J. M., Lieber, M. M. & Jenkins, R. B., 1999, In : Mayo Clinic Proceedings. 74, 12, p. 1214-1220 7 p.

Research output: Contribution to journalArticle

Aneuploidy
Prostate-Specific Antigen
Prostatectomy
Fluorescence In Situ Hybridization
Recurrence
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
Interphase
p53 Genes
DNA Probes
Homozygote
53 Citations (Scopus)

Fluorescence In Situ hybridization with X and Y chromosome probes for cytogenetic studies on bone marrow cells after opposite sex transplantation

Dewald, G. W., Schad, C. R., Christensen, E. R., Law, M. E., Zinsmeister, A. R., Stalboerger, P. G., Jalal, S. M., Ash, R. C. & Jenkins, R. B., 1993, In : Bone Marrow Transplantation. 12, 2, p. 149-154 6 p.

Research output: Contribution to journalArticle

Y Chromosome
X Chromosome
Fluorescence In Situ Hybridization
Cytogenetics
Bone Marrow Cells
8 Citations (Scopus)

Fluorescent in situ hybridization: Use of whole chromosome paint probes to identify unbalanced chromosome translocations

Kraker, W. J., Borell, T. J., Schad, C. R., Pennington, M. J., Karnes, P. S., Dewald, G. W. & Jenkins, R. B., 1992, In : Mayo Clinic Proceedings. 67, 7, p. 658-662 5 p.

Research output: Contribution to journalArticle

Paint
Fluorescence In Situ Hybridization
Chromosomes
Chromosome Aberrations
Staining and Labeling
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
643 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
40 Citations (Scopus)

Frequent deletions within FRA7G at 7q31.2 in Invasive epithelial ovarian cancer

Huang, H., Reed, C. P., Mordi, A., Lomberk, G., Wang, L., Shridhar, V., Hartmann, L., Jenkins, R. B. & Smith, D. I., Jan 1999, In : Genes Chromosomes and Cancer. 24, 1, p. 48-55 8 p.

Research output: Contribution to journalArticle

Loss of Heterozygosity
Neoplasms
Microsatellite Repeats
Aphidicolin
Ovarian epithelial cancer
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
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
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
83 Citations (Scopus)

Frequent occurrence of cytogenetic abnormalities in sporadic nonmedullary thyroid carcinoma

Jenkins, R. B., Hay, I. D., Herath, J. F., Schultz, C. G., Spurbeck, J. L., Grant, C. S., Goellner, J. R. & Dewald, G. W., 1990, In : Cancer. 66, 6, p. 1213-1220 8 p.

Research output: Contribution to journalArticle

Chromosome Aberrations
Papillary Carcinoma
Karyotype
Cytogenetics
Neoplasms
35 Citations (Scopus)

Functional and clinical significance of variants localized to 8q24 in colon cancer

Cicek, M., Slager, S. L., Achenbach, S. J., French, A. J., Blair, H. E., Fink, S. R., Foster, N. R., Kabat, B. F., Halling, K. C., Cunningham, J. M., Cerhan, J. R., Jenkins, R. B., Boardman, L. A., Petersen, G. M., Sargent, D. J., Alberts, S. R., Limburg, P. J. & Thibodeau, S. N., Sep 2009, In : Cancer Epidemiology Biomarkers and Prevention. 18, 9, p. 2492-2500 9 p.

Research output: Contribution to journalArticle

Chromosome Fragility
Colonic Neoplasms
Fluorescence In Situ Hybridization
Alleles
Odds Ratio
11 Citations (Scopus)

Fusion of HMGA1 to the LPP/TPRG1 intergenic region in a lipoma identified by mapping paraffin-embedded tissues

Wang, X., Zamolyi, R. Q., Zhang, H., Pannain, V. L., Medeiros, F., Erickson-Johnson, M., Jenkins, R. B. & Oliveira, A. M., Jan 1 2010, In : Cancer Genetics and Cytogenetics. 196, 1, p. 64-67 4 p.

Research output: Contribution to journalArticle

Intergenic DNA
Lipoma
Paraffin
Cytogenetic Analysis
Abdominal Wall
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

Gene Expression Correlates of Site-specific Metastasis Among Men With Lymph Node Positive Prostate Cancer Treated With Radical Prostatectomy: A Case Series

Sharma, V., Yousefi, K., Haddad, Z., Buerki, C., Jenkins, R. B., Davicioni, E. & Karnes, R. J., Jan 1 2017, (Accepted/In press) In : Urology.

Research output: Contribution to journalArticle

Prostatectomy
Prostatic Neoplasms
Lymph Nodes
Neoplasm Metastasis
Gene Expression
38 Citations (Scopus)

Gene expression profiling of NF-1-associated and sporadic pilocytic astrocytoma identifies aldehyde dehydrogenase 1 family member L1 (ALDH1L1) as an underexpressed candidate biomarker in aggressive subtypes

Rodriguez, F. J., Giannini, C., Asmann, Y., Sharma, M. K., Perry, A., Tibbetts, K. M., Jenkins, R. B., Scheithauer, B. W., Anant, S., Jenkins, S., Eberhart, C. G., Sarkaria, J. N. & Gutmann, D. H., Dec 2008, In : Journal of Neuropathology and Experimental Neurology. 67, 12, p. 1194-1204 11 p.

Research output: Contribution to journalArticle

Astrocytoma
Gene Expression Profiling
Biomarkers
Neurofibromatosis 1
aldehyde dehydrogenase 1
115 Citations (Scopus)

Genetic aberrations defined by comparative genomic hybridization distinguish long-term from typical survivors of glioblastoma

Burton, E. C., Lamborn, K. R., Feuerstein, B. G., Prados, M., Scott, J., Forsyth, P., Passe, S., Jenkins, R. B. & Aldape, K. D., Nov 1 2002, In : Cancer Research. 62, 21, p. 6205-6210 6 p.

Research output: Contribution to journalArticle

Comparative Genomic Hybridization
Glioblastoma
Survivors
Survival
Neoplasms
17 Citations (Scopus)

Genetically defined oligodendroglioma is characterized by indistinct tumor borders at MRI

Johnson, D. R., Diehn, F. E., Giannini, C., Jenkins, R. B., Jenkins, S. M., Parney, I. F. & Kaufmann, T. J., Apr 1 2017, In : American Journal of Neuroradiology. 38, 4, p. 678-684 7 p.

Research output: Contribution to journalArticle

Oligodendroglioma
Neoplasms
Brain Neoplasms
Glioma
Mutation
17 Citations (Scopus)

Genetic alterations and chemotherapeutic response in human diffuse gliomas

Kitange, G. J., Smith, J. S. & Jenkins, R. B., 2001, In : Expert Review of Anticancer Therapy. 1, 4, p. 595-605 11 p.

Research output: Contribution to journalArticle

Glioma
Adjuvant Chemotherapy
Neoplasms
Drug Therapy
Survival
132 Citations (Scopus)
Glioma
Tumors
Astrocytoma
Molecular Models
Survival
58 Citations (Scopus)

Genetic and chromosomal alterations in prostatic intraepithelial neoplasia and carcinoma detected by fluorescence in situ hybridization

Qian, J., Jenkins, R. B. & Bostwick, D. G., 1999, In : European Urology. 35, 5-6, p. 479-483 5 p.

Research output: Contribution to journalArticle

Prostatic Intraepithelial Neoplasia
Carcinoma in Situ
Fluorescence In Situ Hybridization
Carcinoma
Chromosomes, Human, Pair 7
4 Citations (Scopus)

Genetic changes in epithelial ovarian neoplasia

Cliby, W. A. & Jenkins, R. B., 1992, In : Gynecologic Oncology. 47, 2, p. 135-136 2 p.

Research output: Contribution to journalArticle

Heterozygote
Tumor Suppressor Genes
Chromosome Aberrations
Ovarian Neoplasms
Carcinoma
178 Citations (Scopus)

Genetic heterogeneity in HER2 testing in breast cancer panel summary and guidelines

Vance, G. H., Barry, T. S., Bloom, K. J., Fitzgibbons, P. L., Hicks, D. G., Jenkins, R. B., Persons, D. L., Tubbs, R. R. & Hammond, M. E. H., Apr 2009, In : Archives of Pathology and Laboratory Medicine. 133, 4, p. 611-612 2 p.

Research output: Contribution to journalArticle

Genetic Heterogeneity
erbB-2 Genes
Guidelines
Gene Amplification
Breast Neoplasms
20 Citations (Scopus)

Genetics in glioma: Lessons learned from genome-wide association studies

Melin, B. & Jenkins, R. B., Dec 2013, In : Current Opinion in Neurology. 26, 6, p. 688-692 5 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Glioma
Genetic Loci
Neoplasms
Therapeutics
397 Citations (Scopus)

Genetics of adult glioma

Goodenberger, M. L. & Jenkins, R. B., Dec 2012, In : Cancer genetics. 205, 12, p. 613-621 9 p.

Research output: Contribution to journalArticle

Glioma
Histology
Hereditary Neoplastic Syndromes
Oligodendroglioma
Central Nervous System Neoplasms
33 Citations (Scopus)

Genetic variants in telomerase-related genes are associated with an older age at diagnosis in glioma patients: Evidence for distinct pathways of gliomagenesis

Walsh, K. M., Rice, T., Decker, P. A., Kosel, M. L., Kollmeyer, T., Hansen, H. M., Zheng, S., McCoy, L. S., Bracci, P. M., Anderson, E., Hsuang, G., Wiemels, J. L., Pico, A. R., Smirnov, I., Molinaro, A. M., Tihan, T., Berger, M. S., Chang, S. M., Prados, M. D., Lachance, D. H. & 5 others, Sicotte, H., Eckel-Passow, J. E., Wiencke, J. K., Jenkins, R. B. & Wrensch, M. R., Aug 2013, In : Neuro-Oncology. 15, 8, p. 1041-1047 7 p.

Research output: Contribution to journalArticle

Telomerase
Glioma
Genes
Single Nucleotide Polymorphism
Alleles
89 Citations (Scopus)

Genome-wide array CGH analysis of murine neuroblastoma reveals distinct genomic aberrations which parallel those in human tumors

Hackett, C. S., Hodgson, J. G., Law, M. E., Fridlyand, J., Osoegawa, K., De Jong, P. J., Nowak, N. J., Pinkel, D., Albertson, D. G., Jain, A., Jenkins, R. B., Gray, J. W. & Weiss, W. A., Sep 1 2003, In : Cancer Research. 63, 17, p. 5266-5273 8 p.

Research output: Contribution to journalArticle

Neuroblastoma
Genome
Chromosomes, Human, Pair 16
Neoplasms
Chromosomes, Human, Pair 9
158 Citations (Scopus)

Genome-wide association study of glioma and meta-analysis

Rajaraman, P., Melin, B. S., Wang, Z., McKean-Cowdin, R., Michaud, D. S., Wang, S. S., Bondy, M., Houlston, R., Jenkins, R. B., Wrensch, M., Yeager, M., Ahlbom, A., Albanes, D., Andersson, U., Freeman, L. E. B., Buring, J. E., Butler, M. A., Braganza, M., Carreon, T., Feychting, M. & 50 others, Fleming, S. J., Gapstur, S. M., Gaziano, J. M., Giles, G. G., Hallmans, G., Henriksson, R., Hoffman-Bolton, J., Inskip, P. D., Johansen, C., Kitahara, C. M., Lathrop, M., Liu, C., Marchand, L. L., Linet, M. S., Lonn, S., Peters, U., Purdue, M. P., Rothman, N., Ruder, A. M., Sanson, M., Sesso, H. D., Severi, G., Shu, G., Simon, M., Stampfer, M., Stevens, V. L., Visvanathan, K., White, E., Wolk, A., Zeleniuch-Jacquotte, A., Zheng, W., Decker, P., Enciso-Mora, V., Fridley, B., Gao, Y. T., Kosel, M., Lachance, D. H., Lau, C., Rice, T., Swerdlow, A., Wiemels, J. L., Wiencke, J. K., Shete, S., Xiang, Y. B., Xiao, Y., Hoover, R. N., Fraumeni, J. F., Chatterjee, N., Hartge, P. & Chanock, S. J., Dec 2012, In : Human Genetics. 131, 12, p. 1877-1888 12 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Glioma
Meta-Analysis
Cohort Studies
Case-Control Studies
76 Citations (Scopus)

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

GliomaScan Consortium, Mar 27 2017, (Accepted/In press) In : Nature Genetics.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Genetic Predisposition to Disease
Glioblastoma
Glioma
Odds Ratio
33 Citations (Scopus)

Genome-wide high-density SNP linkage search for glioma susceptibility loci: Results from the gliogene consortium

Shete, S., Lau, C. C., Houlston, R. S., Claus, E. B., Barnholtz-Sloan, J., Lai, R., Il'yasova, D., Schildkraut, J., Sadetzki, S., Johansen, C., Bernstein, J. L., Olson, S. H., Jenkins, R. B., Yang, P., Vick, N. A., Wrensch, M., Davis, F. G., McCarthy, B. J., Leung, E. H. C., Davis, C. & 39 others, Cheng, R., Hosking, F. J., Armstrong, G. N., Liu, Y., Yu, R. K., Henriksson, R., Melin, B. S., Bondy, M. L., Amos, C., Aldape, K. D., Gilbert, M. R., Weinberg, J., Man, C., Guerra, R., Gurusiddappa, S., Scheurer, M. E., Robertson, L., Papaemmanuil, E., Sloan, A. E., Barnett, G., Devine, K., Wolinsky, Y., Florendo, E., Rivas, D., Corpuz, C., Yechezkel, G. H., Bruchim, R. B. S., Aslanov, L., Bødtcher, H., Kosteljanetz, M., Broholm, H., Schubert, E., DeAngelis, L., Rynearson, A., Andersson, U., Brännström, T., Wiencke, J., Wiemels, J. & McCoy, L., Dec 15 2011, In : Cancer Research. 71, 24, p. 7568-7575 8 p.

Research output: Contribution to journalArticle

Glioma
Single Nucleotide Polymorphism
Genome
Genetic Heterogeneity
Molecular Epidemiology
118 Citations (Scopus)

Genomic analysis reveals that immune function genes are strongly linked to clinical outcome in the North Central Cancer Treatment Group N9831 adjuvant trastuzumab trial

Perez, E. A., Thompson, E. A., Ballman, K. V., Anderson, S. K., Asmann, Y., Kalari, K. R., Eckel-Passow, J. E., Dueck, A., Tenner, K. S., Jen, J., Fan, J. B., Geiger, X. J., McCullough, A. E., Chen, B., Jenkins, R. B., Sledge, G. W., Winer, E. P., Gralow, J. R. & Reinholz, M. M., Mar 1 2015, In : Journal of Clinical Oncology. 33, 7, p. 701-708 8 p.

Research output: Contribution to journalArticle

Genes
Neoplasms
Recurrence
Survival
Politics
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
88 Citations (Scopus)

Germline mutations in shelterin complex genes are associated with familial glioma

Bainbridge, M. N., Armstrong, G. N., Gramatges, M. M., Bertuch, A. A., Jhangiani, S. N., Doddapaneni, H., Lewis, L., Tombrello, J., Tsavachidis, S., Liu, Y., Jalali, A., Plon, S. E., Lau, C. C., Parsons, D. W., Claus, E. B., Barnholtz-Sloan, J., Il'yasova, D., Schildkraut, J., Ali-Osman, F., Sadetzki, S. & 19 others, Johansen, C., Houlston, R. S., Jenkins, R. B., Lachance, D. H., Olson, S. H., Bernstein, J. L., Merrell, R. T., Wrensch, M. R., Walsh, K. M., Davis, F. G., Lai, R., Shete, S., Aldape, K., Amos, C. I., Thompson, P. A., Muzny, D. M., Gibbs, R. A., Melin, B. S. & Bondy, M. L., Jan 1 2015, In : Journal of the National Cancer Institute. 107, 1, dju384.

Research output: Contribution to journalArticle

Germ-Line Mutation
Glioma
Genes
Mutation
Exome
392 Citations (Scopus)

Germline mutations in the ribonuclease L gene in families showing linkage with HPC1

Carpten, J., Nupponen, N., Isaacs, S., Sood, R., Robbins, C., Xu, J., Faruque, M., Moses, T., Ewing, C., Gillanders, E., Hu, P., Bujnovszky, P., Makalowska, I., Baffoe-Bonnie, A., Faith, D., Smith, J., Stephan, D., Wiley, K., Brownstein, M., Gildea, D. & 21 others, Kelly, B., Jenkins, R. B., Hostetter, G., Matikainen, M., Schleutker, J., Klinger, K., Connors, T., Xiang, Y., Wang, Z., De Marzo, A., Papadopoulos, N., Kallioniemi, O. P., Burk, R., Meyers, D., Grönberg, H., Meltzer, P., Silverman, R., Bailey-Wilson, J., Walsh, P., Isaacs, W. & Trent, J., 2002, In : Nature Genetics. 30, 2, p. 181-184 4 p.

Research output: Contribution to journalArticle

Germ-Line Mutation
Ribonucleases
Genes
Prostatic Neoplasms
Alleles