Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors A Kallioniemi, OP Kallioniemi, D Sudar, D Rutovitz, JW Gray, F Waldman, ... Science 258 (5083), 818-821, 1992 | 4453 | 1992 |
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. D Pinkel, T Straume, JW Gray Proceedings of the National Academy of Sciences 83 (9), 2934-2938, 1986 | 4221 | 1986 |
A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes RM Neve, K Chin, J Fridlyand, J Yeh, FL Baehner, T Fevr, L Clark, ... Cancer cell 10 (6), 515-527, 2006 | 3748 | 2006 |
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays D Pinkel, R Segraves, D Sudar, S Clark, I Poole, D Kowbel, C Collins, ... Nature genetics 20 (2), 207-211, 1998 | 2884 | 1998 |
Somatic activation of KIT in distinct subtypes of melanoma JA Curtin, K Busam, D Pinkel, BC Bastian Journal of clinical oncology 24 (26), 4340-4346, 2006 | 1889 | 2006 |
Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. D Pinkel, J Landegent, C Collins, J Fuscoe, R Segraves, J Lucas, J Gray Proceedings of the National Academy of Sciences 85 (23), 9138-9142, 1988 | 1681 | 1988 |
PIK3CA is implicated as an oncogene in ovarian cancer L Shayesteh, Y Lu, WL Kuo, R Baldocchi, T Godfrey, C Collins, D Pinkel, ... Nature genetics 21 (1), 99-102, 1999 | 1519 | 1999 |
Genomic and transcriptional aberrations linked to breast cancer pathophysiologies K Chin, S DeVries, J Fridlyand, PT Spellman, R Roydasgupta, WL Kuo, ... Cancer cell 10 (6), 529-541, 2006 | 1494 | 2006 |
Fine-scale structural variation of the human genome E Tuzun, AJ Sharp, JA Bailey, R Kaul, VA Morrison, LM Pertz, E Haugen, ... Nature genetics 37 (7), 727-732, 2005 | 1319 | 2005 |
Assembly of microarrays for genome-wide measurement of DNA copy number AM Snijders, N Nowak, R Segraves, S Blackwood, N Brown, J Conroy, ... Nature genetics 29 (3), 263-264, 2001 | 1234 | 2001 |
Segmental duplications and copy-number variation in the human genome AJ Sharp, DP Locke, SD McGrath, Z Cheng, JA Bailey, RU Vallente, ... The American Journal of Human Genetics 77 (1), 78-88, 2005 | 1193 | 2005 |
A tiling resolution DNA microarray with complete coverage of the human genome AS Ishkanian, CA Malloff, SK Watson, RJ DeLeeuw, B Chi, BP Coe, ... Nature genetics 36 (3), 299-303, 2004 | 804 | 2004 |
Array comparative genomic hybridization and its applications in cancer D Pinkel, DG Albertson Nature genetics 37 (Suppl 6), S11-S17, 2005 | 757 | 2005 |
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome AJ Sharp, S Hansen, RR Selzer, Z Cheng, R Regan, JA Hurst, H Stewart, ... Nature genetics 38 (9), 1038-1042, 2006 | 727 | 2006 |
Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene DG Albertson, B Ylstra, R Segraves, C Collins, SH Dairkee, D Kowbel, ... Nature genetics 25 (2), 144-146, 2000 | 726 | 2000 |
Rapid translocation frequency analysis in humans decades after exposure to ionizing radiation JN Lucas, A Awa, T Straume, M Poggensee, Y Kodama, M Nakano, ... International journal of radiation biology 62 (1), 53-63, 1992 | 666 | 1992 |
Classifying melanocytic tumors based on DNA copy number changes BC Bastian, AB Olshen, PE LeBoit, D Pinkel The American journal of pathology 163 (5), 1765-1770, 2003 | 535 | 2003 |
Detection of bcr-abl Fusion in Chronic Myelogeneous Leukemia by in Situ Hybridization DC Tkachuk, CA Westbrook, M Andreeff, TA Donlon, ML Cleary, ... Science 250 (4980), 559-562, 1990 | 517 | 1990 |
Genomic microarrays in human genetic disease and cancer DG Albertson, D Pinkel Human molecular genetics 12 (suppl_2), R145-R152, 2003 | 487 | 2003 |
Mutations and copy number increase of HRAS in Spitz nevi with distinctive histopathological features BC Bastian, PE LeBoit, D Pinkel The American journal of pathology 157 (3), 967-972, 2000 | 462 | 2000 |