The incidence and anatomic site specificity of chromosomal translocations in primary extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) in North America
Remstein, Ellen D, Dogan, Ahmet, Einerson, Richard R, Paternoster, Sarah F, Fink, Stephanie R, Law, Mark, Dewald, Gordon W, Kurtin, Paul J
Published in The American journal of surgical pathology (01.12.2006)
Published in The American journal of surgical pathology (01.12.2006)
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Prospective Evaluation of Clonal Evolution During Long-Term Follow-Up of Patients With Untreated Early-Stage Chronic Lymphocytic Leukemia
SHANAFELT, Tait D, WITZIG, Thomas E, GEYER, Susan, ZENT, Clive S, CALL, Tim G, JELINEK, Diane F, KAY, Neil E, DEWALD, Gordon W, FINK, Stephanie R, JENKINS, Robert B, PATERNOSTER, Sarah F, SMOLEY, Stephanie A, STOCKERO, Kimberly J, NAST, Danielle M, FLYNN, Heather C, TSCHUMPER, Renee C
Published in Journal of clinical oncology (01.10.2006)
Published in Journal of clinical oncology (01.10.2006)
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Papanicolaou test collection with the Papette brush or the spatula with cytobrush: A pragmatic study
O’Laughlin, Danielle J, Strelow, Brittany A, Fellows, Nicole A, Stevens, Joy N, Kelsey, Elizabeth A, Fink, Stephanie R, Peters, Sonya M, Johnson, Jennifer A, Houghton, Jaclyn P, Stolp, Anne M, Fischer, Karen M, Tweedy, Johanna M, DeJesus, Ramona S
Published in Women's health (London, England) (01.01.2023)
Published in Women's health (London, England) (01.01.2023)
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Journal Article
Functional and Clinical Significance of Variants Localized to 8q24 in Colon Cancer
CICEK, Mine S, SLAGER, Susan L, CERHAN, James R, JENKINS, Robert B, BOARDMAN, Lisa A, PETERSEN, Gloria M, SARGENT, Daniel J, ALBERTS, Steven R, LIMBURG, Paul J, THIBODEAU, Stephen N, ACHENBACH, Sara J, FRENCH, Amy J, BLAIR, Hilary E, FINK, Stephanie R, FOSTER, Nathan R, KABAT, Brian F, HALLING, Kevin C, CUNNINGHAM, Julie M
Published in Cancer epidemiology, biomarkers & prevention (01.09.2009)
Published in Cancer epidemiology, biomarkers & prevention (01.09.2009)
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Implementation of preemptive DNA sequence–based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study
Wang, Liewei, Scherer, Steven E., Bielinski, Suzette J., Muzny, Donna M., Jones, Leila A., Black, John Logan, Moyer, Ann M., Giri, Jyothsna, Sharp, Richard R., Matey, Eric T., Wright, Jessica A., Oyen, Lance J., Wiepert, Mathieu, Sullard, Terri, Curry, Timothy B., Rohrer Vitek, Carolyn R., St. Sauver, Jennifer L., Lazaridis, Konstantinos N., Venner, Eric, Qin, Xiang, Kovar, Christie L., Korchina, Viktoriya, Walker, Kimberly, Doddapaneni, HarshaVardhan, Wu, Tsung-Jung, Raj, Ritika, Denson, Shawn, Chandanavelli, Gauthami, Zhang, Lan, Karow, Mary Beth, Harris, Kimberley J., Sicotte, Hugues, Peterson, Sandra E., Barthel, Amy E., Skierka, Jennifer M., Kluge, Michelle L., Kotzer, Katrina E., Kloke, Karen, Vander Pol, Jessica M., Sutton, Joseph A., Kekic, Adrijana, Ebenhoh, Ashley, Bierle, Dennis M., Schuh, Michael J., Grilli, Christopher, Erickson, Sara, Umbreit, Audrey, Ward, Leah, Nelson, Eric A., Levey, Sharon, Elliott, Michelle, Peters, Steve G., Pereira, Naveen, Frye, Mark, Shamoun, Fadi, Goetz, Matthew P., Kullo, Iftikhar J., Wermers, Robert, Anderson, Jan A., Formea, Christine M., El Melik, Razan M., Herges, Joseph R., Krieger, Carrie A., Hoel, Robert W., Taraba, Jodi L., St. Thomas, Scott R., Absah, Imad, Bernard, Matthew E., Fink, Stephanie R., Gossard, Andrea, Grubbs, Pamela L., Jacobson, Therese M., Takahashi, Paul, Buckles, Susan, Bumgardner, Michelle, Gallagher, Colette, Fee-Schroeder, Kelliann, Nicholas, Nichole R., Powers, Melody L., Ragab, Ahmed K., Richardson, Darcy M., Stai, Anthony, Olson, Janet E., Sutton, Erica J., Beck, Annika T., Horrow, Caroline, Kalari, Krishna R., Liu, Hongfang, Wang, Liwei, Zhu, Ye, Jacobson, Debra J., Hathcock, Matthew A., McGree, Michaela E., Koep, Tyler H., Ross, Jason L., Ramey, Bronwyn, Searcy, Isabelle, Boerwinkle, Eric, Gibbs, Richard A., Weinshilboum, Richard M.
Published in Genetics in medicine (01.05.2022)
Published in Genetics in medicine (01.05.2022)
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p16-Cdk4-Rb axis controls sensitivity to a cyclin-dependent kinase inhibitor PD0332991 in glioblastoma xenograft cells
Cen, Ling, Carlson, Brett L, Schroeder, Mark A, Ostrem, Jamie L, Kitange, Gaspar J, Mladek, Ann C, Fink, Stephanie R, Decker, Paul A, Wu, Wenting, Kim, Jung-Sik, Waldman, Todd, Jenkins, Robert B, Sarkaria, Jann N
Published in Neuro-oncology (Charlottesville, Va.) (01.07.2012)
Published in Neuro-oncology (Charlottesville, Va.) (01.07.2012)
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A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation
JENKINS, Robert B, YUANYUAN XIAO, BRACCI, Paige, MCCOY, Lucie S, SMIRNOV, Ivan, PATOKA, Joseph S, HSUANG, George, WIEMELS, Joe L, TIHAN, Tarik, PICO, Alexander R, PRADOS, Michael D, CHANG, Susan M, SICOTTE, Hugues, BERGER, Mitchel S, CARON, Alissa A, FINK, Stephanie R, HALDER, Chandralekha, RYNEARSON, Amanda L, FRIDLEY, Brooke L, BUCKNER, Jan C, O'NEILL, Brian P, GIANNINI, Caterina, LACHANCE, Daniel H, DECKER, Paul A, WIENCKE, John K, ECKEL-PASSOW, Jeanette E, WRENSCH, Margaret R, KOLLMEYER, Thomas M, HANSEN, Helen M, KOSEL, Matthew L, SHICHUN ZHENG, WALSH, Kyle M, RICE, Terri
Published in Nature genetics (01.10.2012)
Published in Nature genetics (01.10.2012)
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Journal Article
MYC gene amplification is often acquired in lethal distant breast cancer metastases of unamplified primary tumors
Singhi, Aatur D, Cimino-Mathews, Ashley, Jenkins, Robert B, Lan, Fusheng, Fink, Stephanie R, Nassar, Hind, Vang, Russell, Fetting, John H, Hicks, Jessica, Sukumar, Saraswati, De Marzo, Angelo M, Argani, Pedram
Published in Modern pathology (01.03.2012)
Published in Modern pathology (01.03.2012)
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Journal Article
Postpartum depression in older women
Strelow, Brittany, Fellows, Nicole, Fink, Stephanie R, OʼLaughlin, Danielle J, Radke, Gladys, Stevens, Joy, Tweedy, Johanna M
Published in JAAPA (Montvale, N.J.) (01.03.2018)
Published in JAAPA (Montvale, N.J.) (01.03.2018)
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Preclinical validation of fluorescence in situ hybridization assays for clinical practice
Wiktor, Anne E., Van Dyke, Daniel L., Stupca, Peggy J., Ketterling, Rhett P., Thorland, Erik C., Shearer, Brandon M., Fink, Stephanie R., Stockero, Kimberly J., Majorowicz, Jason R., Dewald, Gordon W.
Published in Genetics in medicine (01.01.2006)
Published in Genetics in medicine (01.01.2006)
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Journal Article
Validation of a new three-color fluorescence in situ hybridization (FISH) method to detect CHIC2 deletion, FIP1L1/PDGFRA fusion and PDGFRA translocations
Fink, Stephanie R, Belongie, Kimberly J, Paternoster, Sarah F, Smoley, Stephanie A, Pardanani, Animesh D, Tefferi, Ayalew, Van Dyke, Daniel L, Ketterling, Rhett P
Published in Leukemia research (01.06.2009)
Published in Leukemia research (01.06.2009)
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Journal Article
Efficacy of conventional cytogenetics and FISH for EGR1 to detect deletion 5q in hematological disorders and to assess response to treatment with Lenalidomide
Zou, Ying S, Fink, Stephanie R, Stockero, Kimberly J, Paternoster, Sarah F, Smoley, Stephanie A, Tun, Han W, Reeder, Craig B, Tefferi, Ayalew, Dewald, Gordon W
Published in Leukemia research (01.09.2007)
Published in Leukemia research (01.09.2007)
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Journal Article
Fluorescent-labeled DNA probes applied to novel biological aspects of B-cell chronic lymphocytic leukemia
Fink, Stephanie R., Paternoster, Sarah F., Smoley, Stephanie A., Flynn, Heather C., Geyer, Susan M., Shanafelt, Tait D., Lee, You Kyoung, Jelinek, Diane F., Kay, Neil E., Dewald, Gordon W.
Published in Leukemia research (01.03.2005)
Published in Leukemia research (01.03.2005)
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CCDC26 Polymorphisms Are Differentially Expressed in Myeloid Malignancies with Mutant IDH1 Compared to Their IDH2R140-Mutated or IDH-Unmutated Counterparts
Lasho, Terra L, Tefferi, Ayalew, Pardanani, Animesh, Finke, Christy, Fink, Stephanie R, Decker, Paul A, Jenkins, Robert
Published in Blood (18.11.2011)
Published in Blood (18.11.2011)
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Journal Article
Abstract 4207: The germline rs55705857 risk allele is not preferentially gained in gliomas with 8q24 duplication
Rynearson, Amanda L., Schowalter, Kirsten A., Fink, Stephanie R., Kollmeyer, Thomas M., Halder, Chandralekha, Sarkar, Gobinda, Caron, Alissa A., Pauley, Rachel A., Lachance, Daniel H., O'Neill, Brian Patrick, Jenkins, Robert B.
Published in Cancer research (Chicago, Ill.) (15.04.2013)
Published in Cancer research (Chicago, Ill.) (15.04.2013)
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Journal Article
Loss of TP53 is due to rearrangements involving chromosome region 17p10∼p12 in chronic lymphocytic leukemia
Fink, Stephanie R., Smoley, Stephanie A., Stockero, Kimberly J., Paternoster, Sarah F., Thorland, Erik C., Van Dyke, Daniel L., Shanafelt, Tait D., Zent, Clive S., Call, Timothy G., Kay, Neil E., Dewald, Gordon W.
Published in Cancer genetics and cytogenetics (01.06.2006)
Published in Cancer genetics and cytogenetics (01.06.2006)
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Abstract C191: The effect of the cyclin-dependent kinase inhibitor PD 0332991 on glioblastoma cells and relationship with p15INK4B/p16INK4A expression
Cen, Ling, Ostrem, Jamie L., Schroeder, Mark A., Mladek, Ann C., Fink, Stephanie R., Jenkins, Robert B., Sarkaria, Jann N.
Published in Molecular cancer therapeutics (10.12.2009)
Published in Molecular cancer therapeutics (10.12.2009)
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Journal Article
A low frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and IDH1 or IDH2 mutated astrocytomas
Jenkins, Robert B., Xiao, Yuanyuan, Sicotte, Hugues, Decker, Paul A., Kollmeyer, Thomas M., Hansen, Helen M., Kosel, Matthew L., Zheng, Shichun, Walsh, Kyle M., Rice, Terri, Bracci, Paige, McCoy, Lucie S., Smirnov, Ivan, Patoka, Joseph S., Hsuang, George, Wiemels, Joe L., Tihan, Tarik, Pico, Alexander R., Prados, Michael D., Chang, Susan M., Berger, Mitchel S., Caron, Alissa A., Fink, Stephanie R., Halder, Chandralekha, Rynearson, Amanda L., Fridley, Brooke L., Buckner, Jan C., O’Neill, Brian P., Giannini, Caterina, Lachance, Daniel H., Wiencke, John K., Eckel-Passow, Jeanette E., Wrensch, Margaret R.
Published in Nature genetics (26.08.2012)
Published in Nature genetics (26.08.2012)
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Journal Article
Frequency, hematopathology, and detection of a new isodicentric variant of deletion 20q
Smoley, Stephanie A, Fink, Stephanie R, Paternoster, Sarah F, Stockero, Kimberly J, Nguyen, Lai P, Nguyen, Phuong L, Hanson, Curtis A, Dewald, Gordon W
Published in Cancer genetics and cytogenetics (01.03.2007)
Published in Cancer genetics and cytogenetics (01.03.2007)
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Journal Article
Metaphase cells with normal G-bands have cryptic interstitial deletions in 13q14 detectable by fluorescence in situ hybridization in B-cell chronic lymphocytic leukemia
Stockero, Kimberly J., Fink, Stephanie R., Smoley, Stephanie A., Paternoster, Sarah F., Shanafelt, Tait D., Call, Timothy G., Zent, Clive S., Van Dyke, Daniel L., Kay, Neil E., Dewald, Gordon W.
Published in Cancer genetics and cytogenetics (15.04.2006)
Published in Cancer genetics and cytogenetics (15.04.2006)
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