Publications by authors named "Stephanie Fink"

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Improving access to cervical cancer screening: The impact of a Saturday pap smear clinic.
Brittany Strelow, Joy Stevens, Stephanie Fink, Kristin Cole, Danielle O'Laughlin

J Med Screen· June 2025

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Caregiver Wellness after Traumatic Brain Injury (CG-Well): Protocol for a randomized clinical trial.
Natalie Kreitzer, Stephanie Fink, Opeolu Adeoye, Brad Kurowski G, Shari Wade

Contemp Clin Trials Commun· October 2024

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Saturday Pap Smear Clinic: addressing barriers to cervical cancer screening.
Brittany Strelow, Mollie Francis, Gabrielle Gertner, Rachel Olson, Kholood Abuhadid, Stephanie Fink

BMJ Open Qual· July 2023

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Papanicolaou test collection with the Papette brush or the spatula with cytobrush: A pragmatic study.
Danielle J O'Laughlin, Brittany A Strelow, Nicole A Fellows, Joy N Stevens, Elizabeth A Kelsey, Stephanie R Fink

Womens Health (Lond)· May 2023

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Implementation of preemptive DNA sequence-based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study.
Liewei Wang, Steven E Scherer, Suzette J Bielinski, Donna M Muzny, Leila A Jones, Stephanie R Fink

Genet Med· May 2022

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Postpartum depression in older women.
Brittany Strelow, Nicole Fellows, Stephanie R Fink, Danielle J OʼLaughlin, Gladys Radke

JAAPA· March 2018

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Tumorgrafts as in vivo surrogates for women with ovarian cancer.
S John Weroha, Marc A Becker, Sergio Enderica-Gonzalez, Sean C Harrington, Ann L Oberg, Stephanie Fink

Clin Cancer Res· March 2014

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Discovery and validation of a prostate cancer genomic classifier that predicts early metastasis following radical prostatectomy.
Nicholas Erho, Anamaria Crisan, Ismael A Vergara, Anirban P Mitra, Mercedeh Ghadessi, Stephanie Fink

PLoS One· February 2014

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Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology.
Terri Rice, Shichun Zheng, Paul A Decker, Kyle M Walsh, Paige Bracci, Stephanie Fink

Neuro Oncol· May 2013

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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.
Robert B Jenkins, Yuanyuan Xiao, Hugues Sicotte, Paul A Decker, Thomas M Kollmeyer, Stephanie R Fink

Nat Genet· October 2012

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p16-Cdk4-Rb axis controls sensitivity to a cyclin-dependent kinase inhibitor PD0332991 in glioblastoma xenograft cells.
Ling Cen, Brett L Carlson, Mark A Schroeder, Jamie L Ostrem, Gaspar J Kitange, Stephanie R Fink

Neuro Oncol· July 2012

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MYC gene amplification is often acquired in lethal distant breast cancer metastases of unamplified primary tumors.
Aatur D Singhi, Ashley Cimino-Mathews, Robert B Jenkins, Fusheng Lan, Stephanie R Fink

Mod Pathol· March 2012

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Primary central nervous system lymphomas: a validation study of array-based comparative genomic hybridization in formalin-fixed paraffin-embedded tumor specimens.
Esteban Braggio, Ellen Remstein McPhail, William Macon, M Beatriz Lopes, David Schiff, Stephanie Fink

Clin Cancer Res· July 2011

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Distinct germ line polymorphisms underlie glioma morphologic heterogeneity.
Robert B Jenkins, Margaret R Wrensch, Derek Johnson, Brooke L Fridley, Paul A Decker, Stephanie Fink

Cancer Genet· January 2011

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Tubulin polymerization promoting protein (TPPP/p25) as a marker for oligodendroglial changes in multiple sclerosis.
Romana Höftberger, Stephanie Fink, Fahmy Aboul-Enein, Gergö Botond, Judit Olah

Glia· November 2010

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Functional and clinical significance of variants localized to 8q24 in colon cancer.
Mine S Cicek, Susan L Slager, Sara J Achenbach, Amy J French, Hilary E Blair, Stephanie R Fink

Cancer Epidemiol Biomarkers Prev· September 2009

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Fluorescence in situ hybridization to visualize genetic abnormalities in interphase cells of acinar cell carcinoma, ductal adenocarcinoma, and islet cell carcinoma of the pancreas.
Gordon W Dewald, Thomas C Smyrk, Erik C Thorland, Robert R McWilliams, Daniel L Van Dyke, Stephanie R Fink

Mayo Clin Proc· September 2009

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Validation of a new three-color fluorescence in situ hybridization (FISH) method to detect CHIC2 deletion, FIP1L1/PDGFRA fusion and PDGFRA translocations.
Stephanie R Fink, Kimberly J Belongie, Sarah F Paternoster, Stephanie A Smoley, Animesh D Pardanani

Leuk Res· June 2009

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Incidence of TCR and TCL1 gene translocations and isochromosome 7q in peripheral T-cell lymphomas using fluorescence in situ hybridization.
Andrew L Feldman, Mark Law, Karen L Grogg, Erik C Thorland, Stephanie Fink

Am J Clin Pathol· August 2008

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Isochromosome (X)(p10) in hematologic disorders: FISH study of 14 new cases show three types of centromere signal patterns.
Adewale Adeyinka, Stephanie Smoley, Stephanie Fink, Jessica Sanchez, Daniel L Van Dyke

Cancer Genet Cytogenet· November 2007

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Efficacy of conventional cytogenetics and FISH for EGR1 to detect deletion 5q in hematological disorders and to assess response to treatment with Lenalidomide.
Ying S Zou, Stephanie R Fink, Kimberly J Stockero, Sarah F Paternoster, Stephanie A Smoley

Leuk Res· September 2007

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Frequency, hematopathology, and detection of a new isodicentric variant of deletion 20q.
Stephanie A Smoley, Stephanie R Fink, Sarah F Paternoster, Kimberly J Stockero, Lai P Nguyen

Cancer Genet Cytogenet· March 2007

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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.
Ellen D Remstein, Ahmet Dogan, Richard R Einerson, Sarah F Paternoster, Stephanie R Fink

Am J Surg Pathol· December 2006

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Prospective evaluation of clonal evolution during long-term follow-up of patients with untreated early-stage chronic lymphocytic leukemia.
Tait D Shanafelt, Thomas E Witzig, Stephanie R Fink, Robert B Jenkins, Sarah F Paternoster

J Clin Oncol· October 2006

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Loss of TP53 is due to rearrangements involving chromosome region 17p10 approximately p12 in chronic lymphocytic leukemia.
Stephanie R Fink, Stephanie A Smoley, Kimberly J Stockero, Sarah F Paternoster, Erik C Thorland

Cancer Genet Cytogenet· June 2006

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