Stephanie A. Smoley

1.4k total citations
44 papers, 908 citations indexed

About

Stephanie A. Smoley is a scholar working on Genetics, Immunology and Hematology. According to data from OpenAlex, Stephanie A. Smoley has authored 44 papers receiving a total of 908 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 19 papers in Immunology and 17 papers in Hematology. Recurrent topics in Stephanie A. Smoley's work include Chronic Lymphocytic Leukemia Research (24 papers), Immunodeficiency and Autoimmune Disorders (17 papers) and Lymphoma Diagnosis and Treatment (15 papers). Stephanie A. Smoley is often cited by papers focused on Chronic Lymphocytic Leukemia Research (24 papers), Immunodeficiency and Autoimmune Disorders (17 papers) and Lymphoma Diagnosis and Treatment (15 papers). Stephanie A. Smoley collaborates with scholars based in United States, France and China. Stephanie A. Smoley's co-authors include Sarah F. Paternoster, Neil E. Kay, Stephanie Fink, Gordon W. Dewald, Tait D. Shanafelt, Daniel L. Van Dyke, Clive S. Zent, Robert B. Jenkins, Kimberly J. Stockero and Rhett P. Ketterling and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Stephanie A. Smoley

43 papers receiving 893 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Stephanie A. Smoley United States	16	571	407	304	302	226	44	908
Renato Bigoni Italy	20	542 0.9×	492 1.2×	213 0.7×	322 1.1×	167 0.7×	35	939
Lisa Kujawski United States	13	359 0.6×	189 0.5×	208 0.7×	255 0.8×	313 1.4×	21	753
Agnès Daudignon France	13	375 0.7×	290 0.7×	174 0.6×	278 0.9×	195 0.9×	38	687
PM Kluin Netherlands	9	372 0.7×	539 1.3×	214 0.7×	209 0.7×	254 1.1×	15	973
Pascale De Paepe Belgium	15	285 0.5×	564 1.4×	233 0.8×	140 0.5×	268 1.2×	36	999
Sophie Gazzo France	16	448 0.8×	453 1.1×	121 0.4×	136 0.5×	266 1.2×	32	856
Alejandra Martínez‐Trillos Spain	16	514 0.9×	419 1.0×	191 0.6×	207 0.7×	323 1.4×	26	898
Andrés Jerez Spain	17	593 1.0×	358 0.9×	527 1.7×	793 2.6×	639 2.8×	60	1.6k
Johannes Bloehdorn Germany	14	581 1.0×	437 1.1×	320 1.1×	120 0.4×	320 1.4×	34	891
Anna Aventı́n Spain	20	317 0.6×	232 0.6×	147 0.5×	495 1.6×	372 1.6×	58	938

Countries citing papers authored by Stephanie A. Smoley

Since Specialization

Citations

This map shows the geographic impact of Stephanie A. Smoley's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Stephanie A. Smoley with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie A. Smoley more than expected).

Fields of papers citing papers by Stephanie A. Smoley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephanie A. Smoley. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Stephanie A. Smoley. The network helps show where Stephanie A. Smoley may publish in the future.

Co-authorship network of co-authors of Stephanie A. Smoley

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie A. Smoley. A scholar is included among the top collaborators of Stephanie A. Smoley based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stephanie A. Smoley. Stephanie A. Smoley is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Peterson, Jess F., Beth A. Pitel, Stephanie A. Smoley, et al.. (2019). Elucidating a false-negative MYC break-apart fluorescence in situ hybridization probe study by next-generation sequencing in a patient with high-grade B-cell lymphoma with IGH/MYC and IGH/BCL2 rearrangements. Molecular Case Studies. 5(3). a004077–a004077. 15 indexed citations

Peterson, Jess F., Beth A. Pitel, Stephanie A. Smoley, et al.. (2019). Detection of a cryptic NUP214/ABL1 gene fusion by mate-pair sequencing (MPseq) in a newly diagnosed case of pediatric T-lymphoblastic leukemia. Molecular Case Studies. 5(2). a003533–a003533. 7 indexed citations

Peterson, Jess F., Reid G. Meyer, Stephanie A. Smoley, et al.. (2019). Whole Genome Mate-pair Sequencing of Plasma Cell Neoplasm as a Novel Diagnostic Strategy: A Case of Unrecognized t(2;11) Structural Variation. Clinical Lymphoma Myeloma & Leukemia. 19(9). 598–602. 2 indexed citations

Rowsey, Ross, Stephanie A. Smoley, George Vasmatzis, et al.. (2019). Characterization of TCF3 rearrangements in pediatric B-lymphoblastic leukemia/lymphoma by mate-pair sequencing (MPseq) identifies complex genomic rearrangements and a novel TCF3/TEF gene fusion. Blood Cancer Journal. 9(10). 81–81. 15 indexed citations

Peterson, Jess F., Beth A. Pitel, Stephanie A. Smoley, et al.. (2018). Use of mate-pair sequencing to characterize a complex cryptic BCR/ABL1 rearrangement observed in a newly diagnosed case of chronic myeloid leukemia. Human Pathology. 89. 109–114. 6 indexed citations

Peterson, Jess F., Beth A. Pitel, Stephanie A. Smoley, et al.. (2018). Constitutional chromosome rearrangements that mimic the 2017 world health organization “acute myeloid leukemia with recurrent genetic abnormalities”: A study of three cases and review of the literature. Cancer Genetics. 230. 37–46. 8 indexed citations

Johnson, Sarah H., James B. Smadbeck, Stephanie A. Smoley, et al.. (2017). SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq). Cancer Genetics. 221. 1–18. 61 indexed citations

Menke, Joshua, George Vasmatzis, Stephen J. Murphy, et al.. (2017). Mantle cell lymphoma with a novel t(11;12)(q13;p11.2): a proposed alternative mechanism of CCND1 up-regulation. Human Pathology. 64. 207–212. 5 indexed citations

Laurie, Cathy C., Cecelia Laurie, Stephanie A. Smoley, et al.. (2014). Acquired chromosomal anomalies in chronic lymphocytic leukemia patients compared with more than 50,000 quasi-normal participants. Cancer Genetics. 207(1-2). 19–30. 4 indexed citations

10.

Heerema, Nyla A., John C. Byrd, Prasad Koduru, et al.. (2010). Stimulation of chronic lymphocytic leukemia cells with CpG oligodeoxynucleotide gives consistent karyotypic results among laboratories: a CLL Research Consortium (CRC) Study. Cancer Genetics and Cytogenetics. 203(2). 134–140. 38 indexed citations

11.

Smoley, Stephanie A., Daniel L. Van Dyke, Neil E. Kay, et al.. (2010). Standardization of fluorescence in situ hybridization studies on chronic lymphocytic leukemia (CLL) blood and marrow cells by the CLL Research Consortium. Cancer Genetics and Cytogenetics. 203(2). 141–148. 17 indexed citations

12.

Dewald, Gordon W., Thomas C. Smyrk, Erik C. Thorland, et al.. (2009). Fluorescence In Situ Hybridization to Visualize Genetic Abnormalities in Interphase Cells of Acinar Cell Carcinoma, Ductal Adenocarcinoma, and Islet Cell Carcinoma of the Pancreas. Mayo Clinic Proceedings. 84(9). 801–810. 23 indexed citations

13.

Fink, Stephanie, Sarah F. Paternoster, Stephanie A. Smoley, et al.. (2009). Validation of a new three-color fluorescence in situ hybridization (FISH) method to detect CHIC2 deletion, FIP1L1/PDGFRA fusion and PDGFRA translocations. Leukemia Research. 33(6). 843–846. 4 indexed citations

14.

Dyke, Daniel L. Van, Tait D. Shanafelt, Timothy G. Call, et al.. (2009). A comprehensive evaluation of the prognostic significance of 13q deletions in patients with B‐chronic lymphocytic leukaemia. British Journal of Haematology. 148(4). 544–550. 58 indexed citations

15.

Smoley, Stephanie A., Stephanie Fink, Sarah F. Paternoster, et al.. (2007). Frequency, hematopathology, and detection of a new isodicentric variant of deletion 20q. Cancer Genetics and Cytogenetics. 173(2). 144–149. 8 indexed citations

16.

Adeyinka, Adewale, et al.. (2007). Isochromosome (X)(p10) in hematologic disorders: FISH study of 14 new cases show three types of centromere signal patterns. Cancer Genetics and Cytogenetics. 179(1). 25–30. 4 indexed citations

17.

Fink, Stephanie, Stephanie A. Smoley, Kimberly J. Stockero, et al.. (2006). Loss of TP53 is due to rearrangements involving chromosome region 17p10∼p12 in chronic lymphocytic leukemia. Cancer Genetics and Cytogenetics. 167(2). 177–181. 27 indexed citations

18.

Stockero, Kimberly J., Stephanie Fink, Stephanie A. Smoley, et al.. (2006). Metaphase cells with normal G-bands have cryptic interstitial deletions in 13q14 detectable by fluorescence in situ hybridization in B-cell chronic lymphocytic leukemia. Cancer Genetics and Cytogenetics. 166(2). 152–156. 10 indexed citations

19.

Fink, Stephanie, Sarah F. Paternoster, Stephanie A. Smoley, et al.. (2004). Fluorescent-labeled DNA probes applied to novel biological aspects of B-cell chronic lymphocytic leukemia. Leukemia Research. 29(3). 253–262. 27 indexed citations

20.

Smoley, Stephanie A., Stephanie R. Brockman, Sarah F. Paternoster, Reid G. Meyer, & Gordon W. Dewald. (2003). A novel tricolor, dual-fusion fluorescence in situ hybridization method to detect BCR/ABL fusion in cells with t(9;22)(q34;q11.2) associated with deletion of DNA on the derivative chromosome 9 in chronic myelocytic leukemia. Cancer Genetics and Cytogenetics. 148(1). 1–6. 15 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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