Nicole L. Hoppman

1.1k total citations
62 papers, 704 citations indexed

About

Nicole L. Hoppman is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Nicole L. Hoppman has authored 62 papers receiving a total of 704 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Hematology, 19 papers in Molecular Biology and 19 papers in Genetics. Recurrent topics in Nicole L. Hoppman's work include Acute Myeloid Leukemia Research (16 papers), Chronic Myeloid Leukemia Treatments (15 papers) and Acute Lymphoblastic Leukemia research (14 papers). Nicole L. Hoppman is often cited by papers focused on Acute Myeloid Leukemia Research (16 papers), Chronic Myeloid Leukemia Treatments (15 papers) and Acute Lymphoblastic Leukemia research (14 papers). Nicole L. Hoppman collaborates with scholars based in United States, Canada and France. Nicole L. Hoppman's co-authors include Umut Aypar, Hutton M. Kearney, Erik C. Thorland, James B. Smadbeck, George Vasmatzis, Linda B. Baughn, Jess F. Peterson, Patricia T. Greipp, Rhett P. Ketterling and Beth A. Pitel and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Nicole L. Hoppman

58 papers receiving 698 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nicole L. Hoppman United States	14	279	279	173	115	92	62	704
Marie Trková Czechia	13	272 1.0×	145 0.5×	97 0.6×	76 0.7×	60 0.7×	33	589
James Tepperberg United States	15	362 1.3×	532 1.9×	86 0.5×	284 2.5×	84 0.9×	28	889
Periklis Makrythanasis Switzerland	18	402 1.4×	278 1.0×	59 0.3×	59 0.5×	83 0.9×	58	798
Emilie Falconnet Switzerland	15	409 1.5×	251 0.9×	67 0.4×	91 0.8×	161 1.8×	16	672
Giuseppe Calabrese Italy	14	257 0.9×	173 0.6×	135 0.8×	154 1.3×	32 0.3×	45	711
Jonathan J. Waters United Kingdom	17	362 1.3×	439 1.6×	127 0.7×	410 3.6×	69 0.8×	32	1.0k
Pamela Brock United States	15	277 1.0×	286 1.0×	40 0.2×	45 0.4×	103 1.1×	39	712
Silvia Majore Italy	16	427 1.5×	319 1.1×	144 0.8×	33 0.3×	29 0.3×	48	808
M. L. Kwee Netherlands	13	426 1.5×	320 1.1×	55 0.3×	91 0.8×	72 0.8×	24	640
Anita S. Kulharya United States	14	509 1.8×	452 1.6×	72 0.4×	147 1.3×	60 0.7×	31	843

Countries citing papers authored by Nicole L. Hoppman

Since Specialization

Citations

This map shows the geographic impact of Nicole L. Hoppman'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 Nicole L. Hoppman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nicole L. Hoppman more than expected).

Fields of papers citing papers by Nicole L. Hoppman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicole L. Hoppman. 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 Nicole L. Hoppman. The network helps show where Nicole L. Hoppman may publish in the future.

Co-authorship network of co-authors of Nicole L. Hoppman

This figure shows the co-authorship network connecting the top 25 collaborators of Nicole L. Hoppman. A scholar is included among the top collaborators of Nicole L. Hoppman 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 Nicole L. Hoppman. Nicole L. Hoppman 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

Khanna, Cheryl L., James B. Smadbeck, Sarah H. Johnson, et al.. (2024). Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld‐Rieger Syndrome. American Journal of Medical Genetics Part A. 194(5). e63542–e63542. 2 indexed citations

Meyer, Reid G., Patricia T. Greipp, Nicole L. Hoppman, et al.. (2024). Cytogenetic and pathologic characterization of MYC-rearranged B-cell lymphomas in pediatric and young adult patients. Journal of Hematopathology. 17(2). 51–61. 1 indexed citations

Gomes, Maria Aparecida, Laura Morsberger, Nicole L. Hoppman, et al.. (2024). An Integrated Approach Including CRISPR/Cas9-Mediated Nanopore Sequencing, Mate Pair Sequencing, and Cytogenomic Methods to Characterize Complex Structural Rearrangements in Acute Myeloid Leukemia. Biomedicines. 12(3). 598–598. 1 indexed citations

Ding, Qiliang, J. Fine, Nicole L. Hoppman, et al.. (2024). Follow the LINE: A novel case of dilated cardiomyopathy caused by a LINE-1 insertion in the TTN gene. American Journal of Clinical Pathology. 163(4). 511–515.

Polonis, Katarzyna, Stuart Schwartz, Christina Grant, et al.. (2023). Uniparental disomy of multiple chromosomes in two cases with a complex phenotype. American Journal of Medical Genetics Part A. 191(7). 1978–1983. 3 indexed citations

Blackburn, Patrick R., Kaaren K. Reichard, Sarah H. Johnson, et al.. (2022). A Novel USP25::PDGFRA Gene Fusion in a 78 Year Old Patient with a Myeloid Neoplasm. Laboratory Medicine. 53(5). e134–e138.

Rahman, Zaid Abdel, Ricardo Parrondo, Michael G. Heckman, et al.. (2021). Comparative study of therapy‐related and de novo adult b‐cell acute lymphoblastic leukaemia. British Journal of Haematology. 196(4). 963–968. 7 indexed citations

Pitel, Beth A., Kathryn E. Pearce, James B. Smadbeck, et al.. (2020). Characterizing false-positive fluorescence in situ hybridization results by mate-pair sequencing in a patient with chronic myeloid leukemia and progression to myeloid blast crisis. Cancer Genetics. 243. 48–51. 8 indexed citations

Lindsey, Kathryn, Linda B. Baughn, Nicole L. Hoppman, et al.. (2020). Integrated genomic analysis using chromosomal microarray, fluorescence in situ hybridization and mate pair analyses: Characterization of a cryptic t(9;22)(p24.1;q11.2)/BCR-JAK2 in myeloid/lymphoid neoplasm with eosinophilia. Cancer Genetics. 246-247. 44–47. 7 indexed citations

10.

Xu, Xinjie, William R. Sukov, Patricia T. Greipp, et al.. (2020). Siblings with ETV6/RUNX1-positive B-lymphoblastic leukemia: A single site experience and review of the literature. Annals of Diagnostic Pathology. 48. 151588–151588. 1 indexed citations

11.

Polonis, Katarzyna, Matthew Schultz, Horatiu Olteanu, et al.. (2020). Detection of cryptic CCND1 rearrangements in mantle cell lymphoma by next generation sequencing. Annals of Diagnostic Pathology. 46. 151533–151533. 7 indexed citations

12.

Blackburn, Patrick R., Linda B. Baughn, Rhett P. Ketterling, et al.. (2020). Identification of a novel KMT2A/GIMAP8 gene fusion in a pediatric patient with acute undifferentiated leukemia. Genes Chromosomes and Cancer. 60(2). 108–111. 4 indexed citations

13.

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

14.

Smadbeck, James B., Jess F. Peterson, Kathryn E. Pearce, et al.. (2019). Mate pair sequencing outperforms fluorescence in situ hybridization in the genomic characterization of multiple myeloma. Blood Cancer Journal. 9(12). 103–103. 29 indexed citations

15.

Wang, Chen, Amy L. Weaver, Nicole L. Hoppman, et al.. (2019). Combining copy number, methylation markers, and mutations as a panel for endometrial cancer detection via intravaginal tampon collection. Gynecologic Oncology. 156(2). 387–392. 21 indexed citations

16.

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

17.

Hoppman, Nicole L., Kandelaria M. Rumilla, Emily Lauer, Hutton M. Kearney, & Erik C. Thorland. (2018). Patterns of homozygosity in patients with uniparental disomy: detection rate and suggested reporting thresholds for SNP microarrays. Genetics in Medicine. 20(12). 1522–1527. 40 indexed citations

18.

Zou, Ying, et al.. (2017). Novel t(5;11)(q32;q13.4) with NUMA1-PDGFRB fusion in a myeloid neoplasm with eosinophilia with response to imatinib mesylate. Cancer Genetics. 212-213. 38–44. 5 indexed citations

19.

Cao, Yang, et al.. (2016). Two cases with de novo 3q26.31 microdeletion suggest a role for FNDC3B in human craniofacial development. American Journal of Medical Genetics Part A. 170(12). 3276–3281. 4 indexed citations

20.

Aypar, Umut, et al.. (2014). Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader–Willi/Angelman syndrome critical region. American Journal of Medical Genetics Part A. 164(10). 2514–2520. 7 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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