Aaron A. Stence

671 total citations
13 papers, 326 citations indexed

About

Aaron A. Stence is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Aaron A. Stence has authored 13 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Pulmonary and Respiratory Medicine and 3 papers in Genetics. Recurrent topics in Aaron A. Stence's work include Cancer Genomics and Diagnostics (3 papers), Muscle Physiology and Disorders (2 papers) and Molecular Biology Techniques and Applications (2 papers). Aaron A. Stence is often cited by papers focused on Cancer Genomics and Diagnostics (3 papers), Muscle Physiology and Disorders (2 papers) and Molecular Biology Techniques and Applications (2 papers). Aaron A. Stence collaborates with scholars based in United States, Estonia and Canada. Aaron A. Stence's co-authors include Deqin Ma, Aaron Bossler, Chris S. Jensen, Michael P. Gailey, Ramakrishna Sompallae, Natalya V. Guseva, Munir R. Tanas, Anthony N. Snow, Omar Jaber and Steven A. Moore and has published in prestigious journals such as Science Advances, Journal of Clinical Pathology and Histopathology.

In The Last Decade

Aaron A. Stence

13 papers receiving 321 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aaron A. Stence United States	10	119	117	84	77	73	13	326
Frederik Van Dyck Belgium	8	57 0.5×	211 1.8×	88 1.0×	30 0.4×	128 1.8×	8	402
Wayne Engleman United States	8	145 1.2×	143 1.2×	66 0.8×	34 0.4×	27 0.4×	8	376
Manuela Pacyna‐Gengelbach Germany	8	45 0.4×	173 1.5×	62 0.7×	18 0.2×	39 0.5×	9	346
Ryuto Tsuchiya Japan	8	150 1.3×	303 2.6×	45 0.5×	50 0.6×	81 1.1×	45	477
Monisha Dandekar United States	8	77 0.6×	184 1.6×	21 0.3×	110 1.4×	25 0.3×	12	391
Sherie Hodges United States	9	74 0.6×	183 1.6×	78 0.9×	17 0.2×	89 1.2×	15	407
Paul Guilhamon United Kingdom	10	88 0.7×	361 3.1×	135 1.6×	21 0.3×	103 1.4×	13	480
Natália D. Linhares Brazil	10	27 0.2×	168 1.4×	16 0.2×	33 0.4×	102 1.4×	21	350
Mamoru Ozaki Japan	12	53 0.4×	152 1.3×	28 0.3×	25 0.3×	142 1.9×	38	389
Vanesa López‐González Spain	15	55 0.5×	264 2.3×	32 0.4×	85 1.1×	311 4.3×	24	532

Countries citing papers authored by Aaron A. Stence

Since Specialization

Citations

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

Fields of papers citing papers by Aaron A. Stence

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aaron A. Stence. 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 Aaron A. Stence. The network helps show where Aaron A. Stence may publish in the future.

Co-authorship network of co-authors of Aaron A. Stence

This figure shows the co-authorship network connecting the top 25 collaborators of Aaron A. Stence. A scholar is included among the top collaborators of Aaron A. Stence 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 Aaron A. Stence. Aaron A. Stence is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Broeckel, Ulrich, M. Anwar Iqbal, Brynn Levy, et al.. (2024). Detection of Constitutional Structural Variants by Optical Genome Mapping. Journal of Molecular Diagnostics. 26(3). 213–226. 8 indexed citations

Inoue, Kaoru, Hamed Bostan, Carl D. Bortner, et al.. (2023). DUX4 double whammy: The transcription factor that causes a rare muscular dystrophy also kills the precursors of the human nose. Science Advances. 9(7). eabq7744–eabq7744. 5 indexed citations

Iqbal, M. Anwar, Ulrich Broeckel, Brynn Levy, et al.. (2023). Multisite Assessment of Optical Genome Mapping for Analysis of Structural Variants in Constitutional Postnatal Cases. Journal of Molecular Diagnostics. 25(3). 175–188. 23 indexed citations

Stence, Aaron A., Ramakrishna Sompallae, Anthony N. Snow, et al.. (2021). Validation of Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy. Journal of Molecular Diagnostics. 23(11). 1506–1514. 32 indexed citations

Larson, Austin, Peter R. Baker, Miroslav P. Milev, et al.. (2018). TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of α-dystroglycan and muscular dystrophy. Skeletal Muscle. 8(1). 17–17. 41 indexed citations

Guseva, Natalya V., Omar Jaber, Aaron A. Stence, et al.. (2018). Simultaneous detection of single‐nucleotide variant, deletion/insertion, and fusion in lung and thyroid carcinoma using cytology specimen and an RNA‐based next‐generation sequencing assay. Cancer Cytopathology. 126(3). 158–169. 16 indexed citations

Guseva, Natalya V., Munir R. Tanas, Aaron A. Stence, et al.. (2016). The NAB2–STAT6 gene fusion in solitary fibrous tumor can be reliably detected by anchored multiplexed PCR for targeted next-generation sequencing. Cancer Genetics. 209(7-8). 303–312. 24 indexed citations

Stence, Aaron A., et al.. (2016). Single thyroid tumour showing multiple differentiated morphological patterns and intramorphological molecular genetic heterogeneity. Journal of Clinical Pathology. 70(2). 116–119. 13 indexed citations

Guseva, Natalya V., Omar Jaber, Munir R. Tanas, et al.. (2016). Anchored multiplex PCR for targeted next‐generation sequencing reveals recurrent and novel USP6 fusions and upregulation of USP6 expression in aneurysmal bone cyst. Genes Chromosomes and Cancer. 56(4). 266–277. 58 indexed citations

10.

Stence, Aaron A., Michael P. Gailey, Robert A. Robinson, Chris S. Jensen, & Deqin Ma. (2015). Simultaneously Detection of 50 Mutations at 20 Sites in the BRAF and RAS Genes by Multiplexed Single-Nucleotide Primer Extension Assay Using Fine-Needle Aspirates of Thyroid Nodules.. PubMed. 88(4). 351–8. 6 indexed citations

11.

Snow, Anthony N., Aaron A. Stence, Jens C. Pruessner, Aaron Bossler, & Deqin Ma. (2014). A simple and cost-effective method of DNA extraction from small formalin-fixed paraffin-embedded tissue for molecular oncologic testing. BMC Clinical Pathology. 14(1). 30–30. 22 indexed citations

12.

Gailey, Michael P., Aaron A. Stence, Chris S. Jensen, & Deqin Ma. (2014). Multiplatform comparison of molecular oncology tests performed on cytology specimens and formalin‐fixed, paraffin‐embedded tissue. Cancer Cytopathology. 123(1). 30–39. 68 indexed citations

13.

Ma, Deqin, et al.. (2013). Identification of KIT activating mutations in paediatric solitary mastocytoma. Histopathology. 64(2). 218–225. 10 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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