Matthew Kuhar

2.3k total citations · 1 hit paper
16 papers, 1.6k citations indexed

About

Matthew Kuhar is a scholar working on Molecular Biology, Oncology and Surgery. According to data from OpenAlex, Matthew Kuhar has authored 16 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Oncology and 5 papers in Surgery. Recurrent topics in Matthew Kuhar's work include Vascular Tumors and Angiosarcomas (2 papers), Pluripotent Stem Cells Research (2 papers) and DNA Repair Mechanisms (2 papers). Matthew Kuhar is often cited by papers focused on Vascular Tumors and Angiosarcomas (2 papers), Pluripotent Stem Cells Research (2 papers) and DNA Repair Mechanisms (2 papers). Matthew Kuhar collaborates with scholars based in United States, Spain and Italy. Matthew Kuhar's co-authors include James M. Wells, Susanne I. Wells, Scott A. Rankin, Jason R. Spence, Noah F. Shroyer, Jefferson E. Vallance, Aaron M. Zorn, Christopher N. Mayhew, Elizabeth E. Hoskins and Vladimir V. Kalinichenko and has published in prestigious journals such as Nature, Blood and The American Journal of Surgical Pathology.

In The Last Decade

Matthew Kuhar

14 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro

2010 1.4k citations Jason R. Spence, Christopher N. Mayhew et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Matthew Kuhar United States	7	869	577	541	418	262	16	1.6k
Carey L. Watson United States	11	820 0.9×	567 1.0×	627 1.2×	534 1.3×	383 1.5×	16	1.7k
Nambirajan Sundaram United States	13	639 0.7×	451 0.8×	518 1.0×	398 1.0×	235 0.9×	18	1.5k
Holly M. Poling United States	14	635 0.7×	508 0.9×	556 1.0×	398 1.0×	257 1.0×	24	1.4k
Kyle W. McCracken United States	16	1.1k 1.2×	537 0.9×	588 1.1×	615 1.5×	355 1.4×	22	2.0k
Michael A. Schumacher United States	21	969 1.1×	442 0.8×	713 1.3×	660 1.6×	325 1.2×	39	2.2k
Elizabeth E. Hoskins United States	14	1.3k 1.5×	577 1.0×	718 1.3×	362 0.9×	310 1.2×	16	2.0k
Yu-Hwai Tsai United States	16	773 0.9×	472 0.8×	473 0.9×	383 0.9×	167 0.6×	27	1.5k
Yana Zavros United States	21	998 1.1×	378 0.7×	606 1.1×	520 1.2×	251 1.0×	44	1.8k
Katie L. Sinagoga United States	8	608 0.7×	380 0.7×	405 0.7×	314 0.8×	179 0.7×	9	1.1k
Annelise Haft United States	9	720 0.8×	305 0.5×	389 0.7×	582 1.4×	286 1.1×	9	1.5k

Countries citing papers authored by Matthew Kuhar

Since Specialization

Citations

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

Fields of papers citing papers by Matthew Kuhar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew Kuhar. 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 Matthew Kuhar. The network helps show where Matthew Kuhar may publish in the future.

Co-authorship network of co-authors of Matthew Kuhar

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

All Works

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16 of 16 papers shown

Kuhar, Matthew, et al.. (2025). NTRK Fusions in Xanthogranuloma, a Clinicopathologic and Molecular Analysis of 23 Cases. The American Journal of Surgical Pathology. 49(7). 639–645.

Kuhar, Matthew, et al.. (2023). Fatal eosinophilic myocarditis and submassive hepatic necrosis in lamotrigine induced DRESS syndrome. Allergy Asthma and Clinical Immunology. 19(1). 92–92. 3 indexed citations

Kuhar, Matthew, et al.. (2023). Primary mucoepidermoid carcinoma of the external auditory canal with a CRTC1::MAML2 fusion: A case report and a review of literature. Journal of Cutaneous Pathology. 50(11). 947–950.

Hou, Tieying, et al.. (2023). Comparison of PD-L1 IHC 22C3 PharmDx Combined Positive Score (CPS) in Primary Versus Metastatic Nodal Squamous Cell Carcinomas of the Head and Neck: Is There a Significant Difference?. Applied immunohistochemistry & molecular morphology. 31(8). 550–554. 3 indexed citations

Donegan, Diane, et al.. (2022). Hyperphosphatemic Tumoral Calcinosis With Pemigatinib Use. AACE Clinical Case Reports. 8(5). 217–220. 5 indexed citations

Phillips, Carrie L., et al.. (2021). Crystalglobulinemia causing cutaneous vasculopathy and acute nephropathy in a kidney transplant patient. American Journal of Transplantation. 21(6). 2285–2289. 6 indexed citations

Patel, Rajiv M., Jeffrey P. North, Julie Y. Tse, et al.. (2021). Impact of the American Society of Dermatopathology mentorship awards program. Journal of Cutaneous Pathology. 48(11). 1432–1434. 1 indexed citations

Nowrouzi, Ali, Mathieu Sertorio, Damir Krunic, et al.. (2020). Personalized Assessment of Normal Tissue Radiosensitivity via Transcriptome Response to Photon, Proton and Carbon Irradiation in Patient-Derived Human Intestinal Organoids. Cancers. 12(2). 469–469. 12 indexed citations

Alrabadi, Nasr, Liang Cheng, Matthew Kuhar, et al.. (2018). Detection of driver mutations in BRAF can aid in diagnosis and early treatment of dedifferentiated metastatic melanoma. Modern Pathology. 32(3). 330–337. 19 indexed citations

10.

Kuhar, Matthew, et al.. (2017). Epithelioid malignant mesothelioma metastatic to the skin: A case report and review of the literature. Journal of Cutaneous Pathology. 44(12). 1057–1063. 9 indexed citations

11.

Chlon, Timothy M., et al.. (2015). Models of Pluripotent and Somatic Stem Cells to Study Tissue-Specific Sensitivities in Fanconi Anemia. Blood. 126(23). 168–168. 1 indexed citations

12.

Cheng, Liang, Shaobo Zhang, Darrell D. Davidson, et al.. (2014). Laser capture microdissection in molecular diagnostics. 465–482. 3 indexed citations

13.

Spence, Jason R., Christopher N. Mayhew, Scott A. Rankin, et al.. (2010). Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro. Nature. 470(7332). 105–109. 1434 indexed citations breakdown →

14.

Kuhar, Matthew, et al.. (2010). Melanotic Neuroectodermal Tumor of Infancy Presenting in the Subcutaneous Soft Tissue of the Thigh. American Journal of Dermatopathology. 32(3). 282–286. 12 indexed citations

15.

Idrees, Muhammad T., Matthew Kuhar, Thomas M. Ulbright, et al.. (2009). Clonal evidence for the progression of a testicular germ cell tumor to angiosarcoma. Human Pathology. 41(1). 139–144. 13 indexed citations

16.

MacLennan, Gregory T., et al.. (2007). Histogenesis of sarcomatoid urothelial carcinoma of the urinary bladder: evidence for a common clonal origin with divergent differentiation. The Journal of Pathology. 211(4). 420–430. 80 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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