Helmut C. Weigelin

1.3k total citations
17 papers, 878 citations indexed

About

Helmut C. Weigelin is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Helmut C. Weigelin has authored 17 papers receiving a total of 878 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Oncology. Recurrent topics in Helmut C. Weigelin's work include Myeloproliferative Neoplasms: Diagnosis and Treatment (4 papers), Chronic Myeloid Leukemia Treatments (3 papers) and Oral and Maxillofacial Pathology (3 papers). Helmut C. Weigelin is often cited by papers focused on Myeloproliferative Neoplasms: Diagnosis and Treatment (4 papers), Chronic Myeloid Leukemia Treatments (3 papers) and Oral and Maxillofacial Pathology (3 papers). Helmut C. Weigelin collaborates with scholars based in United States and Canada. Helmut C. Weigelin's co-authors include Bryan L. Betz, Kojo S.J. Elenitoba‐Johnson, Noah A. Brown, Megan S. Lim, Larissa V. Furtado, Jonathan B. McHugh, Mark J. Kiel, Michael H. Roh, Lili Zhao and Stewart M. Knoepp and has published in prestigious journals such as Blood, Clinical Cancer Research and Annals of Oncology.

In The Last Decade

Helmut C. Weigelin

16 papers receiving 868 citations

Peers

Helmut C. Weigelin
Noah A. Brown United States
Kim Piper United Kingdom
Nicholas Plowman United Kingdom
S. McCarthy Australia
Andrew S. McDaniel United States
Noah A. Brown United States
Helmut C. Weigelin
Citations per year, relative to Helmut C. Weigelin Helmut C. Weigelin (= 1×) peers Noah A. Brown

Countries citing papers authored by Helmut C. Weigelin

Since Specialization
Citations

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

Fields of papers citing papers by Helmut C. Weigelin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Helmut C. Weigelin. 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 Helmut C. Weigelin. The network helps show where Helmut C. Weigelin may publish in the future.

Co-authorship network of co-authors of Helmut C. Weigelin

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

All Works

17 of 17 papers shown
1.
Betz, Bryan L., et al.. (2024). Optimization of Tumor Dissection Procedures Leads to Measurable Improvement in the Quality of Molecular Testing. Journal of Molecular Diagnostics. 26(10). 876–887.
2.
Betz, Bryan L., et al.. (2019). Comparison of real‐time PCR vs PCR with fragment length analysis for the detection of CALR mutations in suspected myeloproliferative neoplasms. International Journal of Laboratory Hematology. 41(6). e139–e141. 1 indexed citations
3.
Udager, Aaron M., Jonathan B. McHugh, Helmut C. Weigelin, et al.. (2017). Human papillomavirus (HPV) and somatic EGFR mutations are essential, mutually exclusive oncogenic mechanisms for inverted sinonasal papillomas and associated sinonasal squamous cell carcinomas. Annals of Oncology. 29(2). 466–471. 76 indexed citations
4.
Upadhyaya, Santhosh A., Carl Koschmann, Sriram Venneti, et al.. (2016). Brainstem Low-Grade Gliomas in Children—Excellent Outcomes With Multimodality Therapy. Journal of Child Neurology. 32(2). 194–203. 18 indexed citations
5.
Udager, Aaron M., Jonathan B. McHugh, Bryan L. Betz, et al.. (2016). Activating KRAS mutations are characteristic of oncocytic sinonasal papilloma and associated sinonasal squamous cell carcinoma. The Journal of Pathology. 239(4). 394–398. 46 indexed citations
6.
Brown, Noah A., Delphine Rolland, Jonathan B. McHugh, et al.. (2014). Activating FGFR2–RAS–BRAF Mutations in Ameloblastoma. Clinical Cancer Research. 20(21). 5517–5526. 206 indexed citations
7.
Brown, Noah A., Helmut C. Weigelin, Nathanael G. Bailey, et al.. (2014). Requisite Analytic and Diagnostic Performance Characteristics for the Clinical Detection of BRAF V600E in Hairy Cell Leukemia. Applied immunohistochemistry & molecular morphology. 23(8). 590–600. 9 indexed citations
8.
Behdad, Amir, Helmut C. Weigelin, Kojo S.J. Elenitoba‐Johnson, & Bryan L. Betz. (2014). A Clinical Grade Sequencing-Based Assay for CEBPA Mutation Testing. Journal of Molecular Diagnostics. 17(1). 76–84. 21 indexed citations
9.
Brown, Noah A., Larissa V. Furtado, Bryan L. Betz, et al.. (2014). High prevalence of somatic MAP2K1 mutations in BRAF V600E–negative Langerhans cell histiocytosis. Blood. 124(10). 1655–1658. 234 indexed citations
10.
Brown, Noah A., Bryan L. Betz, Helmut C. Weigelin, et al.. (2014). Evaluation of Allele-Specific PCR and Immunohistochemistry for the Detection of BRAF V600E Mutations in Hairy Cell Leukemia. American Journal of Clinical Pathology. 143(1). 89–99. 20 indexed citations
11.
Furtado, Larissa V., Helmut C. Weigelin, Kojo S.J. Elenitoba‐Johnson, & Bryan L. Betz. (2013). A Multiplexed Fragment Analysis-Based Assay for Detection of JAK2 Exon 12 Mutations. Journal of Molecular Diagnostics. 15(5). 592–599. 16 indexed citations
12.
Furtado, Larissa V., Helmut C. Weigelin, Kojo S.J. Elenitoba‐Johnson, & Bryan L. Betz. (2013). Detection of MPL Mutations by a Novel Allele-Specific PCR-Based Strategy. Journal of Molecular Diagnostics. 15(6). 810–818. 32 indexed citations
13.
Betz, Bryan L., et al.. (2013). The use of stained cytologic direct smears for ALK gene rearrangement analysis of lung adenocarcinoma. Cancer Cytopathology. 121(9). 489–499. 55 indexed citations
14.
Bernacki, Kurt D., Bryan L. Betz, Helmut C. Weigelin, et al.. (2012). Molecular Diagnostics of Melanoma Fine-Needle Aspirates. American Journal of Clinical Pathology. 138(5). 670–677. 21 indexed citations
15.
HooKim, Kim, Michael H. Roh, Joseph H. Willman, et al.. (2011). Application of immunocytochemistry and BRAF mutational analysis to direct smears of metastatic melanoma. Cancer Cytopathology. 120(1). 52–61. 36 indexed citations
16.
Betz, Bryan L., Michael H. Roh, Helmut C. Weigelin, et al.. (2011). The Application of Molecular Diagnostic Studies Interrogating EGFR and KRAS Mutations to Stained Cytologic Smears of Lung Carcinoma. American Journal of Clinical Pathology. 136(4). 564–571. 75 indexed citations
17.
Thorson, John, et al.. (2006). Identification of SYT-SSX transcripts from synovial sarcomas using RT-multiplex PCR and capillary electrophoresis. Modern Pathology. 19(5). 641–647. 12 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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