Ryan J. Schmidt

736 total citations
37 papers, 321 citations indexed

About

Ryan J. Schmidt is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Ryan J. Schmidt has authored 37 papers receiving a total of 321 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Ryan J. Schmidt's work include Genomics and Rare Diseases (8 papers), Cancer Genomics and Diagnostics (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). Ryan J. Schmidt is often cited by papers focused on Genomics and Rare Diseases (8 papers), Cancer Genomics and Diagnostics (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). Ryan J. Schmidt collaborates with scholars based in United States, Canada and China. Ryan J. Schmidt's co-authors include Matthew S. Lebo, Birgit Funke, Avni Santani, Diana Mandelker, Mark Bowser, Elizabeth Hynes, Kristin McDonald Gibson, Madhuri Hegde, Himanshu Sharma and Arunkanth Ankala and has published in prestigious journals such as Ophthalmology, The American Journal of Surgical Pathology and Journal of Clinical Pathology.

In The Last Decade

Ryan J. Schmidt

32 papers receiving 317 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ryan J. Schmidt United States 8 121 119 65 54 52 37 321
N. Sertac Kip United States 5 123 1.0× 130 1.1× 129 2.0× 57 1.1× 56 1.1× 9 378
Anna Laura Putignano Italy 11 127 1.0× 130 1.1× 32 0.5× 47 0.9× 54 1.0× 17 316
Annemieke H. van der Hout Netherlands 8 223 1.8× 227 1.9× 88 1.4× 32 0.6× 33 0.6× 13 451
Marlies Sachs Germany 13 77 0.6× 188 1.6× 27 0.4× 48 0.9× 51 1.0× 16 411
Mykyta Artomov United States 9 84 0.7× 157 1.3× 63 1.0× 50 0.9× 25 0.5× 39 382
Chia‐Yun Wu Taiwan 8 69 0.6× 172 1.4× 65 1.0× 36 0.7× 30 0.6× 22 307
Magdalena Koczkowska Poland 12 118 1.0× 157 1.3× 88 1.4× 64 1.2× 37 0.7× 29 310
Kai Ren Ong United Kingdom 7 52 0.4× 150 1.3× 167 2.6× 49 0.9× 28 0.5× 10 351
Beth A. Pitel United States 13 105 0.9× 148 1.2× 105 1.6× 53 1.0× 60 1.2× 37 442
Sarina Sulong Malaysia 10 73 0.6× 157 1.3× 64 1.0× 20 0.4× 32 0.6× 48 378

Countries citing papers authored by Ryan J. Schmidt

Since Specialization
Citations

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

Fields of papers citing papers by Ryan J. Schmidt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ryan J. Schmidt. 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 Ryan J. Schmidt. The network helps show where Ryan J. Schmidt may publish in the future.

Co-authorship network of co-authors of Ryan J. Schmidt

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

All Works

20 of 20 papers shown
1.
Dhar, Vikrom K., et al.. (2025). Standardizing surgical training with objective performance indicators: a prospective cohort study. Surgical Endoscopy. 39(4). 2316–2323. 1 indexed citations
2.
Hahn, Elan, Avinash V. Dharmadhikari, Simran Maggo, et al.. (2025). Copy number variant analysis improves diagnostic yield in a diverse pediatric exome sequencing cohort. npj Genomic Medicine. 10(1). 16–16.
3.
Schmidt, Ryan J., Larissa V. Furtado, Matthew S. Lebo, et al.. (2025). Clinical Bioinformatician Body of Knowledge—Clinical Laboratory Regulation and Data Security Core. Journal of Molecular Diagnostics. 27(7). 583–601. 2 indexed citations
4.
Yang, Bo, Roshan Mahabir, Nick Shillingford, et al.. (2024). Histone H3 trimethylation on lysine 27 immunostaining pattern in DICER1-associated tumors. Translational Pediatrics. 13(4). 624–633.
5.
Roy, Somak, Sabah Kadri, Annette Leon, et al.. (2024). Development of a Body of Knowledge for the Clinical Bioinformatician. Journal of Molecular Diagnostics. 27(7). 541–545. 2 indexed citations
6.
Cushman‐Vokoun, Allison M., Ryan J. Schmidt, Matthew Hiemenz, et al.. (2023). A Primer on Gene Editing: What Does It Mean for Pathologists?. Archives of Pathology & Laboratory Medicine. 148(5). 515–530. 2 indexed citations
7.
Buckley, Jonathan D., Ryan J. Schmidt, Dejerianne Ostrow, et al.. (2023). An Exome Capture-Based RNA-Sequencing Assay for Genome-Wide Identification and Prioritization of Clinically Important Fusions in Pediatric Tumors. Journal of Molecular Diagnostics. 26(2). 127–139. 3 indexed citations
8.
Hu, Zunsong, Alexandra E. Kovach, Venkata D. Yellapantula, et al.. (2023). Transcriptome Sequencing Allows Comprehensive Genomic Characterization of Pediatric B-Acute Lymphoblastic Leukemia in an Academic Clinical Laboratory. Journal of Molecular Diagnostics. 26(1). 49–60. 7 indexed citations
9.
Crooks, Kristy, Kelly D. Farwell Hagman, Diana Mandelker, et al.. (2023). Recommendations for Next-Generation Sequencing Germline Variant Confirmation. Journal of Molecular Diagnostics. 25(7). 411–427. 6 indexed citations
10.
11.
Munabi, Naikhoba C.O., Omar Toubat, Allyn Auslander, et al.. (2022). High prevalence of deleterious mutations in concomitant nonsyndromic cleft and outflow tract heart defects. American Journal of Medical Genetics Part A. 188(7). 2082–2095. 5 indexed citations
12.
Gai, Xiaowu, et al.. (2022). m.3685T>C is a Novel Mitochondrial DNA Variant That Causes Leigh Syndrome. Molecular Case Studies. 8(2). mcs.a006136–mcs.a006136. 2 indexed citations
13.
Chang, Melinda Y., Mark Borchert, Ryan J. Schmidt, & Aaron Nagiel. (2022). Neovascularization of the optic disc and peripheral retinal ischemia in a child with a novel variant in ALMS1 (Alström syndrome). American Journal of Ophthalmology Case Reports. 26. 101506–101506. 1 indexed citations
14.
Berry, Jesse L., David Cobrinik, Matthew A. Deardorff, et al.. (2022). Benign Lobular Inner Nuclear Layer Proliferations of the Retina Associated with Congenital Hypertrophy of the Retinal Pigment Epithelium. Ophthalmology. 130(3). 265–273. 5 indexed citations
15.
Hiemenz, Matthew, Matthew J. Oberley, Andrew Doan, et al.. (2021). A multimodal genomics approach to diagnostic evaluation of pediatric hematologic malignancies. Cancer Genetics. 254-255. 25–33. 7 indexed citations
16.
Sundling, Kaitlin E., et al.. (2021). Developing dashboards for performance improvement in cytopathology. Journal of the American Society of Cytopathology. 10(6). 535–542. 11 indexed citations
17.
Senol-Cosar, Ozlem, Ryan J. Schmidt, Emily Qian, et al.. (2019). Considerations for clinical curation, classification, and reporting of low-penetrance and low effect size variants associated with disease risk. Genetics in Medicine. 21(12). 2765–2773. 15 indexed citations
18.
Seifert, Bryce A., Jennifer McGlaughon, Sarah A. Jackson, et al.. (2018). Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework. Genetics in Medicine. 21(7). 1507–1516. 17 indexed citations
19.
Mandelker, Diana, Ryan J. Schmidt, Arunkanth Ankala, et al.. (2016). Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical next-generation sequencing. Genetics in Medicine. 18(12). 1282–1289. 129 indexed citations
20.
Yamamoto, Masakazu, et al.. (2007). Cloning and characterization of a novel MyoD enhancer-binding factor. Mechanisms of Development. 124(9-10). 715–728. 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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