Kami Wolfe Schneider

1.8k total citations · 1 hit paper
35 papers, 952 citations indexed

About

Kami Wolfe Schneider is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Kami Wolfe Schneider has authored 35 papers receiving a total of 952 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 8 papers in Pediatrics, Perinatology and Child Health and 6 papers in Surgery. Recurrent topics in Kami Wolfe Schneider's work include BRCA gene mutations in cancer (10 papers), Childhood Cancer Survivors' Quality of Life (6 papers) and Neuroblastoma Research and Treatments (5 papers). Kami Wolfe Schneider is often cited by papers focused on BRCA gene mutations in cancer (10 papers), Childhood Cancer Survivors' Quality of Life (6 papers) and Neuroblastoma Research and Treatments (5 papers). Kami Wolfe Schneider collaborates with scholars based in United States, Canada and Germany. Kami Wolfe Schneider's co-authors include Sarah Scollon, Katherine A. Schneider, Junne Kamihara, Uri Tabori, Joyce Turner, Hamish S. Scott, William D. Foulkes, Rose B. McGee, Harriet Druker and Ayelet Erez and has published in prestigious journals such as Clinical Cancer Research, Annals of Oncology and Urology.

In The Last Decade

Kami Wolfe Schneider

32 papers receiving 941 citations

Hit Papers

DICER1 and Associated Conditions: Identification of At-ri... 2018 2026 2020 2023 2018 50 100 150 200
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.

  1. DICER1 and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies
    2018 216 citations Kris Ann P. Schultz, Gretchen M. Williams et al. Clinical Cancer Research profile →

Peers

Kami Wolfe Schneider
Anita Villani Canada
Junne Kamihara United States
Catherine O’Hara United Kingdom
Kristin Zelley United States
Harriet Druker Canada
Bożenna Dembowska–Bagińska Poland
Salvatore Bertolone United States
P.N. Plowman United Kingdom
Ana Novokmet Canada
Kjell Bergfeldt Sweden
Anita Villani Canada
Kami Wolfe Schneider
Citations per year, relative to Kami Wolfe Schneider Kami Wolfe Schneider (= 1×) peers Anita Villani

Countries citing papers authored by Kami Wolfe Schneider

Since Specialization
Citations

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

Fields of papers citing papers by Kami Wolfe Schneider

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kami Wolfe Schneider. 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 Kami Wolfe Schneider. The network helps show where Kami Wolfe Schneider may publish in the future.

Co-authorship network of co-authors of Kami Wolfe Schneider

This figure shows the co-authorship network connecting the top 25 collaborators of Kami Wolfe Schneider. A scholar is included among the top collaborators of Kami Wolfe Schneider 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 Kami Wolfe Schneider. Kami Wolfe Schneider 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.
Rednam, Surya P., Anita Villani, Garrett M. Brodeur, et al.. (2025). Update on Surveillance in Von Hippel–Lindau Disease. Clinical Cancer Research. 31(12). 2271–2277. 1 indexed citations
2.
Rednam, Surya P., Junne Kamihara, Garrett M. Brodeur, et al.. (2025). Update on Tumor Surveillance for Children with Hereditary Pheochromocytoma/Paraganglioma Syndromes. Clinical Cancer Research. 31(16). 3368–3376. 1 indexed citations
3.
Salo‐Mullen, Erin, Julie O. Culver, Pamela Brock, et al.. (2025). Call to action for genetic counseling research in hereditary cancer: Considerations from the evidence‐based guidelines development process. Journal of Genetic Counseling. 34(3). e70026–e70026.
4.
MacFarland, Suzanne P., Kami Wolfe Schneider, Roland P. Kuiper, et al.. (2024). Pediatric Cancer Screening in Hereditary Gastrointestinal Cancer Risk Syndromes: An Update from the AACR Childhood Cancer Predisposition Working Group. Clinical Cancer Research. 30(20). 4566–4571. 6 indexed citations
5.
Zelley, Kristin, Jaclyn Schienda, Bailey Gallinger, et al.. (2024). Update on Genetic Counselor Practice and Recommendations for Pediatric Cancer Predisposition Evaluation and Surveillance. Clinical Cancer Research. 30(18). 3983–3989. 5 indexed citations
6.
Michaeli, Orli, Marjolijn C.J. Jongmans, Jonathan D. Wasserman, et al.. (2024). Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes. Clinical Cancer Research. 31(3). 457–465. 4 indexed citations
7.
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9.
Schneider, Kami Wolfe, et al.. (2023). Early death from childhood cancer: First medical record‐level analysis reveals insights on diagnostic timing and cause of death. Cancer Medicine. 12(19). 20201–20211. 3 indexed citations
10.
Chalmers, David J., Brian Greffe, Timothy Garrington, et al.. (2021). A Cystic Renal Mass in the Setting of a Pneumothorax: More Than Meets the Eye?. Urology. 154. 275–277.
11.
Schneider, Kami Wolfe, et al.. (2021). Lynch syndrome: further defining the pediatric spectrum. Cancer Genetics. 258-259. 37–40. 8 indexed citations
12.
Tsai, Anne Chun-Hui, et al.. (2021). A novel, germline, deactivating CBL variant p.L493F alters domain orientation and is associated with multiple childhood cancers. Cancer Genetics. 254-255. 18–24. 1 indexed citations
13.
Aronson, Melyssa, Chrystelle Colas, Andrew Y. Shuen, et al.. (2021). Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group. Journal of Medical Genetics. 59(4). 318–327. 57 indexed citations
14.
Schneider, Kami Wolfe, et al.. (2021). Incorporating genetic counseling into the evaluation of pediatric bone marrow failure. Journal of Genetic Counseling. 31(2). 433–446. 1 indexed citations
15.
Schneider, Kami Wolfe, et al.. (2020). Germline predisposition to genitourinary rhabdomyosarcoma. Translational Andrology and Urology. 9(5). 2430–2440. 8 indexed citations
16.
Friend, Brian D., Kami Wolfe Schneider, Timothy Garrington, et al.. (2019). Is polycystic kidney disease associated with malignancy in children?. Molecular Genetics & Genomic Medicine. 7(7). e00725–e00725. 4 indexed citations
17.
Schultz, Kris Ann P., Gretchen M. Williams, Junne Kamihara, et al.. (2018). DICER1 and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies. Clinical Cancer Research. 24(10). 2251–2261. 216 indexed citations breakdown →
18.
Evans, D. Gareth, S.P. Hector, Vivian Y. Chang, et al.. (2017). Cancer and Central Nervous System Tumor Surveillance in Pediatric Neurofibromatosis 1. Clinical Cancer Research. 23(12). e46–e53. 114 indexed citations
19.
Senter, Leigha, Robin L. Bennett, Anne C. Madeo, et al.. (2017). National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions. Journal of Genetic Counseling. 27(1). 9–15. 4 indexed citations
20.
Porter, Christopher C., Todd E. Druley, Ayelet Erez, et al.. (2017). Recommendations for Surveillance for Children with Leukemia-Predisposing Conditions. Clinical Cancer Research. 23(11). e14–e22. 69 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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