C. Snyder

2.1k citations
6 papers · 1.4k · 1 hit paper · h-index 5

Impact in

Papers in

C. Snyder

6 papers receiving 1.4k citations

C. Snyder's Hit Papers

Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications 2009 · 562 citations
5620+5+11Years since publication100200300400500

Peers

C. Snyder
Comparison fields: 5 of 57
  • Pathology and Forensic Medicine 586
  • Genetics 805
  • Cancer Research 340
  • Reproductive Medicine 121
  • Oncology 338
Replace Henry T. Lynch with:
Henry T. Lynch United States
Teresa Wagner Austria
Kristen M. Shannon United States
Barbara Weber United States
Susan Randall Armel Canada
Daniela Turchetti Italy
Hanne Meijers-Heijboer Netherlands
Joan H. Marks United States
Louise Izatt United Kingdom
Amie Blanco United States
C. Snyder relative to Henry T. Lynch United States Henry T. Lynch's profile →
Citations per field
00.5×1.5×
Henry T. Lynch · 1×
Citations per year

Countries citing papers authored by C. Snyder

Since Specialization
Citations

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

Fields of papers citing papers by C. Snyder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside C. Snyder, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with C. Snyder Line = papers co-authored together C. Snyder links everyone, so they are left out of the graph.

All Works

6 of 6 papers shown
#Work
1
Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications
Hit paper breakdown →
2009562
2 1999462
3 2014196
4 1998193
5 201334
6 20063

About C. Snyder

C. Snyder is a scholar working on Genetics, Pathology and Forensic Medicine, Oncology, Reproductive Medicine and Infectious Diseases, having authored 6 papers that have together received 1.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genetic factors in colorectal cancer (2 papers), Colorectal Cancer Screening and Detection (1 paper), Ovarian cancer diagnosis and treatment (1 paper) and Colorectal Cancer Treatments and Studies (1 paper). The work is most often cited by research in Pathology and Forensic Medicine (586 citations), Genetics (805 citations), Cancer Research (340 citations), Reproductive Medicine (121 citations) and Oncology (338 citations). C. Snyder has collaborated with scholars based in United States and Canada. Frequent co-authors include Lynch Ht, P. M. Lynch, S. J. Lanspa, J. F. Lynch, Andrea Eisen, Henry T. Lynch, Susan L. Neuhausen, Timothy R. Rebbeck, H. T. Lynch and BL Weber. Their work appears in journals such as Journal of Clinical Oncology, Clinical Genetics, BMJ, Annals of Oncology and JNCI Journal of the National Cancer Institute.

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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