Henry T. Lynch
- Genetics top 1%
- Pathology and Forensic Medicine top 1%
- Oncology top 5%
- Cancer Research top 2%
- Molecular Biology
- Co-authors
- Angélique ChapelleJoseph MarcusDavid L. PagePatrice WatsonSteven A. NarodGilbert LenoirC. SnyderCarolyn Durham
- Topics
- BRCA gene mutations in cancer (16 papers)Genetic factors in colorectal cancer (8 papers)Genomic variations and chromosomal abnormalities (5 papers)
- Partner nations
- United StatesCanadaFrance
In The Last Decade
Henry T. Lynch
25 papers receiving 2.3k citations
Hit Papers
Peers
Comparison fields: 5 of 96
- Genetics 1.4k
- Pathology and Forensic Medicine 1.1k
- Oncology 820
- Cancer Research 782
- Molecular Biology 536
Countries citing papers authored by Henry T. Lynch
This map shows the geographic impact of Henry T. Lynch'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 Henry T. Lynch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Henry T. Lynch more than expected).
Fields of papers citing papers by Henry T. Lynch
This network shows the impact of papers produced by Henry T. Lynch. 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 Henry T. Lynch. The network helps show where Henry T. Lynch may publish in the future.
Co-authorship network of co-authors of Henry T. Lynch
This figure shows the co-authorship network connecting the top 25 collaborators of Henry T. Lynch. A scholar is included among the top collaborators of Henry T. Lynch 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 Henry T. Lynch. Henry T. Lynch is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 196 | |
| 2 | 66 | |
| 3 | 81 | |
| 4 | 86 | |
| 5 | 61 | |
| 6 | GENETIC SUSCEPTIBILITY TO NONPOLYPOSIS COLORECTAL CANCERbreakdown → | 552 |
| 7 | 32 | |
| 8 | 195 | |
| 9 | 13 | |
| 10 | 50 | |
| 11 | 322 | |
| 12 | 104 | |
| 13 | 14 | |
| 14 | Pathology and heredity of breast cancer in younger women. | 75 |
| 15 | Nucleotide sequence polymorphism in a hotspot mutation region of the p53 gene. | 35 |
| 16 | 112 | |
| 17 | 11 | |
| 18 | Abnormal estrogen conjugation in women at risk for familial breast cancer at the periovulatory stage of the menstrual cycle. | 22 |
| 19 | 89 | |
| 20 | 0 |
About Henry T. Lynch
Henry T. Lynch is a scholar working on Genetics, Pathology and Forensic Medicine and Cancer Research, having authored 27 papers that have together received 2.3k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (16 papers), Genetic factors in colorectal cancer (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). The work is most often cited by research in Pathology and Forensic Medicine (1.1k citations), Cancer Research (782 citations) and Genetics (1.4k citations). Henry T. Lynch has collaborated with scholars based in United States, Canada and France. Frequent co-authors include Angélique Chapelle, Joseph Marcus, David L. Page, Patrice Watson, Steven A. Narod, Gilbert Lenoir, C. Snyder, Carolyn Durham, David Main and Caryn Lerman. Their work appears in journals such as The Lancet, Journal of Clinical 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.