Henry T. Lynch
Impact in
- Pathology and Forensic Medicine top 0.01%
- Genetic factors in colorectal cancer
- Cancer Research top 0.02%
- Cancer Genomics and Diagnostics
Papers in
-
- Genetic factors in colorectal cancer 331
- Genetics 316
- BRCA gene mutations in cancer 253
- Genomic variations and chromosomal abnormalities 40
- Co-authors
- Patrice Watson (76 shared papers)Jane F. Lynch (169 shared papers)Albert de la Chapelle (9 shared papers)Jukka‐Pekka Mecklin (11 shared papers)Thomas C. Smyrk (34 shared papers)Steven A. Narod (88 shared papers)Hans F. A. Vasen (17 shared papers)P. Meera Khan (3 shared papers)
- Journals
- Cancer (74 papers)Diseases of the Colon & Rectum (29 papers)Familial Cancer (28 papers)Journal of Clinical Oncology (25 papers)JAMA (22 papers)
- Partner nations
- United StatesCanadaPoland
In The Last Decade
Henry T. Lynch
693 papers receiving 41.5k citations
Henry T. Lynch's Hit Papers
Peers
Comparison fields: 5 of 188
- Pathology and Forensic Medicine 22.2k
- Cancer Research 12.7k
- Oncology 20.9k
- Reproductive Medicine 4.7k
- Genetics 15.3k
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-authors
The 25 scholars most cited alongside Henry T. Lynch, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 707 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) Hit paper breakdown → | 1991 | 1620 |
| 2 | Mutation of a mutL Homolog in Hereditary Colon Cancer Hit paper breakdown → | 1994 | 1450 |
| 3 | Hereditary Colorectal Cancer Hit paper breakdown → | 2003 | 1439 |
| 4 | Colorectal cancer Hit paper breakdown → | 2010 | 1138 |
| 5 | Prophylactic Oophorectomy in Carriers ofBRCA1orBRCA2Mutations Hit paper breakdown → | 2002 | 1025 |
| 6 | Bilateral Prophylactic Mastectomy Reduces Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers: The PROSE Study Group Hit paper breakdown → | 2004 | 812 |
| 7 | Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: An updated review Hit paper breakdown → | 1993 | 792 |
| 8 | Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients Hit paper breakdown → | 1996 | 749 |
| 9 | Accumulation of p53 Tumor Suppressor Gene Protein: An Independent Marker of Prognosis in Breast Cancers Hit paper breakdown → | 1992 | 638 |
| 10 | Extracolonic cancer in hereditary nonpolyposis colorectal cancer Hit paper breakdown → | 1993 | 570 |
| 11 | Milestones of Lynch syndrome: 1895–2015 Hit paper breakdown → | 2015 | 521 |
| 12 | Prophylactic Surgery to Reduce the Risk of Gynecologic Cancers in the Lynch Syndrome Hit paper breakdown → | 2006 | 516 |
| 13 | Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas. | 1996 | 482 |
| 14 | 1993 | 456 | |
| 15 | Genetic instability of microsatellites in endometrial carcinoma. | 1993 | 445 |
| 16 | 2004 | 435 | |
| 17 | Programmed Cell Death 1 (PD-1) and Its Ligand (PD-L1) in Common Cancers and Their Correlation with Molecular Cancer Type Hit paper breakdown → | 2014 | 416 |
| 18 | 2008 | 409 | |
| 19 | 2001 | 406 | |
| 20 | 2000 | 388 |
About Henry T. Lynch
Henry T. Lynch is a scholar working on Pathology and Forensic Medicine, Genetics, Oncology, Cancer Research and Molecular Biology, having authored 707 papers that have together received 43.2k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (331 papers), BRCA gene mutations in cancer (253 papers), Cancer Genomics and Diagnostics (142 papers), Colorectal Cancer Screening and Detection (115 papers), DNA Repair Mechanisms (68 papers), Ovarian cancer diagnosis and treatment (58 papers), Colorectal Cancer Treatments and Studies (54 papers) and Genomic variations and chromosomal abnormalities (40 papers). The work is most often cited by research in Pathology and Forensic Medicine (22.2k citations), Cancer Research (12.7k citations), Oncology (20.9k citations), Reproductive Medicine (4.7k citations) and Genetics (15.3k citations). Henry T. Lynch has collaborated with scholars based in United States, Canada and Poland. Frequent co-authors include Patrice Watson, Jane F. Lynch, Albert de la Chapelle, Jukka‐Pekka Mecklin, Thomas C. Smyrk, Steven A. Narod, Hans F. A. Vasen, P. Meera Khan, Patrick M. Lynch and Anne J. Krush. Their work appears in journals such as Cancer, Diseases of the Colon & Rectum, Familial Cancer, Journal of Clinical Oncology and JAMA.
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.