H. T. Lynch

2.1k total citations · 1 hit paper
11 papers, 1.5k citations indexed

About

H. T. Lynch is a scholar working on Pathology and Forensic Medicine, Oncology and Cancer Research. According to data from OpenAlex, H. T. Lynch has authored 11 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Pathology and Forensic Medicine, 6 papers in Oncology and 6 papers in Cancer Research. Recurrent topics in H. T. Lynch's work include Genetic factors in colorectal cancer (8 papers), Cancer Genomics and Diagnostics (6 papers) and Colorectal Cancer Screening and Detection (4 papers). H. T. Lynch is often cited by papers focused on Genetic factors in colorectal cancer (8 papers), Cancer Genomics and Diagnostics (6 papers) and Colorectal Cancer Screening and Detection (4 papers). H. T. Lynch collaborates with scholars based in United States, Canada and Finland. H. T. Lynch's co-authors include Patrice Watson, Païvi Peltomäki, Martti Juhola, Lauri A. Aaltonen, Jeremy R. Jass, Jukka‐Pekka Mecklin, Heikki Järvinen, G. Tallqvist, BL Weber and M. Daly and has published in prestigious journals such as Gastroenterology, JNCI Journal of the National Cancer Institute and Cancer.

In The Last Decade

H. T. Lynch

11 papers receiving 1.5k citations

Hit Papers

align trajectories

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.

Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients.

1994 510 citations Lauri A. Aaltonen, Païvi Peltomäki et al. PubMed profile →

Peers

H. T. Lynch

PFM

ONCOL

CR

GENET

MB

Peggy Conrad United States

Christopher Arnell United States

Catherine Walsh Vockley United States

Tadashi Nomizu Japan

Ingrid Marino United States

Laura Renkonen‐Sinisalo Finland

Michelle Landon United States

Kaisa Sotamaa United States

Astrid Stormorken Norway

PM Khan Netherlands

Peggy Conrad United States

H. T. Lynch

1.3k ×1.4

PFM

884 ×1.0

ONCOL

504 ×0.9

CR

416 ×0.8

GENET

168 ×0.6

MB

Citations per year, relative to H. T. Lynch H. T. Lynch (= 1×) peers Peggy Conrad

Countries citing papers authored by H. T. Lynch

Since Specialization

Citations

This map shows the geographic impact of H. 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 H. 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 H. T. Lynch more than expected).

Fields of papers citing papers by H. T. Lynch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H. 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 H. T. Lynch. The network helps show where H. T. Lynch may publish in the future.

Co-authorship network of co-authors of H. T. Lynch

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

1.

Tiwari, Ashish K., Hemant K. Roy, & H. T. Lynch. (2015). Lynch syndrome in the 21st century: clinical perspectives. QJM. 109(3). 151–158. 86 indexed citations

2.

Brand, Randall, Markus M. Lerch, Wendy S. Rubinstein, et al.. (2007). Advances in counselling and surveillance of patients at risk for pancreatic cancer: Table 1. Gut. 56(10). 1460–1469. 231 indexed citations

3.

Lynch, H. T., Randall E. Brand, Jane F. Lynch, et al.. (2000). Genetic counseling and testing for germline p16 mutations in two pancreatic cancer–prone families. Gastroenterology. 119(6). 1756–1760. 26 indexed citations

4.

Rebbeck, Timothy R., Albert M. Levin, Andrea Eisen, et al.. (1999). Breast Cancer Risk After Bilateral Prophylactic Oophorectomy in BRCA1 Mutation Carriers. JNCI Journal of the National Cancer Institute. 91(17). 1475–1479. 464 indexed citations

5.

Fujiwara, Takato, Joshua M. Stolker, Toshiaki Watanabe, et al.. (1998). Accumulated Clonal Genetic Alterations in Familial and Sporadic Colorectal Carcinomas with Widespread Instability in Microsatellite Sequences. American Journal Of Pathology. 153(4). 1063–1078. 150 indexed citations

6.

Lynch, H. T., Ramon M. Fusaro, & Jane F. Lynch. (1995). Family History of Cancer. Annals of the New York Academy of Sciences. 768(1). 12–29. 5 indexed citations

7.

Lynch, H. T., S. J. Lanspa, Thomas C. Smyrk, et al.. (1994). Mutation of an mutL Homologue in a Navajo Family With Hereditary Nonpolyposis Colorectal Cancer. JNCI Journal of the National Cancer Institute. 86(18). 1417–1419. 19 indexed citations

8.

Aaltonen, Lauri A., Païvi Peltomäki, Jukka‐Pekka Mecklin, et al.. (1994). Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients.. PubMed. 54(7). 1645–8. 510 indexed citations breakdown →

9.

Lynch, H. T.. (1994). Phenotypic Variation in Hereditary Breast Cancer. Archives of Surgery. 129(8). 806–806. 2 indexed citations

10.

Lynch, H. T., et al.. (1990). Genetic diagnosis of lynch syndrome II in an extended colorectal cancer-prone family. Cancer. 66(10). 2233–2238. 9 indexed citations

11.

Lynch, H. T., Paul Rozen, & Guy S. Schuelke. (1985). Hereditary Colon Cancer: Polyposis and Nonpolyposis Variants. CA A Cancer Journal for Clinicians. 35(2). 95–115. 30 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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