Patrice Watson

19.9k citations
134 papers · 12.5k indexed · 5 hit papers · h-index 51

Impact in

Papers in

Patrice Watson

133 papers receiving 12.1k citations

Hit Papers

Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients 1996 · 749 citations
74919932026200420154008001.2k

Peers

Patrice Watson
Comparison fields: 5 of 148
  • Pathology and Forensic Medicine 8.6k
  • Cancer Research 3.9k
  • Oncology 6.6k
  • Genetics 2.9k
  • Reproductive Medicine 828
Replace Heikki Järvinen with:
Heikki Järvinen Finland
Jukka‐Pekka Mecklin Finland
Sapna Syngal United States
Miguel A. Rodrı́guez-Bigas United States
George Fountzilas Greece
Darryl Carter United States
D. Crowther United Kingdom
Eduardo Díaz‐Rubio Spain
Janine Mansi United Kingdom
Hanneke C. Kluin‐Nelemans Netherlands
Patrice Watson relative to Heikki Järvinen Finland Heikki Järvinen's profile →
Citations per field
00.5×1.5×
Heikki Järvinen · 1×
Citations per year

Countries citing papers authored by Patrice Watson

Since Specialization
Citations

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

Fields of papers citing papers by Patrice Watson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Patrice Watson, 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 Patrice Watson Line = papers co-authored together Patrice Watson links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 201627
2 201143
3 20077
4 200729
5 2005251
6 200426
7 200458
8
Cáncer de mama hereditario: aspectos clínicos
20011
9 199961
10 199965
11 199910
12 1999464
13 1998103
14 199427
15
Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: An updated review
Hit paper breakdown →
1993792
16 199381
17 1993111
18 19897
19 198873
20
Pathology and genetic markers of colorectal cancer in Lynch syndromes I and II
19884

About Patrice Watson

Patrice Watson is a scholar working on Pathology and Forensic Medicine, Oncology, Cancer Research, Reproductive Medicine and Genetics, having authored 134 papers that have together received 12.5k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (68 papers), BRCA gene mutations in cancer (34 papers), Colorectal Cancer Screening and Detection (30 papers), Cancer Genomics and Diagnostics (24 papers), Colorectal Cancer Treatments and Studies (12 papers), Ovarian cancer diagnosis and treatment (10 papers), DNA Repair Mechanisms (9 papers) and Bone health and osteoporosis research (9 papers). The work is most often cited by research in Pathology and Forensic Medicine (8.6k citations), Cancer Research (3.9k citations), Oncology (6.6k citations), Genetics (2.9k citations) and Reproductive Medicine (828 citations). Patrice Watson has collaborated with scholars based in United States, Canada and Finland. Frequent co-authors include Henry T. Lynch, Thomas C. Smyrk, Jane F. Lynch, Jukka‐Pekka Mecklin, Païvi Peltomäki, Patrick M. Lynch, Stephen J. Lanspa, Kenneth W. Kinzler, Nickolas Papadopoulos and Stanley R. Hamilton. Their work appears in journals such as Cancer, Diseases of the Colon & Rectum, Journal of Clinical Oncology, Familial Cancer and Breast Cancer Research and Treatment.

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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