François Eisinger
Impact in
- Genetics top 1%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
- Breast Cancer Treatment Studies
Papers in
- Co-authors
- Hagay Sobol (63 shared papers)Daniel Birnbaum (24 shared papers)Claire Julian‐Reynier (26 shared papers)Michel Longy (9 shared papers)F Kerangueven (8 shared papers)Catherine Noguès (21 shared papers)Dominique Stoppa‐Lyonnet (15 shared papers)Philippe Vennin (12 shared papers)
- Journals
- European Journal of Cancer Prevention (13 papers)Journal of Clinical Oncology (13 papers)Annals of Oncology (8 papers)Current Oncology Reports (6 papers)Familial Cancer (6 papers)
- Partner nations
- FranceUnited StatesSwitzerland
In The Last Decade
François Eisinger
165 papers receiving 2.7k citations
Peers
Comparison fields: 5 of 124
- Genetics 1.3k
- Cancer Research 535
- Pathology and Forensic Medicine 518
- Oncology 741
- Reproductive Medicine 135
Countries citing papers authored by François Eisinger
This map shows the geographic impact of François Eisinger'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 François Eisinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites François Eisinger more than expected).
Fields of papers citing papers by François Eisinger
This network shows the impact of papers produced by François Eisinger. 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 François Eisinger. The network helps show where François Eisinger may publish in the future.
Co-authors
The 25 scholars most cited alongside François Eisinger, 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 180 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 165 | |
| 2 | Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas. | 1997 | 140 |
| 3 | Germ line mutation at BRCA1 affects the histoprognostic grade in hereditary breast cancer. | 1996 | 137 |
| 4 | 2002 | 124 | |
| 5 | Mutations at BRCA1: the medullary breast carcinoma revisited. | 1998 | 121 |
| 6 | Loss of heterozygosity and linkage analysis in breast carcinoma: indication for a putative third susceptibility gene on the short arm of chromosome 8. | 1995 | 109 |
| 7 | 1998 | 105 | |
| 8 | 2000 | 97 | |
| 9 | 1996 | 94 | |
| 10 | 1999 | 81 | |
| 11 | 2006 | 80 | |
| 12 | [Identification and management of hereditary predisposition to cancer of the breast and the ovary (update 2004)]. | 2004 | 68 |
| 13 | 1997 | 57 | |
| 14 | Major improvement in the efficacy of BRCA1 mutation screening using morphoclinical features of breast cancer. | 2000 | 57 |
| 15 | Truncation at conserved terminal regions of BRCA1 protein is associated with highly proliferating hereditary breast cancers. | 1996 | 53 |
| 16 | 2003 | 51 | |
| 17 | 2002 | 49 | |
| 18 | [Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas]. | 2004 | 43 |
| 19 | 1998 | 42 | |
| 20 | 2000 | 41 |
About François Eisinger
François Eisinger is a scholar working on Oncology, Genetics, General Health Professions, Pathology and Forensic Medicine and Cancer Research, having authored 180 papers that have together received 2.9k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (58 papers), Global Cancer Incidence and Screening (31 papers), Colorectal Cancer Screening and Detection (28 papers), Genetic factors in colorectal cancer (18 papers), Nutrition, Genetics, and Disease (15 papers), Cancer Genomics and Diagnostics (11 papers), Healthcare Systems and Practices (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). The work is most often cited by research in Genetics (1.3k citations), Cancer Research (535 citations), Pathology and Forensic Medicine (518 citations), Oncology (741 citations) and Reproductive Medicine (135 citations). François Eisinger has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Hagay Sobol, Daniel Birnbaum, Claire Julian‐Reynier, Michel Longy, F Kerangueven, Catherine Noguès, Dominique Stoppa‐Lyonnet, Philippe Vennin, Florence Allione and Jean‐François Morère. Their work appears in journals such as European Journal of Cancer Prevention, Journal of Clinical Oncology, Annals of Oncology, Current Oncology Reports and Familial Cancer.
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.