Sabine Pagès

1.2k total citations
7 papers, 528 citations indexed

About

Sabine Pagès is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Sabine Pagès has authored 7 papers receiving a total of 528 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Sabine Pagès's work include BRCA gene mutations in cancer (6 papers), CRISPR and Genetic Engineering (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Sabine Pagès is often cited by papers focused on BRCA gene mutations in cancer (6 papers), CRISPR and Genetic Engineering (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Sabine Pagès collaborates with scholars based in France, Austria and Italy. Sabine Pagès's co-authors include Dominique Stoppa‐Lyonnet, Sylvie Mazoyer, Nadine Puget, Olga M. Sinilnikova, Dominique Stoppa-Lyonnet, Henry T. Lynch, Gilbert Lenoir, Therese Sandberg, Teresa Wagner and Peter J. Oefner and has published in prestigious journals such as British Journal of Cancer, Genomics and Genes Chromosomes and Cancer.

In The Last Decade

Sabine Pagès

7 papers receiving 506 citations

Peers

Sabine Pagès

GENET

MB

CR

PFM

ONCOL

Therese Sandberg Sweden

S. Hageman Netherlands

Eva Macháčková Czechia

H. Komatsubara Japan

Dominique Stoppa‐Lyonnet France

Jacopo Azzollini Italy

Sandrine M. Caputo France

F. B. F. Law Hong Kong

Konstantin G. Buslov Russia

Mar Infante Spain

Therese Sandberg Sweden

Sabine Pagès

167 ×0.4

GENET

189 ×0.6

MB

70 ×0.7

CR

46 ×0.6

PFM

81 ×1.8

ONCOL

Citations per year, relative to Sabine Pagès Sabine Pagès (= 1×) peers Therese Sandberg

Countries citing papers authored by Sabine Pagès

Since Specialization

Citations

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

Fields of papers citing papers by Sabine Pagès

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabine Pagès

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

All Works

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7 of 7 papers shown

1.

Gad, Sophie, Alain Aurias, Nadine Puget, et al.. (2001). Color bar coding the BRCA1 gene on combed DNA: A useful strategy for detecting large gene rearrangements. Genes Chromosomes and Cancer. 31(1). 75–84. 50 indexed citations

2.

Pagès, Sabine, et al.. (2001). Screening of male breast cancer and of breast-ovarian cancer families for BRCA2 mutations using large bifluorescent amplicons. British Journal of Cancer. 84(4). 482–488. 10 indexed citations

3.

Wagner, Teresa, Dominique Stoppa‐Lyonnet, Daniela Muhr, et al.. (1999). Denaturing High-Performance Liquid Chromatography Detects Reliably BRCA1 and BRCA2 Mutations. Genomics. 62(3). 369–376. 179 indexed citations

4.

Gad, Sophie, et al.. (1999). GENETIC TESTING FOR BREAST CANCER PREDISPOSITION. Surgical Clinics of North America. 79(5). 1171–1187. 6 indexed citations

5.

Puget, Nadine, Dominique Stoppa-Lyonnet, Olga M. Sinilnikova, et al.. (1999). Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions.. PubMed. 59(2). 455–61. 160 indexed citations

6.

Stoppa‐Lyonnet, Dominique, Pierre Laurent‐Puig, Laurent Essioux, et al.. (1997). BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group.. PubMed. 60(5). 1021–30. 110 indexed citations

7.

Stoppa-Lyonnet, D, Laurent Essioux, Sabine Pagès, et al.. (1996). Segregation of two BRCA1 mutations in a single family.. PubMed. 59(2). 479–81. 13 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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