Pierre Hutter

2.6k total citations
48 papers, 1.2k citations indexed

About

Pierre Hutter is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Cancer Research. According to data from OpenAlex, Pierre Hutter has authored 48 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Pathology and Forensic Medicine, 21 papers in Molecular Biology and 15 papers in Cancer Research. Recurrent topics in Pierre Hutter's work include Genetic factors in colorectal cancer (26 papers), Cancer Genomics and Diagnostics (15 papers) and Colorectal Cancer Screening and Detection (11 papers). Pierre Hutter is often cited by papers focused on Genetic factors in colorectal cancer (26 papers), Cancer Genomics and Diagnostics (15 papers) and Colorectal Cancer Screening and Detection (11 papers). Pierre Hutter collaborates with scholars based in Switzerland, United States and Canada. Pierre Hutter's co-authors include Michael Ashburner, John Roote, Stylianos E. Antonarakis, Pierre O. Chappuis, Michael A. Morris, Claude Lang, C.D. DeLozier-Blanchet, Karl Heinimann, Philippe Maillet and Juul Wijnen and has published in prestigious journals such as Nature, SHILAP Revista de lepidopterología and Journal of the American College of Cardiology.

In The Last Decade

Pierre Hutter

47 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Pierre Hutter Switzerland 18 493 459 352 314 246 48 1.2k
Anne‐Marie Dutrillaux France 15 498 1.0× 125 0.3× 226 0.6× 189 0.6× 309 1.3× 40 907
Philippe Dhordain France 12 1.0k 2.1× 145 0.3× 161 0.5× 202 0.6× 151 0.6× 12 1.4k
Clotilde Deweindt France 8 715 1.5× 549 1.2× 117 0.3× 376 1.2× 115 0.5× 8 1.4k
Madina Sukhanova United States 18 250 0.5× 131 0.3× 206 0.6× 147 0.5× 70 0.3× 68 823
Noopur Thakur India 13 1.0k 2.0× 88 0.2× 172 0.5× 331 1.1× 377 1.5× 54 1.4k
Tommy Gerdes Denmark 20 620 1.3× 89 0.2× 859 2.4× 84 0.3× 201 0.8× 31 1.4k
Anthony Renwick United Kingdom 17 1.7k 3.5× 476 1.0× 1.7k 4.9× 468 1.5× 694 2.8× 21 3.2k
Katsuhiko Endo Japan 23 526 1.1× 58 0.1× 230 0.7× 722 2.3× 283 1.2× 85 1.9k
Sumana Datta United States 13 939 1.9× 54 0.1× 156 0.4× 175 0.6× 78 0.3× 30 1.3k
Klaus Brasch Canada 19 895 1.8× 52 0.1× 313 0.9× 170 0.5× 66 0.3× 37 1.4k

Countries citing papers authored by Pierre Hutter

Since Specialization
Citations

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

Fields of papers citing papers by Pierre Hutter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pierre Hutter

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

All Works

20 of 20 papers shown
1.
Cusin, Isabelle, Daniel Teixeira, Monique Zahn‐Zabal, et al.. (2018). A new bioinformatics tool to help assess the significance of BRCA1 variants. Human Genomics. 12(1). 36–36. 8 indexed citations
2.
Rahner, Nils, Verena Steinke, Brigitte Schlegelberger, et al.. (2012). Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012. European Journal of Human Genetics. 21(1). 118–118. 13 indexed citations
3.
Rahner, Nils, Verena Steinke, Brigitte Schlegelberger, et al.. (2010). Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2). European Journal of Human Genetics. 18(9). 1071–1071. 12 indexed citations
4.
Younan, Rami, Ping Liang, Desirée du Sart, et al.. (2006). Distinct patterns of germ-line deletions inMLH1 andMSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC). Human Mutation. 27(4). 388–388. 43 indexed citations
5.
Soravia, Claudio, Celia D. Delozier, Zuzana Dobbie, et al.. (2005). Double frameshift mutations in APC and MSH2 in the same individual. International Journal of Colorectal Disease. 20(5). 466–470. 16 indexed citations
6.
Russell, Anna, M Buser, Pierre Hutter, et al.. (2005). Evidence for genetic anticipation in hereditary non-polyposis colorectal cancer. Human Genetics. 116(6). 461–465. 23 indexed citations
7.
Tapparel, Caroline, Alexandre Reymond, Christophe Girardet, et al.. (2003). The TPTE gene family: cellular expression, subcellular localization and alternative splicing. Gene. 323. 189–199. 69 indexed citations
8.
Soravia, Claudio, Heleen van der Klift, Marie‐Anne Bründler, et al.. (2003). Prostate cancer is part of the hereditary non‐polyposis colorectal cancer (HNPCC) tumor spectrum. American Journal of Medical Genetics Part A. 121A(2). 159–162. 56 indexed citations
9.
Hutter, Pierre, et al.. (2002). An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1. Journal of Medical Genetics. 39(5). 323–327. 10 indexed citations
10.
Hutter, Pierre. (2002). X-linked small GTPase and OXPHOS genes are candidates for the genetic basis of hybrid inviability in Drosophila. Development Genes and Evolution. 212(10). 504–512. 8 indexed citations
11.
Guipponi, Michel, Caroline Tapparel, Olivier Jousson, et al.. (2001). The murine orthologue of the Golgi-localized TPTE protein provides clues to the evolutionary history of the human TPTE gene family. Human Genetics. 109(6). 569–575. 28 indexed citations
12.
Hutter, Pierre, et al.. (2000). A mutagenic PCR identifies isolates ofBorrelia gariniiresponsible for Lyme borreliosis. FEMS Microbiology Letters. 191(2). 199–203. 1 indexed citations
13.
Maillet, Philippe, Pierre O. Chappuis, Zuzana Dobbie, et al.. (2000). A polymorphism in theATM gene modulates the penetrance of hereditary non-polyposis colorectal cancer. International Journal of Cancer. 88(6). 928–931. 43 indexed citations
14.
Hutter, Pierre, et al.. (2000). Two common forms of the human MLH1gene may be associated with functional differences. Journal of Medical Genetics. 37(10). 776–781. 17 indexed citations
15.
Heinimann, Karl, Rodney J. Scott, Pierre O. Chappuis, et al.. (1999). N-acetyltransferase 2 influences cancer prevalence in hMLH1/hMSH2 mutation carriers.. PubMed. 59(13). 3038–40. 30 indexed citations
16.
Hutter, Pierre, et al.. (1998). Excess ofhMLH1 germline mutations in Swiss families with hereditary non-polyposis colorectal cancer. International Journal of Cancer. 78(6). 680–684. 30 indexed citations
17.
Hutter, Pierre, et al.. (1994). Exon skipping associated with A→G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene. Human Molecular Genetics. 3(4). 663–665. 7 indexed citations
18.
Hutter, Pierre, John Roote, & Michael Ashburner. (1990). A genetic basis for the inviability of hybrids between sibling species of Drosophila.. Genetics. 124(4). 909–920. 108 indexed citations
19.
Hutter, Pierre. (1990). ‘Exceptional sons’ fromDrosophila melanogastermothers carrying a balancerXchromosome. Genetics Research. 55(3). 159–164. 8 indexed citations
20.

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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