Anne Vannier

1.3k total citations
20 papers, 561 citations indexed

About

Anne Vannier is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Anne Vannier has authored 20 papers receiving a total of 561 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Genetics. Recurrent topics in Anne Vannier's work include Cellular transport and secretion (3 papers), CRISPR and Genetic Engineering (3 papers) and Glioma Diagnosis and Treatment (2 papers). Anne Vannier is often cited by papers focused on Cellular transport and secretion (3 papers), CRISPR and Genetic Engineering (3 papers) and Glioma Diagnosis and Treatment (2 papers). Anne Vannier collaborates with scholars based in Switzerland, France and United States. Anne Vannier's co-authors include Stylianos E. Antonarakis, Federico Santoni, Michel Guipponi, Alberto De Iaco, Jeremy Luban, Richard Iggo, Jean‐Marc Limacher, François Waridel, Jean‐Michel Flaman and T Frebourg and has published in prestigious journals such as Nature Communications, Blood and PLoS ONE.

In The Last Decade

Anne Vannier

20 papers receiving 546 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne Vannier Switzerland 12 350 126 100 81 74 20 561
Julia M. Rogers United States 13 659 1.9× 157 1.2× 81 0.8× 104 1.3× 53 0.7× 22 955
Gary Thomas United States 9 290 0.8× 56 0.4× 66 0.7× 83 1.0× 76 1.0× 14 593
Richard Koller United States 14 609 1.7× 128 1.0× 39 0.4× 104 1.3× 42 0.6× 23 775
Claudia Firrito Italy 4 393 1.1× 224 1.8× 62 0.6× 108 1.3× 13 0.2× 8 515
Madapura M. Pradeepa United Kingdom 15 953 2.7× 178 1.4× 59 0.6× 32 0.4× 101 1.4× 19 1.1k
Jun Hasegawa Japan 7 1.0k 2.9× 86 0.7× 140 1.4× 77 1.0× 60 0.8× 8 1.2k
Nina Tonnu United States 5 829 2.4× 225 1.8× 112 1.1× 153 1.9× 87 1.2× 5 954
Normand Groulx Canada 7 634 1.8× 149 1.2× 15 0.1× 89 1.1× 29 0.4× 8 905
A.-P.J. Huovila Finland 8 416 1.2× 98 0.8× 30 0.3× 105 1.3× 70 0.9× 8 899
CE Myers United States 9 216 0.6× 44 0.3× 30 0.3× 113 1.4× 45 0.6× 10 451

Countries citing papers authored by Anne Vannier

Since Specialization
Citations

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

Fields of papers citing papers by Anne Vannier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Vannier

This figure shows the co-authorship network connecting the top 25 collaborators of Anne Vannier. A scholar is included among the top collaborators of Anne Vannier 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 Anne Vannier. Anne Vannier 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.
Laurent, Sacha, Anne Vannier, Corinne Gehrig, et al.. (2024). Improved variant detection using long-read sequencing and optical mapping: Illustration in STRC-related hearing loss. European Journal of Medical Genetics. 73. 104986–104986. 2 indexed citations
2.
Marconi, Caterina, Laure Lemmens, Frédéric G. Masclaux, et al.. (2021). Bi‐allelic loss of ERGIC1 causes relatively mild arthrogryposis. Clinical Genetics. 100(3). 329–333. 4 indexed citations
3.
Laurent, Sacha, Corinne Gehrig, Thierry Nouspikel, et al.. (2021). Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients. Human Mutation. 42(4). 373–377. 13 indexed citations
4.
Vannier, Anne, Frédérique Eber, Virginie Huteau, et al.. (2017). Gene Introgression in Weeds Depends on Initial Gene Location in the Crop:Brassica napus–Raphanus raphanistrumModel. Genetics. 206(3). 1361–1372. 9 indexed citations
5.
Letourneau, Audrey, Gilda Cobellis, Alexandre Fort, et al.. (2015). HSA21 Single-Minded 2 (Sim2) Binding Sites Co-Localize with Super-Enhancers and Pioneer Transcription Factors in Pluripotent Mouse ES Cells. PLoS ONE. 10(5). e0126475–e0126475. 9 indexed citations
6.
Sailani, M. Reza, Federico Santoni, Audrey Letourneau, et al.. (2015). DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins. PLoS ONE. 10(8). e0135555–e0135555. 41 indexed citations
7.
Calvel, Pierre, Kamila Kusz-Zamelczyk, Periklis Makrythanasis, et al.. (2015). A Case of Wiedemann-Steiner Syndrome Associated with a 46,XY Disorder of Sexual Development and Gonadal Dysgenesis. Sexual Development. 9(5). 289–295. 12 indexed citations
8.
Nikolaev, Sergey I., Federico Santoni, Marco Garieri, et al.. (2014). Extrachromosomal driver mutations in glioblastoma and low-grade glioma. Nature Communications. 5(1). 5690–5690. 52 indexed citations
9.
Iaco, Alberto De, Federico Santoni, Anne Vannier, et al.. (2013). TNPO3 protects HIV-1 replication from CPSF6-mediated capsid stabilization in the host cell cytoplasm. Retrovirology. 10(1). 20–20. 119 indexed citations
10.
Nikolaev, Sergey I., Federico Santoni, Anne Vannier, et al.. (2013). Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome. Blood. 122(4). 554–561. 54 indexed citations
11.
Cheeseman, Kevin, Étienne Rouleau, Anne Vannier, et al.. (2012). A diagnostic genetic test for the physical mapping of germline rearrangements in the susceptibility breast cancer genes BRCA1 and BRCA2. Human Mutation. 33(6). 998–1009. 15 indexed citations
12.
Nguyen, Karine, Pierre Walrafen, Rafaëlle Bernard, et al.. (2011). Molecular combing reveals allelic combinations in facioscapulohumeral dystrophy. Annals of Neurology. 70(4). 627–633. 36 indexed citations
13.
Launey, Sophie, Francine Krieg, Pierrick Haffray, et al.. (2003). Twelve new microsatellite markers for gilted seabream (Sparus aurata L.): characterization, polymorphism and linkage. Molecular Ecology Notes. 3(3). 457–459. 38 indexed citations
14.
Aurich‐Costa, Joan, et al.. (2001). IPM-FISH, a new M-FISH approach using IRS-PCR painting probes: Application to the analysis of seven human prostate cell lines. Genes Chromosomes and Cancer. 30(2). 143–143. 5 indexed citations
15.
Aurich‐Costa, Joan, Anne Vannier, Eric Grégoire, Frédérique Nowak, & Dorra Chérif. (2001). IPM-FISH, a new M-FISH approach using IRS-PCR painting probes: Application to the analysis of seven human prostate cell lines. Genes Chromosomes and Cancer. 30(2). 143–160. 23 indexed citations
16.
Flaman, Jean‐Michel, François Waridel, Anne Estreicher, et al.. (1996). The human tumour suppressor gene p53 is alternatively spliced in normal cells.. PubMed. 12(4). 813–8. 75 indexed citations
17.
Vannier, Anne, Françoise Gray, Romain K. Gherardi, et al.. (1986). Diffuse subependymal periventricular metastases:Report of three cases. Cancer. 58(12). 2720–2725. 8 indexed citations
18.
Dougados, Maxime, André Kahan, Anne Vannier, & B Amor. (1983). [Lyme arthritis. 2 new French cases].. PubMed. 50(4). 299–302. 8 indexed citations
19.
Varki, Ajit, et al.. (1982). Demonstration of the heterozygous state for I-cell disease and pseudo-Hurler polydystrophy by assay of N-acetylglucosaminylphosphotransferase in white blood cells and fibroblasts.. PubMed. 34(5). 717–29. 35 indexed citations
20.
Thomas, Gilles, Carol S. Miller, Kathleen Toomey, et al.. (1982). Two clonal cell populations (mosaicism) in a 46,XY male with mucolipidosis II (I-cell disease)--an autosomal recessive disorder.. PubMed. 34(4). 611–22. 3 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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