Maryline Gagnebin

2.6k total citations
11 papers, 743 citations indexed

About

Maryline Gagnebin is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Maryline Gagnebin has authored 11 papers receiving a total of 743 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in Maryline Gagnebin's work include RNA modifications and cancer (4 papers), MicroRNA in disease regulation (4 papers) and Cancer-related molecular mechanisms research (3 papers). Maryline Gagnebin is often cited by papers focused on RNA modifications and cancer (4 papers), MicroRNA in disease regulation (4 papers) and Cancer-related molecular mechanisms research (3 papers). Maryline Gagnebin collaborates with scholars based in Switzerland, United States and Italy. Maryline Gagnebin's co-authors include Stylianos E. Antonarakis, Samuel Deutsch, Christelle Borel, Gregory R. Grant, Terry S. Elton, Praveen Sethupathy, Artemis G. Hatzigeorgiou, Corinne Gehrig, Robert Lyle and Emmanouil T. Dermitzakis and has published in prestigious journals such as PLoS ONE, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Maryline Gagnebin

11 papers receiving 730 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maryline Gagnebin Switzerland	9	465	257	224	132	92	11	743
Robert I. Barnes United States	8	553 1.2×	48 0.2×	210 0.9×	30 0.2×	27 0.3×	12	801
Masanaga Muto Japan	12	362 0.8×	47 0.2×	131 0.6×	159 1.2×	189 2.1×	20	712
Trudi McDevitt Ireland	11	339 0.7×	131 0.5×	127 0.6×	16 0.1×	27 0.3×	19	750
Ilenia Simeoni United Kingdom	12	391 0.8×	36 0.1×	125 0.6×	35 0.3×	16 0.2×	16	608
Yinghui Sui United States	8	554 1.2×	42 0.2×	226 1.0×	50 0.4×	20 0.2×	8	737
Indrani Talukdar India	11	375 0.8×	71 0.3×	35 0.2×	26 0.2×	25 0.3×	18	495
Shixin Tao United States	14	256 0.6×	32 0.1×	139 0.6×	49 0.4×	26 0.3×	20	450
Mengwen Hu China	17	371 0.8×	34 0.1×	102 0.5×	280 2.1×	46 0.5×	52	640
David Monk United Kingdom	18	963 2.1×	64 0.2×	874 3.9×	35 0.3×	646 7.0×	23	1.2k
M Tamura Japan	12	192 0.4×	41 0.2×	128 0.6×	110 0.8×	17 0.2×	23	528

Countries citing papers authored by Maryline Gagnebin

Since Specialization

Citations

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

Fields of papers citing papers by Maryline Gagnebin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maryline Gagnebin

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

All Works

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11 of 11 papers shown

Guipponi, Michel, Federico Santoni, Maude Schneider, et al.. (2017). No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients. Translational Psychiatry. 7(2). e1039–e1039. 7 indexed citations

Coppola, Antonietta, Antonio Romito, Christelle Borel, et al.. (2013). Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications. Stem Cell Research. 12(2). 323–337. 59 indexed citations

Radhakrishna, Uppala, Swapan K. Nath, Ken McElreavey, et al.. (2012). Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. Journal of Medical Genetics. 49(4). 270–276. 9 indexed citations

Attar, Homa, Karen Bedard, Eugenia Migliavacca, et al.. (2012). Extensive Natural Variation for Cellular Hydrogen Peroxide Release Is Genetically Controlled. PLoS ONE. 7(8). e43566–e43566. 3 indexed citations

Borel, Christelle, Eugenia Migliavacca, Audrey Letourneau, et al.. (2012). Tandem repeat sequence variation as causative Cis-eQTLs for protein-coding gene expression variation: The case of CSTB. Human Mutation. 33(8). 1302–1309. 25 indexed citations

Borel, Christelle, Samuel Deutsch, Audrey Letourneau, et al.. (2010). Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts. Genome Research. 21(1). 68–73. 52 indexed citations

Borel, Christelle, Maryline Gagnebin, Corinne Gehrig, et al.. (2008). Mapping of Small RNAs in the Human ENCODE Regions. The American Journal of Human Genetics. 82(4). 971–981. 20 indexed citations

Dahoun, Sophie, Sarantis Gagos, Maryline Gagnebin, et al.. (2008). Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: A complex series of events. American Journal of Medical Genetics Part A. 146A(16). 2086–2093. 29 indexed citations

Sethupathy, Praveen, Christelle Borel, Maryline Gagnebin, et al.. (2007). Human microRNA-155 on Chromosome 21 Differentially Interacts with Its Polymorphic Target in the AGTR1 3′ Untranslated Region: A Mechanism for Functional Single-Nucleotide Polymorphisms Related to Phenotypes. The American Journal of Human Genetics. 81(2). 405–413. 305 indexed citations

10.

Prandini, Paola, Samuel Deutsch, Robert Lyle, et al.. (2007). Natural Gene-Expression Variation in Down Syndrome Modulates the Outcome of Gene-Dosage Imbalance. The American Journal of Human Genetics. 81(2). 252–263. 145 indexed citations

11.

Deutsch, Samuel, Robert Lyle, Emmanouil T. Dermitzakis, et al.. (2005). Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes. Human Molecular Genetics. 14(23). 3741–3749. 89 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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