Danielle Martinet

4.1k total citations
27 papers, 1.1k citations indexed

About

Danielle Martinet is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Danielle Martinet has authored 27 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 14 papers in Genetics and 6 papers in Genetics. Recurrent topics in Danielle Martinet's work include Virus-based gene therapy research (4 papers), RNA Interference and Gene Delivery (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Danielle Martinet is often cited by papers focused on Virus-based gene therapy research (4 papers), RNA Interference and Gene Delivery (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Danielle Martinet collaborates with scholars based in Switzerland, France and United States. Danielle Martinet's co-authors include J. Beckmann, Nicolas Mermod, Marjorie Flahaut, Roland Meier, Annick Mühlethaler‐Mottet, Aurélie Coulon, Felix Niggli, Katya Nardou, Pierre‐Alain Girod and David Calabrese and has published in prestigious journals such as Nucleic Acids Research, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Danielle Martinet

26 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
Danielle Martinet Switzerland 18 767 342 145 144 143 27 1.1k
Christel Kockx Netherlands 20 1.3k 1.7× 227 0.7× 190 1.3× 193 1.3× 150 1.0× 28 1.7k
Klaus K. Wilgenbus Germany 14 736 1.0× 195 0.6× 122 0.8× 214 1.5× 157 1.1× 19 1.2k
Luisa Izzi Canada 14 978 1.3× 196 0.6× 73 0.5× 79 0.5× 237 1.7× 18 1.3k
Fabiola Porro Italy 16 393 0.5× 123 0.4× 119 0.8× 106 0.7× 74 0.5× 24 843
Minke E. Binnerts Netherlands 13 1.0k 1.3× 363 1.1× 72 0.5× 57 0.4× 335 2.3× 14 1.5k
Larissa Savelyeva Germany 23 1.0k 1.3× 461 1.3× 357 2.5× 73 0.5× 273 1.9× 49 1.5k
Najim Ameziane Netherlands 19 1.3k 1.6× 464 1.4× 353 2.4× 100 0.7× 504 3.5× 47 1.7k
Paul Rayhorn United States 11 1.5k 2.0× 397 1.2× 65 0.4× 112 0.8× 238 1.7× 12 1.7k
Xiaosi Han United States 18 489 0.6× 203 0.6× 127 0.9× 208 1.4× 212 1.5× 36 990
Dana N. Levasseur United States 16 1.9k 2.5× 399 1.2× 130 0.9× 252 1.8× 245 1.7× 21 2.2k

Countries citing papers authored by Danielle Martinet

Since Specialization
Citations

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

Fields of papers citing papers by Danielle Martinet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Danielle Martinet

This figure shows the co-authorship network connecting the top 25 collaborators of Danielle Martinet. A scholar is included among the top collaborators of Danielle Martinet 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 Danielle Martinet. Danielle Martinet 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.
Zhao, Min, Charlotte Andrieu‐Soler, Laura Kowalczuk, et al.. (2015). A New CRB1 Rat Mutation Links Müller Glial Cells to Retinal Telangiectasia. Journal of Neuroscience. 35(15). 6093–6106. 49 indexed citations
2.
Fellmann, Florence, Federica Angelini, Jacqueline Wassenberg, et al.. (2015). IL-17 receptor A and adenosine deaminase 2 deficiency in siblings with recurrent infections and chronic inflammation. Journal of Allergy and Clinical Immunology. 137(4). 1189–1196.e2. 50 indexed citations
3.
Dauber, Andrew, Christelle Golzio, Francine M. Jodelka, et al.. (2013). SCRIB and PUF60 Are Primary Drivers of the Multisystemic Phenotypes of the 8q24.3 Copy-Number Variant. The American Journal of Human Genetics. 93(5). 798–811. 58 indexed citations
4.
Kannus, Pekka, et al.. (2013). Post-axial polydactyly type A2, overgrowth and autistic traits associated with a chromosome 13q31.3 microduplication encompassing miR-17-92 and GPC5. European Journal of Medical Genetics. 56(8). 452–457. 16 indexed citations
5.
6.
Zufferey, Flore, Danielle Martinet, Maria‐Chiara Osterheld, et al.. (2011). 16q24.1 microdeletion in a premature newborn: Usefulness of array-based comparative genomic hybridization in persistent pulmonary hypertension of the newborn. Pediatric Critical Care Medicine. 12(6). e427–e432. 13 indexed citations
7.
Valsesia, Armand, Donata Rimoldi, Danielle Martinet, et al.. (2011). Network-Guided Analysis of Genes with Altered Somatic Copy Number and Gene Expression Reveals Pathways Commonly Perturbed in Metastatic Melanoma. PLoS ONE. 6(4). e18369–e18369. 45 indexed citations
8.
Sciuscio, Davide, Annie‐Claire Diserens, Danielle Martinet, et al.. (2010). Extent and Patterns of MGMT Promoter Methylation in Glioblastoma- and Respective Glioblastoma-Derived Spheres. Clinical Cancer Research. 17(2). 255–266. 68 indexed citations
9.
Flahaut, Marjorie, Roland Meier, Aurélie Coulon, et al.. (2009). The Wnt receptor FZD1 mediates chemoresistance in neuroblastoma through activation of the Wnt/β-catenin pathway. Oncogene. 28(23). 2245–2256. 153 indexed citations
10.
Ferrarini, Alberto, Maria‐Chiara Osterheld, Yvan Vial, et al.. (2009). Familial occurrence of an association of multiple intestinal atresia and choanal atresia: A new syndrome?. American Journal of Medical Genetics Part A. 149A(12). 2661–2665.
11.
Campos‐Xavier, Belinda, Danielle Martinet, John F. Bateman, et al.. (2009). Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia. The American Journal of Human Genetics. 84(6). 760–770. 84 indexed citations
12.
Martinet, Danielle, Isabel Filges, Michael A. Morris, et al.. (2008). Subtelomeric 6p deletion: Clinical and array‐CGH characterization in two patients. American Journal of Medical Genetics Part A. 146A(16). 2094–2102. 27 indexed citations
13.
Martinet, Danielle, Nicolas Jaccard, Madiha Derouazi, et al.. (2008). Calcium phosphate transfection generates mammalian recombinant cell lines with higher specific productivity than polyfection. Biotechnology and Bioengineering. 101(5). 937–945. 20 indexed citations
14.
Girod, Pierre‐Alain, David Calabrese, Stefania Puttini, et al.. (2007). Genome-wide prediction of matrix attachment regions that increase gene expression in mammalian cells. Nature Methods. 4(9). 747–753. 114 indexed citations
15.
Flahaut, Marjorie, Annick Mühlethaler‐Mottet, Danielle Martinet, et al.. (2006). Molecular cytogenetic characterization of doxorubicin‐resistant neuroblastoma cell lines: Evidence that acquired multidrug resistance results from a unique large amplification of the 7q21 region. Genes Chromosomes and Cancer. 45(5). 495–508. 19 indexed citations
16.
Martinet, Danielle, et al.. (2006). Fetus with two identical reciprocal translocations: Description of a rare complication of consanguinity. American Journal of Medical Genetics Part A. 140A(7). 769–774. 25 indexed citations
17.
Derouazi, Madiha, Danielle Martinet, Martin Bertschinger, et al.. (2005). Genetic characterization of CHO production host DG44 and derivative recombinant cell lines. Biochemical and Biophysical Research Communications. 340(4). 1069–1077. 108 indexed citations
18.
19.
Reijden, Bert A. van der, Hans G. Dauwerse, Rachel H. Giles, et al.. (1999). Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered. Oncogene. 18(2). 543–550. 25 indexed citations
20.
Martinet, Danielle, Dominique Mühlematter, Matthew F. Leeman, et al.. (1997). Detection of 16 p deletions by FISH in patients with inv(16) or t(16;16) and acute myeloid leukemia (AML). Leukemia. 11(7). 964–970. 26 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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