Danielle Martinet

4.1k citations

27 papers · 1.1k · h-index 18

Impact in

Genetics top 10%
- Virus-based gene therapy research
- Glioma Diagnosis and Treatment
- Genomic variations and chromosomal abnormalities
Molecular Biology top 10%
- Viral Infectious Diseases and Gene Expression in Insects
- CRISPR and Genetic Engineering
- Epigenetics and DNA Methylation
- Wnt/β-catenin signaling in development and cancer
- RNA Interference and Gene Delivery

Papers in

Molecular Biology 20
- CRISPR and Genetic Engineering 4
- RNA Interference and Gene Delivery 4
- Genomics and Chromatin Dynamics 3
- Viral Infectious Diseases and Gene Expression in Insects 3
Genetics 14
- Genomic variations and chromosomal abnormalities 4
- Virus-based gene therapy research 4
- Chronic Lymphocytic Leukemia Research 3

Co-authors: J. Beckmann (17 shared papers)Nicolas Mermod (4 shared papers)Marjorie Flahaut (2 shared papers)Roland Meier (2 shared papers)Annick Mühlethaler‐Mottet (2 shared papers)David Calabrese (3 shared papers)Aurélie Coulon (1 shared paper)Pierre‐Alain Girod (2 shared papers)
Journals: The American Journal of Human Genetics (2 papers)Oncogene (2 papers)Nature Methods (1 paper)Clinical Cancer Research (1 paper)Biotechnology and Bioengineering (1 paper)
Partner nations: Switzerland France United States

In The Last Decade

Danielle Martinet

26 papers receiving 1.1k citations

Peers

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-authors

The 25 scholars most cited alongside Danielle Martinet, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Danielle Martinet Line = papers co-authored together Danielle Martinet links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 27 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The Wnt receptor FZD1 mediates chemoresistance in neuroblastoma through activation of the Wnt/β-catenin pathway Oncogene ·Marjorie Flahaut, Roland Meier, Aurélie Coulon, Katya Nardou, Felix Niggli, Danielle Martinet, J. Beckmann, J-M Joseph, Annick Mühlethaler‐Mottet, (unknown)	2009	153
2	Genome-wide prediction of matrix attachment regions that increase gene expression in mammalian cells Nature Methods ·Pierre‐Alain Girod, Duc-Quang Nguyen, David Calabrese, Stefania Puttini, Mélanie Grandjean, Danielle Martinet, Alexandre Regamey, Damien Saugy, J. Beckmann, Philipp Bücher, Nicolas Mermod	2007	114
3	Genetic characterization of CHO production host DG44 and derivative recombinant cell lines Biochemical and Biophysical Research Communications ·Madiha Derouazi, Danielle Martinet, Nathalie Besuchet Schmutz, R. Flaction, M. Wicht, Martin Bertschinger, David L. Hacker, J. Beckmann, Florian Μ. Wurm	2005	108
4	Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia The American Journal of Human Genetics ·Belinda Campos‐Xavier, Danielle Martinet, John F. Bateman, Dan Belluoccio, Lynn Rowley, Tiong Yang Tan, A Baxová, Karl‐Henrik Gustavson, Zvi Borochowitz, A. Micheil Innes, Sheila Unger, J. Beckmann, Lauréane Mittaz, Diana Ballhausen, Andrea Superti‐Furga, Ravi Savarirayan, Luisa Bonafé	2009	84
5	Presence of an oligodendroglioma-like component in newly diagnosed glioblastoma identifies a pathogenetically heterogeneous subgroup and lacks prognostic value: central pathology review of the EORTC_26981/NCIC_CE.3 trial Acta Neuropathologica ·Monika E. Hegi, Robert-Charles Janzer, Wanyu L. Lambiv, Thierry Gorlia, Mathilde C.M. Kouwenhoven, Christian Hartmann, Andreas von Deimling, Danielle Martinet, Nathalie Besuchet Schmutz, Annie‐Claire Diserens, Marie‐France Hamou, Pierre Bady, Michael Weller, Martin J. van den Bent, Warren Mason, René‐Olivier Mirimanoff, Roger Stupp, Karima Mokhtari, Pieter Wesseling	2012	69
6	Extent and Patterns of MGMT Promoter Methylation in Glioblastoma- and Respective Glioblastoma-Derived Spheres Clinical Cancer Research ·Davide Sciuscio, Annie‐Claire Diserens, Kristof Van Dommelen, Danielle Martinet, Greg Jones, Robert-Charles Janzer, Claudio Pollo, Marie‐France Hamou, Bernd Kaina, Roger Stupp, Marc Levivier, Monika E. Hegi	2010	68
7	SCRIB and PUF60 Are Primary Drivers of the Multisystemic Phenotypes of the 8q24.3 Copy-Number Variant The American Journal of Human Genetics ·Andrew Dauber, Christelle Golzio, Cécile Guenot, Francine M. Jodelka, Maria Kibæk, Susanne Kjærgaard, Bruno Leheup, Danielle Martinet, Małgorzata J.M. Nowaczyk, Jill A. Rosenfeld, Susan Zeesman, Janice Zunich, J. Beckmann, Joel N. Hirschhorn, Michelle L. Hastings, Sébastien Jacquemont, Nicholas Katsanis	2013	58
8	IL-17 receptor A and adenosine deaminase 2 deficiency in siblings with recurrent infections and chronic inflammation Journal of Allergy and Clinical Immunology ·Florence Fellmann, Federica Angelini, Jacqueline Wassenberg, Matthieu Perreau, Natalia Arenas-Ramirez, Gregoire Simon, Onur Boyman, Olivier Demaria, Stéphanie Christen‐Zaech, Daniel Hohl, Marco Belfiore, Annette von Scheven-Gête, Michel Gilliet, Pierre–Yves Bochud, Yannick Perrin, Maya Beck Popovic, Pierre‐Alexandre Bart, J. Beckmann, Danielle Martinet, Michaël Hofer	2015	50
9	A New CRB1 Rat Mutation Links Müller Glial Cells to Retinal Telangiectasia Journal of Neuroscience ·Min Zhao, Charlotte Andrieu‐Soler, Laura Kowalczuk, María Paz Cortés, Marianne Berdugo, Marilyn Dernigoghossian, Francisco Halili, Jean‐Claude Jeanny, Brigitte Goldenberg, Michèle Savoldelli, Mohamed El Sanharawi, Marie‐Christine Naud, Wilfred F. J. van IJcken, Rosanna Pescini Gobert, Danielle Martinet, Alejandro Maass, Jan Wijnholds, Patricia Crisanti, Carlo Rivolta, Francine Béhar‐Cohen	2015	49
10	Network-Guided Analysis of Genes with Altered Somatic Copy Number and Gene Expression Reveals Pathways Commonly Perturbed in Metastatic Melanoma PLoS ONE ·Armand Valsesia, Donata Rimoldi, Danielle Martinet, Mark Ibberson, Paola Benaglio, Manfredo Quadroni, Patrice Waridel, Muriel Gaillard, Mireille Pidoux, Blandine Rapin, Carlo Rivolta, Ioannis Xénarios, Andrew J.G. Simpson, Stylianos E. Antonarakis, J. Beckmann, C. Victor Jongeneel, Christian Iseli, Brian J. Stevenson	2011	45
11	High-level transgene expression by homologous recombination-mediated gene transfer Nucleic Acids Research ·Mélanie Grandjean, Pierre‐Alain Girod, David Calabrese, Kaja Kostyrko, M. Wicht, Florence Yerly, Christian Mazza, J. Beckmann, Danielle Martinet, Nicolas Mermod	2011	44
12	A single epidermal stem cell strategy for safe ex vivo gene therapy EMBO Molecular Medicine ·Stéphanie Droz‐Georget Lathion, Ariane Rochat, Graham Knott, Alessandra Recchia, Danielle Martinet, Sara Benmohammed, Nicolas Grasset, Andrea Zaffalon, Nathalie Besuchet Schmutz, Emmanuelle Savioz-Dayer, J. Beckmann, Jacques Rougemont, Fulvio Mavilio, Yann Barrandon	2015	36
13	Subtelomeric 6p deletion: Clinical and array‐CGH characterization in two patients American Journal of Medical Genetics Part A ·Danielle Martinet, Isabel Filges, Nathalie Besuchet Schmutz, Michael A. Morris, Anne‐Claude Gaide, Sophie Dahoun, Armand Bottani, Marie‐Claude Addor, Stylianos E. Antonarakis, J. Beckmann, Frédérique Béna	2008	27
14	Detection of 16 p deletions by FISH in patients with inv(16) or t(16;16) and acute myeloid leukemia (AML) Leukemia ·Danielle Martinet, Dominique Mühlematter, Matthew F. Leeman, V. Parlier, U Hess, J Gmür, Martine Jotterand	1997	26
15	Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered Oncogene ·Bert A. van der Reijden, Hans G. Dauwerse, Rachel H. Giles, Shantie Jagmohan–Changur, Cisca Wijmenga, P Paul Liu, Bep Smit, Hans W. Wessels, Geoff C. Beverstock, M Jotterand-Bellomo, Danielle Martinet, Dominique Mühlematter, Mårina Lafage‐Pochitaloff, Jean Gabert, Josy Reiffers, Chrystèle Bilhou‐Nabera, Gert‐Jan B. van Ommen, Anne Hagemeijer, Martijn H. Breuning	1999	25
16	Fetus with two identical reciprocal translocations: Description of a rare complication of consanguinity American Journal of Medical Genetics Part A ·Danielle Martinet, Yvan Vial, Francine Thonney, J. Beckmann, Kathleen Meagher‐Villemure, Sheila Unger	2006	25
17	Calcium phosphate transfection generates mammalian recombinant cell lines with higher specific productivity than polyfection Biotechnology and Bioengineering ·Sébastien Chenuet, Danielle Martinet, Nathalie Besuchet‐Schmutz, M. Wicht, Nicolas Jaccard, Anne‐Charlotte Bon, Madiha Derouazi, David L. Hacker, J. Beckmann, Florian Μ. Wurm	2008	20
18	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 ·Marjorie Flahaut, Annick Mühlethaler‐Mottet, Danielle Martinet, Sarah Fattet, Katia Balmas Bourloud, Katya Auderset, Roland Meier, Nathalie Besuchet Schmutz, Olivier Delattre, Jean‐Marc Joseph, Nicole Groß	2006	19
19	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 ·Pekka Kannus, Belinda Campos‐Xavier, Danna Hull, Danielle Martinet, Diana Ballhausen, Luisa Bonafé	2013	16
20	Transcription Factor CTF1 Acts as a Chromatin Domain Boundary That Shields Human Telomeric Genes from Silencing Molecular and Cellular Biology ·Germain Esnault, Stefano Majocchi, Danielle Martinet, Nathalie Besuchet‐Schmutz, J. Beckmann, Nicolas Mermod	2009	14

About Danielle Martinet

Danielle Martinet is a scholar working on Molecular Biology, Genetics, Genetics, Hematology and Surgery, having authored 27 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Virus-based gene therapy research (4 papers), CRISPR and Genetic Engineering (4 papers), RNA Interference and Gene Delivery (4 papers), Chronic Lymphocytic Leukemia Research (3 papers), Genomics and Chromatin Dynamics (3 papers), Chronic Myeloid Leukemia Treatments (3 papers) and Viral Infectious Diseases and Gene Expression in Insects (3 papers). The work is most often cited by research in Genetics (144 citations), Genetics (342 citations), Molecular Biology (767 citations), Cancer Research (145 citations) and Cell Biology (107 citations). Danielle Martinet has collaborated with scholars based in Switzerland, France and United States. Frequent co-authors include J. Beckmann, Nicolas Mermod, Marjorie Flahaut, Roland Meier, Annick Mühlethaler‐Mottet, David Calabrese, Aurélie Coulon, Pierre‐Alain Girod, Felix Niggli and Katya Nardou. Their work appears in journals such as The American Journal of Human Genetics, Oncogene, Nature Methods, Clinical Cancer Research and Biotechnology and Bioengineering.

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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