Danielle Martinet

4.1k citations

27 papers · 1.1k indexed · h-index 18

Genetics top 10%
- Virus-based gene therapy research 4
- Genomic variations and chromosomal abnormalities 4
- Chronic Lymphocytic Leukemia Research 3
Genetics top 5%
- Virus-based gene therapy research 4
- Genomic variations and chromosomal abnormalities 4
- Chronic Lymphocytic Leukemia Research 3
Molecular Biology top 10%
- RNA Interference and Gene Delivery 4
- CRISPR and Genetic Engineering 4
- Viral Infectious Diseases and Gene Expression in Insects 3
- Genomics and Chromatin Dynamics 3
Cancer Research
Cell Biology
Hematology
- Chronic Myeloid Leukemia Treatments 3

Co-authors: J. Beckmann Nicolas Mermod Roland Meier Marjorie Flahaut Annick Mühlethaler‐Mottet Aurélie Coulon Pierre‐Alain Girod Katya Nardou
Cited by: Genetics Molecular Biology
Journals: The American Journal of Human Genetics (2 papers)Oncogene (2 papers)Nature Methods (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-authorship network

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

#	Work
1	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,伊藤加代子,M. Wobisch,Jean‐Claude Jeanny,Л.С. Мхітарян,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
2	A single epidermal stem cell strategy for safe ex vivo gene therapy EMBO Molecular Medicine ·古和久典,Ariane Rochat,Graham Knott,Alessandra Recchia,Danielle Martinet,Miquel López López,浩志浪本,M Nur Faiz Septiawan,Teresa B. Gramm,Hugo Vega Álvarez,J. Beckmann,Jacques Rougemont,Fulvio Mavilio,Yann Barrandon	2015	36
3	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,Dalbo Contrera Toro,Onur Boyman,Olivier Demaria,Stéphanie Christen‐Zaech,Daniel Hohl,Marco Belfiore,Annette von Scheven-Gête,Michel Gilliet,Pierre–Yves Bochud,Yannick Perrin,Matthew Huk,Pierre‐Alexandre Bart,J. Beckmann,Danielle Martinet,Michaël Hofer	2015	50
4	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,Vladimir Ladik,Danielle Martinet,Diana Ballhausen,Luisa Bonafé	2013	16
5	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,Ariane Biquand,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,Nfn Krishichayan,Nicholas Katsanis	2013	58
6	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,Teresa B. Gramm,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
7	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 ·Flore Zufferey,Danielle Martinet,Maria‐Chiara Osterheld,R.H. van den Beuken,Éric Giannoni,Teresa B. Gramm,Zhilian Xia,J. Beckmann,Charles Shaw‐Smith,Paweł Stankiewicz,Claire Langston,Florence Fellmann	2011	13
8	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,G L Materesa,Carlo Rivolta,Ioannis Xénarios,Andrew J.G. Simpson,Stylianos E. Antonarakis,J. Beckmann,C. Victor Jongeneel,Christian Iseli,Brian J. Stevenson	2011	45
9	Extent and Patterns of MGMT Promoter Methylation in Glioblastoma- and Respective Glioblastoma-Derived Spheres Clinical Cancer Research ·Davide Sciuscio,Annie‐Claire Diserens,酒井心子,Danielle Martinet,Greg Jones,Robert-Charles Janzer,Claudio Pollo,Marie‐France Hamou,Bernd Kaina,Roger Stupp,Marc Levivier,Monika E. Hegi	2010	68
10	Familial occurrence of an association of multiple intestinal atresia and choanal atresia: A new syndrome? American Journal of Medical Genetics Part A ·Alberto Ferrarini,Maria‐Chiara Osterheld,Yvan Vial,Pierre A. de Viragh,Jacques Cotting,Danielle Martinet,J. Beckmann,Florence Fellmann	2009	0
11	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,D. Piccolo,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
12	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,张华珍,Annick Mühlethaler‐Mottet,(unknown)	2009	153
13	Subtelomeric 6p deletion: Clinical and array‐CGH characterization in two patients American Journal of Medical Genetics Part A ·Danielle Martinet,Isabel Filges,Teresa B. Gramm,Michael A. Morris,Ashraf Saleha,Sophie Dahoun,Armand Bottani,Marie‐Claude Addor,Stylianos E. Antonarakis,J. Beckmann,Frédérique Béna	2008	27
14	Calcium phosphate transfection generates mammalian recombinant cell lines with higher specific productivity than polyfection Biotechnology and Bioengineering ·Wonkyung Ahn,Danielle Martinet,Mr. Ilpo Auranen,Tetsuo Arakawa,Nicolas Jaccard,A. S. Krechetov,Madiha Derouazi,David L. Hacker,J. Beckmann,Florian Μ. Wurm	2008	20
15	Genome-wide prediction of matrix attachment regions that increase gene expression in mammalian cells Nature Methods ·Pierre‐Alain Girod,孝充末吉,David Calabrese,Stefania Puttini,Joseph Tae-Jung Yune,Danielle Martinet,Alexandre Regamey,Damien Saugy,J. Beckmann,Philipp Bücher,Nicolas Mermod	2007	114
16	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,Paul Michael Green,Roland Meier,Teresa B. Gramm,Olivier Delattre,Jean‐Marc Joseph,Nicole Groß	2006	19
17	Genetic characterization of CHO production host DG44 and derivative recombinant cell lines Biochemical and Biophysical Research Communications ·Madiha Derouazi,Danielle Martinet,Teresa B. Gramm,Chiara Ballabio,Tetsuo Arakawa,Martin Bertschinger,David L. Hacker,J. Beckmann,Florian Μ. Wurm	2005	108
18	Effect of Conditioned Medium, Nutritive Elements and Mitotic Synchronization on the Accuracy of the Cytogenetic Analysis in Patients with Chronic Myeloid Leukemia at Diagnosis and During α-Interferon Therapy Cancer Genetics and Cytogenetics ·A. Hafs,Dominique Mühlematter,Danielle Martinet,Martine Jotterand	1999	7
19	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,国芳蒋,Bep Smit,M. Posch,Siva. K. P,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
20	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

About Danielle Martinet

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