Danielle Martinet

4k citations

42 papers · 3.2k · 1 hit paper · h-index 26

Impact in

Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Glioma Diagnosis and Treatment
- Genomics and Rare Diseases
Developmental Neuroscience top 10%

Papers in

Genetics 20
- Genomic variations and chromosomal abnormalities 16
- Congenital Ear and Nasal Anomalies 2
- Virus-based gene therapy research 2
- Glioma Diagnosis and Treatment 2
Hematology 4
- Acute Myeloid Leukemia Research 3

Co-authors: Jacques Samuel Beckmann (19 shared papers)Nathalie Besuchet Schmutz (10 shared papers)Nicolas Mermod (4 shared papers)Annick Mühlethaler‐Mottet (2 shared papers)Roland Meier (2 shared papers)Marjorie Flahaut (2 shared papers)Katya Nardou (1 shared paper)Florian Maria Wurm (4 shared papers)
Journals: The American Journal of Human Genetics (3 papers)Nature (2 papers)PLoS ONE (2 papers)Oncogene (2 papers)European Journal of Medical Genetics (2 papers)
Partner nations: Switzerland France United States

In The Last Decade

Danielle Martinet

42 papers receiving 3.1k citations

Danielle Martinet's Hit Papers

align trajectories log scale

Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056 2011 · 546 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2011 Science Translational Medicine

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056 Science Translational Medicine ·Sébastien Jacquemont, Aurore Curie, V. des Portes, Maria Giulia Torrioli, Elizabeth Berry‐Kravis, Randi Jenssen Hagerman, Feliciano J. Ramos, Kim M. Cornish Hit paper breakdown →	2011	546
2	A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 Nature ·Robin G. Walters, Sébastien Jacquemont, Armand Valsesia, Adam J. de Smith, Danielle Martinet, Johanna C. Andersson‐Assarsson, Mario Falchi, Fei Chen	2010	424
3	Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Nature ·Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin G. Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen	2011	371
4	A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders Journal of Medical Genetics ·Flore Zufferey, Elliott H. Sherr, Noam D. Beckmann, Ellen M. Hanson, Anne Manuela Maillard, Loyse Hippolyte, Aurélien Macé, Carina Ferrari	2012	240
5	The Wnt receptor FZD1 mediates chemoresistance in neuroblastoma through activation of the Wnt/β-catenin pathway Oncogene ·Marjorie Flahaut, Roland Meier, Katya Nardou, Felix K Niggli, Danielle Martinet, Jacques Samuel Beckmann, J-M Joseph, Annick Mühlethaler‐Mottet +2 others	2009	166
6	Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome European Journal of Medical Genetics ·Nathalie Van der Aa, Liesbeth Rooms, Geert Vandeweyer, Jenneke van den Ende, Edwin Reyniers, Marco Fichera, Corrado Romano, Barbara Delle Chiaie	2009	161
7	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, Marianne Wicht, Martin Bertschinger, David L. Hacker, Jacques Samuel Beckmann	2005	126
8	Genome-wide prediction of matrix attachment regions that increase gene expression in mammalian cells Nature Methods ·Pierre‐Alain Girod, Duc-Quang Nguyen, Stefania Puttini, Mélanie Grandjean, Danielle Martinet, Alexandre Regamey, Damien Saugy, Jacques Samuel Beckmann	2007	122
9	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, Daniele Belluoccio, Lynn Rowley, Tiong Yang Tan, Karl‐Henrik Gustavson, Zvi U Borochowitz	2009	94
10	SCRIB and PUF60 Are Primary Drivers of the Multisystemic Phenotypes of the 8q24.3 Copy-Number Variant The American Journal of Human Genetics ·Andrew Nahum Dauber, Christelle Golzio, Cécile Guenot, Francine M. Jodelka, Maria Kibæk, Susanne Kjærgaard, Bruno Leheup, Danielle Martinet	2013	77
11	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 Johannes Hartmann, Andreas von Deimling, Danielle Martinet	2012	75
12	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, Robert-Charles Janzer, Claudio Pollo, Marie‐France Hamou, Bernd Kaina	2010	73
13	Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization American Journal of Medical Genetics Part A ·Cheryl DeScipio, Laura Kathleen Conlin, Jill Anne Rosenfeld, James H. Tepperberg, Romela M. Pasion, Ankita Patel, Marie McDonald, Swaroop Aradhya	2012	60
14	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	2015	59
15	The phenotype of recurrent 10q22q23 deletions and duplications European Journal of Human Genetics ·Bregje W.M. van Bon, Jorune Balciuniene, Gary Fruhman, Sandesh C. Sreenath Nagamani, Diane L. Broome, Elizabeth Cameron, Danielle Martinet, Eliane Roulet	2011	54
16	A New CRB1 Rat Mutation Links Müller Glial Cells to Retinal Telangiectasia Journal of Neuroscience ·Min Zhao, Charlotte Andrieu‐Soler, Laura Kowalczuk, Marianne Berdugo, Marilyn Dernigoghossian, Francisco Halili, Jean‐Claude Jeanny, Brigitte Thillaye-Goldenberg	2015	52
17	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 R. Ibberson, Paola Benaglio, Manfredo Quadroni, Patrice Waridel, Muriel Gaillard	2011	45
18	A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology The American Journal of Human Genetics ·Eugenia Migliavacca, Christelle Golzio, Katrin Männik, Ian Blumenthal, Edwin C. T. Oh, Louise Harewood, Jack A. Kosmicki, Maria Nicla Loviglio	2015	45
19	High-level transgene expression by homologous recombination-mediated gene transfer Nucleic Acids Research ·Mélanie Grandjean, Pierre‐Alain Girod, Kaja Kostyrko, Marianne Wicht, Florence Yerly, Christian Mazza, Jacques Samuel Beckmann, Danielle Martinet	2011	44
20	Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats Human Mutation ·Paweł Stankiewicz, Shashikant Kulkarni, Avinash V. Dharmadhikari, Srirangan Sampath, Samarth Bhatt, Tamim H. Shaikh, Zhilian Xia, Amber Nolen Pursley	2011	43

About Danielle Martinet

Danielle Martinet is a scholar working on Genetics, Genetics, Hematology, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 42 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Viral Infectious Diseases and Gene Expression in Insects (5 papers), Acute Myeloid Leukemia Research (3 papers), Congenital Ear and Nasal Anomalies (2 papers), Virus-based gene therapy research (2 papers), Neuroblastoma Research and Treatments (2 papers), Genomics and Chromatin Dynamics (2 papers) and Glioma Diagnosis and Treatment (2 papers). The work is most often cited by research in Genetics (1.5k citations), Genetics (152 citations), Developmental Neuroscience (51 citations), Endocrine and Autonomic Systems (81 citations) and Molecular Biology (677 citations). Danielle Martinet has collaborated with scholars based in Switzerland, France and United States. Frequent co-authors include Jacques Samuel Beckmann, Nathalie Besuchet Schmutz, Nicolas Mermod, Annick Mühlethaler‐Mottet, Roland Meier, Marjorie Flahaut, Katya Nardou, Florian Maria Wurm, Madiha Derouazi and Felix K Niggli. Their work appears in journals such as The American Journal of Human Genetics, Nature, PLoS ONE, Oncogene and European Journal of Medical Genetics.

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.

Explore authors with similar magnitude of impact

Danielle Martinet

Impact in

Papers in i

In The Last Decade

Danielle Martinet

Danielle Martinet's Hit Papers

Peers

Countries citing papers authored by Danielle Martinet

Fields of papers citing papers by Danielle Martinet

All Works

About Danielle Martinet

Explore authors with similar magnitude of impact

Papers in