Publications by authors named "Danielle Martinet"

Claim this Profile
I
IL-17 receptor A and adenosine deaminase 2 deficiency in siblings with recurrent infections and chronic inflammation.
Florence Fellmann, Federica Angelini, Jacqueline Wassenberg, Matthieu Perreau, Natalia Arenas Ramirez, Danielle Martinet

J Allergy Clin Immunol· April 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A single epidermal stem cell strategy for safe ex vivo gene therapy.
Stéphanie Droz-Georget Lathion, Ariane Rochat, Graham Knott, Alessandra Recchia, Danielle Martinet

EMBO Mol Med· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A new CRB1 rat mutation links Müller glial cells to retinal telangiectasia.
Min Zhao, Charlotte Andrieu-Soler, Laura Kowalczuk, María Paz Cortés, Marianne Berdugo, Danielle Martinet

J Neurosci· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Chromosomal microarray among children with intellectual disability: a useful diagnostic tool for the clinical geneticist.
Stephanie Capobianco, Sebastiano Ag Lava, Mario G Bianchetti, Danielle Martinet, Marco Belfiore

Dev Med Child Neurol· March 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Potocki-Shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype.
Alessandra Ferrarini, Muriel Gaillard, Frederic Guerry, Gianpaolo Ramelli, Fodstad Heidi, Danielle Martinet

Am J Med Genet A· February 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SCRIB and PUF60 are primary drivers of the multisystemic phenotypes of the 8q24.3 copy-number variant.
Andrew Dauber, Christelle Golzio, Cécile Guenot, Francine M Jodelka, Maria Kibaek, Danielle Martinet

Am J Hum Genet· November 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.
Robin G Walters, Lachlan J M Coin, Aimo Ruokonen, Adam J de Smith, Julia S El-Sayed Moustafa, Danielle Martinet

PLoS One· September 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, Ellen Hanson, Anne M Maillard, Danielle Martinet

J Med Genet· October 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenetic characterization.
Cheryl DeScipio, Laura Conlin, Jill Rosenfeld, James Tepperberg, Romela Pasion, Danielle Martinet

Am J Med Genet A· September 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
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.
Monika E Hegi, Robert-Charles Janzer, Wanyu L Lambiv, Thierry Gorlia, Mathilde C M Kouwenhoven, Danielle Martinet

Acta Neuropathol· June 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.
Paweł Stankiewicz, Shashikant Kulkarni, Avinash V Dharmadhikari, Srirangan Sampath, Samarth S Bhatt, Danielle Martinet

Hum Mutat· January 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
1
16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridization in persistent pulmonary hypertension of the newborn.
Flore Zufferey, Danielle Martinet, Maria-Chiara Osterheld, Florence Niel-Bütschi, Eric Giannoni

Pediatr Crit Care Med· November 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
High-level transgene expression by homologous recombination-mediated gene transfer.
Mélanie Grandjean, Pierre-Alain Girod, David Calabrese, Kaja Kostyrko, Marianne Wicht, Danielle Martinet

Nucleic Acids Res· August 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin G Walters, Danielle Martinet

Nature· August 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The phenotype of recurrent 10q22q23 deletions and duplications.
Bregje W M van Bon, Jorune Balciuniene, Gary Fruhman, Sandesh Chakravarthy Sreenath Nagamani, Diane L Broome, Danielle Martinet

Eur J Hum Genet· April 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanoma.
Armand Valsesia, Donata Rimoldi, Danielle Martinet, Mark Ibberson, Paola Benaglio

PLoS One· April 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Extent and patterns of MGMT promoter methylation in glioblastoma- and respective glioblastoma-derived spheres.
Davide Sciuscio, Annie-Claire Diserens, Kristof van Dommelen, Danielle Martinet, Greg Jones

Clin Cancer Res· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.
Sébastien Jacquemont, Aurore Curie, Vincent des Portes, Maria Giulia Torrioli, Elizabeth Berry-Kravis, Danielle Martinet

Sci Transl Med· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Array CGH: why and to whom].
Alessandra Ferrarini, Sébastien Jacquemont, Maja Beck Popovic, Luisa Bonafé, Danielle Martinet

Rev Med Suisse· February 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Familial occurrence of an association of multiple intestinal atresia and choanal atresia: a new syndrome?
Alessandra Ferrarini, Maria-Chiara Osterheld, Yvan Vial, Pierre A de Viragh, Jacques Cotting, Danielle Martinet

Am J Med Genet A· December 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.
Nathalie Van der Aa, Liesbeth Rooms, Geert Vandeweyer, Jenneke van den Ende, Edwin Reyniers, Danielle Martinet

Eur J Med Genet· September 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia.
Ana Belinda Campos-Xavier, Danielle Martinet, John Bateman, Dan Belluoccio, Lynn Rowley

Am J Hum Genet· June 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Transcription factor CTF1 acts as a chromatin domain boundary that shields human telomeric genes from silencing.
Germain Esnault, Stefano Majocchi, Danielle Martinet, Nathalie Besuchet-Schmutz, Jacques S Beckmann

Mol Cell Biol· May 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Calcium phosphate transfection generates mammalian recombinant cell lines with higher specific productivity than polyfection.
Sebastien Chenuet, Danielle Martinet, Nathalie Besuchet-Schmutz, Marianne Wicht, Nicolas Jaccard

Biotechnol Bioeng· December 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients.
Danielle Martinet, Isabel Filges, Nathalie Besuchet Schmutz, Michael A Morris, Anne-Claude Gaide

Am J Med Genet A· August 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis