Publications by authors named "Frederic Tores"

Claim this Profile
I
Identification of CaVβ1 Isoforms Required for Neuromuscular Junction Formation and Maintenance.
Amélie Vergnol, Aly Bourguiba, Stephanie Bauché, Massiré Traoré, Maxime Gelin, Frederic Tores

Cells· August 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
VNtyper enables accurate alignment-free genotyping of coding VNTR using short-read sequencing data in autosomal dominant tubulointerstitial kidney disease.
Hassan Saei, Vincent Morinière, Laurence Heidet, Olivier Gribouval, Said Lebbah, Frederic Tores

iScience· July 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Complex regulation of Gephyrin splicing is a determinant of inhibitory postsynaptic diversity.
Raphaël Dos Reis, Etienne Kornobis, Alyssa Pereira, Frederic Tores, Judit Carrasco

Nat Commun· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Publisher Correction: Somatic genetic rescue of a germline ribosome assembly defect.
Shengjiang Tan, Laëtitia Kermasson, Christine Hilcenko, Vasileios Kargas, David Traynor, Frédéric Tores

Nat Commun· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence.
Zineb Sbihi, Kay Tanita, Camille Bachelet, Christine Bole, Fabienne Jabot-Hanin, Frederic Tores

J Clin Immunol· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Somatic genetic rescue of a germline ribosome assembly defect.
Shengjiang Tan, Laëtitia Kermasson, Christine Hilcenko, Vasileios Kargas, David Traynor, Frédéric Tores

Nat Commun· August 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Battle of the Sex Chromosomes: Competition between X and Y Chromosome-Encoded Proteins for Partner Interaction and Chromatin Occupancy Drives Multicopy Gene Expression and Evolution in Muroid Rodents.
Charlotte Moretti, Mélina Blanco, Côme Ialy-Radio, Maria-Elisabetta Serrentino, Clara Gobé, Frederic Tores

Mol Biol Evol· December 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology.
Athanasia Stoupa, Frédéric Adam, Dulanjalee Kariyawasam, Catherine Strassel, Sanjay Gawade, Frédéric Tores

EMBO Mol Med· December 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Tetratricopeptide repeat domain 7A is a nuclear factor that modulates transcription and chromatin structure.
Marie-Therese El-Daher, Nicolas Cagnard, Marine Gil, Marie Chansel Da Cruz, Claire Leveau, Frédéric Tores

Cell Discov· November 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency.
Jérémie Rosain, Carmen Oleaga-Quintas, Caroline Deswarte, Hannah Verdin, Stéphane Marot, Frederic Tores

J Clin Immunol· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Expression and epigenomic landscape of the sex chromosomes in mouse post-meiotic male germ cells.
Charlotte Moretti, Daniel Vaiman, Frederic Tores, Julie Cocquet

Epigenetics Chromatin· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.
Lara De Tomasi, Pierre David, Camille Humbert, Flora Silbermann, Christelle Arrondel, Frédéric Tores

Am J Hum Genet· November 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Targeted Exome Sequencing Identifies as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract.
Laurence Heidet, Vincent Morinière, Charline Henry, Lara De Tomasi, Madeline Louise Reilly, Frédéric Tores

J Am Soc Nephrol· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SLY regulates genes involved in chromatin remodeling and interacts with TBL1XR1 during sperm differentiation.
Charlotte Moretti, Maria-Elisabetta Serrentino, Côme Ialy-Radio, Marion Delessard, Tatiana A Soboleva, Frederic Tores

Cell Death Differ· June 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
No correlation between mtDNA amount and methylation levels at the CpG island of exon 2 in wild-type and mutant human differentiated cells.
Julie Steffann, Aurore Pouliet, Houda Adjal, Christine Bole, Cécile Fourrage, Frédéric Tores

J Med Genet· May 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Association of REL polymorphisms and outcome of patients with septic shock.
Julie Toubiana, Emilie Courtine, Frederic Tores, Pierre Asfar, Cédric Daubin

Ann Intensive Care· December 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Antitumour activity of an inhibitor of miR-34a in liver cancer with β-catenin-mutations.
Angélique Gougelet, Chiara Sartor, Laura Bachelot, Cécile Godard, Carmen Marchiol, Frédéric Tores

Gut· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans.
Camille Humbert, Flora Silbermann, Bharti Morar, Mélanie Parisot, Mohammed Zarhrate, Frédéric Tores

Am J Hum Genet· February 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears.
Christopher T Gordon, Florence Petit, Peter M Kroisel, Linda Jakobsen, Roseli Maria Zechi-Ceide, Frédéric Tores

Am J Hum Genet· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects.
Jérôme Carayol, Roberto Sacco, Frédéric Tores, Francis Rousseau, Patricia Lewin

Biol Psychiatry· November 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects.
Cécile Jeanpierre, Guillaume Macé, Mélanie Parisot, Vincent Morinière, Audrey Pawtowsky, Frédéric Tores

J Med Genet· July 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Evaluating diagnostic accuracy of genetic profiles in affected offspring families.
Jerome Carayol, Frédéric Tores, Inke R König, Jörg Hager, Andreas Ziegler

Stat Med· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.
Jerome Carayol, Gerard D Schellenberg, Frederic Tores, Jörg Hager, Andreas Ziegler

Mol Autism· February 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta.
Peter Brooks, Charles Marcaillou, Maud Vanpeene, Jean-Paul Saraiva, Daniel Stockholm, Frédéric Tores

BMC Genet· March 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism.
Gilles Maussion, Jérôme Carayol, Aude-Marie Lepagnol-Bestel, Frédéric Tores, Yann Loe-Mie

Hum Mol Genet· August 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis