Publications by authors named "Philippe Vago"

Claim this Profile
E
Evidence for high breakpoint variability in 46, XX, SRY-positive testicular disorder and frequent ARSE deletion that may be associated with short stature.
Céline Capron, Louis Januel, Gaëlle Vieville, Sylvie Jaillard, Paul Kuentz, Philippe Vago

Andrology· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Reduced telomere length in amniocytes: an early biomarker of abnormal fetal development?
Carole Goumy, Lauren Veronese, Rodrigue Stamm, Quentin Domas, Kamil Hadjab, Philippe Vago

Hum Mol Genet· August 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Further refining the critical region of 10q26 microdeletion syndrome: A possible involvement of INSYN2 and NPS in the cognitive phenotype.
Florian Cherik, Mathis Lepage, Ganaelle Remerand, Christine Francannet, Amélie Delabaere, Philippe Vago

Eur J Med Genet· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Analysis of the cost effectiveness of different strategies for the antenatal diagnosis of chromosomal aberrations in cases of ultrasound-identified fetal abnormalities.
Charline Mourgues, Eléonore Eymard-Pierre, Hélène Laurichesse-Delmas, Laurent Gerbaud, Laëtitia Gouas, Philippe Vago

Ann Biol Clin (Paris)· October 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
1
16p13.11 microduplication in 45 new patients: refined clinical significance and genotype-phenotype correlations.
Laïla Allach El Khattabi, Solveig Heide, Jean-Hubert Caberg, Joris Andrieux, Martine Doco Fenzy, Philippe Vago

J Med Genet· May 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non-homologous Robertsonian translocation. Should we still perform prenatal diagnosis?
Kamran Moradkhani, Laurence Cuisset, Pierre Boisseau, Olivier Pichon, Marine Lebrun, Philippe Vago

Prenat Diagn· October 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, Jonathan Lévy, Julien Buratti, Philippe Vago

NPJ Genom Med· July 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Very long-term molecular follow-up of minimal residual disease in patients with neuroblastoma.
Andrei Tchirkov, Victoria Greze, Dominique Plantaz, Nadège Rouel, Philippe Vago

Pediatr Blood Cancer· December 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Sperm meiotic segregation of a balanced interchromosomal reciprocal insertion resulting in recurrent spontaneous miscarriage.
Gaëlle Salaun, Andrei Tchirkov, Christine Francannet, Hanae Pons, Florence Brugnon, Philippe Vago

Reprod Biomed Online· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spatial organization of chromosome territories in the interphase nucleus of trisomy 21 cells.
Stephan Kemeny, Christophe Tatout, Gaelle Salaun, Céline Pebrel-Richard, Carole Goumy, Philippe Vago

Chromosoma· June 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, Jonathan Lévy, Julien Buratti, Philippe Vago

NPJ Genom Med· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
promoter status and gene copy number gains: effect on expression and association with prognosis in breast cancer.
Mathilde Gay-Bellile, Lauren Véronèse, Patricia Combes, Eleonore Eymard-Pierre, Fabrice Kwiatkowski, Philippe Vago

Oncotarget· September 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Characterization by microarray and meiotic segregation study of a der(10)t(10;18) in a patient with infertility and normal phenotype.
Stephan Kemeny, Florence Brugnon, Eléonore Eymard-Pierre, Carole Goumy, Laurent Janny, Philippe Vago

Asian J Androl· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
ERCC1 and telomere status in breast tumours treated with neoadjuvant chemotherapy and their association with patient prognosis.
Mathilde Gay-Bellile, Pierre Romero, Anne Cayre, Lauren Véronèse, Maud Privat, Philippe Vago

J Pathol Clin Res· October 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardation.
Carole Goumy, Mathilde Gay-Bellile, Gaelle Salaun, Stephan Kemeny, Eleonore Eymard-Pierre, Philippe Vago

Birth Defects Res A Clin Mol Teratol· September 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Telomere status in chronic lymphocytic leukemia with TP53 disruption.
Romain Guièze, Mélanie Pages, Lauren Véronèse, Patricia Combes, Richard Lemal, Philippe Vago

Oncotarget· August 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study.
Nicolas Gruchy, Eleonore Blondeel, Nathalie Le Meur, Géraldine Joly-Hélas, Pascal Chambon, Philippe Vago

Prenat Diagn· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prenatal Screening of 21 Microdeletion/Microduplication Syndromes and Subtelomeric Imbalances by MLPA in Fetuses with Increased Nuchal Translucency and Normal Karyotype.
Laetitia Gouas, Stéphan Kémény, Anne-Marie Beaufrère, Eléonore Eymard-Pierre, Céline Pebrel-Richard, Philippe Vago

Cytogenet Genome Res· March 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prenatal BoBsTM in the cytogenetic analysis of products of spontaneous miscarriage.
Sarah Mellali, Khadidja Haoud, Laetitia Gouas, Meghit Boumediene Khaled, Philippe Vago

S Afr Med J· September 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Philippe Vago

Prenat Diagn· August 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[The right to a chromosomally perfect child].
Philippe Vago

J Int Bioethique· July 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[THE RIGHT TO A CHROMOSOMICALLY PERFECT CHILD].
Philippe Vago

J Int Bioethique Ethique Sci· July 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Congenital diaphragmatic hernia may be associated with 17q12 microdeletion syndrome.
Carole Goumy, Fanny Laffargue, Eléonore Eymard-Pierre, Stéphen Kemeny, Mathilde Gay-Bellile, Philippe Vago

Am J Med Genet A· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay.
Celine Pebrel-Richard, Charles Rouzade, Stephan Kemeny, Eleonore Eymard-Pierre, Mathilde Gay-Bellile, Philippe Vago

Am J Med Genet A· November 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and molecular description of a 17q21.33 microduplication in a girl with severe kyphoscoliosis and developmental delay.
Stéphan Kemeny, Céline Pebrel-Richard, Eléonore Eymard-Pierre, Mathilde Gay-Bellile, Laetitia Gouas, Philippe Vago

Eur J Med Genet· October 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis