François Vialard (F Vialard)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 30

Top Venues

Genes

Biomedicines

Prenatal diagnosis

Journal of assisted reproduction and genetics

Université de Versailles Saint-Quentin-en-Yvelines UFR des sciences de la santé Simone Veil

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Université de Versailles Saint-Quentin-en-Yvelines UFR des sciences de la santé Simone Veil Jan 01 2015

France

Director :: EA4704-GIG

Centre hospitalier intercommunal de Poissy-Saint-Germain-en-Laye Site Hospitalier de Poissy Sep 01 2012

France

Director :: Genetics Federation

Publications

Bérangère Coutanceau, Esther Dos Santos, Nelly Swierkowski Blanchard, Anne Sanchez Louboutin, Florence Boitrelle, François Margueritte, François Vialard, Valérie Serazin, Khadija Fathallah
Should the Treatment of Patients with Repeated Embryo Implantation Failure Be Adapted as a Function of the Endometrial Cytokine Profile? A Single-Center Experience. Biomedicines 11 (3) (2023)
Laurent Galio, Laetitia Bernet, Yoann Rodriguez, Camille Fourcault, Marie-Noëlle Dieudonné, Hélène Pinatel, Céline Henry, Valérie Serazin, Khadija Fathallah, Anissa Gagneux, Zuzana Krupova, François Vialard, Esther Dos Santos
The effect of obesity on uterine receptivity is mediated by endometrial extracellular vesicles that control human endometrial stromal cell decidualization and trophoblast invasion. Journal of extracellular biology 2 (7) (2023)
Cécile Courdier, John Boudjarane, Valérie Malan, Christine Muti, Brian Sperelakis-Beedham, Sylvie Odent, Sylvie Jaillard, Chloé Quelin, Cédric Le Caignec, Olivier Patat, Charlotte Dubucs, Sophie Julia, Caroline Schluth-Bolard, Carole Goumy, Sylvia Redon, Jean-Baptiste Gaillard, Minh Tuan Huynh, Céline Dupont, Anne-Claude Tabet, Guillaume Cogan, François Vialard, Rodolphe Dard, Guillaume Jedraszak, Florence Jobic, Mathilde Lefebvre, Geneviève Quenum, Saori Inai, Mélanie Rama, Fanny Sauvestre, Frédéric Coatleven, Julie Thomas, Caroline Rooryck
Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome). Prenatal diagnosis (2023)
Cécile Courdier, John Boudjarane, Valérie Malan, Christine Muti, Brian Sperelakis-Beedham, Sylvie Odent, Sylvie Jaillard, Chloé Quelin, Cédric Le Caignec, Olivier Patat, Charlotte Dubucs, Sophie Julia, Caroline Schluth-Bolard, Carole Goumy, Sylvia Redon, Jean-Baptiste Gaillard, Minh Tuan Huynh, Céline Dupont, Anne-Claude Tabet, Guillaume Cogan, François Vialard, Rodolphe Dard, Guillaume Jedraszak, Florence Jobic, Mathilde Lefebvre, Geneviève Quenum, Saori Inai, Mélanie Rama, Fanny Sauvestre, Frédéric Coatleven, Julie Thomas, Caroline Rooryck
Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome). Prenatal diagnosis (2023)
Esther Dos Santos, Marta Hita Hernández, Valérie Sérazin, François Vialard, Marie-Noëlle Dieudonné
Human Placental Adaptive Changes in Response to Maternal Obesity: Sex Specificities. International journal of molecular sciences 24 (11) (2023)
N Claudel, M Barrois, Alexandre Joseph Vivanti, J Rosenblatt, Laurent J Salomon, Jean-Marie Jouannic, Olivier Picone, Lionel Carbillon, François Vialard, E Launay, V Tsatsaris, E Curis, L Allach El Khattabi, null null
Non-invasive cell-free DNA prenatal screening for trisomy 21 as part of primary screening strategy in twin pregnancies. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology (2023)
Laurent Galio, Laetitia Bernet, Yoann Rodriguez, Camille Fourcault, Marie-Noëlle Dieudonné, Hélène Pinatel, Céline Henry, Valérie Serazin, Khadija Fathallah, Anissa Gagneux, Zuzana Krupova, François Vialard, Esther Dos Santos
The effect of obesity on uterine receptivity is mediated by endometrial extracellular vesicles that control human endometrial stromal cell decidualization and trophoblast invasion. Journal of extracellular biology 2 (7) (2023)
Bérangère Coutanceau, Esther Dos Santos, Nelly Swierkowski Blanchard, Anne Sanchez Louboutin, Florence Boitrelle, François Margueritte, François Vialard, Valérie Serazin, Khadija Fathallah
Should the Treatment of Patients with Repeated Embryo Implantation Failure Be Adapted as a Function of the Endometrial Cytokine Profile? A Single-Center Experience. Biomedicines 11 (3) (2023)
Malek Bouassida, Matthieu Egloff, Jonathan Levy, Nicolas Chatron, Laura Bernardini, Gwenaël L E Guyader, Anne-Claude Tabet, Caroline Schluth-Bolard, Francesco Brancati, Maria Grazia Giuffrida, Rodolphe Dard, Juliette Clorennec, Juliette Coursimault, François Vialard, Bérénice Hervé
2p25.3 microduplications involving MYT1L: further phenotypic characterization through an assessment of 16 new cases and a literature review. European journal of human genetics : EJHG (2023)
Arthur Clement, Théo Dominot, Jeremy Chammas, Martine Montagnon, Marie Delcroix, Jérôme Pfeffer, Jean Michel Dupont, Aziza Lebbar, Patrice Clement, François Vialard
A Rare Chromosome Rearrangement Leading to de la Chapelle Syndrome with a Mosaic 45,X Cell Line: (46,X,psu dic(X;Y)(p22.13;q11.221)/45,X/45,psu dic(X;Y)(p22.13;q11.221). Genes 14 (1) (2022)
Claire Le Gal, Marie Carbonnel, Vincent Balaya, Christophe Richard, Valerie Gelin, Laurent Galio, Olivier Sandra, Barbara Hersant, Romain Bosc, Johanna Charton, Pascale Chavatte-Palmer, François Vialard, Raphael Coscas, Jean-Marc Ayoubi
Analysis of Predictive Factors for Successful Vascular Anastomoses in a Sheep Uterine Transplantation Model. Journal of clinical medicine 11 (18) (2022)
Jihenne Ben Aissa-Haj, Hugo Pinheiro, François Cornelis, Molka Sebai, Didier Meseure, Adrien Briaux, Philippe Berteaux, Cedric Lefol, Gaëtan Des Guetz, Martine Trassard, Denise Stevens, François Vialard, Ivan Bieche, Catherine Noguès, Roseline Tang, Carla Oliveira, Dominique Stoppat-Lyonnet, Rosette Lidereau, Etienne Rouleau
The Identification of Large Rearrangements Involving Intron 2 of the CDH1 Gene in BRCA1/2 Negative and Breast Cancer Susceptibility. Genes 13 (12) (2022)
Jihenne Ben Aissa-Haj, Hugo Pinheiro, François Cornelis, Molka Sebai, Didier Meseure, Adrien Briaux, Philippe Berteaux, Cedric Lefol, Gaëtan Des Guetz, Martine Trassard, Denise Stevens, François Vialard, Ivan Bieche, Catherine Noguès, Roseline Tang, Carla Oliveira, Dominique Stoppat-Lyonnet, Rosette Lidereau, Etienne Rouleau
The Identification of Large Rearrangements Involving Intron 2 of the CDH1 Gene in BRCA1/2 Negative and Breast Cancer Susceptibility. Genes 13 (12) (2022)
Céline Capron, Louis Januel, Gaëlle Vieville, Sylvie Jaillard, Paul Kuentz, Gaëlle Salaun, Gwenaël Nadeau, Patrice Clement, Marie Pierre Brechard, Bérénice Herve, Jean Michel Dupont, Nicolas Gruchy, Pascal Chambon, Fatma Abdelhedi, Eric Dahlen, Philippe Vago, Radu Harbuz, Ingrid Plotton, Charles Coutton, Marc-Antoine Belaud-Rotureau, Caroline Schluth-Bolard, François Vialard
Evidence for high breakpoint variability in 46, XX, SRY-positive testicular disorder and frequent ARSE deletion that may be associated with short stature. Andrology 10 (8) (2022)
F Ghieh, A L Barbotin, N Swierkowski-Blanchard, C Leroy, J Fortemps, C Gerault, C Hue, H Mambu Mambueni, Sylvie Jaillard, M Albert, M Bailly, V Izard, D Molina-Gomes, F Marcelli, J Prasivoravong, V Serazin, M N Dieudonne, M Delcroix, Henri-Jean Garchon, A Louboutin, Béatrice Mandon-Pépin, Sophie Ferlicot, François Vialard
Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes. Human reproduction (Oxford, England) 37 (6) (2022)
Loren Méar, Emmanuelle Com, Khadija Fathallah, Laetitia Guillot, Régis Lavigne, Blandine Guével, Arnaud Fauconnier, François Vialard, Charles Pineau
The Eutopic Endometrium Proteome in Endometriosis Reveals Candidate Markers and Molecular Mechanisms of Physiopathology. Diagnostics (Basel, Switzerland) 12 (2) (2022)
Jihenne Ben Aissa-Haj, Hugo Pinheiro, François Cornelis, Molka Sebai, Didier Meseure, Adrien Briaux, Philippe Berteaux, Cedric Lefol, Gaëtan Des Guetz, Martine Trassard, Denise Stevens, François Vialard, Ivan Bieche, Catherine Noguès, Roseline Tang, Carla Oliveira, Dominique Stoppat-Lyonnet, Rosette Lidereau, Etienne Rouleau
The Identification of Large Rearrangements Involving Intron 2 of the CDH1 Gene in BRCA1/2 Negative and Breast Cancer Susceptibility. Genes 13 (12) (2022)
Arthur Clement, Théo Dominot, Jeremy Chammas, Martine Montagnon, Marie Delcroix, Jérôme Pfeffer, Jean Michel Dupont, Aziza Lebbar, Patrice Clement, François Vialard
A Rare Chromosome Rearrangement Leading to de la Chapelle Syndrome with a Mosaic 45,X Cell Line: (46,X,psu dic(X;Y)(p22.13;q11.221)/45,X/45,psu dic(X;Y)(p22.13;q11.221). Genes 14 (1) (2022)
Jihenne Ben Aissa-Haj, Hugo Pinheiro, François Cornelis, Molka Sebai, Didier Meseure, Adrien Briaux, Philippe Berteaux, Cedric Lefol, Gaëtan Des Guetz, Martine Trassard, Denise Stevens, François Vialard, Ivan Bieche, Catherine Noguès, Roseline Tang, Carla Oliveira, Dominique Stoppat-Lyonnet, Rosette Lidereau, Etienne Rouleau
The Identification of Large Rearrangements Involving Intron 2 of the CDH1 Gene in BRCA1/2 Negative and Breast Cancer Susceptibility. Genes 13 (12) (2022)
Arthur Clement, Théo Dominot, Jeremy Chammas, Martine Montagnon, Marie Delcroix, Jérôme Pfeffer, Jean Michel Dupont, Aziza Lebbar, Patrice Clement, François Vialard
A Rare Chromosome Rearrangement Leading to de la Chapelle Syndrome with a Mosaic 45,X Cell Line: (46,X,psu dic(X;Y)(p22.13;q11.221)/45,X/45,psu dic(X;Y)(p22.13;q11.221). Genes 14 (1) (2022)
Arthur Clement, Théo Dominot, Jeremy Chammas, Martine Montagnon, Marie Delcroix, Jérôme Pfeffer, Jean Michel Dupont, Aziza Lebbar, Patrice Clement, François Vialard
A Rare Chromosome Rearrangement Leading to de la Chapelle Syndrome with a Mosaic 45,X Cell Line: (46,X,psu dic(X;Y)(p22.13;q11.221)/45,X/45,psu dic(X;Y)(p22.13;q11.221). Genes 14 (1) (2022)
Farah Ghieh, Vincent Izard, Marine Poulain, Johanne Fortemps, Nadia Kazdar, Béatrice Mandon-Pepin, Sophie Ferlicot, Jean Marc Ayoubi, François Vialard
Cryptic splice site poisoning and meiotic arrest caused by a homozygous frameshift mutation in RBMXL2: A case report. Andrologia 54 (11) (2022)
Marion Lesieur-Sebellin, Marianne Till, Philippe Khau Van Kien, Bérénice Herve, Nicolas Bourgon, Céline Dupont, Anne-Claude Tabet, Mathilde Barrois, Aurélie Coussement, Laurence Loeuillet, Eve Mousty, Vuthy Ea, Amal El Assal, Laura Mary, Sylvie Jaillard, Claire Beneteau, Claudine Le Vaillant, Charles Coutton, Françoise Devillard, Carole Goumy, Amélie Delabaere, Sylvia Redon, Yves Laurent, Audrey Lamouroux, Jérôme Massardier, Catherine Turleau, Damien Sanlaville, Vincent Cantagrel, Pascale Sonigo, François Vialard, Laurent J Salomon, Valérie Malan
Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series. Prenatal diagnosis (2021)
Rodolphe Dard, Manon Moreau, Estelle Parizot, Farah Ghieh, Leslie Brehier, Nadim Kassis, Valérie Serazin, Antonin Lamaziere, Chrystèle Racine, Nathalie di Clemente, François Vialard, Nathalie Janel
DYRK1A Overexpression in Mice Downregulates the Gonadotropic Axis and Disturbs Early Stages of Spermatogenesis. Genes 12 (11) (2021)
Manon Moreau, Soukaina Benhaddou, Rodolphe Dard, Stefania Tolu, Rim Hamzé, François Vialard, Jamileh Movassat, Nathalie Janel
Metabolic Diseases and Down Syndrome: How Are They Linked Together? Biomedicines 9 (2) (2021)
Hela Bellil, Farah Ghieh, Emeline Hermel, Béatrice Mandon-Pepin, François Vialard
Human testis-expressed (TEX) genes: a review focused on spermatogenesis and male fertility. Basic and clinical andrology 31 (1) (2021)
Farah Ghieh, Anne-Laure Barbotin, Clara Leroy, François Marcelli, Nelly Swierkowsky-Blanchard, Valérie Serazin, Béatrice Mandon-Pepin, François Vialard
Will whole-genome sequencing become the first-line genetic analysis for male infertility in the near future? Basic and clinical andrology 31 (1) (2021)
Hela Bellil, Bérenice Herve, Elodie Herzog, Jean-Marc Ayoubi, François Vialard, Marine Poulain
A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report. Journal of assisted reproduction and genetics 37 (3) (2020)
Rodolphe Dard, Nathalie Janel, François Vialard
COVID-19 and Down's syndrome: are we heading for a disaster? European journal of human genetics : EJHG 28 (11) (2020)
Estelle Parizot, Rodolphe Dard, Nathalie Janel, François Vialard
Down syndrome and infertility: what support should we provide? Journal of assisted reproduction and genetics 36 (6) (2019)

François Vialard.css-eqlu8i{font-size:small;padding-left:4px;} (F Vialard)

Publication Activity (10 Years)

Top Topics

Top Venues

François Vialard (F Vialard)