Pierre F Ray (Pierre Ray)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 20

Top Venues

Clinical genetics

EMBO molecular medicine

Journal of medical genetics

Scientific reports

University Grenoble Alpes and Centre Hospitalier Universitaire Grenoble Alpes

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

Affiliation History

University Grenoble Alpes and Centre Hospitalier Universitaire Grenoble Alpes Sep 01 2003

France

PU-PH :: Genetics of Infertility and Preimplantation Diagnosis unit

Publications

Zeina Wehbe, Anne-Laure Barbotin, Angèle Boursier, Caroline Cazin, Jean-Pascal Hograindleur, Marie Bidart, Emeline Fontaine, Pauline Plouvier, Florence Puch, Véronique Satre, Christophe Arnoult, Selima Fourati Ben Mustapha, Raoudha Zouari, Nicolas Thierry-Mieg, Pierre F Ray, Zine-Eddine Kherraf, Charles Coutton, Guillaume Martinez
Phenotypic continuum and poor intracytoplasmic sperm injection intracytoplasmic sperm injection prognosis in patients harboring HENMT1 variants. Andrology (2024)
Amir Amiri-Yekta, Sharanya Sen, Florence Hazane-Puch, Célia Tebbakh, Nathalie Roux-Buisson, Caroline Cazin, Nicolas Thierry-Mieg, Ahmed Bouras, Sadighi-Gilani Mohammad Ali, Seyedeh-Hanieh Hosseini, Maedeh Goodarzian, Hamid Gourabi, Pierre F Ray, Zine-Eddine Kherraf
Whole genome sequencing identifies a homozygous splicing variant in TDRKH segregating with non-obstructive azoospermia in an Iranian family. Clinical genetics (2024)
Zine-Eddine Kherraf, Anne-Laure Barbotin, Guillaume Martinez, Aurélien Mazet, Caroline Cazin, Charles Coutton, Christophe Arnoult, Nicolas Thierry-Mieg, Nathalie Rives, Aurélie Rives-Feraille, Pierre F Ray
A splice donor variant of GAS8 induces structural disorganization of the axoneme in sperm flagella and leads to nonsyndromic male infertility. Clinical genetics (2023)
Qing Sang, Pierre F Ray, Lei Wang
Understanding the genetics of human infertility. Science (New York, N.Y.) 380 (6641) (2023)
Fadwa Jreijiri, Emma Cavarocchi, Amir Amiri-Yekta, Caroline Cazin, Seyedeh-Hanieh Hosseini, Elma El Khouri, Catherine Patrat, Nicolas Thierry-Mieg, Pierre F Ray, Emmanuel Dulioust, Marjorie Whitfield, Aminata Toure
CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans. Clinical genetics (2023)
Corinne Loeuillet, Magali Dhellemmes, Caroline Cazin, Zine-Eddine Kherraf, Selima Fourati Ben Mustapha, Raoudha Zouari, Nicolas Thierry-Mieg, Christophe Arnoult, Pierre F Ray
A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females. Clinical genetics 102 (1) (2022)
Guillaume Martinez, Catherine Metzler-Guillemain, Caroline Cazin, Zine-Eddine Kherraf, Odile Paulmyer-Lacroix, Christophe Arnoult, Pierre F Ray, Charles Coutton
Expanding the sperm phenotype caused by mutations in SPATA20: A novel splicing mutation in an infertile patient with partial globozoospermia. Clinical genetics (2022)
Guillaume Martinez, Catherine Metzler-Guillemain, Caroline Cazin, Zine-Eddine Kherraf, Odile Paulmyer-Lacroix, Christophe Arnoult, Pierre F Ray, Charles Coutton
Expanding the sperm phenotype caused by mutations in SPATA20: a novel splicing mutation in an infertile patient with partial globozoospermia. Clinical genetics (2022)
Siyu Liu, Jintao Zhang, Zine Eddine Kherraf, Shuya Sun, Xin Zhang, Caroline Cazin, Charles Coutton, Raoudha Zouari, Shuqin Zhao, Fan Hu, Selima Fourati Ben Mustapha, Christophe Arnoult, Pierre F Ray, Mingxi Liu
CFAP61 is required for sperm flagellum formation and male fertility in human and mouse. Development (Cambridge, England) 148 (23) (2021)
Lucile Ferreux, Mathilde Bourdon, Ahmed Chargui, Alain Schmitt, Laurence Stouvenel, Patrick Lorès, Pierre F Ray, Johanna Lousqui, Khaled Pocate-Cheriet, Pietro Santulli, Emmanuel Dulioust, Aminata Toure, Catherine Patrat
Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum. Human reproduction (Oxford, England) 36 (11) (2021)
Emma Cavarocchi, Marjorie Whitfield, Ahmed Chargui, Laurence Stouvenel, Patrick Lorès, Charles Coutton, Christophe Arnoult, Pietro Santulli, Catherine Patrat, Nicolas Thierry-Mieg, Pierre F Ray, Emmanuel Dulioust, Aminata Toure
The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility. Clinical genetics 99 (5) (2021)
Jiangshan Cong, Xiong Wang, Amir Amiri-Yekta, Lingbo Wang, Zine-Eddine Kherraf, Chunyu Liu, Caroline Cazin, Shuyan Tang, Seyedeh Hanieh Hosseini, Shixiong Tian, Abbas Daneshipour, Jiaxiong Wang, Yiling Zhou, Yuyan Zeng, Shenmin Yang, Xiao-Jin He, Jinsong Li, Yunxia Cao, Li Jin, Pierre F Ray, Feng Zhang
Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice. Journal of medical genetics (2021)
Caroline Cazin, Yasmine Boumerdassi, Guillaume Martinez, Selima Fourati Ben Mustapha, Marjorie Whitfield, Charles Coutton, Nicolas Thierry-Mieg, Pierre Di Pizio, Nathalie Rives, Christophe Arnoult, Aminata Toure, Pierre F Ray, Raoudha Zouari, Christophe Sifer, Zine-Eddine Kherraf
Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa. International journal of molecular sciences 22 (4) (2021)
Nayeralsadat Fatemi, Najmeh Salehi, Laura Pignata, Pietro Palumbo, Maria Vittoria Cubellis, Fariba Ramazanali, Pierre F Ray, Maryam Varkiani, Fakhreddin Reyhani-Sabet, Alireza Biglari, Angela Sparago, Basilia Acurzio, Orazio Palumbo, Massimo Carella, Andrea Riccio, Mehdi Totonchi
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy. Journal of medical genetics 58 (11) (2020)
Tristan Celse, Caroline Cazin, Flore Mietton, Guillaume Martinez, Delphine Martinez, Nicolas Thierry-Mieg, Amandine Septier, Catherine Guillemain, Julie Beurois, Antoine Clergeau, Selima Fourati Ben Mustapha, Mahmoud Kharouf, Abdelali Zoghmar, Ahmed Chargui, Aline Papaxanthos, Béatrice Dorphin, Bernard Foliguet, Chema Triki, Christophe Sifer, Dominique Lauton, Gérard Tachdjian, Gilles Schuler, Hervé Lejeune, Jacques Puechberty, Julien Bessonnat, Laurent Pasquier, Lionel Mery, Marine Poulain, Myriam Chaabouni, Nathalie Sermondade, Rosalie Cabry, Sebti Benbouhadja, Ségolène Veau, Cynthia Frapsauce, Valérie Mitchell, Vincent Achard, Veronique Satre, Sylviane Hennebicq, Raoudha Zouari, Christophe Arnoult, Zine-Eddine Kherraf, Charles Coutton, Pierre F Ray
Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player. Human genetics 140 (1) (2020)
Zine-Eddine Kherraf, Caroline Cazin, Charles Coutton, Amir Amiri-Yekta, Guillaume Martinez, Magalie Boguenet, Selima Fourati Ben Mustapha, Mahmoud Kharouf, Hamid Gourabi, Seyedeh Hanieh Hosseini, Abbas Daneshipour, Aminata Touré, Nicolas Thierry-Mieg, Raoudha Zouari, Christophe Arnoult, Pierre F Ray
Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations. Clinical genetics 96 (5) (2019)
Marie Christou-Kent, Zine-Eddine Kherraf, Amir Amiri-Yekta, Emilie Le Blévec, Thomas Karaouzène, Béatrice Conne, Jessica Escoffier, Said Assou, Audrey Guttin, Emeline Lambert, Guillaume Martinez, Magalie Boguenet, Selima Fourati Ben Mustapha, Isabelle Cedrin Durnerin, Lazhar Halouani, Ouafi Marrakchi, Mounir Makni, Habib Latrous, Mahmoud Kharouf, Charles Coutton, Nicolas Thierry-Mieg, Serge Nef, Serge P Bottari, Raoudha Zouari, Jean Paul Issartel, Pierre F Ray, Christophe Arnoult
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice. EMBO molecular medicine 10 (5) (2019)
Charles Coutton, Alexandra S Vargas, Amir Amiri-Yekta, Zine-Eddine Kherraf, Selima Fourati Ben Mustapha, Pauline Le Tanno, Clémentine Wambergue-Legrand, Thomas Karaouzène, Guillaume Martinez, Serge Crouzy, Abbas Daneshipour, Seyedeh Hanieh Hosseini, Valérie Mitchell, Lazhar Halouani, Ouafi Marrakchi, Mounir Makni, Habib Latrous, Mahmoud Kharouf, Jean-François Deleuze, Anne Boland, Sylviane Hennebicq, Véronique Satre, Pierre-Simon Jouk, Nicolas Thierry-Mieg, Beatrice Conne, Denis Dacheux, Nicolas Landrein, Alain Schmitt, Laurence Stouvenel, Patrick Lorès, Elma El Khouri, Serge P Bottari, Julien Fauré, Jean-Philippe Wolf, Karin Pernet-Gallay, Jessica Escoffier, Hamid Gourabi, Derrick R Robinson, Serge Nef, Emmanuel Dulioust, Raoudha Zouari, Mélanie Bonhivers, Aminata Touré, Christophe Arnoult, Pierre F Ray
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human. Nature communications 9 (1) (2018)
Luiz G Guidi, Zoe G Holloway, Christophe Arnoult, Pierre F Ray, Anthony P Monaco, Zoltán Molnár, Antonio Velayos-Baeza
AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice. Scientific reports 8 (1) (2018)
Zine-Eddine Kherraf, Marie Christou-Kent, Thomas Karaouzene, Amir Amiri-Yekta, Guillaume Martinez, Alexandra S Vargas, Emeline Lambert, Christelle Borel, Béatrice Dorphin, Isabelle Aknin-Seifer, Michael J Mitchell, Catherine Metzler-Guillemain, Jessica Escoffier, Serge Nef, Mariane Grepillat, Nicolas Thierry-Mieg, Véronique Satre, Marc Bailly, Florence Boitrelle, Karin Pernet-Gallay, Sylviane Hennebicq, Julien Fauré, Serge P Bottari, Charles Coutton, Pierre F Ray, Christophe Arnoult
SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes. EMBO molecular medicine 9 (8) (2018)

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

Publication Activity (10 Years)

Top Topics

Top Venues

Pierre F Ray (Pierre Ray)