Aminata Toure (Aminata Touré)

ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 9

Top Venues

International journal of molecular sciences

Clinical genetics

Science (New York, N.Y.)

Human reproduction (Oxford, England)

Intitut Cochin. INSERM U1016, CNRS UMR8104, Université de Paris

Université Paris Descartes (PHD)

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

Affiliation History

Intitut Cochin. INSERM U1016, CNRS UMR8104, Université de Paris

France

Directrice de Recherche, DR2 :: Section 22

MRC, National Institute for Medical Research

United Kingdom

Post-Doctoral fellow (INSERM; Marie-Curie) :: Developmental Genetics

Education History

Université Paris Descartes

France

PHD

Publications

Denis Dacheux, Guillaume Martinez, Christine E Broster Reix, Julie Beurois, Patrick Lores, Magamba Tounkara, Jean-William Dupuy, Derrick Roy Robinson, Corinne Loeuillet, Emeline Lambert, Zeina Wehbe, Jessica Escoffier, Amir Amiri-Yekta, Abbas Daneshipour, Seyedeh-Hanieh Hosseini, Raoudha Zouari, Selima Fourati Ben Mustapha, Lazhar Halouani, Xiaohui Jiang, Ying Shen, Chunyu Liu, Nicolas Thierry-Mieg, Amandine Septier, Marie Bidart, Véronique Satre, Caroline Cazin, Zine Eddine Kherraf, Christophe Arnoult, Pierre F Ray, Aminata Toure, Mélanie Bonhivers, Charles Coutton
Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function. eLife 12 (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)
Emma Cavarocchi, Marjorie Whitfield, Fabrice Saez, Aminata Toure
Sperm Ion Transporters and Channels in Human Asthenozoospermia: Genetic Etiology, Lessons from Animal Models, and Clinical Perspectives. International journal of molecular sciences 23 (7) (2022)
Sudarshan Gadadhar, Gonzalo Alvarez Viar, Jan Niklas Hansen, An Gong, Aleksandr Kostarev, Côme Ialy-Radio, Sophie Leboucher, Marjorie Whitfield, Ahmed Ziyyat, Aminata Toure, Luis Alvarez, Gaia Pigino, Carsten Janke
Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility. Science (New York, N.Y.) 371 (6525) (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)
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)
Patrick Lorès, Zine-Eddine Kherraf, Amir Amiri-Yekta, Marjorie Whitfield, Abbas Daneshipour, Laurence Stouvenel, Caroline Cazin, Emma Cavarocchi, Charles Coutton, Marie-Astrid Llabador, Christophe Arnoult, Nicolas Thierry-Mieg, Lucile Ferreux, Catherine Patrat, Seyedeh-Hanieh Hosseini, Selima Fourati Ben Mustapha, Raoudha Zouari, Emmanuel Dulioust, Pierre F Ray, Aminata Toure
A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome. Human genetics 140 (7) (2021)
Elma El Khouri, Marjorie Whitfield, Laurence Stouvenel, Archana Kini, Brigitte Riederer, Patrick Lores, Dorothee Roemermann, Gabriella di Stefano, Joël R Drevet, Fabrice Saez, Ursula Seidler, Aminata Toure
Slc26a3 deficiency is associated with epididymis dysplasia and impaired sperm fertilization potential in the mouse. Molecular reproduction and development 85 (8-9) (2018)

Aminata Toure.css-eqlu8i{font-size:small;padding-left:4px;} (Aminata Touré)

Publication Activity (10 Years)

Top Topics

Top Venues

Aminata Toure (Aminata Touré)