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authFullName_s : Emmanuel Dulioust

Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse

Frederick Dong , Amir Amiri-Yekta , Guillaume Martinez , Antoine Saut , Julie Tek et al.
American Journal of Human Genetics, 2018, 102 (4), pp.636 - 648. ⟨10.1016/j.ajhg.2018.03.007⟩
Journal articles hal-01877985v1

Mutations in DNAJB13 , Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility

Elma El Khouri , Lucie Thomas , Ludovic Jeanson , Emilie Bequignon , Benoit Vallette et al.
American Journal of Human Genetics, 2016, 99 (2), pp.489-500. ⟨10.1016/j.ajhg.2016.06.022⟩
Journal articles inserm-03875562v1

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility

Chunyu Liu , Haruhiko Miyata , Yang Gao , Yanwei Sha , Shuyan Tang et al.
American Journal of Human Genetics, 2020, 107 (2), pp.330-341. ⟨10.1016/j.ajhg.2020.06.004⟩
Journal articles hal-03004971v1
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Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility

Guillaume Martinez , Julie Beurois , Denis Dacheux , Caroline Cazin , Marie Bidart et al.
Journal of Medical Genetics, 2020, 57 (10), pp.708-716. ⟨10.1136/jmedgenet-2019-106775⟩
Journal articles hal-03004959v1

Zika virus and reproduction: facts, questions and current management

Sylvie Epelboin , Emmanuel Dulioust , Loïc Epelboin , Alexandra Benachi , Françoise Merlet et al.
Human Reproduction Update, 2017, 23 (6), pp.629 - 645. ⟨10.1093/humupd/dmx024⟩
Journal articles hal-01844532v1

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in $Trypanosoma$ and human.

Charles Coutton , Alexandra S. Vargas , Amir Amiri-Yekta , Zine-Eddine Kherraf , Selima Fourati Ben Mustapha et al.
Nature Communications, 2018, 9, pp.686. ⟨10.1038/s41467-017-02792-7⟩
Journal articles hal-01724640v1
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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

Patrick Lorès , Zine-Eddine Kherraf , Amir Amiri-Yekta , Marjorie Whitfield , Abbas Daneshipour et al.
Human Genetics, 2021, 140 (7), pp.1031-1043. ⟨10.1007/s00439-021-02270-7⟩
Journal articles hal-03369854v1
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Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility

Patrick Lorès , Denis Dacheux , Zine-Eddine Kherraf , Jean-Fabrice Nsota Mbango , Charles Coutton et al.
American Journal of Human Genetics, 2019, ⟨10.1016/j.ajhg.2019.10.007⟩
Journal articles hal-02370384v1

Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.

Thassadite Dirami , Baptiste Rode , Mathilde Jollivet , Nathalie da Silva , Denise Escalier et al.
American Journal of Human Genetics, 2013, 92 (5), pp.760-6. ⟨10.1016/j.ajhg.2013.03.016⟩
Journal articles hal-00990664v1
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The sodium/proton exchanger SLC9C1 ( sNHE ) is essential for human sperm motility and fertility

Emma Cavarocchi , Marjorie Whitfield , Ahmed Chargui , Laurence Stouvenel , Patrick Lorès et al.
Clinical Genetics, 2021, 99 (5), pp.684-693. ⟨10.1111/cge.13927⟩
Journal articles hal-03369825v1
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Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia

Patrick Lorès , Charles Coutton , Elma El Khouri , Laurence Stouvenel , Maelle Givelet et al.
Human Molecular Genetics, 2018, 27 (7), pp.1196-1211. ⟨10.1093/hmg/ddy034⟩
Journal articles hal-02346745v1
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Assessment of the frequency of sperm annulus defects in a large cohort of patients presenting asthenozoospermia

Thassadite Dirami , Baptiste Rode , Jean-Philippe Wolf , Gérard Gacon , Emmanuel Dulioust et al.
Basic and clinical andrology, 2015, 25, pp.10 (eCollection 2015). ⟨10.1186/s12610-015-0026-z⟩
Journal articles inserm-01244340v1

Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum

Lucile Ferreux , Mathilde Bourdon , Ahmed Chargui , Alain Schmitt , Laurence Stouvenel et al.
Human Reproduction, 2021, 36 (11), pp.2848-2860. ⟨10.1093/humrep/deab200⟩
Journal articles hal-03873460v1