Works by Amiri-Yekta, Amir

Results: 26
    1
    2

    Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse.

    Published in:
    eLife, 2024, p. 1, doi. 10.7554/eLife.86845
    By:
    • Muroňová, Jana;
    • Kherraf, Zine Eddine;
    • Giordani, Elsa;
    • Lambert, Emeline;
    • Eckert, Simon;
    • Cazin, Caroline;
    • Amiri-Yekta, Amir;
    • Court, Magali;
    • Chevalier, Geneviève;
    • Martinez, Guillaume;
    • Neirijnck, Yasmine;
    • Kühne, Francoise;
    • Wehrli, Lydia;
    • Klena, Nikolai;
    • Hamel, Virginie;
    • De Macedo, Lisa;
    • Escoffier, Jessica;
    • Guichard, Paul;
    • Coutton, Charles;
    • Ben Mustapha, Selima Fourati
    Publication type:
    Article
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    4

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

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02792-7
    By:
    • Coutton, Charles;
    • Vargas, Alexandra S.;
    • Amiri-Yekta, Amir;
    • Kherraf, Zine-Eddine;
    • Ben Mustapha, Selima Fourati;
    • Le Tanno, Pauline;
    • Wambergue-Legrand, Clémentine;
    • Karaouzène, Thomas;
    • Martinez, Guillaume;
    • Crouzy, Serge;
    • Daneshipour, Abbas;
    • Hosseini, Seyedeh Hanieh;
    • Mitchell, Valérie;
    • Halouani, Lazhar;
    • Marrakchi, Ouafi;
    • Makni, Mounir;
    • Latrous, Habib;
    • Kharouf, Mahmoud;
    • Deleuze, Jean-François;
    • Boland, Anne
    Publication type:
    Article
    5

    PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice.

    Published in:
    EMBO Molecular Medicine, 2018, v. 10, n. 5, p. 1, doi. 10.15252/emmm.201708515
    By:
    • Christou‐Kent, Marie;
    • Kherraf, Zine‐Eddine;
    • Amiri‐Yekta, Amir;
    • Le Blévec, Emilie;
    • Karaouzène, Thomas;
    • Conne, Béatrice;
    • Escoffier, Jessica;
    • Assou, Said;
    • Guttin, Audrey;
    • Lambert, Emeline;
    • Martinez, Guillaume;
    • Boguenet, Magalie;
    • Fourati Ben Mustapha, Selima;
    • Cedrin Durnerin, Isabelle;
    • Halouani, Lazhar;
    • Marrakchi, Ouafi;
    • Makni, Mounir;
    • Latrous, Habib;
    • Kharouf, Mahmoud;
    • Coutton, Charles
    Publication type:
    Article
    6

    SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes.

    Published in:
    EMBO Molecular Medicine, 2017, v. 9, n. 8, p. 1132, doi. 10.15252/emmm.201607461
    By:
    • Kherraf, Zine ‐ Eddine;
    • Christou ‐ Kent, Marie;
    • Karaouzene, Thomas;
    • Amiri ‐ Yekta, Amir;
    • Martinez, Guillaume;
    • Vargas, Alexandra S;
    • Lambert, Emeline;
    • Borel, Christelle;
    • Dorphin, Béatrice;
    • Aknin ‐ Seifer, Isabelle;
    • Mitchell, Michael J;
    • Metzler ‐ Guillemain, Catherine;
    • Escoffier, Jessica;
    • Nef, Serge;
    • Grepillat, Mariane;
    • Thierry ‐ Mieg, Nicolas;
    • Satre, Véronique;
    • Bailly, Marc;
    • Boitrelle, Florence;
    • Pernet ‐ Gallay, Karin
    Publication type:
    Article
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    8

    Production of transgenic goats expressing human coagulation factor IX in the mammary glands after nuclear transfer using transfected fetal fibroblast cells.

    Published in:
    Transgenic Research, 2013, v. 22, n. 1, p. 131, doi. 10.1007/s11248-012-9634-y
    By:
    • Amiri Yekta, Amir;
    • Dalman, Azam;
    • Eftekhari-Yazdi, Poopak;
    • Sanati, Mohammad;
    • Shahverdi, Abdol;
    • Fakheri, Rahman;
    • Vazirinasab, Hamed;
    • Daneshzadeh, Mohammad;
    • Vojgani, Mahdi;
    • Zomorodipour, Alireza;
    • Fatemi, Nayeralsadat;
    • Vahabi, Zeinab;
    • Mirshahvaladi, Shahab;
    • Ataei, Fariba;
    • Bahraminejad, Elmira;
    • Masoudi, Najmehsadat;
    • Rezazadeh Valojerdi, Mojtaba;
    • Gourabi, Hamid
    Publication type:
    Article
    9

    Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse.

    Published in:
    Human Genetics, 2021, v. 140, n. 9, p. 1367, doi. 10.1007/s00439-021-02313-z
    By:
    • Shen, Qunshan;
    • Martinez, Guillaume;
    • Liu, Hongbin;
    • Beurois, Julie;
    • Wu, Huan;
    • Amiri-Yekta, Amir;
    • Liang, Dan;
    • Kherraf, Zine-Eddine;
    • Bidart, Marie;
    • Cazin, Caroline;
    • Celse, Tristan;
    • Satre, Véronique;
    • Thierry-Mieg, Nicolas;
    • Whitfield, Marjorie;
    • Touré, Aminata;
    • Song, Bing;
    • Lv, Mingrong;
    • Li, Kuokuo;
    • Liu, Chunyu;
    • Tao, Fangbiao
    Publication type:
    Article
    10

    Correction to: 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.

    Published in:
    2021
    By:
    • Lorès, Patrick;
    • Kherraf, Zine-Eddine;
    • Amiri-Yekta, Amir;
    • Whitfield, Marjorie;
    • Daneshipour, Abbas;
    • Stouvenel, Laurence;
    • Cazin, Caroline;
    • Cavarocchi, Emma;
    • Coutton, Charles;
    • Llabador, Marie-Astrid;
    • Arnoult, Christophe;
    • Thierry-Mieg, Nicolas;
    • Ferreux, Lucile;
    • Patrat, Catherine;
    • Hosseini, Seyedeh-Hanieh;
    • Mustapha, Selima Fourati Ben;
    • Zouari, Raoudha;
    • Dulioust, Emmanuel;
    • Ray, Pierre F.;
    • Touré, Aminata
    Publication type:
    Correction Notice
    11

    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.

    Published in:
    Human Genetics, 2021, v. 140, n. 7, p. 1031, doi. 10.1007/s00439-021-02270-7
    By:
    • Lorès, Patrick;
    • Kherraf, Zine-Eddine;
    • Amiri-Yekta, Amir;
    • Whitfield, Marjorie;
    • Daneshipour, Abbas;
    • Stouvenel, Laurence;
    • Cazin, Caroline;
    • Cavarocchi, Emma;
    • Coutton, Charles;
    • Llabador, Marie-Astrid;
    • Arnoult, Christophe;
    • Thierry-Mieg, Nicolas;
    • Ferreux, Lucile;
    • Patrat, Catherine;
    • Hosseini, Seyedeh-Hanieh;
    • Mustapha, Selima Fourati Ben;
    • Zouari, Raoudha;
    • Dulioust, Emmanuel;
    • Ray, Pierre F.;
    • Touré, Aminata
    Publication type:
    Article
    12
    13

    New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella.

    Published in:
    International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 2559, doi. 10.3390/ijms24032559
    By:
    • Martinez, Guillaume;
    • Barbotin, Anne-Laure;
    • Cazin, Caroline;
    • Wehbe, Zeina;
    • Boursier, Angèle;
    • Amiri-Yekta, Amir;
    • Daneshipour, Abbas;
    • Hosseini, Seyedeh-Hanieh;
    • Rives, Nathalie;
    • Feraille, Aurélie;
    • Thierry-Mieg, Nicolas;
    • Bidart, Marie;
    • Satre, Véronique;
    • Arnoult, Christophe;
    • Ray, Pierre F.;
    • Kherraf, Zine-Eddine;
    • Coutton, Charles
    Publication type:
    Article
    14

    Whole genome sequencing identifies a homozygous splicing variant in TDRKH segregating with non‐obstructive azoospermia in an Iranian family.

    Published in:
    Clinical Genetics, 2024, v. 106, n. 5, p. 625, doi. 10.1111/cge.14584
    By:
    • Amiri‐Yekta, Amir;
    • Sen, Sharanya;
    • Hazane‐Puch, Florence;
    • Tebbakh, Célia;
    • Roux‐Buisson, Nathalie;
    • Cazin, Caroline;
    • Thierry‐Mieg, Nicolas;
    • Bouras, Ahmed;
    • Mohammad Ali, Sadighi‐Gilani;
    • Hosseini, Seyedeh‐Hanieh;
    • Goodarzian, Maedeh;
    • Gourabi, Hamid;
    • Ray, Pierre F.;
    • Kherraf, Zine‐Eddine
    Publication type:
    Article
    15
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    Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations.

    Published in:
    Clinical Genetics, 2019, v. 96, n. 5, p. 394, doi. 10.1111/cge.13604
    By:
    • Kherraf, Zine‐Eddine;
    • Cazin, Caroline;
    • Coutton, Charles;
    • Amiri‐Yekta, Amir;
    • Martinez, Guillaume;
    • Boguenet, Magalie;
    • Fourati Ben Mustapha, Selima;
    • Kharouf, Mahmoud;
    • Gourabi, Hamid;
    • Hosseini, Seyedeh Hanieh;
    • Daneshipour, Abbas;
    • Touré, Aminata;
    • Thierry‐Mieg, Nicolas;
    • Zouari, Raoudha;
    • Arnoult, Christophe;
    • Ray, Pierre F.
    Publication type:
    Article
    18
    19

    Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella.

    Published in:
    2018
    By:
    • Martinez, Guillaume;
    • Kherraf, Zine-Eddine;
    • Zouari, Raoudha;
    • Mustapha, Selima Fourati Ben;
    • Saut, Antoine;
    • Pernet-Gallay, Karin;
    • Bertrand, Anne;
    • Bidart, Marie;
    • Hograindleur, Jean Pascal;
    • Amiri-Yekta, Amir;
    • Fourati Ben Mustapha, Selima;
    • Kharouf, Mahmoud;
    • Karaouzène, Thomas;
    • Thierry-Mieg, Nicolas;
    • Dacheux-Deschamps, Denis;
    • Satre, Véronique;
    • Bonhivers, Mélanie;
    • Touré, Aminata;
    • Arnoult, Christophe;
    • Ray, Pierre F
    Publication type:
    journal article
    20

    Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.

    Published in:
    2016
    By:
    • Amiri-Yekta, Amir;
    • Coutton, Charles;
    • Kherraf, Zine-Eddine;
    • Karaouzène, Thomas;
    • Le Tanno, Pauline;
    • Sanati, Mohammad Hossein;
    • Sabbaghian, Marjan;
    • Almadani, Navid;
    • Gilani, Mohammad Ali Sadighi;
    • Hosseini, Seyedeh Hanieh;
    • Bahrami, Salahadin;
    • Daneshipour, Abbas;
    • Bini, Maurizio;
    • Arnoult, Christophe;
    • Colombo, Roberto;
    • Gourabi, Hamid;
    • Ray, Pierre F.;
    • Sadighi Gilani, Mohammad Ali
    Publication type:
    journal article
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