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Author/Creator Zouari, Raoudha

1. A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females. Issue 1 (1st June 2022)

Authors:
Loeuillet, Corinne; Dhellemmes, Magali; Cazin, Caroline; Kherraf, Zine‐Eddine; Fourati Ben Mustapha, Selima; Zouari, Raoudha; Thierry‐Mieg, Nicolas; Arnoult, Christophe; Ray, Pierre F.
Journal:
Clinical genetics
Issue:
Volume 102:Issue 1(2022)
Page Start:
22
Record Type:
Journal Article
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2. Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility. Issue 10 (11th March 2020)

Authors:
Martinez, Guillaume; Beurois, Julie; Dacheux, Denis; Cazin, Caroline; Bidart, Marie; Kherraf, Zine-Eddine; Robinson, Derrick R; Satre, Véronique; Le Gac, Gerald; Ka, Chandran; Gourlaouen, Isabelle; Fichou, Yann; Petre, Graciane; Dulioust, Emmanuel; Zouari, Raoudha; Thierry-Mieg, Nicolas; Touré, A...
Journal:
Journal of medical genetics
Issue:
Volume 57:Issue 10(2020)
Page Start:
708
Record Type:
Journal Article
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3. PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice. Issue 5 (16th April 2018)

Authors:
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, Lazh...
Journal:
EMBO molecular medicine
Issue:
Volume 10:Issue 5(2018)
Page Start:
n/a
Record Type:
Journal Article
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4. Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations. Issue 5 (17th July 2019)

Authors:
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, Christ...
Journal:
Clinical genetics
Issue:
Volume 96:Issue 5(2019)
Page Start:
394
Record Type:
Journal Article
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5. Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella. Issue 10 (13th August 2018)

Authors:
Martinez, Guillaume; Kherraf, Zine-Eddine; Zouari, Raoudha; Fourati Ben Mustapha, Selima; Saut, Antoine; Pernet-Gallay, Karin; Bertrand, Anne; Bidart, Marie; Hograindleur, Jean Pascal; Amiri-Yekta, Amir; Kharouf, Mahmoud; Karaouzène, Thomas; Thierry-Mieg, Nicolas; Dacheux-Deschamps, Denis; Satre,...
Journal:
Human reproduction
Issue:
Volume 33:Issue 10(2018)
Page Start:
1973
Record Type:
Journal Article
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