日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Phenotypic continuum and poor intracytoplasmic sperm injection intracytoplasmic sperm injection prognosis in patients harboring HENMT1 variants.

表型连续性及携带 HENMT1 变异患者的胞浆内单精子注射预后不良

Wehbe Zeina, Barbotin Anne-Laure, Boursier Angèle, Cazin Caroline, Hograindleur Jean-Pascal, Bidart Marie, Fontaine Emeline, Plouvier Pauline, Puch Florence, Satre Véronique, Arnoult Christophe, Mustapha Selima Fourati Ben, Zouari Raoudha, Thierry-Mieg Nicolas, Ray Pierre F, Kherraf Zine-Eddine, Coutton Charles, Martinez Guillaume

Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia

全外显子组测序可改善非梗阻性无精子症男性患者的诊断和治疗

Kherraf, Zine-Eddine; Cazin, Caroline; Bouker, Amine; Fourati Ben Mustapha, Selima; Hennebicq, Sylviane; Septier, Amandine; Coutton, Charles; Raymond, Laure; Nouchy, Marc; Thierry-Mieg, Nicolas; Zouari, Raoudha; Arnoult, Christophe; Ray, Pierre F

Oligogenic heterozygous inheritance of sperm abnormalities in mouse

小鼠精子异常的寡基因杂合遗传

Martinez, Guillaume; Coutton, Charles; Loeuillet, Corinne; Cazin, Caroline; Muroňová, Jana; Boguenet, Magalie; Lambert, Emeline; Dhellemmes, Magali; Chevalier, Geneviève; Hograindleur, Jean-Pascal; Vilpreux, Charline; Neirijnck, Yasmine; Kherraf, Zine-Eddine; Escoffier, Jessica; Nef, Serge; Ray, Pierre F; Arnoult, Christophe

From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the ZMYND15 gene

从无精子症到巨精子症,ZMYND15基因突变导致的表型连续谱

Kherraf, Zine-Eddine; Cazin, Caroline; Lestrade, Florence; Muronova, Jana; Coutton, Charles; Arnoult, Christophe; Thierry-Mieg, Nicolas; Ray, Pierre F

A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females

一种反复出现的ZP1变异是导致卵母细胞成熟缺陷和不孕女性卵母细胞退化的原因。

Loeuillet, Corinne; Dhellemmes, Magali; Cazin, Caroline; Kherraf, Zine-Eddine; Fourati Ben Mustapha, Selima; Zouari, Raoudha; Thierry-Mieg, Nicolas; Arnoult, Christophe; Ray, Pierre F

Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes C1orf185 and CCT6B

结合全外显子组测序和 CRISPR/Cas9 技术研究非梗阻性无精子症的病因:证实睾丸特异性基因 C1orf185 和 CCT6B 并非必需

Cazin, Caroline; Neirijnck, Yasmine; Loeuillet, Corinne; Wehrli, Lydia; Kühne, Françoise; Lordey, Isabelle; Mustapha, Selima Fourati Ben; Bouker, Amin; Zouari, Raoudha; Thierry-Mieg, Nicolas; Nef, Serge; Arnoult, Christophe; Ray, Pierre F; Kherraf, Zine-Eddine

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

双等位基因DNAH8变异导致精子鞭毛多种形态异常和原发性男性不育

Liu, Chunyu; Miyata, Haruhiko; Gao, Yang; Sha, Yanwei; Tang, Shuyan; Xu, Zoulan; Whitfield, Marjorie; Patrat, Catherine; Wu, Huan; Dulioust, Emmanuel; Tian, Shixiong; Shimada, Keisuke; Cong, Jiangshan; Noda, Taichi; Li, Hang; Morohoshi, Akane; Cazin, Caroline; Kherraf, Zine-Eddine; Arnoult, Christophe; Jin, Li; He, Xiaojin; Ray, Pierre F; Cao, Yunxia; Touré, Aminata; Zhang, Feng; Ikawa, Masahito

Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility

TTC29基因的突变(该基因编码一种进化上保守的轴丝蛋白)会导致弱精子症和男性不育。

Lorès, Patrick; Dacheux, Denis; Kherraf, Zine-Eddine; Nsota Mbango, Jean-Fabrice; Coutton, Charles; Stouvenel, Laurence; Ialy-Radio, Come; Amiri-Yekta, Amir; Whitfield, Marjorie; Schmitt, Alain; Cazin, Caroline; Givelet, Maëlle; Ferreux, Lucile; Fourati Ben Mustapha, Selima; Halouani, Lazhar; Marrakchi, Ouafi; Daneshipour, Abbas; El Khouri, Elma; Do Cruzeiro, Marcio; Favier, Maryline; Guillonneau, François; Chaudhry, Marhaba; Sakheli, Zeinab; Wolf, Jean-Philippe; Patrat, Catherine; Gacon, Gérard; Savinov, Sergey N; Hosseini, Seyedeh Hanieh; Robinson, Derrick R; Zouari, Raoudha; Ziyyat, Ahmed; Arnoult, Christophe; Dulioust, Emmanuel; Bonhivers, Mélanie; Ray, Pierre F; Touré, Aminata