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

Impact of TNF-α (- 308G>A and - 857 C>T) promoter variants on susceptibility to chronic hepatitis B virus infection in a cohort of Mauritanian patients: pilot study

TNF-α (-308G>A 和 -857C>T) 启动子变异对毛里塔尼亚患者慢性乙型肝炎病毒感染易感性的影响:一项初步研究

Ennahoui, Saffiya Mounira; M'Hamed, Abdallah Sid; Veten, Fatimetou; Cheikh Bouna, Sidi M; Barakat, Abdelhamid; Soumbara, Tetou; Houmeida, Ahmed

Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity

马格里布和约旦语前孤立性耳聋和厄舍尔综合征的遗传学:利用纯合子的潜力

Riahi, Zied; Boucher, Sophie; Abdi, Samia; Wong Jun Tai, Fabienne; Singh-Estivalet, Amrit; Aghaie, Asadollah; Niasme-Grare, Magali; Hardelin, Jean-Pierre; Behlouli, Asma; Dahmani, Malika; Talbi, Sonia; Bouyacoub, Yosra; Mkaouar, Rahma; Charfeddine, Cherine; Amalou, Ghita; Bakhchane, Amina; Bousfiha, Amale; Salime, Sara; Elrharchi, Soukaina; Salame, Malak; Hadrami, Mouna; Boussaty, Ely; Charoute, Hicham; Detsouli, Mustapha; Snoussi, Khalid; Rouba, Hassan; Hachmi, Hala El; Veten, Fatimetou; Meiloud, Ghlana; Marrakchi, Jihene; Zainine, Rim; Chahed, Houda; Besbes, Ghazi; Trabelsi, Mediha; Mrad, Ridha; Kraoua, Ichraf; Ouhab, Sofiane; Djennaoui, Djamel; Boudjenah, Farid; Chouery, Eliane; Mustapha, Mirna; Houmeida, Ahmed; Barakat, Abdelhamid; Khodja, Fatima Ammar; Makrelouf, Mohamed; Zenati, Akila; Beltaief, Najeh; Abdelhak, Sonia; Petit, Christine; Bonnet, Crystel

Prevalence and genetic etiology of poly-cystic ovarian syndrome (PCOS) in Mauritania

毛里塔尼亚多囊卵巢综合征(PCOS)的患病率和遗传病因

Elwafi, Marieme; Ahmed, Abdi; Akhouayri, Omar; Zein, Ahmed; Abdelkader, Hamma; Selman, Roughaya; Houmeida, Ahmed

Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment

毛里塔尼亚一个患有非综合征性听力障碍的家族中,PJVK基因存在剪接改变变异。

Salame, Malak; Bonnet, Crystel; Singh-Estivalet, Amrit; Brahim, Selma Mohamed; Roux, Solene; Boussaty, Ely Cheikh; Hadrami, Mouna; Hamed, Cheikh Tijani; Sidi, Abdellahi M'hamed; Veten, Fatimetou; Petit, Christine; Houmeida, Ahmed

Genetic variation of TLR3 gene is associated with the outcome of hepatitis b infection in mauritanian patients: case control study

TLR3基因的遗传变异与毛里塔尼亚乙型肝炎患者的预后相关:病例对照研究

Soumbara, Tetou; Bonnet, Crystel; Hamed, Cheikh Tijani; Veten, Fatimetou; Hemeyine, Mohamed; Fall-Malick, F-Zahra; El Yezid, Mohamed Mahmoud; Diallo, Aichetou; Mounah, Moustapha Mouhamedou; Houmeida, Ahmed

Genomic Evidence of Multiple Introductions of SARS-CoV-2 in Mauritania

毛里塔尼亚多次引入 SARS-CoV-2 的基因组证据

Abdelmalick Abdelmalick, Sofia Sehli, Abdellah Idrissi Azami, Nihal Habib, Najib Al Idrissi, Lahcen Belyamani, Ahmed Houmeida, Hassan Ghazal

Screening of BRCA1/2 variants in Mauritanian breast cancer patients

对毛里塔尼亚乳腺癌患者进行BRCA1/2变异筛查

Brahim, Selma Mohamed; Zein, Ekht Elbenina; Bonnet, Crystel; Hamed, Cheikh Tijani; Salame, Malak; Zein, Mohamed Vall; Khyatti, Meriem; Tolba, Ahmedou; Houmeida, Ahmed

Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma

毛里塔尼亚原发性先天性青光眼家族中青光眼候选基因的突变谱

Hadrami, Mouna; Bonnet, Crystel; Zeitz, Christina; Veten, Fatimetou; Biya, Med; Hamed, Cheikh T; Condroyer, Christel; Wang, Panfeng; Sidi, Med Mahmoud; Cheikh, Sidi; Zhang, Qingjiong; Audo, Isabelle; Petit, Christine; Houmeida, Ahmed

HLA class I (-A, -B, -C) and class II (-DR, -DQ) polymorphism in the Mauritanian population

毛里塔尼亚人群中HLA I类(-A、-B、-C)和II类(-DR、-DQ)多态性

Hamed, Cheikh Tijani; Meiloud, Ghlana; Veten, Fatimetou; Hadrami, Mouna; Ghaber, Sidi M; Boussaty, Ely C; Habti, Norddine; Houmeida, Ahmed

Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness.

CDC14A 基因突变编码一种参与毛细胞纤毛发生的蛋白磷酸酶,导致常染色体隐性遗传的重度至极重度耳聋

Delmaghani Sedigheh, Aghaie Asadollah, Bouyacoub Yosra, El Hachmi Hala, Bonnet Crystel, Riahi Zied, Chardenoux Sebastien, Perfettini Isabelle, Hardelin Jean-Pierre, Houmeida Ahmed, Herbomel Philippe, Petit Christine