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

Novel Perspectives on ATP8A2 Regulation: Evidence for Parental Imprinting and Chimeric Transcript Formation

ATP8A2调控的新视角：亲本印记和嵌合转录本形成的证据

期刊:Epigenomes
影响因子:3.5
doi:10.3390/epigenomes10020026
Bouramtane, Abdelhamid; Elmakhzen, Badreddine; Ouskri, Amal; Ahakoud, Mohamed; Bouguenouch, Laila; Ouldim, Karim; Askander, Omar
信号转导
发表日期：2026
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The genetic landscape of breast cancer in young women from Morocco: implications for diagnosis and treatment

摩洛哥年轻女性乳腺癌的遗传图谱：对诊断和治疗的启示

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-026-02343-4
El Hejjioui, Brahim; Bouramtane, Abdelhamid; Bouguenouch, Laila; Elmakhzen, Badreddine; Ahakoud, Mohamed; Melhouf, Moulay Abdelilah; Ouldim, Karim; Bennis, Sanae
肿瘤
乳腺癌
肿瘤免疫
发表日期：2026
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A De Novo 13q21.33-q31.1 Interstitial Deletion in a Child With Megalocornea and Neurodevelopmental Delay: A Clinico-Genomic Correlation

一名患有巨角膜和神经发育迟缓的儿童的13q21.33-q31.1新生间质缺失：临床基因组相关性

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.90646
Elmakhzen, Badreddine; Nedbour, Ayoub; Bouguenouch, Laila; Ahakoud, Mohamed
发育与干细胞
神经科学
发表日期：2025
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In-depth exploration of differences of sex development: 5-year experience in a tertiary center

深入探究性别发育差异：一家三级医疗中心五年的经验

期刊:Endocrine Connections
影响因子:2.8
doi:10.1530/EC-24-0236
Hssaini, Mohamed; Abourazzak, Sana; El Otmani, Ihsane; Ahakoud, Mohamed; Ameli, Amina; Bouguenouch, Laila; Bekkari, Hicham
发育与干细胞
发表日期：2024
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A Case Report of a Rare 46,XX/47,XXY Mosaicism With Ovotesticular Disorder of Sex Development and a Literature Review

罕见46,XX/47,XXY嵌合性卵睾性发育障碍病例报告及文献综述

期刊:Cureus Journal of Medical Science
影响因子:1
doi:10.7759/cureus.65856
Mohamed Hssaini, Ghita Bourkadi, Mohamed Ahakoud, Laila Bouguenouch, Sanae Abourazzak, Hicham Bekkari, Amina Ameli
发育与干细胞
发表日期：2024
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Impact of Deletion on Angelman Syndrome Phenotype Variability: Phenotype-Genotype Correlation in 97 Patients with Motor Developmental Delay

基因缺失对安格曼综合征表型变异的影响：97例运动发育迟缓患者的表型-基因型相关性研究

期刊:Journal of Pediatric Genetics
影响因子:0.4
doi:10.1055/s-0042-1751268
Belghiti, Hanae Daha; Abbassi, Meriame; Sayel, Hanane; Ahakoud, Mohamed; El Makhzen, Badr Eddine; Lee, Norman; Russo, Silvia; Chaouki, Sana; Bouguenouch, Laila
发育与干细胞
发表日期：2024
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Rare and Atypical Case of Turner Syndrome With Three Cell Lines

罕见且非典型的特纳综合征病例，涉及三种细胞系

期刊:Cureus Journal of Medical Science
影响因子:1.3
doi:10.7759/cureus.41128
Essouabni, Amal; Ahakoud, Mohamed; Aynaou, Hayat; Bouguenouch, Laila; Salhi, Houda; Karim, Ouldim; Elouahabi, Hanan
细胞生物学
发表日期：2023
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The Diagnosis and Genetic Mechanisms of Prader-Willi Syndrome: Findings From a Moroccan Population Study

普拉德-威利综合征的诊断和遗传机制：来自摩洛哥人口研究的结果

期刊:Cureus Journal of Medical Science
影响因子:1
doi:10.7759/cureus.37866
Mohamed Ahakoud, Hanae Daha Belghiti, Ayoub Nedbour, Abdelhamid Bouramtane, Sana Chaouki, Laila Bouguenouch, Karim Ouldim
信号转导
发表日期：2023
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