الرئيسية › دليل الباحثين › Amal Tazzite
Amal Tazzite
الانتماء : Instituts Supérieurs des Professions Infirmières et Techniques de Santé · Institut Supérieur des Professions Infirmières et Techniques de Santé de Casablanca · University of Hassan II Casablanca
- 52منشورات (انتماء مغربي)
- 67مجموع المنشورات
- 286الاستشهادات
- 10مؤشر h
الملف البحثي
لدى Amal Tazzite 52 منشور(ات) مفهرسة (2009–2026). تُنشر أعماله أساسًا في «(IJRE) International Journal of Research and Ethics»، «Figshare» و«Egyptian Journal of Medical Human Genetics». أكثر مقالاته استشهادًا هو «BRCA1 and BRCA2 germline mutations in Moroccan breast/ovarian cancer families: Novel mutations and unclassified variants» (2012)، وقد استُشهد به 63 مرة. 16 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Epilepsy research and treatment
- Breast Lesions and Carcinomas
المنشورات (52)
- Duplication of the 15q11-13 region in a Moroccan patient with autism, intellectual deficiency and absence of speech - A case report
- Severe sepsis and genetic predisposition: systematic review
- Additional file 3 of Severe sepsis and genetic predisposition: systematic review
- Severe sepsis and genetic predisposition: systematic review
- Additional file 4 of Severe sepsis and genetic predisposition: systematic review
- Additional file 1 of Severe sepsis and genetic predisposition: systematic review
- Additional file 2 of Severe sepsis and genetic predisposition: systematic review
- Two adult Moroccan women with phenotypes suggestive of TRRAPrelated neurodevelopmental disorder carrying TRRAP variants of uncertain significance: a case report of two patients
- Genetics of cardiotoxicity induced by anti-HER2 therapies: a systematic review
- Impact of CYP17A1 Gene Polymorphisms on Abiraterone Efficacy in Prostate Cancer: A Systematic Review
- Gene’s Association with Coronary Stent Stenosis After Drug Eluting Stent: Review
- Gene’s Association with Coronary Stent Stenosis After Drug Eluting Stent: Mini-review
- A novel variant of ATRX gene is potentially associated with alpha-thalassemia X-linked intellectual disability syndrome: Case report and literature review
- Fanconi anemia diagnosed by genetic testing
- Epilepsy in a Moroccan patient with Pitt-Hopkins syndrome
- Next-generation technology in epilepsy diagnostic: First Moroccan pediatric case series and literature review.
- Impact of CYP2D6, CYP2C9/19, CYP3A4, UGT , and SULT Variability on Tamoxifen Metabolism in Breast Cancer Treatment
- A novel SCN8A variant of unknown significance in pediatric epilepsy: a case report
- Prognostic value of residual disease detection in acute myeloid leukemia with normal karyotype and negative FLT3-ITD
- Ring chromosome 13 and sexual ambiguity: Case report
- Terminal deletion of 18q: A case report
- Novel FREM1 homozygous variant in an individual with an intermediate phenotype between Bifid Nose with or without Anorectal and Renal Anomalies and Manitoba-oculo-tricho-anal syndromes
- R306X Mutation in the MECP2 Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report
- Involvement of APOE polymorphism in Alzheimer's disease susceptibility and Donepezil response in Moroccan patients
- Complement Factor I deficiency: A novel homozygous CFI gene mutation
- Neurological manifestations in Tuberous Sclerosis Complex
- Tuberous Sclerosis Complex: Clinical Case Presentation and Literature Review
- Huntington disease and the mechanisms of neuronal death
- Molecular diagnosis of Duchene Muscular dystrophy
- Ring chromosome 9 and chromosome 9p deletion associated with neurological and malformative syndrome
- Clinical exome sequencing identifies a novel variant in SCN1A gene in a Moroccan patient with Dravet syndrome
- Neurological manifestations in Patau syndrome
- Fragile X Syndrome: role of the FMR1 gene in neurodevelopmental disorders
- Molecular study of infantile Spinal Muscular Atrophy
- Postnatal Edward’s syndrome
- Next-generation sequencing of BRCA1 and BRCA2 genes in Moroccan prostate cancer patients with positive family history
- The impact of ABCB1 gene polymorphism (C3435T) and its expression on response to Donepezil in Moroccan patients with Alzheimer's disease
- An extensive meta-analysis of the association of MTHFR c.677C > T and c.1298A > C polymorphisms with gliomas
- Cutting-Edge Technologies for Ovarian Cancer: An Overview of the Impact of Genetic Testing, Next-Generation Sequencing, and Single-Cell Analysis
- BRCA Mutational Status is a Promising Predictive Biomarker for Platinum- based Chemotherapy in Triple-Negative Breast Cancer
- Germline variants in the ATM gene and breast cancer susceptibility in Moroccan women: A meta-analysis
- Association between ABCB1 C3435T polymorphism and breast cancer risk: a Moroccan case-control study and meta-analysis
- Clinical and pathological features of BRCA1/2 tumors in a sample of high-risk Moroccan breast cancer patients
- The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population
- Specific BRCA1 gene variations amongst young Moroccan breast cancer patients
- Association of TP53 PIN3 polymorphism with breast cancer in Moroccan population
- Large scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,297 individuals
- Relationship between family history of breast cancer and clinicopathological features in Moroccan patients.
- Effect of the novel Moroccan BRCA1 and BRCA2 frameshift mutations
- BRCA1 and BRCA2 germline mutations in Moroccan breast/ovarian cancer families: Novel mutations and unclassified variants
- Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals
- Chapitre 5. Les implications éthiques de la conservation des échantillons biologiques
مجلات النشر
- (IJRE) International Journal of Research and Ethics × 15
- Figshare × 5
- Egyptian Journal of Medical Human Genetics × 3
- Gene Reports × 3
- Indian journal of human genetics × 3
- European Journal of Medical Case Reports × 2
المنشورات حسب السنة
- 20268
- 20252
- 20246
- 20235
- 202214
- 20214
- 20201
- 20171
- 20162
- 20151
التعاون العلمي
المؤسسات الشريكة : Centre Hospitalier Universitaire Ibn Rochd · Laboratoire de Recherche et d’Analyses Médicales de la Fraternelle de la Gendarmerie Royale · Université Sultan Moulay Slimane · Moroccan Foundation for Advanced Science, Innovation and Research · Institut Pasteur du Maroc
المؤلفون المشاركون
- Hind Dehbi
- Bouchaïb Gazzaz
- Sarah Berrada
- Wafaa Bouzroud
- H. Jouhadi
- Sellama Nadifi
- Fatima Maarouf
- Abdellatif Benider
- Bouchra Oukkache
- Hind Dehbi
- Hanane Ezzouine
- Hind Dehbi
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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