Accueil › Annuaire des chercheurs › Amal Tazzite
Amal Tazzite
Affiliation : 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
- 52Publications (affiliation marocaine)
- 67Publications au total
- 286Citations
- 10Indice h
Profil de recherche
Amal Tazzite compte 52 publications référencées (2009–2026). Ses travaux paraissent principalement dans « (IJRE) International Journal of Research and Ethics », « Figshare » et « Egyptian Journal of Medical Human Genetics ». Son article le plus cité, « BRCA1 and BRCA2 germline mutations in Moroccan breast/ovarian cancer families: Novel mutations and unclassified variants » (2012), a été cité 63 fois. 16 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Epilepsy research and treatment
- Breast Lesions and Carcinomas
Publications (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
Revues de publication
- (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
Publications par année
- 20268
- 20252
- 20246
- 20235
- 202214
- 20214
- 20201
- 20171
- 20162
- 20151
Collaborations
Établissements partenaires : 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
Co-auteurs
- Hind Dehbi
- Bouchaïb Gazzaz
- Sarah Berrada
- Wafaa Bouzroud
- H. Jouhadi
- Sellama Nadifi
- Fatima Maarouf
- Abdellatif Benider
- Bouchra Oukkache
- Hind Dehbi
- Hanane Ezzouine
- Hind Dehbi
Données bibliographiques issues d’OpenAlex (base ouverte).
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