الرئيسية › دليل الباحثين › Hamza Dallali
Hamza Dallali
الانتماء : University of Carthage · Institut Pasteur de Tunis · National Institute of Applied Science and Technology
- 35منشورات (انتماء تونسي)
- 52مجموع المنشورات
- 307الاستشهادات
- 11مؤشر h
الملف البحثي
لدى Hamza Dallali 35 منشور(ات) مفهرسة (2017–2026). تُنشر أعماله أساسًا في «Frontiers in Genetics»، «PLoS ONE» و«Bioscience Reports». أكثر مقالاته استشهادًا هو «Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort» (2017)، وقد استُشهد به 28 مرة. 7 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في فرنسا، جنوب أفريقيا.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Diabetes, Cardiovascular Risks, and Lipoproteins
- Nutrition, Genetics, and Disease
- BRCA gene mutations in cancer
المنشورات (35)
- Metataxonomic strategy to decipher gut bacteriome biomarkers of type 2 diabetes and obesity in Tunisian population
- Genomic Insights into Unspecified Monogenic Forms of Diabetes and Their Associated Comorbidities: Implication for Treatment
- Hemoglobin Disorders Associated with Neurological Impairment: First Report of ATR-X Syndrome and Recessive Congenital Methemoglobinemia Type II in Tunisia
- Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing
- Pharmacogenetic landscape of pain management variants among Mediterranean populations
- Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
- Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
- Decoding the genetic relationship between Alzheimer’s disease and type 2 diabetes: potential risk variants and future direction for North Africa
- Whole-exome sequencing reveals novel variants of monogenic diabetes in Tunisia: impact on diagnosis and healthcare management
- The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes
- PHINDaccess Hackathons for COVID‐19 and Host‐Pathogen Interaction: Lessons Learned and Recommendations for Low‐ and Middle‐Income Countries
- Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis
- Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
- Correction to: Development of a custom next-generation sequencing panel for the determination of bladder cancer risk in a Tunisian cohort
- Multiallelic Rare Variants in BBS Genes Support an Oligogenic Ciliopathy in a Non-obese Juvenile-Onset Syndromic Diabetic Patient: A Case Report
- Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia
- Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis
- A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa
- Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
- Development of a custom next-generation sequencing panel for the determination of bladder cancer risk in a Tunisian cohort
- Development of a Custom NGS Panel for the Determination of Bladder Cancer Risk
- Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa
- Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young
- Clinical and Genetic Heterogeneity in Six Tunisian Families With Horizontal Gaze Palsy With Progressive Scoliosis: A Retrospective Study of 13 Cases
- Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family
- Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk
- Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk
- Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing
- Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins
- Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome
- Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family
- Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations
- Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort
- Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis
- Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population
مجلات النشر
- Frontiers in Genetics × 5
- PLoS ONE × 4
- Bioscience Reports × 3
- Molecular Biology Reports × 3
- Current Issues in Molecular Biology × 1
- International Journal of Molecular Sciences × 1
المنشورات حسب السنة
- 20261
- 20252
- 20244
- 20234
- 20223
- 20217
- 20206
- 20194
- 20181
- 20173
التعاون العلمي
المؤسسات الشريكة : Tunis El Manar University · Tunis University · Faculté de médecine de Tunis · Hôpital Charles-Nicolle · Institut National de Nutrition et de Technologie Alimentaire
بلدان المؤلفين المشاركين : فرنسا · جنوب أفريقيا
المؤلفون المشاركون
- Sonia Abdelhak
- Rym Kéfi
- Meriem Hechmi
- Haifa Jmel
- Olfa Messaoud
- H. Jamoussi
- Abdelmajid Abid
- Yosr Hamdi
- Nadia Kheriji
- Lilia Romdhane
- Ridha Mrad
- Ismail Gouiza
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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