الرئيسية › دليل الباحثين › Khalid Sadki
Khalid Sadki
الانتماء : Mohammed V University
- 51منشورات (انتماء مغربي)
- 66مجموع المنشورات
- 1242الاستشهادات
- 16مؤشر h
الملف البحثي
لدى Khalid Sadki 51 منشور(ات) مفهرسة (2000–2026). تُنشر أعماله أساسًا في «Mechanisms of Ageing and Development»، «Egyptian Journal of Medical Human Genetics» و«BMC Infectious Diseases». أكثر مقالاته استشهادًا هو «Platelets Can Associate With SARS-CoV-2 RNA and Are Hyperactivated in COVID-19» (2020)، وقد استُشهد به 496 مرة. 16 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في كندا، فرنسا، بلجيكا، الولايات المتحدة.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Tuberculosis Research and Epidemiology
- Genetic Associations and Epidemiology
- Infectious Diseases and Tuberculosis
- vaccines and immunoinformatics approaches
- Lung Cancer Treatments and Mutations
المنشورات (51)
- Antiretroviral raltegravir, a selective human immunodeficiency virus type 1 integrase inhibitor, shows anti-Alzheimer’s potential against amyloid-beta1–42-induced neurodegeneration
- Mechanistic insights into the neuroprotective potential of gut microbiota-derived urolithins in Alzheimer’s disease
- Genetic variations on influenza virus infection outcomes in Moroccan patients
- Bacteriophages in the environmental control of antimicrobial resistance: opportunities, risks, and surveillance challenges
- Polyphenol-Microbiota Interactions in Atherosclerosis: The Role of Hydroxytyrosol and Tyrosol in Modulating Inflammation and Oxidative Stress
- Meta-analysis of EGFR gene polymorphisms and lung cancer risk
- Endemic scorpion species and subspecies in Morocco: A comprehensive overview
- Exome sequencing reveals new insights into the germline landscape of inflammatory breast cancer among Tunisian patients
- Unveiling the Genomic Landscape: Architectural Insights into Triple-Negative Breast Cancer in Moroccan Patients Through Whole-Exome Sequencing
- HLA molecules: Another challenge for CAR T cell therapy
- Genetic insights from whole-exome sequencing in Moroccan patients with non-small cell lung cancer: a case report
- Impact of IFITM3 rs12252 and IFNAR2 rs2236757 SNP polymorphisms on influenza virus infection outcomes in Moroccan patients
- Prevalence of HBsAg among Moroccan HIV-1 infected patients and APOBEC3G variant frequencies in HIV-1/HBV co-infection
- Application of Genomic Medicine in Africa: 14th Conference of the African Society of Human Genetics and the 2nd International Congress of the Moroccan Society of Genomics and Human Genetics, Rabat, Morocco 2022
- Design of SARS-CoV-2 protein S peptides recognized by the most frequent HLA alleles in the Moroccan population using an immunoinformatics approach
- A prospective epidemiological investigation of human leukocyte antigen-B*57:01 in HIV-1-infected Moroccan subjects
- HLA alleles associated with COVID-19 susceptibility and severity in different populations: a systematic review
- HLA-C Genotyping Reveals Haplotype C*07 as a Potential Biomarker of Late Psoriasis Onset in Moroccan Patients
- Assessment of the Association of Chlamydia e pneumoniae Infection with Lung Cancer in a Moroccan Patients’ Cohort
- The APOBEC3G gene rs2294367(C>G) variant is associated with HIV-1 infection in Moroccan subjects
- Bioscreening and pre-clinical evaluation of the impact of bioactive molecules from Ptychotis verticillata on the multilineage potential of mesenchymal stromal cells towards immune- and inflammation-mediated diseases
- New Anti-Leukemic Effect of Carvacrol and Thymol Combination through Synergistic Induction of Different Cell Death Pathways
- Genetic diversity and genomic epidemiology of SARS-CoV-2 in Morocco
- 15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review
- Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
- Research of the Philadelphia Chromosome in Chronic Myeloid Leukemia: Diagnostic and Prognostic Interests
- Platelets Can Associate With SARS-CoV-2 RNA and Are Hyperactivated in COVID-19
- Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy
- Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy
- Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
- Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
- Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report.
- The biological response of mesenchymal stromal cells to thymol and carvacrol in comparison to their essential oil: An innovative new study
- Development of Bioinformatics Infrastructure for Genomics Research
- Low plasma vitamin A concentration is associated with tuberculosis in Moroccan population: a preliminary case control study
- New variant identified in major susceptibility locus to tuberculosis on chromosomal region 8q12-q13 in Moroccan population: a case control study
- ABI Base Recall: Automatic Correction and Ends Trimming of DNA Sequences
- Current immunogenetic predisposition to tuberculosis in the Moroccan population
- H3ABioNet, a sustainable pan-African bioinformatics network for human heredity and health in Africa
- Molecular Typing of Mycobacterium Tuberculosis Complex by 24-Locus Based MIRU-VNTR Typing in Conjunction with Spoligotyping to Assess Genetic Diversity of Strains Circulating in Morocco
- Prevalence of HLA-B27 in Moroccan healthy subjects and patients with ankylosing spondylitis and mapping construction of several factors influencing AS diagnosis by using multiple correspondence analysis
- Rotavirus and Norovirus infections among acute gastroenteritis children in Morocco
- The CYP7A1 gene rs3808607 variant is associated with susceptibility of tuberculosis in Moroccan population
- COMPARISON OF A DNA BASED PCR APPROACH WITH CONVENTIONAL METHODS FOR THE DETECTION OF MYCOBACTERIUM TUBERCULOSIS IN MOROCCO
- Analysis of MIF, FCGR2A and FCGR3A gene polymorphisms with susceptibility to pulmonary tuberculosis in Moroccan population
- Serodiagnosis of tuberculosis using nine in silico predicted B-cell epitopes peptides derived from Mycobacterium tuberculosis proteins
- Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population
- Design of immunogenic peptides from Mycobacterium tuberculosis genes expressed during macrophage infection
- CD209Promoter Single Nucleotide Polymorphism -336A/G and the Risk of Susceptibility to Tuberculosis Disease in the Moroccan Population
- Erratum to “Design of immunogenic peptides from Mycobacterium tuberculosis genes expressed during macrophage infection” [Tuberculosis 89 (3) (May 2009) 210–217]
- A novel HLA‐B*51 allele (B*5116) identified by nucleotide sequencing
مجلات النشر
- Mechanisms of Ageing and Development × 2
- Egyptian Journal of Medical Human Genetics × 2
- BMC Infectious Diseases × 2
- Tissue Antigens × 2
- Tuberculosis × 2
- Iranian Journal of Microbiology × 1
المنشورات حسب السنة
- 20264
- 20258
- 20244
- 20234
- 20221
- 20215
- 20206
- 20191
- 20175
- 20153
التعاون العلمي
المؤسسات الشريكة : Institut National d'Hygiène du Maroc · Institut Pasteur du Maroc · Ministère de la Santé · Mohamed I University · University of Hassan II Casablanca
بلدان المؤلفين المشاركين : كندا · فرنسا · بلجيكا · الولايات المتحدة
المؤلفون المشاركون
- Rajae El Aouad
- Meryem Fakhkhari
- Hicham Oumzil
- Yahya BENBOUCHTA
- Ikram Salih
- Abdelaziz Sefiani
- Imane Cherkaoui Jaouad
- Abdelali Zrhidri
- Mouna Ouhenach
- Jaber Lyahyai
- Fouzia Radouani
- Elmir Elharti
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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