الرئيسية › دليل الباحثين › Majdi Nagara

Majdi Nagara

الانتماء : Inserm · Aix-Marseille Université

• 26منشورات (انتماء تونسي)
• 63مجموع المنشورات
• 614الاستشهادات
• 15مؤشر h

OpenAlex

مجالات البحث

• Cancer Immunotherapy and Biomarkers
• Genetic Associations and Epidemiology
• Colorectal Cancer Treatments and Studies
• Forensic and Genetic Research
• Immune Cell Function and Interaction

المنشورات (26)

• The implication of Epstein-Barr virus latent membrane protein 1 on the composition and prognostic significance of the tumor microenvironment of classical Hodgkin lymphoma
  2023 · Research Square
• FOXP3+/CD68+ ratio within the tumor microenvironment may serve as a potential prognostic factor in classical Hodgkin lymphoma
  2022 · Human Immunology · استُشهد به 2 مرة
• Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young
  2020 · Herz · استُشهد به 12 مرة
• Findings of Whole-Exome Sequencing in a Tunisian Man with Congenital Anomalies of Kidney and Ureteral Tract and Dilated Cardiomyopathy
  2020 · Journal of the American Society of Nephrology
• A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci
  2018 · BMC Cancer · استُشهد به 19 مرة
• Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis
  2017 · Journal of Dermatological Science · استُشهد به 18 مرة
• Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population
  2017 · Annales d Endocrinologie · استُشهد به 16 مرة
• Lactase persistence in Tunisia as a result of admixture with other Mediterranean populations
  2017 · Genes & Nutrition · استُشهد به 14 مرة
• Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance
  2017 · European Journal of Medical Genetics · استُشهد به 8 مرة
• Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome
  2016 · Metabolic Syndrome and Related Disorders · استُشهد به 30 مرة
• Gender-specific associations of genetic variants with metabolic syndrome components in the Tunisian population
  2016 · Endocrine Research · استُشهد به 23 مرة
• CO-13: Association du gène FTO au syndrome métabolique ou à ses composantes chez la population tunisienne
  2016 · Diabetes & Metabolism
• Differential impact of consanguineous marriages on autosomal recessive diseases in T unisia
  2015 · American Journal of Human Biology · استُشهد به 31 مرة
• Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia
  2015 · British Journal of Dermatology · استُشهد به 25 مرة
• Association of genetic variants in the FTO gene with metabolic syndrome: A case-control study in the Tunisian population
  2015 · Journal of Diabetes and its Complications · استُشهد به 24 مرة
• Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity
  2015 · Annals of Human Genetics · استُشهد به 22 مرة
• Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population
  2015 · Neurological Sciences · استُشهد به 13 مرة
• History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation
  2015 · Mitochondrial DNA Part A · استُشهد به 5 مرة
• Specific Aspects of Consanguinity: Some Examples from the Tunisian Population
  2014 · Human Heredity · استُشهد به 25 مرة
• Molecular Investigation of Distal Renal Tubular Acidosis in Tunisia, Evidence for Founder Mutations
  2014 · Genetic Testing and Molecular Biomarkers · استُشهد به 16 مرة
• A Tunisian Patient with Two Rare Syndromes: Triple A Syndrome and Congenital Hypogonadotropic Hypogonadism
  2014 · Hormone Research in Paediatrics · استُشهد به 12 مرة
• A novel splice-site mutation in ATP6V0A4 gene in two brothers with distal renal tubular acidosis from a consanguineous Tunisian family
  2014 · Journal of Genetics · استُشهد به 4 مرة
• Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: Implication for diagnosis in North Africa
  2013 · Gene · استُشهد به 22 مرة
• A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families
  2013 · International Journal of Pediatric Otorhinolaryngology · استُشهد به 3 مرة
• Biotinidase deficiency: Novel mutations in Algerian patients
  2013 · Gene · استُشهد به 3 مرة
• Adult gaucher disease in southern Tunisia: report of three cases
  2012 · Diagnostic Pathology · استُشهد به 8 مرة

مجلات النشر

• Gene × 2
• Research Square × 1
• Human Immunology × 1
• Herz × 1
• Journal of the American Society of Nephrology × 1
• BMC Cancer × 1

المنشورات حسب السنة

• 20231
• 20221
• 20202
• 20181
• 20174
• 20163
• 20156
• 20144
• 20133
• 20121

التعاون العلمي

المؤسسات الشريكة : Institut Pasteur de Tunis · Tunis El Manar University · Institut National de Nutrition et de Technologie Alimentaire · Hôpital La Rabta · Faculté de médecine de Tunis

بلدان المؤلفين المشاركين : فرنسا · الهند

المؤلفون المشاركون

• Sonia Abdelhak
• Rym Kéfi
• Olfa Messaoud
• Nizar Ben Halim
• Lilia Romdhane
• Yosra Bouyacoub
• Sahar Elouej
• Faten Ben Rhouma
• Mariem Chargui
• Mariem Ben Rekaya
• H. Jamoussi
• Insaf Rejeb

البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).