Accueil › Annuaire des chercheurs › Amina Bibi
Amina Bibi
Affiliation : Children's Hospital · Institut National de Nutrition et de Technologie Alimentaire
- 29Publications (affiliation tunisienne)
- 83Publications au total
- 1230Citations
- 16Indice h
Profil de recherche
Amina Bibi compte 29 publications référencées (2009–2023). Ses travaux paraissent principalement dans « Clinical Chemistry and Laboratory Medicine (CCLM) », « Annales de biologie clinique » et « Molecular Biology Reports ». Son article le plus cité, « Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-c » (2013), a été cité 47 fois. 5 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de France.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Hemoglobinopathies and Related Disorders
- Maternal Mental Health During Pregnancy and Postpartum
- Mental Health Treatment and Access
- Genetic Associations and Epidemiology
- Iron Metabolism and Disorders
Publications (29)
- Risk of metabolic syndrome in patients with chronic hepatitis C.
- Effect of flax seeds on lipids: Insulin and ghrelin in type 2 diabetic women with metabolic syndrome
- Kefir milk consumption decreases sperm alterations due to the high‐fat diet in adult male rats
- Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations
- Association of Vitamin D Receptor Gene Polymorphisms With the Evolution of MODY Diabetes: Study in Tunisian Patients
- A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del
- Salivary cortisol levels during Ramadan fasting in hydrocortisone-treated secondary adrenal insufficiency patients
- Evaluation of free thyroxine determination based on one-step fluorometric immunoassay technique and the suboptimal concordance with two-step immunoassay
- Determination of glucose-6-phosphate dehydrogenase cut-off values in a Tunisian population
- Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA1c quantification
- Molecular identification of Gd A- and Gd B- G6PD deficient variants by ARMS-PCR in a Tunisian population
- First description of the rs45496295 polymorphism of theC/EBPEgene in β-thalassemia intermedia patients
- Setup of a Protocol of Molecular Diagnosis of β‐Thalassemia Mutations in Tunisia using Denaturing High‐Performance Liquid Chromatography (DHPLC)
- Angiotensin-converting enzyme insertion/deletion gene polymorphism in cystic fibrosis patients
- Fortuitous description of haemoglobin A2’ [δ16 (A13) Gly→Arg (GGC→CGC)] in a Tunisian family: study of the molecular defect and its origin
- First study of angiotensin converting enzyme in cystic fibrosis Tunisian patients
- Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia
- Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia
- Identification of a cystic fibrosis mutation W19X in Tunisia
- New frameshift CF mutation 3729delAinsTCT in a Tunisian cystic fibrosis patient
- No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population
- Association Between Alzheimer Disease and the −491T Allele of Regulatory Region Polymorphism of Apolipoprotein E in a Tunisian Population
- Detection of a novel splicing mutation causing analbuminemia in a Libyan family
- Identification of candidate genes involved in clinical variability among Tunisian patients with β-thalassemia
- Fortuitous description of hemoglobin Hope in a high-level Tunisian athlete: molecular diagnosis and origin
- δ0-Thalassemia in cis of βKnossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients
- Molecular analysis of mucopolysaccharidosis type I in Tunisia: identification of novel mutation and eight Novel polymorphisms
- Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults
- The epidemiology of abnormal hemoglobins in Mediterranean high-level athletes
Revues de publication
- Clinical Chemistry and Laboratory Medicine (CCLM) × 5
- Annales de biologie clinique × 4
- Molecular Biology Reports × 2
- Journal of Genetics × 2
- PubMed Central × 1
- GSC Biological and Pharmaceutical Sciences × 1
Publications par année
- 20232
- 20221
- 20212
- 20202
- 20181
- 20172
- 20164
- 20151
- 20141
- 20136
Collaborations
Établissements partenaires : Tunis El Manar University · Faculté de médecine de Tunis · Tunis University · Hôpital La Rabta · University of Monastir
Pays des co-auteurs : France
Co-auteurs
- Taieb Ben Messaoud
- Hajer Siala
- Sondess Hadj Fredj
- Chaima Abdelhafidh Sahli
- Faida Ouali
- Latifa Jouini
- Slaheddine Fattoum
- Rahma Mahjoub
- Naouel Laouini
- Nour El Houda Toumi
- Sabrine Oueslati
- Sondes Hadj Fredj
Données bibliographiques issues d’OpenAlex (base ouverte).
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