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Amina Bibi
Affiliation : Children's Hospital · Institut National de Nutrition et de Technologie Alimentaire
- 29Publications (affiliation in Tunisia)
- 83Total publications
- 1230Citations
- 16h-index
Research profile
Amina Bibi has 29 indexed publications (2009–2023). Their work appears mainly in “Clinical Chemistry and Laboratory Medicine (CCLM)”, “Annales de biologie clinique” and “Molecular Biology Reports”. Their most cited article, “Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-c” (2013), has been cited 47 times. 5 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in France.
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Create my free profile Add my publicationsResearch areas
- 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
Publication venues
- 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 per year
- 20232
- 20221
- 20212
- 20202
- 20181
- 20172
- 20164
- 20151
- 20141
- 20136
Collaborations
Partner institutions : Tunis El Manar University · Faculté de médecine de Tunis · Tunis University · Hôpital La Rabta · University of Monastir
Co-authors’ countries : France
Co-authors
- 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
Bibliographic data from OpenAlex (open database).
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