Author

Miniar Kalai

Observed names: Kalai M, Kalai Miniar, M. Kalai, Miniar Kalai1

Institutions: Tunis University, Institut Pasteur de Tunis, Tunis El Manar University

Observed institutions: Tunis University, Institut Pasteur de Tunis, Tunis El Manar University

ORCID: 0000-0003-1345-6456

Observed ORCID: 0000-0003-1345-6456

OpenAlex ID: A5011633627

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients

2015 · Leila Chaouch, Imen Moumni, et al. · Hematology · 24

Early Complication in Sickle Cell Anemia Children due toA(TA)nTAAPolymorphism at the Promoter ofUGT1A1Gene

2013 · Leila Chaouch, Emna Talbi, et al. · Disease Markers · 15

Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among Sickle Cell Aneamia patients

2013 · Leila Chaouch, Miniar Kalai, et al. · Biomedical Papers · 13

Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia

2013 · Miniar Kalai, Leila Chaouch, et al. · Polish Journal of Pathology · 12

The role of rs1984112_G atCD36gene in increasing reticulocyte level among sickle cell disease patients

2016 · Miniar Kalai, Marwa Dridi, et al. · Hematology · 10

Molecular basis of pyruvate kinase deficiency among Tunisians: description of new mutations affecting coding and noncoding regions in the PKLR gene

2017 · M. Jaouani, L. Manco, et al. · International Journal of Laboratory Hematology · 8

New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level

2019 · Leila Chaouch, Houssem Sellami, et al. · Journal of Pediatric Hematology/Oncology · 5

Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn

2022 · Miniar Kalai, Imen Moumni, et al. · American Journal of Perinatology · 4

Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients.

2015 · Leila Chaouch, Miniar Kalai, et al. · PubMed · 4

Association of MCP1-2518A/G and CCR2 ?V64I Polymorphisms and Vasoocclusive Crisis among Sickle Cell Anemia Tunisian Patients

2014 · Chaouch L, Kalai M, et al. · Interdisciplinary Journal of Microinflammation · 3

Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.

2016 · Leila Chaouch, Miniar Kalai1, et al. · PubMed · 2

Phenotypic and molecular genetic analysis of Pyruvate Kinase deficiency in a Tunisian family

2015 · Jaouani Mouna, Hamdi Nadia, et al. · Egyptian Journal of Medical Human Genetics · 2

Implication of rs1026611 in the MCP-1 Gene and V64I of CCR2 in Stroke among SCA Tunisian Patients: A Brief Study

2022 · Leila Chaouch, Miniar Kalai, et al. · Book Publisher International (a part of SCIENCEDOMAIN International) · 1

Association of rs1319868, rs1567811 and rs8041224 of IGF1R gene with infection among sickle cell anemia Tunisian patients

2016 · Mouna Ben Sassi, Leila Chaouch, et al. · Acta Haematologica Polonica · 1

Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ) 0 -Thalassemia among Tunisian family

2022 · Miniar Kalai, Imen Moumni, et al. · Annals of Clinical Biochemistry International Journal of Laboratory Medicine

Works count: 15

Citation count: 104

H-index: 6

I10-index: 5