Yessine Amri - Publications, H-index & Citations

Yessine Amri

universite de tunis-el-manar

8H指数

43论文数

131被引数

收录论文 15

发表时间

Glucose-6-phosphate dehydrogenase activity and genetic variants in tunisian diabetic populations: A case-control study 葡萄糖-6-磷酸脱氢酶活性和基因变异在突尼斯糖尿病人群中的研究：一项病例对照研究

Journal of the National Medical Association

IF2.3

2026-08-01

PREAI

Amri, Yessine; Othmani, Mariem; Hannachi, Nada; Tombari, Sarra; Chelbi, Siwar; Dridi, Amira; Zmerli, Nesrine; Fredj, Sondess Hadj; Messaoud, Taieb; Dabboubi, Rym

A hybrid machine learning and deep learning framework for non-invasive blood pressure estimation from rPPG signals 基于混合机器学习和深度学习框架的非侵入式血压估计rPPG信号方法

Biomedical Signal Processing and Control

IF4.9

2026-05-28

PREAI

Zouhair Mbarki; Yessine Amri; Amine Ben Slama; Lassaad Sfina; Hedi Trabelsi; Hassene Seddik

Integrative Biochemical and In Silico Characterization of Congenital Bisalbuminemia and Its Impact on Albumin Structure and Ligand Transport 先天性双白蛋白血症的生化与计算机模拟表征及其对白蛋白结构和配体转运的影响

Scientific African

IF3.3

2026-04-08

OAAI

Yessine Amri; Mariem Atallah; Sarra Tombari; Siwar Chelbi; Mariem Othmani; Sondess Hadj Fredj; Taieb Messaoud; Rym Dabboubi

Vitamin D deficiency in sickle cell disease: a neglected comorbidity in Tunisia

Annals of Hematology

IF2.4

2026-01-12

OAAI

Mariem Othmani; Yessine Amri; Yosr Jouini; Faida Ouali; Siwar Chelbi; Sondess Hadj Fredj; Rym Dabboubi; Taieb Messaoud

Discrepancies in Sigma Metrics Driven by Total Allowable Error Variability: Implications for QC Strategy and Laboratory Efficiency 由总允许误差变异性驱动的西格玛指标差异：对质量控制策略和实验室效率的影响

JOURNAL OF APPLIED LABORATORY MEDICINE

IF1.9

2025-11-01

OAAI

Othmani, Mariem; Amri, Yessine; Chelbi, Siwar; Hadj Fredj, Sondess; Messaoud, Taieb; Dabboubi, Rym

Challenges in Serum Albumin Measurements: A Comparative Study of the Bromocresol Green and the Capillary Zone Electrophoretic Method 血清白蛋白测量的挑战：溴甲酚绿法与毛细管区带电泳法的比较研究

PROTEIN JOURNAL

IF1.4

2025-11-01

PREAI

Othmani, Mariem; Amri, Yessine; Chelbi, Siwar; Hadj Fredj, Sondes; Messaoud, Taieb; Dabboubi, Rym

Respiratory Chain Complex I Deficiency in Leber Hereditary Optic Neuropathy: Insights from Ophthalmologic and Molecular Investigations in Tunisia

BMC GENOMICS

IF3.7

2024-11-22

OAAI

Chkioua, Latifa; Amri, Yessine; Sahli, Chayma; Nasri, Tawfik; Miladi, Mohamed Omar; Massoud, Taieb; Laradi, Sandrine; Ghorbel, Mohamed; Ben Abdennebi, Hassen

Mucopolysaccharidosis type I: founder effect of the p.P533R mutation in North Africa

BMC GENOMICS

IF3.7

2024-10-09

OAAI

Chkioua, Latifa; El Fissi, Houda; Amri, Yessine; Sahli, Chayma; Bouzid, Fadoua; Boudabous, Hela; Tbib, Neji; Ferchichi, Salima; Massoud, Taieb; Alif, Najat; Laradi, Sandrine; Ben Abdennebi, Hassen

Vitamin D status and VDR gene polymorphisms in patients with growth hormone deficiency: A case control Tunisian study

HELIYON

IF3.6

2024-07-01

OAAI

Tombari, Sarra; Amri, Yessine; Hasni, Yosra; Fredj, Sondess Hadj; Salem, Yesmine; Ferchichi, Salima; Essaddam, Leila; Messaoud, Taieb; Dabboubi, Rym

Identification of a new mutation in the MEN1 gene responsible for familial primary hyperparathyroidism in a Tunisian family

CLINICA CHIMICA ACTA

IF2.9

2024-05-01

PREAI

Oueslati, S.; Mahjoub, R.; Hammami, S.; Amri, Y.; Fredj, S. Hadgj; Kammoun, I.; Messaoud, T.; Talbi, E.

Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b

DIABETOLOGY & METABOLIC SYNDROME

IF3.9

2023-04-28

OAAI

Chkioua, Latifa; Amri, Yessine; Sahli, Chayma; Ben Rhouma, Ferdawes; Ben Chehida, Amel; Tebib, Neji; Messaoud, Taieb; Ben Abdennebi, Hassen; Laradi, Sandrine

Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6-10_16delTTTG deletion

HAEMOPHILIA

IF3

2020-03-23

PREAI

Amri, Yessine; Dabboubi, Rym; Mghaieth, Fathia; Zili, Mohamed; Messaoud, Taieb; Casini, Alessandro; De Moerloose, Philippe; Toumi, Nour El Houda

Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization

HAEMOPHILIA

IF3

2017-06-08

PREAI

Amri, Y.; Jouini, H.; Becheur, M.; Dabboubi, R.; Mahjoub, B.; Messaoud, T.; Sfar, M. T.; Casini, A.; de Moerloose, P.; Toumi, N. E. H.

Hypodysfibrinogenemia: A novel abnormal fibrinogen associated with bleeding and thrombotic complications

CLINICA CHIMICA ACTA

IF2.9

2016-09-01

PREAI

Amri, Yessine; Kallel, Choumous; Becheur, Mariem; Dabboubi, Rym; Elloumi, Moez; Belaaj, Hatem; Kammoun, Sami; Messaoud, Taieb; de Moerloose, Philippe; Toumi, Nour El Houda

Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families

THROMBOSIS RESEARCH

IF3.4

2016-07-01

PREAI

Amri, Yessine; Toumi, Nour El Houda; Fredj, Sondess Hadj; de Moerloose, Philippe

研究方向