M. Hachicha

1.8k total citations
136 papers, 1.2k citations indexed

About

M. Hachicha is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, M. Hachicha has authored 136 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 25 papers in Surgery and 25 papers in Genetics. Recurrent topics in M. Hachicha's work include Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (10 papers) and Diabetes and associated disorders (8 papers). M. Hachicha is often cited by papers focused on Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (10 papers) and Diabetes and associated disorders (8 papers). M. Hachicha collaborates with scholars based in Tunisia, France and Portugal. M. Hachicha's co-authors include Shaun R. McColl, Thomas J. Schall, Palaniswami Rathanaswami, M D Sadick, Paul H. Naccache, Hajer Aloulou, I. Chabchoub, L. Sfaihi, S. Levasseur and Kuldeep Neote and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Experimental Medicine and The Journal of Immunology.

In The Last Decade

M. Hachicha

125 papers receiving 1.2k citations

Peers

Countries citing papers authored by M. Hachicha

Since Specialization

Citations

This map shows the geographic impact of M. Hachicha's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by M. Hachicha with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Hachicha more than expected).

Fields of papers citing papers by M. Hachicha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Hachicha. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by M. Hachicha. The network helps show where M. Hachicha may publish in the future.

Co-authorship network of co-authors of M. Hachicha

This figure shows the co-authorship network connecting the top 25 collaborators of M. Hachicha. A scholar is included among the top collaborators of M. Hachicha based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M. Hachicha. M. Hachicha is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Title	Journal	Authors	Indexed citations
1	Autoantibodies to Zinc Transporter 8 and SLC30A8 Genotype in Type 1 Diabetes Childhood: A Pioneering Study in North Africa	Journal of Diabetes Research	R. Fakhfakh, Olfa Abida et al.	1
2	Mitochondrial disease patients with novel ND4 12058A > C and ND1 m.3911A > G variations: implications for a role in the phenotype following a bioinformatic investigation	Molecular Biology Reports	Emna Mkaouar‐Rebai, L. Sfaihi et al.	1
3	High Diagnostic Yield of Targeted Next-Generation Sequencing in a Cohort of Patients With Congenital Hypothyroidism Due to Dyshormonogenesis	Frontiers in Endocrinology	Athanasia Stoupa, Dulanjalee Kariyawasam et al.	17
4	Epidémiologie des accidents domestiques de l’enfant: expérience d’un Service de Pédiatrie Générale du sud tunisien	Pan African Medical Journal	S. Yaïch, Jamel Damak et al.	7
5	A novel TBX1 missense mutation in patients with syndromic congenital heart defects	Biochemical and Biophysical Research Communications	I. Chabchoub, Leila Keskes et al.	11
6	Improved SSCP Analysis through Primers Addition to Screen Hotspot Exons in DNAH5 gene	International Journal of Medical Research & Health Sciences	M. Hachicha, Khadija Boussetta et al.	1
7	Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion	Clinica Chimica Acta	L. Sfaihi, Majida Charif et al.	14
8	Factor XIII deficiency in south of Tunisia	Blood Coagulation & Fibrinolysis	Hajer Aloulou, Moez Elloumi et al.	1
9	Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance	European Journal of Medical Genetics	Majdi Nagara, Gregory Papagregoriou et al.	7
10	Caractérisation de la contamination spatiale par le Pb, Zn et Cd de l’ancienne mine de Lakhouat (Siliana-Tunisie)	Journal of New Sciences	M. Hachicha et al.	3
11	Chediak-Higashi syndrome presenting in accelerated phase	Hematology/Oncology and Stem Cell Therapy	I. Mâaloul, I. Chabchoub et al.	18
12	Hemolytic Anemia and Progressive Neurologic Impairment: Think About Triosephosphate Isomerase Deficiency	Fetal and Pediatric Pathology	L. Sfaihi, Hajer Aloulou et al.	12
13	Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis	Indian Journal of Endocrinology and Metabolism	Mahdi Kamoun, Fatma Mnif et al.	18
14	Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency	Indian Journal of Endocrinology and Metabolism	Fatma Mnif, Nadia Charfi et al.	15
15	Création et rapport du registre tunisien de l’anémie de Fanconi (TFAR)	Archives de Pédiatrie	Yosra Ben Youssef, Ahlem Amouri et al.	5
16	A case of Kearns–Sayre syndrome with two novel deletions (9.768 and 7.253kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles	Mitochondrion	Emna Mkaouar‐Rebai, I. Chabchoub et al.	12
17	Association lithiase vésiculaire et cavernome porte chez l’enfant : « à propos de 2 observations »	Archives de Pédiatrie	H. Turki, Hajer Aloulou et al.	1
18	Ganglioneuroma of adrenal gland in a patient with Turner syndrome	Annals of Diagnostic Pathology	Mahdi Kamoun, Mouna Mnif et al.	12
19	Inflammatory microcrystals differentially regulate the secretion of macrophage inflammatory protein 1 and interleukin 8 by human neutrophils: a possible mechanism of neutrophil recruitment to sites of inflammation in synovitis.	The Journal of Experimental Medicine	M. Hachicha, Paul H. Naccache et al.	116
20	Une méthode de cartographie de la salinité des sols: conductivité électromagnétique et interpolation par krigeage		Pascal Boivin, M. Hachicha et al.	4

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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