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 — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
M. Hachicha Tunisia 15 400 313 204 163 145 136 1.2k
Lori Steiner United States 22 284 0.7× 407 1.3× 108 0.5× 297 1.8× 89 0.6× 35 1.4k
Elizabeth Whalen United States 16 314 0.8× 725 2.3× 157 0.8× 184 1.1× 96 0.7× 27 1.4k
Vijay Saxena United States 19 278 0.7× 495 1.6× 120 0.6× 130 0.8× 202 1.4× 39 1.5k
Sumio Miyazaki Japan 21 371 0.9× 300 1.0× 175 0.9× 119 0.7× 49 0.3× 103 1.5k
Afig Berdelı Türkiye 23 369 0.9× 290 0.9× 105 0.5× 93 0.6× 190 1.3× 102 1.4k
Nollaig A. Parfrey Ireland 24 240 0.6× 401 1.3× 225 1.1× 235 1.4× 68 0.5× 43 1.8k
W. A. Buurman Netherlands 22 318 0.8× 431 1.4× 115 0.6× 85 0.5× 51 0.4× 43 1.6k
Ronald M. Allen United States 15 516 1.3× 717 2.3× 124 0.6× 59 0.4× 115 0.8× 22 1.4k
Quan Sha United States 16 320 0.8× 666 2.1× 222 1.1× 53 0.3× 86 0.6× 30 1.5k
B. Uring‐Lambert France 20 235 0.6× 556 1.8× 57 0.3× 155 1.0× 98 0.7× 46 1.2k

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

20 of 20 papers shown
1.
Fakhfakh, R., et al.. (2022). Autoantibodies to Zinc Transporter 8 and SLC30A8 Genotype in Type 1 Diabetes Childhood: A Pioneering Study in North Africa. Journal of Diabetes Research. 2022. 1–10. 1 indexed citations
2.
3.
Stoupa, Athanasia, Dulanjalee Kariyawasam, Gabor Szinnai, et al.. (2021). High Diagnostic Yield of Targeted Next-Generation Sequencing in a Cohort of Patients With Congenital Hypothyroidism Due to Dyshormonogenesis. Frontiers in Endocrinology. 11. 545339–545339. 17 indexed citations
4.
Yaïch, S., et al.. (2019). Epidémiologie des accidents domestiques de l’enfant: expérience d’un Service de Pédiatrie Générale du sud tunisien. Pan African Medical Journal. 33. 108–108. 7 indexed citations
5.
Chabchoub, I., et al.. (2018). A novel TBX1 missense mutation in patients with syndromic congenital heart defects. Biochemical and Biophysical Research Communications. 499(3). 563–569. 11 indexed citations
6.
Hachicha, M., et al.. (2018). Improved SSCP Analysis through Primers Addition to Screen Hotspot Exons in DNAH5 gene. International Journal of Medical Research & Health Sciences. 7(9). 120–126. 1 indexed citations
7.
Sfaihi, L., Majida Charif, Valérie Desquiret‐Dumas, et al.. (2018). 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. 488. 104–110. 14 indexed citations
8.
Aloulou, Hajer, et al.. (2017). Factor XIII deficiency in south of Tunisia. Blood Coagulation & Fibrinolysis. 28(6). 485–489. 1 indexed citations
9.
Nagara, Majdi, Gregory Papagregoriou, Zied Landoulsi, et al.. (2017). Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance. European Journal of Medical Genetics. 61(1). 1–7. 7 indexed citations
10.
Hachicha, M., et al.. (2016). Caractérisation de la contamination spatiale par le Pb, Zn et Cd de l’ancienne mine de Lakhouat (Siliana-Tunisie). Journal of New Sciences. 3 indexed citations
11.
Mâaloul, I., I. Chabchoub, Lobna Ayadi, et al.. (2015). Chediak-Higashi syndrome presenting in accelerated phase. Hematology/Oncology and Stem Cell Therapy. 9(2). 71–75. 18 indexed citations
12.
Sfaihi, L., et al.. (2014). Hemolytic Anemia and Progressive Neurologic Impairment: Think About Triosephosphate Isomerase Deficiency. Fetal and Pediatric Pathology. 33(4). 234–238. 12 indexed citations
13.
Kamoun, Mahdi, Fatma Mnif, Nadia Charfi, et al.. (2013). 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. 17(1). 121–127. 18 indexed citations
14.
Mnif, Fatma, et al.. (2012). Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Indian Journal of Endocrinology and Metabolism. 16(6). 939–946. 15 indexed citations
15.
Youssef, Yosra Ben, Ahlem Amouri, Hatem Elghezal, et al.. (2012). Création et rapport du registre tunisien de l’anémie de Fanconi (TFAR). Archives de Pédiatrie. 19(5). 467–475. 5 indexed citations
16.
17.
Turki, H., et al.. (2010). Association lithiase vésiculaire et cavernome porte chez l’enfant : « à propos de 2 observations ». Archives de Pédiatrie. 17(5). 507–510. 1 indexed citations
18.
Kamoun, Mahdi, Mouna Mnif, N. Rekik, et al.. (2009). Ganglioneuroma of adrenal gland in a patient with Turner syndrome. Annals of Diagnostic Pathology. 14(2). 133–136. 12 indexed citations
19.
20.
Boivin, Pascal, et al.. (1989). Une méthode de cartographie de la salinité des sols: conductivité électromagnétique et interpolation par krigeage. 27(1). 69–72. 4 indexed citations

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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