Malek Louha

2.0k total citations · 1 hit paper
25 papers, 1.3k citations indexed

About

Malek Louha is a scholar working on Sensory Systems, Molecular Biology and Otorhinolaryngology. According to data from OpenAlex, Malek Louha has authored 25 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Sensory Systems, 7 papers in Molecular Biology and 5 papers in Otorhinolaryngology. Recurrent topics in Malek Louha's work include Hearing, Cochlea, Tinnitus, Genetics (10 papers), Ear Surgery and Otitis Media (5 papers) and Vestibular and auditory disorders (5 papers). Malek Louha is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (10 papers), Ear Surgery and Otitis Media (5 papers) and Vestibular and auditory disorders (5 papers). Malek Louha collaborates with scholars based in France, Algeria and Türkiye. Malek Louha's co-authors include Patrizia Paterlini-Bréchot, Christian Bréchot, Dominique Franco, Frédérique Capron, Giovanna Vona, Abdelmajid Sabile, Bernard Lacour, Serge Romana, Véronique Sitruk and Mario Pazzagli and has published in prestigious journals such as PLoS ONE, Hepatology and Neurology.

In The Last Decade

Malek Louha

25 papers receiving 1.3k citations

Hit Papers

Isolation by Size of Epithelial Tumor Cells 2000 2026 2008 2017 2000 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Isolation by Size of Epithelial Tumor Cells
    2000 870 citations Giovanna Vona, Abdelmajid Sabile et al. American Journal Of Pathology profile →

Peers

Malek Louha
Rajender Nandigama Germany
Ingeborg Fischer United States
Ruey‐Jen Lin Taiwan
Yasuyuki Fujita Japan
Lesang Shen China
Olga Ilina Netherlands
Milan G. Chheda United States
Jenny J. Hong United States
Shusaku Kurisu Japan
Jill Schartner United States
Rajender Nandigama Germany
Malek Louha
Citations per year, relative to Malek Louha Malek Louha (= 1×) peers Rajender Nandigama

Countries citing papers authored by Malek Louha

Since Specialization
Citations

This map shows the geographic impact of Malek Louha'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 Malek Louha with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Malek Louha more than expected).

Fields of papers citing papers by Malek Louha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Malek Louha. 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 Malek Louha. The network helps show where Malek Louha may publish in the future.

Co-authorship network of co-authors of Malek Louha

This figure shows the co-authorship network connecting the top 25 collaborators of Malek Louha. A scholar is included among the top collaborators of Malek Louha 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 Malek Louha. Malek Louha 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.
Bonnet, Crystel, et al.. (2018). Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa province. International Journal of Pediatric Otorhinolaryngology. 112. 1–5. 14 indexed citations
2.
Doummar, Diane, Fathi Moussa, Claudia Ravelli, et al.. (2018). Monoamine neurotransmitters and movement disorders in children and adults. Revue Neurologique. 174(9). 581–588. 17 indexed citations
3.
Takçı, Şahin, Deniz Anuk İnce, Malek Louha, et al.. (2017). A rare large mutation involving two exons of the SP-B gene in an infant with severe respiratory distress. The Turkish Journal of Pediatrics. 59(4). 483–486. 1 indexed citations
4.
Amat, Flore, Malek Louha, Marta Benet, et al.. (2017). The IL‐4 rs2070874 polymorphism may be associated with the severity of recurrent viral‐induced wheeze. Pediatric Pulmonology. 52(11). 1435–1442. 2 indexed citations
5.
Bonnet, Crystel, et al.. (2016). A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family. International Journal of Pediatric Otorhinolaryngology. 87. 28–33. 10 indexed citations
6.
Koht, Jeanette, et al.. (2016). Benign hereditary chorea, not only chorea: a family case presentation. PubMed. 3(1). 3–3. 9 indexed citations
7.
Bahloul, Amel, Jean‐Pierre Hardelin, Mohamed Makrelouf, et al.. (2016). Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome. PLoS ONE. 11(9). e0161893–e0161893. 17 indexed citations
8.
Bonnet, Crystel, Yosra Bouyacoub, Jean‐Pierre Hardelin, et al.. (2015). Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients. PLoS ONE. 10(3). e0120584–e0120584. 18 indexed citations
9.
Bonnet, Crystel, Malek Louha, Yosra Bouyacoub, et al.. (2014). Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness. PLoS ONE. 9(6). e99797–e99797. 21 indexed citations
10.
Bonnet, Crystel, Aïcha Bouaita, Andrea Lelli, et al.. (2014). EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness. Orphanet Journal of Rare Diseases. 9(1). 55–55. 41 indexed citations
11.
Hadchouel, Alice, Aurore Coulomb, Laureline Berteloot, et al.. (2014). Pulmonary alveolar proteinosis in children on La Réunion Island: a new inherited disorder?. Orphanet Journal of Rare Diseases. 9(1). 85–85. 28 indexed citations
12.
Marlin, Sandrine, Sandra Chantot‐Bastaraud, Albert David, et al.. (2013). Discovery of a Large Deletion of KAL1 in 2 Deaf Brothers. Otology & Neurotology. 34(9). 1590–1594. 8 indexed citations
13.
Deterding, Robin R., Megan K. Dishop, Rémy Couderc, et al.. (2013). Survival of an infant with homozygous surfactant protein C (SFTPC) mutation. Pediatric Pulmonology. 49(3). E112–5. 9 indexed citations
14.
Bonnet, Crystel, Malek Louha, Natalie Loundon, et al.. (2013). Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment. Gene. 527(2). 537–540. 19 indexed citations
15.
Jonard, Laurence, Sandrine Marlin, Malek Louha, et al.. (2011). Molecular diagnosis of genetic deafness. Clinical Biochemistry. 44(7). 510–511. 2 indexed citations
16.
Couderc, Rémy, Laurence Jonard, & Malek Louha. (2011). Next generation sequencing: The technology we need in pediatric laboratories?. Clinical Biochemistry. 44(7). 514–515. 3 indexed citations
17.
Vona, Giovanna, Abdelmajid Sabile, Malek Louha, et al.. (2000). Isolation by Size of Epithelial Tumor Cells. American Journal Of Pathology. 156(1). 57–63. 870 indexed citations breakdown →
18.
Louha, Malek, Jérôme Nicolet, Hervé Zylberberg, et al.. (1999). Liver Resection and Needle Liver Biopsy Cause Hematogenous Dissemination of Liver Cells. Hepatology. 29(3). 879–882. 66 indexed citations
19.
Sabile, Abdelmajid, Malek Louha, Eric Bonté, et al.. (1999). Efficiency of Ber-EP4 Antibody for Isolating Circulating Epithelial Tumor Cells Before RT-PCR Detection. American Journal of Clinical Pathology. 112(2). 171–178. 27 indexed citations
20.
Louha, Malek, Karine Poussin, H. Zylberberg, et al.. (1997). Spontaneous and iatrogenic spreading of liver-derived cells into peripheral blood of patients with primary liver cancer. Hepatology. 26(4). 998–1005. 68 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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