Maher Kharrat

987 citations
48 papers · 516 indexed · h-index 14

Impact in

  • Genetics top 10%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Hormonal and reproductive studies

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
    • BRCA gene mutations in cancer 5
    • Genomic variations and chromosomal abnormalities 4
    • Genetics and Neurodevelopmental Disorders 3

Maher Kharrat

44 papers receiving 500 citations

Peers

Maher Kharrat
Comparison fields: 5 of 77
  • Genetics 222
  • Endocrinology, Diabetes and Metabolism 107
  • Urology 29
  • Molecular Biology 287
  • Clinical Biochemistry 27
Replace Kristi L. Rupert with:
Kristi L. Rupert United States
Christopher Roy United States
Quentin B. Vincent France
Claudine Beauchamp Canada
Pierre‐Yves Le Pennec France
Qiusha Guo United States
Allison Dane Australia
Toshihiro Kishikawa Japan
Л. А. Лившиц Ukraine
Cushla McKinney New Zealand
Maher Kharrat relative to Kristi L. Rupert United States Kristi L. Rupert's profile →
Citations per field
00.5×4.8×
Kristi L. Rupert · 1×
Citations per year

Countries citing papers authored by Maher Kharrat

Since Specialization
Citations

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

Fields of papers citing papers by Maher Kharrat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Maher Kharrat, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Maher Kharrat Line = papers co-authored together Maher Kharrat links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20250
2 20251
3 20250
4 20242
5 20244
6 20231
7 20231
8 20221
9 20221
10 20213
11 202019
12 201927
13 20189
14 20155
15
Non-syndromic autosomal recessive mental retardation in Tunisian families : exclusion of GRIK2 and TUSC3 genes.
20112
16 201024
17 200918
18 20079
19 200474
20
Controlateral axillary nodal metastases of breast cancer
19983

About Maher Kharrat

Maher Kharrat is a scholar working on Genetics, Developmental Biology, Endocrinology, Diabetes and Metabolism, Molecular Biology and Cancer Research, having authored 48 papers that have together received 516 indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (9 papers), Hormonal and reproductive studies (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), BRCA gene mutations in cancer (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Phylogenetic Studies (3 papers), Fractal and DNA sequence analysis (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (222 citations), Endocrinology, Diabetes and Metabolism (107 citations), Urology (29 citations), Molecular Biology (287 citations) and Clinical Biochemistry (27 citations). Maher Kharrat has collaborated with scholars based in Tunisia, France and Germany. Frequent co-authors include Habiba Chaâbouni, Ridha Mrad, Faouzi Mâazoul, Lamia Ben Jemâa, Yves Morel, Véronique Tardy, Mohamed Irfan Mohamed Refai, Zied Lachiri, S Boubaker and Henda Triki. Their work appears in journals such as Diagnostic Molecular Pathology, L Encéphale, Clinical Genetics, Familial Cancer and Seminars in Arthritis and Rheumatism.

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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2026